Worker Ants: You Could Have Been Queens
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Model Organisms
RESEARCH HIGHLIGHTS Nature Reviews Genetics | Published online 30 Aug 2017; doi:10.1038/nrg.2017.70 P. Morgan/Macmillan Publishers Limited Morgan/Macmillan P. its caste-specific RNA expression is conserved in other insect species with different social systems. In ants undergoing the worker–gamergate transition, high corazonin peptide levels promoted worker-specific behaviour and inhibited behaviours associated with progression to the MODEL ORGANISMS gamergate caste; as expected, short interfering RNA (siRNA) knockdown of the corazonin receptor (CrzR) gene New tools, new insights — had the opposite phenotypic effect. The researchers went on to identify the vitellogenin gene as a key regula- probing social behaviour in ants tory target of corazonin; its expres- sion is consistently downregulated Eusocial insects display complex strategy of Harpegnathos saltator to in response to increased corazonin social behaviours, but the underlying increase the number of reproducing levels, suggesting that corazonin and Until now, molecular mechanisms are largely ants to enable them to establish orco vitellogenin have opposing effects functional unknown. Now, a trio of papers in mutant lines. In the absence of a on caste identity. Consistent with genetic studies Cell decribe two genes (orco and queen, non-reproductive H. saltator this hypothesis, siRNA knockdown corazonin) that control social behav- workers can become ‘gamergates’, of vitellogenin gene expression pro- have not been iour in ants. Furthermore, two of which lay fertilized eggs. This caste moted worker-specific behaviours. possible in the studies describe the first mutant transition can be replicated in the lab Based on these observations, the ants lines in ants, which were generated by simply by isolating workers. -
Genetic Mechanisms Underlying the Evolutionary Success of Eusocial Insects
insects Review (Epi)Genetic Mechanisms Underlying the Evolutionary Success of Eusocial Insects Kayli R. Sieber 1 , Taylor Dorman 1, Nicholas Newell 1 and Hua Yan 1,2,* 1 Department of Biology, University of Florida, Gainesville, FL 32611, USA; kayli.sieber@ufl.edu (K.R.S.); taylor.dorman@ufl.edu (T.D.); nicholas.newell@ufl.edu (N.N.) 2 Center for Smell and Taste, University of Florida, Gainesville, FL 32611, USA * Correspondence: hua.yan@ufl.edu; Tel.: +1-352-273-4983 Simple Summary: Social insects, namely ants, bees, and termites, are among the most numerous and successful animals on Earth. This is due to a variety of features: highly cooperative behavior performed by colony members and their specialization on a variety of tasks. Diverse physiological and behavioral specializations are regulated not only by the genetic system, but also by the epige- netic system which alters gene expressions without modifying the genetic code. This review will summarize recent advancements in such studies in eusocial insects. Abstract: Eusocial insects, such as bees, ants, and wasps of the Hymenoptera and termites of the Blattodea, are able to generate remarkable diversity in morphology and behavior despite being genetically uniform within a colony. Most eusocial insect species display caste structures in which reproductive ability is possessed by a single or a few queens while all other colony members act Citation: Sieber, K.R.; Dorman, T.; as workers. However, in some species, caste structure is somewhat plastic, and individuals may Newell, N.; Yan, H. (Epi)Genetic switch from one caste or behavioral phenotype to another in response to certain environmental cues. -
Convergent Evolution of the Army Ant Syndrome and Congruence in Big-Data Phylogenetics
Copyedited by: YS MANUSCRIPT CATEGORY: Systematic Biology Syst. Biol. 68(4):642–656, 2019 © The Author(s) 2019. Published by Oxford University Press, on behalf of the Society of Systematic Biologists. All rights reserved. For permissions, please email: [email protected] DOI:10.1093/sysbio/syy088 Advance Access publication January 3, 2019 Convergent Evolution of the Army Ant Syndrome and Congruence in Big-Data Phylogenetics , , ,∗ MAREK L. BOROWIEC1 2 3 1Department of Entomology, Plant Pathology and Nematology, 875 Perimeter Drive, University of Idaho, Moscow, ID 83844, USA; 2School of Life Sciences, Social Insect Research Group, Arizona State University, Tempe, AZ 85287, USA; and 3Department of Entomology and Nematology, One Shields Avenue, University of California at Davis, Davis, CA 95616, USA ∗ Correspondence to be sent to: Department of Entomology, Plant Pathology and Nematology, 875 Perimeter Drive, University of Idaho, Moscow, ID 83844, USA; Downloaded from https://academic.oup.com/sysbio/article-abstract/68/4/642/5272507 by Arizona State University West 2 user on 24 July 2019 E-mail: [email protected]. Received 24 May 2018; reviews returned 9 November 2018; accepted 15 December 2018 Associate Editor: Brian Wiegmann Abstract.—Army ants are a charismatic group of organisms characterized by a suite of morphological and behavioral adaptations that includes obligate collective foraging, frequent colony relocation, and highly specialized wingless queens. This army ant syndrome underlies the ecological success of army ants and its evolution has been the subject of considerable debate. It has been argued to have arisen once or multiple times within the ant subfamily Dorylinae. To address this question in a phylogenetic framework I generated data from 2166 loci and a comprehensive taxon sampling representing all 27 genera and 155 or approximately 22% of doryline species. -
Mechanisms for the Evolution of Superorganismality in Ants
Rockefeller University Digital Commons @ RU Student Theses and Dissertations 2021 Mechanisms for the Evolution of Superorganismality in Ants Vikram Chandra Follow this and additional works at: https://digitalcommons.rockefeller.edu/ student_theses_and_dissertations Part of the Life Sciences Commons MECHANISMS FOR THE EVOLUTION OF SUPERORGANISMALITY IN ANTS A Thesis Presented to the Faculty of The Rockefeller University in Partial Fulfillment of the Requirements for the degree of Doctor of Philosophy by Vikram Chandra June 2021 © Copyright by Vikram Chandra 2021 MECHANISMS FOR THE EVOLUTION OF SUPERORGANISMALITY IN ANTS Vikram Chandra, Ph.D. The Rockefeller University 2021 Ant colonies appear to behave as superorganisms; they exhibit very high levels of within-colony cooperation, and very low levels of within-colony conflict. The evolution of such superorganismality has occurred multiple times across the animal phylogeny, and indeed, origins of multicellularity represent the same evolutionary process. Understanding the origin and elaboration of superorganismality is a major focus of research in evolutionary biology. Although much is known about the ultimate factors that permit the evolution and persistence of superorganisms, we know relatively little about how they evolve. One limiting factor to the study of superorganismality is the difficulty of conducting manipulative experiments in social insect colonies. Recent work on establishing the clonal raider ant, Ooceraea biroi, as a tractable laboratory model, has helped alleviate this difficulty. In this dissertation, I study the proximate evolution of superorganismality in ants. Using focussed mechanistic experiments in O. biroi, in combination with comparative work from other ant species, I study three major aspects of ant social behaviour that provide insight into the origin, maintenance, and elaboration of superorganismality. -
The Adaptive Significance of Phasic Colony Cycles in Army Ants
bioRxiv preprint doi: https://doi.org/10.1101/091934; this version posted December 6, 2016. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 The adaptive significance of phasic colony cycles in army ants 2 3 Simon Garnier1 & Daniel J. C. Kronauer2 4 5 1Department of Biological Sciences, New Jersey Institute of Technology, Newark, NJ 07102, USA; 6 [email protected] 7 2Laboratory of Social Evolution and Behavior, The Rockefeller University, New York, NY 10065, USA; 8 [email protected] 9 10 Keywords: Dorylinae; Evolution; Foraging; Formicidae; Group predation; Modelling; Nomadism; 11 Reproductive cycle 12 1 bioRxiv preprint doi: https://doi.org/10.1101/091934; this version posted December 6, 2016. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 13 Abstract: 14 Army ants are top arthropod predators in tropical forests around the world. The colonies of many army 15 ant species undergo stereotypical behavioral and reproductive cycles, alternating between brood care 16 and reproductive phases. In the brood care phase, colonies contain a cohort of larvae that are 17 synchronized in their development and have to be fed. In the reproductive phase larvae are absent and 18 oviposition takes place. Despite these colony cycles being a striking feature of army ant biology, their 19 adaptive significance is unclear. -
Genomic and Brain Expansion Provide Ants with Refined Sense of Smell
COMMENTARY Genomic and brain expansion provide ants with refined sense of smell COMMENTARY Patrizia d’Ettorrea,1 Chemical communication is the most ancient way of and individuals belonging to the worker caste are typ- information transfer among organisms, and chemical ically not able to disperse and found their own colonies senses, although universal, are particularly developed (5). To maintain and optimize such extreme division of in social species. Many animals use odors in circum- labor among society members, an efficient transfer of stances that are critical for survival and reproduction: information is of critical importance. This is usually to detect suitable food sources and nest sites, to avoid achieved in ants and other social animals by means of predators, and to find mates. Social animals use chemical messengers. chemical communication also to regulate interactions Pheromones are chemical signals transmitted be- within a social group and to distinguish group members tween individuals of the same species that produce a from strangers. Chemical communication is exquisitely behavioral and/or physiological response in the re- developed and multifaceted in some insects, usually ceiver (6). They can be single molecules or a precise described with the idiosyncratic term of “eusocial” in- combination of molecules, and they represent spe- sects (from Greek eu- meaning “well” or “good”). These cies-wide signals, which do not require learning be- include all known species of ants and termites, and cause the response is typically hardwired (7). Many some bees and wasps, and represent the most ad- pheromones are volatile, such as alarm pheromones vanced and evolutionarily successful social organisms. -
Genomic and Brain Expansion Provide Ants with Refined Sense of Smell
COMMENTARY Genomic and brain expansion provide ants with refined sense of smell COMMENTARY Patrizia d’Ettorrea,1 Chemical communication is the most ancient way of and individuals belonging to the worker caste are typ- information transfer among organisms, and chemical ically not able to disperse and found their own colonies senses, although universal, are particularly developed (5). To maintain and optimize such extreme division of in social species. Many animals use odors in circum- labor among society members, an efficient transfer of stances that are critical for survival and reproduction: information is of critical importance. This is usually to detect suitable food sources and nest sites, to avoid achieved in ants and other social animals by means of predators, and to find mates. Social animals use chemical messengers. chemical communication also to regulate interactions Pheromones are chemical signals transmitted be- within a social group and to distinguish group members tween individuals of the same species that produce a from strangers. Chemical communication is exquisitely behavioral and/or physiological response in the re- developed and multifaceted in some insects, usually ceiver (6). They can be single molecules or a precise described with the idiosyncratic term of “eusocial” in- combination of molecules, and they represent spe- sects (from Greek eu- meaning “well” or “good”). These cies-wide signals, which do not require learning be- include all known species of ants and termites, and cause the response is typically hardwired (7). Many some bees and wasps, and represent the most ad- pheromones are volatile, such as alarm pheromones vanced and evolutionarily successful social organisms. -
Colony Expansions Underlie the Evolution of Army Ant Mass Raiding
Colony expansions underlie the evolution of army ant mass raiding Vikram Chandraa,1,2, Asaf Gala,1, and Daniel J. C. Kronauera,1 aLaboratory of Social Evolution and Behavior, The Rockefeller University, New York, NY 10065 Edited by Joan E. Strassmann, Washington University in St. Louis, St. Louis, MO, and approved April 8, 2021 (received for review January 7, 2021) The mass raids of army ants are an iconic collective phenomenon, in much smaller colonies of only hundreds of workers. They are which many thousands of ants spontaneously leave their nest to hunt rarely encountered in the field, and little is known about their for food, mostly other arthropods. While the structure and ecology of behavior. Sporadic and usually partial observations suggest that these raids have been relatively well studied, how army ants evolved many non-army ant dorylines display a different form of foraging such complex cooperative behavior is not understood. Here, we show called group raiding (SI Appendix, Supplementary Note 1 and that army ant mass raiding has evolved from a different form of Table S1), in which scouts find prey before recruiting a raiding cooperative hunting called group raiding, in which a scout directs a party from the nest (4, 11). W. M. Wheeler, who first observed small group of ants to a specific target through chemical communi- these group raids in 1918, noted similarities in diet and foraging cation. We describe the structure of group raids in the clonal raider behavior with army ants and suggested that this had evolutionary ant, a close relative of army ants in the subfamily Dorylinae. -
Complex Outcomes…
HARVARD UNIVERSITY Waring “Buck” Trible Faculty of Arts and Sciences [email protected] Trible Lab, Division of Science 52 Oxford Street NW 369.20 Z John Harvard Distinguished Science Fellow Cambridge, MA 02138 The Trible Lab at Harvard University is looking to hire a postdoctoral researcher with expertise in collecting and analyzing functional genomic data. The successful candidate will seek to understand molecular mechanisms of ant biology and evolution using emerging technologies including genome editing, long read sequencing, single cell genomics, and chromatin binding and architecture measurements. The position will start as soon as March 1, 2020 and no later than September 1, 2020. The position is initially for 2 years and may be extended up to 4 years total. Potential candidates are encouraged to contact me, Buck Trible ([email protected]), with a cover letter, a CV including contact information for 3 references, and the link to your Google Scholar page. Background A colony of ants cannot be accurately described as a collection of single individuals. Instead, it is a superorganism in which each ant depends on and contributes to the function of the group. An ant colony is therefore analogous to a unitary organism, like a plant or animal, whose cells cooperate to form a larger whole. Like cells, group behavior in ants is orchestrated by continuous communication between individuals, which is largely achieved via a wide range of pheromones. Also similar to cells, the ants in a colony typically differentiate into a germ line (the reproductive queen caste) and a soma (the non-reproductive worker caste(s)) via phenotypic plasticity. -
Draft Aphaenogaster Genomes Expand Our View of Ant
bioRxiv preprint doi: https://doi.org/10.1101/302679; this version posted September 4, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Draft Aphaenogaster genomes expand our 2 view of ant genome size variation across 3 climate gradients 1 1 2,3 4,5 4 Matthew K. Lau , Aaron M. Ellison , Andrew D. Nguyen , Clint Penick , 6 2 7 5 Bernice DeMarco , Nicholas J. Gotelli , Nathan J. Sanders , Robert R. 4 2 6 Dunn , and Sara Helms Cahan 1 7 Harvard Forest, Harvard University, Petersham, MA, USA 2 8 Department of Biology, University of Vermont, Burlington, VT, USA 3 9 Department of Entomology and Nematology, University of Florida, Gainesville, FL, 10 USA 4 11 Department of Applied Ecology, North Carolina State University, Raleigh, NC, USA 5 12 The Biomimicry Center, Arizona State University, Tempe, AZ, USA 6 13 Smithsonian Institution, Washington, DC, USA 7 14 Environmental Program, Rubenstein School of Environment and Natural Resources, 15 University of Vermont, Burlington, VT, USA 16 Corresponding author: 17 Matthew K. Lau 18 Email address: [email protected] 19 ABSTRACT 20 Given the abundance, broad distribution, and diversity of roles that ants play in many ecosystems, they are 21 an ideal group to serve as ecosystem indicators of climatic change. At present, only a few whole-genome 22 sequences of ants are available (19 of > 16,000 species), mostly from tropical and sub-tropical species. -
The Gene Expression Network Regulating Queen Brain Remodeling After Insemination and Its Parallel Use in Ants with Reproductive Workers
The gene expression network regulating queen brain remodeling after insemination and its parallel use in ants with reproductive workers Nagel, Manuel; Qiu, Bitao; Brandenborg, Lisa Eigil; Larsen, Rasmus Stenbak; Ning, Dongdong; Boomsma, Jacobus Jan; Zhang, Guojie Published in: Science Advances DOI: 10.1126/sciadv.aaz5772 Publication date: 2020 Document version Publisher's PDF, also known as Version of record Document license: CC BY-NC Citation for published version (APA): Nagel, M., Qiu, B., Brandenborg, L. E., Larsen, R. S., Ning, D., Boomsma, J. J., & Zhang, G. (2020). The gene expression network regulating queen brain remodeling after insemination and its parallel use in ants with reproductive workers. Science Advances, 6(38), [eaaz5772]. https://doi.org/10.1126/sciadv.aaz5772 Download date: 26. sep.. 2021 SCIENCE ADVANCES | RESEARCH ARTICLE EVOLUTIONARY BIOLOGY Copyright © 2020 The Authors, some rights reserved; The gene expression network regulating queen brain exclusive licensee American Association remodeling after insemination and its parallel use for the Advancement of Science. No claim to in ants with reproductive workers original U.S. Government Manuel Nagel1*, Bitao Qiu1,2*, Lisa Eigil Brandenborg1, Rasmus Stenbak Larsen1, Works. Distributed 3 1,2 1,3,4,5† under a Creative Dongdong Ning , Jacobus Jan Boomsma , Guojie Zhang Commons Attribution NonCommercial Caste differentiation happens early in development to produce gynes as future colony germlines and workers as License 4.0 (CC BY-NC). present colony soma. However, gynes need insemination to become functional queens, a transition that initiates reproductive role differentiation relative to unmated gynes. Here, we analyze the anatomy and transcriptomes of brains during this differentiation process within the reproductive caste of Monomorium pharaonis. -
Implications of Orco on Olfaction, Neural Development, and Social Behavior in Ants: a Review of the Literature
Implications of orco on olfaction, neural development, and social behavior in ants: A review of the literature Item Type text; Electronic Thesis Authors Agosttini, Joseph Anthony Publisher The University of Arizona. Rights Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. Download date 26/09/2021 19:00:24 Item License http://rightsstatements.org/vocab/InC/1.0/ Link to Item http://hdl.handle.net/10150/626733 IMPLICATIONS OF ORCO ON OLFACTION, NEURAL DEVELOPMENT, AND SOCIAL BEHAVIOR IN ANTS: A REVIEW OF THE LITERATURE By JOSEPH ANTHONY AGOSTTINI ____________________ A Thesis Submitted to The Honors College In Partial Fulfillment of the Bachelors degree With Honors in Neuroscience & Cognitive Science THE UNIVERSITY OF ARIZONA D E C E M B E R 2 0 1 7 Approved by: ____________________________ Dr. Wulfila Gronenberg Department of Neuroscience Abstract Olfaction is one of the most essential sensory modalities amongst insects. Not only is this behaviorally observed, but it is also anatomically evidenced. A range of social behaviors, including communication, foraging, and reproduction to name a few, immensely rely upon chemosensation. However, studies examining the genetics and neuroethology underlying this sociality in eusocial species, such as bees and ants, have been scarce, thus limiting our understanding of the molecular mechanisms needed for these species to thrive. This review examined the current literature on the orco-encoding gene and the effects that its mutagenesis had on ant olfaction, neural development, and behavior, specifically on Harpegnathos saltator and Ooceraea biroi ants.