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From hunting and foraging to clearing land for agriculture, humans modify forest biodiversity, landscapes, and climate. Forests constantly undergo disturbance–recovery dynamics and understanding them is a major objective of ecologists and conservationists. Chronosequences are a useful tool for understanding global restoration efforts. They represent a space-for-time substitution approach suited for the quantification of the resistance of ecosystem properties to withstand disturbance and the resilience of these properties until reaching pre-disturbance levels. Here we introduce a newly established chronosequence with 62 plots (50 ⍰ 50 m) in active cacao plantations and pastures, early and late regeneration, and mature old-growth forests, across a 200 km2 area in the extremely wet Chocó rainforest. Our chronosequence covers by far the largest total area of plots compared to others in the Neotropics. Plots ranged from 159–615 masl in a forested landscape with 74 ± 2.8 % forest cover within a 1-km radius including substantial old-growth forest cover. Land-use legacy and regeneration time were not confounded by elevation. We tested how six forest structure variables (maximum tree height and DBH, basal area, number of stems, vertical vegetation heterogeneity, and light availability), aboveground biomass (AGB), and rarefied tree species richness change along our chronosequence. Forest structure variables, AGB, and tree species richness increased with regeneration time and are predicted to reach similar levels to those in old-growth forests after ca. 30–116, 202, and 108 yrs, respectively. Compared to previous work in the Neotropics, old-growth forests in Canandé accumulate high AGB that takes one of the largest time spans reported until total recovery. Our chronosequence comprises one of the largest tree species pools, covers the largest total area of regenerating and old-growth forests, and has higher forest cover than other Neotropical chronosequences. Hence, our chronosequence can be used to determine the time for recovery and stability (resistance and resilience) of different taxa and ecosystem functions, including species interaction networks. This integrative effort will ultimately help to understand how one of the most diverse forests on the planet recovers from large-scale disturbances.
Two new species of Strandesia Stuhlmann, 1888 are described from the northeastern part of Thailand: S. karanovicae sp. nov. and S. amnatcharoenensis sp. nov. Strandesia karanovicae is characterized by a tumid carapace in dorsal view, a small anterior overlap, the absence of a dorso-subapical seta on the first segment of the antennule (A1), a large aesthetasc Y on the antenna, an α seta shape with a needle-like tip and a large β seta on the mandibular palp (Md-palp), serrated bristles on the maxilla, a long h1 seta on the second thoracopod (T2) and a slender caudal ramus (CR). Strandesia amnatcharoenensis has a small compressed posterior part of the right valves (RV) which makes it closely related to S. pholpunthini Savatenalinton, 2015. The new species can be distinguished primarily by a considerably small anterior overlap of the left valve over the right valve (RV), a postero-ventral flange of the RV, a remarkably large claw Ga of the CR and the chaetotaxy of the limbs, especially A1, Md-palp and T2. In addition, in the present study, the sexual population of S. martensi Savatenalinton, 2015 is recorded for the first time, and thus the first description of the male is provided here. Moreover, the morphological examination of both males and females revealed differences between asexual and sexual females and also points to the fact that S. martensi is a mixed reproduction species. This is the first record of the mixed reproductive mode in the genus Strandesia or even in the Cypricercinae.
A comprehensive checklist of Habenaria from Chapada dos Veadeiros, State of Goiás, was performed alongside morphologic and molecular phylogenetic studies, revealing three new taxa endemic to this region. A total of 61 taxa (59 species and two varieties) of Habenaria are recorded for Chapada dos Veadeiros, representing a two-fold increase compared to previous lists and comprising one of the greatest diversities of the genus in Brazil. Of this total, four taxa are locally endemic. Habenaria cultellifolia, until recently known only from the type collection, was rediscovered in the region after 127 years without records and represents this species’ only known extant population. Three proposed new taxa of Habenaria (H. minuticalcar J.A.N. Bat. & Bianch. sp. nov., H. proiteana J.A.N. Bat., A.A. Vale & Bianch. sp. nov., and H. lavrensis var. xanthodactyla J.A.N. Bat. & Bianch. var. nov.) are corroborated by molecular phylogenetic analyses based on nuclear and plastid markers. They are described, illustrated, tentatively assessed as threatened, and compared to phylogenetically and morphologically related species. Since some areas of this mountain range have not yet been floristically sampled, additional taxonomic novelties and new records are still expected in the future.
Description of three new Acanthocinini (Coleoptera: Cerambycidae: Lamiinae) species from Ecuador
(2023)
Three new species of Acanthocinini (Coleoptera: Cerambycidae: Lamiinae) are described from Napo province, Ecuador: Anisopodus micromaculatus new species; Parabaryssinus katerinae new species; and Paracleodoxus minutus new species. A key to species of Paracleodoxus Monné and Monné (2010) is provided.
ZooBank registration. urn:lsid:zoobank.org:pub:E7C66DA1-6F5F-4F94-922E-43E0B83331DD
This review covers Parageron Paramonov s. lat., including 36 species. Three new genera are proposed: Ectopusia gen. nov., Protypusia gen. nov. and Parusia gen. nov.; Parageron s. str. more narrowly defined. Eleven new species are described: Parageron longilingua sp. nov., Protypusia argentata gen. et sp. nov., Pro. separata Gibbs & Theodor gen. et sp. nov., Pro. flavipalpis gen. et sp. nov., Pro. kerkini gen. et sp. nov., Pro. strymonas gen. et sp. nov., Parusia almeria gen. et sp. nov., Pru. benoisti gen. et sp. nov., Pru. cyrenaica gen. et sp. nov., Pru. faesae gen. et sp. nov. and Pru. propinqua gen. et sp. nov. Two species raised from synonymy Par. orientalis Paramonov stat. rev. and Pru. taeniolata (Costa) stat. rev. Two species synonymised Pro. major Macquart syn. nov. and Usia arida Báez syn. nov. Eight species removed from Usiini to Apolysini, Apolysis bicolor (Efflatoun) comb. nov., A. elbae (Efflatoun) comb. nov., A. flavipes (Efflatoun) comb. nov., A. marginata (Brunetti) comb. nov., A. minuscula (Efflatoun) comb. nov., A. parvula (Efflatoun) comb. nov., A. turkmenica (Paramonov) comb. nov. and A. volkovitshi (Zaitzev) comb. nov. Apolysis melanderi Gibbs nom. nov. replaces A. bicolor (Melander) (was in Oligodranes) and A. hessei Gibbs nom. nov. replaces A. minuscula Hesse. Two neotypes and nine lectotypes are designated.
In this paper are presented notes on the primary types of some species of the oil-collecting bees of the genus Centris described by the European naturalists and entomologists Amédée Louis Michel Lepeletier de Saint-Fargeau, Anders Christian Jensen-Haarup, Arthur Louis Marie Joseph Vachal, Charles Émile Blanchard, Embrik Strand, Félix Édouard Guérin-Méneville, Guillaume-Antoine Olivier, Jean Guillaume Audinet-Serville, Jean Pérez, Johann Christoph Friedrich Klug, Johann Ludwig Christ, John Obadiah Westwood, Josef Anton Maximilian Perty, Jules Dominique, Karl Hermann Konrad Burmeister, Karl Wilhelm von Dalla Torre, Massimiliano Spinola, Peter Cameron, and Wilhelm Ferdinand Erichson. Information on the type status, type locality and depository are provided. In order to stabilize some names, lectotype designations were made for Centris rhodophthalma, C. sponsa var. asuncionis, C. transversa, Hemisia byssina and Ptilotopus americanus. Centris sponsa var. asuncionis is withdrawn from the synonymy of C. sponsa, revalidated and raised to species level. Centris byssina is proposed as nomen oblitum and as a new junior synonym of C. trigonoides, nomen protectum.
A new state record of Eucera (Xenoglossa) kansensis (Hymenoptera: Apidae) in South Dakota, USA
(2023)
Eucera (Xenoglossa) kansensis (Cockerell, 1905) (Hymenoptera: Apidae) is newly recorded for the state of South Dakota, USA. The bees were sampled predominantly with blue vane traps, and E. kansensis was associated with a wide range of habitats that did not include its primary floral resources of Cucurbita L. and Ipomoea L. Further study is warranted to determine the basis for the association of E. kansensis within the wide range of habitats in this study.
ZooBank registration. urn:lsid:zoobank.org:pub:4504A68E-8629-4CE7-996B-1D0EA793C944
An annotated catalogue of the type specimens of the family Cerambycidae Latreille, 1802 (Coleoptera) housed at the Zoological Museum of Hamburg (ZMH), Leibniz Institute for the Analysis of Biodiversity Change (LIB) is provided: one holotype and nine secondary types were found deposited at the ZHM. A list of the primary types lost during the bombardment in the Second World War is also provided, including types of 103 names, 14 of Cerambycinae, 87 of Lamiinae, and two of Prioninae. In addition, we report secondary types that have been found, corresponding to names of subspecific rank and unavailable names with infrasubspecific rank.
Analyses of whole genomic shotgun datasets, COI barcodes, morphology, and historical literature suggest that the following 13 butterfly species from the family Hesperiidae (Lepidoptera: Papilionoidea) in Texas, USA are distinct from their closest named relatives and therefore are described as new (type localities are given in parenthesis): Spicauda atelis Grishin, new species (Hidalgo Co., Mission), Urbanus (Urbanus) rickardi Grishin, new species (Hidalgo Co., nr. Madero), Urbanus (Urbanus) oplerorum Grishin, new species (Hidalgo Co., Mission/Madero), Telegonus tsongae Grishin, new species (Starr Co., Roma), Autochton caballo Grishin, new species (Hidalgo Co., 6 mi W of Hidalgo), Epargyreus fractigutta Grishin, new species (Hidalgo Co., McAllen), Aguna mcguirei Grishin, new species (Cameron Co., Brownsville), Polygonus pardus Grishin, new species (Hidalgo Co., McAllen), Arteurotia artistella Grishin, new species (Hidalgo Co., Mission), Heliopetes elonmuski Grishin, new species (Cameron Co., Boca Chica), Hesperia balcones Grishin, new species (Travis Co., Volente), Troyus fabulosus Grishin, new species (Hidalgo Co., Peñitas), and Lerema ochrius Grishin, new species (Hidalgo Co., nr. Relampago). Most of these species are known in the US almost exclusively from the Lower Rio Grande Valley in Texas. Nine of the holotypes were collected in 1971-1975, a banner period for butterfly species newly recorded from the Rio Grande Valley of Texas; five of them collected by William W. McGuire, and one by Nadine M. McGuire. At the time, these new species have been recorded under the names of their close relatives. A Neotype is designated for Papilio fulminator Sepp, [1841] (Suriname). Lectotypes are designated for Goniurus teleus Hübner, 1821 (unknown, likely in South America), Goniloba azul Reakirt, [1867] (Mexico: Veracruz) and Eudamus misitra Plötz, 1881 (Mexico). Several taxonomic changes are proposed. The following taxa are species (not subspecies): Spicauda zalanthus (Plötz, 1880), reinstated status (not Spicauda teleus (Hübner, 1821)), Telegonus fulminator (Sepp, [1841]), reinstated status (not Telegonus fulgerator (Walch, 1775), Telegonus misitra (Plötz, 1881), reinstated status (not Telegonus azul (Reakirt, [1867])), Autochton reducta (Mabille and Boullet, 1919), new status (not Autochton potrillo (Lucas, 1857)), Epargyreus gaumeri Godman and Salvin, 1893, reinstated status (not Epargyreus clavicornis (Herrich-Schäffer, 1869)), and Polygonus punctus E. Bell and W. Comstock, 1948, new status (not Polygonus savigny (Latreille, [1824])). Urbanus ehakernae Burns, 2014 and Epargyreus socus chota Evans, 1952 are junior subjective synonyms of Urbanus alva Evans, 1952 and Epargyreus clavicornis (Herrich-Schäffer, 1869), respectively, and Epargyreus gaumeri tenda Evans, 1955, new combination is not a subspecies of E. clavicornis.
ZooBank registration. https://zoobank.org/D5462F9E-E08D-46C6-898D-76EE7466DD19
Abstract. More than 1300 specimens of Eucnemidae collected from Heredia Province in Costa Rica during the 1990s Arthropods of La Selva (ALAS) survey were studied from 2018 through 2022. One new genus of false click beetle, Absensiugum Otto, Muona and Córdoba-Alfaro, is described. Nematodes teres Horn, from the Nearctic and Caribbean regions, is transferred to this new genus to form Absensiugum teres, new combination. Sixteen new species of false click beetle (Coleoptera: Eucnemidae) are described from Costa Rica. These new species are: Adelothyreus brevis, Adelothyreus costaricensis, Adelothyreus totus, Quirsfeldia stethonoides, Lacus pectinatus, Maelodrus costaricensis, Onichodon confluentus, Onichodon rufus, Isarthrus striatus, Absensiugum brunneum, Dromaeolus americanus, Dromaeolus brunneus, Dromaeolus herediensis, Dromaeolus holdridgei, Deltometopus bicolor and Nematodes apicalis. Three additional records outside of the Heredia Province from the Osa Peninsula and Panama for Lacus pectinatus are included in this study. Identification keys are provided for species of Adelothyreus Chevrolat, Onichodon Newman, Dromaeolus Kiesenwetter, Deltometopus Bonvouloir and Nematodes Berthold in Costa Rica. Diagnostic differences are briefly noted for each species within the Neotropical region. A list of Eucnemidae from Heredia Province is provided.
ZooBank registration. urn:lsid:zoobank.org:pub:C1D5B819-A964-4679-B090-84CDBBC59D6A
A century and a half since the time of Hewitson, we are experiencing a renaissance in species discovery fueled by whole genome sequencing. A large-scale genomic analysis of Hesperiidae Latreille, 1809 (Lepidoptera), including primary type specimens, reveals a deluge of species new to science. One hundred of them (one in a new genus) are described here from the New World (type localities are given in parenthesis): Drephalys (Drephalys) diovalis Grishin, new species (Ecuador: Napo), Euriphellus panador Grishin, new species (Ecuador: Esmeraldas), Euriphellus panamicus Grishin, new species (Panama: Panama), Cecropterus (Thorybes) viridissimus Grishin, new species (Ecuador: Zamora-Chinchipe), Cecropterus (Murgaria) dariensis Grishin, new species (Panama: Darien), Urbanus (Urbanus) mericuti Grishin, new species (Ecuador: Napo), Telegonus (Telegonus) pastus Grishin, new species (Panama: Panama), Autochton (Autochton) dora Grishin, new species (Ecuador: Pastaza), Astraptes centralis Grishin, new species (Panama: Colón), Aguna claxonica Grishin, new species (Ecuador: Napo), Aguna esmeralda Grishin, new species (Ecuador: Esmeraldas), Aguna lata Grishin, new species (Guyana), Ridens angulinea Grishin, new species (Peru: Cuzco), Pythonides lera Grishin, new species (Peru: Cuzco), Pythonides latemarginatus Grishin, new species (Panama: Panama), Gindanes variegatus Grishin, new species (Brazil: Mato Grosso), Milanion (Milanion) virga Grishin, new species (Brazil: Rondônia), Milanion (Milanion) furvus Grishin, new species (Panama: Panama), Milanion (Milanion) laricus Grishin, new species (Ecuador: Napo), Charidia ronda Grishin, new species (Brazil: Rondônia), Pseudodrephalys tinas Grishin, new species (Peru: Loreto), Pseudodrephalys argus Grishin, new species (Suriname: Para), Achlyodes calvus Grishin, new species (Brazil: Santa Catarina), Spioniades artemis Grishin, new species (Panama: Panama), Spioniades artemidoides Grishin, new species (Brazil: Santa Catarina), Myrinia orieca Grishin, new species (Ecuador: Orellana), Myrinia aragua Grishin, new species (Venezuela: Aragua), Myrinia maculosa Grishin, new species (Guatemala), Myrinia manchada Grishin, new species (Guyana), Polyctor (Fenops) lamperus Grishin, new species (Panama: Darien), Nisoniades (Nisoniades) lutum Grishin, new species (Mexico: Guerrero. ), Bolla (Stolla) vena Grishin, new species (Venezuela: Aragua), Staphylus (Vulga) vula Grishin, new species (Mexico: Veracruz), Staphylus (Vulga) vulga Grishin, new species (Panama: Darien), Staphylus (Staphylus) rotundalus Grishin, new species (Ecuador: Napo), Staphylus (Staphylus) yucatanus Grishin, new species (Mexico: Quintana Roo/Yucatan), Heliopetes (Heliopetes) lana Grishin, new species (Guatemala), Canesia ella Grishin, new species (Venezuela: Barinas), Paches (Paches) loxeca Grishin, new species (Ecuador: Morona-Santiago), Clito congruens Grishin, new species (Panama: Colón), Cycloglypha corax Grishin, new species (Brazil: Rio de Janeiro), Festivia peruvia Grishin, new species (Peru: Huánuco), Decinea notata Grishin, new species (Ecuador: Napo), Pompeius fuscus Grishin, new species (Brazil: Minas Gerais), Vernia clara Grishin, new species (Panama: Chiriquí), Oligoria (Oligoria) obtena Grishin, new species (Ecuador: Napo), Thespieus mandal Grishin, new species (Brazil: Rio de Janeiro), Psoralis (Saniba) magnamacus Grishin, new species (Panama: Darien), Alychna ayonis Grishin, new species (Ecuador: Napo), Wahydra banios Grishin, new species (Ecuador: Tungurahua), Wahydra cuzcona Grishin, new species (Peru: Cuzco), Cynea (Cynea) aureofimbra Grishin, new species (Ecuador), Cynea (Nycea) quada Grishin, new species (Ecuador: Napo), Cynea (Quinta) achirae Grishin, new species (Mexico: Tamaulipas), Eutus amazonicus Grishin, new species (Peru: Madre de Dios), Eutus incus Grishin, new species (Peru: Cuzco), Eutus septemaculatus Grishin, new species (Brazil: Mato Grosso), Godmia viridicapita Grishin, new species (Ecuador: Napo), Rhomba pulla Grishin, new species (Peru: Cuzco), Niconiades victoria Grishin, new species (Mexico: Tamaulipas), Lancephallus purpurus Grishin, new genus and new species (Guyana), Mnasicles (Remella) ecua Grishin, new species (Ecuador: Pichincha), Amblyscirtes (Amblyscirtes) aeratus Grishin, new species (Mexico: Oaxaca), Amblyscirtes (Mastor) chrysoplea Grishin, new species (Mexico: Oaxaca), Amblyscirtes (Mastor) chrysomisa Grishin, new species (Mexico: Chiapas), Amblyscirtes (Flor) meridus Grishin, new species (Mexico: Veracruz), Rectava chiriquensis Grishin, new species (Panama: Chiriquí), Cobalopsis adictys Grishin, new species (Panama: Veraguas), Cymaenes melaporphyrus Grishin, new species (Mexico: San Luis Potosí), Lerema (Morys) ecuadorica Grishin, new species (Ecuador: Pichincha), Saturnus obscurior Grishin, new species (Panama: Darien), Cantha zoirodicta Grishin, new species (Peru: Madre de Dios), Cantha meiodicta Grishin, new species (Peru: Madre de Dios), Phlebodes duplex Grishin, new species (Guatemala: Cayuga), Lychnuchus (Enosis) valle Grishin, new species (Colombia: Valle), Eutychide ochoides Grishin, new species (Peru: Cuzco), Dion bora Grishin, new species (Panama: Darien), Dion occida Grishin, new species (Peru: Madre de Dios), Eprius (Eprius) veledinus Grishin, new species (Ecuador: Pichincha), Radiatus panamensis Grishin, new species (Panama: Panama), Pheraeus pulcher Grishin, new species (Peru: Madre de Dios), Callimormus rades Grishin, new species (Panama: Panama), Gubrus lubens Grishin, new species (Ecuador: Loja), Ludens labens Grishin, new species (Panama: Darien), Rigga isa Grishin, new species (Ecuador: Napo), Flaccilla lactea Grishin, new species (Peru: Cuzco), Falga athena Grishin, new species (Panama: Darien), Panoquina jay Grishin, new species (Peru: Loreto), Calpodes salianus Grishin, new species (Peru: Madre de Dios), Calpodes stingo Grishin, new species (Ecuador: Sucumbíos), Aides nobra Grishin, new species (Panama: Colón), Thracides pavo Grishin, new species (Mexico: Tabasco), Talides eluta Grishin, new species (Peru: Cuzco), Talides laeta Grishin, new species (Peru: Cuzco), Neoxeniades angustior Grishin, new species (Brazil: Rio de Janeiro), Damas zea Grishin, new species (Guyana), Tromba xantha Grishin, new species (Mexico: Veracruz), Perichares fura Grishin, new species (Ecuador: Pichincha), Carystoides (Balma) goliath Grishin, new species (Colombia: Valle), and Agathymus galeana Grishin, new species (Mexico: Nuevo Leon). Additionally, we present evidence to support 22 taxa as species (not subspecies or synonyms) and synonymize one genus and four species. Namely, the following taxa are species: Milanion pilta Evans, 1953 (not Milanion pilumnus Mabille and Boullet, 1917), Milanion latior Mabille and Boullet, 1917 (not a synonym of Milanion marciana Godman and Salvin, 1895), Charidia pilea Evans, 1953, and Charidia pocus Evans, 1953 (not Charidia lucaria (Hewitson, 1868)), Paches (Paches) gloriosus Röber, 1925 and Paches (Paches) loxana Evans, 1953 (not Paches (Paches) loxus (Westwood, 1852)), Spioniades anta Evans, 1953 (not Spioniades abbreviata (Mabille, 1888)), Decinea onasima (Hewitson, 1877) and Decinea formosus (Hayward, 1940) (not Decinea dama (Herrich-Schäffer, 1869)), Thespieus guerreronis (Dyar, 1913) (not Thespieus dalman (Latreille, [1824])), Cynea (Nycea) erebina (Möschler, 1879) and Cynea (Nycea) cleochares (Mabille, 1891) (not Cynea (Cynea) diluta (Herrich-Schäffer, 1869)), Amblyscirtes (Mastor) repta Evans, 1955 (not Amblyscirtes (Flor) florus (Godman, 1900)), Saturnus tiberius (Möschler, 1883), Saturnus conspicuus (E. Bell, 1941), Saturnus meton (Mabille, 1891), and Saturnus obscurus (E. Bell, 1941) (not Saturnus reticulata (Plötz, 1883)), Phlebodes sifax Evans, 1955 (not Phlebodes campo (E. Bell, 1947)), Eutychide ochus Godman, 1900 and Eutychide rogersi (Kaye, 1914) (not a subspecies and a synonym, respectively, of Eutychide subcordata (Herrich-Schäffer, 1869)), Falga mirabilis Evans, 1955, Falga jacta Evans, 1955, and Falga ombra Evans, 1955 (not Falga jeconia (A. Butler, 1870)); and the following taxa are junior subjective synonyms: Libra Evans, 1955 (of Phemiades Hübner, [1819]), Papilio clito Fabricius, 1787 of Milanion hemes hemes (Cramer, 1777), Pamphila hycsos Mabille, 1891 of Cynea (Nycea) erebina (Möschler, 1879), Hesperia olympia Plötz, 1882 of Eutychide subcordata (Herrich-Schäffer, 1869), and Hesperia ocrinus Plötz, 1882 of Aides aegita (Hewitson, 1866). Furthermore, we propose new combinations for genus-species: Lychnuchus (Enosis) ponka (Evans, 1955) (not Thoon Godman, 1900), and species-subspecies: Charidia pocus mayo Evans, 1953 (not Charidia lucaria (Hewitson, 1868)), Decinea onasima boliviensis (E. Bell, 1930) (not Decinea dama (Herrich-Schäffer, 1869)), Cynea (Nycea) erebina somba Evans, 1955 (not Pamphila hycsos Mabille, 1891), Saturnus tiberius suffuscus (Hayward, 1940) (not Saturnus reticulata (Plötz, 1883)), and Falga mirabilis odol Evans, 1955 (not Falga jeconia (A. Butler, 1870)). Then, Milanion pilumnus var. hemestinus Mabille and Boullet, 1917 is a junior subjective synonym of Milanion pilumnus pilumnus Mabille and Boullet, 1917, not of Milanion leucaspis (Mabille, 1878). Lectotypes are designated for nine taxa (names in original combinations below): Pellicia bromias Godman and Salvin, 1894 (Mexico: Veracruz, Atoyac), Nisoniades perforata Möschler, 1879 (Colombia), Helias ascalaphus Staudinger, 1876 (central Panama), Pamphila hycsos Mabille, 1891 (Colombia), Amblyscirtes fluonia Godman, 1900 (Mexico: Guerrero, Xocomanatlan), Mastor anubis Godman, 1900 (Mexico: Guerrero, Omiltemi), Eutychide ochus Godman, 1900 (Mexico: Veracruz, Atoyac), Cobalus subcordata Herrich-Schäffer, 1869 (Southeast Brazil), and Thracides xanthura Godman, 1901 (Panama: Chiriquí Province, Bugaba). A neotype is designated for Eudamus briccius Plötz, 1881 (Guyana: Iwokrama Forest).
ZooBank registration. urn:lsid:zoobank.org:pub:ACDF923B-906D-460E-9707-259E0ECDBCA8
Genomic analysis of Pyrginae Burmeister, 1878 (Lepidoptera: Hesperiidae Latreille, 1809) with an emphasis on the tribes Achlyodini Burmeister, 1878 and Carcharodini Verity, 1940 reveals many inconsistencies between the resulting phylogeny and the current classification. These problems are corrected by proposing new taxa, changing the ranks of others, or synonymizing them, and transferring species between genera. As a result, five subtribes, one genus, 20 subgenera, and one species are proposed as new: Cyclosemiina Grishin, new subtribe (type genus Cyclosemia Mabille, 1878), Ilianina Grishin, new subtribe (type genus Iliana E. Bell, 1937), Nisoniadina Grishin, new subtribe (type genus Nisoniades Hübner, [1819]), Burcina Grishin, new subtribe (type genus Burca E. Bell and W. Comstock, 1948), and Pholisorina Grishin, new subtribe (type genus Pholisora Scudder, 1872), all in Carcharodini; Lirra Grishin, new genus (type species Leucochitonea limaea Hewitson, 1868) in Pythonidina Grishin, 2019; Trifa Grishin, new subgenus (type species Tagiades jacobus Plötz, 1884), Tuberna Grishin, new subgenus (type species Pythonides contubernalis Mabille, 1883), Ebona Grishin, new subgenus (type species Quadrus eboneus E. Bell, 1947), Noctis Grishin, new subgenus (type species Achlyodes accedens Mabille, 1895), and Cyrna Grishin, new subgenus (type species Achlyodes cyrna Mabille, 1895) of Quadrus Lindsey, 1925; Liddia Grishin, new subgenus (type species Helias pallida R. Felder, 1869), Minna Grishin, new subgenus (type species Achlyodes minna Evans, 1953), and Thilla Grishin, new subgenus (type species Eurypterus later Mabille, 1891) of Eantis Boisduval, 1836; Torgus Grishin, new subgenus (type species Ouleus gorgus E. Bell, 1937) of Iliana E. Bell, 1937; Fenops Grishin, new subgenus (type species Cabares enops Godman and Salvin, 1894) of Polyctor Evans, 1953; Bezus Grishin, new subgenus (type species Pellicia bessus Möschler, 1877) and Macarius Grishin, new subgenus (type species Pellicia macarius Herrich-Schäffer, 1870) of Nisoniades Hübner, [1819]; Quadralis Grishin, new subgenus (type species Pterygospidea extensa Mabille, 1891) of Gorgopas Godman and Salvin, 1894; Menuda Grishin, new subgenus (type species Nisoniades menuda Weeks, 1902) and Narycus Grishin, new subgenus (type species Pythonides narycus Mabille, 1889) of Perus Grishin, 2019; Bovaria Grishin, new subgenus (type species Achlyodes cyclops Mabille, 1876), Sebia Grishin, new subgenus (type species Nisoniades eusebius Plötz, 1884), and Stolla Grishin, new subgenus (type species Pholisora balsa E. Bell, 1937) of Bolla Mabille, 1903; Vulga Grishin, new subgenus (type species Achlyodes vulgata Möschler, 1879) and Capilla Grishin, new subgenus (type species Helias aurocapilla Staudinger, 1876, currently a junior subjective synonym of Hesperia musculus Burmeister, 1875) of Staphylus Godman and Salvin, 1896; and Quadrus (Zera) vivax Grishin, new species (type locality in Brazil: Rio de Janeiro). The following 10 are subgenera, not genera or synonyms: Ouleus Lindsey, 1925 and Zera Evans, 1953 of Quadrus Lindsey, 1925; Atarnes Godman and Salvin, 1897 and Eburuncus Grishin, 2012 of Milanion Godman and Salvin, 1895; Pachyneuria Mabille, 1888 and Austinus O. Mielke and Casagrande, 2016 of Sophista Plötz, 1879; Hemipteris Mabille, 1889 and Mictris Evans, 1955 of Pellicia Herrich-Schäffer, 1870; and Hesperopsis Dyar, 1905 and Scantilla Godman and Salvin, 1896 of Staphylus Godman and Salvin, 1896. The following 7 are species, not subspecies: Quadrus (Ebona) cristatus (Steinhauser, 1989) (not Quadrus (Ebona) negrus (Nicolay, 1980)), Quadrus (Quadrus) ophia (A. Butler, 1870) (not Quadrus (Quadrus) lugubris (R. Felder, 1869)), Quadrus (Zera) gellius (Mabille, 1903) and Quadrus (Zera) servius (Plötz, 1884) (not Quadrus (Zera) hyacinthinus (Mabille, 1877)), Mimia pazana Evans,1953 (not Mimia phidyle (Godman and Salvin, 1894)), Polyctor (Polyctor) dagua Evans, 1953 (not Polyctor (Polyctor) polyctor (Prittwitz, 1868)), and Staphylus (Vulga) satrap Evans, 1953 (not Staphylus (Vulga) saxos Evans, 1953); and these 8 are species, not synonyms: Quadrus (Zera) menedemus (Godman and Salvin, 1894) (not Quadrus (Zera) tetrastigma (Sepp, [1847])), Pellicia (Pellicia) bilinea Mabille, 1889 (not Pellicia (Pellicia) dimidiata Herrich-Schäffer, 1870), Pellicia (Hemipteris) nema Williams and Bell, 1939 (not Pellicia (Pellicia) theon Plötz, 1882), Bolla (Bovaria) sodalis Schaus, 1913 (not Bolla (Bolla) imbras (Godman and Salvin, 1896)), Bolla (Bovaria) aplica (E. Bell, 1937) (not Bolla (Sebia) eusebius (Plötz, 1884)), Bolla (Sebia) chilpancingo (E. Bell, 1937) (not Bolla (Bolla) subapicatus (Schaus, 1902)), and Bolla (Stolla) madrea (R. Williams and E. Bell, 1940) and Bolla (Stolla) hazelae (Hayward, 1940) (not Bolla (Stolla) zorilla (Plötz, 1886)). The following 2 are junior subjective synonyms: Achlyodes erisichthon Plötz, 1884 of Quadrus (Zera) servius (Plötz, 1884) (not a subspecies of Quadrus (Zera) tetrastigma (Sepp, [1847]) and Staphylus subapicatus Schaus, 1902 of Bolla (Bolla) imbras (Godman and Salvin, 1896). Furthermore, we propose the following additional new genus-species combination: Gindanes homer (Evans, 1953), Gindanes nides (O. Mielke and Casagrande, 2002), Gindanes maraca (O. Mielke and Casagrande, 1992), Gindanes jenmorrisae (Shuey and Ramírez. 2022), Gindanes tullia (Evans, 1953), Gindanes herennius (Geyer, [1838]), Gindanes proxenus (Godman and Salvin, 1895), Gindanes parallelus (Mabille, 1898), Gindanes braga (Evans, 1953), Gindanes hampa (Evans, 1953), Gindanes rosa (Steinhauser, 1989), Gindanes neivai (Hayward, 1940), Gindanes mundo (H. Freeman, 1979), Gindanes eminus (E. Bell, 1934), Quadrus (Trifa) francesius Freeman, 1969, Quadrus (Trifa) ineptus (Draudt, 1922), Quadrus (Trifa) jacobus (Plötz, 1884), Quadrus (Tuberna) lancea (Hewitson, 1868), Quadrus (Ebona) pescada (E. Bell, 1956), Lirra pteras (Godman and Salvin, 1895), and Lirra limaea (Hewitson, 1868) (not Pythonides Hübner, 1819); Quadrus (Cyrna) zora (Evans, 1953) (not Bolla Mabille, 1903); Eantis later (Mabille, 1891) and Eantis haber (Mabille, 1891) (not Aethilla Hewitson, 1868); Iliana (Torgus) gorgus (E. Bell, 1937) and Iliana (Torgus) taurus (Evans, 1953) (not Eantis Boisduval, 1836); Bolla (Stolla) evemerus (Godman and Salvin, 1896), Bolla (Stolla) chlora (Evans, 1953), Bolla (Stolla) astra (R. Williams and E. Bell, 1940), Bolla (Stolla) balsa (E. Bell, 1937), Bolla (Stolla) tridentis (Steinhauser, 1989), Bolla (Stolla) esmeraldus (L. Miller, 1966), Bolla (Stolla) chlorocephala (Latreille, [1824]), and Bolla (Stolla) incanus (E. Bell, 1932) (not Staphylus Godman and Salvin, 1896). Finally, lectotypes are designated for Achlyodes servius Plötz, 1884 (type locality in Brazil: Rio de Janeiro), Pellicia theon Plötz, 1882 (type locality in South America), and Nisoniades eusebius Plötz, 1884 (type locality in Central America). Unless stated otherwise, all subgenera, species, subspecies, and synonyms of mentioned genera and species are transferred with their parent taxa, and others remain as previously classified.
ZooBank registration. http://zoobank.org/B9AFA1A9-8664-4F31-B4D9-ACF7780C7CC6
New and notable stomatopods are reported on and added to the Mozambican faunal list, based principally on material housed in the collections of the Iziko South African Museum. Seven species are reported for the first time from Mozambican waters including one undescribed species of Clorida Eydoux & Souleyet, 1842, bringing the total known Mozambican stomatopod fauna to 22 species, comprising 17 genera and eight families. The known fauna is tabulated and taxonomic accounts of eight species are given, seven of these representing the new species records including one undescribed species, while the eighth species account is of the previously poorly documented Erugosquilla woodmasoni (Kemp, 1911), which is reported on from unpublished material. The new record of Manningia australiensis Manning, 1970 represents the first record of the family Eurysquillidae from southern Africa.
The article presents a potentially obligate association of a pleustid amphipod of the genus Pleusymtes (Crustacea: Amphipoda: Pleustidae) with the large sea anemone Urticina eques (Gosse, 1858) (Anthozoa: Actiniaria: Actiniidae) from shallow waters of the Barents Sea. The new species shows a conspicuously striped (disruptive or aposematic) colouration, unlike other Arctic species of the genus, which shows a potential for its permanent connection with anemones. It is possible that this is the first known possibly obligatory anemone-associated species, within the genus and the family Pleustidae. The article discusses the taxonomy, morphological differences from congeners and ecological features of the new species, as well as the known symbiotic associations of sea anemones (as hosts) in Arctic and sub-Arctic waters.
The Chapada dos Veadeiros National Park is a conservation unit established to preserve the highest savannahs of Central Brazil and their unique biodiversity. Eriocaulaceae are a relevant and conspicuous family in such high savannahs, but its diversity is poorly known, documented solely in general lists or in isolated efforts aimed at small groups. After a structured series of field expeditions and analysis of specimens from the relevant herbaria, we provide nomenclatural novelties, a first identification key, and an illustrated checklist for the species of Paepalanthoideae (Eriocaulaceae) in the area. We recorded 42 species of Paepalanthoideae from the Chapada dos Veadeiros National Park: Actinocephalus (Körn.) Sano (2 spp.), Comanthera L.B.Sm. (1 sp.), Paepalanthus Mart. (24 spp.), and Syngonanthus Ruhland (15 spp.). Actinocephalus brevifolius Trovó & Echtern. sp. nov. and P. irwinii Trovó & Echtern. sp. nov. are newly described species and P. politus Trovó stat. et nom. nov. is a variety of P. elongatus (Bong.) Körn. raised to the species status with a new name. The generic and specific composition shows predominance of Paepalanthus and Syngonanthus, and with a low representation of Actinocephalus and Comanthera, as expected, outside of the Espinhaço Range. More than 50% of the species (22 spp.) are endemic to the area and 25 species are endemic to Central Brazil, the area being the main center of diversity for dimerous-flowered groups. The non-endemic diversity is a combination of widespread species and marginal distribution of species typical from the Amazon and southeastern savannahs. The species are unevenly distributed in the area, with their occurrence correlated to altitude, water availability, and lithology. We reinforce that the savannahs from Central Brazil are a secondary center of diversity for Eriocaulaceae, playing a central role in the conservation of an unique and irreplaceable piece of its diversity and the Cerrado biome as well.
Our expanded efforts in genomic sequencing to cover additional skipper butterfly (Lepidoptera: Hesperiidae) species and populations, including primary type specimens, call for taxonomic changes to restore monophyly and correct misidentifications by moving taxa between genera and proposing new names. Reconciliation between phenotypic characters and genomic trees suggests three new tribes, two new subtribes, 23 new genera, 17 new subgenera and 10 new species that are proposed here: Psolosini Grishin, new tribe (type genus Psolos Staudinger, 1889), Ismini Grishin, new tribe (type genus Isma Distant, 1886), Eetionini Grishin, new tribe (type genus Eetion de Nicéville, 1895), Orphina Grishin, new subtribe (type genus Orphe Godman, 1901), Carystoidina Grishin, new subtribe (type genus Carystoides Godman, 1901), Fulvatis Grishin, new genus (type species Telegonus fulvius Plötz, 1882), Adina Grishin, new genus (type species Nascus adrastor Mabille and Boullet, 1912), Ornilius Grishin, new genus (type species Ornilius rotundus Grishin, new species), Tolius Grishin, new genus (type species Antigonus tolimus Plötz, 1884), Lennia Grishin, new genus (type species Leona lena Evans, 1937), Trida Grishin, new genus (type species Cyclopides barberae Trimen, 1873), Noxys Grishin, new genus (type species Oxynthes viricuculla Hayward, 1951), Gracilata Grishin, new genus (type species Enosis quadrinotata Mabille, 1889), Hermio Grishin, new genus (type species Falga ? hermione Schaus, 1913), Eutus Grishin, new genus (type species Cobalus rastaca Schaus, 1902), Gufa Grishin, new genus (type species Phlebodes gulala Schaus, 1902), Godmia Grishin, new genus (type species Euroto chlorocephala Godman, 1900), Rhomba Grishin, new genus (type species Eutychide gertschi Bell, 1937), Rectava Grishin, new genus (type species Megistias ignarus Bell, 1932), Contrastia Grishin, new genus (type species Hesperia distigma Plötz, 1882), Mit Grishin, new genus (type species Mnasitheus badius Bell, 1930), Picova Grishin, new genus (type species Vorates steinbachi Bell, 1930), Lattus Grishin, new genus (type species Eutocus arabupuana Bell, 1932), Gubrus Grishin, new genus (type species Vehilius lugubris Lindsey, 1925), Koria Grishin, new genus (type species Hesperia kora Hewitson, 1877), Corta Grishin, new genus (type species Eutychide lycortas Godman, 1900), Calvetta Grishin, new genus (type species Hesperia calvina Hewitson, 1866), Oz Grishin, new genus (type species Astictopterus ozias Hewitson, 1878), Praxa Grishin, new subgenus (type species Nascus prax Evans, 1952), Bron Grishin, new subgenus (type species Papilio broteas Cramer, 1780), Turis Grishin, new subgenus (type species Pyrgus 1955, and Synale Mabille, 1904 of Carystus Hübner, [1819]. The following 20 genera are treated as junior subjective synonyms: Leucochitonea Wallengren, 1857 of Abantis Hopffer, 1855; Sapaea Plötz, 1879 and Netrobalane Mabille, 1903 of Caprona Wallengren, 1857; Parasovia Devyatkin, 1996 of Sebastonyma Watson, 1893; Pemara Eliot, 1978 of Oerane Elwes and Edwards, 1897; Ankola Evans, 1937 of Pardaleodes Butler, 1870; Arotis Mabille, 1904 of Mnaseas Godman, 1901; Chalcone Evans, 1955, Hansa Evans, 1955, and Propertius Evans, 1955 of Metrocles Godman, 1900; Jongiana O. Mielke and Casagrande, 2002 of Cobaloides Hayward, 1939; Pamba Evans, 1955 of Psoralis Mabille, 1904; Brownus Grishin, 2019 of Styriodes Schaus, 1913; Mnasilus Godman, 1900 of Papias Godman, 1900; Sucova Evans, 1955 of Mnasitheus Godman, 1900; Pyrrhocalles Mabille, 1904 and Asbolis Mabille, 1904 of Choranthus Scudder, 1872; Miltomiges Mabille, 1903 of Methionopsis Godman, 1901; Sacrator Evans, 1955 of Thracides Hübner, [1819]; and Lychnuchoides Godman, 1901 of Perichares Scudder, 1872. Arunena Swinhoe, 1919 is a junior subjective synonym of Stimula de Nicéville, 1898 (not of Koruthaialos Watson, 1893). The following 27 names are species-level taxa (some in new combinations) reinstated from synonymy: Salantoia gildo (Mabille, 1888) (not Salatis cebrenus (Cramer, 1777)), Bungalotis corentinus (Plötz, 1882) (not Bungalotis midas (Cramer, 1775)), Telegonus cretellus (Herrich-Schäffer, 1869) (not Telegonus cassander (Fabricius, 1793)), Santa palica (Mabille, 1888) (not Chiothion asychis (Stoll, 1780)), Camptopleura cincta Mabille and Boullet, 1917 (not Camptopleura auxo (Möschler, 1879)), Camptopleura orsus (Mabille, 1889) (not Nisoniades mimas (Cramer, 1775)), Metron voranus (Mabille, 1891) and Metron fasciata (Möschler, 1877) (not Metron zimra (Hewitson, 1877)), Limochores catahorma (Dyar, 1916) (not Limochores pupillus (Plötz, 1882)), Pares viridiceps (Mabille, 1889) (not Thoon modius (Mabille, 1889)), Tigasis wellingi (Freeman, 1969) (not Tigasis arita (Schaus, 1902)), Rectava sobrinus (Schaus, 1902) (not Papias phainis Godman, 1900), Nastra subsordida (Mabille, 1891) (not Adlerodea asema (Mabille, 1891), previously in Eutychide Godman, 1900), Lerema pattenii Scudder, 1872 (not Lerema accius (J. E. Smith, 1797)), Lerema (Morys) ancus (Möschler, 1879) (not Cymaenes tripunctus theogenis (Capronnier, 1874)), Cobalopsis zetus (Bell, 1942) (not Cobalopsis nero (Herrich-Schäffer, 1869)), Lerema (Geia) etelka (Schaus, 1902) (not Lerema (Geia) geisa (Möschler, 1879), previously in Morys Godman, 1900), Cymaenes isus (Godman, 1900) (not Cymaenes trebius (Mabille, 1891)), Vehilius labdacus (Godman, 1900) (not Vehilius inca (Scudder, 1872)), Papias amyrna (Mabille, 1891) (not Papias allubita (Butler, 1877), previously in Mnasilus Godman, 1900), Papias integra (Mabille, 1891) (not Papias subcostulata (Herrich-Schäffer, 1870)), Metiscus atheas Godman, 1900 (not Hesperia achelous Plötz, 1882), Dion agassus (Mabille, 1891) (not Dion uza (Hewitson, 1877), previously in Enosis Mabille, 1889), Picova incompta (Hayward, 1942) (not Lerema (Morys) micythus (Godman, 1900), previously in Morys Godman, 1900), Lucida melitaea (Draudt, 1923) (not Lucida lucia (Capronnier, 1874)), Methionopsis modestus Godman, 1901 (not Methionopsis ina (Plötz, 1882)), and Thargella (Volus) volasus (Godman, 1901) (not Eutocus facilis (Plötz, 1884)). The following 57 taxa are elevated from subspecies to species, new status (some in new combinations): Dyscophellus doriscus (Hewitson, 1867) (not Dyscophellus porcius (C. Felder and R. Felder, 1862), Phocides vida (A. Butler, 1872) (not Phocides urania (Westwood, 1852)), Tagiades (Daimio) ceylonica Evans, 1932 (not Tagiades litigiosa Möschler, 1878), Tagiades (Daimio) tubulus Fruhstorfer, 1910 (not Tagiades sambavana Elwes and Edwards, 1897), Tagiades (Daimio) kina Evans, 1934, Tagiades (Daimio) sheba Evans, 1934, Tagiades (Daimio) martinus Plötz, 1884, Tagiades (Daimio) sem Mabille, 1883, and Tagiades (Daimio) neira Plötz, 1885 (not Tagiades trebellius (Hopffer, 1874)), Tagiades (Daimio) korela Mabille, 1891 and Tagiades (Daimio) presbyter Butler, 1882 (not Tagiades nestus (C. Felder, 1860)), Tagiades obscurus Mabille, 1876, Tagiades ravi (Moore, [1866]), Tagiades atticus (Fabricius, 1793), Tagiades titus Plötz, 1884, Tagiades janetta Butler, 1870, Tagiades inconspicua Rothschild, 1915, and Tagiades hovia Swinhoe, 1904 (not Tagiades japetus (Stoll, [1781])), Tagiades silvia Evans, 1934 and Tagiades elegans Mabille, 1877 (not Tagiades gana (Moore, [1866])), Tapena bornea Evans, 1941 and Tapena minuscula Elwes and Edwards, 1897 (not Tapena thwaitesi Moore, [1881]), Darpa dealbata (Distant, 1886) (not Darpa pteria (Hewitson, 1868)), Perus manx (Evans, 1953) (not Perus minor (Schaus, 1902)), Canesia pallida (Röber, 1925) (not Carrhenes canescens (R. Felder, 1869)), Carrhenes conia Evans, 1953 (not Carrhenes fuscescens (Mabille, 1891)), Anisochoria extincta Hayward, 1933 and Anisochoria polysticta Mabille, 1876 (not Anisochoria pedaliodina (Butler, 1870)), Anisochoria verda Evans, 1953 (not Anisochoria minorella Mabille, 1898), Bralus alco (Evans, 1953) (not Bralus albida (Mabille, 1888)), Ephyriades jamaicensis (Möschler, 1879) (not Ephyriades brunnea (Herrich-Schäffer, 1865)), Koruthaialos (Stimula) frena Evans, 1949 (not Koruthaialos focula (Plötz, 1882)), Euphyes kiowah (Reakirt, 1866) (not Euphyes vestris (Boisduval, 1852)), Mnaseas inca Bell, 1930 (not Mnaseas bicolor (Mabille, 1889)), Metron hypochlora (Draudt, 1923) (not Metrocles schrottkyi (Giacomelli, 1911), previously in Metron Godman, 1900), Decinea huasteca (H. Freeman, 1969), Decinea denta Evans, 1955, and Decinea antus (Mabille, 1895) (not Decinea decinea (Hewitson, 1876)), Xeniades pteras Godman, 1900 (not Xeniades chalestra (Hewitson, 1866)), Xeniades difficilis Draudt, 1923 (not Xeniades orchamus (Cramer, 1777)), Xeniades hermoda (Hewitson, 1870) (not Tisias quadrata (HerrichSchäffer, 1869)), Hermio vina (Evans, 1955) (not Hermio hermione (Schaus, 1913), previously in Lento Evans, 1955), Cymaenes loxa Evans, 1955, (not Cymaenes laureolus (Schaus, 1913)), Niconiades peri (Evans, 1955) (not Rhinthon bajula (Schaus, 1902), previously in Neoxeniades Hayward, 1938), Gallio danius (Bell, 1941) (not Vehilius seriatus (Mabille, 1891)), Gallio massarus (E. Bell, 1940) (not Gallio garima (Schaus, 1902) previously in Tigasis Godman, 1900), Cymaenes edata (Plötz, 1882), Cymaenes miqua (Dyar, 1913) and Cymaenes aequatoria (Hayward, 1940) (not Cymaenes odilia (Burmeister, 1878)), Lychnuchus (Enosis) demon (Evans, 1955) (not Lychnuchus (Enosis) immaculata (Hewitson, 1868), previously in Enosis Mabille, 1889), Naevolus naevus Evans, 1955 (not Naevolus orius (Mabille, 1883)), Lucida scopas (Mabille, 1891), Lucida oebasus (Godman, 1900), and Lucida leopardus (Weeks, 1901) (not Lucida lucia (Capronnier, 1874)), Corticea schwarzi (E. Bell, 1941) and Corticea sylva (Hayward, 1942) (not Corticea mendica (Mabille, 1898)), and Choranthus orientis (Skinner, 1920) (not Choranthus antiqua (Herrich-Schäffer, 1863), previously in Pyrrhocalles Mabille, 1904). Borbo impar bipunctata (Elwes and J. Edwards, 1897) is a valid subspecies, not a synonym of Borbo impar tetragraphus (Mabille, 1891), here placed in synonymy with Lotongus calathus (Hewitson, 1876), new synonym. We confirm the species status of Telegonus cassius (Evans, 1952) and Lerema (Morys) valda Evans, 1955. Euphyes chamuli Freeman, 1969 is placed as a subspecies of Euphyes kiowah (Reakirt, 1866), new status. The following 41 taxa are junior subjective synonyms, either newly proposed or transferred from synonymy with other species or subspecies: Telegonus mutius Plötz, 1882 of Euriphellus phraxanor (Hewitson, 1876), Telegonus erythras Mabille, 1888 of Dyscophellus damias (Plötz, 1882), Aethilla jaira Butler, 1870 of Telegonus cretellus (Herrich-Schäffer, 1869), Paches era Evans, 1953 of Santa palica (Mabille, 1888), Antigonus alburnea Plötz, 1884 of Tolius tolimus robigus (Plötz, 1884) (not of Echelatus sempiternus simplicior (Möschler, 1877)), Echelatus depenicillus Strand, 1921 of E. sempiternus simplicior (not of T. tolimus robigus), Antigonus aura Plötz, 1884 of Theagenes dichrous (Mabille, 1878) (not of Helias phalaenoides palpalis (Latreille, [1824])), Achlyodes impressus Mabille, 1889 of Camptopleura orsus (Mabille, 1889), Augiades tania Schaus, 1902 of Metron voranus (Mabille, 1891), Pamphila verdanta Weeks, 1906 of Metron fasciata (Möschler, 1877), Niconiades viridis vista Evans, 1955 of Niconiades derisor (Mabille, 1891), Pamphila binaria Mabille, 1891 of Conga chydaea (A. Butler, 1877) (not of Cynea cynea (Hewitson, 1876)), Psoralis concolor Nicolay, 1980 of Ralis immaculatus (Hayward, 1940), Hesperia dido Plötz, 1882 of Cynea (Quinta) cannae (Herrich-Schäffer, 1869) (not of Lerema lochius (Plötz, 1882)), Proteides osembo Möschler, 1883 of Cynea (Cynea) diluta (Herrich-Schäffer, 1869) (not of Cynea (Quinta) cannae (Herrich-Schäffer, 1869)), Cobalopsis brema E. Bell, 1959 of Eutus rastaca (Schaus, 1902), Psoralis panamensis Anderson and Nakamura, 2019 of Rhomba gertschi (Bell, 1937), Cobalus asella Herrich-Schäffer, 1869 of Amblyscirtes alternata (Grote and Robinson, 1867) (not of Amblyscirtes vialis (W. H. Edwards, 1862)), Papias trimacula Nicolay, 1973 of Nastra subsordida (Mabille, 1891), Pamphila bipunctata Mabille, 1889 and Sarega staurus Mabille, 1904 of Lerema pattenii Scudder, 1872 (not of Cymaenes lumina (Herrich-Schäffer, 1869), previously in Lerema Scudder, 1872), Hesperia aethra Plötz, 1886 of Lerema lineosa (Herrich-Schäffer, 1865) (not of Lerema (Morys) compta Butler, 1877), Megistias miaba Schaus, 1902 of Cobalopsis valerius (Möschler, 1879), Phanis sylvia Kaye, 1914 of Lerema etelka (Schaus, 1902) (not of Lerema (Geia) geisa (Möschler, 1879), previously in Morys Godman, 1900), Carystus odilia Burmeister, 1878, Pamphila trebius Mabille, 1891 and Megistias corescene Schaus, 1902 of Cymaenes lumina (Herrich-Schäffer, 1869), Hesperia phocylides Plötz, 1882 of Cymaenes edata (Plötz, 1882) (not of Lerema accius (J. E. Smith, 1797)), Pamphila xenos Mabille, 1898 of Vehilius inca (Scudder, 1872), Mnasilus guianae Lindsey, 1925 of Papias amyrna (Mabille, 1891), Pamphila nubila Mabille, 1891 of Papias integra (Mabille, 1891) (not of Cynea corisana (Plötz, 1882)), Enosis matheri H. Freeman, 1969 of Metiscus atheas Godman, 1900 (previously in Enosis Mabille, 1889), Hesperia infuscata Plötz, 1882 of Mnaseas derasa derasa (Herrich-Schäffer, 1870) (previously Arotis Mabille, 1904), (not of Papias subcostulata (Herrich-Schäffer, 1870)), Pamphila astur Mabille, 1891 of Metiscus angularis (Möschler, 1877) (not of Cymaenes tripunctus theogenis (Capronnier, 1874)), Anthoptus macalpinei H. Freeman, 1969 of Anthoptus inculta (Dyar, 1918), Methionopsis typhon Godman, 1901 of Methionopsis ina (Plötz, 1882), Methionopsis dolor Evans, 1955 of Thargella volasus (Godman, 1901), Hesperia cinica Plötz, 1882 of Dubiella dubius (Stoll, 1781), Cobalus disjuncta Herrich-Schäffer, 1869 of Dubiella dubius (Stoll, 1781) (not of Vettius lafrenaye (Latreille, [1824])), and Saliana vixen Evans, 1955 of Neoxeniades parna (Evans, 1955). The following are new and revised genusspecies combinations: Euriphellus cebrenus (Cramer, 1777) (not Salatis Evans, 1952), Gorgopas extensa (Mabille, 1891) (not Polyctor Evans, 1953), Clytius shola (Evans, 1953) (not Staphylus Godman and Salvin, 1896), Perus narycus (Mabille, 1889) (not Ouleus Lindsey, 1925), Perus parvus (Steinhauser and Austin, 1993) (not Staphylus Godman and Salvin, 1896), Pholisora litus (Dyar, 1912) (not Bolla Mabille, 1903), Carrhenes decens (A. Butler, 1874) (not Antigonus Hübner, [1819]), Santa palica (Mabille, 1888) (not Chiothion Grishin, 2019), Bralus nadia (Nicolay, 1980) (not Anisochoria Mabille, 1876), Acerbas sarala (de Nicéville, 1889) (not Lotongus Distant, 1886), Caenides sophia (Evans, 1937) (not Hypoleucis Mabille, 1891), Hypoleucis dacena (Hewitson, 1876) (not Caenides Holland, 1896), Dotta tura (Evans, 1951) (not Astictopterus C. Felder and R. Felder, 1860), Nervia wallengrenii (Trimen, 1883) (not Kedestes Watson, 1893), Testia mammaea (Hewitson, 1876) (not Decinea Evans, 1955), Oxynthes trinka (Evans, 1955) (not Orthos Evans, 1955), Metrocles argentea (Weeks, 1901) (not Paratrytone Godman, 1900), Metrocles scitula (Hayward, 1951) (not Mucia Godman, 1900), Metrocles schrottkyi (Giacomelli, 1911) (not Metron Godman, 1900), Niconiades derisor (Mabille, 1891) (not Decinea Evans, 1955), Paratrytone samenta (Dyar, 1914) (not Ochlodes Scudder, 1872), Oligoria (Cobaloides) locutia (Hewitson, 1876) (not Quinta Evans, 1955), Psoralis (Saniba) laska (Evans, 1955) (not Vidius Evans, 1955), Psoralis (Saniba) arva (Evans, 1955) and Psoralis (Saniba) umbrata (Erschoff, 1876) (not Vettius Godman, 1901), Psoralis (Saniba) calcarea (Schaus, 1902) and Psoralis (Saniba) visendus (E. Bell, 1942) (not Molo Godman, 1900), Alychna gota (Evans, 1955) (not Psoralis Mabille, 1904), Adlerodea asema (Mabille, 1891) and Adlerodea subpunctata (Hayward, 1940) (not Eutychide Godman, 1900), Ralis immaculatus (Hayward, 1940) (not Mucia Godman, 1900), Rhinthon braesia (Hewitson, 1867) and Rhinthon bajula (Schaus, 1902) (not Neoxeniades Hayward, 1938), Cymaenes lochius Plötz, 1882 (not Lerema Scudder, 1872), Paracarystus ranka (Evans, 1955) (not Thoon Godman, 1900), Tricrista aethus (Hayward, 1951), Tricrista canta (Evans, 1955), Tricrista slopa (Evans, 1955), Tricrista circellata (Plötz, 1882), and Tricrista taxes (Godman, 1900) (not Thoon Godman, 1900), Gallio madius (E. Bell, 1941) and Gallio seriatus (Mabille, 1891) (not Vehilius Godman, 1900), Gallio garima (Schaus, 1902) (not Tigasis Godman, 1900), Tigasis corope (HerrichSchäffer, 1869) (not Cynea Evans, 1955), Tigasis perloides (Plötz, 1882) (not Cymaenes Scudder, 1872), Amblyscirtes (Flor) florus (Godman, 1900) (not Repens Evans, 1955), Vidius fraus (Godman, 1900) (not Cymaenes Scudder, 1872), Nastra celeus (Mabille, 1891) (not Vehilius Godman, 1900), Nastra nappa (Evans, 1955) (not Vidius Evans, 1955), Vehilius warreni (Weeks, 1901) and Vehilius limae (Lindsey, 1925) (not Cymaenes Scudder, 1872), Cymaenes lumina (Herrich-Schäffer, 1869) (not Lerema Scudder, 1872), Cobalopsis valerius (Möschler, 1879) (not Cobalopsis Godman, 1900), Cobalopsis dictys (Godman, 1900) (not Papias Godman, 1900), Lerema (Morys) venias (Bell, 1942) (not Cobalopsis Godman, 1900), Papias latonia (Schaus, 1913) (not Cobalopsis Godman, 1900), Dion iccius (Evans, 1955) and Dion uza (Hewitson, 1877) (not Enosis Mabille, 1889), Vistigma (Vistigma) opus (Steinhauser, 2008) (not Thoon Godman, 1900), Saturnus fartuga (Schaus, 1902) (not Parphorus Godman, 1900), Phlebodes fuldai (E. Bell, 1930) (not Vettius Godman, 1901), Mnasitheus padus (Evans, 1955) (not Moeris Godman, 1900), Naevolus brunnescens (Hayward, 1939) (not Psoralis Mabille, 1904), Lamponia ploetzii (Capronnier, 1874) (not Vettius Godman, 1901), Mnestheus silvaticus Hayward, 1940 (not Ludens Evans, 1955), Rigga spangla (Evans, 1955) (not Sodalia Evans, 1955), Corticea vicinus (Plötz, 1884) (not Lento Evans, 1955), Mnasalcas thymoetes (Hayward, 1942) (not Mnasicles Godman, 1901), Mnasalcas boyaca (Nicolay, 1973) (not Pamba Evans, 1955), Vertica brasta (Evans, 1955) (not Lychnuchus Hübner, [1831]), Carystina discors Plötz, 1882 (not Cobalus Hübner, [1819]), Zetka irena (Evans, 1955) (not Neoxeniades Hayward, 1938), and Neoxeniades parna (Evans, 1955) (not Niconiades Hübner, [1821]). The following are new or revised species-subspecies combinations: Tagiades neira moti Evans, 1934, Tagiades neira canonicus Fruhstorfer, 1910, Tagiades sheba vella Evans, 1934, Tagiades sheba lola Evans, 1945, Tagiades korela biakana Evans, 1934, Tagiades korela mefora Evans, 1934, Tagiades korela suffusus Rothschild, 1915, Tagiades korela brunta Evans, 1949, Tagiades ravi ravina Fruhstorfer, 1910, Tagiades atticus carnica Evans, 1934, Tagiades atticus nankowra Evans, 1934, Tagiades atticus helferi C. Felder, 1862, Tagiades atticus balana Fruhstorfer, 1910, Tagiades inconspicua mathias Evans, 1934, Tagiades hovia kazana Evans, 1934, Tagiades elegans fuscata de Jong and Treadaway, 2007, Tagiades elegans semperi Fruhstorfer, 1910, Metron hypochlora tomba Evans, 1955, Decinea denta pruda Evans, 1955, and Choranthus orientis eleutherae (Bates, 1934) (previously in Pyrrhocalles Mabille, 1904). In addition to the abovementioned changes, the following new combinations involve newly proposed genus group names: Fulvatis fulvius (Plötz, 1882) and Fulvatis scyrus (E. Bell, 1934) (not Salatis Evans, 1952); Adina adrastor (Mabille and Boullet, 1912) (not Bungalotis Watson, 1893); Nascus (Praxa) prax Evans, 1952, Nascus (Bron) broteas (Cramer, 1780), and Nascus (Bron) solon (Plötz, 1882) (not Pseudonascus Austin, 2008); Chirgus (Turis) veturius (Plötz, 1884); Paches (Tiges) liborius (Plötz, 1884), and Paches (Tiges) mutilatus (Hopffer, 1874) (not Antigonus Hübner, [1819]); Paches (Tiges) exosa (A. Butler, 1877); Tolius tolimus (Plötz, 1884) and Tolius luctuosus (Godman & Salvin, 1894) (not Echelatus Godman and Salvin, 1894); Ancistroides (Ocrypta) caerulea (Evans, 1928), Ancistroides (Ocrypta) renardi (Oberthür, 1878), Ancistroides (Ocrypta) waigensis (Plötz, 1882), Ancistroides (Ocrypta) aluensis (Swinhoe, 1907), Ancistroides (Ocrypta) flavipes (Janson, 1886), and Ancistroides (Ocrypta) maria (Evans, 1949) (not Notocrypta de Nicéville, 1889); Lennia lena (Evans, 1937), Lennia binoevatus (Mabille, 1891), Lennia maracanda (Hewitson, 1876), and Lennia lota (Evans, 1937) (not Leona Evans, 1937); Trida barberae (Trimen, 1873) and Trida sarahae (Henning and Henning, 1998) (not Kedestes Watson, 1893); Noxys viricuculla (Hayward, 1951) (not Oxynthes Godman, 1900); Xeniades (Tixe) quadrata (Herrich-Schäffer, 1869), Xeniades (Tixe) rinda (Evans, 1955), Xeniades (Tixe) putumayo (Constantino and Salazar, 2013) (not Tisias Godman, 1901); Gracilata quadrinotata (Mabille, 1889) (not Styriodes Schaus, 1913); Hermio hermione (Schaus, 1913) (not Lento Evans, 1955); Cynea (Nycea) hycsos (Mabille, 1891), Cynea (Nycea) corisana (Plötz, 1882), Cynea (Nycea) popla Evans, 1955, Cynea (Nycea) iquita (E. Bell, 1941), Cynea (Nycea) robba Evans, 1955, Cynea (Nycea) melius (Geyer, 1832), and Cynea (Nycea) irma (Möschler, 1879); Eutus rastaca (Schaus, 1902) (not Eutychide Godman, 1900); Eutus yesta (Evans, 1955) (not Thoon Godman, 1900); Eutus mubevensis (E. Bell, 1932) (not Tigasis Godman, 1900); Gufa gulala (Schaus, 1902) (not Mucia Godman, 1900); Gufa fusca (Hayward, 1940) (not Tigasis Godman, 1900); Godmia chlorocephala (Godman, 1900) (not Onophas Godman, 1900); Rhomba gertschi (E. Bell, 1937) (not Justinia Evans, 1955); Mnasicles (Nausia) nausiphanes (Schaus, 1913) (not Tigasis Godman, 1900); Amblyscirtes (Flor) florus (Godman, 1900) (not Repens Evans, 1955); Rectava ignarus (E. Bell, 1932) (not Papias Godman, 1900); Rectava vorgia (Schaus, 1902) (not Cobalopsis Godman, 1900); Rectava nostra (Evans, 1955) (not not Vidius Evans, 1955); Lerema (Geia) geisa (Möschler, 1879) and Lerema (Geia) lyde (Godman, 1900) (not Morys Godman, 1900); Contrastia distigma (Plötz, 1882) (not Cymaenes Scudder, 1872); Mit (Mit) badius (E. Bell, 1930) (not Styriodes Schaus, 1913); Mit (Mit) gemignanii (Hayward, 1940), (not Mnasitheus Godman, 1900); Mit (Rotundia) schausi (Mielke and Casagrande, 2002), (not Enosis Mabille, 1889); Picova steinbachi (E. Bell, 1930) (not Saturnus Evans, 1955); Lattus arabupuana (E. Bell, 1932) (not Eutocus Godman, 1901); Gubrus lugubris (Lindsey, 1925) (not Vehilius Godman, 1900); Thargella (Pseudopapias) tristissimus (Schaus, 1902) (not Papias Godman, 1900); Koria kora (Hewitson, 1877) (not Justinia Evans, 1955); Justinia (Septia) septa Evans, 1955; Corta lycortas (Godman, 1900) (not Orthos Evans, 1955); Vertica (Brasta) brasta (Evans, 1955) (not Lychnuchus Hübner, [1831]); Calvetta calvina (Hewitson, 1866) (not Cobalus Hübner, [1819]); Neoxeniades (Bina) gabina (Godman, 1900) (not Orthos Evans, 1955); Oz ozias (Hewitson, 1878) and Oz sebastiani Salazar and Constantino, 2013 (not Lychnuchoides Godman, 1901); and Carystoides (Balma) balza Evans, 1955 and Carystoides (Balma) maroma (Möschler, 1877). Finally, unless stated otherwise, all subgenera, species, subspecies and synonyms of mentioned genera and species are transferred together with their parent taxa, and taxa not mentioned in this work remain as previously classified.
Four new species of limnoterrestrial rhabdocoels (‘Typhloplanidae’ Graff, 1905) are described. One of these – Faunulus nielsi Houben, Proesmans & Artois gen. et sp. nov. – could not be unambiguously placed within an existing genus. Faunulus nielsi most closely resembles species of the genus Adenocerca Reisinger, 1924 but can be clearly distinguished by the position of the testes. The three other new species described are Bryoplana belgica Houben, Proesmans & Artois sp. nov., Hoplopera isis Houben, Proesmans & Artois sp. nov., and Protoplanella leiae Houben, Proesmans & Artois sp. nov. All three belong to the subfamily ‘Protoplanellinae’ Reisinger, 1924 and are distinguished based on a detailed description of the reproductive system. Finally, new data are provided for nine other, known typhloplanids: Adenocerca minima Kolasa, 1981; Chorizogynopora italica Kolasa, 1981; Hoplopera opaca Reisinger, 1924; K. subterranea Reisinger, 1933; Krumbachia virginiana (Kepner & Carter, 1931) Ruebush, 1938; Olisthanellinella rotundula Reisinger, 1924; Prorhynchella minuta Ruebush, 1939; Protoplanella simplex Reisinger, 1924; and Ventrociliella romanae Kolasa, 1977. A detailed comparison of our material of V. romanae to what is described for Bockia deses Reisinger, 1924, leads us to consider the latter a nomen dubium.
Review of the Panorpa wormaldi group (Mecoptera: Panorpidae), with descriptions of two new species
(2022)
Panorpa Linnaeus, 1758 is the largest genus in the scorpionfly family Panorpidae. In this paper, a taxonomic review of the Panorpa wormaldi group is provided, with two new species described from China: Panorpa fengyanga Wang & Suzuki, sp. nov. from Zhejiang, and Panorpa zhuohengi Wang & Suzuki, sp. nov. from Guangdong. The male of Panorpa implicata Cheng, 1957 is discovered and described for the first time. A distributional map and keys to species are also provided for this group. Species number in this group is updated from 17 to 19. In addition, their biogeographical and evolutionary implications are briefly discussed.
We describe two new species of Cyrtodactylus Gray, 1827, each from the Indian states of Meghalaya and Mizoram based on morphology and ND2 gene sequences. The new species are a part of the Cyrtodactylus khasiensis group. Both species represent the highland clade within the south of Brahmaputra clade of Indo-Burmese Cyrtodactylus. Based on ND2 gene sequence, the species from Meghalaya have an uncorrected p-distance of 4.21%–4.25% from a lowland species C. guwahatiensis Agarwal, Mahony, Giri, Chaitanya & Bauer, 2018 and is a sister taxon to C. septentrionalis Agarwal, Mahony, Giri, Chaitanya & Bauer, 2018. The species from Mizoram differ from its sister species C. bengkhuaiai Purkayastha, Lalremsanga, Bohra, Biakzuala, Decemson, Muansanga, Vabeiryureilai, Chauhan & Rathee, 2021 by a p-distance of 8.33%.
A checklist with preliminary conservation assessments of native South American species of Acalypha is presented. This work is supported by the study of ca 6500 herbarium specimens and an in-depth literature review. As a result, 87 species (83 native and four introduced) and eight subspecies are accepted, and a further 395 names are considered synonyms. Geographical distribution, habitat, and altitudinal range for all species are also indicated. Brazil is the richest country in number of species of Acalypha (40), followed by Peru (32), Bolivia (29), Colombia and Ecuador—including Galapagos Islands—(24), Venezuela (18), Argentina (17), Paraguay (13), Guyana (8), Uruguay (5), French Guiana (4), and Suriname (3). The presence of the genus Acalypha in Chile is reported for the first time, alongside new country records of A. poiretii in Peru and A. venezuelica in Guatemala. The specimens previously identified as A. plicata from Colombia and Venezuela, are here considered belonging to A. cuspidata. The red list provided follows IUCN criteria and includes 39 species and three subspecies, 47% of total native species of Acalypha in South America: 16 species and one subspecies Critically Endangered (nine of them probably extinct), 15 species and two subspecies Endangered, and eight species Vulnerable.
New taxa in Hesperiidae (Lepidoptera: Papilionoidea) are traditionally proposed after inspection of male genitalia, which largely form the basis for Hesperiidae taxonomy. However, with genomic DNA sequencing, even a single female specimen can be placed in a phylogenetic context of existing classification and taxonomically assigned with confidence. Genomic sequencing of an unusually patterned Hesperiidae female from San Martin, Peru, characterized by pearly spots outlining an inverted heart pattern on the rust-colored ventral hindwing, reveals that it represents an undescribed genus and species named here as Gemmia buechei Brockmann and Grishin, new genus and new species.
ZooBank registration. https://zoobank.org/2FA538FA-7D65-4097-9BBA-71CD1B2795E5
Elusive flaws are identified in techniques widely adopted to organize the Material Examined sections in taxonomic publications, mostly regarding the usage of the term ibidem and the nesting of information such as country and states. Logical errors are identified that prevent objective retrieval of the original information and can hinder or block its interpretation, even in case-by-case analyses. It is demonstrated that the free usage of ibidem in the sense of “same as previous except as follows” compromises the interpretation of data, characterizing bad practice. Solutions are proposed for the precise usage of both the term ibidem and the nesting technique. A new technique for organizing, compressing, and presenting information, called grid-setting, is described and evaluated. Its most notable practical effect is that the Material Examined section becomes literally a coded data sheet, which can be accurately converted back to spreadsheet format. In addition, the grid-setting technique was able to generate texts up to 30% shorter than those edited with the best-known traditional techniques. The new ideas and fixes are incorporated into a new software, flexible enough to process varied and unlimited data into largely user-defined texts, which remain nevertheless universal in their format and logical interpretation.
The Bittacidae fauna in Guizhou Province, China is reviewed. Eleven species in the genera Terrobittacus Tan & Hua, 2009 and Bittacus Latreille, 1805 of Bittacidae are documented in Guizhou, including three new species: Bittacus dilobus sp. nov. and Bittacus leigongshanicus sp. nov. from Leigongshan, and Bittacus multisetus sp. nov. from Yushe. A key to species of Bittacidae in Guizhou is provided.
This study presents the inventory of sea spiders (Pycnogonida) sampled during the Madibenthos Expedition in Martinique (West Indies). Species were discriminated leaning on morphological and molecular data. A total of 761 specimens are classified in 72 species, 16 genera and nine families. Thirteen new species are described: Ammothella dirbergi sp. nov., A. krappi sp. nov., Tanystylum boucheti sp. nov., T. ingrallis sp. nov., Ascorhynchus iguanarum sp. nov., Eurycyde kaiouti sp. nov., Nymphon dorlis sp. nov., N. ludovici sp. nov., N. martinicum sp. nov., N. timons sp. nov., Anoplodactylus madibenthos sp. nov., Pycnogonum cesairei sp. nov. and Rhynchothorax sidereus sp. nov. We describe a neotype for Anoplodactylus micros Bourdillon, 1955 from the type locality. Martinique now includes 79 species of sea spiders, mostly endemic to the Tropical Northwestern Atlantic, cosmopolitan or shared with the South America Atlantic coast. Some species are potentially introduced. However, our knowledge of the distribution of species found in Martinique is probably biased by the scarcity of diagnostic morphological characters. Also, nine potentially cryptic species (discriminated on genetic data alone), are identified, shedding light on the overlooked diversity of sea spiders in the Tropical Northwestern Atlantic. Therefore, we call for a more widespread use of barcoding in sea spiders.
A new polynoid, Webbnesia maculata gen. et sp. nov., was discovered during benthic surveys conducted around the Canary Islands. Its generic characters (absence of cephalic peaks, ventrally inserted lateral antennae, reduced notopodium and chaetae all stout) place it close to Antinoe Kinberg, 1856, Hermadion Kinberg, 1856 and Malmgrenia McIntosh, 1874, but the combination is unique and justifies the erection of a new genus. The new genus and species are described, figured and discussed in detail. An updated list of taxa and an identification key to all genera of Polynoinae Kinberg, 1856 sensu lato currently reported from the extended Northeast Atlantic are given.
The description in 1891 of the sea pen genus Gyrophyllum Studer, 1891 and also the type species G. hirondellei Studer, 1891 was based on a single colony collected in the Azores Archipelago. During the 19th and 20th centuries, the family placement of this genus became controversial as the set of morphological features present in Gyrophyllum could justify its assignation to both the families Pennatulidae Ehrenberg, 1834 and Pteroeididae Kölliker, 1880. Deliberations over this intermediate set of characters finally ended in the reunification of the genera and species of both families under Pennatulidae by principle of priority. The use of molecular sources of information based on a series of sequencing techniques presents a different but promising phylogenetic scenario in order to go further in the understanding of pennatulacean systematics. In this paper, a complementary morphological and molecular study (multiloci sequences with three mitochondrial and one nuclear markers) based mainly on newly collected material is carried out. This study re-confirms from a molecular point of view previously published results that indicate the position of Gyrophyllum as being distant from Pennatula Linnaeus, 1758 and Pteroeides Herklots, 1858 (type genera of the families Pennatulidae and Pteroeididae, respectively). This fact together with the results of a detailed morphological examination strongly supports the placement of the enigmatic genus Gyrophyllum in a separate family: Gyrophyllidae fam. nov. and resolves the nomenclatural uncertainty at family level for this genus. Moreover, the characters previously considered useful in the distinction of the two currently recognised species G. hirondellei in the Atlantic and G. sibogae Hickson, 1916 in the Indo-western Pacific are revisited.
Martensina thailandica gen. et sp. nov., a freshwater ostracod species representing a new subfamily, Martensininae subfam. nov., in the family Cyprididae, is here described from a swamp in Maha Sarakham Province, Thailand. The new genus and species is mainly characterized by the 7-segmented antennula which has a Rome organ and remarkably long aesthetasc ya, the morphology of the sexually dimorphic antenna (A2), the markedly elongated A2 terminal segment, the short and thin α- and β-setae on the mandibular palp, the elongated terminal segment of the maxillula, the obviously 2-segmented male prehensile palp, the presence of d1 and d2 setae on the protopod of the second thoracopod (T2), the sexually dimorphic T2, the distinctive terminal segment of the third thoracopod bearing three long setae, the well-developed caudal ramus, the large hemipenis which has a complex internal structure, and the Zenker organ with funnel-shaped ends and numerous spiny whorls.
The pseudoscorpion (Arachnida: Pseudoscorpiones) fauna of mainland Ecuador, excluding the Galápagos Islands, is poorly known, with only 41 described species in 9 families. The family Syarinidae has a pantropical distribution and presently comprises ca 120 species in 17 valid genera that are found in leaf litter and subterranean habitats, mostly in tropical and subtropical climates. Four syarinid species have been recorded from Ecuador, including the Galápagos, in two widespread genera, Ideobisium and Ideoblothrus, but field collections suggest that these pseudoscorpions are common and abundant in all forest systems across the country. Here, we review field collections of syarinids from mainland Ecuador and describe five new species in these genera: Ideobisium kichwa sp. nov. (Napo Province, Colonso Chalupas Natural Reserve), I. sonqo sp. nov. (Napo Province, Colonso Chalupas Natural Reserve), I. susanae sp. nov. (Napo Province, Jatun Sacha Natural Reserve), Ideoblothrus nadineae sp. nov. (Napo Province, Colonso Chalupas Natural Reserve) and I. safinai sp. nov. (Pichincha Province, Otongachi Natural Reserve) based on morphology. These species seem to have narrow distributions and we therefore restrict the ranges of two species previously recorded from Ecuador (Ideobisium crassimanum Balzan, 1892 and Ideoblothrus costaricensis (Beier, 1931)) to their countries of origin, which is Costa Rica and Venezuela, respectively.
Erebaces woodruffi Anderson, new species (Curculionidae: Molytinae: Cryptorhynchini), from Palawan (Philippines) is described and illustrated. This is the second species of the genus Erebaces Pascoe described from the Philippines. It can be separated from Erebaces kidapawanus Pancini by the pair of divergent dorsal pale-scaled lines on the pronotum extended onto the elytra and by the form of the elytral tubercles.
A new genus, Thaicypris gen. nov., in the tribe Herpetocypridini Kaufmann, 1900 of the subfamily Herpetocypridinae Kaufmann, 1900 is established to accommodate a new species from Thailand. The present contribution deals with the description of a new genus and species, Thaicypris panhai gen. et sp. nov., which is mainly characterized by the distinctive and raised, inwardly displaced selvage at the postero-ventral part of the right valve (RV) that is not parallel to the valve margin, the absence of an anterior inner list on the RV, the prominent and elevated double inner list on the posterior part of the left valve, the small and three-segmented Rome organ on the first antenna (A1), the spatulated terminal segment of the maxillular (Mx1) palp, the slender caudal ramus (CR) with long and thin Sp seta, the presence of basal triangle on the CR attachment, and the pointed projection at the terminal segment base of the prehensile palps. The hemipenis of the new genus and species is outstanding, especially the medial lateral shield which has a long, beak-shaped protrusion on the distal part. The discovery of this Thai taxon is the first record of the tribe Herpetocypridini in Thailand and the second species of the tribe in Southeast Asia.
A global synonymical checklist of the species and higher taxa of the insect order Megaloptera is provided. The checklist includes both extant and extinct taxa, and recognizes 2 families, 4 subfamilies, 48 genera, 425 species, and 6 subspecies. Both families (Corydalidae and Sialidae), and three of the four subfamilies (Corydalinae, Chauliodinae, and Sialinae) are known from both extant and extinct species; the Sharasialinae (Sialidae) is entirely extinct. Country-level geographic distribution data are provided for all species and subspecies. Synoptic type data are provided for taxa in the family and genus groups. Summary data are given for the numbers of megalopteran species currently known to occur in each of the major biogeographical regions of the world, and for the world fauna. Increase of knowledge about the diversity of the world Megaloptera fauna is summarized in counts of valid species described per decade and in a global taxonomic description curve. An updated set of keys to the world families, subfamilies, and genera of the Megaloptera is also provided.
The whip spider family Charinidae Quintero, 1986 is the most speciose and widely distributed in the arachnid order Amblypygi Thorell, 1883. It comprises three genera and 95 species distributed across all tropical continents and the eastern Mediterranean. Despite recent advances in the taxonomy of the family, a global revision of all its species, necessary to advance understanding of its systematics, biogeography and evolution, has never been conducted. In the present contribution, the family is revised in its entirety for the first time, including all previous names and 33 new species, 24 in the genus Charinus Simon, 1892: C. alagoanus sp. nov., C. apiaca sp. nov., C. carinae sp. nov., C. carioca sp. nov., C. carvalhoi sp. nov., C. cearensis sp. nov., C. diamantinus sp. nov., C. euclidesi sp. nov., C. goitaca sp. nov., C. guayaquil sp. nov., C. imperialis sp. nov., C. loko sp. nov., C. magalhaesi sp. nov., C. miskito sp. nov., C. mocoa sp. nov., C. monasticus sp. nov., C. palikur sp. nov., C. perquerens sp. nov., C. puri sp. nov., C. renneri sp. nov., C. sooretama sp. nov., C. souzai sp. nov., C. susuwa sp. nov., C. una sp. nov.; eight in the genus Sarax Simon, 1892: S. bilua sp. nov., S. dunni sp. nov., S. gravelyi sp. nov., S. indochinensis sp. nov., S. lembeh sp. nov., S. palau sp. nov., S. rahmadii sp. nov., S. tiomanensis sp. nov.; and one in the genus Weygoldtia Miranda et al., 2018: W. consonensis sp. nov. Taxonomic keys to the 132 species (excluding four nomina dubia) are presented and several taxonomic rearrangements implemented. Four subspecies are elevated to species level: Charinus cavernicolus Weygoldt, 2006, C. elegans Weygoldt, 2006, C. longipes Weygoldt, 2006, and Sarax bispinosus (Nair, 1934). Sarax batuensis Roewer, 1962 is removed from synonymy with Sarax buxtoni (Gravely, 1915) and S. buxtoni newly synonymized with Sarax rimosus (Simon, 1901). Stygophrynus moultoni Gravely, 1915 is transferred to Sarax, resulting in Sarax moultoni (Gravely, 1915) comb. nov. Ten species are transferred from Charinus to Sarax, resulting in new combinations: S. abbatei (Delle Cave, 1986) comb. nov., S. bengalensis (Gravely, 1911) comb. nov., S. dhofarensis (Weygoldt, Pohl & Polak, 2002) comb. nov., S. ioanniticus (Kritscher, 1959) comb. nov., S. israelensis (Miranda et al., 2016) comb. nov., S. omanensis (Delle Cave, Gardner & Weygoldt, 2009) comb. nov., S. pakistanus (Weygoldt, 2005) comb. nov., S. seychellarum (Kraepelin, 1898) comb. nov., S. socotranus (Weygoldt, Pohl & Polak, 2002) comb. nov. and S. stygochthobius (Weygoldt & Van Damme, 2004) comb. nov.
Integrative taxonomy was employed to exploit the differences between the known Metaphire anomala (Michaelsen, 1907) and other specimens collected in Vietnam. The results brought to light two new species, namely Metaphire iranomala sp. nov. and Metaphire decemtheca sp. nov. The former is easily recognised by having male pores on xix and four pairs of spermathecal pores on 5/6/7/8/9 while the latter is distinguished by having five pairs of spermathecal pores on 4/5/6/7/8/9. The K2P distances of the fragment of the cytochrome c oxidase subunit I (COI) gene are 13.1% between M. iranomala sp. nov. and M. anomala (Michaelsen, 1907) and 18% between M. decemtheca sp. nov. and Metaphire grandiverticulata Nguyen & Lam, 2017. The intraspecific divergences are 1.5%–10.6% for M. iranomala sp. nov. and 2.1%–11.4% for M. decemtheca sp. nov.
Two new species of the subfamily Cypricercinae McKenzie, 1971 are described from the Western part of Thailand: Pseudostrandesia ratchaburiensis sp. nov. and Strandesia prachuapensis sp. nov. Pseudostrandesia ratchaburiensis sp. nov. is mainly characterized by a flange on the antero-ventral part of the left valve (LV), a markedly large β seta on the mandibular (Md) palp, serrated bristles on the third endite of the maxillula (Mx1), a slender caudal ramus (CR) with a long claw Ga (length ca half that of the ramus) and a relatively low number (13) of spiny whorls in the Zenker’s organ. The discovery of both males and females of Pseudostrandesia ratchaburiensis sp. nov. in the present study constitutes the first report of a sexual population in this genus, thereby allowing for a comparison of the male reproductive organs (hemipenis and Zenker’s organ) from a new species with those of other genera of Cypricercinae. Strandesia prachuapensis sp. nov. is most closely related to Strandesia odiosa (Moniez, 1892) and Strandesia flavescens Klie, 1932 as they bear similar anterior flanges on the right valve (RV). The key diagnostic features of the new Strandesia species are a large carapace (ca 1.5 mm), an angulated antero-ventral part of the LV, a weak and small anterior inner list on the LV, an anterior flange on the RV, a markedly small aesthetasc Y on the second antenna, a large β seta on the Md-palp, smooth bristles on the third endite of the Mx1 and a slender CR with a short claw Ga (length ca ⅓ of the ramus). In addition, Pseudostrandesia complexa (Victor & Fernando, 1981) comb. nov. is here proposed.
A rare fairyfly (Hymenoptera, Mymaridae) genus, Ganomymar De Santis, 1972, is revised and rediagnosed based on both sexes; its males were previously unknown. This genus, which has remarkable structures on the propodeum and peculiar fore wings in females, is known only from Madagascar in the Afrotropical region. Its type species, Ganomymar dessarti De Santis, 1972, is redescribed and illustrated based on a non-type female specimen. Three new species of Ganomymar are described: G. caslot sp. nov., G. libertatium sp. nov., and G. zuparkoi sp. nov. The species are placed in two distinct species groups. A key to females of the four species is provided.
In the Indo-West Pacific, intertidal slugs of the genus Platevindex Baker, 1938 are common in mangrove forests, where they typically live on the roots and trunks of mangrove trees. These slugs are easily distinguished from most onchidiids by their hard notum and narrow foot, but despite their large size and abundance, species diversity and geographic distributions have remained a mystery. With the aid of new collections from across the entire Indo-West Pacific, the taxonomy of Platevindex is revised using an integrative approach (natural history field observations, re-examination of type specimens, mitochondrial and nuclear DNA sequences, and comparative anatomy). In this monograph, nine species of Platevindex are recognized, including one new to science: P. amboinae (Plate, 1893), P. applanatus (Simroth, 1920) comb. nov., P. aptei Goulding & Dayrat sp. nov., P. burnupi (Collinge, 1902) comb. nov., P. coriaceus (Semper, 1880), P. latus (Plate, 1893), P. luteus (Semper, 1880), P. martensi (Plate, 1893) and P. tigrinus (Stoliczka, 1869) comb. nov. Five species names are recognized as junior synonyms, four of which are new, and two Platevindex names are regarded as nomina dubia. One new subspecies is also recognized: P. coriaceus darwinensis Goulding & Dayrat subsp. nov. Most species were previously known only from the type material and many new geographic records are provided across the Indo-West Pacific, from South Africa to the West Pacific (Japan, New Ireland and New Caledonia).
Aim: The identification of the mechanisms determining spatial variation in biological diversity along elevational gradients is a central objective in ecology and biogeography. Here, we disentangle the direct and indirect effects of abiotic drivers (climatic conditions, and land use) and biotic drivers (vegetation structure and food resources) on functional diversity and composition of bird and bat assemblages along a tropical elevational gradient. Location: Southern slopes of Mt. Kilimanjaro, Tanzania, East Africa. Methods: We counted birds and recorded bat sonotypes on 58 plots distributed in near-natural and anthropogenically modified habitats from 700 to 4,600 m above sea level. For the recorded taxa, we compiled functional traits related to movement, foraging and body size from museum specimens and databases. Further, we recorded mean annual temperature, precipitation, vegetation complexity as well as the number of fruits, flowers, and insect biomass as measures of resource availability on each study site. Results: Using path analyses, we found similar responses of bird and bat functional diversity to the variation in abiotic and biotic drivers along the elevational gradient. In contrast, the functional composition of both taxa showed distinct responses to abiotic and biotic drivers. For both groups, direct temperature effects were most important, followed by resource availability, precipitation and vegetation complexity. Main Conclusions: Our findings indicate that physiological and metabolic constraints imposed by temperature and resource availability determine the functional diversity of bird and bat assemblages, whereas the composition of individual functional traits is driven by taxon-specific processes. Our study illustrates that distinct filtering mechanisms can result in similar patterns of functional diversity along broad environmental gradients. Such differences need to be taken into account when it comes to conserving the functional diversity of flying vertebrates on tropical mountains.
Aim: Recent studies in southern Africa identified past biome stability as an important predictor of biodiversity. We aimed to assess the extent to which past biome stability predicts present global biodiversity patterns, and the extent to which projected climatic changes may lead to eventual biome changes in areas with constant past biome.
Location: Global.
Taxon: Spermatophyta; terrestrial vertebrates.
Methods: Biome constancy was assessed and mapped using results from 89 dynamic global vegetation model simulations, driven by outputs of palaeoclimate experiments spanning the past 140 ka. We tested the hypothesis that terrestrial vertebrate diversity is predicted by biome constancy. We also simulated potential future vegetation, and hence potential future biome patterns, and quantified and mapped the extent of projected eventual future biome change in areas of past constant biome.
Results: Approximately 11% of global ice-free land had a constant biome since 140 ka. Apart from areas of constant Desert, many areas with constant biome support high species diversity. All terrestrial vertebrate groups show a strong positive relationship between biome constancy and vertebrate diversity in areas of greater diversity, but no relationship in less diverse areas. Climatic change projected by 2100 commits 46%–66% of global ice-free land, and 34%–52% of areas of past constant biome (excluding areas of constant Desert) to eventual biome change.
Main conclusions: Past biome stability strongly predicts vertebrate diversity in areas of higher diversity. Future climatic changes will lead to biome changes in many areas of past constant biome, with profound implications for biodiversity conservation. Some projected biome changes will result in substantial reductions in biospheric carbon sequestration and other ecosystem services.
Two new species of giant pill-millipedes, Zephronia viridisoma Rosenmejer & Wesener sp. nov. and Sphaerobelum aesculus Rosenmejer & Wesener sp. nov., are described based on museum samples from southern Thailand. Zephronia viridisoma sp. nov. comes from Khao Lak, while the type locality of S. aesculus sp. nov. is on Phuket Island. Both species are described integratively, combining light microscopy, scanning electron microscopy, multi-layer photography, micro-CT scans and genetic barcoding. Genetic barcoding was successfully conducted for holotypes of both new species, which could be added to a dataset of all published sequences of the family Zephroniidae, including all described species from Thailand, Laos and Cambodia up to 2020. Genetic barcoding of the COI gene revealed another female of S. aesculus sp. nov., 160 km east of the type locality. Both new species are genetically distant from all other Zephroniidae from Thailand and surrounding countries, showing uncorrected p-distances of 16.8–23.1%. A virtual cybertype of a paratype of Z. viridisoma sp. nov. was created and made publically accessible.
Invasive alien species are a well-known and pervasive threat to global biodiversity and human well-being. Despite substantial impacts of invasive alien species, quantitative syntheses of monetary costs incurred from invasions in national economies are often missing. As a consequence, adequate resource allocation for management responses to invasions has been inhibited, because cost-benefit analysis of management actions cannot be derived. To determine the economic cost of invasions in Germany, a Central European country with the 4th largest GDP in the world, we analysed published data collected from the first global assessment of economic costs of invasive alien species. Overall, economic costs were estimated at US$ 9.8 billion between 1960 and 2020, including US$ 8.9 billion in potential costs. The potential costs were mostly linked to extrapolated costs of the American bullfrog Lithobates catesbeianus, the black cherry Prunus serotina and two mammals: the muskrat Ondatra zibethicus and the American mink Neovison vison. Observed costs were driven by a broad range of taxa and mostly associated with control-related spending and resource damages or losses. We identified a considerable increase in costs relative to previous estimates and through time. Importantly, of the 2,249 alien and 181 invasive species reported in Germany, only 28 species had recorded economic costs. Therefore, total quantifications of invasive species costs here should be seen as very conservative. Our findings highlight a distinct lack of information in the openly-accessible literature and governmental sources on invasion costs at the national level, masking the highly-probable existence of much greater costs of invasions in Germany. In addition, given that invasion rates are increasing, economic costs are expected to further increase. The evaluation and reporting of economic costs need to be improved in order to deliver a basis for effective mitigation and management of invasions on national and international economies.
Ishtarella Martens new genus (Hymenoptera: Braconidae: Aphidiinae) and I. thailandica Martens new species are described and illustrated from Doi Phu Kha National Park, Nan Province, Thailand. The genus is assigned to the tribe Aphidiini, subtribe Trioxina. Based on morphology, Ishtarella appears most closely related to Binodoxys Mackauer. An updated checklist of the aphidiine fauna of Thailand, based on published records, is presented.
A strong decline and thinning of the Arctic sea-ice cover over the past five decades has been documented. The former multiyear sea-ice system has largely changed to an annual system and with it the dynamics of sea-ice transport across the Arctic Ocean. Less sea ice is reaching the Fram Strait and more ice and ice-transported material is released in the northern Laptev Sea and the central Arctic Ocean. This trend is expected to have a decisive impact on ice associated (“sympagic”) communities. As sympagic fauna plays an important role in transmitting carbon from the ice-water interface to the pelagic and benthic food webs, it is important to monitor its community composition under the changing environmental conditions. We investigated the taxonomic composition, abundance and distribution of sea-ice meiofauna (here heterotrophs >10 μm; eight stations) and under-ice fauna (here metazoans >300 μm; fourteen stations) in Arctic 1.5 year-old pack ice north of Svalbard. Sampling was conducted during spring 2015 by sea-ice coring and trawling with a Surface and Under-Ice Trawl. We identified 42 taxa associated with the sea ice. The total abundance of sea-ice meiofauna ranged between 580 and 17,156 ind.m–2 and was dominated by Ciliophora (46%), Copepoda nauplii (29%), and Harpacticoida (20%). In contrast to earlier studies in this region, we found no Nematoda and few flatworms in our sea-ice samples. Under-ice fauna abundance ranged between 15 and 6,785 ind.m–2 and was dominated by Appendicularia (58%), caused by exceptionally high abundance at one station. Copepoda nauplii (23%), Calanus finmarchicus (9%), and Calanus glacialis (6%) were also very abundant while sympagic Amphipoda were comparatively rare (0.35%). Both sympagic communities showed regional differences in community composition and abundance between shelf and offshore stations, but only for the under-ice fauna those differences were statistically significant. Selected environmental variables moderately explained variations in abundances of both faunas. The results of this study are consistent with predictions of diversity shifts in the new Arctic.
An inventory of Sciaridae (Diptera: Sciaroidea) from a eutrophic fen and a spring brook in Viidumäe Nature Reserve (Estonia, Saaremaa Island) recorded a total of 60 species, of which 57 are new records for Estonia, including two that are new to science and described herein as Cratyna (Diversicratyna) palustricola sp. nov. (Estonia) and Sciara bryophila sp. nov. (Estonia, Finland). This has raised the number of Sciaridae known from Estonia from 6 to 63.
This paper describes rare Cardiomya species from Brazil which have been hitherto misidentified as Cardiomya cleryana (d’Orbigny, 1842) in literature or museum collections. Cardiomya minerva sp. nov. is proposed as new species and is characterized by its quadrangular shell, short and truncated rostrum, and external ornamentation composed of six radial ribs on the posterior half of the shell flank. Cardiomya striolata (Locard, 1897) described from the Mediterranean Sea and northwestern Atlantic Ocean, is reported from Brazil for the first time; although previously regarded as a junior synonym of Cardiomya costellata (Deshayes, 1835), it is herein considered as a full species and redescribed. This species is characterized by its trapezoidal shell flank, elongated rostrum, tapering towards the tip, and external ornamentation composed of 18–53 radial ribs, the 3–4 posterior ones being the strongest and more widely spaced. Other three previously unknown species are illustrated but not formally named due to the lack of well-preserved articulated shells.
Meiofauna sampling in the proximity of Syd-Hällsö Island (Strömstad, Sweden) revealed a new species of Kinorhyncha from the Skagerrak. The species, Setaphyes elenae sp. nov., is distinguished from its congeners by the arrangement of the middorsal cuticular specializations (it has shortened, distally rounded middorsal processes on segments 1 and 9 and middorsal elevations throughout segments 2–8), as well as by the presence of paired laterodorsal setae on segments 3, 5, 7 and 9 and ventromedial setae on segments 3, 5 and 7 in both males and females. The finding of a new species from the northeastern Atlantic Ocean, provides new valuable information for the recently established genus in the Allomalorhagida.
A new cypridopsine genus, Cyprettadopsis gen. nov., described here, is principally characterized by the reduced caudal ramus, the strongly serrated claw G2 of the antenna (A2), the A2 subquadrate terminal segment, the undivided penultimate segment of the second thoracopod (T2), the morphology of the third thoracopod bearing a distinctly separated terminal segment, the complete septa on the posteroventral margin and the incomplete septa on the anterior margin of both valves. Based on a combination of these characters, a new tribe, Cyprettadopsini trib. nov., is created in the subfamily Cypridopsinae Kaufmann, 1900 to accommodate this new genus, and one new species, Cyprettadopsis sutura gen. et sp. nov., is described as the type species. Apart from the above generic characters, the following features are also typical of the new species: the tiny needlepoint-like pores along the anterior and ventral margins of both valves, the remarkably large β-seta on the mandibular palp and the considerably short d2 seta on the T2. The presence of marginal septa in the new genus is a distinctive character and constitutes the first record of this feature within Cypridopsinae. The taxonomically relevant characters in the new taxon and related taxa are briefly discussed.
Nemoura Latreille, 1796 and Amphinemura Ris, 1902 are the two largest genera of Nemouridae in China. In this paper, two new species are described and illustrated from China: Nemoura lixiana sp. nov. from Sichuan Province and Amphinemura jiaoheensis sp. nov. from Jilin Province. The two new species are diagnostic from congeners by the genitalic structures in males and females.
The present study aims to fulfill the gap of taxonomic knowledge on Triphoridae from Brazil. We describe five new species (Isotriphora uncia sp. nov., Isotriphora leo sp. nov., Monophorus verecundus sp. nov., Sagenotriphora albocaput sp. nov., Similiphora lucida sp. nov.), report five species previously known only from the Caribbean and related areas (Cheirodonta dupliniana (Olsson, 1916), Eutriphora auffenbergi Rolán & Lee, 2008, Isotriphora tricingulata Rolán & Fernández-Garcés, 2015, Marshallora ostenta Rolán & Fernández-Garcés, 2008, Monophorus caracca (Dall, 1927) comb. nov.) and describe six morphotypes at the generic level (Isotriphora sp. 1, Marshallora sp. 1, Nanaphora sp. 1, Sagenotriphora sp. 1, Sagenotriphora sp. 2, Similiphora sp. 1). Remarks are made to some species previously recorded from Brazil, including the invalidation of records, problems of generic allocation and geographical range extensions. Maps of the geographical distribution are provided for the 65 currently recognized species of Triphoridae from Brazil. Of these, 31 species are endemic to Brazil and 58 inhabit the continental shelf vs only seven from the continental slope. A distinct geographical zone occurs in southeastern Brazil. A few species occur exclusively near the mouth of the Amazon River, whereas others inhabit a local biogenic reef, possibly serving as a biogeographical corridor that connects western Atlantic populations. Species of Isotriphora from Brazil are particularly common around oceanic islands, probably due to adopting intracapsular metamorphosis, which may have evolved in more than one evolutionary event.
Sea pens (Cnidaria: Anthozoa: Pennatulacea) constitute a distinctive group of colonial marine invertebrates. They inhabit the world`s oceans, from shallow to deep waters. Studies about this group in Argentina are scarce, and no species have been described in the area in over a decade. Based on samples collected in Mar del Plata Submarine Canyon at about 3000 m deep we describe a new species of sea pen, Umbellula pomona Risaro, Williams & Lauretta sp. nov. This is a spiculate Umbellula that differs from other species of Umbellula with sclerites, by the number, development and distribution of the autozooids in its terminal cluster, as well as the shape of its axis. Molecular data also distinguishes it from other known species. Of the forty-three described species approximately ten are considered valid for the genus Umbellula, four of them are registered for the South Atlantic Ocean and only three are described for the Antarctic region. Since sampling efforts in this area have been scarce, the number of species of sea pens from the region is likely to increase substantially in the coming years.
The Chinese fauna of the pselaphine genus Sathytes Westwood (Batrisitae: Batrisini) currently includes 20 species. In this paper, 15 new species from various provinces of the country are described: S. alpicola sp. nov. (Xizang), S. australis sp. nov. (Guangdong, Guangxi), S. chayuensis sp. nov. (Xizang), S. chengzhifeii sp. nov. (Yunnan), S. huapingensis sp. nov. (Guangxi), S. linzhiensis sp. nov. (Xizang), S. maoershanus sp. nov. (Guangxi), S. nujiangensis sp. nov. (Yunnan), S. panzhaohuii sp. nov. (Xizang), S. shennong sp. nov. (Hubei), S. tianquanus sp. nov. (Sichuan), S. transversus sp. nov. (Xizang), S. valentulus sp. nov. (Guangxi), S. xingdoumontis sp. nov. (Hubei) and S. xizangensis sp. nov. (Xizang). New collection records are provided for S. longitrabis Yin & Li, 2012, S. tangliangi Yin & Li, 2012 and S. yunnanicus Yin & Li, 2012. Maps showing the distribution of the genus in China, and an updated checklist of the world species are provided.
We report on fourteen species and four genera of Tischeriidae recorded from Las Cuevas, a single tropical forest locality in Belize, Central America. This is the highest number of species of Tischeriidae recorded from a single locality worldwide, exceeding the species and generic diversity of the entire Tischeriidae fauna of Europe and accounting for about 9% of the documented global fauna for this family. We describe and name six new species: Astrotischeria papilloma Diškus & Stonis sp. nov., mining on Lasianthaea fruticosa (L.) K.M.Becker (Asteraceae); A. scutifera Diškus & Stonis sp. nov., mining on Sida glabra Mill. (Malvaceae); A. basilobata Remeikis & Stonis sp. nov., mining on Lasianthaea fruticosa; Paratischeria robinsoni Diškus & Stonis sp. nov., mining on Otopappus verbesinoides Benth. (Asteraceae); P. tubifex Diškus & Stonis sp. nov., mining on Lasianthaea fruticosa; and P. belizensis Remeikis & Stonis sp. nov. (host plant unknown). Additionally, we review eight previously described species from the same period of collecting at Las Cuevas in 1997–1998: A. selvica Diškus, Carvalho-Filho & Stonis, 2018, mining on Sphagneticola trilobata (L.) Pruski and Synedrella nodiflora (L.) Gaertn. (Asteraceae); A. casila Diškus & Stonis, 2018, mining on Montanoa atriplicifolia (Pers.) Sch.Bip. (Asteraceae); A. furcata Diškus & Stonis, 2018 (host plant unknown); Paratischeria neotropicana (Diškus & Stonis, 2015), mining on Sida L. (Malvaceae), including S. rhombifolia L.; Dishkeya gouaniae (Stonis & Diškus, 2007), mining on Gouania polygama (Jacq.) Urb. (Rhamnaceae); Coptotriche pulverea (Walsingham, 1897), mining on Terminalia amazonia (J.F.Gmel.) Exell (Combretaceae); C. forsteroniae Stonis & Diškus, 2008, mining on Forsteronia myriantha Donn Sm. (Apocynaceae); and C. singularis Stonis & Diškus, 2008 (host plant unknown). All taxa, except for C. singularis, are illustrated with photographs of the adults and their genitalia. We also briefly discuss the discovery of some novel characters for Astrotischeria Puplesis & Diškus, 2003 and Paratischeria Diškus & Stonis, 2017, Tischeriidae, and provide the first photographic documentation of Coptotriche pulverea and C. forsteroniae.
Dichromatobolus, a new genus of spirobolidan millipedes from Madagascar (Spirobolida, Pachybolidae)
(2020)
A new genus, Dichromatobolus gen. nov., belonging to the genus-rich mainly southern hemisphere family Pachybolidae of the order Spirobolida, is described based on D. elephantulus gen. et sp. nov., illustrated with color pictures, line drawings, and scanning electron micrographs. The species is recorded from the spiny bush of southwestern Madagascar. Dichromatobolus elephantulus gen. et sp. nov. shows an unusual color pattern, sexual dichromatism with males being red with black legs and females being grey. Males seem to be more surface active, as mainly males were collected with pitfall traps. Females mainly come from the pet trade. The body of this species is short and very wide, being only 8 times longer than wide in the males. Live observations show the species is a very slow mover, digging in loose soil almost as fast as walking on the surface. The posterior gonopods of Dichromatobolus gen. nov. are unusually simple and well-rounded, displaying some similarities to the genera Corallobolus Wesener, 2009 and Granitobolus Wesener, 2009, from which the new genus differs in numerous other characters, e.g., size, anterior gonopods and habitus. Despite several attempts with fresh tissue samples and different primers, molecular barcoding did not work for Dichromatobolus gen. nov. Any relationships to the other 15 genera of Pachybolidae indigenous to Madagascar remain unknown.
Making agriculture sustainable is a global challenge. In the European Union (EU), the Common Agricultural Policy (CAP) is failing with respect to biodiversity, climate, soil, land degradation as well as socio‐economic challenges.
The European Commission's proposal for a CAP post‐2020 provides a scope for enhanced sustainability. However, it also allows Member States to choose low‐ambition implementation pathways. It therefore remains essential to address citizens' demands for sustainable agriculture and rectify systemic weaknesses in the CAP, using the full breadth of available scientific evidence and knowledge.
Concerned about current attempts to dilute the environmental ambition of the future CAP, and the lack of concrete proposals for improving the CAP in the draft of the European Green Deal, we call on the European Parliament, Council and Commission to adopt 10 urgent action points for delivering sustainable food production, biodiversity conservation and climate mitigation.
Knowledge is available to help moving towards evidence‐based, sustainable European agriculture that can benefit people, nature and their joint futures.
The statements made in this article have the broad support of the scientific community, as expressed by above 3,600 signatories to the preprint version of this manuscript. The list can be found here (https://doi.org/10.5281/zenodo.3685632).
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The arboreal click beetle fauna (Coleoptera: Elateridae) in a lowland tropical rainforest in southern Venezuela was observed and collected by means of a tower crane for a full year. The evaluation of the elaterid assemblage is part of a general survey of Coleoptera associated with several canopy trees. The Elateridae represented the tenth most species-rich beetle family in the canopy of the crane plot and was therefore selected for a detailed analysis of host-use patterns. In total, 20 species of Elateridae with 402 adult individuals were sampled, including seven singletons. Species were either flower visiting (Aeolus Eschscholtz and Cosmesus Candèze) or fed mainly on extrafloral nectaries (Chalcolepidius Eschscholtz, Crepidius Candèze, Lacon Castelnau, Lissomus Dalman, and Semiotus Eschscholtz). The most abundant species was Aeolus sp. 1 (N = 306) feeding on flowers of nine different host-tree species. This species was found often in high abundances during the entire flowering period of a single tree species with highest abundances coinciding with the maximum of open flowers. Aeolus sp. 1 was recorded almost every month of the year moving usually from one flowering tree species to another comprising possibly the entire local population. This species showed preferences between different tree species and occurred there only at night. Tree species that supported the most species-rich elaterid assemblages were Ruizterania trichanthera (Spruce ex Warm.) Marc.-Berti (Vochysiaceae) (N = 8) and Goupia glabra Aubl. (Goupiaceae) (N = 6). Only one elaterid species with at least two collected individuals was found restricted to one tree species.
Two new species of Carpophilus Stephens, 1829 in the subgenus Ecnomorphus Motschulsky, 1858 (Coleoptera: Nitidulidae) were recovered in material from the Caribbean. Descriptions and detailed diagnoses are provided for Carpophilus (Ecnomorphus) jamaicensis Powell and Schnepp, new species and Carpophilus (Ecnomorphus) thomasi Powell and Schnepp, new species. A key to the Carpophilus (Ecnomorphus) of the West Indies is appended.
Aim: Predicting future changes in species richness in response to climate change is one of the key challenges in biogeography and conservation ecology. Stacked species distribution models (S‐SDMs) are a commonly used tool to predict current and future species richness. Macroecological models (MEMs), regression models with species richness as response variable, are a less computationally intensive alternative to S‐SDMs. Here, we aim to compare the results of two model types (S‐SDMS and MEMs), for the first time for more than 14,000 species across multiple taxa globally, and to trace the uncertainty in future predictions back to the input data and modelling approach used.
Location: Global land, excluding Antarctica.
Taxon: Amphibians, birds and mammals.
Methods: We fitted S‐SDMs and MEMs using a consistent set of bioclimatic variables and model algorithms and conducted species richness predictions under current and future conditions. For the latter, we used four general circulation models (GCMs) under two representative concentration pathways (RCP2.6 and RCP6.0). Predicted species richness was compared between S‐SDMs and MEMs and for current conditions also to extent‐of‐occurrence (EOO) species richness patterns. For future predictions, we quantified the variance in predicted species richness patterns explained by the choice of model type, model algorithm and GCM using hierarchical cluster analysis and variance partitioning.
Results: Under current conditions, species richness predictions from MEMs and S‐SDMs were strongly correlated with EOO‐based species richness. However, both model types over‐predicted areas with low and under‐predicted areas with high species richness. Outputs from MEMs and S‐SDMs were also highly correlated among each other under current and future conditions. The variance between future predictions was mostly explained by model type.
Main conclusions: Both model types were able to reproduce EOO‐based patterns in global terrestrial vertebrate richness, but produce less collinear predictions of future species richness. Model type by far contributes to most of the variation in the different future species richness predictions, indicating that the two model types should not be used interchangeably. Nevertheless, both model types have their justification, as MEMs can also include species with a restricted range, whereas S‐SDMs are useful for looking at potential species‐specific responses.
We present an updated, subjective list of the extant, non-marine ostracod genera and species of the world, with their distributions in the major zoogeographical regions, as well as a list of the genera in their present hierarchical taxonomic positions. The list includes all taxa described and taxonomic alterations made up to 1 July 2018. Taxonomic changes include 17 new combinations, 5 new names, 1 emended specific name and 11 new synonymies (1 tribe, 4 genera, 6 species). Taking into account the recognized synonymies, there are presently 2330 subjective species of non-marine ostracods in 270 genera. The most diverse family in non-marine habitats is the Cyprididae, comprising 43.2% of all species, followed by the Candonidae (29.0%), Entocytheridae (9.1%) and the Limnocytheridae (7.0%). An additional 13 families comprise the remaining 11.8% of described species. The Palaearctic zoogeographical region has the greatest number of described species (799), followed by the Afrotropical region with 453 species and the Nearctic region with 439 species. The Australasian and Neotropical regions each have 328 and 333 recorded species, respectively, while the Oriental region has 271. The vast majority of non-marine ostracods (89.8%) are endemic to one zoogeographical region, while only six species are found in six or more regions. We also present an additional list with 'uncertain species', which have neither been redescribed nor re-assessed since 1912, and which are excluded from the main list; a list of taxonomic changes presented in the present paper; a table with the number of species and % per family; and a table with numbers of new species described in the 20-year period between 1998 and 2017 per zoogeographical region. Two figures visualize the total number of species and endemic species per zoogeographical region, and the numbers of new species descriptions per decade for all families and the three largest families since 1770, respectively.
Invasive plant species are increasingly altering species composition and the functioning of ecosystems from a local to a global scale. The grass species Pennisetum setaceum has recently raised concerns as an invader on different archipelagos worldwide. Among these affected archipelagos are the Canary Islands, which are a hotspot of endemism. Consequently, conservation managers and stakeholders are interested in the potential spreading of this species in the archipelago. We identify the current extent of the suitable habitat for P. setaceum on the island of La Palma to assess how it affects island ecosystems, protected areas (PAs), and endemic plant species richness. We recorded in situ occurrences of P. setaceum from 2010 to 2018 and compiled additional ones from databases at a 500 m × 500 m resolution. To assess the current suitable habitat and possible distribution patterns of P. setaceum on the island, we built an ensemble model. We projected habitat suitability for island ecosystems and PAs and identified risks for total as well as endemic plant species richness. The suitable habitat for P. setaceum is calculated to cover 34.7% of the surface of La Palma. In open ecosystems at low to mid elevations, where native ecosystems are already under pressure by land use and human activities, the spread of the invader will likely lead to additional threats to endemic plant species. Forest ecosystems (e.g., broadleaved evergreen and coniferous forests) are not likely to be affected by the spread of P. setaceum because of its heliophilous nature. Our projection of suitable habitat of P. setaceum within ecosystems and PAs on La Palma supports conservationists and policymakers in prioritizing management and control measures and acts as an example for the potential threat of this graminoid invader on other islands.
Polysyncraton Nott, 1892 is the second largest genus of didemnid ascidians; it has a wide distribution ranging from temperate to tropical waters. Seventy-one specimens of Polysyncraton from eight museum collections and recently collected samples were analyzed. This resulted in the description of three new species (P. cabofriense Oliveira & Rocha sp. nov. from Brazil, P. globosum Oliveira & Rocha sp. nov. from Australia and P. snelliusi Oliveira & Rocha sp. nov. from Suriname) and emended descriptions of three further species (P. amethysteum (Van Name, 1902), P. magnilarvum (Millar, 1962) and P. purou C. Monniot & F. Monniot, 1987).
Genomic sequencing and analysis of worldwide skipper butterfly (Lepidoptera: Hesperiidae) fauna points to imperfections in their current classification. Some tribes, subtribes and genera as they are circumscribed today are not monophyletic. Rationalizing genomic results from the perspective of phenotypic characters suggests two new tribes, two new subtribes and 50 new genera that are named here: Ceratrichiini Grishin, trib. n., Gretnini Grishin, trib. n., Falgina Grishin, subtr. n., Apaustina Grishin, subtr. n., Flattoides Grishin, gen. n., Aurivittia Grishin, gen. n., Viuria Grishin, gen. n., Clytius Grishin, gen. n., Incisus Grishin, gen. n., Perus Grishin, gen. n., Livida Grishin, gen. n., Festivia Grishin, gen. n., Hoodus Grishin, gen. n., Anaxas Grishin, gen. n., Chiothion Grishin, gen. n., Crenda Grishin, gen. n., Santa Grishin, gen. n., Canesia Grishin, gen. n., Bralus Grishin, gen. n., Ladda Grishin, gen. n., Willema Grishin, gen. n., Argemma Grishin, gen. n., Nervia Grishin, gen. n., Dotta Grishin, gen. n., Lissia Grishin, gen. n., Xanthonymus Grishin, gen. n., Cerba Grishin, gen. n., Avestia Grishin, gen. n., Zetka Grishin, gen. n., Turmosa Grishin, gen. n., Mielkeus Grishin, gen. n., Coolus Grishin, gen. n., Daron Grishin, gen. n., Barrolla Grishin, gen. n., Brownus Grishin, gen. n., Tava Grishin, gen. n., Rigga Grishin, gen. n., Haza Grishin, gen. n., Dubia Grishin, gen. n., Pares Grishin, gen. n., Chitta Grishin, gen. n., Artonia Grishin, gen. n., Lurida Grishin, gen. n., Corra Grishin, gen. n., Fidius Grishin, gen. n., Veadda Grishin, gen. n., Tricrista Grishin, gen. n., Viridina Grishin, gen. n., Alychna Grishin, gen. n., Ralis Grishin, gen. n., Testia Grishin, gen. n., Buzella Grishin, gen. n., Vernia Grishin, gen. n., and Lon Grishin, gen. n. In addition, the following taxonomic changes are suggested. Prada Evans is transferred from Hesperiinae to Trapezitinae. Echelatus Godman and Salvin, Systaspes Weeks, and Oenides Mabille are removed from synonymy and are treated as valid genera. The following genera are new junior subjective synonyms: Tosta Evans of Eantis Boisduval; Turmada Evans of Neoxeniades Hayward, Arita Evans of Tigasis Godman, and Alera Mabille of Perichares Scudder. Eantis pallida (R. Felder) (not Achlyodes Hübner), Gindanes kelso (Evans) (not Onenses Godman and Salvin), Isoteinon abjecta (Snellen) (not Astictopterus C. and R. Felder), Neoxeniades ethoda (Hewitson) (not Xeniades Godman), Moeris anna (Mabille) (not Vidius Evans), and Molo pelta Evans (not Lychnuchus Hübner) are new genus-species combinations. The following are species-level taxa: Livida assecla (Mabille) (not a subspecies of Livida grandis (Mabille), formerly Pythonides Hübner) and Alychna zenus (E. Bell) (not a junior subjective synonym of Alychna exclamationis (Mabille), formerly Psoralis Mabille); and Barrolla molla E. Bell (formerly Vacerra Godman) is a junior subjective synonym of Barrolla barroni Evans (formerly Paratrytone Godman). All these changes to taxonomic status of names are propagated to all names currently treated as subspecies (for species), subgenera (for genera) and synonyms of these taxa. Finally, taxa not mentioned in this work are considered to remain at the ranks and in taxonomic groups they have been previously assigned to.
The concept of the jumping spider genus Pochytoides Berland & Millot, 1941 is reviewed, based on the examination of described and undescribed species. Pochytoides is elevated from the subgeneric to the generic rank and a short diagnosis and description of the genus are presented. Redescriptions or descriptions of all species are provided together with a key to the species. Two new combinations are proposed: Pochytoides perezi (Berland & Millot, 1941) comb. nov. and P. poissoni (Berland & Millot, 1941) comb. nov. (both from Pochyta). Pochyta remyi Berland & Millot, 1941 originally placed in the subgenus Pochytoides is excluded; new combination Thiratoscirtus remyi (Berland & Millot, 1941) comb. nov. is proposed for it (but its generic status is uncertain). Six new species are described: Pochytoides monticola sp. nov., P. obstipa sp. nov., P. lamottei sp. nov., P. patellaris sp. nov., P. securis sp. nov. and P. spiniger sp. nov. The genus has a West African distribution.
A new species of the genus Birdantis Stål, 1863 (Hemiptera: Fulgoridae), B. bhaskarai sp. nov. from Larat Island (Tanimbar), is described. Birdantis collaris (Walker, 1870) stat. rev. and B. trilineata (Schmidt, 1926) stat. rev. are reinstated as valid species, respectively from status of subspecies and as junior synonym of B. delibuta Stål, 1863. These four species, as well as the other one previously described from the Maluku Islands, B. decens Stål, 1863, are illustrated from their type specimens. An identification key, a distribution map, illustrations of habitus and details of male genitalia are provided. The synonymy between Myrilla Distant, 1888 and Birdantis is formally reinstated and all species formerly placed in the subgenus Birdantis (Myrilla) are transferred to Birdantis sensu stricto. Birdantis is transferred to the subfamily Aphaeninae Blanchard, 1847 and now contains eighteen species distributed in Maluku (five species), New Guinea and neighbouring islands (ten species) and Australia
(three species).
The nesting biology of the potter wasp Pachymenes ghilianii (Spinola) (Hymenoptera: Vespidae: Eumeninae) is described based on observations made in the Cerro Turega Hydric Reserve, Penonome, Panama. The collection of building material, the architecture of the nest, the process of building a cell and cell provision with geometrid larvae (Lepidoptera: Geometridae), and the emergence time of the adults are recorded.
We present an abundance-based checklist of Pennsylvania planthoppers (Hemiptera: Auchenorrhyncha: Fulgoroidea) compiled from available literature and 13,718 specimens. A substantial portion of the latter were bycatch from Lindgren funnel and panel traps intended to intercept wood-boring beetle species, and a directed survey for the spotted lanternfly (Lycorma delicatula (White)). The known planthopper fauna of Pennsylvania consists of 10 families, 54 genera and 139 species including 34 new state species records (and 12 new genera). In an attempt to assess the level of completeness of this survey, we compiled an abundance-based checklist of planthopper species found in states adjacent to Pennsylvania and found similar numbers of planthopper species for each state (viz. Delaware 138 species, Maryland 147, New Jersey 145, New York 162 and Ohio 126), but the cumulative species list is comprised of 240 planthopper species, suggesting that the inventory for Pennsylvania and all adjacent states may be substantially incomplete.
Solenogastres (Aplacophora) is a small clade of marine, shell-less worm-molluscs with close to 300 valid species. Their distribution ranges across all oceans, and whereas the vast majority of species has been collected and described from the continental shelf and slope, only few species are known from depths below 4,000 m. Following traditional taxonomy, identification of specimens to species level is complex and time-consuming and requires detailed investigations of morphology and anatomy—often resulting in the exclusion of the clade in biodiversity or biogeographic studies. During the KuramBio expedition (Kuril-Kamchatka Biodiversity Studies) to the abyssal plain of the Northwest Pacific and the Kuril-Kamchatka Trench, 33 solenogaster specimens were sampled from 4,830 m to 5,397 m. Within this study we present an efficient workflow to address solenogaster diversity, even when confronted with a high degree of singletons and minute body sizes, hampering the use of single individuals for multiple morphological and molecular approaches. We combine analyses of external characters and scleritome with molecular barcoding based on a self-designed solenogaster specific set of mitochondrial primers. Overall we were able to delineate at least 19 solenogaster lineages and identify 15 species to family level and beyond. Based on our approach we identified three key lineages from the two regionally most species-rich families (Acanthomeniidae and Pruvotinidae) for deeper taxonomic investigations and describe the novel abyssal species Amboherpia abyssokurilensis sp. nov. (Cavibelonia, Acanthomeniidae) using microanatomical 3D-reconstructions. Our study more than doubles the previous records of solenogaster species from the Northwest Pacific and its marginal seas. Almost all lineages are reported for the first time from the region of the (Northwest) Pacific, vastly expanding distribution ranges of the respective clades. Moreover it doubles the number of Solenogastres collected from abyssal depths on a global scale and underlines the lack of exploratory α-diversity work in the abyssal zone for reliable species estimates in marine biodiversity.
Siamopsis gen. nov., described here, belongs to a group of genera with the right valve overlapping the left valve in the subfamily Cypridopsinae Kaufmann, 1900 of the family Cyprididae Baird, 1845. The distinguishing characters of the new genus are in the morphology of its valves and soft parts. The postero-dorsal margin of the internal left valve is plate-like protruded. The morphology of this plate varies in different species, e.g., some species bear a tooth-like tubercle on the plate. The posterior margin of the right valve is recurved inwardly at ca mid-height, resulting in the occurrence of a lobe-like expansion that can clearly be seen in the dorsal and caudal views of the carapace. In addition, the other diagnostic soft part features of the new genus are the cylindrical caudal ramus, the presence of two t-setae on the female A2 penultimate segment, the very elongated terminal segment of the Mx1 palp, the morphology of the two large bristles (tooth bristles) of the Mx1 third endite (one smooth, one serrated) and the absence of d-seta on T1. In the present paper, five new species are described under this new genus: Siamopsis renateae gen. et sp. nov., S. suttajiti gen. et sp. nov., S. conspecta gen. et sp. nov., S. khoratensis gen. et sp. nov. and Siamopsis planitia gen. et sp. nov. A key to the species of Siamopsis gen. nov. is also provided.
A new species of Ctilodes Murray, 1864 (Coleoptera: Nitidulidae) was recovered in material from Vietnam during a large study of Carpophilinae. A description and detailed diagnosis of Ctilodes clinei Powell and Duffy new species is presented here along with a key to identify all currently known species of Ctilodes.
Cette étude analyse les stratégies locales de dénomination des espèces végétales par les Mossé des régions du nord, du centre nord, du centre et du Plateau Central du Burkina Faso et leurs perceptions des plantes. A travers des interviews semi directes auprès de 1437 personnes âgées d’au moins 60 ans et des jeunes de moins de 40 ans des différentes localités, l’étude a pu montrer les critères de dénomination, les conceptions que les populations ont des espèces végétales ainsi que l‘impact de ces connaissances dans la conservation de la phytodiversité. 72 espèces au total ont été décrites. Elles sont réparties en 51 genres et 29 familles. Les familles dominantes sont les Commelinaceae et les Fabaceae-Mimosoideae. Dans la taxonomie locale faite sur les plantes en milieu rural Mossé, 16 critères sont utilisés. Les critères les plus cités par la population sont l’usage fait de la plante (94 %), le mysticisme lié à l’espèce (86 %), l’écologie ou le milieu de vie de l’espèce (83 %), la dualité mâle/femelle (83 %), la couleur des organes ou parties de la plante (81 %), l’origine de la plante (80 %), la morphologie foliaire (76 %), la présence d’organes saillants sur la plante (75 %) et le mode de dissémination des fruits ou des graines (74 %). Les noms botaniques attribués aux plantes varient d’une région à une autre. Les populations ont des perceptions vis-à-vis de nombreuses espèces. Ainsi, les espèces comme Stereospermum kunthianum, Calotropis procera, Ozoroa insignis, Faidherbia albida, Maytenus senegalensis et Biophytum umbraculum sont frappées de mysticisme. Elles sont toutes craintes par les populations et sont dans certaines localités à l’abri d’exploitations multiformes humaines. Cela contribue à une meilleure conservation de la biodiversité.
Ten new species belonging to three new genera (Atlantisina gen. nov., Bathycyclopora gen. nov., Calvetopora gen. nov.) of umbonulomorph bryozoans from northeastern Atlantic seamounts, islands, and the continental slope are introduced. We furthermore erect the new family Atlantisinidae fam. nov. for these genera. Eight new species belong to the new genus Atlantisina: Atlantisina atlantis gen. et sp. nov. (type species), A. acantha gen. et sp. nov., A. gorringensis gen. et sp. nov., A. inarmata gen. et sp. nov., A. lionensis gen. et sp. nov., A. meteor gen. et sp. nov., A. seinensis gen. et sp. nov., and A. tricornis gen. et sp. nov. The genus Bathycyclopora gen. nov. is introduced for ?Phylactella vibraculata Calvet from the Azores, and also includes Bathycyclopora suroiti gen. et sp. nov. The type species of Calvetopora gen. nov. is Lepralia inflata Calvet from the Gulf of Cadiz; this genus also includes Calvetopora otapostasis gen. et sp. nov. and another species left in open nomenclature. Of the 13 species described herein, 11 occur on seamounts and islands, and nine species are endemic to a single seamount, island or station. The present results show that bryozoans provide striking examples of the function of seamounts as areas of endemism, most likely intrinsically linked to the low dispersal abilities of bryozoan larvae.
Twelve new species are assigned to the genus Otitoma Jousseaume, 1898 in the family Pseudomelatomidae Morrison, 1966 and herein described: O. hadra sp. nov., O. neocaledonica sp. nov., O. rubiginostoma sp. nov and O. tropispira sp. nov. from New Caledonia; O. boucheti sp. nov., O. nereidum sp. nov. and O. sororcula sp. nov. from the Fiji Islands; O. xantholineata sp. nov. from the Solomon to the Fiji Islands; O. crassivaricosa sp. nov. from Fiji to Hiva Oa Island (Marquesas Archipelago); O. philpoppei sp. nov. from the Philippines but also reported from the Fiji Islands; O. elegans sp. nov. from the Fiji Islands and O. philippinensis sp. nov. from the Philippines. New data on O. carnicolor (Hervier, 1896) are provided. Otitoma mitra (Kilburn, 1986), from Southern Mozambique, is here considered a synonym of O. cyclophora (Deshayes, 1863). Drillia batjanensis Schepman, 1913, previously assigned to the genus Maoritomella Powell, 1942 in the family Borsoniidae Bellardi, 1875, is here assigned to the genus Otitoma. Photographs of the holotype of Drillia batjanensis are provided for the first time. In addition, color photographs of the type specimens of the following species are provided: Drillia kwandangensis Schepman, 1913, D. timorensis Schepman, 1913 and Mitrellatoma mitra Kilburn, 1986.
Two new species of hangingflies, Terrobittacus rostratus sp. nov. and Terrobittacus angustus sp. nov., are described and illustrated from Yunnan, southwestern China, increasing the species number of Terrobittacus Tan & Hua, 2009 to six. Terrobittacus rostratus sp. nov. differs from its congeners by wings devoid of markings and epandrial appendages slightly longer than half the length of the gonocoxites. Terrobittacus angustus sp. nov. can be recognized by wing markings along R5 distally. A key to species of the genus is updated to include the two new species.
Elevational gradients in high mountain ranges are particularly suitable to study and understand patterns and drivers of plant community diversity and composition, yet there are only few studies that explicitly addressed this topic for the European Alps. Here we analysed an elevational gradient in grasslands of the Gran Paradiso National Park (NW Italy) from c. 1,700 to 3,100 m a.s.l. We recorded vascular plant species composition in 13 100-m² plots, each with two series of nested subplots from 0.0001 to 10 m², as well as a set of environmental parameters (topography, soil). Beta-diversity was assessed via the z-values of power-law species-area relationships, both across all plot sizes and from one plot size to the next bigger one. Diversity-environment relationships were assessed with multi-model inference based on Akaike information criterion (AIC), while scale dependence in z-values across plot sizes was analysed with an ANOVA. Life forms and three major functional traits (specific leaf area = SLA, canopy height, seed mass) were derived from trait databases to calculate fractions of life forms and community-weighted means for the metric traits. Species richness on 100 m² ranged from 17 to 65, with a mean of 43.5. The z-values were within a typical range known for European grasslands (mean: 0.227), with non-significant scale dependence. The importance of environmental factors for richness changed across grain sizes, with inclination (positive effect), mean soil depth and soil skeleton content (both: negative effect) being most influential at grain sizes of 0.0001–1 m². By contrast, soil pH was most important (with a unimodal relationship) for 10 and 100 m². After account-ing for the other environmental factors, elevation showed a moderate unimodal relationship only for the two largest grain sizes. By contrast, functional composition showed strong and mostly significant rela-tionships with elevation: hemicryptophytes and geophytes became rarer and chamaephytes more fre-quent, while community-weighted means of SLA, canopy height and seed mass decreased. Our findings highlight the scale dependence of biodiversity patterns, thus pointing to the need of multi-scale sampling to reach comprehensive understanding. Further, we could provide one of the first documentations of biodiversity and functional composition along an elevational gradient in the Alps, some in agreement with expectations, others not. This suggests that more extensive studies with a similar design in this and other regions of the Alps could be a valuable contribution to the understanding of how environmental factors drive components of biodiversity as well a functional community assembly.
The spider diversity of the family Anyphaenidae in premontane, low evergreen montane and cloud forest from the Chocó region of Ecuador is examined. A total of 287 adult specimens were collected and 19 morphospecies were identified based on male specimens. Thirteen new species are described and one new genus is proposed. Five new species are described in the genus Katissa Brescovit, 1997: Katissa kurusiki sp. nov., K. puyu sp. nov., K. tamya sp. nov., K. yaya sp. nov. and K. guyasamini sp. nov. The new genus Shuyushka gen. nov. is proposed and includes three species: Shuyushka achachay gen. et sp. nov., S. moscai gen. et sp. nov. and S. wachi gen. et sp. nov. Finally, five species are described in the genus Patrera Simon, 1903: P. hatunkiru sp. nov., P. philipi sp. nov., P. suni sp. nov., P. shida sp. nov. and P. witsu sp. nov. New records are provided for Patrera fulvastra Simon, 1903 and Josa nigrifrons Simon, 1897.
Harpactea dufouri (Thorell, 1873) was collected in the Gavarres protected natural area in Catalonia, Spain. The specimens were compared with specimens from Mallorca, Balearic Islands,
and found to be conspecific. The female of the species is described here for the first time. The new finding proves that Harpactea dufouri occurs outside the Balearic Islands. The species, however, may be endemic to Catalonia.
Diplura C.L. Koch, 1850 is a mygalomorph genus with putative records from Central and South America. The type-species Diplura macrura (C.L. Koch, 1841), originally described from West Indies, is poorly known and represented only by its holotype. Most of the 20 species currently included in the genus lack modern taxonomic descriptions, as D. lineata (Lucas, 1857), from Rio de Janeiro state, Brazil. Males and females of Diplura macrura and D. lineata are herein redescribed. New junior synonyms of D. macrura are identified (Linothele bicolor (Simon, 1889), Diplura uniformis Mello- Leitão, 1923, and the two junior synonyms of the latter species, Thalerothele minensis Mello-Leitão, 1926 and T. aurantiaca Mello-Leitão, 1943). Also, two junior synonyms are established for D. lineata: Diplura fasciata (Bertkau, 1880) and Diplura nigridorsi (Mello-Leitão, 1924). The type-locality of D. macrura is corrected to São João del Rei, Minas Gerais state, Brazil. D. macrura is restricted to the state of Minas Gerais and D. lineata to the state of Rio de Janeiro. The type-locality of D. parallela (Mello-Leitão, 1923) is also corrected from Argentina to Paraná state, Brazil. The distribution of Diplura is now restricted from south Panama to north Argentina, excluding previous erroneous records for Cuba and West Indies. The six synonymies herein established help to clarify the genus composition, which includes now 17 valid species.
The salticid genera Bristowia Reimoser, 1934, Habrocestum Simon, 1876 and Macaroeris Wunderlich 1992 are reported from Sri Lanka for the first time. One new species of Bristowia, B. gandhii sp. nov. (♂♀), and three new species of Habrocestum, H. hantaneensis sp. nov. (♂♀), H. kodigalaensis sp. nov. (♂♀) and H. ohiyaensis sp. nov. (♂), are described and diagnosed. The male of Macaroeris nidicolens Walckenaer, 1802 is redescribed and illustrated, based on new material from Sri Lanka.
Termites are important ecosystem engineers of the savanna biome, with the large mounds of fungus-cultivating termites being sources of habitat heterogeneity and structural complexity in African savanna landscapes. Studies from different localities throughout Africa have shown that termite mounds have a strong influence of diversity and composition of plant communities. However, most research has been conducted only at the local scale, and integrating knowledge across Africa is hampered by different methodology of studies and differing environmental context. Little is known about the variation in vegetation composition on termite mounds compared to the surrounding savanna at the regional scale and at the landscape scale, and the main determinants of plant communities on mounds are yet to be ascertained.
This thesis aimes at better understanding the influence of termite mounds on vegetation compared to the surrounding savanna across spatial scales. Three research projects analyse vegetation data and soil data from paired mound and savanna plots in West Africa. The first project examines the influence of termite-induced heterogeneity on plant diversity and vegetation composition at a regional scale, following a bioclimatic gradient from the Sahel of Burkina Faso to the Sudanian vegetation zone in North Benin. The second Project analysed variation of vegetation on and off mounds at the landscape scale in Pendjari National Park, North Benin. The third is a monitoring study over the course of two years, exploring dynamics of juvenile woody plant communities on mounds and in the surrounding savanna at a local scale. The thesis thus provides the first comparative quantitative analysis across scales of mound and savanna vegetation and the drivers of the mound–savanna difference in vegetation.
Synthesizing across scales, its results confirm that termite mounds strongly contribute to savanna plant diversity, even though mounds are not generally more species rich than the surrounding savanna. Variation in mound vegetation is much higher along climatic and soil gradients than previously acknowledged. Mound vegetation differs from the surrounding savanna in the whole study area and in each sampled savanna type, with the strongest differences occurring at the most humid study sites. A large proportion of the differences between mound and savanna vegetation is explained by clay enrichment and related soil factors, such as cation concentrations. Plants on mounds thus benefit from favourable soil conditions, including higher fertility and higher water availability, which is also mirrored by the higher abundance and basal area of juvenile woody plants found on mounds. The variation in mound vegetation between study sites across scales results in part from local differences in soil composition and from climatic differences that influence the regional distribution of species. Different sets of characteristic mound species are identified in each project. Specific plant families and traits like succulency, lianescence, and adaptations to zoochory are found to be overrepresented in mound communities.
In addition to the findings in this thesis, remaining parts of the variation in mound vegetation between study sites could likely be explained by investigating further factors. Specifically, mound vegetation depends on habitat context, which includes available species pools, spatial distribution of mounds, biotic interactions with dispersers and herbivores, fire, and also anthropogenic influence. The high proportion of species with adaptations to zoochory found on mounds, for example, indicates that animal dispersers should be of particular importance for vegetation on termite mounds. Herbivory and fire regime, which are known to contribute to the diversity and community composition of the mound–savanna system, also show strong local variation, not least because of anthropogenic influence.
In conclusion, termite mounds play a crucial role in maintaining heterogeneity and plant diversity in the savanna across scales. Ecosystem services provided by termites, especially considering long-term effects on soil fertility and ecosystem resilience, are most likely undervalued. Mounds should be considered in management plans from local to regional, transnational scales as a matter of course, accompanied by further research on the role of termite mounds in savanna ecology on a longer temporal scale. The research presented here thus provides a basis for future studies on termite mound vegetation that should specifically consider the biotic and abiotic context of the mound–savanna system.
Four species of Bradysia Winnertz (Diptera, Sciaridae) from the Northern Holarctic are described and illustrated for the first time: Bradysia bigeminata sp. nov. (Finland, Canada), B. falciceps sp. nov. (Finland, Canada), B. oelandica sp. nov. (Sweden) and B. plusiospina sp. nov. (Finland). A few Bradysia species, described previously and now found in Northern Europe, are also redefined and illustrated.
The ostracod genus Bennelongia De Deckker & McKenzie, 1981 occurs in Australia and New Zealand. We redescribe B. nimala from the Northern Territory and describe six new species from Western Australia belonging to the B. nimala (five species) and B. triangulata sp. nov. (one species) lineages: B. tirigie sp. nov., B. koendersae sp. nov., B. pinderi sp. nov., B. muggon sp. nov., B. shieli sp. nov. and B. triangulata sp. nov. For six of these seven species, we could construct molecular phylogenies and parsimonious networks based on COI sequences. We tested for specific status and for potential cryptic diversity of clades with Birky’s 4 theta rule. The analyses support the existence of these six species and the absence of cryptic species in these lineages. Bennelongia triangulata sp. nov. is a common species in the turbid claypans of the Murchison/Gascoyne region. Bennelongia nimala itself is thus far known only from the Northern Territory. Bennelongia tirigie sp. nov., B. pinderi sp. nov. and B. muggon sp. nov. occur in the Murchison/Gascoyne region, whereas B. koendersae sp. nov. and B. shieli sp. nov. are described from the Pilbara. With the six new species described here, the genus Bennelongia now comprises 31 nominal species.
The study of the Portuguese marine ichthyofauna has a long historical tradition, rooted back in the 18th Century. Here we present an annotated checklist of the marine fishes from Portuguese waters, including the area encompassed by the proposed extension of the Portuguese continental shelf and the Economic Exclusive Zone (EEZ). The list is based on historical literature records and taxon occurrence data obtained from natural history collections, together with new revisions and occurrences. It comprises a total of 1191 species, distributed among 3 superclasses, 4 classes, 42 orders, 212 families and 617 genera. If considering only the EEZ and present territorial waters, this list represents an increase of 230 species (27.8%) and of 238 species (29.0%), when compared to the information available in FishBase (2012) and in the last checklist of marine and estuarine fishes of Portugal (1993), respectively. The order Perciformes shows the highest diversity, with 54 families, 162 genera and 299 species. Stomiidae (80 species), Myctophidae (71 species) and Macrouridae (37 species) are the richest families. From the listed species, 734 are present off mainland Portugal, 857 off the Azores and 766 off Madeira. Within the limits of the examined area, three species are reported for the first time in mainland Portugal and twenty-nine records are identified as doubtful. A total of 133 species have been recorded from the extended Portuguese continental shelf (2 off mainland Portugal, 117 off the Azores and 14 off Madeira), two of which are common to the Azores and Madeira extensions. Biogeographically, the Atlantic group is the most important (548 species – 46.01%), followed by the Lusitanian group (256 species – 21.49%), the African group (71 species – 5.96%), the Boreal group (34 species – 2.85%), the Mediterranean group (31 species – 2.60%), the Macaronesian group (21 species – 1.76%), the Atlantic/African group (19 species – 1.60%) and the Mediterranean/African and the Arctic groups, each with only 1 species (0.08%). Regarding the preferences for vertical habitat, the demersal fishes are the most important group (305 species – 25.61%), followed by the mesopelagic group (228 species – 19.14%), the bathypelagic group (164 species – 13.77%), the benthopelagic group (147 species – 12.34%), the bathydemersal group (115 species – 9.66%), the reef-associated group (88 species – 7.39%), the pelagic group (74 species – 6.21%), the epipelagic group (58 species – 4.87%) and 1 species (0.08%) of the benthic group. The oceanic habitat is the best represented group comprising 446 species (37.45%), followed by the shelf group (199 species – 16.71%), the slope group (164 species – 13.77%), the inner shelf group (89 species – 7.47%), the coastal group (70 species – 5.88%), the outer shelf group (29 species – 2.43%) and the oceanic/shelf group (7 species – 0.59%).
Flächenbezogene Artenzahlen sind besonders im Kontext von Monitoringprojekten grundlegend für die Beurteilung von Veränderungen der Biodiversität. Diese Studie vergleicht die von neun Bearbeitern (5 Einzelbearbeiter, 2 Zweierteams) erfasste Zahl an Gefäßpflanzenarten bei Vegetationserhebungen auf markierten Flächen von 4, 100 und 400 m2 Größe in einem artenreichen Kalkbuchenwald im Göttinger Stadtwald. Dabei wurden Bearbeiter- und Zeiteffekte untersucht, sowie artspezifische Übersehensraten, Fehlbestimmungsraten und Ungenauigkeiten bei der Zuordnung von Pflanzenindividuen zur jeweiligen Aufnahmefläche (Fehlzuordnungsraten) abgeschätzt.
Protokollierte Fragen ließen keine systematischen Unterschiede bei der Vertrautheit der Bearbeiter mit der Vegetation vor Ort erkennen, so dass Ausbildung und Erfahrung für gefundene Unterschiede ausschlaggebend sein dürften. Bei den 4 m2 großen Erhebungseinheiten ergaben sich bei der Artenzahl relative Abweichungen der Bearbeiter vom Erwartungswert von 8 bis 26 % (1 bis 4 Arten absolut). Diese waren bei den 100 m2 großen Erhebungseinheiten mit 9 bis 27 % (2 bis 6 Arten absolut) höher. Mit zunehmender Flächengröße nahm der Flächenidentitätseffekt tendenziell ab und der Bearbeitereffekt signifikant zu. Bei den 100 m2 großen Flächen hatte eine längere Bearbeitungszeit einen positiven Effekt auf die Artenzahl.
Mit Hilfe artbezogener Auswertungen wurden Übersehens-, Fehlbestimmungs- und Fehlzuordnungsraten ermittelt. Nicht eine Art wurde von allen Bearbeitern auf allen Flächen gefunden, auf denen sie jeweils auftrat. Schwer differenzierbare Arten sowie Arten in ungünstigen Entwicklungsstadien wiesen höhere Übersehens-, aber auch höhere Fehlbestimmungsraten auf. Bei morphologisch gut charakterisierten Arten wurde bei Einzelfunden von einer Fehlzuordnung zur Erhebungseinheit ausgegangen.
Die erzielten Ergebnisse sind auch für andere Projekte zur Erfassung der Biodiversität relevant und Bemühungen zur Reduzierung entsprechender Bearbeitereffekte sollten unternommen werden. Eine organisatorische Einbindung entsprechender Bemühungen wird vorgeschlagen.
Results of an Odonata survey carried out in the peatlands of Central Kalimantan, Indonesia, in 2012
(2014)
The results of a survey of Odonata (dragonflies and damselflies) in the peat lands of Central Kalimantan, Indonesia, in 2012 are presented. Fifty four species of Odonata found in the area in June-July 2012 are listed, along with brief notes and the locations in which they were found. Of the species found, twelve had not been recorded in Central Kalimantan previously, and of these at least four are completely new to science. Six species, originally described from Central Kalimantan and not recorded any- where since 1953, were rediscovered. At least sixteen of the species found during the survey are considered to be of conservation concern. The discovery of at least four new species to science in a relatively short survey indicates a high probability of occurrence of many more species that are awaiting discovery, and that many un-discovered species may be lost or highly threatened because of the rapid demise of peat swamp forest habitats. A checklist of the Odonata known from Central Kalimantan is provided in an appendix.
Dynamics of juvenile woody plant communities on termite mounds in a West African savanna landscape
(2014)
Termites are keystone species in savanna ecology, and their mounds are thought to be an important source of habitat heterogeneity and structural complexity of the savanna. Macrotermes termitaria have been shown to allow woody plant colonisation of landscapes otherwise dominated by C4 grasses. In this study, we assess how resource-rich Macrotermes mounds affect juvenile woody plant and non-woody plant species diversity, community composition, biomass and population dynamics. We repeatedly sampled paired termite mound and savanna plots in Pendjari National Park (Sudanian vegetation zone, North Benin, West Africa) over the course of two years. Despite considerable overlap in their species pools, plant communities of mound and savanna plots were clearly separated in ordinations. Species richness and diversity of juvenile woody plants was consistently higher on termite mounds, while no differences could be detected for non-woody plants. Evenness of juvenile woody plants was generally lower on mounds, whereas density and basal area were higher on mounds. In contrast, we did not detect any influence of the mound microhabitat on colonisation, mortality and turnover of woody juveniles. Therefore, we suggest that differences in the communities on and off mounds should be strongly influenced by directed diaspore dispersal through zoochory.
Auf dem Plateau des Göttinger Waldes wurden 1980 12 ha eines artenreichen, heute etwa 145 Jahre alten, submontanen Kalkbuchenwaldes (Hordelymo-Fagetum lathyretosum) für ein Ökosystemforschungsprojekt eingezäunt. In diesem Bereich wurde ein großer Transekt (GT) von 2,81 ha mit 281 10x10m-Quadraten als Dauerfläche zur Untersuchung der natürlichen Vegetationsentwicklung ausge-wählt. Von 1981 bis 2011 wurden alle 10 Jahre Flora und Vegetation sehr detailliert in allen Quadraten erfasst (Schichtung, Deckungsgradschätzung aller Arten in %, Vegetationskartierung). Die Ergebnisse werden in Tabellen der Krautschicht, in quantitativen Verteilungskarten einzelner Arten und in Vegetationskarten dargestellt. – Schon in den ersten 10 Jahren hatte sich teilweise eine Strauchschicht, vor-wiegend aus jungen Bäumen, entwickelt. Auch in der Krautschicht gab es deutliche Veränderungen. Eine Frequenztabelle aller 83 gefundenen Arten (Tab. 1) zeigt zahlreiche Pflanzen (33) mit Abnahme-tendenz, dazu einen Grundstock konstanter Arten. Deutlich zugenommen haben nur Allium ursinum, Cardamine bulbifera, Dryopteris carthusiana, Hedera helix und Neottia nidusavis. Für die Vegetationskartierung wurden verschiedene Einheiten nach Dominanz oder Mischung einzelner Arten benutzt, mit den Schlüsselarten Aconitum lycoctonum, Allium ursinum, Anemone nemorosa und Mercurialis perennis. – Insgesamt war lange Zeit der Antagonismus von Allium (deutliche Zunahme) und Mer-curialis (starke Abnahme) besonders auffällig. So hat sich auch der Allium ursinum-Dominanztyp über 30 Jahre stark ausgedehnt. Während sich kleinflächig in den Quadraten (Mikroskala) deutliche Veränderungen der Artenzusammensetzung zeigten, war im gesamten Bestand (Mesoskala) teilweise auch floristische Konstanz zu erkennen. – In der Diskussion werden mögliche Ursachen für die festgestellten Veränderungen erörtert. Neben lokalen Wirkungen wie Einzäunung oder der Konkurrenzkraft von Allium ursinum lassen sich im Literaturvergleich großräumig wirksame Faktoren erkennen. Seit langem vollzieht sich vor allem in forstlich wenig oder gar nicht beeinflussten Laubwäldern eine Verdichtung des Kronendaches mit Ausbildung eines stärker schattig-luftfeuchten Mikroklimas. Seit einigen Jahrzehnten können stärkere Stickstoffeinträge für nährstoffliebende Arten wirksam sein. In den letzten 20 Jahren lassen sich zunehmend Auswirkungen einer Klimaerwärmung erkennen, z. B. eine Verlängerung der Vegetationsperiode. Als neues Phänomen wird das Eschentriebsterben durch Pilzbefall beschrieben.
The ostracod genus Bennelongia De Deckker & McKenzie, 1981 is endemic to Australia and New Zealand. Extensive sampling in Western Australia (WA) revealed a high specific and largely undescribed diversity. Here, we describe seven new species belonging to the B. barangaroo lineage: B. timmsi sp. nov., B. gnamma sp. nov., B. hirsuta sp. nov., B. ivanae sp. nov., B. mcraeae sp. nov., B. scanloni sp. nov. and B. calei sp. nov., and confirm the presence of an additional species, B. dedeckkeri, in WA. For five of these eight species, we could construct molecular phylogenies and parsimonious networks based on COI sequences. We also tested for cryptic diversity and specific status of clusters with a statistical method based on the evolutionary genetic species concept, namely Birky’s 4 theta rule. The analyses support the existence of these five species and a further three cryptic species in the WA B. barangaroo lineage. The molecular evidence was particularly relevant because most species described herein have very similar morphologies and can be distinguished from each other only by the shape, size and position of the antero-ventral lapel on the right valve, and, in sexual populations, by the small differences in shape of the hemipenes and the prehensile palps in males. Four species of the WA B. barangaroo lineage occur in small temporary rock pools (gnammas) on rocky outcrops. The other four species are mainly found in soft bottomed seasonal water bodies. One of the latter species, B. scanloni sp. nov., occurs in both claypans and deeper rock pools (pit gnammas). All species, except for B. dedeckkeri, originally described from Queensland, have quite clearly delimited distributions in WA. With the seven new species described here, the genus Bennelongia now comprises 25 nominal species but several more await formal description.
It is common knowledge that plants have been the world-wide most important source of medicines and that they still play this role in developing countries. However, up to now, complete lists of medicinal and aromatic plants (MAP) exist for comparatively few countries. A review of all lists know to the authors reveals the following results: A total of 20.7 % of the plant species analyzed by either publications or own research are or were used as MAP. However, regarding single countries, the differences are considerably high. Absolutely leading the list are China (36.2 %), Burkina Faso (35.2 %) and the Korean Republic (34.5 %). Also ahead of other countries or regions are the North of Benin (32.8 %) and the entire Pakistan (30.3 %). Still above average rank Great Britain (26.7 %) and Nepal (23.3 %), while the figures for Bul¬garia (21.0 %), Germany (20.2 %) and France (19.4 %) almost represent the average. Jordan (17.3 %), Vietnam (17.1 %), Sri Lanka (16.6 %), India (16.1 %) and Thailand (15.5 %) rank slightly beneath. Clearly below the average are the percentages of MAP for Hungary (12.2 %) and the USA (11.8 %). The average numbers of MAP in the Philippines (9.5 %) and Malaysia (7.7 %) fall far behind. Calculated on a worldwide scale, every fifth plant can be regarded as MAP. This number matches that from Bulgaria, France and Germany. In northern Benin, Burkina Faso, Korea, China and Pakistan, however, every third plant is or was used as MAP, whereas in Hungary and the USA only every eighth plant can be regarded as MAP. This number drops even further for the Philippines ore Malaysia where only every tenth or thirteenth plant can be attributed to medicinal or aromatic use. These differences might be due to various factors. A geographical component of the results is obvious: in most cases geographically close countries show similar percentages. A correlation between the total number of species and the fraction of those used as MAP cannot be confirmed. The countries with percentage of MAP > 30 % in common show that they belong either entirely (Burkina Faso, Benin) or at least in their rural areas to the poorest countries of the world so that it is (was) impossible for the majority of the people to buy "modern" MAP. In those countries the number of traditional healers outnumbers largely the number of modern doctors. Therefore, the tradition of folk medicine was maintained until today. Additionally, China, Korea and partially Pakistan have a very old and well documented tradition of folk medicine. Due to this documentation even in areas where today "modern MAP" are used, the knowledge was not lost. In neighboring countries or regions, which differ with respect to a more arid or a more humid climate, for the arid country (region) more MAPs are reported than for the humid one. The potential reasons for this phenomenon are discussed in the paper. For many countries the percentage given for MAP in literature is too low. But even these low values represent a striking argument for the importance of a world-wide conservation of biodiversity.
New Zealand species of Iphimediidae, Amphipoda, are revised. Based on new material from the Chatham Rise, east of New Zealand, two new species are described in detail: Labriphimedia meikae sp. nov. and Labriphimedia martinae sp. nov. A key to the six species belonging to three genera of New Zealand Iphimediidae is provided.
Australia is predicted to have a high number of currently undescribed ostracod taxa. The genus Bennelongia De Deckker & McKenzie, 1981 (Crustacea, Ostracoda) occurs in Australia and New Zealand, and has recently shown potential for high speciosity, after the description of nine new species from Western Australia. Here, we focus on Bennelongia from eastern Australia, with the objectives of exploring likely habitats for undiscovered species, genetically characterising published morphological species and scanning classical species for cryptic diversity. Two traditional (morphological) species are confi rmed to be valid using molecular evidence (B. harpago De Deckker & McKenzie, 1981 and B. pinpi De Deckker, 1981), while three new species are described using both morphological and molecular evidence. Two of the new species belong to the B. barangaroo lineage (B. dedeckkeri sp. nov. and B. mckenziei sp. nov.), while the third is a member of the B. nimala lineage (B. regina sp. nov.). Another species was found to be genetically distinct, but is not formally described here owing to a lack of distinguishing morphological features from the existing species B. cuensis Martens et al., 2012. Trends in diversity and radiation of the genus are discussed, as well as implications these results have for the conservation of temporary pool microfauna and our understanding of Bennelongia’s evolutionary origin.
Three different male and female super-specific types are distinguished according to variations in the morphology of the bulb and spermathecae within the genus Nemesia Audouin, 1826. Plotting the distributions of these sexual types on a map of the Mediterranean indicates the existence of geography-related sub-generic diversity in which the Nemesia fauna of the eastern Mediterranean differs markedly from that of the western Mediterranean. While the eastern Mediterranean Nemesia fauna is highly homogeneous, the fauna of the western Mediterranean is very diverse. The eastern and western Nemesia faunae appear to overlap in the central Mediterranean. Efforts to relate the specific bulb types to the particular types of spermathecae described here were only partly successful.
The genus Bennelongia De Deckker & McKenzie, 1981 is most likely endemic to Australia and New Zealand and, up to now, only two described species in this genus had been reported from Western Australia. Extensive sampling in Western Australia revealed a much higher specifi c diversity. Here, we describe nine new species in three lineages, within the genus Bennelongia: B. cygnus sp. nov. and B. frumenta sp. nov. in the B. cygnus lineage, B. gwelupensis sp. nov., B. coondinerensis sp. nov., B. cuensis sp. nov., B. lata sp. nov. and B. bidgelangensis sp. nov. in the B. australis lineage, and B. strellyensis sp. nov. and B. kimberleyensis sp. nov. (from the Pilbara and Kimberley regions respectively) in the B. pinpi-lineage. For six of the nine species, we were also able to construct molecular phylogenies and to test for cryptic diversity with two different methods based on the evolutionary genetic species concept, namely Birky’s 4 x rule and the GYMC model. These analyses support the specifi c nature of at least four of the fi ve new species in the B. australis lineage and of the two new species in the B. pinpi lineage. We also describe Bennelongiinae n.subfam. to accommodate the genus. With the nine new species described here, the genus Bennelongia now comprises 15 species, but several more await formal description.
The continuous decline in biodiversity in some European landscapes has led recently to the (re-) implementation of low-intensity grazing systems as an alternative to more cost-intensive conservation practices. This approach aims at developing habitat complexes comprising various successional stages and increasing plant species diversity on local (a-diversity) and landscape scales (b-, y-diversity). The primary objectives of this review were to uncover ecological processes in which large domestic herbivores (cattle, equids, sheep, goats, pigs) have a key function in affecting plant diversity and to provide a framework for future research and conservation practices. The reviewed literature covers a wide range of ecosystem types in various temperate regions of Europe with a main focus on recent results from Central Europe. Low-intensity grazing enhances existing environmental gradients and generates manifold disturbance patterns on various spatial scales resulting in high habitat diversity. Livestock trampling has a so far underestimated impact on plant species composition and richness. Additionally, selective herbivore behavior facilitates the coexistence of plant species representing different functional types including a considerable number of threatened and grazing-sensitive species. Co-occurrence of progressive and regressive successional processes on low-intensive pastures results in a high b- and y-diversity, an effect that has been observed soon after the (re-)implementation of grazing. Persistence of speciespoor successional stages of dominant competitive graminoid and herb species can in many cases be inhibited by grazing. Large domestic herbivores serve as effective vectors for the dispersal of diaspores, thus improving the connectivity of isolated plant populations. There is a combined effect of diaspore dispersal and microsite creation which can increase the probability of diaspores to successfully germinate and establish. Overall, low-intensity grazing represents a highly flexible concept to maintain and restore plant diversity in cultivated landscapes; general management implications are given.
Naturschutzfachlich wertvolles extensiv genutztes Feuchtgrünland der Auen ist durch Maßnahmen des Gewässerausbaus, des Hochwasserschutzes sowie durch Entwässerung und Melioration in Mitteleuropa sehr selten geworden. Renaturierungsmaßnahmen von Gewässern und Auen werden in der jüngeren Vergangenheit gezielt eingesetzt, um die gefährdeten Tier- und Pflanzenarten des offenen Feuchtgrünlandes zu fördern. Dabei werden häufig ehemals intensiv genutzte Wiesen renaturiert. Die Frage des Flächenmanagements nach der Wiedervernässung ist sowohl aus praktischer und ökonomischer als auch aus naturschutzfachlicher Sicht wichtig. Eine extensive Beweidung ist auf den wiedervernässten Auestandorten oft praktikabler als eine Mahdnutzung, aber durch die Umstellung der Nutzung aus naturschutzfachlicher Sicht oft umstritten. Im Rahmen der vorliegenden Studie werden unterschiedliche Landnutzungsregime für Feuchtgrünland in der Luxemburger Syr-Aue sechs Jahre nach der Wiedervernässung durch ein Renaturierungsprojekt vegetationsökologisch verglichen. Ziel ist es, Unterschiede in der Vegetationszusammensetzung zwischen den Nutzungsvarianten der extensiven Beweidung, der einschürigen Mahd mit Beweidung und der zweischürigen Mahd zu analysieren und Rückschlüsse für ein künftiges Management von wiedervernässtem Auengrünland zu ziehen. Entlang der Nutzungsgrenze Weide – Mahdflächen wurden anhand von gepaarten Probeflächen, die standörtlich ähnliche Verhältnisse gewährleisten sollten, Vegetationsaufnahmen durchgeführt. Neben Parametern der floristischen Diversität und Seltenheit wurden die gewonnenen Vegetationsdaten mit Hilfe von Zeigerwerten und funktionallen Arteigenschaften analysiert. Eine NMDS-Ordination unterscheidet die Vegetationszusammensetzung der Nutzungsvarianten entlang einer Dimension signifikant voneinander. Haupteinflussfaktor ist hier die unterschiedliche Nutzung. Auf den untersuchten Weideflächen konnten insgesamt im Vergleich zu den Mahdflächen mehr Arten beobachtet werden. Die durchschnittlichen Artenzahlen, Diversitätsindizes und strukturellen Vegetationsparameter pro Aufnahmeeinheit deuten auf eine größere räumliche Heterogenität der Vegetation unter den Nutzungseinflüssen der Weidetiere hin. Bei den seltenen und naturschutzrelevanten Pflanzenarten konnten keine signifikanten Unterschiede zwischen den Varianten nachgewiesen werden. Dagegen unterscheiden sich die Arteigenschaften der vorkommenden Pflanzenarten der zweischürigen Wiesen von der Standweide im Hinblick auf die Lebensformen, den Reproduktionstyp und den Blühbeginn bereits signifikant voneinander. Die Ergebnisse dieser Studie decken sich nicht mit dem beobachteten Artenrückgang durch einen Bewirtschaftungswechsel von Mahd zu Beweidung, der bei verschiedenen Vergleichsstudien auf anderen Stand orten von Mahd- und Weidenutzungen festgestellt wurde. Die extensive Mahd- und Weidenutzung im Syrtal kommt historischen Bewirtschaftungsformen im Gebiet sehr nahe, die zunehmend zur Erhaltung und Entwicklung von artenreichen Habitattypen gefordert werden. Die unterschiedlichen Nutzungsregime ergänzen sich im Syrtal auf engstem Raum und bieten Habitatnischen für Pflanzenarten mit unterschiedlichen Ansprüchen.
Die Kartierung von 25 Arten der Pilzgattung Hygrocybe im Großraum Trier während der Herbstmonate 2010 hat klar gezeigt, dass die meisten sehr eng an mageres altes Grasland gebunden sind. Durch die genaue Kenntnis der Verbreitung solcher Mähwiesen war es möglich, auf 16 Topographischen Karten (1:25.000) einen großen Teil der Vorkommen auf 165 Wiesen zu dokumentieren. Da dieses Magergrasland durch Nutzungsänderungen und N-Eintrag aus der Atmosphäre stark gefährdet ist, sind neben den dort lebenden Pflanzen und Tieren auch eine größere Anzahl von Pilzen akut bedroht. Schon jetzt stehen fast alle diese Arten auf den Roten Listen. Die Auswertung der Funde zeigt, dass im Untersuchungsraum die Mehrzahl der Hygrocybe-Arten einen Verbreitungsschwerpunkt in der collinen bis submontanen Höhenstufe hat. Mit Hilfe der ungewichteten mittleren Zeigerwerte (nach Ellenberg) der von den Wiesen erstellten Pflanzenlisten konnte deutlich gemacht werden, dass diese Pilze überwiegend auf trockenen bis leicht frischen Böden (F-Zahl: 4,5–5,0) mit guter Basenversorgung (R-Zahl: 5,5–6,5) und niedrigen Nährstoffgehalten (N-Zahl: 3,5–4,5) Fruchtkörper bilden. Die mittleren Artenzahlen der zugrunde liegenden Gesamt - artenlisten umfassen Werte von 40 bis 55. Die Flächengrößen waren uneinheitlich, weil jeweils vollständige, einheitlich genutzte Wiesenparzellen für Pflanzenlisten und Pilze als Bezugsgröße dienten. Viele der Pilze haben weite ökologische Amplituden in Bezug auf Wasser- und Basenversorgung. Aber die N-Zahlen überschreiten selten den Wert 5. Unter den selten beobachteten Hygrocybe-Arten sind einige an Extremstandorte gebunden, nämlich an sehr saure, sehr kalkreiche bzw. nasse Böden. Da die Arten der Gattung Hygrocybe durch ihre vielfältigen Farben auffallen, relativ leicht zu bestimmen sind und sehr klare Indikatoreigenschaften für mageres altes Grasland haben, sollten sie überall zur Bewertung von dessen Schutzwürdigkeit mit herangezogen werden. Die heute schon seltenen Pflanzen, Tiere und Pilze werden sich von alleine nach Umbruch, Ackernutzung bzw. intensiver Düngung nur sehr langsam oder gar nicht mehr ansiedeln können, auch wenn versucht wird, die Böden auszuhagern.
In einem teilweise stillgelegten Steinbruch in Bad Deutsch-Altenburg nahe Hainburg/Donau (NÖ) wurde die epigäische Spinnenfauna auf sechs Untersuchungsflächen unterschiedlichen Sukzessionsalters mittels Barberfallen in der Zeit von 27. März bis 29. Oktober 2006 untersucht. Es wurden 79 Arten mit 845 adulten Individuen aus 18 Familien gefangen. Sieben Arten kamen auf allen Untersuchungsflächen vor. 28 Arten werden in den Roten Listen Tschechiens und/oder der Slowakei in einer der Gefährdungskategorie eingestuft. Die wenig bekannte Arten Thanatus pictus L. Koch, 1881 und Xysticus embriki Kolosváry, 1935 werden genauer vorgestellt. Der Vergleich der sechs Spinnengemeinschaften des untersuchten Steinbruchs mit 16 geographisch benachbarten Spinnengemeinschaften aus dem Gebiet der Parndorfer Platte zeigt einen kontinuierlichen Sukzessionsverlauf innerhalb der Ruderalfluren von den jüngsten zur ältesten Fläche und weiter zu intakten gepflegten Trockenrasen, und über verbrachende und verbuschende Trockenrasen sowie Hecken und Gebüsch-Standorten zu natürlichenWäldern der Region.
In der Mittelgebirgslandschaft des Mittleren Schwarzwaldes werden wenig ertragreiche Weideflächen zunehmend aufgelassen oder aufgeforstet. Ertragreichere Flächen werden gedüngt und intensiver genutzt. Der Flächenanteil magerer Weideflächen in mittleren Höhenlagen geht immer weiter zurück. Im Mittleren Schwarzwald sind dies Besenginsterweiden oder Borstgrasrasen, die beide als FFH-Lebensraumtyp naturschutzfachlich von Bedeutung sind. In diesem Kontext wurde unter sucht, ob Kleinstrukturen in der Landschaft, wie z. B. Böschungen oder Weidezaunbereiche, für die Artenvielfalt im Raum von Bedeutung sind und ob sich diese Strukturen als Refugien für die Arten der Magerweiden eignen. In zwei Tälern wurden die Kleinstrukturen in Höhenlagen von 400 bis 800 m ü. NN kartiert. An 60 stratifiziert zufällig auf den Kleinstrukturen verteilten Punkten wurden Vegetationsaufnahmen gemacht. Die Vegetationsdaten wurden klassifiziert und einer Korrespondenzanalyse (CA) unterzogen. Auf den untersuchten Kleinstrukturen lassen sich fünf verschiedene Vegetationseinheiten unter scheiden, die nicht an spezielle Typen von Kleinstrukturen gebunden sind. Vier dieser Einheiten können den montanen Borstgrasrasen zugeordnet werden, die fünfte ist eher als Saumgesellschaft anzusprechen. Die Vegetation der Kleinstrukturen wurde mit der Vegetation von Magerweiden in der gleichen Region und der gleichen Höhenlage mit Hilfe einer weiteren Ordination (CA) verglichen. Die beiden Vegetationsdatensätze sind auf der ersten Ordinationsachse weitgehend voneinander getrennt. Die Vegetation der Kleinstrukturen hat einige Gemeinsamkeiten mit der Vegetation magerer Weideflächen, wird darüber hinaus aber von der umgebenden Vegetation stark beeinflusst. So finden sich z. B. Ajuga reptans, Filipendula ulmaria und Hieracium lachenalii eher in den Kleinstrukturen als auf den Magerweiden. Aber auch Kennarten der Nardetalia wie Galium saxatile, Luzula multiflora oder Meum athamanticum haben dort ihren Schwerpunkt. Kleinstrukturen sind artenreicher als Weideflächen. Hier heben sich insbesondere Felsflächen und Böschungen am Wegrand deutlich ab. Dieser Sachverhalt wird zum einen der strukturellen Vielfalt und zum anderen Randeffekten, die bei Kleinstrukturen aufgrund ihrer Geometrie eine große Rolle spielen, zugeschrieben. Kleinstrukturen können so zu einem gewissen Grad eine Rolle als Refugium für Arten der Magerweiden spielen. Die Artenkombination weicht aber in den meisten Fällen deutlich von derjenigen der Magerweiden ab.