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A Catalogue of Coleoptera Specimens with Potential Forensic Interest in the Goulandris Natural History Museum Collection
ENTOMOLOGIA HELLENICA Vol. 25, 2016 A catalogue of Coleoptera specimens with potential forensic interest in the Goulandris Natural History Museum collection Dimaki Maria Goulandris Natural History Museum, 100 Othonos St. 14562 Kifissia, Greece Anagnou-Veroniki Maria Makariou 13, 15343 Aghia Paraskevi (Athens), Greece Tylianakis Jason Zoology Department, University of Canterbury, Private Bag 4800, Christchurch, New Zealand http://dx.doi.org/10.12681/eh.11549 Copyright © 2017 Maria Dimaki, Maria Anagnou- Veroniki, Jason Tylianakis To cite this article: Dimaki, M., Anagnou-Veroniki, M., & Tylianakis, J. (2016). A catalogue of Coleoptera specimens with potential forensic interest in the Goulandris Natural History Museum collection. ENTOMOLOGIA HELLENICA, 25(2), 31-38. doi:http://dx.doi.org/10.12681/eh.11549 http://epublishing.ekt.gr | e-Publisher: EKT | Downloaded at 27/12/2018 06:22:38 | ENTOMOLOGIA HELLENICA 25 (2016): 31-38 Received 15 March 2016 Accepted 12 December 2016 Available online 3 February 2017 A catalogue of Coleoptera specimens with potential forensic interest in the Goulandris Natural History Museum collection MARIA DIMAKI1’*, MARIA ANAGNOU-VERONIKI2 AND JASON TYLIANAKIS3 1Goulandris Natural History Museum, 100 Othonos St. 14562 Kifissia, Greece 2Makariou 13, 15343 Aghia Paraskevi (Athens), Greece 3Zoology Department, University of Canterbury, Private Bag 4800, Christchurch, New Zealand ABSTRACT This paper presents a catalogue of the Coleoptera specimens in the Goulandris Natural History Museum collection that have potential forensic interest. Forensic entomology can help to estimate the time elapsed since death by studying the necrophagous insects collected on a cadaver and its surroundings. In this paper forty eight species (369 specimens) are listed that belong to seven families: Silphidae (3 species), Staphylinidae (6 species), Histeridae (11 species), Anobiidae (4 species), Cleridae (6 species), Dermestidae (14 species), and Nitidulidae (4 species). -
Diversity and Resource Choice of Flower-Visiting Insects in Relation to Pollen Nutritional Quality and Land Use
Diversity and resource choice of flower-visiting insects in relation to pollen nutritional quality and land use Diversität und Ressourcennutzung Blüten besuchender Insekten in Abhängigkeit von Pollenqualität und Landnutzung Vom Fachbereich Biologie der Technischen Universität Darmstadt zur Erlangung des akademischen Grades eines Doctor rerum naturalium genehmigte Dissertation von Dipl. Biologin Christiane Natalie Weiner aus Köln Berichterstatter (1. Referent): Prof. Dr. Nico Blüthgen Mitberichterstatter (2. Referent): Prof. Dr. Andreas Jürgens Tag der Einreichung: 26.02.2016 Tag der mündlichen Prüfung: 29.04.2016 Darmstadt 2016 D17 2 Ehrenwörtliche Erklärung Ich erkläre hiermit ehrenwörtlich, dass ich die vorliegende Arbeit entsprechend den Regeln guter wissenschaftlicher Praxis selbständig und ohne unzulässige Hilfe Dritter angefertigt habe. Sämtliche aus fremden Quellen direkt oder indirekt übernommene Gedanken sowie sämtliche von Anderen direkt oder indirekt übernommene Daten, Techniken und Materialien sind als solche kenntlich gemacht. Die Arbeit wurde bisher keiner anderen Hochschule zu Prüfungszwecken eingereicht. Osterholz-Scharmbeck, den 24.02.2016 3 4 My doctoral thesis is based on the following manuscripts: Weiner, C.N., Werner, M., Linsenmair, K.-E., Blüthgen, N. (2011): Land-use intensity in grasslands: changes in biodiversity, species composition and specialization in flower-visitor networks. Basic and Applied Ecology 12 (4), 292-299. Weiner, C.N., Werner, M., Linsenmair, K.-E., Blüthgen, N. (2014): Land-use impacts on plant-pollinator networks: interaction strength and specialization predict pollinator declines. Ecology 95, 466–474. Weiner, C.N., Werner, M , Blüthgen, N. (in prep.): Land-use intensification triggers diversity loss in pollination networks: Regional distinctions between three different German bioregions Weiner, C.N., Hilpert, A., Werner, M., Linsenmair, K.-E., Blüthgen, N. -
A Phylogenetic Analysis of the Megadiverse Chalcidoidea (Hymenoptera)
UC Riverside UC Riverside Previously Published Works Title A phylogenetic analysis of the megadiverse Chalcidoidea (Hymenoptera) Permalink https://escholarship.org/uc/item/3h73n0f9 Journal Cladistics, 29(5) ISSN 07483007 Authors Heraty, John M Burks, Roger A Cruaud, Astrid et al. Publication Date 2013-10-01 DOI 10.1111/cla.12006 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Cladistics Cladistics 29 (2013) 466–542 10.1111/cla.12006 A phylogenetic analysis of the megadiverse Chalcidoidea (Hymenoptera) John M. Heratya,*, Roger A. Burksa,b, Astrid Cruauda,c, Gary A. P. Gibsond, Johan Liljeblada,e, James Munroa,f, Jean-Yves Rasplusc, Gerard Delvareg, Peter Jansˇtah, Alex Gumovskyi, John Huberj, James B. Woolleyk, Lars Krogmannl, Steve Heydonm, Andrew Polaszekn, Stefan Schmidto, D. Chris Darlingp,q, Michael W. Gatesr, Jason Motterna, Elizabeth Murraya, Ana Dal Molink, Serguei Triapitsyna, Hannes Baurs, John D. Pintoa,t, Simon van Noortu,v, Jeremiah Georgea and Matthew Yoderw aDepartment of Entomology, University of California, Riverside, CA, 92521, USA; bDepartment of Evolution, Ecology and Organismal Biology, Ohio State University, Columbus, OH, 43210, USA; cINRA, UMR 1062 CBGP CS30016, F-34988, Montferrier-sur-Lez, France; dAgriculture and Agri-Food Canada, 960 Carling Avenue, Ottawa, ON, K1A 0C6, Canada; eSwedish Species Information Centre, Swedish University of Agricultural Sciences, PO Box 7007, SE-750 07, Uppsala, Sweden; fInstitute for Genome Sciences, School of Medicine, University -
Alfalfa Leafcutter
Pest Profile Alfalfa leafcutter bee adult Alfalfa leafcutter bee adult on alfalfa Photo credit: Arlo Pelegrin; bugguide.net Photo credit: www.ars.usda.gov Common Name: Alfalfa leafcutter bee Scientific Name: Megachile rotundata Order and Family: Hymenoptera: Megachilidae Size and Appearance: Length (mm) Appearance Egg Larva Overwinter as mature larvae with approx. 4 larval instars Pupa Females are dark gray with light yellow bands across the abdomen and a gray ventral side. The body has special white Adult 6-9 (Females) hairs for carrying pollen (called scopa). Males are much smaller and have cream-colored, white to yellow spots on the abdomen. Type of feeder: Adults feed on and gather pollen and nectar for provision of individual nest cells, but do not feed on vegetation. Female alfalfa leafcutter bees are very effective pollinators of alfalfa, canola, legumes, flowers, berries, and some vegetables and fruits. Adult female leafcutter bees will cut smooth, semicircular pieces from leaves to use in the formation of nests in which eggs will be laid. Lifecycle: This solitary bee, which was introduced from Europe in the late 1930s, has a short life span with females living a few weeks during the summer, and males dying soon after mating. Most leafcutter bees only have a single generation each year. Female alfalfa leafcutter bees will construct tube-like tunnels from leaf material and within each approx. 8-inch long tube may build up to 2 dozen individual nest cells in which the female will lay a single egg. Each nest cell is provisioned with nectar and pollen for the larvae to feed after hatching. -
Chalcid Forum Chalcid Forum
ChalcidChalcid ForumForum A Forum to Promote Communication Among Chalcid Workers Volume 23. February 2001 Edited by: Michael E. Schauff, E. E. Grissell, Tami Carlow, & Michael Gates Systematic Entomology Lab., USDA, c/o National Museum of Natural History Washington, D.C. 20560-0168 http://www.sel.barc.usda.gov (see Research and Documents) minutes as she paced up and down B. sarothroides stems Editor's Notes (both living and partially dead) antennating as she pro- gressed. Every 20-30 seconds, she would briefly pause to Welcome to the 23rd edition of Chalcid Forum. raise then lower her body, the chalcidoid analog of a push- This issue's masthead is Perissocentrus striatululus up. Upon approaching the branch tips, 1-2 resident males would approach and hover in the vicinity of the female. created by Natalia Florenskaya. This issue is also Unfortunately, no pre-copulatory or copulatory behaviors available on the Systematic Ent. Lab. web site at: were observed. Naturally, the female wound up leaving http://www.sel.barc.usda.gov. We also now have with me. available all the past issues of Chalcid Forum avail- The second behavior observed took place at Harshaw able as PDF documents. Check it out!! Creek, ~7 miles southeast of Patagonia in 1999. Jeremiah George (a lepidopterist, but don't hold that against him) and I pulled off in our favorite camping site near the Research News intersection of FR 139 and FR 58 and began sweeping. I knew that this area was productive for the large and Michael W. Gates brilliant green-blue O. tolteca, a parasitoid of Pheidole vasleti Wheeler (Formicidae) brood. -
Weiblen, G.D. 2002 How to Be a Fig Wasp. Ann. Rev. Entomol. 47:299
25 Oct 2001 17:34 AR ar147-11.tex ar147-11.sgm ARv2(2001/05/10) P1: GJB Annu. Rev. Entomol. 2002. 47:299–330 Copyright c 2002 by Annual Reviews. All rights reserved ! HOW TO BE A FIG WASP George D. Weiblen University of Minnesota, Department of Plant Biology, St. Paul, Minnesota 55108; e-mail: [email protected] Key Words Agaonidae, coevolution, cospeciation, parasitism, pollination ■ Abstract In the two decades since Janzen described how to be a fig, more than 200 papers have appeared on fig wasps (Agaonidae) and their host plants (Ficus spp., Moraceae). Fig pollination is now widely regarded as a model system for the study of coevolved mutualism, and earlier reviews have focused on the evolution of resource conflicts between pollinating fig wasps, their hosts, and their parasites. Fig wasps have also been a focus of research on sex ratio evolution, the evolution of virulence, coevolu- tion, population genetics, host-parasitoid interactions, community ecology, historical biogeography, and conservation biology. This new synthesis of fig wasp research at- tempts to integrate recent contributions with the older literature and to promote research on diverse topics ranging from behavioral ecology to molecular evolution. CONTENTS INTRODUCING FIG WASPS ...........................................300 FIG WASP ECOLOGY .................................................302 Pollination Ecology ..................................................303 Host Specificity .....................................................304 Host Utilization .....................................................305 -
Drivers of Parasitoid Wasps' Community Composition in Cacao Agroforestry Practice in Bahia State, Brazil
3 Drivers of Parasitoid Wasps' Community Composition in Cacao Agroforestry Practice in Bahia State, Brazil Carlos Frankl Sperber1, Celso Oliveira Azevedo2, Dalana Campos Muscardi3, Neucir Szinwelski3 and Sabrina Almeida1 1Laboratory of Orthoptera, Department of General Biology, Federal University of Viçosa, Viçosa, MG, 2Department of Biology, Federal University of Espírito Santo, Vitória, ES, 3Department of Entomolgy, Federal University of Viçosa, Viçosa, MG, Brazil 1. Introduction The world’s total forest area is just over 4 billion hectares, and five countries (the Russian Federation, Brazil, Canada, the United States of America and China) account for more than half of the total forest area (FAO, 2010). Apart from their high net primary production, the world’s forests harbour at least 50% of the world’s biodiversity, which underpins the ecosystem services they provide (MEA, 2005). Primarily the plants, through their physiological processes, such as evapotranspiration, essential to the ecosystem's energy budget, physically dissipate a substantial portion of the absorbed solar radiation (Bonan, 2002), and sequester carbon from the atmosphere. The carbon problem, considered a trend concern around the world due to global warming (Botkin et al, 2007), can be minimized through the carbon sequestration by forests. Forests have the potential of stabilizing, or at least contributing to the stabilization of, atmospheric carbon in the short term (20–50 years), thereby allowing time for the development of more long-lasting technological solutions that reduce carbon emission sources (Sedjo, 2001). Brazil's forests comprise 17 percent of the world's remaining forests, making it the third largest block of remaining frontier forest in the world and ranks first in plant biodiversity among frontier forest nations. -
Indirect Mutualism: Ants Protect Fig Seeds and Pollen Dispersers from Parasites Ecological Entomology, 2015 K
Ecological Entomology (2015), DOI: 10.1111/een.12215 Indirect mutualism: ants protect fig seeds and pollen dispersers from parasites K. CHARLOTTE JANDÉR1,2,3 1Department of Ecology and Evolutionary Biology, Yale University, New Haven, Connecticut, U.S.A., 2Department of Ecology and Genetics, Evolutionary Biology Centre, Uppsala University, Uppsala, Sweden and 3Smithsonian Tropical Research Institute, Panama City, Panama Abstract. 1. Mutualisms are ubiquitous and ecologically important, but may be particularly vulnerable to exploitation by species outside of the mutualism owing to a combination of an attractive reward and potentially limited defence options. For some mutualisms, ants can offer dynamic and relatively selective protection against herbivores and parasites. 2. The mutualism between fgtreesandtheirpollinatingwasps,akeystonemutualism in tropical forests, is particularly well suited for ant protection because pollinators are protected inside hollow inforescences but parasites are exposed on the outside. 3. In the present study, it was shown that the presence of ants provides a ftness beneft for both the pollinators and the hosting fgtree.Thepresenceofants(i)reducedabortions of developing fgs, (ii) reduced herbivory of fgs, and (iii) reduced parasitic wasp loads, resulting in more pollinators and more seeds in ant-protected fgs. Even when taking costs such as ant predation on emerging pollinators into account, the total ftness increase of hosting ants was threefold for the tree and fvefold for the pollinators. 4. It was further shown that the seemingly most vulnerable parasitic wasps, of the genus Idarnes,haveaspecifcbehaviourthatallowsthemtoevadeantattackwhilecontinuing to oviposit. 5. Ants were present on 79% of surveyed Panamanian fgtrees.Togetherwithprevious studies from the Old World, the results found here imply that ants are both powerful and common protectors of the fgmutualismworldwide. -
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, Cleroidea, Cleridae)
ISSN: 1578-1666; 2254-8777 Boletín de la SAE Nº 27 (2017): 01-09. Aportaciones a la corología de algunos Cleridae de Andalucía (España) (Coleoptera, Cleroidea, Cleridae) Marcos A. LÓPEZ VERGARA 1, Manuel BAENA 2 & Alejandro CASTRO TOVAR 3 1. C/ Pilar de la Imprenta 5, 2º; 23002 Jaén (ESPAÑA). E-mail: [email protected] 2. Departamento de Biología y Geología; I.E.S. Alhaken II; C/ Manuel Fuentes “Bocanegra”; 14005 Córdoba (ESPAÑA). E-mail: [email protected] 3. C/ Bernardas 1, 4º; 23001 Jaén (ESPAÑA). E-mail: [email protected] Resumen: Se amplía el área de distribución conocida en Andalucía de siete especies de cléridos: Tillus ibericus Bahillo, López-Colón & García-París, 2003, Opilo domesticus (Sturm, 1837), Tilloidea unifasciata (Fabricius, 1787), Korynetes pusillus Klug, 1842, Clerus mutillarius africanus Kocher, 1955, Allonyx quadrimaculatus (Schaller, 1783) y Necrobia violacea (Linnaeus, 1758). Tres especies, T. ibericus T. unifasciata y K. pusillus, son primeras citas para la provincia de Jaén. T. ibericus se registra por primera vez en la provincia de Granada y O. domesticus (Sturm, 1837) en la provincia de Málaga. Palabras clave: Coleoptera, Cleridae, distribución, Jaén, Granada, Málaga, Andalucía, España. Contribution to the chorology of some Cleridae in Andalusia (Spain) (Coleoptera, Cleroidea, Cleridae) Abstract: The known range of distribution in Andalusia of seven species of Cleridae: Tillus ibericus Bahillo, López-Colón & García París, 2003, Opilo domesticus (Sturm, 1837), Tilloidea unifasciata (Fabricius, 1787), Korynetes pusillus Klug, 1842, Clerus mutillarius africanus Kocher, 1955, Allonyx quadrimaculatus (Schaller, 1783) and Necrobia violacea (Linnaeus, 1758), is expanded. Three species, T. ibericus T. unifasciata and K. pusillus, are recorded first time in Jaen province. -
A Comment on Iranian Fig Wasps (Chalcidoidea: Agaonidae, Pteromalidae)
© Biologiezentrum Linz/Austria; download unter www.biologiezentrum.at Linzer biol. Beitr. 43/2 1247-1252 19.12.2011 A comment on Iranian fig wasps (Chalcidoidea: Agaonidae, Pteromalidae) H. GHAHARI & S. VAN NOORT Abstract: A total of 5 species of fig wasps from 5 genera including, Blastophaga, Elisabethiella (Agaonidae), and Apocrypta, Sycophaga, Apocryptophagus (Pteromalidae) are recorded from Iran. Among the collected fig wasps, Apocryptophagus gigas (MAYR) is a new record for the Iranian fauna. Key words: Fig wasp, Agaonidae, Pteromalidae, Ficus, Iran. Introduction Fig wasps include the pollinating fig wasps (Chalcidoidea: Agaonidae) and a diverse assemblage of non-pollinating fig wasps (Chalcidoidea: Pteromalidae, Eurytomidae, Ormyridae) that are also associated with individual fig tree species (VAN NOORT & VAN HARTEN 2006). The relationship between pollinating fig wasps (Chalcidoidea, Agaoni- dae) and their host fig trees (Ficus L. 1753, Moraceae) is a classic example of an obligate mutualism, where neither partner can reproduce without the other, the wasp providing a pollination service and the fig tree in turn providing a breeding site for the pollinating wasp’s progeny (JANZEN 1979). The obligate mutualism between pollinating fig wasps and their host fig trees (Ficus, Moraceae) has historically been considered to be a one-to- one relationship (RAMIREZ 1970; WIEBES 1979; WIEBES & COMPTON 1990; VAN NOORT 2004), but increasing evidence is suggesting that the relationship is not as tight as has previously been supposed, with records of more than one species of pollinator associated with a single host and, conversely, of a single pollinator species associated with more than one host fig species (COMPTON & VAN NOORT 1992; WEST & HERRE 1994; WEST et al. -
Insects of the Idaho National Laboratory: a Compilation and Review
Insects of the Idaho National Laboratory: A Compilation and Review Nancy Hampton Abstract—Large tracts of important sagebrush (Artemisia L.) Major portions of the INL have been burned by wildfires habitat in southeastern Idaho, including thousands of acres at the over the past several years, and restoration and recovery of Idaho National Laboratory (INL), continue to be lost and degraded sagebrush habitat are current topics of investigation (Ander- through wildland fire and other disturbances. The roles of most son and Patrick 2000; Blew 2000). Most restoration projects, insects in sagebrush ecosystems are not well understood, and the including those at the INL, are focused on the reestablish- effects of habitat loss and alteration on their populations and ment of vegetation communities (Anderson and Shumar communities have not been well studied. Although a comprehen- 1989; Williams 1997). Insects also have important roles in sive survey of insects at the INL has not been performed, smaller restored communities (Williams 1997) and show promise as scale studies have been concentrated in sagebrush and associated indicators of restoration success in shrub-steppe (Karr and communities at the site. Here, I compile a taxonomic inventory of Kimberling 2003; Kimberling and others 2001) and other insects identified in these studies. The baseline inventory of more habitats (Jansen 1997; Williams 1997). than 1,240 species, representing 747 genera in 212 families, can be The purpose of this paper is to present a taxonomic list of used to build models of insect diversity in natural and restored insects identified by researchers studying cold desert com- sagebrush habitats. munities at the INL.