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The evolution and interrelationships of carnivorous squamates (mosasaurs, snakes, monitor lizards, Gila Monsters) are a contentious part of reptile systematics and go to the heart of conflict between morphological and molecular data in inferring evolutionary history. One of the best-preserved fossils in this motley grouping is “Saniwa” feisti Stritzke, 1983, represented by complete skeletons from the early-middle Eocene of Messel, Germany. We re-describe it on the basis of superficial examination, stereoradiography, and high-resolution X-ray computed tomography of new and published specimens. The scalation of the lizard is unique, consisting of small, keeled scales on the head (including a row of enlarged medial supraorbitals) and large, rhomboidal, keeled scales (invested by osteoderms) that covered the rest of the body. Two paired longitudinal rows of enlarged scales ran down the neck. The head was laterally compressed and box-shaped due to the presence of a strong canthal-temporal ridge; the limbs and tail were very long. Notable osteological features include: a toothed, strap-like vomer; septomaxilla with a long posterior process; palpebral with a long posterolateral process; a lacrimal boss and a single lacrimal foramen; a well-developed cultriform process of the parabasisphenoid; two hypoglossal (XII) foramina in addition to the vagus; a lack of resorption pits for replacement teeth; and possibly the presence of more than one wave of developing replacement teeth per locus. There are no osteological modifications suggestive of an intramandibular hinge, but postmortem displacement of the angular-prearticular-surangular complex in multiple specimens suggests that there might have been some degree of mobility in the lower jaw based on soft-tissue modifications. Using phylogenetic analyses on a data-set comprising 473 morphological characters and 46 DNA loci, we infer that a monophyletic Palaeovaranidae Georgalis, 2017, including Eosaniwa Haubold, 1977, lies on the stem of Varanidae Merrem, 1820, basal to various Cretaceous Mongolian taxa. We transfer feisti to the new genus Paranecrosaurus n. gen. Analysis of gut contents reveals only the second known specimen of the cryptozoic lizard Cryptolacerta hassiaca Müller, Hipsley, Head, Kardjilov, Hilger, Wuttke & Reisz, 2011, confirming a diet that was at least partly carnivorous; the preservation of the teeth of C. hassiaca suggests that the gastric physiology of Paranecrosaurus feisti (Stritzke, 1983) n. comb. had high acidity but low enzyme activity. Based on the foregoing and linear discriminant function analysis, we reconstruct P. feisti n. comb., as a powerful, widely roaming, faunivorous-carnivorous stem monitor lizard with a sensitive snout. If the molecular phylogeny of anguimorphs is correct, then many of the features shared by Helodermatidae Gray, 1837 and Varanidae must have arisen convergently, partly associated with diet. In that case, a reconciliation of morphological and molecular data would require the discovery of equally primitive fossils on the helodermatid stem.
A list of taxa belonging to Xylotrupes Hope (Scarabaeidae: Dynastinae: Dynastini) is presented which incorporates several taxonomic actions: X. australicus darwinia Rowland comb. nov.; X. damarensis Rowland stat. nov.; X. lorquini zideki Rowland comb. nov.; X. macleayi szekessyi Endrödi comb. nov.; X. pachycera Rowland stat. nov.; X. philippinensis philippinensis Endrödi stat. nov.; X. philippinensis peregrinus Rowland comb. nov.; X. sumatrensis tanahmelayu Rowland comb. nov.; X. tadoana Rowland stat. nov.; X. telemachos Rowland stat. nov.; X. wiltrudae Silvestre stat. nov. Two new taxa are described: X. carinulus sp. nov. and X. clinias buru ssp. nov. Lectotypes are designated for X. lamachus Minck and X. clinias Schaufuss. Xylotrupes lamachus is found to be a junior subjective synonym of X. ulysses (Guérin-Méneville), new synonymy.
A new genus of Lebinthina (Orthoptera: Gryllidae: Eneopterinae) is erected based on species from Maluka Islands near northern Sulawesi (Indonesia): Platybinthus gen. nov. This new genus currently consists of three species. Platybinthus punctatus (Brunner von Wattenwyl, 1898) gen. et comb. nov. from Halmahera Island is assigned as the type species. Platybinthus striolatus gen. et comb. nov., also from Halmahera Island, is redescribed. We also describe a new species: Platybinthus sandyi gen. et sp. nov. from Morotai Island.
Nomenclatural changes are made in three previously described genera in the planthopper tribe Hemisphaeriini (Hemiptera: Fulgoromorpha: Issidae: Issinae), viz Gergithus Stål, 1870, Mongoliana Distant, 1909 and Hemisphaeroides Melichar, 1903. In addition, a new genus, Gnezdilovius gen. nov., with Gergithus lineatus Kato, 1933 as its type species, is described for 40 species formerly included in Gergithus, and the generic characteristics of the latter genus is revised. One new species, Gergithus frontilongus sp. nov. from China (Yunnan), is described and illustrated. One additional Gergithus species, previously misidentified as G. signatifrons Melichar, 1906 from Siberut Island, is mentioned and illustrated. Gergithus contusus Walker, 1851 is transferred to Mongoliana and Hemisphaerius atromaculatus Distant, 1916 and H. fuscoclypeatus Distant, 1916 are transferred to Hemisphaeroides. Checklists for all four genera are provided detailing the nomenclatural changes and a key to the 19 genera of Hemisphaeriini is provided. Morphological diversity and distribution of the genera are briefly discussed.
During verifications of museum material for the Catalogue of the Palaearctic Coleoptera, the type specimen of Hylobius huguenini Reitter, 1891 conserved in the Hungarian National Museum was examined. The type specimen had been found by Gustav Huguenin in the Emmental region in Switzerland. The species was never found again and remained therefore mysterious. After the examination of the type specimen, it became clear that Hylobius huguenini belongs to the American genus Heilipodus Kuschel, 1955 (comb. nov.), and there it ranks as a good species next to Heilipodus goeldii sp. nov., described here, and H. polyspilus (Pascoe, 1889), both from Brazil. The type specimens of Heilipodus goeldii sp. nov. were found in the Emil August Göldi-collection in the Natural History Museum of the Burgergemeinde Bern.
A systematic redefinition of the species belonging to the genus Geomyphilus Gordon and Skelley, 2007 (Coleoptera: Scarabaeidae: Aphodiinae) of Mexico and neighboring countries is presented. The new species G. tuzincola of Mexico is described and figured. The new combination Coelotrachelus macgregori (Islas, 1955) is proposed.
Differential diagnoses, updates on distribution ranges, and an illustrated identification key are given for all species of Agamopus. The first record for A. castaneus from Brazil is given. Type specimens of all valid species-group names are studied and illustrated. Notes on the natural history of Agamopus species, as well as brief phylogenetic comments, are presented. The new species Agamopus joker sp. nov. is described based on a male from Paraná, southern Brazil. Lectotypes are designated for Canthon unguicularis Harold, 1883 and Agamopus lampros Bates, 1887. We also propose the transfer of Agamopus convexus Balthasar, 1965 to the Ateuchus ovalis species group (Ateuchus convexus comb. nov.) based on morphological features of the protibiae, clypeal teeth, and the posterior margin of the pronotum and pygidium.
Walter Biese described Littoridina santiagensis Biese, 1944 (Cochliopidae) from Estero Dehesa in 1944 based exclusively on external shell features and a second allopatric population in Yeso Spring three years later. Since 2011 different samplings have been carried out at the type locality and have only provided specimens of the morphologically similar invasive mudsnail Potamopyrgus antipodarum Gray, 1843 (Tateidae), raising doubts about the identity of the species. The recent finding of two snail morphotypes in Yeso Spring, a thick shelled form congruent with type specimens of L. santiagensis and a slender one morphologically associable to P. antipodarum, allowed comparative studies, including the taxonomic analysis of additional populations with similar shell morphology occurring in central Chile. A DNA barcoding (COI) approach identified the slender form from Yeso Spring in Maipo Basin and a second population from the contiguous Rapel Basin indeed as the invasive P. antipodarum; however, L. santiagensis was recovered among species of Potamolithus Pilsbry, 1896 (Tateidae), justifying the Potamolithus santiagensis (Biese, 1944) comb. nov. Besides recognition of three other populations as belonging to Potamolithus, the molecular analysis also suggests trans-Andean dispersal of this group of snails in the Southern Cone of South America.
The taxonomic history of the rhinotragine genera Phygopoda Thomson, 1864 and Pseudophygopoda Tavakilian and Peñaherrera-Leiva, 2007 (Coleoptera: Cerambycidae: Cerambycinae) are discussed, and evidence is presented to suggest that some recent taxonomic changes made by Carelli and Monné (2015) were unjustified. Consequently, Phygopoda nigritarsis Gounelle, 1911 is moved to the genus Neophygopoda Melzer, 1933, creating the new combination Neophygopoda nigritarsis, the genera Panamapoda Clarke, 2014 and Paraphygopoda Clarke, 2014 are revalidated, and the species Paraphygopoda viridimicans (Fisher, 1952) and Paraphygopoda nappae Clarke, 2014 are also revalidated.
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.
The classification of the genera belonging to the doryctine tribe Rhaconotini (Braconidae) is updated. The following new taxa are described: Troporhaconotus gen. nov. (with 12 species), Afroipodoryctes subgen. nov. (of Ipodoryctes Granger, 1949) (with three species), Hexarhaconotinus subgen. nov. (of Rhaconotinus Hedqvist, 1965) (with ten species), Bathycentor zimbabwensis sp. nov., Ipodoryctes (Afroipodoryctes) reunionus sp. nov., I. (A.) saintphilippensis sp. nov., Platyspathius (Platyspathius) venezuelicus sp. nov., P. (P.) ranomafanus sp. nov., Rhacontsira haeselbarthi sp. nov., Rh. mozambiquensis sp. nov., Rh. saigonensis sp. nov. and Rh. toamasina sp. nov. The generic status of Euryphrymnus Cameron, 1910 is resurrected. The generic name Aptenobracon Marsh, 1965 is synonymised under Rhaconotus Ruthe, 1854 (syn. nov.); Rhaconotus asiaticus Belokobylskij, 1990 is synonymised under Rh. kerzhneri Belokobylskij, 1985 (syn. nov.). The new name, Rhaconotinus austrochinensis nom. nov., is suggested for the preoccupied name Rhaconotus chinensis Chen & Shi, 2004 (December) not Rhaconotus chinensis Belokobylskij & Chen, 2004 (June). New species contents, in many cases with numerous new combinations, are suggested for the genera Bathycentor Saussure, 1892, Euryphrymnus Cameron, 1910, Ipodoryctes Granger, 1949, Rhaconotinus Hedqvist, 1965 and Rhaconotus. The tribe Leptorhaconotini is synonymised with Rhaconotini based on previously published molecular phylogenetic studies, though we leave this group within the subtribe Leptorhaconotina.
A new jumping spider genus, Manzuma gen. nov. (Salticidae Blackwall, 1841), is described, type species is Manzuma nigritibia (Caporiacco, 1941). Aelurillus reconditus Wesołowska & van Harten, 1994 is synonymized with Rafalus nigritibiis (Caporiacco, 1941). Four new combinations are proposed: M. jocquei gen. et comb. nov. (ex Aelurillus), M. kenyaensis gen. et comb. nov. (ex Langelurillus), M. lympha gen. et comb. nov. (ex Rafalus) and M. nigritibia gen. et comb. nov. (ex Rafalus). Three species, M. botswana gen. et sp. nov. (♂♀, Botswana and Republic of South Africa), M. petroae gen. et sp. nov. (♂♀, Republic of South Africa) and M. tanzanica gen. et sp. nov. (♂, Tanzania), are described. The male of M. kenyaensis gen. et comb. nov. and female of M. lympha gen. et comb. nov. are described for the first time. A new aelurilline synapomorphy is proposed. Identification key for males is provided.