Revision of the genus Hemisaprinus Kryzhanovskij, 1976 (Coleoptera,Histeridae, Saprininae)

The monophyletic genus Hemisaprinus Kryzhanovskij in Kryzhanovskij & Reichardt, 1976 is revised herein. All three species Hemisaprinus subvirescens (Ménétries, 1832), H. lutshniki (Reichardt, 1941) and H. cyprius (Dahlgren, 1981) are found to be correctly assigned to the genus and their monophyly is supported by the synapomorphy of the presence of prosternal foveae. The three species are re-described and supplemented with colour photographs as well as SEM micrographs outlining their differences. Male genitalia drawing of H. subvirescens and H. lutshniki are provided and a key to the species is given. Hemisaprinus subvirescens (Ménétries, 1832) is newly reported from Armenia, Azerbaijan, Kyrgyzstan, Uzbekistan, Turkmenistan, Tajikistan, Jordan, Cyprus and Mongolia. The lectotypes and paralectotypes of the following species are designated herein: Saprinus foveisternus Schmidt, 1884, Saprinus syriacus Marseul, 1855 and Saprinus viridulus Marseul, 1855.     

New genera and species of Neotropical Exosternini (Coleoptera,Histeridae)

We describe the following 8 new genera and 23 new species of Neotropical Exosternini. Conocassis gen. n. (Conocassis minor sp. n. [type species], Conocassis dromedaria sp. n., Conocassis trisulcata sp. n., and Conocassis invaginata sp. n.), Enkyosoma gen. n. (Enkyosoma rockwelli sp. n.), Pluricosta gen. n. (Pluricosta onthophiloides sp. n.), Pyxister gen. n. (Pyxister devorator sp. n. [type species] and Pyxister labralis sp. n.), Chapischema gen. n. (Chapischema doppelganger sp. n.), Scaptorus gen. n. (Scaptorus pyramus sp. n.), Lacrimorpha gen. n. (Lacrimorpha glabra sp. n. [type species], Lacrimorpha balbina sp. n., Lacrimorpha subdepressa sp. n., and Lacrimorpha acuminata sp. n.), Crenulister gen. n. (Crenulister grossus sp. n. [type species], Crenulister explanatus sp. n., Crenulister dentatus sp. n., Crenulister impar sp. n., Crenulister umbrosus sp. n., Crenulister simplex sp. n., Crenulister paucitans sp. n., Crenulister spinipes sp. n., and Crenulister seriatus sp. n.) These all represent highly distinctive and phylogenetically isolated forms, almost invariably known from very few specimens. All but one species have been collected only by passive flight intercept traps, and nothing significant is known about the biology of any of them.     

Phylogeny of European Pyrochroa (Coleoptera,Pyrochroidae) reveals cryptic taxa and different glacial histories

Only three saproxylic species of Pyrochroinae (Coleoptera: Pyrochroidae) are distributed in Europe, two of which belonging to Pyrochroa: P. coccinea and P. serraticornis. However, P. serraticornis is polytypic, for the presence of the endemic subspecies P. s. kiesenwetteri in southern Italy. Using both molecular and morphological data, we explored the phylogeny of the European Pyrochroa species. A multilocus (COI, CAD, 28S) phylogenetic analysis helped highlight different evolutionary histories for the two examined species. First, P. coccinea, distributed throughout Europe, showed a high differentiation among Italian and European populations. Furthermore, three different taxonomic entities were identified within P. serraticornis, among which the cryptic species Pyrochroa bifoveata sp. n. from central Europe is described and illustrated. A comprehensive identification key to the European Pyrochroinae is also provided. Our results also suggested an historical survival of P. coccinea and P. s. kiesenwetteri in glacial refugia in Italy, and a subsequent post-glacial spread of the former species throughout the Peninsula. In contrast, the current distribution of P. s. serraticornis likely originated from a post-glacial colonization of western European relict populations, while the survival of P. bifoveata plausibly occurred in more eastern glacial refugia (e.g. Carpathian or Balkan regions). Similarly, the European populations of P. coccinea could have originated from relict populations in glacial refugia out from the Italian Peninsula. More comprehensive data on the taxonomy, ecology and biogeography of Pyrochroa are needed to learn more about these species and to help preserve the European saproxylic fauna.     

Phylogeny of subfamily Epidendroideae (Orchidaceae) inferred from ndhF chloroplast gene sequences

This project undertakes the first molecular-based phylogenetic study of subfamily Epidendroideae (Orchidaceae). Approximately 1200 nucleotides (from the 3' half of the chloroplast gene ndhF for 34 orchid taxa and a lilioid monocot, Clivia miniata (Amaryllidaceae), were subjected to phylogenetic analysis using parsimony and maximum likelihood methods. Oryza sativa (Poaceae), a nonlilioid monocot, was designated as outgroup. Trees from both parsimony and maximum likelihood methods suggest that subfamily Epidendroideae is monophyletic, with Listera (Neottieae) as sister. Although subtribal relationships are typically well resolved and have strong branch support, intertribal relationships are generally poorly resolved. Perhaps this general lack of resolution among tribes reflects a rapid species radiation that coincided with anatomical, physiological, and anatomical adaptations that initiated large-scale epiphytism in the ancestral Epidendroideae. Six taxa in this study exhibit deletions that are not evenly divisible by three and result in extensive sequence frameshifts. For example, one deletion is 227 bp in length and is flanked by the short direct repeat sequence; TCAATAGGAATTTCTTTT. Multiple deletions and frameshifts suggest that ndhF may be a pseudogene, in at least some orchid taxa.     

Phylogenetic reassessment and biogeography of the Ectateus generic group (Coleoptera: Tenebrionidae: Platynotina)

Owing to the reinterpretation of its morphological synapomorphies, the taxonomic composition of the Ectateus generic group had been ambiguous. The present study scrutinized all existing taxonomic concepts of the group based on a cladistic analysis of the adult morphology of all of the Afrotropical platynotoid Platynotina genera. The phylogenetic relationships were reconstructed using parsimony and Bayesian inference. The results show that all previous taxonomic concepts of the Ectateus generic group concerned paraphyletic entities. The cladistic analysis revealed the following synapomorphies for the taxon: (1) presence of basal indentations of the pronotal disc, (2) ratio of prothorax width to its maximal height > 6.0, and (3) ratio of maximal height of the prothorax to total height < 0.3. Moreover, phylogenetic studies revealed the existence of the Upembarus generic group, a sister‐taxon group to the Ectateus generic group, within the Afrotropical platynotoid Platynotina. Autapomorphic and synapomorphic character mapping show that several taxonomic and nomenclatural changes are needed to consider the particular generic‐level entities traditionally assigned to Afrotropical platynotoid Platynotina as monophyletic lineages. The following taxonomic and nomenclatural adjustments are made in this paper: P teroselinus gen. nov. is erected to accommodate a single species that was previously assigned to Zidalus: Pteroselinus insularis comb. nov. Additionally, the following synonymies are proposed: Anchophthalmops (= Platykochius syn. nov. ), Angolositus (= Aberlencus syn. nov. , = Platymedvedevia syn. nov. ), Glyptopteryx (= Microselinus syn. nov. , = Quadrideres syn. nov. , = Synquadrideres syn. nov. ). In addition, Kochogaster is lowered in rank and is treated as one of the subgenera of Anchophthalmus. Moreover, Pseudoselinus is treated as a subgenus of Upembarus. An identification key to all Afrotropical platynotoid Platynotina genera and subgenera is presented. Zoogeographical analyses revealed the following dispersal barriers for the Ectateus generic group: (1) the Sahara (northern barrier); (2) the dry ecosystems of Botswana, Namibia, and South Africa (southern barrier); and (3) the Congolian rainforests (internal distributional gap). The ancestor of the taxon probably originated in East African ecoregions that predominantly contained wattletrees (acacias) and Commiphora Jacq. Moreover, past climate changes seem to have had a great impact on the observed generic distribution. © 2015 The Linnean Society of London     

Phylogeny and evolutionary history of the Aplodontoidea (Mammalia: Rodentia)

Athough over a hundred species of fossil aplodontoids have been described since the extant species, Aplodontia rufa (the mountain beaver), was first described by Rafinesque in 1817, a thorough survey of the relationships among all the species in this clade has not been undertaken since McGrew's study in 1941. Here, a complete phylogenetic analysis of all published species of aplodontoids is used to reconstruct the evolutionary relationships within the clade, and to present an updated classification of the Aplodontoidea. Several of the traditionally recognized subfamilies are found to be paraphyletic, namely the Prosciurinae, the Allomyinae, and the Meniscomyinae. Others, however, including the Aplodontinae and the Mylagaulidae, appear to be monophyletic. These latter two taxa, which include all of the hypsodont members of the aplodontoid clade, seem to be sister taxa. The history of the aplodontoid clade shows several episodes of rapid diversification in the Early Oligocene, the Late Oligocene, and the Early to Middle Miocene. The Ansomyinae and Aplodontinae show comparatively low speciation rates. The patterns of change in morphology and evolutionary rates suggest a need for a more detailed study of the causes of diversification, extinction, and ecological change in this lineage.  © 2008 The Linnean Society of London, Zoological Journal of the Linnean Society, 2008, 153 , 769–838.     

Female genitalia are moderately informative for phylogenetic inference and not concerted with male genitalia in Saprininae beetles (Coleoptera: Histeridae)

Our study – the first of its kind within Histeridae (Coleoptera) – deals with the female genitalia in the subfamily Saprininae, with respect to their variation and utility for phylogenetic reconstruction. Morphology of female genitalia (chiefly characters of the spermatheca, and variation of the gonocoxites, articulating sclerites and gonostyli) is herein described and depicted. We perform parsimony‐based morphological phylogenetic analyses of Saprininae using combined datasets that comprise somatic, male and female genitalia characters. We assess phylogenetic utility of female genital characters and test for their correlation with male genital characters. We found that female genitalia are generally moderately informative for phylogenetic reconstruction. The somatic and male genitalia characters (on average) possess higher phylogenetic signal; female genitalia provide better support and diagnoses for particular clades (emphasizing their importance for systematics), in which the evolution of female genitalia can be linked to environmental factors imposed by the mode of life. Regardless of the degree of informativeness, structures of female genitalia represent an additional interesting and important source of information for systematics and taxonomy. We did not find any evidence of correlated evolution between male and female genitalia.     

Are we doomed to repeat history? A model of the past using tiger beetles (Coleoptera: Cicindelidae) and conservation biology to anticipate the future

Studies of conservation biology involving tiger beetles have become increasingly common in the last 15 years. Governments and NGOs in several countries have considered tiger beetles in making policy decisions of national conservation efforts and have found tiger beetles useful organisms for arguing broad conservation issues. We trace the evolution of the relationship between tiger beetle studies and conservation biology and propose that this history may in itself provide a model for anticipating developments and improvements in the ability of conservation biology to find effective goals, gather appropriate data, and better communicate generalizations to non-scientific decision makers, the public, and other scientists. According to the General Continuum of Scientific Perspectives on Nature model, earliest biological studies begin with natural history and concentrate on observations in the field and specimen collecting, followed by observing and measuring in the field, manipulations in the field, observations and manipulations in the laboratory, and finally enter theoretical science including systems analysis and mathematical models. Using a balance of historical and analytical approaches, we tested the model using scientific studies of tiger beetles (Coleoptera: Cicindelidae) and the field of conservation biology. Conservation biology and tiger beetle studies follow the historical model, but the results for conservation biology also suggest a more complex model of simultaneous parallel developments. We use these results to anticipate ways to better meet goals in conservation biology, such as actively involving amateurs, avoiding exclusion of the public, and improving language and style in scientific communication. CXLV, Studies of Tiger Beetles     

New or interesting Laboulbeniales (Ascomycetes) on Japanese chlaeniine beetles (Coleoptera,Carabidae)

Four species ofLaboulbenia were isolated from Japanese chlaeniines and are reported.Laboulbenia habui is described as a new species; it is possibly related toL. fasciculata. Laboulbenia habui is characterized by the proliferation and division of cell V, resulting in the formation of an obliquely superposed series of cells from which short, cylindrical cells arise in a double row, whereas there is a single row of cubical cells inL. fasciculata. Laboulbenia humilis is new for the Japanese mycoflora; antheridia of this fungus were observed for the first time; shape of the perithecial apex, persistent antheridia and the spore size suggest thatL. humilis is not closely related toL. exigua and its related taxa. ForL. proliferans andL. fasciculata, new chlaeniine hosts are listed and some supplemental notes are given.     

Phylogeny of the Cocculinoidea (Mollusca, Gastropoda)

Abstract. The superfamily Cocculinoidea is a group of marine, deep-water, limpet-like gastropods. Recent speculation surrounding their affinities has concentrated on their placement within the Gastropoda. However, phylogenetic relationships within the Cocculinoidea, especially the monophyly of families and genera within the group, remain poorly understood. Phylogenetic analysis of 31 morphological characters for 15 cocculinoidean taxa and 2 outgroups resulted in a single most parsimonious tree, length=70, CI=0.62, and RI=0.71. Monophyly of the Cocculinoidea, Cocculinidae, and the genera Cocculina and Coccopigya was supported; Paracocculina and Coccocrater were found to be paraphyletic. Character optimization demonstrates that many characters often cited as diagnostic of various taxa, are often homoplastic and/or synapomorphies at different hierarchical levels.     

Phylogeny and evolution of Mesozoic and extant lineages of Histeridae (Coleoptera), with discovery of a new subfamily Antigracilinae from the Lower Cretaceous

In order to place a newly discovered species Antigracilus costatus gen. sp. n. from the Lower Cretaceous Yixian Formation (China) and to assess previously unplaced fossil taxa, we investigated the relationships of extant and extinct lineages of Histeridae based on three data sets: (i) 69 morphological characters belonging to 48 taxa (representing all 11 subfamilies and 15 of 17 tribes of modern Histeridae); (ii) partitioned alignment of 6030 bp from downloaded nucleotide sequences (28S, CAD, COI, 18S) of 50 taxa (representing 10 subfamilies and 15 of 17 tribes of modern Histeridae); and (iii) a combined morphological and molecular dataset for 75 taxa. Phylogenetic analyses of the morphology and combined matrices recovered the new Lower Cretaceous taxon as a sister group to remaining Histeridae and it is placed in †Antigracilinae subfam. n. †Antigracilinae constitutes the earliest record of Histeridae from the Lower Cretaceous Yixian Formation (∼125 Myr), backdating the minimum age of the family by 25 Myr from the earliest Cenomanian (~99 Myr) to the Barremian of the Cretaceous Period. Our molecular phylogeny supports Histeridae to be divided into seven different clades, with currently recognised subfamilies Abraeinae (sensu lato), Saprininae, Chlamydopsinae, and Histerinae (sensu lato) recovered as monophyletic, while Dendrophilinae, Onthophilinae, and Tribalinae are polyphyletic taxa. The Burmese amber species †Pantostictus burmanicus Poinar & Brown is placed as a sister group to the tribe Plegaderini (Abraeinae) and was assigned as a new tribe Pantostictini trib. n. Both molecular and combined phylogenies recovered the subfamilies Trypanaeinae and Trypeticinae deeply within the subfamily Abraeinae (sensu lato), and they are downgraded into Trypanaeini stat. n. and Trypeticini stat. n.     

Thermoregulatory strategies in two closely related sympatric Scarabaeus species (Coleoptera: Scarabaeinae)

Abstract. The thermoregulation strategies of Scarabaeus sacer L. and Scarabaeus cicatricosus Lucas were studied in the Doñana National Park, Spain. In this area, both species coexist, showing the same habitat and food preferences. However, S. cicatricosus is active during warmer parts of the day compared to S. sacer. Both species thermoregulate their thoracic temperature but, whereas the abdomen of S. sacer is a passive thermal window, S. cicatricosus actively thermoregulates abdominal temperature by increasing heat transfer from the thorax to the abdomen at high T_a values. In the case of S. sacer, their endothermy indicates an adaptive capacity to thorax heat retention, as occurs mainly in winter‐flying insects. This mechanism, possibly related to the aerodynamic flight posture in Scarabaeinae, could be an effective barrier to retard the rate of abdominal heat loss during flight. This endothermic strategy makes flight difficult at higher temperatures, although it allows flight during cooler periods of the day. On the other hand, S. cicatricosus showed a different adaptive behaviour to S. sacer. In this case, a significant decrease in abdominal heat loss at higher ambient temperatures would indicate a decrease in heat transfer from the thorax to the abdomen, as occurs in some desert and semiarid insects. This ‘heat exchanger’ mechanism observed in S. cicatricosus could be due to the irregular posture adopted during flight, with the posterior legs clearly extended and separate from the body. This behaviour increases turbulence and convective cooling, favouring exposure of the soft abdominal tergal cuticle and, subsequently, water loss. Thus, for S. cicatricosus, the well‐adapted ‘heat exchanger’ permits flight during periods of the day when temperatures would possibly be lethal for those species with high endothermy. From an adaptive viewpoint, these mechanisms of thermoregulation may explain how both closely‐related sympatric species respond in different ways to environmental temperature, favouring their coexistence.     

Cladistic analysis of Omalodini Kryzhanovskij (Coleoptera: Histeridae: Histerinae)

According to the current Histeridae classification, Omalodini is composed of 100 species described in 12 genera distributed in the Neotropical, Afrotropical, Afrotemperate and Oriental regions: Asolenus Lewis; Atribalus Bickhardt; Blypotehus Vienna, Ebonius Lewis; Lewisister Bickhardt; Notolister Lewis; Omalodes Erichson, divided in Omalodes (Omalodes), O. (Diplogrammicus) Lewis and O. (Cornillus) Lewis; Perfidolenus Vienna; Rhypochares Marseul; Scapomegas Lacordaire; Sphyracus Marseul; Theropatina Mazur. Our aims were to test the monophyly of Omalodini, using cladistic analysis, and propose a hypothesis of the phylogeny of the tribe. The matrix was composed of 49 terminal taxa (34 from the ingroup and 15 from the outgroup) and 131 characters of the adult morphology. The data were analysed under equal weights and implied weights. In both analyses, Omalodini represents a polyphyletic group and the trees obtained from equal weights analysis (two most parsimonious trees) were chosen in order to recover the tribe's monophyly. We recognize three lineages in Omalodini: Ebonius, undescribed genus and Omalodes, being supported by six transformations (Ebonius + (undescribed genus + Omalodes)). The sister group of Omalodini was defined as a clade composed of Histerini, Platysomatini and Hololeptini. The subgenera of Omalodes were not resolved consistently under different implied weight analyses. It is necessary to emphasize that Omalodes (Omalodes) comprises the largest group of Omalodini and requires an analysis with better sampling for more precise resolution of the internal phylogeny of the genus. The groups excluded a posteriori from Omalodini, Theropatina, Asolenus, Atribalus, Blypotehus, Lewisister, Notolister, Perfidolenus, Rhypochares, Sphyracus and Scapomegas, could not be allocated to any of the existing tribes of Histerinae.     

Taxonomic review of Agraphydrus from Japan (Coleoptera: Hydrophilidae: Acidocerinae)

The Japanese species of the genus Agraphydrus are revised. Five species are recognized, including Agraphydrus ogatai sp. nov. from Honshu, Shikoku and Kyushu. The new species can be distinguished by the coarse ground punctures on the pronotum and elytra, and by the shape of parameres. All species except A. luteilateralis are redescribed. All species are diagnosed, relevant morphological characters are illustrated, distributional records are summarized and an updated key is provided.     

Phylogeny and classification of tribe Aedini (Diptera: Culicidae)

The phylogeny and classification of tribe Aedini are delineated based on a cladistic analysis of 336 characters from eggs, fourth‐instar larvae, pupae, adult females and males, and immature stage habitat coded for 270 exemplar species, including an outgroup of four species from different non‐aedine genera. Analyses of the data set with all multistate characters treated as unordered under implied weights, implemented by TNT version 1.1, with values of the concavity constant K ranging from 7 to 12 each produced a single most parsimonious cladogram (MPC). The MPCs obtained with K values of 7–9 were identical, and that for K = 10 differed only in small changes in the relationships within one subclade. Because values of K < 7 and > 10 produced large changes in the relationships among the taxa, the stability of relationships exemplified by the MPC obtained from the K = 9 analysis is used to interpret the phylogeny and classification of Aedini. Clade support was assessed using parsimony jackknife and symmetric resampling. Overall, the results reinforce the patterns of relationships obtained previously despite differences in the taxa and characters included in the analyses. With two exceptions, all of the groups represented by two or more species were once again recovered as monophyletic taxa. Thus, the monophyly of the following genera and subgenera is corroborated: Aedes, Albuginosus, Armigeres (and its two subgenera), Ayurakitia, Bothaella, Bruceharrisonius, Christophersiomyia, Collessius (and its two subgenera), Dahliana, Danielsia, Dobrotworskyius, Downsiomyia, Edwardsaedes, Finlaya, Georgecraigius (and its two subgenera), Eretmapodites, Geoskusea, Gilesius, Haemagogus (and its two subgenera), Heizmannia (and subgenus Heizmannia), Hopkinsius (and its two subgenera), Howardina, Hulecoeteomyia, Jarnellius, Kenknightia, Lorrainea, Macleaya, Mucidus (and its two subgenera), Neomelaniconion, Ochlerotatus (subgenera Chrysoconops, Culicelsa, Gilesia, Pholeomyia, Protoculex, Rusticoidus and Pseudoskusea), Opifex, Paraedes, Patmarksia, Phagomyia, Pseudarmigeres, Rhinoskusea, Psorophora (and its three subgenera), Rampamyia, Scutomyia, Stegomyia, Tanakaius, Udaya, Vansomerenis, Verrallina (and subgenera Harbachius and Neomacleaya), Zavortinkius and Zeugnomyia. In addition, the monophyly of Tewarius, newly added to the data set, is confirmed. Heizmannia (Mattinglyia) and Verrallina (Verrallina) were found to be paraphyletic with respect to Heizmannia (Heizmannia) and Verrallina (Neomacleaya), respectively. The analyses were repeated with the 14 characters derived from length measurements treated as ordered. Although somewhat different patterns of relationships among the genera and subgenera were found, all were recovered as monophyletic taxa with the sole exception of Dendroskusea stat. nov. Fifteen additional genera, three of which are new, and 12 additional subgenera, 11 of which are new, are proposed for monophyletic clades, and a few lineages represented by a single species, based on tree topology, the principle of equivalent rank, branch support and the number and nature of the characters that support the branches. Acartomyia stat. nov. , Aedimorphus stat. nov. , Cancraedes stat. nov. , Cornetius stat. nov. , Geoskusea stat. nov. , Levua stat. nov. , Lewnielsenius stat. nov. , Rhinoskusea stat. nov. and Sallumia stat. nov., which were previously recognized as subgenera of various genera, are elevated to generic status. Catageiomyia stat. nov. and Polyleptiomyia stat. nov. are resurrected from synonymy with Aedimorphus, and Catatassomyia stat. nov. and Dendroskusea stat. nov. are resurrected from synonymy with Diceromyia. Bifidistylus gen. nov. (type species: Aedes lamborni Edwards) and Elpeytonius gen. nov. (type species: Ochlerotatus apicoannulatus Edwards) are described as new for species previously included in Aedes (Aedimorphus), and Petermattinglyius gen. nov. (type species: Aedes iyengari Edwards) and Pe. (Aglaonotus) subgen. nov. (type species: Aedes whartoni Mattingly) are described as new for species previously included in Aedes (Diceromyia). Four additional subgenera are recognized for species of Ochlerotatus, including Oc. (Culicada) stat. nov. (type species: Culex canadensis Theobald), Oc. (Juppius) subgen. nov. (type species: Grabhamia caballa Theobald), Oc. (Lepidokeneon) subgen. nov. (type species: Aedes spilotus Marks) and Oc. (Woodius) subgen. nov. (type species: Aedes intrudens Dyar), and seven are proposed for species of Stegomyia: St. (Actinothrix) subgen. nov. (type species: Stegomyia edwardsi Barraud), St. (Bohartius) subgen. nov. (type species: Aedes pandani Stone), St. (Heteraspidion) subgen. nov. (type species: Stegomyia annandalei Theobald), St. (Huangmyia) subgen. nov. (type species: Stegomyia mediopunctata Theobald), St. (Mukwaya) subgen. nov. (type species: Stegomyia simpsoni Theobald), St. (Xyele) subgen. nov. (type species: Stegomyia desmotes Giles) and St. (Zoromorphus) subgen. nov. (type species: Aedes futunae Belkin). Due to the unavailability of specimens for study, many species of Stegomyia are without subgeneric placement. As is usual with generic‐level groups of Aedini, the newly recognized genera and subgenera are polythetic taxa that are diagnosed by unique combinations of characters. The analysis corroborates the previous observation that ‘Oc. (Protomacleaya)’ is a polyphyletic assemblage of species.     

Afroprinus cavicola gen. et sp. n. from the Afrotropical region with notes on cave-dwelling Saprininae (Coleoptera,Histeridae)

A new genus and species from Kenya, Afroprinus cavicola is herein described and illustrated and its systematic position is discussed. By the prosternal pre-apical foveae connected by marginal prosternal stria it resembles most of the Afrotropical species of the genus Chalcionellus Reichardt, 1932, or some species of the genus Pholioxenus Reichardt, 1932 from South Africa and Namibia. Afroprinus can be distinguished from Chalcionellus chiefly by the lack of pronotal depressions and a coarsely sculptured, non-metallic dorsum; from Afrotropical species of Pholioxenus it can be most easily distinguished by the asetose pronotal hypomeron. The new taxon was discovered in a cave, but lacks obvious troglophilic adaptations. Notes on other Saprininae taxa found in caves are given. An identification key to the genera of Afrotropical Saprininae is provided.