Order Hymenoptera, Family Formicidae
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Ants in French Polynesia and the Pacific: Species Distributions and Conservation Concerns
Ants in French Polynesia and the Pacific: species distributions and conservation concerns Paul Krushelnycky Dept of Plant and Environmental Protection Sciences, University of Hawaii, Honolulu, Hawaii Hervé Jourdan Centre de Biologie et de Gestion des Populations, INRA/IRD, Nouméa, New Caledonia The importance of ants • In most ecosystems, form a substantial portion of a communities’ biomass (1/3 of animal biomass and ¾ of insect biomass in Amazon rainforest) Photos © Alex Wild The importance of ants • In most ecosystems, form a substantial portion of a communities’ biomass (1/3 of animal biomass and ¾ of insect biomass in Amazon rainforest) • Involved in many important ecosystem processes: predator/prey relationships herbivory seed dispersal soil turning mutualisms Photos © Alex Wild The importance of ants • Important in shaping evolution of biotic communities and ecosystems Photos © Alex Wild Ants in the Pacific • Pacific archipelagoes the most remote in the world • Implications for understanding ant biogeography (patterns of dispersal, species/area relationships, community assembly) • Evolution of faunas with depauperate ant communities • Consequent effects of ant introductions Hypoponera zwaluwenburgi Ants in the Amblyopone zwaluwenburgi Pacific – current picture Ponera bableti Indigenous ants in the Pacific? Approx. 30 - 37 species have been labeled “wide-ranging Pacific natives”: Adelomyrmex hirsutus Ponera incerta Anochetus graeffei Ponera loi Camponotus chloroticus Ponera swezeyi Camponotus navigator Ponera tenuis Camponotus rufifrons -
Effects on Brood Development in the Carpenter Ant Camponotus Vicinus Mayr After Exposure to the Yeast Associate Schwanniomyces Polymorphus Kloecker
insects Article Effects on Brood Development in the Carpenter Ant Camponotus vicinus Mayr after Exposure to the Yeast Associate Schwanniomyces polymorphus Kloecker Mark E. Mankowski 1,*, Jeffrey J. Morrell 2 and Patricia K. Lebow 3 1 Forest Products Laboratory Starkville, USDA Forest Service, Starkville, MS 39759, USA 2 Centre Timber Durability and Design Life, University of the Sunshine Coast, Sippy Downs, QLD 4102, Australia; [email protected] 3 Forest Products Laboratory Madison, USDA Forest Service, Madison, WI 53726, USA; [email protected] * Correspondence: [email protected] Simple Summary: Carpenter ants are important to ecosystem services as they assist in the breakdown of course woody debris when excavating wood for nests. Feeding on a variety of carbohydrate and protein sources, they have an infrabuccal filter that limits passage of large food particles to their gut. A variety of yeasts have been found associated with the infrabuccal pocket and the nests of these ants. The yeast Schwanniomyces polymorphus is associated with the carpenter ant Camponotus vicinus. To examine a possible nutritional association between this yeast and ant, we reared small sub-colonies of defaunated and non-defaunated C. vincus brood on several artificial diets where various nutritional components were removed. Part of the testing involved exposure of brood to these diets and cells of S. polymorphus. Dietary treatments that were augmented with yeast generally had deleterious Citation: Mankowski, M.E.; Morrell, J.J.; effects on brood development compared to diets without yeast. However, increased brood weight Lebow, P.K. Effects on Brood and increased number of adult ants from initial brood was observed in non-defaunated ants fed a Development in the Carpenter Ant diet where B vitamins and sterols were absent, but augmented with live yeast. -
Climate Change Impacts Vulnerability Adaptation
Acknowledgements The authors are deeply indebted to several individuals who made important contributions to this report. First of all, I would like to thank Mr. Majid Al Mansour Al Mansouri and Dr. Jaber Al Jaberi for their initiative in calling for this study and their continual support throughout the effort. Dr El Waleed Mohamed Hamad El Malik was instrumental in facilitating the many meetings and assisting with the acquisition of needed databases and other information. There were many individuals who provided invaluable support in obtaining the data and information needed by the models used in the study. Dr. Mohamed Dawoud provided extensive water resource information on water supply and demand that helped in the assessment about the impact of climate change on water resources. Mr. Khaldoun Kiwan, Mr. Maher Kabshawi, and Mr. Mayas Qarqaz, specialists in the Terrestrial Environmental Research Centre were very helpful in helping me to understand the types of data and information available for assessing the impact of climate change on terrestrial ecosystems in Abu Dhabi. Mr. Abdessalaam Thabit provided an essential orientation to information on marine resources and the marine environment in the Abu Dhabi region. In a study where baseline information on coastal zones, water resources and dryland ecosystems played such a crucial role, Mark Sorensen, Joseph Abdo, Anil Kumar were instrumental in orientation and access to the Environmental Agency’s environmental database under the AGEDI framework. Rashed Mohammed Amin Karkain from Dubai and Nabil Alolaqi, Sultan Zaidi, and Rashed Alkaabi from the Abu Dhabi Environmental Agency provided excellent facilitation in arranging meetings. Contributors Author William W. -
Zootaxa, Hymenoptera, Formicidae, Dolichoderinae
Zootaxa 776: 1–10 (2004) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA 776 Copyright © 2004 Magnolia Press ISSN 1175-5334 (online edition) A new species of the genus Bothriomyrmex Emery, 1869 (Hymenoptera: Formicidae: Dolichoderinae) from Costa Rica DMITRY A. DUBOVIKOFF1 & JOHN T. LONGINO2 1 Department of Entomology, Faculty of Biology and Soil Sciences, Saint Petersburg State University, 7/9 Uni- versiteskaya nab., St. Petersburg, 199034, Russia, [email protected] 2 The Evergreen State College, Olympia WA 98505 USA, [email protected] Abstract Bothriomyrmex paradoxus Dubovikov and Longino sp. nov. is described from Costa Rica, based on two collections from widely separated localities. These are the first collections of the genus Bothri- omyrmex in the Americas. The genus Bothriomyrmex can be divided into Palearctic species (Both- riomyrmex s.s.) and Oriental and Australian species, based on differences in palp formula and queen wing venation. Bothriomyrmex paradoxus shares palp and wing characters with the Palearc- tic species. It is probably native to Central America and long separated from its Old World relatives. Key words: Bothriomyrmex, Formicidae, Dolichoderinae, Costa Rica Introduction The subfamily Dolichoderinae is comprised of 22 genera, the majority of which are Old World (Shattuck 1992, Bolton 2003, Brandão et al. 1999). The dolichoderine genera with significant indigenous radiations in the New World are Azteca, Dolichoderus, Dory- myrmex, Forelius, Linepithema, Liometopum, and Tapinoma. Three additional genera have been reported as rare or introduced elements. Technomyrmex, a diverse genus in the Old World, is represented in the New World by one introduced tramp species and, paradoxi- cally, one native species from Panama and Costa Rica (Wheeler 1934, Longino pers. -
Diversity and Organization of the Ground Foraging Ant Faunas of Forest, Grassland and Tree Crops in Papua New Guinea
- - -- Aust. J. Zool., 1975, 23, 71-89 Diversity and Organization of the Ground Foraging Ant Faunas of Forest, Grassland and Tree Crops in Papua New Guinea P. M. Room Department of Agriculture, Stock and Fisheries, Papua New Guinea; present address: Cotton Research Unit, CSIRO, P.M.B. Myallvale Mail Run, Narrabri, N.S.W. 2390. Abstract Thirty samples of ants were taken in each of seven habitats: primary forest, rubber plantation, coffee plantation, oilpalm plantation, kunai grassland, eucalypt savannah and urban grassland. Sixty samples were taken in cocoa plantations. A total of 156 species was taken, and the frequency of occurrence of each in each habitat is given. Eight stenoecious species are suggested as habitat indicators. Habitats fell into a series according to the similarity of their ant faunas: forest, rubber and coffee, cocoa and oilpalm, kunai and savannah, urban. This series represents an artificial, discontinuous succession from a complex stable ecosystem to a simple unstable one. Availability of species suitably preadapted to occupy habitats did not appear to limit species richness. Habitat heterogeneity and stability as affected by human interference did seem to account for inter-habitat variability in species richness. Species diversity was compared between habitats using four indices: Fisher et al.; Margalef; Shannon; Brillouin. Correlation of diversity index with habitat hetero- geneity plus stability was good for the first two, moderate for Shannon, and poor for Brillouin. Greatest diversity was found in rubber, the penultimate in the series of habitats according to hetero- geneity plus stability ('maturity'). Equitability exceeded the presumed maximum in rubber, and was close to the maximum in all habitats. -
List of Indian Ants (Hymenoptera: Formicidae) Himender Bharti
List of Indian Ants (Hymenoptera: Formicidae) Himender Bharti Department of Zoology, Punjabi University, Patiala, India - 147002. (email: [email protected]/[email protected]) (www.antdiversityindia.com) Abstract Ants of India are enlisted herewith. This has been carried due to major changes in terms of synonymies, addition of new taxa, recent shufflings etc. Currently, Indian ants are represented by 652 valid species/subspecies falling under 87 genera grouped into 12 subfamilies. Keywords: Ants, India, Hymenoptera, Formicidae. Introduction The following 652 valid species/subspecies of myrmecology. This species list is based upon the ants are known to occur in India. Since Bingham’s effort of many ant collectors as well as Fauna of 1903, ant taxonomy has undergone major myrmecologists who have published on the taxonomy changes in terms of synonymies, discovery of new of Indian ants and from inputs provided by taxa, shuffling of taxa etc. This has lead to chaotic myrmecologists from other parts of world. However, state of affairs in Indian scenario, many lists appeared the other running/dynamic list continues to appear on web without looking into voluminous literature on http://www.antweb.org/india.jsp, which is which has surfaced in last many years and currently periodically updated and contains information about the pace at which new publications are appearing in new/unconfirmed taxa, still to be published or verified. Subfamily Genus Species and subspecies Aenictinae Aenictus 28 Amblyoponinae Amblyopone 3 Myopopone -
Copyrighted Material
Index Note: page numbers in italics refer to figures, those in bold refer to tables Abu Al Abyad (Abu Dhabi, UAE) cyanobacterial mats 22–3, 47–8, evaporative-pumping barrier island 71 85 model 245–6, 252 coral reefs 65–6 depositional environments 93, geomorphology 209 Abu Dhabi (UAE) 1–2, 3, 4–8 209–12 Holocene age sediments 247 algal mangrove flats 224 dolomite 27 Holocene age sediments barrier islands 20, 21, 22–3, 46, dunes 223 organic matter 48–9, 50, 51, 52, 208 early Holocene sediments 48 distribution 277–97 sabkha 71 evaporite distribution 177 Holocene barriers 271–2 sediment accumulation facies 93 Holocene coastal gypsum and 222–3 geology 222–4 anhydrite 268, 269 beaches 223 gypsum 29 Holocene coastal halite carbonate muds 22, 47–8 Holocene 101–2, 103, 104–5, accumulations/ carbonate sediment engineering 106, 107 salinas 267–8 properties 221–40 carbonates 205–17 hydrogeological chemical 229–32, 233, 234–9 geomorphology 45–86 framework 246–53 engineering intertidal flats 224 microbial mats 295–6 considerations 239–40 intertidal sediment organic mixing with aquifer 251, 252 engineering description/ matter accumulation organic matter classification 224–5, 296 distribution 294–6 226–7, 227–9 lagoons 21, 22–3, 46, 48–9, 50, rainfall events 251 geotechnical 229–32, 233, 51, 52, 92, 208–9 sea-level change impact on 234–9 carbonate sediment ramp margin site data 231–2, 233, 234–9 accumulation 222–3, deposition 89–108 terminology 241–2 223–4 seawater flooding model 245 carbonates mainland coastal plain 209 seawater trapping 246 cementation 23–4 -
Liquid Baits Control Argentine Ants Sustainably in Coastal Vineyards
UC Agriculture & Natural Resources California Agriculture Title Liquid baits control Argentine ants sustainably in coastal vineyards Permalink https://escholarship.org/uc/item/64z229kw Journal California Agriculture, 62(4) ISSN 0008-0845 Authors Cooper, Monica L Daane, Kent M Nelson, Erik H et al. Publication Date 2008-10-01 Peer reviewed eScholarship.org Powered by the California Digital Library University of California REVIEW ARTICLE ▼ Liquid baits control Argentine ants sustainably in coastal vineyards by Monica L. Cooper, Kent M. Daane, Erik H. Nelson, Lucia G. Varela, Mark C. Battany, Wild Alex Neil D. Tsutsui and Michael K. Rust Liquid ant baits are an alterna- tive to broad-spectrum insecticide sprays conventionally used to con- trol Argentine ants. We review the development of liquid ant baits, which capitalize on the ants’ sugar- feeding requirements and social structure to deliver small doses of toxicant throughout the colony. The ant bait program described here, developed for commercial vine- yards, also has the potential to fa- cilitate the use of biological controls for mealybug and scale pests. The implementation of an Argentine ant bait program will enable grape growers to target other pests more selectively with insecticides, further contributing to their sustainable An Argentine ant tends an adult mealybug. A drop of honeydew, the sugar-rich viticulture practices. mealybug excretion, can be seen in the ant’s mouthparts. he Argentine ant is an invasive pest grape mealybug (Pseudococcus maritimus out the colony. We also discuss future that has spread throughout Cali- [Ehrhorn]), obscure mealybug (P. viburni avenues of study to further control forniaT since it was fi rst reported from [Signoret]) (Daane et al. -
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. -
Chromosome Numbers in Spanish Formicidae (Hymenoptera) IV
331 Chromosome Numbers in Spanish Formicidae (Hymenoptera) IV. New data of Species from the Genera Camponotus, Formica, Lasius, Messor, and Monomorium by Pedro Lorite1, Jose A. Carrillo1, Alberto Tinaut2 and Teresa Palomeque1 ABSTRACT In this paper we report new karyological data from seven species belonging to subfamilies Formicinae and Myrmicinae. Among them we include two that are considered as endemic Iberian species, Formica frontalis and Formica subrufa. Also the chromosome number of Formica gerardi is reported. In Lasius brunneus, a variation on chromosome number probably due to the presence of B-chromosomes was detected. For two other species (Camponotus cruentatus and Messor barbarus) we found different chromosome numbers from those previously published. Also we confirm the chromosome number reported for Monomorium subopacum. INTRODUCTION Hymenoptera form one of the most distinct and well-defined insect orders and have long been perceived as a natural group. Haplo-diploidy or male haploidy is the main characteristic of the order (Crozier 1975, Gauld & Bolton 1988). Several studies have been carried about cytogenetic aspects of ants. A wide variation has been observed in relation to the chromosome number (n=1 to n=42). Karyological analysis has proved to be useful to determine the karyotypic relationship and evolution between related species (Imai 1971, Loiselle et al. 1990, Palomeque et al. 1988, 1993) as well for the establishment and characterization of new species (Imai et al. 1994). In recent years our group have performed studies in Spanish Formicidae. In relation to this, we have published several reviews of chromosome numbers (Lorite et al. 1998a, 1998b, 2000). In this paper we report new karyological data from seven species from the Formicinae 1 Departamento de Biología Experimental. -
Of Abu Dhabi Emirate, United Arab Emirates MARINE and COASTAL ENVIRONMENTS of ABU DHABI EMIRATE, UNITED ARAB EMIRATES
of Abu Dhabi Emirate, United Arab Emirates MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES Page . II of Abu Dhabi Emirate, United Arab Emirates Page . III MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES Page . IV MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES H. H. Sheikh Khalifa bin Zayed Al Nahyan President of the United Arab Emirates Page . V MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES Page . VI MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES H. H. Sheikh Mohammed bin Zayed Al Nahyan Crown Prince of Abu Dhabi, Deputy Supreme Commander of the UAE Armed Forces Page . VII MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES Page . VIII MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES H. H. Sheikh Hamdan bin Zayed Al Nahyan Deputy Prime Minister Page . IX MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES s\*?*c*i]j6.%;M"%&9+~)#"$*&ENL`\&]j6. =';78G=%1?%&'12= !"##$" 9<8*TPEg-782#,On%O)6=]KL %&'( )*+,-. 2#,On#X%3G=FON&$4#*.%&9+~)#"$*&XNL %?)#$*&E, &]1TL%&9+%?)':5=&4O`(.#`g-78 %!/ اﻷوراق اﻟﻘﻄﺎﻋﻴﺔ fJT=V-=>?#Fk9+*#$'&= /%*?%=*<(/8>OhT7.F 012(.%34#56.%-78&9+:;(<=>=?%@8'-/ABC $L#01i%;1&&!580.9,q@EN(c D)=EF%3G&H#I7='J=:KL)'MD*7.%&'-(8=';78G=NO D)$8P#"%;QI8ABCRI7S;<#D*T(8%.I7)=U%#$#VW'.X JG&Bls`ItuefJ%27=PE%u%;QI8)aEFD)$8%7iI=H*L YZZ[\&F]17^)#G=%;/;!N_-LNL`%3;%87VW'.X NL]17~Is%1=fq-L4"#%;M"~)#"G=,|2OJ*c*TLNLV(ItuG= )aE0@##`%;Kb&9+*c*T(`d_-8efJG=g-78012 -
Hymenoptera: Formicidae
16 The Weta 30: 16-18 (2005) Changes to the classification of ants (Hymenoptera: Formicidae) Darren F. Ward School of Biological Sciences, Tamaki Campus, Auckland University, Private Bag 92019, Auckland ([email protected]) Introduction This short note aims to update the reader on changes to the subfamily classification of ants (Hymenoptera: Formicidae). Although the New Zealand ant fauna is very small, these changes affect the classification and phylogeny of both endemic and exotic ant species in New Zealand. Bolton (2003) has recently proposed a new subfamily classification for ants. Two new subfamilies have been created, a revised status for one, and new status for four. Worldwide, there are now 21 extant subfamilies of ants. The endemic fauna of New Zealand is now classified into six subfamilies (Table 1), as a result of three subfamilies, Amblyoponinae, Heteroponerinae and Proceratiinae, being split from the traditional subfamily Ponerinae. Bolton’s (2003) classification also affects several exotic species in New Zealand. Three species have been transferred from Ponerinae: Amblyopone australis to Amblyoponinae, and Rhytidoponera chalybaea and R. metallica to Ectatomminae. Currently there are 28 exotic species in New Zealand (Table 1). Eighteen species have most likely come from Australia, where they are native. Eight are global tramp species, commonly transported by human activities, and two species are of African origin. Nineteen of the currently established exotic species are recorded for the first time in New Zealand as occurring outside their native range. This may result in difficulty in obtaining species-specific biological knowledge and assessing their likelihood of becoming successful invaders. In addition to the work by Bolton (2003), Phil Ward and colleagues at UC Davis have started to resolve the phylogenetic relationships among subfamilies and genera of all ants using molecular data (Ward et al, 2005).