(Coleoptera, Coccinelloidea, Discolomatidae) from Vietnam

Total Page:16

File Type:pdf, Size:1020Kb

(Coleoptera, Coccinelloidea, Discolomatidae) from Vietnam Elytra, Tokyo, New Series, 11 (1): 85–92 August 16, 2021 New Aphanocephalus from Vietnam 85 A New Species of the Genus Aphanocephalus (Coleoptera, Coccinelloidea, Discolomatidae) from Vietnam 1) 2), 3) Hiroyuki YOSHITOMI and Thai Hong PHAM 1) Entomological Laboratory, Faculty of Agriculture, Ehime University, Tarumi 3–5–7, Matsuyama, 790–8566 Japan 2) Mientrung Institute for Scientific Research, Vietnam Academy of Science and Technology, 321 Huynh Thuc Khang, Hue, Vietnam 3) Vietnam National Museum of Nature & Graduate School of Science and Technology, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet, Hanoi, Vietnam Abstract A new species of the genus Aphanocephalus, A. hiranoi sp. nov., is described from Vietnam. Three known species from Vietnam and Laos are briefly redescribed. An identification key to species and the list of previous records of Aphanocephalus from Vietnam and Laos are provided. Keywords: Taxonomy, Aphanocephalinae, Aphanocephalini, male genitalia, Laos. Introduction The family Discolomatidae includes about 400 species, 16 genera, within five subfamilies C( LINE & Ślipiński, 2010), and is distributed throughout tropical to temperate regions in the Old World, but only tropical areas in the New World. They are mycophagous or saprophagous, and some genera are known as a myrmecophiles (CLINE & Ślipiński, 2010). The genus Aphanocephalus Wollaston, 1873 (Aphanocephalinae, Aphanocephalini) is one of the largest genera in the family (JOHN, 1959), and is represented by more than 100 species from Central and East Africa, East to Southeast Asia, Pacific Islands, and northern Australia p( al, 1992). From Vietnam and Laos, nine species have been recorded, but most species are known from a few sites (Table 1). In the present paper, a new species from Vietnam is described, and three previously known species are recorded and briefly redescribed based on the additional specimens. Material and Methods The materials examined in this paper are located in Ehime University Museum, Matsuyama, Japan (EUMJ) and Vietnam National Museum of Nature (VNMN). The numbers in the specimen data (e.g. LA35, VN49) indicate the collecting sites, and their additional information and photos of the collection sites are available in: https://sites.google.com/site/waterbeetlesofjapan/home/field- investigation. General observations, dissections and observations of microstructures of dissected parts were made under a Leica MZ95. After observation, the dissected parts were mounted on the same card with the specimen. Photographs were taken with a Leica MZ95. The male genitalia of this family are complicated. Some species possess asymmetrical genitalia with extra appendages, but the male genitalia were examined and figured under condition of con- necting penis and tegmen in the previous study. In this paper, we disarticulated the penis and tegmen and figured them independently for the purpose of better discerning diagnostic features. 86 Hiroyuki YOSHITOMI and Thai Hong PHAM Table 1. Records of Aphanocephalus spp. from Vietnam and Laos. Species Country Locality Altitude Reference A. annamensis Vietnam Goa, Annam (type loc.) JOHN (1956) Vietnam Tonkin, Hoa Binh JOHN (1956) A. decoomani Laos betw. Vientiane and Luang Prabang (type loc.) JOHN (1954) Vietnam Tonkin, Hoa Binh JOHN (1956) Vietnam Ha Son Binh, Da Bac schaWaller (1993) Vietnam Kui-Tshau 200 m schaWaller (1993) Laos LA35 575 m present study A. ebeninus Vietnam Tonkin, Reg. de Hoa-Binh JOHN (1956) Vietnam 40 km NE Thai-Nguen 700–800 m schaWaller (1993) Vietnam NE Thai-Nguen schaWaller (1993) Vietnam Bakshon 600 m schaWaller (1993) Vietnam Shan-Hoa, Ngoklak schaWaller (1993) Vietnam VN49 Cuc Phuong NP., Ninh Bình Prov. 369 m present study Vietnam VN50 Cuc Phuong, Ninh Bình Prov. 165 m present study A. formosanus Vietnam Tam-Dao 900 m schaWaller (1993) Vietnam VN43 Tam Dao, Vinh Phuc Prov. 960 m present study Vietnam VN45 Tam Dao, Vinh Phuc Prov. 1,023 m present study A. hiranoi sp. nov. Vietnam Deo O Quy Ho, Lao Cai (type loc.) 1,750 m present study A. poesi Vietnam Prov. Ha-Tinh, forestiere Huong-son (type loc.) 200 m JOHN (1965) Vietnam Prov. Ha-Tinh, forestiere Huong-son 150 m JOHN (1965) A. pseudatomus Vietnam Tonkin, Hoa Binh (type loc.) JOHN (1954) Vietnam Tonkin, Hoa Binh JOHN (1956) A. pubescens Vietnam 30 km SE Hanoi schaWaller (1993) A. tonkinensis Vietnam Tonkin, Hoa Binh (type loc.) JOHN (1954) Vietnam Tonkin, Hoa Binh JOHN (1956) Vietnam 125 km NW Than-Hoa, Batok 500 m schaWaller (1993) A. wollastoni Vietnam Tonkin, Hoa Binh JOHN (1956) Vietnam 100 km W Shan-Hoa, Lang-Gang 100 m schaWaller (1993) Morphological abbreviations used in this study are as follows: EL — elytral length from anterior margin to elytral apex; EW — maximum elytral width; PL — pronotal length in median line; PW — pronotal maximum width; TL — total length (PL + EL). The average is given in parenthesis after the range. Taxonomy Genus Aphanocephalus Wollaston, 1873 Aphanocephalus Wollaston, 1873: 278 [type species: Aphanocephalus hemisphaericus Wollaston, 1873]; JOHN, 1956: 1; 1959: 34; Fukuda, 1969: 20 [description of larva]; pal, 1992: 46. Diagnosis. Body oval to circular, hemispherical, shiny, glabrous or pubescent. Coloration of body evenly brown or black in most species, with weak greenish luster in some species; elytra with 2 to 6 spots in some species. Head completely obscured by pronotum, not visible in dorsal view. Anten- New Aphanocephalus from Vietnam 87 Fig. 1. Habitus of Aphanocephalus spp. — A, A. decoomani; B, A. ebeninus; C, A. formosanus; D, A. hiranoi sp. nov. Scale bar = 1.0 mm. nae 9-segmented, with 1-segmented apical club. Pronotum transverse, with two pairs of tubular gland openings near front and hind angles; anterior margin gently arcuate; anterior angles broadly rounded; posterior angles acute. Elytra with six pairs of tubular gland openings along lateral margins. Legs short; tarsal formula 3-3-3; claws simple; empodium well developed, bisetose. Key to the Species of Aphanocephalus from Vietnam and Laos 1. Elytra black, with a pair of reddish brown spots. ························ A. pseudatomus JOHN, 1954 — Elytra fully black. ··························································································· 2 2. Pronotum and elytra bearing long setae. ································································· 3 — Pronotum and elytra glabrous or bearing sparsely distributed short setae. ·························· 4 3. Elytral punctures evenly small. ······································· A. pubescens Grouvelle, 1912 — Elytra closely and irregularly covered with small and moderate punctures. ························ 5 88 Hiroyuki YOSHITOMI and Thai Hong PHAM 4. Punctures in basal area of elytra consisting of three size, large, moderate and small. ················ ························································································· A. pocsi JOHN, 1965 — Punctures in basal area of elytra consisting of two size, small and moderate. ························· ················································································· A. annamensis JOHN, 1956 5. Small body size species, TL ˂ 1.5 mm. ·································································· 6 — Large size species, TL > 2.2 mm. ········································································· 7 6. Tegmen reduced, smaller than penis. ········································ A. tonkinensis JOHN, 1954 — Tegmen developed, larger than penis. ········································· A. wollastoni rye, 1873 7. Apex of tegmen simply acute. ············································································· 8 — Apex of tegmen with two or three pairs of lateral projections. ······································· 9 8. Smaller species, TL ˂ 2.2 mm; penis short, projecting dorsally in apico-lateral parts. ··············· ····················································································· A. ebeninus JOHN, 1956 — Larger species, TL > 2.5 mm; penis long, projecting apically. ···················· A. hiranoi sp. nov. 9. Apical part of tegmen distinctly asymmetrical; apex of penis with large projection in right-dorsal corner. ········································································· A. decoomani JOHN, 1954 — Apical part of tegmen slightly asymmetrical; apex of penis flat dorsally. ······························ ················································································· A. formosanus JOHN, 1956 Aphanocephalus decoomani JOHN, 1954 (Figs. 1A & 2A–E) Aphanocephalus decoomani JOHN, 1954: 302. schaWaller, 1993: 32. Specimens examined. 2 males, 4 females & 3 exs. (EUMJ), “[LA35] Hot Spring, Xieng Kh- ouang Prov., Laos, 28. IV. 2018, 19.332993, 103.411440 575 m, H. Yoshitomi leg.”. Redescription. For full description see JOHN (1954). PW/PL 1.93–2.14 (2.05); EL/EW 0.90–0.97 (0.94); EL/PL 2.32–2.57 (2.46); EW/PW 1.19–1.33 (1.28); TL/EW 1.28–1.37 (1.32). Tegmen (Fig. 2A–C) distinctly asymmetrical; right paramere with three projections, inner one long and pointed at apex, middle and outer ones obtuse; left paramere with two obtuse projections. Penis (Fig. 2D & E) long, asymmetrical, with large projection in right-dorsal corner of apex. Measurement (N = 7). TL 2.28–2.80 (2.56) mm; PW 1.40–1.70 (1.52) mm; PL 0.68–0.82 (0.74) mm; EL 1.60–1.98 (1.82) mm; EW 1.78–2.12 (1.94) mm. Distribution. Laos, Vietnam. Aphanocephalus ebeninus JOHN, 1956 (Figs. 1B & 2F–I) Aphanocephalus ebeninus JOHN, 1956: 8. schaWaller, 1993: 32. Specimens
Recommended publications
  • The Evolution and Genomic Basis of Beetle Diversity
    The evolution and genomic basis of beetle diversity Duane D. McKennaa,b,1,2, Seunggwan Shina,b,2, Dirk Ahrensc, Michael Balked, Cristian Beza-Bezaa,b, Dave J. Clarkea,b, Alexander Donathe, Hermes E. Escalonae,f,g, Frank Friedrichh, Harald Letschi, Shanlin Liuj, David Maddisonk, Christoph Mayere, Bernhard Misofe, Peyton J. Murina, Oliver Niehuisg, Ralph S. Petersc, Lars Podsiadlowskie, l m l,n o f l Hans Pohl , Erin D. Scully , Evgeny V. Yan , Xin Zhou , Adam Slipinski , and Rolf G. Beutel aDepartment of Biological Sciences, University of Memphis, Memphis, TN 38152; bCenter for Biodiversity Research, University of Memphis, Memphis, TN 38152; cCenter for Taxonomy and Evolutionary Research, Arthropoda Department, Zoologisches Forschungsmuseum Alexander Koenig, 53113 Bonn, Germany; dBavarian State Collection of Zoology, Bavarian Natural History Collections, 81247 Munich, Germany; eCenter for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, 53113 Bonn, Germany; fAustralian National Insect Collection, Commonwealth Scientific and Industrial Research Organisation, Canberra, ACT 2601, Australia; gDepartment of Evolutionary Biology and Ecology, Institute for Biology I (Zoology), University of Freiburg, 79104 Freiburg, Germany; hInstitute of Zoology, University of Hamburg, D-20146 Hamburg, Germany; iDepartment of Botany and Biodiversity Research, University of Wien, Wien 1030, Austria; jChina National GeneBank, BGI-Shenzhen, 518083 Guangdong, People’s Republic of China; kDepartment of Integrative Biology, Oregon State
    [Show full text]
  • CDFA-PPDC, 3294 Meadowview Rd., Sacramento, CA 95758, U.S.A. [email protected]
    The Coleopterists Bulletin, 66(2): 93–99. 2012. ANEW SPECIES OF FALLIA SHARP (CUCUJOIDEA:DISCOLOMATIDAE) FROM THE WEST INDIES, WITH A WORLD CHECKLIST FOR FALLIA ANDREW R. CLINE CDFA-PPDC, 3294 Meadowview Rd., Sacramento, CA 95758, U.S.A. [email protected] AND FLOYD W. SHOCKLEY Department of Entomology, National Museum of Natural History Smithsonian Institution, P.O. Box 37012, MRC-165 Washington, DC 20013–7012, U.S.A. [email protected] ABSTRACT A new discolomatid species, Fallia iviei Cline and Shockley, new species, is described from the Dominican Republic. A distribution map, habitus and character images, and discussion of its biology are provided. The new species represents the first known member of the genus from the West Indies. A species checklist for all nine described species of Fallia Sharp is presented. Key Words: taxonomy, catalog, Hispaniola, Dominican Republic, Caribbean Discolomatidae is a family of small cucujoid likelyremaininmuseums’ undetermined Cerylonidae, beetles (1–8 mm long) with a mostly circumtropical Endomychidae, Corylophidae, and Latridiidae, with distribution. These beetles generally are thought to which Discolomatidae has shared an intertwined be saprophagous as they are commonly found in taxonomic history. leaf litter, compost heaps, and other areas of decom- Fallia is a small genus of Discolomatidae within position, including subcortical spaces of decaying the subfamily Aphanocephalinae (see Cline and logs (Arrow 1939; Costa Lima 1953; Crowson 1967; Ślipiński 2010 for discussion of discolomatid phy- Lawrence 1982; Scholtz and Holm 1985; Lawrence logeny). The genus contains nine species, includ- 1989; Ide and Costa 1990; Lawrence 1991; Lawrence ing the new one described herein (see checklist and Britton 1994; Peck 2006).
    [Show full text]
  • Review of the Tribe Hyperaspidini Mulsant (Coleoptera: Coccinellidae) from Iran
    Zootaxa 4236 (2): 311–326 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2017 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4236.2.6 http://zoobank.org/urn:lsid:zoobank.org:pub:01F6A715-AA19-4A2A-AD79-F379372ACC65 Review of the tribe Hyperaspidini Mulsant (Coleoptera: Coccinellidae) from Iran AMIR BIRANVAND1, WIOLETTA TOMASZEWSKA2,11, OLDŘICH NEDVĚD3,4, MEHDI ZARE KHORMIZI5, VINCENT NICOLAS6, CLAUDIO CANEPARI7, JAHANSHIR SHAKARAMI8, LIDA FEKRAT9 & HELMUT FÜRSCH10 1Young Researchers and Elite Club, Khorramabad Branch, Islamic Azad University, Khorramabad, Iran. E-mail: amir.beiran@gmail 2Museum and Institute of Zoology, Polish Academy of Sciences, Warszawa, Poland. E-mail: [email protected] 3Faculty of Science, University of South Bohemia, Branišovská 1760, CZ-37005 České Budějovice, Czech Republic. E-mail: [email protected] 4Institute of Entomology, Biology Centre, Branišovská 31, 37005 České Budějovice, Czech Republic. 5Department of Entomology, College of Agricultural Sciences, Shiraz Branch, Islamic Azad University, Shiraz, Iran. E-mail: [email protected] 627 Glane, 87200 Saint-Junien, France. E-mail: [email protected] 7Via Venezia 1, I-20097 San Donato Milanese, Milan, Italy. E-mail: [email protected] 8Plant Protection Department, Lorestan University, Agricultural faculty, Khorramabad, Iran. E-mail: [email protected] 9Department of Plant Protection, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iran. E-mail: [email protected] 10University Passau, Didactics of Biology, Germany. E-mail: [email protected] 11Corresponding author. E-mail: [email protected] Abstract The Iranian species of the tribe Hyperaspidini Mulsant, 1846 (Coleoptera: Coccinellidae) are reviewed.
    [Show full text]
  • Phylogeny and Classification of Cucujoidea and the Recognition of A
    Systematic Entomology (2015), 40, 745–778 DOI: 10.1111/syen.12138 Phylogeny and classification of Cucujoidea and the recognition of a new superfamily Coccinelloidea (Coleoptera: Cucujiformia) JAMES A. ROBERTSON1,2,ADAM SL´ I P I NS´ K I3, MATTHEW MOULTON4, FLOYD W. SHOCKLEY5, ADRIANO GIORGI6, NATHAN P. LORD4, DUANE D. MCKENNA7, WIOLETTA TOMASZEWSKA8, JUANITA FORRESTER9, KELLY B. MILLER10, MICHAEL F. WHITING4 andJOSEPH V. MCHUGH2 1Department of Entomology, University of Arizona, Tucson, AZ, U.S.A., 2Department of Entomology, University of Georgia, Athens, GA, U.S.A., 3Australian National Insect Collection, CSIRO, Canberra, Australia, 4Department of Biology and M. L. Bean Museum, Brigham Young University, Provo, UT, U.S.A., 5Department of Entomology, National Museum of Natural History, Smithsonian Institution, Washington, DC, U.S.A., 6Faculdade de Ciências Biológicas, Universidade Federal do Pará, Altamira, Brasil, 7Department of Biological Sciences, University of Memphis, Memphis, TN, U.S.A., 8Museum and Institute of Zoology, Polish Academy of Sciences, Warszawa, Poland, 9Chattahoochee Technical College, Canton, GA, U.S.A. and 10Department of Biology and Museum of Southwestern Biology, University of New Mexico, Albuquerque, NM, U.S.A. Abstract. A large-scale phylogenetic study is presented for Cucujoidea (Coleoptera), a diverse superfamily of beetles that historically has been taxonomically difficult. This study is the most comprehensive analysis of cucujoid taxa to date, with DNA sequence data sampled from eight genes (four nuclear, four mitochondrial) for 384 coleopteran taxa, including exemplars of 35 (of 37) families and 289 genera of Cucujoidea. Maximum-likelihood analyses of these data present many significant relationships, some proposed previously and some novel.
    [Show full text]
  • Phylogenetic Systematics of the Cerylonid Series of Cucujoidea
    PHYLOGENETIC SYSTEMATICS OF THE CERYLONID SERIES OF CUCUJOIDEA (COLEOPTERA) by JAMES A. ROBERTSON (Under the Direction of Joseph V. McHugh) ABSTRACT We conduct a large-scale phylogenetic investigation of the Cerylonid Series (C.S.) of Cucujoidea, a diverse group of cucujoid beetles comprising 9,600 species classified in eight families, using morphological data (76 taxa ! 147 adult and larval characters), molecular data (341 taxa ! 9 genes: 18S, 28S, H3, 12S, 16S, COI, COII, CAD and ArgK) and a combination of the two datasets. In total, our analyses suggest the following: the C.S. is a monophyletic group based on both morphological and molecular evidence; the superfamily Cucujoidea is paraphyletic with respect to the remaining superfamilies in the series Cucujiformia; the C.S. represents a unique clade within Cucujiformia and should be recognized as its own supferfamily, Coccinelloidea, within the series; Byturidae and Biphyllidae should be transferred to Cleroidea; the C.S. families Corylophidae, Coccinellidae, Latridiidae, and Discolomatidae, are monophyletic; Cerylonidae, Endomychidae, and Bothrideridae are paraphyletic. Bothrideridae is split into two distinct families comprising the former Bothriderinae (as Bothrideridae) and the other including the remaining subfamilies (as Teredidae); the cerylonid subfamily Euxestinae is included within Teredidae; the new concept of Cerylonidae includes the following subfamilies: Ceryloninae, Ostomopsinae, Murmidiinae, Discolomatinae and Loeblioryloninae (inserte sedis); the status of the putative
    [Show full text]
  • Characterization of the Complete Mitochondrial Genomes from Two Nitidulid Pests with Phylogenetic Implications
    insects Article Characterization of the Complete Mitochondrial Genomes from Two Nitidulid Pests with Phylogenetic Implications Xiaoxiao Chen, Qing Song and Min Huang * Key Laboratory of Plant Protection Resources and Pest Management of the Ministry of Education, Entomological Museum, College of Plant Protection, Northwest A&F University, Yangling 712100, Shanxi, China; [email protected] (X.C.); [email protected] (Q.S.) * Correspondence: [email protected]; Tel.: +86-029-87092705 Received: 26 September 2020; Accepted: 7 November 2020; Published: 11 November 2020 Simple Summary: Nitidulidae is the most diverse group of Cucujoidea. In this study, we sequence and analyze two mitochondrial genomes of the nitidulid species, Xenostrongylus variegatus and Epuraea sp. Both genomes are highly conserved in their size, base content, codon usage, and secondary structure of tRNAs. Phylogenetic analyses of Nitidulidae and related families in Cucujoidea are carried out based on three outgroups and fourteen ingroups. The results of the Bayesian inference and maximum likelihood methods support the monophyly of Nitidulidae and the sister-group relationship of Kateretidae + (Monotomidae + Nitidulidae). Abstract: The complete mitochondrial genomes of Xenostrongylus variegatus and Epuraea sp. were sequenced and analyzed. The total genome lengths are 17,657 and 16,641 bp, with an A + T content of 77.2% and 76.4%, respectively. Each mitochondrial genome consists of 37 coding genes and a non-coding (AT-rich) region. All protein-coding genes (PCGs) start with the standard start codon, ATN, and end with complete stop codons, TAA and TAG, or an incomplete stop codon, T. All tRNAs can be folded into the typical clover-leaf secondary structure, with the exception of trnS1 in both species with a reduced dihydrouridine (DHU) arm.
    [Show full text]
  • Mckenna2009chap34.Pdf
    Beetles (Coleoptera) Duane D. McKenna* and Brian D. Farrell and Polyphaga (~315,000 species; checkered beetles, Department of Organismic and Evolutionary Biology, 26 Oxford click beetles, A reP ies, ladybird beetles, leaf beetles, long- Street, Harvard University, Cambridge, MA 02138, USA horn beetles, metallic wood-boring beetles, rove beetles, *To whom correspondence should be addressed scarabs, soldier beetles, weevils, and others) (2, 3). 7 e ([email protected]) most recent higher-level classiA cation for living beetles recognizes 16 superfamilies and 168 families (4, 5). Abstract Members of the Suborder Adephaga are largely preda- tors, Archostemata feed on decaying wood (larvae) and Beetles are placed in the insect Order Coleoptera (~350,000 pollen (adults), and Myxophaga are aquatic or semi- described species). Recent molecular phylogenetic stud- aquatic and feed on green and/or blue-green algae ( 6). ies defi ne two major groups: (i) the Suborders Myxophaga Polyphaga exhibit a diversity of habits, but most spe- and Archostemata, and (ii) the Suborders Adephaga and cies feed on plants or dead and decaying plant parts Polyphaga. The time of divergence of these groups has (1–3). 7 e earliest known fossil Archostemata are from been estimated with molecular clocks as ~285–266 million the late Permian (7), and the earliest unequivocal fossil years ago (Ma), with the Adephaga–Polyphaga split at ~277– Adephaga and Polyphaga are from the early Triassic (1). 266 Ma. A majority of the more than 160 beetle families Myxophaga are not known from the fossil record, but are estimated to have originated in the Jurassic (200–146 extinct possible relatives are known from the Permian Ma).
    [Show full text]
  • Fossil Perspectives on the Evolution of Insect Diversity
    FOSSIL PERSPECTIVES ON THE EVOLUTION OF INSECT DIVERSITY Thesis submitted by David B Nicholson For examination for the degree of PhD University of York Department of Biology November 2012 1 Abstract A key contribution of palaeontology has been the elucidation of macroevolutionary patterns and processes through deep time, with fossils providing the only direct temporal evidence of how life has responded to a variety of forces. Thus, palaeontology may provide important information on the extinction crisis facing the biosphere today, and its likely consequences. Hexapods (insects and close relatives) comprise over 50% of described species. Explaining why this group dominates terrestrial biodiversity is a major challenge. In this thesis, I present a new dataset of hexapod fossil family ranges compiled from published literature up to the end of 2009. Between four and five hundred families have been added to the hexapod fossil record since previous compilations were published in the early 1990s. Despite this, the broad pattern of described richness through time depicted remains similar, with described richness increasing steadily through geological history and a shift in dominant taxa after the Palaeozoic. However, after detrending, described richness is not well correlated with the earlier datasets, indicating significant changes in shorter term patterns. Corrections for rock record and sampling effort change some of the patterns seen. The time series produced identify several features of the fossil record of insects as likely artefacts, such as high Carboniferous richness, a Cretaceous plateau, and a late Eocene jump in richness. Other features seem more robust, such as a Permian rise and peak, high turnover at the end of the Permian, and a late-Jurassic rise.
    [Show full text]
  • Searching for Natural Lineages Within the Cerylonid Series (Coleoptera: Cucujoidea)
    ARTICLE IN PRESS Available online at www.sciencedirect.com Molecular Phylogenetics and Evolution xxx (2007) xxx–xxx www.elsevier.com/locate/ympev Searching for natural lineages within the Cerylonid Series (Coleoptera: Cucujoidea) James A. Robertson a,*, Michael F. Whiting b, Joseph V. McHugh a a Department of Entomology, University of Georgia, 413 Biological Sciences Building, Athens, GA 30602-2603, USA b Department of Biology, M.L. Bean Museum, Brigham Young University, 401 Widtsoe Building Provo, UT 84602, USA Received 19 April 2007; revised 6 August 2007; accepted 26 September 2007 Abstract Phylogenetic relationships within the diverse beetle superfamily Cucujoidea are poorly known. The Cerylonid Series (C.S.) is the larg- est of all proposed superfamilial cucujoid groups, comprising eight families and representing most of the known cucujoid species diver- sity. The monophyly of the C.S., however, has never been formally tested and the higher-level relationships among and within the constituent families remain equivocal. Here we present a phylogenetic study based on 18S and 28S rDNA for 16 outgroup taxa and 61 C.S. ingroup taxa, representing seven of the eight C.S. families and 20 of 39 subfamilies. We test the monophyly of the C.S., inves- tigate the relationships among the C.S. families, and test the monophyly of the constituent families and subfamilies. Phylogenetic recon- struction of the combined data was achieved via standard static alignment parsimony analyses, Direct Optimization using parsimony, and partitioned Bayesian analysis. All three analyses support the paraphyly of Cucujoidea with respect to Tenebrionoidea and confirm the monophyly of the C.S.
    [Show full text]
  • A Case Study from Kepulauan Seribu Marine National Park
    Biogeography and ecology of beetles in a tropical archipelago: A case study from Kepulauan Seribu Marine National Park Thesis submitted for the degree of Doctor of Philosophy University College London by Shinta Puspitasari Department of Geography University College London April 2016 1 I, Shinta Puspitasari, confirm that the work presented in this thesis is my own. Where information has been derived from other sources, I confirm that this has been indicated in the thesis. Shinta Puspitasari April 2016 2 Abstract Beetles comprise not only the most diverse group of insects, but also contribute significantly to vital ecological functions. A quantitative formula to determine the optimal level of investment in the beneficial beetle conservation is still not available. I aim to establish specific attention to beetles and their role in tropical island ecosystems in small archipelago in Indonesia. The study aims to give further insights into beetle diversity patterns on islands in the Kepulauan Seribu Marine National Park and on Java, and how island isolation and area affect assemblage composition. My research also provides insights into the effects of anthropogenic activities on beetle diversity on these islands. A first important result is the substantial number of highly abundant island species and a high number of unique island species found in the study areas, indicating islands as potentially important for the global conservation of genetic resources. My results also highlight the highly varied results relating to the use of two different types of traps, pitfall traps and FITs, for sampling beetles. It underscores the need for complementary trapping strategies using multiple methods for beetle community surveys in tropical islands.
    [Show full text]
  • General Overview of Saproxylic Coleoptera
    Chapter 2 General Overview of Saproxylic Coleoptera Matthew L. Gimmel and Michael L. Ferro Abstract A broad survey of saproxylic beetles (Coleoptera) from literature and personal observations was conducted, and extensive references were included to serve as a single resource on the topic. Results are summarized in a table featuring all beetle families and subfamilies with saproxylicity indicated for both adults and larvae (where known), along with information on diversity, distribution, habits, habitat, and other relevant notes. A discussion about the prevalence of and evolu- tionary origins of beetles in relation to the saproxylic habitat, as well as the variety of saproxylic beetle habits by microhabitat, is provided. This initial attempt at an overview of the entire order shows that 122 (about 65%) of the 187 presently recognized beetle families have at least one saproxylic member. However, the state of knowledge of most saproxylic beetle groups is extremely fragmentary, particularly in regard to larval stages and their feeding habits. 2.1 Introduction to Beetles There are nearly 400,000 described species of beetles, which comprise 40% of all described insect species (Zhang 2011). In fact, one in every four animal species (from jellyfish to Javan rhinos) is a beetle. The dominance of this group in terrestrial ecosystems can hardly be overstated—and the dead wood habitat is no exception in this regard. The largest (see Acorn 2006), longest-lived, and geologically oldest beetles are saproxylic. Of the roster of saproxylic insect pests in forests, beetles M. L. Gimmel (*) Department of Invertebrate Zoology, Santa Barbara Museum of Natural History, Santa Barbara, CA, USA e-mail: [email protected] M.
    [Show full text]
  • Coleoptera: Cucujoidea)
    Available online at www.sciencedirect.com Molecular Phylogenetics and Evolution 46 (2008) 193–205 www.elsevier.com/locate/ympev Searching for natural lineages within the Cerylonid Series (Coleoptera: Cucujoidea) James A. Robertson a,*, Michael F. Whiting b, Joseph V. McHugh a a Department of Entomology, University of Georgia, 413 Biological Sciences Building, Athens, GA 30602-2603, USA b Department of Biology, M.L. Bean Museum, Brigham Young University, 401 Widtsoe Building Provo, UT 84602, USA Received 19 April 2007; revised 6 August 2007; accepted 26 September 2007 Available online 4 October 2007 Abstract Phylogenetic relationships within the diverse beetle superfamily Cucujoidea are poorly known. The Cerylonid Series (C.S.) is the larg- est of all proposed superfamilial cucujoid groups, comprising eight families and representing most of the known cucujoid species diver- sity. The monophyly of the C.S., however, has never been formally tested and the higher-level relationships among and within the constituent families remain equivocal. Here we present a phylogenetic study based on 18S and 28S rDNA for 16 outgroup taxa and 61 C.S. ingroup taxa, representing seven of the eight C.S. families and 20 of 39 subfamilies. We test the monophyly of the C.S., inves- tigate the relationships among the C.S. families, and test the monophyly of the constituent families and subfamilies. Phylogenetic recon- struction of the combined data was achieved via standard static alignment parsimony analyses, Direct Optimization using parsimony, and partitioned Bayesian analysis. All three analyses support the paraphyly of Cucujoidea with respect to Tenebrionoidea and confirm the monophyly of the C.S.
    [Show full text]