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This study was conducted to describe and illustrate two new species of groundwater amphipods from the northern parts of the Zagros Mountains in West Azerbaijan Province, Iran. Mitochondrial (COI) and nuclear (28S rDNA) fragments as well as several morphological traits were used to characterize Niphargus urmiensis sp. nov. and Niphargus fiseri sp. nov. The phylogenetic analyses showed that the nucleotide differences between the recently described species and their close allies are attributed to their distinctiveness. The molecular analysis also introduced that the new species are placed within the clade comprising Iranian species as a sister taxon. The genetic distances between N. urmiensis sp. nov. and N. fiseri sp. nov. are 7.6% and 1.6%, respectively based on the COI and 28S rDNA gene fragments.
Eleven species of Ctenopelma Holmgren, 1857 are reported from China. Five species are new to science: C. labiatum Sheng, Sun & Li sp. nov., from Ningxia Hui Autonomous Region, C. lii Sheng, Sun & Li sp. nov., from Liaoning province, C. rufofasciatum Sheng, Sun & Li sp. nov., reared from Cephalcia lariciphila (Wachtl, 1898) from Beijing, C. pineatum Sheng, Sun & Li sp. nov., reared from Acantholyda posticalis (Matsumura, 1912) and Cephalcia lariciphila from Beijing and Henan, Shanxi, Shan’xi, Liaoning, Jilin and Heilongjiang provinces, and C. spiraculare Sheng, Sun & Li sp. nov., reared from Cephalcia lariciphila from Henan and Shanxi provinces. One species, C. nigrum Holmgren, 1857, reared from Cephalcia lariciphila in Beijing, is a new record for China. Ctenopelma tomentosum (Desvignes, 1856) was reared from Neurotoma sibirica Gussakovskij, 1935 (new host record) in Liaoning province. A key to species of Ctenopelma known in China is provided.
The birdwing butterfly Trogonoptera brookiana (Wallace, 1855) is a well-known conservation icon, yet questions remain about the infraspecific status of regional populations. The eastern Peninsular Malaysian population has been described as the subspecies mollumar d’Abrera, Doggett & Parker, 1976, but its status as a subspecies distinguishable from the taxon trogon (Vollenhoven, 1860) in Sumatra has been disputed. Wing characters and measurements of specimens from the two regions were therefore examined quantitatively using discriminant function and correspondence analyses. Eastern Peninsular specimens differ on average from Sumatran specimens in having more extensive green, especially in the female. This is reflected in many of the measurements and characters analysed. Females from the Peninsula also have a characteristically blacker upperside ground colour in which the outer areas of both wings barely contrast with the black veins and forewing cell. The extent of these differences enables a reliable differentiation of the females of both regions. The magnitude and consistency of differences are comparable to that between other subspecies of undisputed status. Behavioural differences also exist. The name mollumar therefore merits subspecific status. In addition, we consider the male forms walshi Haugum & Low, 1982 and walshoides Haugum & Low, 1982 to be chemically discoloured specimens of trogon rather than biological forms.
Revision of the genus Cerapanorpa (Mecoptera: Panorpidae) with descriptions of four new species
(2019)
The genus Cerapanorpa Gao, Ma & Hua, 2016 is taxonomically revised. Cerapanorpa is confirmed to be endemic to the mountain regions in central China. Nineteen species are recognized in the genus, including four new species: Cerapanorpa baimaensis sp. nov., Cerapanorpa xuebaodinga sp. nov., and Cerapanorpa yanggashana sp. nov. from the Minshan Mountains, and Cerapanorpa taizishana sp. nov. from the northeastern margin of the Qinghai-Tibetan Plateau. Six species are transferred from Cerapanorpa back to Panorpa Linnaeus, 1758. An updated key to species is presented.
Neopanorpa van der Weele, 1909 is the second largest genus in Panorpidae, and over 170 Oriental species have been reported hitherto. In this paper, we describe two new species: Neopanorpa luojishana sp. nov. and Neopanorpa xingmini sp. nov. from Southwest China. We also report the first discovery of the male of Neopanorpa ocellaris (Navás, 1908) from Guangxi and Guizhou, China, a species recorded from Sikkim previously. Neopanorpa brevivalvae Chou & Wang, 1988 is synonymized with Neopanorpa lungtaushana Cheng, 1957. In addition, Neopanorpa furcula nom. nov. is proposed for Neopanorpa furcata Zhou, 2005, a junior homonym preoccupied by Neopanorpa furcata (Hardwicke, 1825). The biogeographical implications of some Neopanorpa species are discussed in brief.
A cladistic analysis of the genus Atlantodesmus Hoffman, 2000 is presented. With a total of 11 taxa and 30 morphological characters, and under implied weighting (k = 3), two equally most parsimonious trees (length = 58 steps; total fit = 23.150; CI = 0.64; RI = 0.64) recovered the monophyly of the genus. The resulting synapomorphies are: absence of a ventral projection on the post-gonopodal sternites; presence of folds on the dorsal edge of the prefemoral region of the gonopod; and one homoplastic transformation: presence of a cingulum. In addition, Atlantodesmus sierwaldae sp. nov. is described from the state of Minas Gerais, in the Brazilian Cerrado, and a key to the males of the genus is provided.
We examined the type specimens and historical collections holding puzzling Atlantic and Mediterranean material belonging to the genus Schizoretepora Gregory, 1893. We performed a detailed study of the colonial characters and re-describe the resulting species and those that have rarely been found or have poor original descriptions. As a result of this revision, nine species are found in the northeast Atlantic and Mediterranean. Six of them are re-described and illustrated: S. aviculifera (Canu & Bassler, 1930), S. calveti d’Hondt, 1975, S. imperati (Busk, 1884), S. sp. nov.? (= S. imperati sensu O'Donoghue & de Watteville 1939) (in open nomenclature, specimen lacks ovicells), S. pungens (Canu & Bassler, 1928) and S. solanderia (Risso, 1826). For S. dentata (Calvet, 1931), no material remains; furthermore, S. hassi Harmelin, Bitar & Zibrowius, 2007 and S. serratimargo (Hincks, 1886) have recently been described and redescribed, respectively. This new arrangement attains a coherent geographical distribution: S. imperati seems restricted to the eastern Atlantic, S. dentata and S. calveti are deepwater species from Atlantic islands, S. pungens and S. aviculifera dwell on the African coasts of the Western Mediterranean, S. hassi and S. sp. nov.? (=S. imperati sensu O’Donogue & de Wateville 1939) are confined to the Eastern Mediterranean, and S. solanderia and S. serratimargo live on the European coasts of the Mediterranean.
Macrostemum is the second largest genus of Macronematinae with about 104 described species distributed in the Neotropical (18), Afrotropical (20), Australasian (7), Palearctic (2), Nearctic (3) and Oriental (54) regions. Despite its great diversity, knowledge about its immature stages is scarce: worldwide, only 7 species (6.7%) have larvae and/or pupae described. From the Neotropics, only one species, Macrostemum ulmeri (Banks, 1913), has described larvae and pupae. The objectives of this study are to describe and illustrate a new species, Macrostemum araca sp. nov., based on adult males and females from Serra do Aracá, Amazonas, Brazil, and the larvae and pupae of M. brasiliense (Fischer, 1970) from an Atlantic Forest fragment in São Paulo state using the metamorphotype method. In addition, this species is recorded for the first time for Minas Gerais state.
The gigas species group of the subgenus Canthidium (Neocanthidium) is defi ned and described. This species group is composed of three described species [C. gigas Balthasar, 1939, Brazilian Atlantic Forest, including intrusions into Cerrado, C. bokermanni (Martínez et al., 1964), Chaco and western Cerrado in Brazil, Bolivia, Paraguay, and Argentina, and C. kelleri (Martínez et al., 1964), Brazilian Cerrado and neighbouring open areas] and three new species: Canthidium stofeli sp. nov. from the western and southern regions of the Brazilian Amazon, Canthidium feeri sp. nov. from French Guiana, and Canthidium ayri sp. nov. from the Brazilian Atlantic Forest. We present descriptions and redescriptions, illustrations, an identifi cation key and comments on the distributions of the species of the gigas group.
Three new species of the genus Mimetus Hentz, 1832 are described and named as M. bucerus sp. nov. (♂), M. lingbaoshanensis sp. nov. (♂♀) and M. yinae sp. nov. (♂♀). Detailed morphological descriptions, photos of the body and copulatory organs, line drawings of copulatory organs, as well as the distribution maps are provided.
Several taxonomic groups within Empidoidea Latreille, 1809 have been subject to unclear phylogenetic assignments along with multiple parallel hypotheses causing difficulties in classification and morphological identification. This study reviews the internal classification of the Ragadidae and includes a diagnosis and description of all included subfamilies and genera based on the results of an analysis of morphological characters using maximum parsimony. Illustration of important characters and a key to all genera in the family is given. The genus Hormopeza Zetterstedt, 1838 is found to be most closely related to Anthepiscopus Becker, 1891 and Iteaphila Zetterstedt, 1838, and the subfamily Iteaphilinae Wahlberg & Johanson, 2018 is therefore expanded to also include that genus. Hormopeza is consequently excluded from Ragadinae Sinclair, 2016. This study provides diagnoses, descriptions and keys in a contribution to a thorough classification of the empidoid groups and increased ease in morphological recognition.
The African shieldbug genus Afrius Stål, 1870 is revised. Cantheconidea migratoria Distant, 1913 and A. williamsi Miller, 1952 are proposed as junior synonyms of A. (Subafrius) flavirostrum (Signoret, 1861) whereas Canthecona marmorata Dallas, 1851, Canthecona annulipes Dallas, 1851 and A. rubromarginatus Bergroth, 1903 are proposed as junior synonyms of A. (Afrius) purpureus (Westwood, 1837) based on the general morphology and genitalia of the species. The three valid species, viz. A. (Subafrius) flavirostrum, A. (Afrius) kolleri Schouteden, 1911 and A. (Afrius) purpureus, are redescribed with details of male and female genitalia morphology, and a lectotype is designated for A. (Afrius) kolleri. A key to identify the species as well as an update of the geographical distribution for each species are provided, including new records for A. (Afrius) purpureus.
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).
The new genus and species Campydoroides manautei Holovachov gen. et sp. nov. is placed in the suborder Campydorina and is characterised by a transversely striated cuticle without lateral alae, body pores or epidermal glands; somatic sensilla only on pharyngeal region and on tail; a truncate labial region with papilliform inner labial, outer labial and cephalic sensilla; a stirrup-shaped amphid with transverse slit-like opening; a conoid stoma with strongly cuticularised walls and large protrusible dorsal tooth; a cylindrical pharynx with distinct basal bulb but without valves; a large ovoid cardia; didelphic, amphidelphic female gonads with antidromously reflexed ovaries and without spermatheca; a transverse vulva; a straight vagina without pars refringens vaginae or epiptygmata; an elongate tail with caudal glands and spinneret. The new genus is similar to the genera Campydora Cobb, 1920 and Udonchus Cobb, 1913 in having papilliform labial and cephalic sensilla, a stirrup-shaped amphid with a transverse slit-like opening, a stoma with a well-developed protrusible dorsal tooth, and a muscular pharynx with a strongly developed basal bulb, but can be easily separated from both in details of a stoma morphology. The systematics of the suborder Campydorina is revised. Halirhabdolaimus Siddiqi, 2012 is synonymised with Syringolaimus de Man, 1888.
Two new Brazilian sharpshooter species of the genus Tretogonia Melichar, 1926 are described and illustrated: Tretogonia diminuta sp. nov. and T. elegantula sp. nov., both from the State of Paraná. A redescription of T. dentalis Emmrich, 1988 is provided based on a male from the State of Mato Grosso do Sul. This is the first Brazilian record of T. dentalis, a species originally described from Paraguay. Photographs and line drawings are provided for the three species, as well as notes on the taxonomy and biology of the genus.
The majority of Ceraphronoidea (Insecta: Hymenoptera) species were described in the late 1800s and early 1900s, with most of these early descriptions relying on text alone. Few type specimens have been illustrated and even fewer have been photographed, posing a challenge to taxonomists working on the group today. Here, we attempt to remove the barriers obstructing Ceraphronoidea research by creating a photographic catalog of the type specimens present at the Muséum national d'Histoire naturelle (MNHN) in Paris, France. We discuss the history of the ceraphronoid specimens present in the collection and provide comments on unpublished species notes from former Ceraphronoidea taxonomist Paul Dessart. We synonymize Ceraphron myrmecophilus Kieffer, 1913 syn. nov. with Aphanogmus abdominalis (Thomson, 1858) (Hymenoptera: Ceraphronidae) based on the male genitalia morphology, body shape and presence of foveae on the median length of the mesoscutellum. We also report the discovery of the missing male holotype of Ceraphron testaceus (Risbec, 1953) (Hymenoptera: Ceraphronidae) and several potential types of Aphangomus aphidi (Risbec, 1955) (Hymenoptera: Ceraphronidae).
The taxa of Cryptocephalinae (Clytrini), Synetinae and part of Galerucinae introduced by Carl Peter Thunberg are reviewed based on the examination of primary type specimens deposited in the Museum of Evolution, Uppsala University. The following taxonomic changes are proposed: Coptocephala unifasciata unifasciata (Scopoli, 1763) = Cryptocephalus melanocephalus Thunberg, 1787 syn. nov.; Melitonoma decemnotata (Thunberg, 1787) comb. nov. (from Cryptocephalus Geoffroy, 1762); Miopristis flexuosa (Thunberg, 1821) = Miopristis namaquensis Medvedev, 1993 syn. nov.; Protoclytra ( Lacordairella) taeniata (Thunberg, 1821) comb. nov. (from Camptolenes Chevrolat, 1836) = Camptolenes fastuosa (Lacordaire, 1848) syn. nov.; Smeia undata (Thunberg, 1821) comb. nov. (from Miopristis Lacordaire, 1848) = Smeia virginea (Lacordaire, 1848) syn. nov. = Melitonoma pictipennis Jacoby, 1898 syn. nov.; Teinocera catenata (Thunberg, 1821) comb. nov. (from Miopristis) = Teinocera subclathrata (Lacordaire, 1848) syn. nov.; Exosoma lusitanica (Linnaeus, 1767) = Crioceris haemorrhoa Thunberg, 1827 syn. nov.; Megalognatha festiva (Fabricius, 1781) = Crioceris virens Thunberg, 1827 syn. nov.; Monolepta bioculata (Fabricius, 1781) = Cryptocephalus bioculatus Thunberg, 1827 syn. nov.; Monolepta melanogaster (Wiedemann, 1823) = Cryptocephalus capensis Thunberg, 1827 syn. nov.; Palaeophylia tricolor (Fabricius, 1781) = Crioceris tetrapuncta Thunberg, 1787 syn. nov. = Crioceris dimidiata Thunberg, 1827 syn. nov. Lectotypes are designated for Cryptocephalus bioculatus Thunberg, 1827 and Crioceris dimidiata Thunberg, 1827. Melitonoma decemnotata comb. nov. is redescribed. Labidostomis insidiosa Péringuey, 1888 is resurrected from synonymy with Teinocera catenata comb. nov. and provisionally placed as a valid species in the genus Miopristis Lacordaire, 1848. Crioceris betulina Thunberg, 1787 is proposed as nomen oblitum for Syneta betulae (Fabricius, 1792) (nomen protectum). Colour photographs of the type specimens of all taxa are provided.
Five new species of the genus Drosophila Fallén, 1823 belonging to the tripunctata group are described and illustrated: D. warmi sp. nov., D. kurillakta sp. nov., D. chichu sp. nov., D. saraguru sp. nov. and D. ayauma sp. nov. from the forests of Podocarpus National Park. The first species is ascribed to subgroup II of Frota-Pessoa (1954), the second species to subgroup IV, and the last three species are not assigned to any subgroup. The flies were captured using plastic bottles containing pieces of yeast fermented banana.
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.