This paper reports the collecting of adult beetles and third-instar larvae of Coelocorynus desfontainei Antoine, 1999 in Cameroon and provides new data on the biology of this high-altitude Afromontane genus. It also presents the first diagnosis of this genus based on larval characters and examination of its systematic position in a phylogenetic context using 78 parsimony informative larval and adult characters. Based on the results of our analysis we (1) support the hypothesis that the tribe Trichiini is paraphyletic with respect to both Valgini and the rest of the Cetoniinae, and (2) propose that the Trichiini subtribe Cryptodontina, represented by Coelocorynus, is a sister group of the Valgini: Valgina, represented by Valgus. The larvae-only analyses were about twofold better than the adults-only analyses in providing a phylogenetic resolution consistent with the larvae + adults analyses. Only one of the ten clades was consistently supported by the analyses of both the larval and adult datasets, while the remaining nine were invariably strongly supported by one but not the other analysis, thus highlighting the importance of employing different data sources.
First and third instar larvae of Aepopsis robini (Laboulbène, 1849) are studied, redescribed, and illustrated. The larvae are characterised by three unique and likely autapomorphic character states within known members of the supertribe Trechitae: (1) apex of antennomere 4 has only one conical sensillun 1; (2) setae FR10 and FR11 on frontale are removed basally on dorsal surface from the apical margin; (3) terga of meso- and metathorax lack pore MEa, and abdominal terga 1-8 lack pore TEa.
Ant-like stone beetles (Coleoptera: Scydmaenidae) include more than 4,850 described species in about 90 genera maintained as a separate cosmopolitan family since 1815. Recent authors have hypothesised that Scydmaenidae might be rooted deep inside rove-beetles (Staphylinidae). To test this hypothesis we analysed 206 parsimoniously informative larval and adult morphological characters scored for 38 taxa. Strict consensus topologies from the shortest trees in all 12 analyses consistently placed Scydmaenidae as sister to (Steninae + Euaesthetinae) in a monophyletic Staphylinine Group (with or without Oxyporinae). The single fully resolved and most consistently supported topology maintains a monophyletic Staphylinine Group consisting of Oxyporinae + (Megalopsidiinae + (("Scydmaenidae" + (Steninae + Euaesthetinae)) + (Leptotyphlinae + (Pseudopsinae + (Paederinae + Staphylininae))))); Solierius lacks larval data and is ambiguously placed within the Group. Eight analyses of variably aligned 18S rDNA data for 93 members of Staphylinoidea under parsimony, neighbour-joining and Bayesian approaches were markedly inconsistent, although partly congruent with the Scydmaenidae + (Steninae + Euaesthetinae) hypothesis. Our results strongly suggest that ant-like stone beetles do not form an independent family, but are morphologically modified members of Staphylinidae and, consequently, should be treated as a 32nd recent subfamily within the megadiverse Staphylinidae sensu latissimo. Formal taxonomic acts are: Scydmaeninae Leach, 1815, status novus (= Scydmaenidae Leach, 1815); Scydmaenitae Leach, 1815, status novus (= Scydmaeninae Leach, 1815); Mastigitae Fleming, 1821, status novus (= Mastiginae Fleming, 1821); Hapsomelitae Poinar & Brown, 2004, status novus (= Hapsomelinae Poinar & Brown, 2004). The family Staphylinidae sensu latissimo becomes the largest in Coleoptera and in the whole of the Animal Kingdom, with 55,440 described species (extant plus extinct), thus surpassing Curculionidae with an estimated 51,000 described species.
The recently described and originally monotypic genus Discheramocephalus Johnson, 2007 from the Solomon Islands is revised. Six new species are described, illustrated and keyed: Discheramocephalus brucei sp. n. (Cameroon), D. elisabethae sp. n. (Cameroon), D. mikaeli sp. n. (Tanzania), D. stewarti sp. n. (Bolivia), D. jarmilae sp. n. (Bolivia), D. minutissimus sp. n. (Indonesia). Adults of D. minutissimus have a body length of about 400-426 µm, which is at the lower limit among non-egg-parasitoid insects. Evidence is provided that an egg size large enough to produce a viable larva is the main factor limiting miniaturisation of female insects. Females and males of egg-parasitoids are able to overcome the 400 µm threshold and reach limits of 180 µm and 130 µm, respectively. Brain size is likely the second most important factor limiting miniaturisation in insects.
Tomicus piniperda and T. destruens are sibling species which are extremely difficult to separate by morphological characters. Although several papers report differences between the two species, many characters need confirmation or better description. Moreover, new morphological characters are required for correct species determination. For these purposes, eight populations of T. destruens from Italy, Greece, Spain and Algeria, and ten of T. piniperda from Finland, Poland, Czech Republic, Austria, Sweden and Italy, were investigated considering eleven morphological characters. The morphological differences most useful for the species separation include four previously described characters (colour of the elytra, colour of the antennal club, distribution of the antennal setae, distribution of the punctures along the elytral declivity), and four new characters (body proportions, setation of the first antennal club suture, sculpture of the elytral declivity and striae density of the pars stridens). Distribution of the two species is discussed and an illustrated key is included.
Larvae of three genera representing the staphylinid subfamily Pseudopsinae are described for the first time and illustrated with 33 morphological drawings: Pseudopsis Newman, Zalobius LeConte and Nanobius Herman. Thirty-six characters (mainly of larval morphology) were scored for representatives of six staphylinid subfamilies and a phylogenetic analysis was carried out. The monophyly of the subfamily Pseudopsinae is supported by the presence of a short oblique ridge on ventral side of larval head capsule laterad of maxillary foramina. The monophyly of each of the subfamilies Paederinae and Staphylininae is discussed based on the characters of the immature stages. The subfamily Pseudopsinae is confirmed to be a sister-group of the subfamilies Paederinae + Staphylininae on the basis of six larval synapomorphies. The latter clade is confirmed to be monophyletic on the basis of five larval synapomorphies. A larval identification key to the studied Pseudopsinae genera is provided.
This paper presents a synthesis of morphological information on larvae of the beetle suborder Archostemata. Larvae of the following families and species were studied: Ommatidae: Omma sp.; Micromalthidae: Micromalthus debilis LeConte, 1878; Cupedidae: Priacma serrata LeConte, 1861, Distocupes varians (Lea, 1902), Rhipsideigma raffrayi (Fairmaire, 1884), Tenomerga cinerea (Say, 1831) and Tenomerga mucida (Chevrolat, 1829). Morphological characters of the suborder and three families are described. Monophyly of the suborder is strongly supported by more than 10 larval autapomorphies. A close relationship between Micromalthidae and Cupedidae is confirmed. New larval characters are introduced, including chaetotaxy of first instar larvae of Micromalthus LeConte, 1878, Priacma LeConte, 1874 and Distocupes Neboiss, 1984. An identification key to families and subfamilies of Archostematan larvae is provided, along with a checklist of extant Archostemata taxa. The work is illustrated with 120 morphological drawings.
A new genus, Trurlia Jałoszyński, in the tribe Cephenniini (Scydmaenidae: Scydmaeninae) is described. The type species is T. insana sp. n. from Sumatra; females of an undescribed species are also reported to occur in W Malaysia. Trurlia most closely resembles Cephennomicrus Reitter, but it is the first genus of the Scydmaenidae with entirely fused antennomeres 10 and 11, forming a large, oval, abruptly separated club. Based on a disarticulated female of Trurlia sp., the detailed morphology of the new genus is described and illustrated, and possible relationships with other genera of the tribe are discussed. Comments on evolution, polarity of characters and feeding strategy of the Cephenniini are included.