Invertebrate Species List E Xcluding Papilionoidea (Butterflies )
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In Indonesian Grasslands with Special Focus on the Tropical Fire Ant, Solenopsis Geminata
The Community Ecology of Ants (Formicidae) in Indonesian Grasslands with Special Focus on the Tropical Fire Ant, Solenopsis geminata. By Rebecca L. Sandidge A dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Environmental Science, Policy, and Management in the Graduate Division of the University of California, Berkeley Committee in charge: Professor Neil D. Tsutsui, Chair Professor Brian Fisher Professor Rosemary Gillespie Professor Ellen Simms Fall 2018 The Community Ecology of Ants (Formicidae) in Indonesian Grasslands with Special Focus on the Tropical Fire Ant, Solenopsis geminata. © 2018 By Rebecca L. Sandidge 1 Abstract The Community Ecology of Ants (Formicidae) in Indonesian Grasslands with Special Focus on the Tropical Fire Ant, Solenopsis geminata. by Rebecca L. Sandidge Doctor of Philosophy in Environmental Science Policy and Management, Berkeley Professor Neil Tsutsui, Chair Invasive species and habitat destruction are considered to be the leading causes of biodiversity decline, signaling declining ecosystem health on a global scale. Ants (Formicidae) include some on the most widespread and impactful invasive species capable of establishing in high numbers in new habitats. The tropical grasslands of Indonesia are home to several invasive species of ants. Invasive ants are transported in shipped goods, causing many species to be of global concern. My dissertation explores ant communities in the grasslands of southeastern Indonesia. Communities are described for the first time with a special focus on the Tropical Fire Ant, Solenopsis geminata, which consumes grass seeds and can have negative ecological impacts in invaded areas. The first chapter describes grassland ant communities in both disturbed and undisturbed grasslands. -
The Predatory Mite (Acari, Parasitiformes: Mesostigmata (Gamasina); Acariformes: Prostigmata) Community in Strawberry Agrocenosis
Acta Universitatis Latviensis, Biology, 2004, Vol. 676, pp. 87–95 The predatory mite (Acari, Parasitiformes: Mesostigmata (Gamasina); Acariformes: Prostigmata) community in strawberry agrocenosis Valentîna Petrova*, Ineta Salmane, Zigrîda Çudare Institute of Biology, University of Latvia, Miera 3, Salaspils LV-2169, Latvia *Corresponding author, E-mail: [email protected]. Abstract Altogether 37 predatory mite species from 14 families (Parasitiformes and Acariformes) were collected using leaf sampling and pit-fall trapping in strawberry fi elds (1997 - 2001). Thirty- six were recorded on strawberries for the fi rst time in Latvia. Two species, Paragarmania mali (Oud.) (Aceosejidae) and Eugamasus crassitarsis (Hal.) (Parasitidae) were new for the fauna of Latvia. The most abundant predatory mite families (species) collected from strawberry leaves were Phytoseiidae (Amblyseius cucumeris Oud., A. aurescens A.-H., A. bicaudus Wainst., A. herbarius Wainst.) and Anystidae (Anystis baccarum L.); from pit-fall traps – Parasitidae (Poecilochirus necrophori Vitz. and Parasitus lunaris Berl.), Aceosejidae (Leioseius semiscissus Berl.) and Macrochelidae (Macrocheles glaber Müll). Key words: agrocenosis, diversity, predatory mites, strawberry. Introduction Predatory mites play an important ecological role in terrestrial ecosystems and they are increasingly being used in management for biocontrol of pest mites, thrips and nematodes (Easterbrook 1992; Wright, Chambers 1994; Croft et al. 1998; Cuthbertson et al. 2003). Many of these mites have a major infl uence on nutrient cycling, as they are predators on other arthropods (Santos 1985; Karg 1993; Koehler 1999). In total, investigations of mite fauna in Latvia were made by Grube (1859), who found 28 species, Eglītis (1954) – 50 species, Kuznetsov and Petrov (1984) – 85 species, Lapiņa (1988) – 207 species, and Salmane (2001) – 247 species. -
Newly Discovered Sister Lineage Sheds Light on Early Ant Evolution
Newly discovered sister lineage sheds light on early ant evolution Christian Rabeling†‡§, Jeremy M. Brown†¶, and Manfred Verhaagh‡ †Section of Integrative Biology, and ¶Center for Computational Biology and Bioinformatics, University of Texas, 1 University Station C0930, Austin, TX 78712; and ‡Staatliches Museum fu¨r Naturkunde Karlsruhe, Erbprinzenstr. 13, D-76133 Karlsruhe, Germany Edited by Bert Ho¨lldobler, Arizona State University, Tempe, AZ, and approved August 4, 2008 (received for review June 27, 2008) Ants are the world’s most conspicuous and important eusocial insects and their diversity, abundance, and extreme behavioral specializations make them a model system for several disciplines within the biological sciences. Here, we report the discovery of a new ant that appears to represent the sister lineage to all extant ants (Hymenoptera: Formicidae). The phylogenetic position of this cryptic predator from the soils of the Amazon rainforest was inferred from several nuclear genes, sequenced from a single leg. Martialis heureka (gen. et sp. nov.) also constitutes the sole representative of a new, morphologically distinct subfamily of ants, the Martialinae (subfam. nov.). Our analyses have reduced the likelihood of long-branch attraction artifacts that have trou- bled previous phylogenetic studies of early-diverging ants and therefore solidify the emerging view that the most basal extant ant lineages are cryptic, hypogaeic foragers. On the basis of morpho- logical and phylogenetic evidence we suggest that these special- EVOLUTION ized subterranean predators are the sole surviving representatives of a highly divergent lineage that arose near the dawn of ant diversification and have persisted in ecologically stable environ- ments like tropical soils over great spans of time. -
Ticks (Parasitiformes: Ixodida) on New World Wild Primates in Brazil
International Journal of Acarology ISSN: (Print) (Online) Journal homepage: https://www.tandfonline.com/loi/taca20 Ticks (Parasitiformes: Ixodida) on new world wild primates in Brazil Thiago F. Martins, Rodrigo H. F. Teixeira, Julio C. Souza Jr, Hermes R. Luz, Mônica M. Montenegro, Leandro Jerusalinsky, Marina G. Bueno, Valeria C. Onofrio, Marinete Amorim, Gilberto S. Gazêta, Paula De J. Da Silva, Karla Bitencourth, Ana B. P. Borsoi, Sandro Marques, Marco O. Mattos Jr, Leandra S. I. Hernandes, Alessandra Scofild, Rafael F. C. Vieira, Richard C. Pacheco, Maurício C. Horta, Valéria P. da Silva, Patrícia W. Silva, Claudia A. Igayara, Thais C. Sanches, Marcello S. Nardi, Camile Lugarini, Natasha L. Maia, Cláudio L. M. de Siqueira, Juliana M. Ferreira, João F. Soares & Marcelo B. Labruna To cite this article: Thiago F. Martins, Rodrigo H. F. Teixeira, Julio C. Souza Jr, Hermes R. Luz, Mônica M. Montenegro, Leandro Jerusalinsky, Marina G. Bueno, Valeria C. Onofrio, Marinete Amorim, Gilberto S. Gazêta, Paula De J. Da Silva, Karla Bitencourth, Ana B. P. Borsoi, Sandro Marques, Marco O. Mattos Jr, Leandra S. I. Hernandes, Alessandra Scofild, Rafael F. C. Vieira, Richard C. Pacheco, Maurício C. Horta, Valéria P. da Silva, Patrícia W. Silva, Claudia A. Igayara, Thais C. Sanches, Marcello S. Nardi, Camile Lugarini, Natasha L. Maia, Cláudio L. M. de Siqueira, Juliana M. Ferreira, João F. Soares & Marcelo B. Labruna (2021): Ticks (Parasitiformes: Ixodida) on new world wild primates in Brazil, International Journal of Acarology, DOI: 10.1080/01647954.2020.1870554 To link to this article: https://doi.org/10.1080/01647954.2020.1870554 Published online: 03 Mar 2021. -
Alternative Reproductive Tactics in the Ant Genus Hypoponera
Alternative reproductive tactics in the ant genus Hypoponera Dissertation zur Erlangung des Doktorgrades der Naturwissenschaften an der Fakultät für Biologie der Ludwig-Maximilians-Universität München vorgelegt von Markus H. Rüger aus Marktoberdorf 2007 Erklärung Diese Dissertation wurde im Sinne von § 12 der Promotionsordnung von Frau Prof. Dr. Susanne Foitzik betreut. Ich erkläre hiermit, dass die Dissertation keiner anderen Prüfungskommission vorgelegt worden ist und dass ich mich nicht anderweitig einer Doktorprüfung ohne Erfolg unterzogen habe. Ehrenwörtliche Versicherung Ich versichere hiermit ehrenwörtlich, dass die vorgelegte Dissertation von mir selbständig und ohne unerlaubte Hilfe angefertigt wurde. München den 9. Oktober 2007 ........................................................................... Markus H. Rüger Dissertation eingereicht am: 9. Oktober 2007 1. Gutachter: Prof. Dr. Susanne Foitzik 2. Gutachter: Prof. Dr. Bart Kempenaers Mündliche Prüfung am: 20. Februar 2008 Table of Contents General Introduction…………………………………………………………………. 9 Chapter I: Alternative reproductive tactics and sex allocation in the bivoltine ant Hypoponera opacior…………………………………….... 21 Abstract………………………………………………………………………… 23 Introduction……………………………………………………………………. 25 Material & Methods…………………………………………………………… 27 Results.………………………………………………………………………… 30 Discussion……………………………………………………........................... 38 Conclusions......................................................................................................... 43 Acknowledgements……………………………………………………………. -
Community Structure of Mites (Acari: Acariformes and Parasitiformes) in Nests of the Semi-Collared Flycatcher (Ficedula Semitorquata) R
International Research Journal of Natural Sciences Vol.3, No.3, pp.48-53, December 2015 ___Published by European Centre for Research Training and Development UK (www.eajournals.org) COMMUNITY STRUCTURE OF MITES (ACARI: ACARIFORMES AND PARASITIFORMES) IN NESTS OF THE SEMI-COLLARED FLYCATCHER (FICEDULA SEMITORQUATA) R. Davidova, V. Vasilev, N. Ali, J. Bakalova Konstantin Preslavsky University of Shumen, 115, Universitetska Str., Shumen, 9700, Bulgaria. ABSTRACT: The aims of the present paper are to establish the specific structure of communities of prostigmatic and mesostigmatic mites in nests of the semi-collared flycatcher (Ficedula semitorquata) and to compare the fauna with the mites in nests of two other European flycatchers. For analysis of community structure of mites were used the indices: prevalence, relative density, mean intensity and dominance. Mite communities are strongly dominated by the species Dermanyssus gallinae and Ornithonyssus sylviarum, which were found with the highest frequency and dominance. The mite communities are characterized by a large number of subrecedent species. KEYWORDS: Acariformes, Parasitiformes, Nest of Bird, Community Structure INTRODUCTION The nests of different species of birds are an example of a fairly unstable and isolated habitat, with its own dependent on it specific fauna which involves different groups of invertebrate animals. One of the components of this fauna which demonstrates particular abundance is the arthropods, and more specifically, the mites. The studies of Parasitiformes show that mesostigmatic mites living in birds' nests vary both in terms of their species affiliation and the structure of their communities [4, 8]. Highly important with respect to veterinary science and medicine are a number of species, such as Ornithonyssus bursa, Ornithonyssus sylviarum, Dermanyssus gallinae harboured by birds, Ornithonyssus bacoti, harboured by rodents, etc. -
Ants (Hymenoptera: Formicidae) of Bermuda
212 Florida Entomologist 87(2) June 2004 ANTS (HYMENOPTERA: FORMICIDAE) OF BERMUDA JAMES K. WETTERER1 AND ANDREA L. WETTERER2 1Wilkes Honors College, Florida Atlantic University, 5353 Parkside Drive, Jupiter, FL 33458 2Department of Ecology, Evolution, and Environmental Biology, Columbia University, New York, NY 10027 ABSTRACT For more than 50 years, two exotic ant species, Linepithema humile (Mayr) and Pheidole megacephala (F.), have been battling for ecological supremacy in Bermuda. Here we summa- rize known ant records from Bermuda, provide an update on the conflict between the domi- nant ant species, and evaluate the possible impact of the dominant species on the other ants in Bermuda. We examined ant specimens from Bermuda representing 20 species: Brachy- myrmex heeri Forel, B. obscurior Forel, Camponotus pennsylvanicus (De Geer), Cardio- condyla emeryi Forel, C. obscurior Wheeler, Crematogaster sp., Hypoponera opaciceps (Mayr), H. punctatissima (Roger), L. humile, Monomorium monomorium Bolton, Odontomachus rug- inodis Smith, Paratrechina longicornis (Latreille), P. vividula (Nylander), P. megacephala, Plagiolepis alluaudi Forel, Solenopsis (Diplorhoptrum) sp., Tetramorium caldarium Roger, T. simillimum (Smith), Wasmannia auropunctata (Roger), and an undetermined Dacetini. Records for all but three (H. punctatissima, P. vividula, W. auropunctata) include specimens from 1987 or later. We found no specimens to confirm records of several other ant species, in- cluding Monomorium pharaonis (L.) and Tetramorium caespitum (L.). Currently, L. humile dominates most of Bermuda, while P. megacephala appear to be at its lowest population lev- els recorded. Though inconspicuous, B. obscurior is common and coexists with both dominant species. Paratrechina longicornis has conspicuous populations in two urban areas. Three other ant species are well established, but inconspicuous due to small size (B. -
The Functions and Evolution of Social Fluid Exchange in Ant Colonies (Hymenoptera: Formicidae) Marie-Pierre Meurville & Adria C
ISSN 1997-3500 Myrmecological News myrmecologicalnews.org Myrmecol. News 31: 1-30 doi: 10.25849/myrmecol.news_031:001 13 January 2021 Review Article Trophallaxis: the functions and evolution of social fluid exchange in ant colonies (Hymenoptera: Formicidae) Marie-Pierre Meurville & Adria C. LeBoeuf Abstract Trophallaxis is a complex social fluid exchange emblematic of social insects and of ants in particular. Trophallaxis behaviors are present in approximately half of all ant genera, distributed over 11 subfamilies. Across biological life, intra- and inter-species exchanged fluids tend to occur in only the most fitness-relevant behavioral contexts, typically transmitting endogenously produced molecules adapted to exert influence on the receiver’s physiology or behavior. Despite this, many aspects of trophallaxis remain poorly understood, such as the prevalence of the different forms of trophallaxis, the components transmitted, their roles in colony physiology and how these behaviors have evolved. With this review, we define the forms of trophallaxis observed in ants and bring together current knowledge on the mechanics of trophallaxis, the contents of the fluids transmitted, the contexts in which trophallaxis occurs and the roles these behaviors play in colony life. We identify six contexts where trophallaxis occurs: nourishment, short- and long-term decision making, immune defense, social maintenance, aggression, and inoculation and maintenance of the gut microbiota. Though many ideas have been put forth on the evolution of trophallaxis, our analyses support the idea that stomodeal trophallaxis has become a fixed aspect of colony life primarily in species that drink liquid food and, further, that the adoption of this behavior was key for some lineages in establishing ecological dominance. -
James K. Wetterer
James K. Wetterer Wilkes Honors College, Florida Atlantic University 5353 Parkside Drive, Jupiter, FL 33458 Phone: (561) 799-8648; FAX: (561) 799-8602; e-mail: [email protected] EDUCATION UNIVERSITY OF WASHINGTON, Seattle, WA, 9/83 - 8/88 Ph.D., Zoology: Ecology and Evolution; Advisor: Gordon H. Orians. MICHIGAN STATE UNIVERSITY, East Lansing, MI, 9/81 - 9/83 M.S., Zoology: Ecology; Advisors: Earl E. Werner and Donald J. Hall. CORNELL UNIVERSITY, Ithaca, NY, 9/76 - 5/79 A.B., Biology: Ecology and Systematics. UNIVERSITÉ DE PARIS III, France, 1/78 - 5/78 Semester abroad: courses in theater, literature, and history of art. WORK EXPERIENCE FLORIDA ATLANTIC UNIVERSITY, Wilkes Honors College 8/04 - present: Professor 7/98 - 7/04: Associate Professor Teaching: Biodiversity, Principles of Ecology, Behavioral Ecology, Human Ecology, Environmental Studies, Tropical Ecology, Field Biology, Life Science, and Scientific Writing 9/03 - 1/04 & 5/04 - 8/04: Fulbright Scholar; Ants of Trinidad and Tobago COLUMBIA UNIVERSITY, Department of Earth and Environmental Science 7/96 - 6/98: Assistant Professor Teaching: Community Ecology, Behavioral Ecology, and Tropical Ecology WHEATON COLLEGE, Department of Biology 8/94 - 6/96: Visiting Assistant Professor Teaching: General Ecology and Introductory Biology HARVARD UNIVERSITY, Museum of Comparative Zoology 8/91- 6/94: Post-doctoral Fellow; Behavior, ecology, and evolution of fungus-growing ants Advisors: Edward O. Wilson, Naomi Pierce, and Richard Lewontin 9/95 - 1/96: Teaching: Ethology PRINCETON UNIVERSITY, Department of Ecology and Evolutionary Biology 7/89 - 7/91: Research Associate; Ecology and evolution of leaf-cutting ants Advisor: Stephen Hubbell 1/91 - 5/91: Teaching: Tropical Ecology, Introduction to the Scientific Method VANDERBILT UNIVERSITY, Department of Psychology 9/88 - 7/89: Post-doctoral Fellow; Visual psychophysics of fish and horseshoe crabs Advisor: Maureen K. -
James K. Wetterer
James K. Wetterer Wilkes Honors College, Florida Atlantic University 5353 Parkside Drive, Jupiter, FL 33458 Phone: (561) 799-8648; FAX: (561) 799-8602; e-mail: [email protected] EDUCATION UNIVERSITY OF WASHINGTON, Seattle, WA, 9/83 - 8/88 Ph.D., Zoology: Ecology and Evolution; Advisor: Gordon H. Orians. MICHIGAN STATE UNIVERSITY, East Lansing, MI, 9/81 - 9/83 M.S., Zoology: Ecology; Advisors: Earl E. Werner and Donald J. Hall. CORNELL UNIVERSITY, Ithaca, NY, 9/76 - 5/79 A.B., Biology: Ecology and Systematics. UNIVERSITÉ DE PARIS III, France, 1/78 - 5/78 Semester abroad: courses in theater, literature, and history of art. WORK EXPERIENCE FLORIDA ATLANTIC UNIVERSITY, Wilkes Honors College 8/04 - present: Professor 7/98 - 7/04: Associate Professor Teaching: Principles of Ecology, Behavioral Ecology, Human Ecology, Environmental Studies, Tropical Ecology, Biodiversity, Life Science, and Scientific Writing 9/03 - 1/04 & 5/04 - 8/04: Fulbright Scholar; Ants of Trinidad and Tobago COLUMBIA UNIVERSITY, Department of Earth and Environmental Science 7/96 - 6/98: Assistant Professor Teaching: Community Ecology, Behavioral Ecology, and Tropical Ecology WHEATON COLLEGE, Department of Biology 8/94 - 6/96: Visiting Assistant Professor Teaching: General Ecology and Introductory Biology HARVARD UNIVERSITY, Museum of Comparative Zoology 8/91- 6/94: Post-doctoral Fellow; Behavior, ecology, and evolution of fungus-growing ants Advisors: Edward O. Wilson, Naomi Pierce, and Richard Lewontin 9/95 - 1/96: Teaching: Ethology PRINCETON UNIVERSITY, Department of Ecology and Evolutionary Biology 7/89 - 7/91: Research Associate; Ecology and evolution of leaf-cutting ants Advisor: Stephen Hubbell 1/91 - 5/91: Teaching: Tropical Ecology, Introduction to the Scientific Method VANDERBILT UNIVERSITY, Department of Psychology 9/88 - 7/89: Post-doctoral Fellow; Visual psychophysics of fish and horseshoe crabs Advisor: Maureen K. -
Generalized Antifungal Activity and 454-Screening of Pseudonocardia and Amycolatopsis Bacteria in Nests of Fungus-Growing Ants
Generalized antifungal activity and 454-screening SEE COMMENTARY of Pseudonocardia and Amycolatopsis bacteria in nests of fungus-growing ants Ruchira Sena,1, Heather D. Ishaka, Dora Estradaa, Scot E. Dowdb, Eunki Honga, and Ulrich G. Muellera,1 aSection of Integrative Biology, University of Texas, Austin, TX 78712; and bMedical Biofilm Research Institute, 4321 Marsha Sharp Freeway, Lubbock, TX 79407 Edited by Raghavendra Gadagkar, Indian Institute of Science, Bangalore, India, and approved August 14, 2009 (received for review May 1, 2009) In many host-microbe mutualisms, hosts use beneficial metabolites origin (12–14). Many of the ant-associated Pseudonocardia species supplied by microbial symbionts. Fungus-growing (attine) ants are show antibiotic activity in vitro against Escovopsis (13–15). A thought to form such a mutualism with Pseudonocardia bacteria to diversity of actinomycete bacteria including Pseudonocardia also derive antibiotics that specifically suppress the coevolving pathogen occur in the ant gardens, in the soil surrounding attine nests, and Escovopsis, which infects the ants’ fungal gardens and reduces possibly in the substrate used by the ants for fungiculture (16, 17). growth. Here we test 4 key assumptions of this Pseudonocardia- The prevailing view of attine actinomycete-Escovopsis antago- Escovopsis coevolution model. Culture-dependent and culture- nism is a coevolutionary arms race between antibiotic-producing independent (tag-encoded 454-pyrosequencing) surveys reveal that Pseudonocardia and Escovopsis parasites (5, 18–22). Attine ants are several Pseudonocardia species and occasionally Amycolatopsis (a thought to use their integumental actinomycetes to specifically close relative of Pseudonocardia) co-occur on workers from a single combat Escovopsis parasites, which fail to evolve effective resistance nest, contradicting the assumption of a single pseudonocardiaceous against Pseudonocardia because of some unknown disadvantage strain per nest. -
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ISSN 1997-3500 Myrmecological News myrmecologicalnews.org Myrmecol. News 30: 27-52 doi: 10.25849/myrmecol.news_030:027 16 January 2020 Original Article Unveiling the morphology of the Oriental rare monotypic ant genus Opamyrma Yamane, Bui & Eguchi, 2008 (Hymeno ptera: Formicidae: Leptanillinae) and its evolutionary implications, with first descriptions of the male, larva, tentorium, and sting apparatus Aiki Yamada, Dai D. Nguyen, & Katsuyuki Eguchi Abstract The monotypic genus Opamyrma Yamane, Bui & Eguchi, 2008 (Hymeno ptera, Formicidae, Leptanillinae) is an ex- tremely rare relictual lineage of apparently subterranean ants, so far known only from a few specimens of the worker and queen from Ha Tinh in Vietnam and Hainan in China. The phylogenetic position of the genus had been uncertain until recent molecular phylogenetic studies strongly supported the genus to be the most basal lineage in the cryptic subterranean subfamily Leptanillinae. In the present study, we examine the morphology of the worker, queen, male, and larva of the only species in the genus, Opamyrma hungvuong Yamane, Bui & Eguchi, 2008, based on colonies newly collected from Guangxi in China and Son La in Vietnam, and provide descriptions and illustrations of the male, larva, and some body parts of the worker and queen (including mouthparts, tentorium, and sting apparatus) for the first time. The novel morphological data, particularly from the male, larva, and sting apparatus, support the current phylogenetic position of the genus as the most basal leptanilline lineage. Moreover, we suggest that the loss of lancet valves in the fully functional sting apparatus with accompanying shift of the venom ejecting mechanism may be a non-homoplastic synapomorphy for the Leptanillinae within the Formicidae.