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Basic Biology and Applications of Actinobacteria
Edited by Shymaa Enany Basic Biology and Applications of ActinobacteriaBasic of Biology and Applications Actinobacteria have an extensive bioactive secondary metabolism and produce a huge Basic Biology and amount of naturally derived antibiotics, as well as many anticancer, anthelmintic, and antifungal compounds. These bacteria are of major importance for biotechnology, medicine, and agriculture. In this book, we present the experience of worldwide Applications of Actinobacteria specialists in the field of Actinobacteria, exploring their current knowledge and future prospects. Edited by Shymaa Enany ISBN 978-1-78984-614-0 Published in London, UK © 2018 IntechOpen © PhonlamaiPhoto / iStock BASIC BIOLOGY AND APPLICATIONS OF ACTINOBACTERIA Edited by Shymaa Enany BASIC BIOLOGY AND APPLICATIONS OF ACTINOBACTERIA Edited by Shymaa Enany Basic Biology and Applications of Actinobacteria http://dx.doi.org/10.5772/intechopen.72033 Edited by Shymaa Enany Contributors Thet Tun Aung, Roger Beuerman, Oleg Reva, Karen Van Niekerk, Rian Pierneef, Ilya Korostetskiy, Alexander Ilin, Gulshara Akhmetova, Sandeep Chaudhari, Athumani Msalale Lupindu, Erasto Mbugi, Abubakar Hoza, Jahash Nzalawahe, Adriana Ribeiro Carneiro Folador, Artur Silva, Vasco Azevedo, Carlos Leonardo De Aragão Araújo, Patricia Nascimento Da Silva, Jorianne Thyeska Castro Alves, Larissa Maranhão Dias, Joana Montezano Marques, Alyne Cristina Lima, Mohamed Harir © The Editor(s) and the Author(s) 2018 The rights of the editor(s) and the author(s) have been asserted in accordance with the Copyright, Designs and Patents Act 1988. All rights to the book as a whole are reserved by INTECHOPEN LIMITED. The book as a whole (compilation) cannot be reproduced, distributed or used for commercial or non-commercial purposes without INTECHOPEN LIMITED’s written permission. -
The Conservation Management and Ecology of Northeastern North
THE CONSERVATION MANAGEMENT AND ECOLOGY OF NORTHEASTERN NORTH AMERICAN BUMBLE BEES AMANDA LICZNER A DISSERTATION SUBMITTED TO THE FACULTY OF GRADUATE STUDIES IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY GRADUATE PROGRAM IN BIOLOGY YORK UNIVERSITY TORONTO, ONTARIO September 2020 © Amanda Liczner, 2020 ii Abstract Bumble bees (Bombus spp.; Apidae) are among the pollinators most in decline globally with a main cause being habitat loss. Habitat requirements for bumble bees are poorly understood presenting a research gap. The purpose of my dissertation is to characterize the habitat of bumble bees at different spatial scales using: a systematic literature review of bumble bee nesting and overwintering habitat globally (Chapter 1); surveys of local and landcover variables for two at-risk bumble bee species (Bombus terricola, and B. pensylvanicus) in southern Ontario (Chapter 2); identification of conservation priority areas for bumble bee species in Canada (Chapter 3); and an analysis of the methodology for locating bumble bee nests using detection dogs (Chapter 4). The main findings were current literature on bumble bee nesting and overwintering habitat is limited and biased towards the United Kingdom and agricultural habitats (Ch.1). Bumble bees overwinter underground, often on shaded banks or near trees. Nests were mostly underground and found in many landscapes (Ch.1). B. terricola and B. pensylvanicus have distinct habitat characteristics (Ch.2). Landscape predictors explained more variation in the species data than local or floral resources (Ch.2). Among local variables, floral resources were consistently important throughout the season (Ch.2). Most bumble bee conservation priority areas are in western Canada, southern Ontario, southern Quebec and across the Maritimes and are most often located within woody savannas (Ch.3). -
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. -
Symbiotic Adaptations in the Fungal Cultivar of Leaf-Cutting Ants
ARTICLE Received 15 Apr 2014 | Accepted 24 Oct 2014 | Published 1 Dec 2014 DOI: 10.1038/ncomms6675 Symbiotic adaptations in the fungal cultivar of leaf-cutting ants Henrik H. De Fine Licht1,w, Jacobus J. Boomsma2 & Anders Tunlid1 Centuries of artificial selection have dramatically improved the yield of human agriculture; however, strong directional selection also occurs in natural symbiotic interactions. Fungus- growing attine ants cultivate basidiomycete fungi for food. One cultivar lineage has evolved inflated hyphal tips (gongylidia) that grow in bundles called staphylae, to specifically feed the ants. Here we show extensive regulation and molecular signals of adaptive evolution in gene trancripts associated with gongylidia biosynthesis, morphogenesis and enzymatic plant cell wall degradation in the leaf-cutting ant cultivar Leucoagaricus gongylophorus. Comparative analysis of staphylae growth morphology and transcriptome-wide expressional and nucleotide divergence indicate that gongylidia provide leaf-cutting ants with essential amino acids and plant-degrading enzymes, and that they may have done so for 20–25 million years without much evolutionary change. These molecular traits and signatures of selection imply that staphylae are highly advanced coevolutionary organs that play pivotal roles in the mutualism between leaf-cutting ants and their fungal cultivars. 1 Microbial Ecology Group, Department of Biology, Lund University, Ecology Building, SE-223 62 Lund, Sweden. 2 Centre for Social Evolution, Department of Biology, University of Copenhagen, Universitetsparken 15, DK-2100 Copenhagen, Denmark. w Present Address: Section for Organismal Biology, Department of Plant and Environmental Sciences, University of Copenhagen, Thorvaldsensvej 40, DK-1871 Frederiksberg, Denmark. Correspondence and requests for materials should be addressed to H.H.D.F.L. -
CATALOG of SPECIES
ARSARSARSARSARSARS ARSARS CollectionCollectionef ofof EntomopathogenicEntomopathogenic FungalFungal CulturesCultures CATALOG of SPECIES FULLY INDEXED [INCLUDES 9773 ISOLAtes] USDA-ARS Biological Integrated Pest Management Research Robert W. Holley Center for Agriculture and Health 538 Tower Road Ithaca, New York 14853-2901 28 July 2011 Search the ARSEF catalog online at http://www.ars.usda.gov/Main/docs.htm?docid=12125 ARSEF Collection Staff Richard A. Humber, Curator phone: [+1] 607-255-1276 fax: [+1] 607-255-1132 email: [email protected] Karen S. Hansen phone: [+1] 607-255-1274 fax: [+1] 607-255-1132 email: [email protected] Micheal M. Wheeler phone: [+1] 607-255-1274 fax: [+1] 607-255-1132 email: [email protected] USDA-ARS Biological IPM Research Unit Robert W. Holley Center for Agriculture & Health 538 Tower Road Ithaca, New York 14853-2901, USA IMPORTANT NOTE Recent phylogenetically based reclassifications of fungal pathogens of invertebrates Richard A. Humber Insect Mycologist and Curator, ARSEF UPDATED July 2011 Some seemingly dramatic and comparatively recent changes in the classification of a number of fungi may continue to cause confusion or a degree of discomfort to many of the clients of the cultures and informational resources provided by the ARSEF culture collection. This short treatment is an attempt to summarize some of these changes, the reasons for them, and to provide the essential references to the literature in which the changes are proposed. As the Curator of the ARSEF collection I wish to assure you that these changes are appropriate, progressive, and necessary to modernize and to stabilize the systematics of the fungal pathogens affecting insects and other invertebrates, and I urge you to adopt them into your own thinking, teaching, and publications. -
The Coexistence
Myrmecological News 13 37-55 2009, Online Earlier Natural history and phylogeny of the fungus-farming ants (Hymenoptera: Formicidae: Myrmicinae: Attini) Natasha J. MEHDIABADI & Ted R. SCHULTZ Abstract Ants of the tribe Attini comprise a monophyletic group of approximately 230 described and many more undescribed species that obligately depend on the cultivation of fungus for food. In return, the ants nourish, protect, and disperse their fungal cultivars. Although all members of this tribe cultivate fungi, attine ants are surprisingly heterogeneous with regard to symbiont associations and agricultural system, colony size and social structure, nesting behavior, and mating system. This variation is a key reason that the Attini have become a model system for understanding the evolution of complex symbioses. Here, we review the natural-history traits of fungus-growing ants in the context of a recently published phylo- geny, collating patterns of evolution and symbiotic coadaptation in a variety of colony and fungus-gardening traits in a number of major lineages. We discuss the implications of these patterns and suggest future research directions. Key words: Hymenoptera, Formicidae, fungus-growing ants, leafcutter ants, colony life, natural history, evolution, mating, agriculture, review. Myrmecol. News 13: 37-55 (online xxx 2008) ISSN 1994-4136 (print), ISSN 1997-3500 (online) Received 12 June 2009; revision received 24 September 2009; accepted 28 September 2009 Dr. Natasha J. Mehdiabadi* (contact author) & Dr. Ted R. Schultz* (contact author), Department of Entomology and Laboratories of Analytical Biology, National Museum of Natural History, Smithsonian Institution, P.O. Box 37012, NHB, CE518, MRC 188, Washington, DC 20013-7012, USA. E-mail: [email protected]; [email protected] * Both authors contributed equally to the work. -
Reconstructing the Functions of Endosymbiotic Mollicutes in Fungus
RESEARCH ARTICLE Reconstructing the functions of endosymbiotic Mollicutes in fungus- growing ants Panagiotis Sapountzis*, Mariya Zhukova, Jonathan Z Shik, Morten Schiott, Jacobus J Boomsma* Centre for Social Evolution, Department of Biology, University of Copenhagen, Copenhagen, Denmark Abstract Mollicutes, a widespread class of bacteria associated with animals and plants, were recently identified as abundant abdominal endosymbionts in healthy workers of attine fungus- farming leaf-cutting ants. We obtained draft genomes of the two most common strains harbored by Panamanian fungus-growing ants. Reconstructions of their functional significance showed that they are independently acquired symbionts, most likely to decompose excess arginine consistent with the farmed fungal cultivars providing this nitrogen-rich amino-acid in variable quantities. Across the attine lineages, the relative abundances of the two Mollicutes strains are associated with the substrate types that foraging workers offer to fungus gardens. One of the symbionts is specific to the leaf-cutting ants and has special genomic machinery to catabolize citrate/glucose into acetate, which appears to deliver direct metabolic energy to the ant workers. Unlike other Mollicutes associated with insect hosts, both attine ant strains have complete phage-defense systems, underlining that they are actively maintained as mutualistic symbionts. DOI: https://doi.org/10.7554/eLife.39209.001 *For correspondence: [email protected] (PS); Introduction [email protected] (JJB) Bacterial endosymbionts, defined here as comprising both intra- and extra-cellular symbionts Competing interests: The (Bourtzis and Miller, 2006), occur in all eukaryotic lineages and range from parasites to mutualists authors declare that no (Bourtzis and Miller, 2006; Martin et al., 2017). -
Ecology of a Costa Rican Leaf-Cutting Ant 61
Wetterer et al.: Ecology of a Costa Rican Leaf-cutting Ant 61 FORAGING AND NESTING ECOLOGY OF ACROMYRMEX OCTOSPINOSUS (HYMENOPTERA: FORMICIDAE) IN A COSTA RICAN TROPICAL DRY FOREST JAMES K. WETTERER,1 DANIEL S. GRUNER2 AND JORGÉ E. LOPEZ3 1Center for Environmental Research & Conservation, Columbia University New York, NY 10027 2Department of Zoology, University of Hawaii, Honolulu, HI 96822 3Department of Ecology and Evolution, University of Chicago, Chicago, IL 60637 ABSTRACT Leaf-cutting ants (Acromyrmex sp. and Atta sp.) in Costa Rica show many intra- and interspecific differences in ecology. Recent taxonomic studies question whether the Acromyrmex octospinosus populations on the Pacific and Atlantic slopes of Costa Rica are a single species. We therefore examined the foraging and nesting ecology of A. octospinosus in the tropical dry forest of Palo Verde National Park on the Pacific slope of Costa Rica and compared our findings with published data on the ecology of A. octospinosus in the tropical moist forest of La Selva Biological Station on the At- lantic slope. The Pacific A. octospinosus foraged primarily on the leaves of herbs and other small plants, fallen leaves, fruit, flowers, and insect frass, but does not cut the leaves of large trees. Worker size distribution within colonies was bimodal with only 62 Florida Entomologist 81(1) March, 1998 the larger workers leaving the nest to forage. Nests were shallow and generally under a few centimeters of organic debris at the base of trees and woody shrubs or in crev- ices. The foraging and nesting ecology of the Pacific A. octospinosus appeared to be very similar to that of the Atlantic A. -
Recent Human History Governs Global Ant Invasion Dynamics
ARTICLES PUBLISHED: 22 JUNE 2017 | VOLUME: 1 | ARTICLE NUMBER: 0184 Recent human history governs global ant invasion dynamics Cleo Bertelsmeier1*, Sébastien Ollier2, Andrew Liebhold3 and Laurent Keller1* Human trade and travel are breaking down biogeographic barriers, resulting in shifts in the geographical distribution of organ- isms, yet it remains largely unknown whether different alien species generally follow similar spatiotemporal colonization patterns and how such patterns are driven by trends in global trade. Here, we analyse the global distribution of 241 alien ant species and show that these species comprise four distinct groups that inherently differ in their worldwide distribution from that of native species. The global spread of these four distinct species groups has been greatly, but differentially, influenced by major events in recent human history, in particular historical waves of globalization (approximately 1850–1914 and 1960 to present), world wars and global recessions. Species in these four groups also differ in six important morphological and life- history traits and their degree of invasiveness. Combining spatiotemporal distribution data with life-history trait information provides valuable insight into the processes driving biological invasions and facilitates identification of species most likely to become invasive in the future. hallmark of the Anthropocene is range expansion by alien been introduced outside their native range). For each species, we species around the world1, facilitated by the construction of recorded the number of countries where it had established (spatial transport networks and the globalization of trade and labour richness) and estimated spatial diversity taking into account pair- A 2 16 markets since the beginning of the Industrial Revolution . -
Foraging Ecology of the Desert Leaf-Cutting Ant, Acromyrmex Versicolor, in Arizona (Hymenoptera: Formicidae)
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/256979550 Foraging ecology of the desert leaf-cutting ant, Acromyrmex versicolor, in Arizona (Hymenoptera: Formicidae) Article in Sociobiology · January 2001 CITATIONS READS 13 590 3 authors, including: James K. Wetterer Florida Atlantic University 184 PUBLICATIONS 3,058 CITATIONS SEE PROFILE Some of the authors of this publication are also working on these related projects: Ant stuff View project Systematics and Evolution of the Tapinoma ants (Formicidae: Dolichoderinae) from the Neotropical region View project All content following this page was uploaded by James K. Wetterer on 17 May 2014. The user has requested enhancement of the downloaded file. 1 Foraging Ecology of the Desert Leaf-Cutting Ant, Acromyrmex versicolor, in Arizona (Hymenoptera: Formicidae) by James K. Wetterer1,2, Anna G. Himler1, & Matt M. Yospin1 ABSTRACT The desert would seem to be an inhospitable place for leaf-cutting ants (Acromyrmex spp. and Atta spp.), both because the leaves of desert perennials are notably well-defended, both chemically and physically, and because leaf-cutters grow a fungus that requires constant high humidity. We investigated strategies that leaf-cutters use to survive in arid environments by examining foraging activity, resource use, forager size, load size, and nesting ecology of the desert leaf-cutting ant, Acromyrmex versicolor, at 12 colonies from 6 sites in Arizona during June, August, and November 1997, and March 1998. The ants showed striking seasonal changes in materials harvested, apparently in response to changes in the availability of preferred resources. Acromyrmex versicolor foragers (n = 800) most commonly collected dry vegetation (54.3% of all loads), but also harvested ephem- eral resources, such as dry flowers (18.6%), fresh young leaves (18.5%), fruits and seeds (4.0%), and fresh flowers (3.5%), when seasonally available. -
Multiple Paternity, Relatedness and Genetic Diversity in Acromyrmex Leaf-Cutter Ants
Multiple paternity, relatedness and genetic diversity in Acromyrmex leaf-cutter ants Jacobus J. Boomsma, Else J. Fjerdingstad{ and Jane Frydenberg Department of Ecology and Genetics, University of Aarhus, 8000 Aarhus C, Denmark ([email protected]) Multiple queen-mating occurs in many social insects, but high degrees of multiple paternity have only been found in honeybees and some yellowjacket wasps. Here we report the ¢rst case of an ant species where multiple mating reduces relatedness among female o¡spring to values signi¢cantly lower than 0.5. Genetic analysis of a Panamanian population of the leaf-cutter ant Acromyrmex octospinosus showed that queens mate with at least 4^10 males. The detected (minimum) genetically e¡ective paternity of nestmate females was 3.9 and estimates of mean relatedness among nestmate females were ca. 0.33. This implies that multiple queen-mating in Acromyrmex octospinosus reduces relatedness to 44% of the value in full-sib colonies (0.75), realizing 84% of the maximum reduction (to 0.25) that would be obtained with an in¢nite number of matings. Queens of Panamanian Acromyrmex octospinosus mate with more males than sympatric queens of Atta colombica, which is contrary to the positive relationship between queen-mating frequency and colony size found across more distantly related ant species. Possible selective forces that maintain high queen-mating frequencies in leaf-cutter ants are discussed. Keywords: Acromyrmex; leaf-cutter ants; multiple mating; paternity; relatedness; social evolution been documented for leaf-cutter ants: ca. three fathers per 1. INTRODUCTION colony in Acromyrmex versicolor (Reichardt & Wheeler The evolution and maintenance of multiple queen-mating 1996), 1^5 fathers per colony in Atta colombica (Fjerding- in the eusocial Hymenoptera (ants, some bees and some stad et al. -
Trophallaxis: 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 (Hymeno ptera: 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.