Patterns and Drivers of Ant Biodiversity Along Urbanization Gradients

Total Page:16

File Type:pdf, Size:1020Kb

Patterns and Drivers of Ant Biodiversity Along Urbanization Gradients PATTERNS AND DRIVERS OF ANT BIODIVERSITY ALONG URBANIZATION GRADIENTS by JAIME ABRAHAM PEREZ Submitted in partial fulfillment of requirements For the degree of Doctor of Philosophy Advisor: Dr. Sarah E. Diamond Department of Biology CASE WESTERN RESERVE UNIVERSITY CASE WESTERN RESERVE UNIVERSITY SCHOOL OF GRADUATE STUDIES We hereby approve the thesis/dissertation of Jaime A. Perez candidate for the Doctor of Philosophy degree. Committee Chair: Karen Abbott Committee Member: Sarah Diamond Committee Member: Jean Burns Committee Member: Michael Benard Committee Member: Andrew Suarez Date of Defense: April 28th, 2020 ii DEDICATION To Terry McGlynn - without you, none of this would have been possible. Thank you for believing in me and introducing me to the little things that run the world iii TABLE OF CONTENTS List of Tables ............................................................................................................vii List of Figures ...........................................................................................................viii Acknowledgements ..................................................................................................ix Abstract .....................................................................................................................1 Chapter 1: Introduction ..........................................................................................3 Chapter 2: Idiosyncrasies in cities: evaluating patterns and drivers of ant biodiversity along urbanization gradients .............................................................7 Abstract ......................................................................................................................7 Introduction ................................................................................................................8 Materials and Methods:..............................................................................................10 Study area and sampling design .............................................................................10 Ant species assemblages and diversity ...................................................................13 Statistical analyses: .................................................................................................14 Characterizing biodiversity patterns across urbanization gradients.....................14 Evaluating the mechanisms of urban biodiversity patterns .................................16 Results and Discussion: ............................................................................................17 Positive, but mixed support for the maintenance of urban biodiversity in ants ......18 Non-native species introductions can contribute positively to species diversity, but do not entirely explain the maintenance of urban biodiversity .........................19 No indication of differential phenologies in communities along urbanization gradients ..................................................................................................................21 Study limitations and future directions ...................................................................23 Tables .........................................................................................................................25 Figures........................................................................................................................28 Supplementary Tables ................................................................................................33 iv Supplementary Figures ..............................................................................................43 Chapter 3: Urbanization shifts ant communities towards thermophilic species across multiple cities ............................................................................................................46 Abstract ......................................................................................................................46 Introduction ................................................................................................................46 Materials and Methods:..............................................................................................49 Study area and sampling design ..............................................................................49 Trait assignments: ...................................................................................................51 Estimating species geographic range location .....................................................51 Quantifying species mean heat tolerance and aridity tolerance ...........................52 Statistical Analyses: ................................................................................................53 The effect of urbanization on species geographic range location ........................53 The effect of urbanization on species tolerance traits ..........................................54 Results: .......................................................................................................................55 Urbanization consistently favors ant species from southerly and westerly distributions.............................................................................................................55 Urbanization consistently favors thermophilic species ...........................................55 Discussion: .................................................................................................................56 Implications and future directions ..........................................................................59 Tables ........................................................................................................................62 Figures........................................................................................................................64 Supplementary Table ................................................................................................68 Chapter 4: Urbanization dampens the latitude-diversity cline in ants ...............69 Abstract ......................................................................................................................69 Introduction ................................................................................................................69 Materials and Methods:..............................................................................................72 v Developing the ant species richness and community composition database ..........72 Controlling for intercity variation in the degree of urbanization ............................74 Statistical analyses: .................................................................................................74 The effect of urbanization on the latitude-diversity cline ....................................74 The effect of urbanization on community composition .......................................77 Results: .......................................................................................................................79 Urbanization dampens the latitude-diversity cline in ants ......................................77 Urban community composition is similar to nonurban at high latitude, but very divergent at low latitude..........................................................................................79 Discussion ..................................................................................................................79 Tables .........................................................................................................................85 Figures........................................................................................................................88 Supplementary Table .................................................................................................93 Supplementary Figure ................................................................................................101 Chapter 5: Conclusions: ..........................................................................................102 Future directions .....................................................................................................102 Figure ......................................................................................................................105 Bibliography: ............................................................................................................106 vi LIST OF TABLES Chapter 2: Table 2.1: ...............................................................................................................25 Table 2.2 .................................................................................................................26 Table 2.3 .................................................................................................................27 Table S2.1...............................................................................................................33 Table S2.2...............................................................................................................35 Table S2.3...............................................................................................................36 Table S2.4...............................................................................................................37 Table S2.5...............................................................................................................39
Recommended publications
  • Trofička Niša Mirmekofagnog Predatora Tijekom Ontogenetičkog Razvoja
    Trofička niša mirmekofagnog predatora tijekom ontogenetičkog razvoja Gajski, Domagoj Master's thesis / Diplomski rad 2019 Degree Grantor / Ustanova koja je dodijelila akademski / stručni stupanj: University of Zagreb, Faculty of Science / Sveučilište u Zagrebu, Prirodoslovno-matematički fakultet Permanent link / Trajna poveznica: https://urn.nsk.hr/urn:nbn:hr:217:211948 Rights / Prava: In copyright Download date / Datum preuzimanja: 2021-09-26 Repository / Repozitorij: Repository of Faculty of Science - University of Zagreb University of Zagreb Faculty of Science Department of Biology Domagoj Gajski Trophic niche of an ant-eating predator during its ontogenetic development Graduation Thesis Zagreb, 2019. This thesis was made during an internship at the Masaryk University (Brno, Czech Republic) under the supervision of Prof. Mgr. Stanislav Pekár, Ph.D. and Assoc. Prof. Dr. sc. Damjan Franjević from University of Zagreb, and submitted for evaluation to the Department of Biology, Faculty of Science, University of Zagreb in order to acquire the title Master of molecular biology. I would first like to thank my thesis advisors Prof. dr. mgr. Stanislav Pekar and dr. mgr. Lenka Petrakova of the arachnological lab at the Masaryk University. The door to their offices was always open whenever I ran into questions about my research or writing. They consistently allowed this paper to be my own work but steered me in the right direction whenever they thought I needed it. I would like to thank all the co-workers at the arachnological lab, that made each day of work more interesting by losing their spiders in the lab. They somehow always landed on my work desk.
    [Show full text]
  • Range Expansion in an Introduced Social Parasite-Host Species Pair Abstract Keywords
    1 Range expansion in an introduced social parasite-host species pair 2 Jackson A. Helms IV1*, Selassie E. Ijelu2, Nick M. Haddad1 3 1 Kellogg Biological Station, Department of Integrative Biology, Michigan State University, 3700 E Gull 4 Lake Dr, Hickory Corners, MI 49060, USA 5 2 University of Saint Francis, 2701 Spring St, Fort Wayne, IN 46808, USA 6 * Corresponding author: orcid.org/0000-0001-6709-6770, [email protected] 7 Abstract 8 Dispersal in social parasites is constrained by the presence of suitable host populations, limiting 9 opportunities for rapid range expansion. For this reason, although hundreds of ant species have 10 expanded their ranges through human transport, few obligate social parasites have done so. We 11 test the hypothesis that social parasites expand their ranges more slowly than their hosts by 12 examining the spread of an introduced social parasite-host species pair in North America—the 13 workerless ant Tetramorium atratulum and the pavement ant T. immigrans. In doing so we 14 report a new range extension of T. atratulum in the interior US. Consistent with host limitation 15 on dispersal, we found a time lag ranging from several years to over a century between the 16 arrivals of the host and parasite to a new region. The estimated maximum rate of range 17 expansion in the parasite was only a third as fast as that of the host. We suggest that relative to 18 free-living social insects, social parasites may be less able to rapidly shift their ranges in 19 response to changes in habitat or climate.
    [Show full text]
  • 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.
    [Show full text]
  • A Review of the Ant Genera Leptothorax Mayr and Temnothorax Mayr (Hymenoptera, Formicidae) of the Eastern Palaearctic
    Acta Zoologica Academiae Scientiarum Hungaricae 50 (2), pp. 109–137, 2004 A REVIEW OF THE ANT GENERA LEPTOTHORAX MAYR AND TEMNOTHORAX MAYR (HYMENOPTERA, FORMICIDAE) OF THE EASTERN PALAEARCTIC A. RADCHENKO Museum and Institute of Zoology, Polish Academy of Sciences 64, Wilcza str., 00–679, Warsaw, Poland; E-mail: [email protected] Nineteen species of the genera Leptothorax and Temnothorax are distributed from Mongolia to the Pacific Ocean, these are revised and a key to their identification is provided. Four new species, Temnothorax cuneinodis, T. xanthos, T. pisarskii and T. michali are described from North Korea. L. galeatus WHEELER is synonymised with T. nassonovi (RUZSKY) and L. wui WHEELER is raised to species rank (in the genus Temnothorax). Key words: ants, Leptothorax, Temnothorax, taxonomy, new species, key, East Palaearctic INTRODUCTION The genus Leptothorax was described by MAYR in 1855, and a few years later he described the closely related genus Temnothorax (MAYR, 1861). For many years, the latter was regarded by different authors either as a good genus or as a subgenus of Leptothorax, but during the last decade it was considered to be a junior synonym of Leptothorax (BOLTON, 1995). BINGHAM (1903) designated Formica acervorum FABRICIUS, 1793 as the type-species of the genus Leptothorax. About the same time RUZSKY (1904) de- scribed the genus Mychothorax, to which F. acervorum was also assigned as type species (by original designation); later Mychothorax was considered as a subgenus of Leptothorax, insomuch that EMERY (1912, 1921) designated Myrmica clypeata MAYR, 1853 as the type species of Leptothorax. All subsequent authors placed the species with 11-jointed antennae in the subgenus Mychothorax and those with 12-jointed antennae in the subgenus Leptothorax s.
    [Show full text]
  • Taxonomic Studies on Ant Genus Hypoponera (Hymenoptera: Formicidae: Ponerinae) from India
    ASIAN MYRMECOLOGY Volume 7, 37 – 51, 2015 ISSN 1985-1944 © HIMENDER BHARTI, SHAHID ALI AKBAR, AIJAZ AHMAD WACHKOO AND JOGINDER SINGH Taxonomic studies on ant genus Hypoponera (Hymenoptera: Formicidae: Ponerinae) from India HIMENDER BHARTI*, SHAHID ALI AKBAR, AIJAZ AHMAD WACHKOO AND JOGINDER SINGH Department of Zoology and Environmental Sciences, Punjabi University, Patiala – 147002, India *Corresponding author's e-mail: [email protected] ABSTRACT. The Indian species of the ant genus Hypoponera Santschi, 1938 are treated herewith. Eight species are recognized of which three are described as new and two infraspecific taxa are raised to species level. The eight Indian species are: H. aitkenii (Forel, 1900) stat. nov., H. assmuthi (Forel, 1905), H. confinis (Roger, 1860), H. kashmirensis sp. nov., H. shattucki sp. nov., H. ragusai (Emery, 1894), H. schmidti sp. nov. and H. wroughtonii (Forel, 1900) stat. nov. An identification key based on the worker caste of Indian species is provided. Keywords: New species, ants, Formicidae, Ponerinae, Hypoponera, India. INTRODUCTION genus with use of new taxonomic characters facilitating prompt identification. The taxonomy of Hypoponera has been in a From India, three species and two state of confusion and uncertainty for some infraspecific taxa ofHypoponera have been reported time. The small size of the ants, coupled with the to date (Bharti, 2011): Hypoponera assmuthi morphological monotony has led to the neglect (Forel, 1905), Hypoponera confinis (Roger, of this genus. The only noteworthy revisionary 1860), Hypoponera confinis aitkenii (Forel, 1900), work is that of Bolton and Fisher (2011) for Hypoponera confinis wroughtonii (Forel, 1900) and the Afrotropical and West Palearctic regions. Hypoponera ragusai (Emery, 1894).
    [Show full text]
  • A Survey of Ground-Dwelling Ants (Hymenoptera: Formicidae) in Georgia
    Ipser et al.: Ground-Dwelling Ants in Georgia 253 A SURVEY OF GROUND-DWELLING ANTS (HYMENOPTERA: FORMICIDAE) IN GEORGIA REID M. IPSER, MARK A. BRINKMAN, WAYNE A. GARDNER AND HAROLD B. PEELER Department of Entomology, University of Georgia, College of Agricultural and Environmental Sciences Griffin Campus, 1109 Experiment Street, Griffin, GA 30223-1797, USA ABSTRACT Ground-dwelling ants (Hymenoptera: Formicidae) were sampled at 29 sites in 26 counties in Georgia with pitfall traps, leaf litter extraction, visual searching, and bait stations. We found 96 ant taxa including nine species not previously reported from Georgia: Myrmica ameri- cana Weber, M. pinetorum Wheeler, M. punctiventris Roger, M. spatulata Smith, Pyramica wrayi (Brown), Stenamma brevicorne (Mayr), S. diecki Emery, S. impar Forel, and S. schmitti Wheeler, as well as three apparently undescribed species (Myrmica sp. and two Ste- namma spp.). Combined with previous published records and museum records, we increased the total number of ground-dwelling ants known from Georgia to 144 taxa. Key Words: ground-dwelling ants, Formicidae, survey, Georgia, species. RESUMEN Hormigas que habitan en el suelo (Hymenoptera: Formicidae) fueron recolectadas en 29 si- tios en 26 condados del estado de Georgia con trampas de suelo, extración de hojarasca, bus- queda visual, y trampas de cebo. Nosotros encontramos 96 taxa de hormigas incluyendo nueve especies no informadas anteriormente en Georgia: Myrmica americana Weber, M. pin- etorum Wheeler, M. punctiventris Roger, M. spatulata Smith, Pyramica wrayi (Brown), Ste- namma brevicorne (Mayr), S. diecki Emery, S. impar Forel, y S. schmitti Wheeler, además de tres especies aparentemente no descritas (Myrmica sp. y dos Stenamma spp.).
    [Show full text]
  • Pavement Ants (Tetramorium Immigrans Santschi) Ryan S
    Published by Utah State University Extension and Utah Plant Pest Diagnostic Laboratory ENT-219-20 June 2020 Pavement Ants (Tetramorium immigrans Santschi) Ryan S. Davis, Arthropod Diagnostician • Lori Spears, Cooperative Agricultural Pest Survey Coordinator • Austin Taylor, Entomology Assistant Quick Facts • Pavement ants are the most common pest ant in and around structures in Utah. • Worker pavement ants are all the same size and have only one queen. • Pavement ants feed on many foods, but prefer sweet and greasy foods. • Occasionally, pavement ants will injure plants. • Indoor problems with pavement ants are worst in spring and early summer. • Indoors, manage pavement ants using baits coupled with habitat modification, cleaning, Fig. 1. (left) Swarm of pavement ant workers in spring (Ryan proper food storage, and exclusion. Davis, Utah State University). Fig. 2. (right) Two workers fighting • Outside, use habitat modification, exclusion, (Ryan Davis, Utah State University). bait, and residual/nonresidual insecticides to manage pavement ants. or structure. They are attracted indoors by food, garbage and moisture, or swarm indoors when they nest in or near foundation cracks or voids. Pavement ants can also be abundant in gardens, and occasionally injure plants. They INTRODUCTION are found throughout the U.S. from the West Coast to the Pavement ants (Formicidae, Tetramorium immigrans) are Northeast. northern Utah’s most common pest ant in and around homes and structures. Until recently, the pavement IDENTIFICATION ant’s scientific name was Tetramorium caespitum, but recent genetic work has clarified that our common pest Pavement ants are most commonly recognized by their Tetramorium species in the U.S. is from Europe and has habit of gathering in large groups near cracks in the been given the name T.
    [Show full text]
  • Radiation in Socially Parasitic Formicoxenine Ants
    RADIATION IN SOCIALLY PARASITIC FORMICOXENINE ANTS DISSERTATION ZUR ERLANGUNG DES DOKTORGRADES DER NATURWISSENSCHAFTEN (D R. R ER . N AT .) DER NATURWISSENSCHAFTLICHEN FAKULTÄT III – BIOLOGIE UND VORKLINISCHE MEDIZIN DER UNIVERSITÄT REGENSBURG vorgelegt von Jeanette Beibl aus Landshut 04/2007 General Introduction II Promotionsgesuch eingereicht am: 19.04.2007 Die Arbeit wurde angeleitet von: Prof. Dr. J. Heinze Prüfungsausschuss: Vorsitzender: Prof. Dr. S. Schneuwly 1. Prüfer: Prof. Dr. J. Heinze 2. Prüfer: Prof. Dr. S. Foitzik 3. Prüfer: Prof. Dr. P. Poschlod General Introduction I TABLE OF CONTENTS GENERAL INTRODUCTION 1 CHAPTER 1: Six origins of slavery in formicoxenine ants 13 Introduction 15 Material and Methods 17 Results 20 Discussion 23 CHAPTER 2: Phylogeny and phylogeography of the Mediterranean species of the parasitic ant genus Chalepoxenus and its Temnothorax hosts 27 Introduction 29 Material and Methods 31 Results 36 Discussion 43 CHAPTER 3: Phylogenetic analyses of the parasitic ant genus Myrmoxenus 46 Introduction 48 Material and Methods 50 Results 54 Discussion 59 CHAPTER 4: Cuticular profiles and mating preference in a slave-making ant 61 Introduction 63 Material and Methods 65 Results 69 Discussion 75 CHAPTER 5: Influence of the slaves on the cuticular profile of the slave-making ant Chalepoxenus muellerianus and vice versa 78 Introduction 80 Material and Methods 82 Results 86 Discussion 89 GENERAL DISCUSSION 91 SUMMARY 99 ZUSAMMENFASSUNG 101 REFERENCES 103 APPENDIX 119 DANKSAGUNG 120 General Introduction 1 GENERAL INTRODUCTION Parasitism is an extremely successful mode of life and is considered to be one of the most potent forces in evolution. As many degrees of symbiosis, a phenomenon in which two unrelated organisms coexist over a prolonged period of time while depending on each other, occur, it is not easy to unequivocally define parasitism (Cheng, 1991).
    [Show full text]
  • First Confirmed Record of the Ant Genus Myrmecina (Hymenoptera, Formicidae) from the Malay Peninsula: Description of a New Sp
    JHR 50: 129–140First (2016) confirmed record of the ant genusMyrmecina (Hymenoptera, Formicidae)... 129 doi: 10.3897/JHR.50.8652 RESEARCH ARTICLE http://jhr.pensoft.net First confirmed record of the ant genus Myrmecina (Hymenoptera, Formicidae) from the Malay Peninsula: description of a new species and a key to Myrmecina species from Sundaland Mark K. L. Wong1, Benoit Guénard2 1 National Parks Board, Singapore Botanic Gardens, 1 Cluny Road, Singapore 2 School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong Corresponding author: Benoit Guénard ([email protected]) Academic editor: Michael Ohl | Received 29 March 2016 | Accepted 20 April 2016 | Published 27 June 2016 http://zoobank.org/8B72E213-BFDC-4334-AD6E-C2ED1067C231 Citation: Wong MKL, Guénard B (2016) First confirmed record of the ant genus Myrmecina (Hymenoptera, Formicidae) from the Malay Peninsula: description of a new species and a key to Myrmecina species from Sundaland. Journal of Hymenoptera Research 50: 129–140. doi: 10.3897/JHR.50.8652 Abstract We present the first confirmed record of the little known and uncommon ant genusMyrmecina for the Malay Peninsula. Myrmecina magnificenssp. n., a new species displaying unique anteriorly pointing pro- podeal spines, is described from specimens of the worker caste collected in a selectively logged primary rainforest in Singapore. We also provide the first key to Myrmecina species of the Sundaland region. Keywords Myrmecina, Southeast Asia, Malay Peninsula, Singapore, Leaf litter Copyright Mark K.L. Wong, Benoit Guénard. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
    [Show full text]
  • Formicidae, Ponerinae), a Predominantly Nocturnal, Canopy-Dwelling
    Behavioural Processes 109 (2014) 48–57 Contents lists available at ScienceDirect Behavioural Processes jo urnal homepage: www.elsevier.com/locate/behavproc Visual navigation in the Neotropical ant Odontomachus hastatus (Formicidae, Ponerinae), a predominantly nocturnal, canopy-dwelling predator of the Atlantic rainforest a,1 b,∗ Pedro A.P. Rodrigues , Paulo S. Oliveira a Graduate Program in Ecology, Universidade Estadual de Campinas, 13083-862 Campinas, SP, Brazil b Departamento de Biologia Animal, C.P. 6109, Universidade Estadual de Campinas, 13083-862 Campinas, SP, Brazil a r t a b i s c l e i n f o t r a c t Article history: The arboreal ant Odontomachus hastatus nests among roots of epiphytic bromeliads in the sandy forest Available online 24 June 2014 at Cardoso Island (Brazil). Crepuscular and nocturnal foragers travel up to 8 m to search for arthropod prey in the canopy, where silhouettes of leaves and branches potentially provide directional information. Keywords: We investigated the relevance of visual cues (canopy, horizon patterns) during navigation in O. hastatus. Arboreal ants Laboratory experiments using a captive ant colony and a round foraging arena revealed that an artificial Atlantic forest canopy pattern above the ants and horizon visual marks are effective orientation cues for homing O. has- Canopy orientation tatus. On the other hand, foragers that were only given a tridimensional landmark (cylinder) or chemical Ponerinae marks were unable to home correctly. Navigation by visual cues in O. hastatus is in accordance with other Trap-jaw ants diurnal arboreal ants. Nocturnal luminosity (moon, stars) is apparently sufficient to produce contrasting Visual cues silhouettes from the canopy and surrounding vegetation, thus providing orientation cues.
    [Show full text]
  • Social Foraging in Temnothorax Ants by Zachary Shaffer A
    The Wisdom of the Acorn: Social Foraging in Temnothorax Ants by Zachary Shaffer A Dissertation Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy Approved April 2014 by the Graduate Supervisory Committee: Stephen Pratt, Chair Bert Hölldobler Marco Janssen Jennifer Fewell Juergen Liebig ARIZONA STATE UNIVERSITY May 2014 ABSTRACT The coordination of group behavior in the social insects is representative of a broader phenomenon in nature, emergent biological complexity. In such systems, it is believed that large- scale patterns result from the interaction of relatively simple subunits. This dissertation involved the study of one such system: the social foraging of the ant Temnothorax rugatulus. Physically tiny with small population sizes, these cavity-dwelling ants provide a good model system to explore the mechanisms and ultimate origins of collective behavior in insect societies. My studies showed that colonies robustly exploit sugar water. Given a choice between feeders unequal in quality, colonies allocate more foragers to the better feeder. If the feeders change in quality, colonies are able to reallocate their foragers to the new location of the better feeder. These qualities of flexibility and allocation could be explained by the nature of positive feedback (tandem run recruitment) that these ants use. By observing foraging colonies with paint-marked ants, I was able to determine the ‘rules’ that individuals follow: foragers recruit more and give up less when they find a better food source. By altering the nutritional condition of colonies, I found that these rules are flexible – attuned to the colony state. In starved colonies, individual ants are more likely to explore and recruit to food sources than in well-fed colonies.
    [Show full text]
  • 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 - =- .
    [Show full text]