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Zootaxa, Coleoptera, Attelabidae, Apoderinae, Hoplapoderini
Zootaxa 1089: 37–47 (2005) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA 1089 Copyright © 2005 Magnolia Press ISSN 1175-5334 (online edition) A new genus and species of Hoplapoderini from Madagascar (Coleoptera: Attelabidae: Apoderinae) SILVANO BIONDI Via E. di Velo 137, I-36100 Vicenza - Italy. email: [email protected] Abstract Madapoderus pacificus, a new genus and species of hoplapoderine attelabid beetles, is described from Madagascar. A key to the genera of Hoplapoderini and field observations on the host plant and reproductive behaviour of the new species are provided. Key words: Attelabidae, Apoderinae, Hoplapoderini, Madagascar, new genus, new species, Grewia Introduction In May 2002, among specimens of Attelabidae collected in Madagascar by David Hauck some months earlier, I received two males belonging to the apoderine tribe Hoplapoderini that could not be assigned to any known genus. A study of the rich collection of Madagascan attelabids at the Muséum National d’Histoire Naturelle, Paris, a few months later confirmed this diagnosis. During a month-long collecting expedition in Madagascar in December 2003 and January 2004, I collected the new taxon again, at a different locality, and could carry out some observations on its behaviour. Systematics Tribe Hoplapoderini Voss, 1926 Voss (1926) defined his tribe Hoplapoderini largely on the basis of features of the head and elytra. The new Madagascan genus fits into this tribe due to its tapered head, with maximum width near the basis, and its tuberculate elytra. Voss also provided a key to the Accepted by Q. Wang: 7 Oct. 2005; published: 2 Dec. 2005 37 ZOOTAXA genera of the tribe, but this is largely inadequate because of its heavy reliance on the 1089 presence and shape of what he called “abdominal lobes” (“Abdominallappen”). -
Fossil History of Curculionoidea (Coleoptera) from the Paleogene
geosciences Review Fossil History of Curculionoidea (Coleoptera) from the Paleogene Andrei A. Legalov 1,2 1 Institute of Systematics and Ecology of Animals, Siberian Branch, Russian Academy of Sciences, Ulitsa Frunze, 11, 630091 Novosibirsk, Novosibirsk Oblast, Russia; [email protected]; Tel.: +7-9139471413 2 Biological Institute, Tomsk State University, Lenin Ave, 36, 634050 Tomsk, Tomsk Oblast, Russia Received: 23 June 2020; Accepted: 4 September 2020; Published: 6 September 2020 Abstract: Currently, some 564 species of Curculionoidea from nine families (Nemonychidae—4, Anthribidae—33, Ithyceridae—3, Belidae—9, Rhynchitidae—41, Attelabidae—3, Brentidae—47, Curculionidae—384, Platypodidae—2, Scolytidae—37) are known from the Paleogene. Twenty-seven species are found in the Paleocene, 442 in the Eocene and 94 in the Oligocene. The greatest diversity of Curculionoidea is described from the Eocene of Europe and North America. The richest faunas are known from Eocene localities, Florissant (177 species), Baltic amber (124 species) and Green River formation (75 species). The family Curculionidae dominates in all Paleogene localities. Weevil species associated with herbaceous vegetation are present in most localities since the middle Paleocene. A list of Curculionoidea species and their distribution by location is presented. Keywords: Coleoptera; Curculionoidea; fossil weevil; faunal structure; Paleocene; Eocene; Oligocene 1. Introduction Research into the biodiversity of the past is very important for understanding the development of life on our planet. Insects are one of the Main components of both extinct and recent ecosystems. Coleoptera occupied a special place in the terrestrial animal biotas of the Mesozoic and Cenozoics, as they are characterized by not only great diversity but also by their ecological specialization. -
Bulletin UASVM Agriculture 69(2)/2012
Bulletin UASVM serie Agriculture 69(2)/2012 Print ISSN 1843-5246; Electronic ISSN 1843-5386 Parameters Researches Regarding the Structural Parameters of the Populations of Rhynchitidae and Attelabidae in Romania Iuliana ANTONIE “Lucian Blaga” University, The Faculty of Agricultural Sciences, Food Industry and the Protection of the Environment, Sibiu, 7-9 Dr. Ion Raţiu, 550012, Sibiu, Romania: [email protected] Abstract. The study of the two families took into account the economic factor, because there are not few species of Rhynchitidae and Attelabidae that produced important damages in the vine, orchard, and forest areas as well as in the agricultural cultures. The researches took place during 1996-2006. The fauna material was collected during the travels to different localities in the country. In some investigated localities the collecting and the observations in the field were extended for at least 2-3 days and for the vine ecosystems with a great attack of Byctiscus betulae the researches lasted for 3-4 years, at regulated intervals of 3-4 weeks. In order to establish the structural parameters there was processed a rich material of over 1300 adult samples belonging to 17 species from a total of 29, which are to be found in Romania. The material comes from 42 localities. The way of collecting was: directly with the hand, with the entomologic net, by drillings in the soil and by using the device of obtaining the zoophagous parasites. Keywords: Ecology, structural parameters, Rhynchitidae and Attelabidae INTRODUCTION The species Rhynchitidae and Attelabidae (Coleoptera, Curculionoidea) are a relatively small group of insects, whose research represents both a scientific and practical interest (Becker, 1954). -
Coleoptera: Attelabidae)
Fragmenta entomologica, 49 (2): 159-163 (2017) eISSN: 2284-4880 (online version) pISSN: 0429-288X (print version) Research article Submitted: April 28th, 2017 - Accepted: November 24th, 2017 - Published: December 29th, 2017 Ecology and life history of Paratomapoderus brachypterus in Gabon (Coleoptera: Attelabidae) Silvano BIONDI 1,*, Carlo MASSARONE 2, Cosmin-Ovidiu MANCI 3 1 Via G.E. di Velo 137, 36100 Vicenza, Italy - [email protected] 2 Vicolo del Frantoio 8, 50060 San Godenzo (FI), Italy - [email protected] 3 PostRestant, OP Tomesti, Tomesti (IS), Romania - [email protected] * Corresponding author Abstract On the base of data collected during four expeditions in Gabon (West Africa) from 2012 to 2016, the authors provide new information on trophic activity and reproductive behaviour of Paratomapoderus brachypterus (Voss, 1926) (Attelabidae: Apoderinae, Hoplapoder- ini), with emphasis on leaf-roll realisation; host plant, leaf roll, larva and pupa are illustrated for the first time. Key words: Attelabidae, Paratomapoderus, Gabon, Combretum, biology, host plant, distribution, Afrotropic. Introduction 1839) is given as a pest on Eucalyptus maculata in South Af ri ca (Anonymous 1976); Parapoderus flavoebenus Tomapoderus Voss, 1926, Paratomapoderus Voss, 1926 (Thomson, 1858) is reported as feeding on Terminalia su and Parapoderus Voss 1926 (that Legalov (2007) regards perba and Khaya ivorensis in Cameroon (Foahom 2002), as a synonym of Paratomapoderus) are nearly exclusively or Theo bro ma cacao in Ghana (Cotterell 1927) and Ivo- African genera, together including more than one hundred ry Coast (Alibert 1951); again in Ivory Coast Parapoder species. Their systematics is still unclear and is in need of us clivi col lis (Marshall, 1948) is reported as feeding on a revision. -
Weevils) of the George Washington Memorial Parkway, Virginia
September 2020 The Maryland Entomologist Volume 7, Number 4 The Maryland Entomologist 7(4):43–62 The Curculionoidea (Weevils) of the George Washington Memorial Parkway, Virginia Brent W. Steury1*, Robert S. Anderson2, and Arthur V. Evans3 1U.S. National Park Service, 700 George Washington Memorial Parkway, Turkey Run Park Headquarters, McLean, Virginia 22101; [email protected] *Corresponding author 2The Beaty Centre for Species Discovery, Research and Collection Division, Canadian Museum of Nature, PO Box 3443, Station D, Ottawa, ON. K1P 6P4, CANADA;[email protected] 3Department of Recent Invertebrates, Virginia Museum of Natural History, 21 Starling Avenue, Martinsville, Virginia 24112; [email protected] ABSTRACT: One-hundred thirty-five taxa (130 identified to species), in at least 97 genera, of weevils (superfamily Curculionoidea) were documented during a 21-year field survey (1998–2018) of the George Washington Memorial Parkway national park site that spans parts of Fairfax and Arlington Counties in Virginia. Twenty-three species documented from the parkway are first records for the state. Of the nine capture methods used during the survey, Malaise traps were the most successful. Periods of adult activity, based on dates of capture, are given for each species. Relative abundance is noted for each species based on the number of captures. Sixteen species adventive to North America are documented from the parkway, including three species documented for the first time in the state. Range extensions are documented for two species. Images of five species new to Virginia are provided. Keywords: beetles, biodiversity, Malaise traps, national parks, new state records, Potomac Gorge. INTRODUCTION This study provides a preliminary list of the weevils of the superfamily Curculionoidea within the George Washington Memorial Parkway (GWMP) national park site in northern Virginia. -
The Fallen-Letter Beetle, a Red Weevil, Alas the Wrong Colour, Nevertheless It Gave Me an Important Clue: the Family Attelabidae (Leaf-Roller Weevils)
Volume 19 • December 2011 23 TThhee ffaalllleenn--lleetttteerr bbeeeettllee by Maria Fremlin Back in early May 2009 I was hiking in a forest with my family when I spotted some neatly rolled leaves on the ground. At first, considering that we were in Japan, the land of origami, I thought that they were the work of someone rather fidgety. But, as they kept cropping up and all looked very similar (Figure 1a & 1b) my curiosity got the better of me and I decided to investigate. Figure 1a & 1b - Leaf-rolls. Chiba Peninsula, Honshu Island, Japan. Photo taken on 13.05.2009. 24 The Bug Club Magazine The first step was to see what was inside. As the leaves were very fresh I had no trouble unrolling one and was rewarded with a lovely yellow egg suspended by a thread at the very tip of it (Figure 2); after that I could not resist keeping some to see the final results. Figure 2 - Underside of an unrolled leaf and the egg, inset. Note the regular notches along the midrib (one is arrowed); they make it easier to roll. And in less than three weeks out popped some rather fetching little beetles, leaving behind neat emergence holes on the rolled leaves (Figures 3-4). Some had more than one hole; remarkably the larvae ate very little. TTuurrnn tthhee ppaaggee ttoo sseeee tthhee bbeeeettlleess Volume 19 • December 2011 25 Figure 3 - Freshly emerged beetle, ~ 7 mm. Photo taken on 30.05.2009. The next challenge was to find out what they were and for that I did some searching in the Internet. -
Insect Egg Size and Shape Evolve with Ecology but Not Developmental Rate Samuel H
ARTICLE https://doi.org/10.1038/s41586-019-1302-4 Insect egg size and shape evolve with ecology but not developmental rate Samuel H. Church1,4*, Seth Donoughe1,3,4, Bruno A. S. de Medeiros1 & Cassandra G. Extavour1,2* Over the course of evolution, organism size has diversified markedly. Changes in size are thought to have occurred because of developmental, morphological and/or ecological pressures. To perform phylogenetic tests of the potential effects of these pressures, here we generated a dataset of more than ten thousand descriptions of insect eggs, and combined these with genetic and life-history datasets. We show that, across eight orders of magnitude of variation in egg volume, the relationship between size and shape itself evolves, such that previously predicted global patterns of scaling do not adequately explain the diversity in egg shapes. We show that egg size is not correlated with developmental rate and that, for many insects, egg size is not correlated with adult body size. Instead, we find that the evolution of parasitoidism and aquatic oviposition help to explain the diversification in the size and shape of insect eggs. Our study suggests that where eggs are laid, rather than universal allometric constants, underlies the evolution of insect egg size and shape. Size is a fundamental factor in many biological processes. The size of an 526 families and every currently described extant hexapod order24 organism may affect interactions both with other organisms and with (Fig. 1a and Supplementary Fig. 1). We combined this dataset with the environment1,2, it scales with features of morphology and physi- backbone hexapod phylogenies25,26 that we enriched to include taxa ology3, and larger animals often have higher fitness4. -
Coleoptera) of the World Fauna
Acta Biol. Univ. Daugavp. 8 (2) 2008 ISSN 1407 - 8953 TO THE KNOWLEDGE OF ATTELABID-BEETLES (COLEOPTERA) OF THE WORLD FAUNA Andrei A. Legalov Legalov A.A. 2008. To the knowledge of Attelabid-beetles (Coleoptera) of the world fauna. Acta Biol.Univ. Daugavpil. 8 (2): 193 - 226. New genera: Jekelitrahelus Legalov, gen.n. (type species: Trachelophorus elegans Voss, 1929) and Metriotracheloides Legalov, gen.n. (type species: Apoderus holoxanthus Fairmaire, 1902), new subgenera: Chinphialodes Legalov, subgen.n (type species: Phialodes hubeiensis Legalov, sp.n.) of the genus Phialodes Roelofs, 1874, Protrachelophorus Legalov, subgen.n. (type species: Trachelophoridius minutus Voss, 1929) of the genus Trachelophoridius Voss, 1929, and new species: Vossieuscelus loretoensis Legalov, sp.n. (Peru), Omolabus kirschi Legalov, sp.n. (Colombia), O. westerduijni Legalov, sp.n. (Peru), Phialodes hubeiensis Legalov, sp.n. (Hubei), Humerilabus alleni Legalov, sp.n. (Laos), H. borneoensis Legalov, sp.n. (Sabah), Henicolaboides nanlingensis Legalov, sp.n. (China) and Paroplapoderus alleni Legalov, sp.n. (Bhutan) are described. New synonyms: subtribe Phialodina Legalov, 2003, syn.n. (type genus: Phialodes Roelofs, 1874) for subtribe Attelabina Billberg, 1820, Henicolaboides nigrocapitus Legalov, 2007, syn.n. for H. spinipes (Schilsky, 1906), Eoclitostylus Legalov, 2003, syn.n.; (type species: Apoderus tenuissimus Pascoe, 1881) for Trachelismus Motschulsky, 1870, Trachelophorus fausti Voss, 1929, syn.n. for T. signatus Voss, 1929, Apoderus cinctipectoralis Voss, 1930, syn.n. for Leptapoderus affinis (Schilsky, 1906), Apoderus papei Voss, 1927, syn.n. for L. nigroapicatus (Jekel, 1860). New status: Madagasocycnelus ater (Faust, 1890), stat.n. from variation of M. humeralis Olivier, 1807. Resurrected status Omolabus deceptor (Jekel, 1860), stat.res. from synonym to O. -
125. NEMONYCHIDAE Bedel 1882
692 · Family 125. Nemonychidae Superfamily CURCULIONOIDEA 125. NEMONYCHIDAE Bedel 1882 by Robert S. Anderson Family common name: The pine flower snout beetles mong the weevils, these rarely collected beetles are easily recognized by their straight antennae, and elongate rostrum combined with the presence of a distinct labrum. Adults are found in association with the male pollen- Abearing flowers of Pinus species. Description (based on ing four pairs of setae. Antenna of a single membranous article Lawrence 1982). Shape elon- bearing an accessory appendage. Mandible with two apical teeth, gate, slightly convex; length an obtuse protuberance on cutting edge, a distinctly produced 3.0-5.5 mm; color pale brown molar area with a flattened grinding surface, and one pair of setae. to black; vestiture of fine short Hypopharyngeal bracon present. Maxillary palp with three ar- to moderately long appressed ticles, palpiger present or absent. Labial palp of two articles. or suberect pubescence. Ros- Premental sclerite present, may be divided medially. Thorax with trum moderately to very long pronotal sclerite transverse, lightly pigmented or unpigmented, and mostly narrow. Antennae sparsely covered with setae. Legs very small, subconical, of two or straight, ending in a weak, three segments, with or without a terminal claw. Abdomen with loose club of three articles; an- first eight segments with two dorsal folds and bearing annular or tennal insertions lateral at the bicameral spiracles. Anal opening terminal. middle or near the apex of the Pupae are undescribed. rostrum. Labrum distinct, not Habits and habitats. These beetles are rarely collected, likely fused with clypeus. Mandibles because of their specialized habits and life history. -
Molecular Phylogenetics of the Superfamily Curculionoidea (Insecta: Coleoptera)
Molecular Phylogenetics of the Superfamily Curculionoidea (Insecta: Coleoptera) Conrad Paulus Dias Trafford Gillett A thesis submitted in fulfilment of the requirements for the degree of Doctor of Philosophy University of East Anglia Norwich, Norfolk, England March 2014 © This copy of the thesis has been supplied on condition that anyone who consults it is understood to recognise that its copyright rests with the author and that use of any information derived there-from must be in accordance with current UK Copyright Law. In addition, any quotation or extract must include full attribution. 1 Molecular Phylogenetics of the Superfamily Curculionoidea (Insecta: Coleoptera) Conrad Paulus Dias Trafford Gillett March 2014 Thesis abstract This thesis examines higher-level evolutionary history within the superfamily Curculionoidea, the most speciose family-level taxon, which includes beetles commonly known as weevils. This is achieved using a phylogenetic approach incorporating the largest datamatrix yet employed for weevil molecular systematics, and includes an investigation into the prospect of obtaining short phylogenetically informative amplicons from archival museum specimens. Newly obtained DNA sequence data is analysed from a variety of mitochondrial and nuclear loci, including 92 mitogenomes assembled through the approach of next-generation sequencing of pooled genomic DNA. The resulting trees are used to test previous morphological- and molecular-based hypotheses of weevil relationships and classification schemes. Mitogenomic-derived trees reveal topologies that are highly congruent with previous molecular studies, but that conflict with some morphological hypotheses. Strong nodal support strengthens inferences into the relationships amongst most weevil families and suggests that the largest family, the Curculionidae, is monophyletic, if the subfamily Platypodinae is excluded. -
The Mitochondrial Genome of Apion Squamigerum (Coleoptera, Curculionoidea, Brentidae) and the Phylogenetic Implications
The mitochondrial genome of Apion squamigerum (Coleoptera, Curculionoidea, Brentidae) and the phylogenetic implications Nan Song1, Xinxin Li1, Xinming Yin1, Xinghao Li1, Shengjun Yin2 and Mingsheng Yang3 1 College of Plant Protection, Henan Agricultural University, Zhengzhou, China 2 Department of Chinese Medicine, The Second Hospital of Tianjin Medical University, Tianjin, China 3 College of Life Science and Agronomy, Zhoukou Normal University, Zhoukou, China ABSTRACT In this article, we present the nearly complete mitochondrial genome (mitogenome) of the weevil beetle Apion squamigerum (Curculionoidea, Brentidae), assembled using data from Illumina next generation sequencing (NGS). This mitogenome was found to be very large, with the total length of 18,562 bp. Two trnM genes were identified. A large non-coding intergenic spacer spanning 1,949 bp occurred between trnI and trnM2. Combined with 111 existing weevil mitogenomes, we conducted phylogenetic recon- structions based on various datasets under maximum likelihood and Bayesian inference. Firstly, phylogenetic analyses robustly supported a sister group of A. squamigerum and Rhopalapion longirostre, namely, that two species of Apioninae (Brentidae) formed a clade. Within the entire Curculionoidea, the Nemonychidae diverged firstly, following the families Anthribidae and Attelabidae. In addition, a large clade comprising the sister families Brentidae and Curculionidae was strongly supported in all trees. Subjects Biodiversity, Entomology, Evolutionary Studies, Taxonomy Keywords Mitogenome, Brentid beetle, Large intergenic spacer, Phylogeny Submitted 23 September 2019 Accepted 11 December 2019 Published 13 January 2020 INTRODUCTION Corresponding author Nan Song, [email protected] Weevil beetles (Curculionoidea), with approximately 62,000 species in 5,800 described genera, are one of the most diverse groups in the order Coleoptera (Oberprieler, Marvaldi Academic editor Jia-Yong Zhang & Anderson, 2007). -
Contradictory Effects of Leaf Rolls in a Leaf-Mining Weevil
www.nature.com/scientificreports OPEN Contradictory efects of leaf rolls in a leaf‑mining weevil Chisato Kobayashi1*, Kazunori Matsuo2 & Masakado Kawata1 Leaf rolls by herbivorous insects evolved in various lepidopteran groups, aphids, and some attelabid weevil species. Leaf rolls are known to have a positive efect on the survival of immature insects, protecting them from natural enemies such as birds, ants, predatory wasps, and parasitoids as well as environmental stress. On the other hand, leaf rolls are considered to have a negative efect on immature survival, attracting natural enemies because of their noticeability and subsequent learning or specialization. In this study, we directly tested the efects of leaf rolls using an attelabid species by comparing the fate of immature insects between artifcial leaf rolls and unrolled leaves. The results showed the following positive efects of leaf rolls: avoidance of parasitism by eulophid wasps and avoidance of egg predation by unknown predators. On the other hand, a negative efect of leaf rolls was also detected, specifcally and increase in mortality via leaf roll herbivory. This study indicated that leaf shelters are not only protective refuges but are also sometimes risky hiding places, although total survival rates increased in leaf shelters. Herbivorous insects are one of the most diverse organisms in terrestrial ecosystems, and have evolved various types of feeding niches such as leaf chewers, leaf gallers, leaf miners, and stem borers 1–4. Leaf roller is one of various feeding niches of herbivorous insects and many species in diferent taxa, for examples, tortricid moths, pyralid moths, gelechiid moths, aphids, and attelabid weevils, all show leaf rolling traits and grow in leaf rolls during their immature period or the adult period.