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The taxonomy of Nearctic tiger beetles (Coleoptera: Carabidae: Cicindelinae) is reviewed in light of modern systematics research. Despite decades of published molecular phylogenies, the taxonomic nomenclature has not been formally updated since the 1950s. We generated a maximum likelihood phylogenetic tree based on three mitochondrial gene fragments (16S, COX3 and CytB) to address the placement of Nearctic taxa that were not included in recent studies; these species were historically contained within Cylindera Westwood, 1831, a polyphyletic genus. Here we describe Parvindela Duran and Gough, new genus, and propose 20 new combinations based on a plurality of data, including our topology, prior molecular phylogenetic studies, morphology and ecology: Apterodela unipunctata (Fabricius, 1775) new combination; Brasiella praecisa (Bates, 1890) new combination; Brasiella viridisticta (Bates, 1881) new combination; Cicindela amargosae (Dahl, 1939) new combination; Cicindela senilis (G. Horn, 1866) new combination; Cicindela willistoni (LeConte, 1879) new combination; Eunota californica (Menetries, 1883) new combination; Eunota circumpicta (LaFerte, 1841) new combination; Eunota fulgoris (Casey, 1913) new combination; Eunota gabbii (G. Horn, 1866) new combination; Eunota pamphila (LeConte, 1873) new combination; Eunota praetextata (LeConte, 1854) new combination; Eunota severa (LaFerte, 1841) new combination; Eunota striga (LeConte, 1875) new combination; Parvindela debilis (Bates, 1890) new combination; Parvindela celeripes (LeConte, 1848) new combination; Parvindela cursitans (LeConte, 1860) new combination; Parvindela terricola (Say, 1824) new combination; Parvindela nephelota (Bates, 1882) new combination; Parvindela lunalonga (Schaupp, 1884) new combination.
The Cyrtodactylus irregularis group, originally considered to consist of only one taxon, has been split into 26 species. We herein present the distribution of all species within the group in Cambodia, Laos and Vietnam and describe two new species based on integrative analyses. Cyrtodactylus chumuensis sp. nov. is discovered from Dak Lak Province and distinguished from the remaining taxa by more than 11.86% genetic divergence and by the following distinct morphological characters: size medium (SVL 67.5 mm); enlarged femoral scales on each thigh 4–5, femoral pores 0–2 in males; precloacal pores 6–7 in males; ventral scale rows 43–45; lamellae under toe IV 17–21. Cyrtodactylus arndti sp. nov. is described from Binh Dinh Province and genetically differentiated from its congeners by a minimum of 11.42% and by the following characters: adult size medium (SVL 73.4–80.8 mm); enlarged femoral scales on each thigh 5–11; femoral pores 0–2 in males; 6 precloacal pores in males, females with 6 pitted precloacal pores; ventral scale rows 26–38; lamellae under toe IV 17–22; subcaudal scales transversely enlarged. Additionally, we highlight the potential cryptic diversity with the taxon currently regarded as C. pseudoquadrivirgatus and understudied areas in Vietnam where new species will likely be discovered.
Phylogenetic inference, based on five molecular markers (COI, 28S, AATS, 12S, PGD), corroborates the synonymy of the flightless genera Pieltainia Arias, 1919 and Ariasella Gil, 1923 with Tachydromia Meigen, 1803. The secondary structure of the 28S rRNA gene is used for the first time in this family to align the multiple sequences. Molecular and morphological data are largely congruent for all known species of flightless Tachydromia. This paper treats ten western Mediterranean species (nine Iberian and one Italian) in detail, including the description of four new species: T. ebejeri Gonçalves, Grootaert & Andrade sp. nov., T. stenoptera Gonçalves, Grootaert & Andrade sp. nov., T. cantabrica Gonçalves, Grootaert & Andrade sp. nov. and T. nigrohirta Gonçalves, Grootaert & Andrade sp. nov. The male of Tachydromia pieltaini (Gil Collado, 1936) and the female of Tachydromia apterygon Plant & Deeming, 2006 are described for the first time, while a lectotype is assigned to Tachydromia pandellei (Séguy, 1941). A key to all non-macropterous Tachydromia is supplied. Knowledge on the geographic distribution of most species is considerably enhanced. The mating behaviour of Tachydromia semiaptera (Gil Collado, 1923) and Tachydromia iberica (Arias, 1919) is documented for the first time, and we propose a change in the definition of terms apterous and micropterous to properly accommodate the diversity of wing states in this cluster of species.
The genus Pseudolatirus Bellardi, 1884, with the Miocene type species Fusus bilineatus Hörnes, 1853, has been used for 13 Miocene to Early Pleistocene fossil species and eight Recent species and has traditionally been placed in the fasciolariid subfamily Peristerniinae Tryon, 1880. Although the fossil species are apparently peristerniines, the Recent species were in their majority suspected to be most closely related to Granulifusus Kuroda & Habe, 1954 in the subfamily Fusininae Wrigley, 1927. Their close affinity was confirmed by the molecular phylogenetic analysis of Couto et al. (2016). In the molecular phylogenetic section we present a more detailed analysis of the relationships of 10 Recent Pseudolatirus-like species, erect two new fusinine genera, Okutanius gen. nov. (type species Fusolatirus kuroseanus Okutani, 1975) and Vermeijius gen. nov. (type species Pseudolatirus pallidus Kuroda & Habe, 1961). Five species are described as new for science, three of them are based on sequenced specimens (Granulifusus annae sp. nov., G. norfolkensis sp. nov., Okutanius ellenae gen. et sp. nov.) and two (G. tatianae sp. nov., G. guidoi sp. nov.) are attributed to Granulifusus on the basis of conchological similarities to sequenced species. New data on radular morphology is presented for examined species.
The molecular phylogeny of Miliusa (Annonaceae) is reconstructed, with 27 (of ca. 50) species included, using a combination of seven plastid markers (rbcL exon, trnL intron, trnL-F spacer, matK exon, ndhF exon, psbA-trnH spacer, and ycf1 exon) constituting ca. 7 kb. In addition, two new species of Miliusa are described from the Malesian area: M. butonensis sp. nov. from Buton Island, Indonesia and M. viridifl ora sp. nov. from Papua New Guinea. The former is included in the molecular phylogenetic analysis. The reconstructed phylogeny corresponds well to the informal morphological grouping proposed earlier. A revised key to 13 Austro-Malesian species of Miliusa is provided.
Die Grabwespen (Sphecidae sensu Bohart & Menke 1976; Sphecidae sensu lato in neueren, phylogenetischen Arbeiten), zu denen nach Day (1984) und späteren Autoren auch die Heterogynaidae zählen, umfassen derzeit 266 Gattungen mit 9559 beschriebene Arten (Pulawski 2006). Zusammen mit den Bienen (= Apiformes nach Michener 2000, bzw. Anthophila nach Engel 2005) bilden die Grabwespen ein gut begründetes Monophylum, das nach Michener (1986) den Namen Apoidea trägt und eine der drei Hauptlinien innerhalb der aculeaten Hymenoptera ist. Die Monophylie der aculeaten Hymenoptera, der Apoidea sowie die der Bienen ist jeweils gut begründet (z.B. Brothers 1975, Königsmann 1978, Lomholdt 1982, Alexander 1992, Brothers & Carpenter 1993). Anders verhält es sich mit den Grabwespen. Neben der phylogenetischen Untersuchung von Brothers & (1993), die die Monophylie der Grabwespen unterstützt, haben andere morphologische als auch molekularsystematische Analysen starken Zweifel an dieser Hypothese aufkommen lassen (z.B. Königsmann 1978, Lomholdt 1982, Alexander 1992, Prentice 1998, Melo 1999, Ohl & Bleidorn 2006).
Previous phylogenetic analyses of the grass-specialist leafhopper tribe Chiasmini have resolved relationships among genera but have included few representatives of individual genera. Here the phylogeny of 20 Chinese species belonging to 8 chiasmine genera was investigated by combining DNA sequence data from two mitochondrial genes (COI, 16S) and two nuclear genes (H3, 28S). In both maximum likelihood (ML) and Bayesian inference (BI) analyses, relationships among genera were largely consistent with prior analyses, with most members of the tribe placed into two sister clades: (Exitianus + Nephotettix) and the remaining five sampled genera. To examine morphology-based species definitions in the taxonomically difficult genus Exitianus Ball, 1929, one mitochondrial gene (COI) and one nuclear gene (ITS2) were used to infer the phylogenetic relationships and status of two common and widespread species and compare the performance of different molecular species-delimitation methods. These analyses divide the included populations into two well-supported clades corresponding to current morphological species concepts but some inconsistencies occurred under the jMOTU, ABGD and bPTP methods depending on the which gene and analytical parameter values were selected. Considering the variable results yielded by methods employing single loci, the BPP method, which combines data from multiple loci, may be more reliable in Exitianus.
The following new taxa are described from the Philippines: Mioscarta nubisa Crispolon & Soulier-Perkins sp. nov., M. translucida Crispolon & Yap sp. nov. and Trigonoschema Crispolon & Soulier-Perkins gen. nov. with three new species: T. manoborum Crispolon & Soulier-Perkins sp. nov. (as type species), T. negrosensis Crispolon & Yap sp. nov and T. rubercella Crispolon &Guilbert sp. nov. Trigonoschema pallida (Lallemand, 1927) comb. nov. is transferred from Mioscarta Breddin, 1901. Descriptions of male genitalia are illustrated and keys to species of Philippine Mioscarta and Trigonoschema gen. nov. are provided. Although phylogenetic results confirm the monophyly of all genera and Trigonoschema being a distinct genus from Mioscarta, relationships between genera remain uncertain. A checklist of the genera and species of Cercopidae found in the Philippines is included.
A new species of abyssal Neanthes Kinberg, 1865, N. goodayi sp. nov., is described from the Clarion-Clipperton Zone in the central Pacific Ocean, a region targeted for seabed mineral exploration for polymetallic nodules. It is a relatively large animal found living inside polymetallic nodules and in xenophyophores (giant Foraminifera) growing on nodules, highlighting the importance of the mineral resource itself as a distinct microhabitat. Neanthes goodayi sp. nov. can be distinguished from its congeners primarily by its distinctive, enlarged anterior pair of eyes in addition to characters of the head, pharynx and parapodia. Widespread, abundant, and easily recognisable, N. goodayi sp. nov. is also considered to be a suitable candidate as a potential indicator taxon for future monitoring of the impacts of seabed mining.
Lycosa Latreille, 1804 (Araneae, Lycosidae) of Israel, with a note on Geolycosa Montgomery, 1904
(2022)
Lycosa (Araneae, Lycosidae) is a wolf spider genus typical of subtropical latitudes in the western Palearctic. Despite being erected over 200 years ago, the taxonomy of Lycosa is still unclear. Many species formerly ascribed to it are currently being moved to other genera, while new species are still being described. The species of Lycosa of the western Mediterranean basin are relatively well known, yet the Levantine region, the easternmost part of the Mediterranean basin, has not received much attention since the early 20th century. Here, we study Lycosa from the southern Levant using morphological, molecular and behavioral characteristics, to delimit the species found in this region. We describe two new species: L. hyraculus sp. nov. and L. gesserit sp. nov. We re-describe the widespread and polymorphic species, Lycosa piochardi Simon, 1876. Lycosa piochardi infraclara Strand, 1913 is synonymized with Lycosa piochardi. By adding novel data to the molecular phylogeny of Lycosa created by Planas et al. (2013) and re-analyzing it, we explore the relationship of the Levantine species to other Mediterranean species of Lycosa. We discuss habitat preferences of the two species of Lycosa. Additionally, we report the burrowing species Geolycosa vultuosa (C.L. Koch, 1838) as a new record to Israel, thus extending the distribution of this species and genus into the Levant.