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.
The genus Berchmansus Navás, which was previously assigned to the tribe Leucochrysini, consists of three very rare species, all described from the Neotropics and all poorly known. Our report (1) provides the first description of a Berchmansus larva, the first instar of Berchmansus elegans (Guérin Méneville), (2) illustrates and redescribes the B. elegans adult, with emphasis on male and female genitalia, and (3) examines the larval and adult characters vis-à-vis the tribal affiliation of the genus. Given that the B. elegans adult and first instar share many apomorphies with other belonopterygine genera, this species belongs in the cosmopolitan tribe Belonopterygini, rather than the New World tribe Leucochrysini. Although Berchmansus larvae have not been collected in the field, we suspect that, like other belonopterygines, they are associated with ant nests. B. elegans exhibits a number of highly modified and unusual structures, some of which (#1 to #5) are not reported for any other chrysopids. Specifically: Males have (1) a unique, quadrate, dome-like hood above the gonarcus and (2) large, coiled parameres on the gonosaccus. First instars have (3) a greatly enlarged subapical seta on the flagellum, (4) a transverse row of long, hooked setae along the dorso-anterior margin of the pronotum, and (5) setose laterodorsal tubercles on the meso- and metathorax, with (6) multi-pronged, hooked setae.
Selected representatives of Cucujoidea, Cleroidea, Tenebrionoidea, Chrysomelidae, and Lymexylidae were examined. External and internal head structures of larvae of Sphindus americanus and Ericmodes spp. are described in detail. The data were analyzed cladistically. A sister group relationship between Sphindidae and Protocucujidae is suggested by the vertical position of the labrum. The monophyly of Cucujiformia is supported by the reduced dorsal and anterior tentorial arms, fusion of galea and lacinia, and the presence of tube-like salivary glands. Absence of M. tentoriopraementalis inferior and presence of a short prepharyngeal tube are potential synapomorphies of Cleroidea, Cucujoidea and Tenebrionoidea. The monophyly of Cleroidea and Cucujoidea is suggested by the unusual attachment of the M. tentoriostipitalis to the ventral side of the posterior hypopharynx. Cucujoidea are paraphyletic. The families Endomychidae, Coccinellidae and Nitidulidae are more closely related to the monophyletic Cleroidea, than to other cucujoid groups. Separation of the posterior tentorial arms from the tentorial bridge and presence of a maxillolabial complex are synapomorphic features of Cleroidea and these cucujoid families. For a reliable reconstruction of cucujoid interrelationships, further characters and taxa need to be studied.
External and internal head structures and external structures of the thorax and abdomen of larval representatives of Melandryidae (Orchesia), Ulodidae (Meryx), Oedemeridae (Pseudolycus) and Pythidae (Pytho) are described. The obtained data were compared to characters of other tenebrionoid larvae and to larval characters of other representatives of Cucujiformia. Characters potentially relevant for phylogenetic reconstruction are listed and were analysed cladistically. The data set is characterised by a high degree of homoplasy and the resolution of the strict consensus trees of 2650 or 815 (second analysis) minimal length trees is low. The monophyly of Tenebrionoidea is supported by several larval autapomorphies, e.g. posteriorly diverging gula, anteriorly shifted posterior tentorial arms, asymmetric mandibles and the origin of several bundles of M. tentoriopharyngalis from the well-developed gular ridges. Several features of the larval head are plesiomorphic compared to the cleroid-cucujoid lineage. The interrelationships of most tenebrionoid families not belonging to the pythid-salpingid and anthicid-scraptiid groups were not resolved. Synchroidae were placed as sister group of a clade comprising these two lineages and Prostomidae. A sistergroup relationship between Trictenotomidae and Pythidae seems to be well supported and the monophyly of the anthicid-scraptiid lineage was also confirmed. Another potential clade comprises Prostomidae, Mycteridae and Boridae, and possibly Pyrochroidae (s.str.) and Inopeplinae. The monophyly of Salpingidae (incl. Othniinae and Inopelinae) and Pyrochroidae (incl. Pedilinae) was not supported. Many features such as the shape of the head and body, sutures and ridges of the head capsule, the endocarina, the mandibles, the maxillary apex, and also characters of the terminal abdominal apex are highly variable, even within families. Especially the families Tetratomidae, Melandryidae, Colydiidae and Zopheridae show a high degree of variation in the larval stages. Several taxa appear isolated in terms of larval morphology within the families they are assigned to, e.g. Orchesia within Melandryidae, Sphindocis (Sphindocinae) within Ciidae, Calopus (Calopinae) within Oedemeridae and Penthe (Penthinae) within Tetratomidae. A broader spectrum of characters and a stepwise approach will be needed for a reliable clarification of the relationships within a very complex group like Tenebrionoidea.
Five flightless species of Micromus are known from the Hawaiian Archipelago; only one, the rare Micromus usingeri, is reported from the Island of Hawai'i. Herein, we report the natural occurrence of intermediates between this brachypterous species and its near relative, the macropterous Micromus longispinosus. We compare some morphological and life-history characteristics of the two species and the intermediates. Our study shows that: (1) The two closely related species are broadly distributed on Hawai'i, but they appear to be allopatric altitudinally. (2) M. usingeri is associated with a cool, misty, high-altitude environment, M. longispinosus with warmer, rainy conditions at lower elevations. The intermediates occur in both types of situations and generally at intermediate elevations. (3) The macropterous M. longispinosus has large, oblong, flexible, membranous forewings and hind wings. In contrast, the brachypterous M. usingeri has convex, shortened, elytra-like forewings with reticulate venation, and very small, thick, triangular, stub-like hind wings with greatly reduced venation. The wings of intermediate specimens exhibit a broad range of variation between the two species. (4) Several characteristics of wing venation are highly correlated with reduced wing size; others are not. (5) Aside from the wings, adults of M. usingeri and M. longispinosus differ in relatively few morphological features, most notably the antennal and metatibial length, prothoracic length, mesothoracic length and width, and the length of the spine-covered process on the posteroventral margin of the male T9+ectoproct. The intermediate specimens are variable in adult characteristics, but they generally fall between the two species. (6) Egg size and larval characteristics (except the body length of the fully-fed first and third instars) do not differ between the two species. (7) The evolution of the wing variation is discussed.
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.
Odontomyia ochropa Thomson, 1869, is redescribed and found to be identical with O. dorsoangulata Brunetti, 1920, which is proposed as a new synonym. The female holotype of O. ochropa from the Philippines was examined and compared with specimens from India, Thailand and Singapore. Terminalia and other diagnostic characters of both sexes are illustrated. The larva of O. ochropa is described in detail. The larval characters are in accordance with the characters of O. dorsoangulata mentioned by Brunetti (1920). The larva of O. ochropa is compared with that of O. cyanea described by Mathur (1933). Cuticular structures and diagnostic characters of both larvae are documented by drawings and SEM micrographs. A new identification key to larvae of Odontomyia known from the Oriental Region is provided.
The larval morphology of Aphodius (Plagiogonus) nanus Fairmaire, 1860 and A. (P.) arenarius (Olivier, 1789) are described and redescribed, respectively. The common characters of both species, and the specific diagnostic characters are provided and discussed. The most important morphological characters of the larvae of Plagiogonus Mulsant, 1842 are the longitudinal alignment of the anterior setae of the stipes, the spatulate form of the posterior-lateral setae of the glossae of the hypopharynx, the slight development of the anal lobe slit, the form of the epitorma of the epipharynx, the slight sclerotization of the pternotormae and the relative length of second antennal segment. A key to the larvae of both species of Plagiogonus is presented along with life history data and the preferred food of these species. This study shows that A. arenarius and A. nanus feeding habits are closer to saprophagy than to coprophagy.
The third instar larvae of three Anisoplia species, Anisoplia baetica Erichson, 1847, Anisoplia depressa Erichson, 1847 and Anisoplia remota Reitter, 1889 are described and illustrated to show the diagnostic characters of the species. The third instar larva of the monospecific genus Anthoplia, represented by Anthoplia floricola (F., 1787) is also described and illustrated. These four species are included in a revised key to the larvae of Anisopliini, which now includes four genera, and ten species. The taxonomic status of Anthoplia based on the larval morphology, is discussed.
A provisional larval groundplan of the family Hygrobiidae is provided through descriptions of internal and external features of three of six extant species, Hygrobia hermanni (Fabricius, 1775), H. wattsi Hendrich 2001 and H. australasiae (Clark, 1862) and phylogenetic interpretations. Hygrobiidae larvae are morphologically differing dramatically from all other known Adephaga by 20 autapomorphies. Structures involved with feeding, i.e., mouthparts, prepharynx and foregut are highly modified as a result of a specialisation on small tubificid worms and chironomid larvae. A placement of Hygrobiidae within Dytiscoidea is well supported by the reduced condition of the terminal abdominal segments, and the presence of 10 ancestral setae on femur and a clade comprising Hygrobiidae, Amphizoidae, and Dytiscidae by the presence of thin and elongate caudal tentorial arms, a very strong musculus verticopharyngalis and a longitudinally divided adductor tendon of the mandible. A highly modified foregut, reduced terminal spiracles VIII and the presence of tubular gills are features which distinguish hygrobiid larvae from those of other groups of Dytiscoidea (i.e, Amphizoidae, Noteridae, Dytiscidae). A sister-group relationship between Hygrobiidae and Dytiscidae is indicated by a distinctly shortened and transverse prepharynx and a cerebrum and suboesophaeal ganglion shifted to the anterior third of the head. Larvae of the Australian species H. wattsi and H. australasiae share the presence of a bluntly rounded mandible and an apical position of the primary pore MNd in instar I as potential synapomorphies.