A Comparison of the Effectiveness of Pitfall Traps and Winkler Litter Samples for Characterization of Terrestrial Ant (Formicidae) Communities in Temperate Savannas
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Diversity from the Lower Kennebec Valley Region of Maine
J. Acad. Entomol. Soc. 8: 48-51 (2012) NOTE Formicidae [Hymenoptera] diversity from the Lower Kennebec Valley Region of Maine Gary D. Ouellette and André Francoeur Ants [Hymenoptera: Formicidae] occupy an important ecological position in most terrestrial habitats and have been investigated for evaluating the effects of ecosystem characteristics such as soil, vegetation, climate and habitat disturbance (Sanders et al., 2003; Rios-Casanova et al., 2006). At present, Maine’s myrmecofauna has not been extensively studied (Ouellette et al., 2010). Early in the 20th century, Wheeler (1908) presented results from a small survey of the Casco Bay region and Wing (1939) published a checklist of ant species recorded from the state. Both Procter (1946) and Ouellette et al. (2010) reported ant species surveyed from the Mount Desert Island region. The importance of expanding this knowledge base is highlighted by a recent discovery of the invasive ant species Myrmica rubra (Linnaeus) (Garnas 2004; Groden et al. 2005; Garnas et al. 2007; McPhee et al. 2012). The present study represents the first evaluation and characterization of Formicidae from a White Pine- Mixed Hardwoods Forest (WPMHF) ecosystem (Gawler & Cutko 2010) located in the lower Kennebec Valley region. The species reported here provide a baseline condition and a means for future biodiversity comparison. Fifteen study sites, located in the lower Kennebec Valley region, were sampled 1 to 8 times between May 1998 and July 2011 (Figure 1). Habitats comprised of a closed-canopy, WPMHF ecosystem covered by hemlock forests, mixed beech forests, red-oak-northern-hardwood-white pine-forests, and white pine mixed conifer forests. -
Raid Organization and Behavioral Development in the Slave-Making Ant Polyergus Lucidus Mayr E
Insectes Sociaux, Paris Masson, Paris, 1984 1984, Volume 31, n ~ 4, pp. 361-374 RAID ORGANIZATION AND BEHAVIORAL DEVELOPMENT IN THE SLAVE-MAKING ANT POLYERGUS LUCIDUS MAYR E. COOL-KWAIT (1) and H. TOPOFF (2) (1) Department of Biology, City College of Cuny, New York, N.Y. I003i, U.S.A. (2) Department of Psychology, Hunter College of Cuny, New York, N.Y. 10021, U.S.A and The American Museum of Natural History, New York, N.Y. 10024, U.S.A. Requ le 5 septembre 1983. Accept6 le 18 juin 1984. SUMMARY Mixed-species colonies of Polyergus lucidus and Fdrmica schaufussi xvere studied in New York. Slave raids were conducted in late afternoon, past the peak in diurnal temperature. Multiple raids on different Formica colonies xvere common, as ~vere re-raids on the same colony. In laboratory nests, about 75 % of the raided Formica brood was eaten. Of 27 days on ,which raids occurred in the laboratory, 25 ~vere on Formica nests scouted on the day of the raid. Polyergus scouts are among the oldest individuals in the colony, and call~ws do not participate in scouting during the entire season of their eclosion. The group of Polyergus workers that circle on the surface near the nest prior to raiding has a dynamic composition.. The most frequent behavioral transition ~vas from circling on one day to scouting on the next. The next most common change was from SCOUting to circling. The first scouting of the spring season occurred only one day after the appearance of Polyergus larvae. The first slave raid 'was conducted 4 days later. -
A Thesis Entitled the Short-Term Impacts of Burning and Mowing on Prairie Ant Communities of the Oak Openings Region by Russell
A Thesis entitled The Short-term Impacts of Burning and Mowing on Prairie Ant Communities of the Oak Openings Region by Russell L. Friedrich Submitted to the Graduate Faculty as partial fulfillment of the requirements for the degree of Master of Science in Biology (Ecology track) ________________________________________________ Dr. Stacy Philpott, Committee Chair ________________________________________________ Dr. Jonathan Bossenbroek, Committee Member ________________________________________________ Dr. Daniel Pavuk, Committee Member ________________________________________________ Dr. Patricia Komuniecki, Dean College of Graduate Studies The University of Toledo May 2010 Copyright 2010, Russell L. Friedrich This document is copyrighted material. Under copyright law, no parts of this document may be reproduced without the expressed permission of the author. An Abstract of The Short-term Impacts of Land Management Techniques on Prairie Ant Communities by Russell L. Friedrich Submitted to the Graduate Faculty in partial fulfillment of the requirements for the degree of Master of Science in Biology (Ecology track) The University of Toledo May 2010 Controlled burning and mowing are among the most common forms of disturbance in prairie grasslands. Extensive studies on vegetative responses to fire, grazing, and mowing have been investigated, however, there is a lack of information on how animals and particularly insects are affected by these disturbances. Ants in particular play vital ecological roles in nutrient cycling, soil structure and turnover, predation, and seed dispersal, but few studies have assessed ant response to land management practices in prairie ecosystems. This research will assess the short-term impacts of controlled burning and mowing on ant communities. Ants were sampled in 17 prairie sites, divided into three treatments (burn, control, mow) within the Oak Openings Region in Ohio. -
Five New Records of Ants (Hymenoptera: Formicidae)
The Prairie Naturalist 44(1):63–65; 2012 FIVE NEW RECORDS OF ANTS (HYMENOPTERA: Formica incerta, F. montana, F. pallidefulva, Lasius FORMICIDAE) FOR NEBRASKA—Ants are ubiquitous interjectus, L. neoniger, Myrmica americana, M. and influential organisms in terrestrial ecosystems. About brevispinosa, Nylanderia parvula, Pheidole pilfera pilfera, 1,000 ant species occur in North America, where they are Ponera pennsylvanica, Prenolepis imparis, Solenopsis found in nearly every habitat (Fisher and Cover 2007). Ants molesta, and Tapinoma sessile. K. T. Nemec [KTN] are critical to ecological processes and structure. Ants collected all ant specimens. For each record, the person affect soils via tunneling activity (Baxter and Hole 1967), who determined the identity of the specimen is preceded by disperse plant seeds (Lengyel et al. 2009), prey upon a the abbreviation “det.” Voucher specimens are either variety of insects and other invertebrates (Way and Khoo located at the Nebraska State Museum [NSM] or with KTN. 1992, Folgarait 1998), are often effective primary Aphaenogaster rudis Enzmann is common in deciduous consumers through their prodigious consumption of floral woodlands and nests in soil, under stones or logs, in and especially extrafloral nectar, and honeydew (Tobin decaying wood, leaf litter, hollow stems of plants, or under 1994), and serve as prey for invertebrates (Gotelli 1996, bark at bases of trees (Smith 1979). Like most members of Gastreich 1999) and vertebrates (Reiss 2001). Aphaenogaster, it is not characteristic of prairies (Trager In Nebraska, ants have been the subject of relatively few 1998), but may be found in prairie remnants or restorations in-depth analyses, including theses (Bare 1929, Henzlik that are adjacent to deciduous trees (Kittelson et al. -
Hymenoptera: Formicidae)
SYSTEMATICS Phylogenetic Analysis of Aphaenogaster Supports the Resurrection of Novomessor (Hymenoptera: Formicidae) 1 B. B. DEMARCO AND A. I. COGNATO Department of Entomology, Michigan State University, 288 Farm Lane, East Lansing, MI 48824. Ann. Entomol. Soc. Am. 108(2): 201–210 (2015); DOI: 10.1093/aesa/sau013 ABSTRACT The ant genus Aphaenogaster Mayr is an ecologically diverse group that is common throughout much of North America. Aphaenogaster has a complicated taxonomic history due to variabil- ity of taxonomic characters. Novomessor Emery was previously synonymized with Aphaenogaster, which was justified by the partial mesonotal suture observed in Aphaenogaster ensifera Forel. Previous studies using Bayesian phylogenies with molecular data suggest Aphaenogaster is polyphyletic. Convergent evolution and retention of ancestral similarities are two major factors contributing to nonmonophyly of Aphaenogaster. Based on 42 multistate morphological characters and five genes, we found Novomessor more closely related to Veromessor Forel and that this clade is sister to Aphaenogaster. Our results confirm the validity of Novomessor stat. r. as a separate genus, and it is resurrected based on the combi- nation of new DNA, morphological, behavioral, and ecological data. KEY WORDS Aphaenogaster, Novomessor, phylogenetics, resurrection Introduction phylogenetic analyses resolved Aphaenogaster as polyphyletic, including Messor Forel, 1890 and Sten- The ant genus Aphaenogaster Mayr, 1853 is a speciose amma (Brady et al. 2006, Moreau and Bell 2013). group,whichhasnotbeentaxonomicallyreviewedin Ward (2011) suggested that convergent evolution and over 60 years (Creighton 1950). Aphaenogaster con- retention of ancestral similarities were two major fac- tains 227 worldwide species (Bolton 2006), with 23 tors contributing to polyphyly of Aphaenogaster. valid North American species reduced from 31 original Aphaenogaster taxonomy was further complicated species descriptions. -
Akes an Ant an Ant? Are Insects, and Insects Are Arth Ropods: Invertebrates (Animals With
~ . r. workers will begin to produce eggs if the queen dies. Because ~ eggs are unfertilized, they usually develop into males (see the discus : ~ iaplodiploidy and the evolution of eusociality later in this chapter). =- cases, however, workers can produce new queens either from un ze eggs (parthenogenetically) or after mating with a male ant. -;c. ant colony will continue to grow in size and add workers, but at -: :;oint it becomes mature and will begin sexual reproduction by pro· . ~ -irgin queens and males. Many specie s produce males and repro 0 _ " females just before the nuptial flight . Others produce males and ---: : ._ tive fem ales that stay in the nest for a long time before the nuptial :- ~. Our largest carpenter ant, Camponotus herculeanus, produces males _ . -:= 'n queens in late summer. They are groomed and fed by workers :;' 0 it the fall and winter before they emerge from the colonies for their ;;. ights in the spring. Fin ally, some species, including Monomoriurn : .:5 and Myrmica rubra, have large colonies with multiple que ens that .~ ..ew colonies asexually by fragmenting the original colony. However, _ --' e polygynous (literally, many queens) and polydomous (literally, uses, referring to their many nests) ants eventually go through a -">O=- r' sexual reproduction in which males and new queens are produced. ~ :- . ant colony thus functions as a highly social, organ ized "super _ _ " 1." The queens and mo st workers are safely hidden below ground : : ~ - ed within the interstices of rotting wood. But for the ant workers ~ '_i S ' go out and forage for food for the colony,'life above ground is - =- . -
Description of a New Genus of Primitive Ants from Canadian Amber
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida 8-11-2017 Description of a new genus of primitive ants from Canadian amber, with the study of relationships between stem- and crown-group ants (Hymenoptera: Formicidae) Leonid H. Borysenko Canadian National Collection of Insects, Arachnids and Nematodes, [email protected] Follow this and additional works at: http://digitalcommons.unl.edu/insectamundi Part of the Ecology and Evolutionary Biology Commons, and the Entomology Commons Borysenko, Leonid H., "Description of a new genus of primitive ants from Canadian amber, with the study of relationships between stem- and crown-group ants (Hymenoptera: Formicidae)" (2017). Insecta Mundi. 1067. http://digitalcommons.unl.edu/insectamundi/1067 This Article is brought to you for free and open access by the Center for Systematic Entomology, Gainesville, Florida at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Insecta Mundi by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. INSECTA MUNDI A Journal of World Insect Systematics 0570 Description of a new genus of primitive ants from Canadian amber, with the study of relationships between stem- and crown-group ants (Hymenoptera: Formicidae) Leonid H. Borysenko Canadian National Collection of Insects, Arachnids and Nematodes AAFC, K.W. Neatby Building 960 Carling Ave., Ottawa, K1A 0C6, Canada Date of Issue: August 11, 2017 CENTER FOR SYSTEMATIC ENTOMOLOGY, INC., Gainesville, FL Leonid H. Borysenko Description of a new genus of primitive ants from Canadian amber, with the study of relationships between stem- and crown-group ants (Hymenoptera: Formicidae) Insecta Mundi 0570: 1–57 ZooBank Registered: urn:lsid:zoobank.org:pub:C6CCDDD5-9D09-4E8B-B056-A8095AA1367D Published in 2017 by Center for Systematic Entomology, Inc. -
The Evolution of Social Parasitism in Formica Ants Revealed by a Global Phylogeny – Supplementary Figures, Tables, and References
The evolution of social parasitism in Formica ants revealed by a global phylogeny – Supplementary figures, tables, and references Marek L. Borowiec Stefan P. Cover Christian Rabeling 1 Supplementary Methods Data availability Trimmed reads generated for this study are available at the NCBI Sequence Read Archive (to be submit ted upon publication). Detailed voucher collection information, assembled sequences, analyzed matrices, configuration files and output of all analyses, and code used are available on Zenodo (DOI: 10.5281/zen odo.4341310). Taxon sampling For this study we gathered samples collected in the past ~60 years which were available as either ethanol preserved or pointmounted specimens. Taxon sampling comprises 101 newly sequenced ingroup morphos pecies from all seven species groups of Formica ants Creighton (1950) that were recognized prior to our study and 8 outgroup species. Our sampling was guided by previous taxonomic and phylogenetic work Creighton (1950); Francoeur (1973); Snelling and Buren (1985); Seifert (2000, 2002, 2004); Goropashnaya et al. (2004, 2012); Trager et al. (2007); Trager (2013); Seifert and Schultz (2009a,b); MuñozLópez et al. (2012); Antonov and Bukin (2016); Chen and Zhou (2017); Romiguier et al. (2018) and included represen tatives from both the New and the Old World. Collection data associated with sequenced samples can be found in Table S1. Molecular data collection and sequencing We performed nondestructive extraction and preserved samespecimen vouchers for each newly sequenced sample. We remounted all vouchers, assigned unique specimen identifiers (Table S1), and deposited them in the ASU Social Insect Biodiversity Repository (contact: Christian Rabeling, [email protected]). -
AN UPDATED LIST of the ANTS (HYMENOPTERA FORMICIDAE) of OHIO KAL IVANOV DEPARTMENT of RECENT INVERTEBRATES; [email protected]
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/324042927 ONHC 2018 Ants of Ohio Feb 24 2018 Poster · March 2018 DOI: 10.13140/RG.2.2.33148.44162 CITATIONS READS 0 145 1 author: Kaloyan Ivanov Virginia Museum of Natural History 38 PUBLICATIONS 185 CITATIONS SEE PROFILE Some of the authors of this publication are also working on these related projects: Ants of Virginia View project Ants of Ohio View project All content following this page was uploaded by Kaloyan Ivanov on 27 March 2018. The user has requested enhancement of the downloaded file. AN UPDATED LIST OF THE ANTS (HYMENOPTERA FORMICIDAE) OF OHIO KAL IVANOV DEPARTMENT OF RECENT INVERTEBRATES; [email protected] 1, 2, 8, 9, Introduction 10, 15, 16, 3, 6, 7, 18, 19, 21 In 2005, Coovert summarized all previously known information and published the first 8, 14 21 • 15 comprehensive list of the ants of Ohio • In the following thirteen years, a considerable amount of information has become available 16 as a result of survey work, as well as recent taxonomic descriptions and revisions Huron-Erie Lake 5, 14, 16 • Here I update Ohio’s list to accommodate 23 additional species, and 32 name changes in Plains 15, 16 species already on the list Glaciated Allegheny • The new additions are based on published accounts (13 species), museum databases (3 5 Plateau species), and newly collected material (7 species), (Table 1, Figs. 1 and 2) Till Plains • Two species, previously on the list, have been removed as a result of taxonomic changes Allegheny Plateau (Formica nitidiventris Emery), or because the records are likely based on misidentifications (Dorymyrmex insanus (Buckley)) 5 Species Accounts 5, 18 20 1, 8 Table 1. -
View a Presentation
A modest study on biodiversity in Hartford community gardens Premise: Urban gardens will be hotspots of biodiversity in an otherwise degraded urban landscape. Because Hartford has an extensive set of diverse community gardening sites, and because my CTP partner Lucia was keen on an insect project, we initiated a study, looking at ant and arthropod diversity in the city. Why diversity in gardens? Plant diversity – crops, weeds Structural diversity – e.g., corn, vining plants, trellis Moisture variability with extensive irrigation Pollinators attracted to long season of blooms Plant and woody debris Typical small garden LargeEarle garden Street - Knox Large Garden Earle Street Sampling scheme Sampled ants 3 dates Sampled for ants+arthropods 1 date - 3 large gardens (>5000 m2) - 3 matched “controls” (old field) - 3 small gardens (<600 m2) - 3 matched “controls” (turf) Units: Six 40 dram pitfalls per site per date. Analysis: Ant species identified for garden sites on 3 dates. Arthropod (morphospecies + ants) identified for garden sites and controls on Aug 24. The ants ca. 20 species Large and small gardens with similar species counts Common species Myrmica nr rubra Premolepis imparis “Rare” Formica incerta Crematogaster cerasi Extremes Camponotus chromaiodes Solenopsis Nylanderia sp. Manhattan Study - High stress medians: 21 species (!) - Urban forests 32 species Savage, A. M., Hackett, B., Guénard, B., Youngsteadt, E. K., Dunn, R. R. (2014), "Fine-scale heterogeneity across Manhattan's urban habitat mosaic is associated with variation in ant composition and richness." Insect Conservation and Diversity. Camponotus herculeanus Camponotus novaeboracensis We expect the same difference here. 2 species observed in Keney Park, and absent from all other urban sites. -
Effects of Forest Edges, Exotic Ants and Nonnative Plants on Local Ant (Hymenoptera: Formicidae) Diversity in Urban Forest Fragments of Northeastern Ohio
Cleveland State University EngagedScholarship@CSU ETD Archive 2010 Effects of Forest Edges, Exotic Ants and Nonnative Plants on Local Ant (Hymenoptera: Formicidae) Diversity in Urban Forest Fragments of Northeastern Ohio Kaloyan Ivanov Cleveland State University Follow this and additional works at: https://engagedscholarship.csuohio.edu/etdarchive Part of the Environmental Sciences Commons How does access to this work benefit ou?y Let us know! Recommended Citation Ivanov, Kaloyan, "Effects of Forest Edges, Exotic Ants and Nonnative Plants on Local Ant (Hymenoptera: Formicidae) Diversity in Urban Forest Fragments of Northeastern Ohio" (2010). ETD Archive. 141. https://engagedscholarship.csuohio.edu/etdarchive/141 This Dissertation is brought to you for free and open access by EngagedScholarship@CSU. It has been accepted for inclusion in ETD Archive by an authorized administrator of EngagedScholarship@CSU. For more information, please contact [email protected]. EFFECTS OF FOREST EDGES, EXOTIC ANTS AND NONNATIVE PLANTS ON LOCAL ANT (HYMENOPTERA: FORMICIDAE) DIVERSITY IN URBAN FOREST FRAGMENTS OF NORTHEASTERN OHIO KALOYAN IVANOV Master of Science in Entomology Sofia University Sofia, Bulgaria 2000 Submitted in partial fulfillment of requirements for the degree DOCTOR OF PHILOSOPHY IN REGULATORY BIOLOGY at the CLEVELAND STATE UNIVERSITY December, 2010 This dissertation has been approved for the Department of Biological, Geological, and Environmental Sciences and for the College of Graduate Studies by Date: Dr. Joe B. Keiper, Virginia Museum of Natural History Major Advisor Date: Dr. B. Michael Walton, BGES / CSU Advisory Committee Member Date: Dr. Robert A. Krebs, BGES / CSU Advisory Committee Member Date: Dr. Jaharul Haque, The Cleveland Clinic Advisory Committee Member Date: Dr. -
1 the RESTRUCTURING of ARTHROPOD TROPHIC RELATIONSHIPS in RESPONSE to PLANT INVASION by Adam B. Mitchell a Dissertation Submitt
THE RESTRUCTURING OF ARTHROPOD TROPHIC RELATIONSHIPS IN RESPONSE TO PLANT INVASION by Adam B. Mitchell 1 A dissertation submitted to the Faculty of the University of Delaware in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Entomology and Wildlife Ecology Winter 2019 © Adam B. Mitchell All Rights Reserved THE RESTRUCTURING OF ARTHROPOD TROPHIC RELATIONSHIPS IN RESPONSE TO PLANT INVASION by Adam B. Mitchell Approved: ______________________________________________________ Jacob L. Bowman, Ph.D. Chair of the Department of Entomology and Wildlife Ecology Approved: ______________________________________________________ Mark W. Rieger, Ph.D. Dean of the College of Agriculture and Natural Resources Approved: ______________________________________________________ Douglas J. Doren, Ph.D. Interim Vice Provost for Graduate and Professional Education I certify that I have read this dissertation and that in my opinion it meets the academic and professional standard required by the University as a dissertation for the degree of Doctor of Philosophy. Signed: ______________________________________________________ Douglas W. Tallamy, Ph.D. Professor in charge of dissertation I certify that I have read this dissertation and that in my opinion it meets the academic and professional standard required by the University as a dissertation for the degree of Doctor of Philosophy. Signed: ______________________________________________________ Charles R. Bartlett, Ph.D. Member of dissertation committee I certify that I have read this dissertation and that in my opinion it meets the academic and professional standard required by the University as a dissertation for the degree of Doctor of Philosophy. Signed: ______________________________________________________ Jeffery J. Buler, Ph.D. Member of dissertation committee I certify that I have read this dissertation and that in my opinion it meets the academic and professional standard required by the University as a dissertation for the degree of Doctor of Philosophy.