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Our knowledge of early evolution of snakes is improving, but all that we can infer about the evolution of modern clades of snakes such as boas (Booidea) is still based on isolated bones. Here, we resolve the phylogenetic relationships of Eoconstrictor fischeri comb. nov. and other booids from the early-middle Eocene of Messel (Germany), the best-known fossil snake assemblage yet discovered. Our combined analyses demonstrate an affinity of Eoconstrictor with Neotropical boas, thus entailing a South America-to-Europe dispersal event. Other booid species from Messel are related to different New World clades, reinforcing the cosmopolitan nature of the Messel booid fauna. Our analyses indicate that Eoconstrictor was a terrestrial, medium- to large-bodied snake that bore labial pit organs in the upper jaw, the earliest evidence that the visual system in snakes incorporated the infrared spectrum. Evaluation of the known palaeobiology of Eoconstrictor provides no evidence that pit organs played a role in the predator–prey relations of this stem boid. At the same time, the morphological diversity of Messel booids reflects the occupation of several terrestrial macrohabitats, and even in the earliest booid community the relation between pit organs and body size is similar to that seen in booids today.
Three species of Lophogastrida and eight Mysida are documented for samples from 5161–5497 m bottom depth in the Angola Basin. Previously known latitudinal ranges are extended southward for five species, and bathymetric ranges extended beyond 5000 m for six species. Upon revision of the subfamily Petalophthalminae (Mysidae), four species previously attributed to the genus Petalophthalmus are integrated into Ipirophthalmus gen. nov. as I. liui gen. et comb. nov., I. caribbeanus gen. et comb. nov., I. oculatus gen. et comb. nov., and I. macrops gen. et comb. nov., mainly based on the structure of eyes and presence of setae on the telson. Petalophthalmus cristatus sp. nov. is described based on its reduced cornea and the structure of eyestalks, rostrum, mandibles, and telson. The structure of mouthparts, foregut and maxillipeds suggests an omnivorous mode of life. The diagnosis of the tribe Calyptommini (Mysidae: Erythropinae) is widened to cover the 3-segmented, uniramous fourth male pleopod and the non-incised eyeplate with horn-like rudiments of eyestalks in Abyssomysis cornuta gen. et sp. nov. The structure of mandibles, foregut, and second maxilliped suggest detritus feeding in this species. Keys to the Calyptommini and Petalophthalminae are given.
Features of the Maechidiini (Scarabaeidae: Melolonthinae) genera Maechidius Macleay, 1819, Epholcis Waterhouse, 1875 and Paramaechidius Frey, 1969 are critically revised and a new synonymy is proposed: Maechidius = Epholcis syn. nov. = Paramaechidius syn. nov. A key to and an annotated checklist of Maechidiini from the Indo-Australian transition zone are presented for the first time. Thirty-five new species are described, namely Maechidius aiyura sp. nov., M. alesbezdeki sp. nov., M. awu sp. nov., M. babyrousa sp. nov., M. bintang sp. nov., M. boessnecki sp. nov., M. brocki sp. nov., M. caperatus sp. nov., M. ciliatus sp. nov., M. crypticus sp. nov., M. dani sp. nov., M. deltouri sp. nov., M. dendrolagus sp. nov., M. hamatus sp. nov., M. kazantsevi sp. nov., M. konjo sp. nov., M. lapsus sp. nov., M. legalovi sp. nov., M. leucopsar sp. nov., M. longipes sp. nov., M. mailu sp. nov., M. maleo sp. nov., M. merdeka sp. nov., M. miklouhomaclayi sp. nov., M. nepenthephilus sp. nov., M. owenstanleyi sp. nov., M. riedeli sp. nov., M. similis sp. nov., M. skalei sp. nov., M. sougb sp. nov., M. suwawa sp. nov., M. trivialis sp. nov., M. ursus sp. nov., M. weigeli sp. nov. and M. yamdena sp. nov. Six new synonyms are proposed: Maechidius Macleay, 1819 = Epholcis Waterhouse, 1875 syn. nov. = Paramaechidius Frey, 1969 syn. nov., Maechidius esau Heller, 1914 = M. setosus Moser, 1920 syn. nov. = M. setosellus Frey, 1969 syn. nov., Maechidius heterosquamosus Heller, 1910 comb. rest. = Paramaechidius clypeatus Frey, 1969 syn. nov. and Maechidius paupianus Heller, 1910 = M. arrowi Frey, 1969 syn. nov. The first records of Maechidiini from the Tanimbar Islands (Yamdena), Sangihe Islands (Sangir) and Lesser Sunda Islands (Bali) are documented, of which the latter two are the northern- and westernmost known records of Maechidius and of the tribe Maechidiini. Lectotypes are designated for 23 species. Fifteen new combinations are proposed and the original combination to Maechidius is restored for four species. Ecological data are presented for the first time for selected Papuan and Wallacean species. Type material of Wallacean and Papuan Maechidiini is depicted for the first time. A key to species is given. In total, 78 species of Maechidiini are confirmed for the Indo-Australian transition zone.
The geographical range of the typically host-specific species of chewing lice (Phthiraptera) is often assumed to be similar to that of their hosts. We tested this assumption by reviewing the published records of twelve species of chewing lice parasitizing wild and domestic chicken, one of few bird species that occurs globally. We found that of the twelve species reviewed, eight appear to occur throughout the range of the host. This includes all the species considered to be native to wild chicken, except Oxylipeurus dentatus (Sugimoto, 1934). This species has only been reported from the native range of wild chicken in Southeast Asia and from parts of Central America and the Caribbean, where the host is introduced. Potentially, this discontinuous distribution is due to a low tolerance for dry environments, possibly exacerbated by competitive exclusion by Cuclotogaster heterographus (Nitzsch, 1866). Our examinations of O. dentatus also revealed that this species differs significantly from other species of Oxylipeurus in the male and female genitalia, head structure and chaetotaxy, and other morphological characters. We therefore here erect the monotypic genus Gallancyra gen. nov. for O. dentatus, and redescribe the type species.
Cloeon perkinsi was described from South Africa in 1932 by Barnard. Despite being relatively common in Africa, it was mentioned in the literature quite rarely, and its known distribution to date includes most of sub-Saharan Africa. Material collected recently in Ethiopia, Israel, Saudi Arabia, and Yemen extends its distribution in East Africa, Arabian Peninsula and the Levant. We examined this material, and provide a re-description of adults (females and males) and nymphs of the species. It represents a much-needed urge mainly due to inconsistencies in literature reports regarding colouration, and sometimes incomplete morphological description of all stages. We demonstrate the intraspecific morphological variability that we have witnessed, and provide information regarding the range of habitats colonised by C. perkinsi. Based on geological and climatic history of the studied region, taken together with among countries genetic distances of the mitochondrial barcoding gene COI, we propose colonisation mechanisms for the north-easternmost limit of distribution. The fragmented distribution pattern of the species highlights the conservation importance of isolated aquatic habitats in the region, as well as current knowledge gaps.
Revision of the endemic Malagasy leafhopper tribe Platyjassini (Hemiptera: Cicadellidae: Iassinae)
(2020)
The leafhopper tribe Platyjassini, endemic to Madagascar, is revised, largely based on specimens obtained in a recent bioinventory project led by the California Academy of Sciences. Platyjassini was previously known based on the type genus, Platyjassus Evans, 1953, and four described species. Betsileonas marmorata (Blanchard, 1840), the largest leafhopper recorded from Madagascar, presently known from a few specimens collected > 100 years ago and recently considered a genus and species incertae sedis within Cicadellidae, is newly placed in Platyjassini. Fourteen new genera and 54 new species are described and illustrated, and three new combinations are proposed. Pachyjassus gen. nov. includes three new species: Pachyjassus alatus sp. nov., Pachyjassus basifurcatus sp. nov. and Pachyjassus ranomafanensis sp. nov. Pallijassus gen. nov. is erected to include two species previously placed in Platyjassus, Pallijassus reticulatus (Evans, 1959) comb. nov. and Pallijassus stenospatulatus (Evans, 1959) comb. nov. Petalojassus gen. nov. includes one new species, Petalojassus ochrescens sp. nov. Phaiojassus gen. nov. includes seven new species: Phaiojassus acutus sp. nov., Phaiojassus bispinosus sp. nov., Phaiojassus constrictus sp. nov., Phaiojassus grandis sp. nov., Phaiojassus spatulatus sp. nov., Phaiojassus undulatus sp. nov. and Phaiojassus unispinosus sp. nov. Pictojassus gen. nov. includes three new species: Pictojassus kirindiensis sp. nov., Pictojassus productus sp. nov. and Pictojassus tulearensis sp. nov. Platyjassella gen. nov. includes six new species: Platyjassella ancora sp. nov., Platyjassella andohahelensis sp. nov., Platyjassella attenuata sp. nov., Platyjassella cormorana sp. nov., Platyjassella emarginata sp. nov. and Platyjassella immaculata sp. nov. Platyjassula gen. nov. includes four new species: Platyjassula cyclura sp. nov., Platyjassula heterofurca sp. nov., Platyjassula isofurca sp. nov. and Platyjassula mahajangensis sp. nov. In addition to the type species, Platyjassus viridis Evans, 1953, Platyjassus includes 11 new species: Platyjassus acutus sp. nov., Platyjassus asymmetricus sp. nov., Platyjassus fisheri sp. nov., Platyjassus griswoldi sp. nov., Platyjassus harinhalai sp. nov., Platyjassus irwini sp. nov., Platyjassus pedistylus sp. nov., Platyjassus pennyi sp. nov., Platyjassus pictipennis sp. nov., Platyjassus symmetricus sp. nov. and Platyjassus vestigius sp. nov. Plerujassus gen. nov. includes one new species, Plerujassus brunnescens sp. nov., in addition to Plerujassus appendiculatus (Evans, 1959) comb. nov., previously placed in Platyjassus. Plexijassus gen. nov. includes one new species, Plexijassus caliginosus sp. nov. Pseudocurtara gen. nov. includes three new species: Pseudocurtara minima sp. nov., Pseudocurtara nigripicta sp. nov. and Pseudocurtara quadrata sp. nov. Pseudocyrta gen. nov. includes one new species, Pseudocyrta hyalina sp. nov. Pseudomarganana gen. nov. includes two new species: Pseudomarganana olivacea sp. nov. and Pseudomarganana rosea sp. nov. Pulchrijassus gen. nov. includes eight new species: Pulchrijassus anjozorobensis sp. nov., Pulchrijassus eunsunae sp. nov., Pulchrijassus pallescens sp. nov., Pulchrijassus roseus sp. nov., Pulchrijassus rubrilineatus sp. nov., Pulchrijassus sindhuae sp. nov., Pulchrijassus talatakelyensis sp. nov. and Pulchrijassus toamasinensis sp. nov. Punctijassus gen. nov. includes three new species: Punctijassus circularis sp. nov., Punctijassus compressus sp. nov. and Punctijassus ivohibensis sp. nov. Illustrated keys to genera and species are provided.