Redefinition of the parastenocaridid genus Proserpinicaris (Copepoda: Harpacticoida), with description of three new species from Korea

Proserpinicaris young sp. nov., Proserpinicaris wangpi sp. nov. and Proserpinicaris imjin sp. nov. are described from subterranean waters of South Korea. They are short-range endemics, allopatric in distribution and closely related to each other, and to two other Far Eastern congeners. Distinguishing features are limited to the general habitus shape, proportions of the caudal rami and degree of sexual dimorphism. The genus Proserpinicaris Jakobi, 1972 Jakobi, H. 1972. Trends (Enp.P4 Mänchen) innerhalb der Parastenocarididen (Copepoda Harpacticoidea). Crustaceana, 22: 127–146. [Crossref] , [Google Scholar], as redefined here, is Palaearctic in distribution, with the centre of diversity in southern Europe, and 20 valid members, all of which share a large hyaline spiniform structure on the male fourth leg basis as a synapomorphy. A key to species is provided. Genera Niponnicaris Jakobi, 1972 Jakobi, H. 1972. Trends (Enp.P4 Mänchen) innerhalb der Parastenocarididen (Copepoda Harpacticoidea). Crustaceana, 22: 127–146. [Crossref] , [Google Scholar] and Pannonicaris Jakobi, 1972 Jakobi, H. 1972. Trends (Enp.P4 Mänchen) innerhalb der Parastenocarididen (Copepoda Harpacticoidea). Crustaceana, 22: 127–146. [Crossref] , [Google Scholar] are established as its junior subjective synonyms, Lacustricaris Jakobi, 1972 Jakobi, H. 1972. Trends (Enp.P4 Mänchen) innerhalb der Parastenocarididen (Copepoda Harpacticoidea). Crustaceana, 22: 127–146. [Crossref] , [Google Scholar] is formally synonymized with Parastenocaris Kessler, 1913, and Parastenocaris lacustris Chappuis, 1958 Chappuis, PA. 1958. Le genre Parastenocaris Kessler. Vie Milieu, 8: 423–432.  [Google Scholar] is designated as incertae sedis in Fontinalicaridinae Schminke, 2010 Schminke, HK. 2010. High-level phylogenetic relationships within Parastenocarididae (Copepoda, Harpacticoida). Crustaceana, 83: 343–367. [Crossref], [Web of Science ®] , [Google Scholar].     

On Paranacypris samambaiensis gen. nov., sp. nov. (Crustacea,Ostracoda), the first South American psychrodromid from the alluvial valley of the Upper Paraná River,Brazil

Paranacypris samambaiensis gen. nov., sp. nov. is here described from closed lakes in the alluvial valley of the Upper Paraná River. The new genus, characterized by a large frontally overlapping left valve, belongs in the Psychrodromini, and is the first representative of this tribe described in South America. Nevertheless, it has some different character states, and the diagnosis of the tribe had to be adapted. The species is rare and restricted to closed lakes (not in contact with the main channels of the river). It mostly occurs in benthic littoral habitats, and far less in the pleuston communities, the most common habitat in this floodplain. The behaviour of P. samambaiensis gen. nov., sp. nov. is enigmatic because it combines long natatory setae on the antennae (swimming behaviour) with a very stout caudal ramus, including the spine‐like posterior seta (crawling behaviour). We present a key to the genera of the Herpetocypridinae.     

Nine new species of the subgenus Stegana (Oxyphortica) from the Oriental region,with morphological and molecular evidence based on Chinese species (Diptera: Drosophilidae)

Nine new species of the subgenus Stegana (Oxyphortica) have been discovered from the Oriental Region: S. (O.) chuanjiangi Zhang and Chen, sp. nov., S (O.) dainuo Wang and Chen, sp. nov., S. (O.) dawa Zhang and Chen, sp. nov., S. (O.) laohlie Zhang and Chen, sp. nov., S. (O.) luchun Wang and Chen, sp. nov., S. (O.) mengwan Wang and Chen, sp. nov., S. (O.) triodonta Cheng and Chen, sp. nov. from southern China; S. (O.) dehiscens Cheng and Chen, sp. nov. and S. (O.) spinosa Cheng and Chen, sp. nov. from eastern Malaysia. One newly recorded species from China: S. (O.) maichouensis Sidorenko is re-described. The DNA sequences of the mitochondrial COI gene with BOLD Process ID and GenBank accession numbers are provided for the above seven new species and five known species from China: S. (O.) acutipenis Xu, Gao and Chen, S. (O.) adentata Toda and Peng, S. (O.) hirtipenis Xu, Gao and Chen, S. (O.) latipenis Xu, Gao and Chen, and S. (O.) maichouensis Sidorenko. Intra- and interspecific pairwise K-2P distances among these species are summarized and the phylogenetic relationships are reconstructed based on the neighbour-joining (NJ) analyses.

www.zoobank.org/urn:lsid:zoobank.org:pub:2FA403F6-5535-40A4-9FD0-ADB9913EDE83.     

Description of Rathkea lizzioides sp. nov. (Hydromedusae: Rathkeidae) from Antarctica and a key to the genus

A new species of hydromedusa from the Antarctic, Rathkea lizzioides sp. nov. is described and illustrated. The species is characterized by its rounded bell-shaped form, being almost as broad as high, the presence of an apical dome and a gastric peduncle, the 4 unbranched oral arms, the number of nematocyst clusters (7 to 18 in specimens 1·5 mm or greater in height), the occasional presence of 1 or more nematocyst clusters near the mouth margin, the 5 to 7 tentacles in each perradial tentacular bulb, the 3 to 5 tentacles in each interradial tentacular bulb, and the ovoid shape of the tentacular bulb. A key to the known species of Rathkea is provided.     

A revision and phylogenetic re-evaluation of the family Schizopodidae (Coleoptera,Buprestoidea)

The Schizopodidae (formerly subfamily Schizopodinae, family Buprestidae) is elevated to family status, based on a review of its morphology including wing venation, male and female genitalia, larvae, and also a cladistic analysis of in-group and out-group comparisions. Two tribes are recognized: Schizopodini LeConte with one genus, Schizopus LeConte and Dystaxiini Théry with two genera: Dystaxia LeConte and Glyptoscelimorpha Horn. The genus Schizopus contains two species: S. laetus LeConte and S. sallei Horn with one new subspecies, S. sallei nigricans Nelson. The genus Dystaxia includes two species: D. murrayi LeConte, and D. elegans Fall. The genus Glyptoscelimorpha is separated into two subgenera: G. (s. str.) with two species, G. marmorata Horn, and G. viridis Chamberlin; and G. (Dystaxiella) Knull, new status, with one species, G. (D.) juniperae (Knull), new combination, with a new subspecies, G. (D.) juniperae viridiceps Nelson. All taxa are described and information on variation, type localities, distribution, biology, and comparisons are given for each species. Keys to taxa for tribes to subspecies are provided. Illustrations for all species, including habitus, male and female genitalia and other parts, as well as cladograms of relationships are presented. Lectotypes are designated for the following: Yermoella helferi Obenberger, Dystaxia elegans Fall and Glyptoscelimorpha marmorata Horn. Tables of taxa, characters and character states used in the cladistic analysis are included.     

The morphological and molecular analyses of a new South American urban tardigrade offer new insights on the biological meaning of the Macrobiotus hufelandi group of species (Tardigrada: Macrobiotidae)

Worldwide knowledge of tardigrade fauna is still limited, and many areas such as South America are not well studied. The collection of new substrates in Argentinean urban areas provided an opportunity to describe the new tardigrade species Macrobiotus kristenseni sp. nov. This species has been studied with an integrative taxonomic approach, analysing its morphology by light and scanning electron microscopy, and considering two genes (cox1 and 18S rRNA) for DNA barcoding and phylogenetic purposes. The species belongs to the Macrobiotus hufelandi group of species, and it is characterized by egg processes in the shape of elongated cones with truncated and enlarged apexes, and by a high genetic distance with respect to closely related species (cox1: 18.2–33.4%). Morphological and molecular data show that the Macrobiotus hufelandi group of species has to be considered a true biological entity; one of the more widespread tardigrade lineages in continental environments. http://www.zoobank.org/urn:lsid:zoobank.org:pub:2CA51ABA-5570-4AFB-8182-CE499D97B0F1     

The parasitic wasp genera Skiapus,Hellwigia, Nonnus,Chriodes, and Klutiana (Hymenoptera,Ichneumonidae): Recognition of the Nesomesochorinae stat. rev. and Nonninae stat. nov. and transfer of Skiapus and Hellwigia to the Ophioninae

The ichneumonid wasp genera Skiapus Morley, Hellwigia Gravenhorst, Nonnus Cresson, Chriodes Förster, and Klutiana Betrem are each formally removed from the Campopleginae on the basis of morphological, molecular, and simultaneous analyses using PAUP* and the optimization alignment program POY. Skiapus and Hellwigia are shown to form a monophyletic group with the Ophioninae to which they are transferred. Nonnus is treated as comprising the Nonninae stat. nov. and Chriodes and Klutiana (sometimes treated as a junior synonym of Chriodes) are treated as comprising the Nesomesochorinae stat. rev. The status of Nesomesochorinae and Nonninae is not fully resolved as they are not consistently recovered as separate groups, forming a single clade in some analyses. We keep them separate because of this uncertainty. Molecular synapomorphies within the D2–3 expansion region of the 28S rDNA gene show the utility of this gene region in determining subfamily‐level placement within the higher Ophioniformes.     

Ciplakastacus gen. nov., a primitive genus of Leptastacidae (Copepoda,Harpacticoida) from the Mediterranean coast of Turkey

Both sexes of Ciplakastacus mersinensis gen. et sp. nov. (Copepoda, Harpacticoida, Leptastacidae) are described in detail based on intertidal material collected from the Mediterranean coast of Turkey (Mersin Province). Plesiomorphic character states displayed by the antenna and P1–P2 indicate Ciplakastacus diverged before the crown group Leptastacidae diversified. The new genus is placed in a basal clade (currently encompassing Archileptastacus and Meloriastacus) defined by eight synapomorphies: (1) caudal ramus with strongly developed seta I flanked by two elongate spinules; (2) caudal ramus with posteriorly directed spinous outgrowth of outer distal corner; (3) caudal ramus seta III vestigial; (4) P5 exopod and baseoendopod forming single plate in both sexes; (5) P2–P4 exp‐3 with one outer spine; (6) dorsal posterior margin of anal somite bilaterally serrate; (7) rostrum triangular or bell‐shaped, and (8) sexually dimorphic ornamentation on the anal somite. Within this clade Ciplakastacus appears most closely related to Meloriastacus on account of the shared presence of the extremely elongate second antennulary segment, an allobasis on the antenna, the strongly reduced accessory seta on the maxillipedal endopod, the subcylindrical sternal process between the maxillipeds and P1, and paired laterodorsal, posteriorly directed, serrate extensions on the anal somite. Both genera can be distinguished from each other by P5 morphology (both sexes), armature of P4 enp‐2 and abdominal hyaline frill structure. The phylogenetic relationships between the basal taxa of the Leptastacidae are briefly outlined.     

Champsodontidae (Pisces: Trachinoidei) in the Eastern Mediterranean: how many species are there?

ABSTRACT

Three marine fish species of the Indo-Pacific genus Champsodon were reported as invasive species in the Eastern Mediterranean between 2009 and 2012; Champsodon nudivittis, C. vorax, and C. capensis. These are presumed to invade through the Suez Canal, but only C. nudivittis is known from the Red Sea, so the presence of C. vorax and C. capensis is surprising. To test the validity of the taxonomic identification of these two species, this study combined traditional morphology, genetic barcoding, and photography investigation. Our results demonstrate that only one species, C. nudivittis, has migrated into the Eastern Mediterranean.     

On the taxonomic position of Indiacypridinae (Crustacea,Ostracoda), with the description of a new species of Indiacypris Hartmann, 1964 from Chalakkudy River (Kerala,India)

A new species of Indiacypris, I. chalakkudensis n. sp., is described from Chalakkudy River in Kerala, India; an asexual population of I. dispar occurred sympatrically with the new species and is here briefly redescribed. This is only the third species reported in this genus, and indeed also in the subfamily. The taxonomic position of this lineage is discussed in light of new morphological evidence. The subfamily could either belong to Cyprididae, or to Ilyocyprididae, or could represent an intermediate branch. Until molecular phylogeny can test these hypotheses, the subfamily remains in Ilyocyprididae.     

A new karst-dwelling gecko of the Gekko petricolus group (Reptilia: Gekkonidae) from Phitsanulok Province,central Thailand

We describe a new species of the genus Gekko from Phitsanulok Province, central Thailand. Gekko flavimaritus sp. nov. can be distinguished from its congeners by a combination of morphological characters: medium size for Gekko (snout–vent length 76.0–84.5 mm in six adult males, 67.5–78.3 mm in 11 adult females); nares in contact with rostral; two enlarged postmentals; 12–16 dorsal tubercle rows; 27–35 ventral scale rows; 10–15 subdigital lamellae on first toe, 15–18 on fourth toe; finger and toe webbing weakly developed; tubercle absent on dorsal surface of forelimbs and hindlimbs; adult male with 7–8 precloacal pores, in continuous row; precloacal pores absent in females; single postcloacal tubercle on each side; tubercles present on dorsal surface of tail base; subcaudals enlarged; sexual dimorphism present (colouration on dorsum in life — yellow in adult males and brownish grey in adult females); dorsum with whitish vertebral blotches between nape and base of tail. Genetically, the new species is nested within the G. petricolus group and is closely related to G. boehmei and G. petricolus. The new species has uncorrected pairwise divergences of ≥ 18.57% of the ND2 gene from other species of G. petricolus group. Additionally, we present the first genetic data for G. lauhachindai, and verify its morphological assignment to the G. petricolus group.

urn:lsid:zoobank.org:pub:06420ACC-2A05-4CE5-AF94-86B5D550E907