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In this paper we describe Macrobiotus canaricus sp. nov., a new tardigrade species of the Macrobiotus hufelandi group from the Canary Islands. Moreover, with the use of DNA sequencing, we confirm that Macrobiotus recens Cuénot, 1932 represents the hufelandi group, even though eggs laid by this species do not exhibit the typical hufelandi group morphology. Our study is based on both classical taxonomic methods that include morphological and morphometric analyses conducted with the use of light and scanning electron microscopy, and on the analysis of nucleotide sequences of four molecular markers (three nuclear: 18S rRNA, 28S rRNA, ITS-2, and one mitochondrial: COI). Our analyses revealed that M. canaricus sp. nov. is most similar to Macrobiotus almadai Fontoura et al., 2008 from the Archipelago of the Azores, from which it differs by the absence of granulation patches on the external and internal surfaces of legs I–III as well as by the absence of a cuticular pore in the centre of the external patch on legs I–III. Molecular sequences allowed us to pinpoint the phylogenetic positions of M. canaricus sp. nov. and M. recens within the M. hufelandi group.
We describe two new frog species of the genus Guibemantis Dubois, 1992 (Mantellidae) from northern Madagascar. Both species are placed in the subgenus Pandanusicola Glaw & Vences, 1994 and, like most of their relatives, appear to only inhabit the leaf axils of Pandanus plants. Guibemantis albomaculatus sp. nov. is distinguished from other closely related species by light colored dorsolateral stripes and abundant small white spots found on its flanks and limbs. Guibemantis woosteri sp. nov. also has light-colored dorsolateral stripes and small white spots, but differs by having strongly banded forelimbs and a reddish coloration around the eye orbits. Mitochondrial DNA sequences corroborate the identity of these two new species, which appear to be regional endemics in northern and north-eastern Madagascar, respectively. These descriptions bring the species count in Pandanusicola to thirteen.
Glemparon Jaschhof, 2013, a previously monotypic genus confined to Sweden, is shown here to be considerably richer in species, with most species found to occur in the Australasian region. Eighteen new species are described: G. tomelilla sp. nov. (from Sweden); G. aotearoa sp. nov., G. birhojohmi sp. nov., G. cervus sp. nov., G. didhami sp. nov, G. kaikoura sp. nov., G. nativitas sp. nov., G. orautahi sp. nov., G. otago sp. nov., G. pureora sp. nov., G. rakiura sp. nov., G. rotoiti sp. nov., G. rotoroa sp. nov., G. tewaipounamu sp. nov., G. waipapa sp. nov., G. waipoua sp. nov. (all from New Zealand); G. manuka sp. nov. and G. warra sp. nov. (both from Tasmania, Australia). Glemparon sagittifer Jaschhof, 2013 is redescribed. Genitalic illustrations are provided allowing for the effective identification of all the species known thus far. Morphological data obtained here are used for revising the generic definition. Dicerura Kieffer, 1898 is hypothesized as the sister group to Glemparon. The case of Glemparon is discussed as a perfect example of the fact that our collective ignorance of porricondyline diversity in most parts of the world is a major impediment to a better understanding of the European species.
Four new species of Lobolibethra Hennemann & Conle, 2007 (Diapheromerinae: Diapheromerini: “Clonistria-group”) are described and illustrated. Lobolibethra carbonelli sp. nov. and L. pozuzoae sp. nov. from eastern Peru are described from both sexes and the eggs, L. tricarinata sp. nov. from southeast Ecuador is described from the female and male, and L. verruculosa sp. nov. from eastern Peru is described from the male. The previously unknown males of the Peruvian L. mainerii (Giglio-Tos, 1910) and L. mutica Hennemann & Conle, 2007 are described and illustrated. Dyme iconnicoffi Caudell, 1918 is shown to represent the previously unknown male of L. mainerii (Giglio-Tos, 1910) and is synonymised (syn. nov.). An updated key is presented for the eleven known species of Lobolibethra.
Flower flies (Diptera, Syrphidae) of French Polynesia, with the description of two new species
(2018)
The flower flies (Diptera, Syrphidae) of French Polynesia are revised. A total of nine syrphid species were recorded from the five archipelagos of French Polynesia. Among them are two species new to science, Allograpta jacqi Mengual & Ramage sp. nov. and Melanostoma polynesiotes Mengual & Ramage sp. nov., and a new record for this country, Syritta aenigmatopatria Hardy, 1964. We provide DNA barcodes for all flower fly species of French Polynesia, making the syrphid fauna of this country the first one in the world to be entirely barcoded. New data on biology, flowers visited and some taxonomic notes are provided. An identification key for the species of Syrphidae in French Polynesia is given, as well as an identification key for the species of Melanostoma Schiner, 1860 in the Australasian and Oceanian Regions.
Afrocampe gen. nov. is described for its only species, A. prinslooi gen. et sp. nov., from Eastern and Western Cape, South Africa. This new genus is recognized as a member of the subfamily Tetracampinae Förster, 1856 of Tetracampidae Förster, 1856 based on the possession of 5-segmented tarsi in females and 4-segmented tarsi in males, the short straight calcar, the mesoscutum with distinct notauli, the mesoscutellum with two pairs of setae, the reduced mesopleural suture and the short stigmal and long postmarginal veins of the fore wing. Afrocampe gen. nov. is characterized by a large mesosoma, a non-convex first gastral tergite, an evenly acute calcar, a 5-segmented antennal funicle, a head lacking occipital carina and facial grooves and a long fore wing with distinctly delimited speculum, a bare admarginal area with a distinct admarginal row of setae on the underside and with 3 setal tracks (hair rows) radiating from the apex of the stigmal vein. The combination of these characters suggests a special status of the new genus within the subfamily Tetracampinae. Moreover, Afrocampe gen. nov. bears some resemblance to the Australian tetracampine genus Niticampe Bouček, 1988. The position of the latter in Tetracampinae, as well as habitus features of the former, are discussed.
Based on a study of 2150 specimens of the genus Trechus Clairville, 1806 from the Bale Mts, Mount Chillalo, and Mount Enkuolo, southern Ethiopia, the current knowledge regarding systematics and distribution of the genus in the area is summarized. Twenty-six new species are described and figured in detail: Trechus abalkhasimi sp. nov. (southeastern slope of Bale Mts, below Mt Abalkhasim); T. adaba sp. nov. (western Bale Mts, above Adaba); T. angavoensis sp. nov. (western Bale Mts, above Dodola); T. balesilvestris sp. nov. (western Bale Mts, above Adaba); T. bombi sp. nov. (southern escarpment of Bale Mts, Harenna Forest); T. colobus sp. nov. (western Bale Mts); T. depressipennis sp. nov. (northeastern margin of Sanetti Plateau, Bale Mts); T. dodola sp. nov. (western Bale Mts, above Dodola); T. fisehai sp. nov. (northern slope of Bale Mts, above Goba); T. grandipennis sp. nov. and T. hagenia sp. nov. (southern escarpment of Bale Mts, Harenna Forest); T. haggei sp. nov. (northeastern margin of Sanetti Plateau); T. harenna sp. nov. and T. harryi sp. nov. (southern escarpment of Bale Mts, Harenna Forest); T. iridescens sp. nov. (southeastern slope of Bale Mts, below Mt Abalk-hasim); T. mattisi sp. nov. (southern escarpment of Bale Mts, Harenna Forest); T. mekbibi sp. nov. (southern and western part of Bale Mts); T. minitrechus sp. nov. (northeastern slope of Mt Enkuolo); T. nanulus sp. nov. (southern escarpment of Bale Mts, Harenna Forest); T. nigrifemoralis sp. nov. and T. oppositus sp. nov. (western Bale Mts, above Dodola); T. rira sp. nov. (southern escarpment of Bale Mts, upper Rira Valley); T. sanettii sp. nov. (southeastern slope of Sanetti Plateau, Bale Mts); T. tragelaphus sp. nov. (western Bale Mts, above Dodola); T. transversicollis sp. nov. (southern escarpment of Bale Mts, Harenna Forest); T. wiersbowskyi sp. nov. (southern escarpment of Bale Mts, upper Rira Valley). New distributional data are provided for T. baleensis (Basilewsky, 1974), T. bastianinii Magrini & Sciaky, 2006, T. batuensis Magrini & Sciaky, 2006, T. chillalicus Jeannel, 1936, T. clarkeianus (Basilewsky, 1974), T. culminicola Jeannel, 1936, T. ericalis Magrini, Quéinnec & Vigna Taglianti, 2013, T. gallorites Jeannel, 1936, T. gypaeti Vigna Taglianti & Magrini, 2010, T. oromiensis Magrini, Quéinnec & Vigna Taglianti, 2012, T. relictus Magrini, Quéinnec & Vigna Taglianti, 2012 and T. rotundicollis (Basilewsky, 1974). Cothresia robini Basilewsky, 1974 is considered a junior synonym of T. chillalicus Jeannel, 1936. A key to all species known to occur in the Bale Mts and adjacent volcanos is presented.
Twenty-two new species of the genus Eviulisoma Silvestri, 1910, from the Eastern Arc Mountains, Tanzania, are described: E. acaciae sp. nov., E. aequilobatum sp. nov., E. akkariae sp. nov., E. angulatum sp. nov., E. articulatum sp. nov., E. biquintum sp. nov., E. breviscutum sp. nov., E. cetafi sp. nov., E. chitense sp. nov., E. commelina sp. nov., E. coxale sp. nov., E. ejti sp. nov., E. grumslingslak sp. nov., E. kalimbasiense sp. nov., E. navuncus sp. nov., E. nessiteras sp. nov., E. ottokrausi sp. nov., E. paradisiacum sp. nov., E. sternale sp. nov. and E. zebra sp. nov. from the Udzungwa Mts, E. culter sp. nov. from the Rubeho Mts and E. kangense sp. nov. from the Kanga Mts. Eviulisoma kwabuniense Kraus, 1958, and E. dabagaense Kraus, 1958, both from the Udzungwa Mts, are redesribed based on new material. Notes are provided on E. iuloideum (Verhoeff, 1941) based on type material. Eoseviulisoma Brolemann, 1920, is synonymized under Eviulisoma, based on newly collected material of E. julinum (Attems, 1909), type species of Eoseviulisoma. New material of Suohelisoma ulugurense Hoffman, 1964, type species of Suohelisoma Hoffman, 1964, has revealed that the gonopod structure is more similar to that of Eviulisoma than originally thought, but Suohelisoma is retained as a valid genus. Four species groups are recognized among Eviulisoma species from the Udzungwa Mts, but the need for a revision of the entire genus is emphasized. Two types of epizootic fungi are recorded from Eviulisoma spp., and an enigmatic amorphous mass, which may be a kind of plugging substance, is recorded from the gonopod tips and excavated sixth sternum of several species.
A new genus of jumping spiders, Bavirecta gen. nov. is proposed to include the type species B. flavopuncta gen. et sp. nov. and Bavirecta exilis (Cao et al., 2016) gen. et comb. nov. Distinguishing characters of Bavirecta gen. nov. include: 1) tubular abdomen, 2) enlarged front legs, 3) straight and
pointed embolus, broadest proximal lobe with black blotches, 4) prolateral tegular lobe, 5) widely separated anterior atria. Furthermore, two new species, Schenkelia aurantia sp. nov. (♂♀) and Brancus calebi (♂) sp. nov., are described and diagnosed. Mogrus frontosus (Simon, 1871) is redescribed based on a male collected from Mandaitivu Island of Jaffna District in Sri Lanka. The genera Brancus Simon, 1902, Mogrus Simon, 1882 and Schenkelia Lessert, 1927 are reported for the first time from Sri Lanka
(Brancus and Schenkelia are recorded for the first time outside Africa).
The systematic position of Tonza Walker, 1864 is re-evaluated, based on the characteristics of immature stages and DNA barcodes. Larvae and pupae of Tonza citrorrhoa Meyrick, 1905 are described and illustrated for the first time. Larvae of this species form a loose web among the leaves and branches of the host plant, Putranjiva matsumurae Koidz. (Putranjivaceae Endl.). The immature stages of Tonza exhibit four unique apomorphies including: in the larva, the prolegs on A5 and A6 absent, and the seta L2 on the A1–A8 very small; in the pupa, four minute knobs are positioned in the middle portion on abdominal segments V and VI; while its caudal processes possess a W-shaped spine with numerous minute spines. These characteristics clearly distinguish Tonza from other yponomeutoid families and hence, we propose a new family group name, Tonzidae Kobayashi & Sohn fam. nov., for the genus Tonza. Existing DNA barcode data suggest a relationship with Glyphipterigidae Stainton, 1854. The family level status of Tonzidae fam. nov. provides a hypothesis that needs to be tested with larger molecular data.