Social insects Ch. 11 Eusocial: co-operate in reproduction and have division of reproductive effort division of labor, with a caste system involving sterile.

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Social insects Ch. 11 Eusocial: co-operate in reproduction and have division of reproductive effort division of labor, with a caste system involving sterile or non-reproductive individuals assisting those that reproduce; co-operation among colony members in tending the young; overlap of generations capable of contributing to colony functioning. – Daughters help mom raise daughters

Subsocial insects Heterogeneous behavioral traits that include some but not all of the elements of eusociality – Nonbreeding aggregations – Parental care – Division of labor, particularly defense Quasisocial: Cooperative nesting, all females reproducing Semisocial: Cooperative nesting, division of reproductive labor, but only one generation – All sisters

Eusocial insects

Eusociality Hymenoptera – evolved (probably) 10 separate times – All ants (Formicidae) – Several lineages of Bees Apidae (three times) Halictidae (three times) – Several lineages of Wasps Vespidae (twice) Sphecidae (once) All termites (Isoptera within Blattodea) Hemiptera (Aphids) Coleoptera (Cuculionidae)

Eusociality Castes – Morphologically and behaviorally different individuals within a colony Queen (reproductive) Workers Soldiers Drone/King

Vespidae castes

Eciton

How do castes form? Caste is trophigenic: Determined by food quantity & quality during immature stages

Apis mellifera Queens compared to workers – Larger – Lack wax glands – Sting is NOT barbed Fed on Royal Jelly – Food supply differs in quantity and quality – Royal jelly rich in Pantothenic acid, Biopterin, sugar Queen maintains control of workers via pheromone – Inhibits worker ovarian development – Queen+pheromone more effective than pheromone only

Honey bee workers Monomorphic Polyethic – Young: hive bees Feed brood Clean cells – Old: Foragers – Change determined by Juvenile hormone III Low in young bees (Hive) Higher in field bees (Foragers)

Experiment: Role of JH? Sullivan et al Hormones & Behavior 37:1-14 Corpora allata (CA) secrete JH Allatectomy: remove CA; remove JH JH replacement therapy What does this do to behavior? – CA- (sugically remove CA) – Sham (surgery, no removal) – CA- with Methoprene (Synthetic JH) – Untreated % Foragers

JH not necessary for foraging JH regulates timing of transition Remove JH, Timing of transition delayed Even CA- bees eventually become foragers Replace JH, return unmanipulated timing Colonies varied in their responses to allatectomy and to JH analog

Colony founding Newly mated queen Produces brood of daughters Reproduction suppressed in daughers – Help mother raise more daughters Reproductive offspring (queens, males) produced later in season

Nest construction in Hymenoptera Wasps (Vespidae) – “paper” – Plant fibers chewed and modified into papery substance – Cellulose Bees (Apidae, Halictidae) – Wax – Produced by glands on abdomen

Nest construction in Hymenoptera Ants (Formicidae) – Subterranean – “carton”; Fungus galleries – Living plants Weaver ants use silk Domatia-dwelling ants – None (army ants)

New colonies Reproduction in social insects = new colonies Founding new colonies varies among social insect taxa Wasps (Vespidae) – Mostly annual Bees (Apidae – particularly Apis) - >Annual Ants (Formicidae) – Variable Termites (Isoptera) - variable

Vespidae Queens and males produced in fall Existing colonies break down and die Females mate; reproductive diapause Locate overwintering site Spring – Queens feed – Locate nest site – Constructs first cells – Produces workers

Apidae (Apis mellifera) Colonies overwinter; queens live multiple years Spring: Queen leaves with majority of workers – Swarming; often in 2 nd year of colony life Locates new nest site; founds “new” colony Existing site retained by a daughter queen – Daughter queens fight; one survivor – Daughter queens go on mating flights (possibly >1)

Ants (Formicidae) Typically seasonal production of alates (male, female) Mating flights Single-queen colonies Multi-queen colonies – Primary [found colony together] – Secondary [daughter queens join mom as reproductives] – Facultative or obligate Budding: Founding new colonies by splitting of existing multi-queen colony

Reproduction by workers Across hymenoptera Highly variable Unmated produce males In some species workers may mate and produce females Workers may “move up” if queens die

Legionary or Army ants Traits – Obligate collective foraging – Nomadism – Robust wingless queens – Abdominal distension during egg production Three well defined subfamilies – Dorylinae ~150 spp. (E. Africa, Asia) – Aenictinae ~100 spp. (Africa, Asia, Australia) – Ecitoninae ~70 spp. (N., C., S. America)

Traditional Hypothesis – Two lineages (old world, new world) – Evolved Army ant habit independently (Homoplasy) New information: – Brady, S Proc. Natl. Acad. Sci. USA 100: – Molecular, Morphological, Fossil evidence – Nuclear genes (18S rDNA, 28S rDNA, and wingless) – mtDNA (Cytochrome Oxidase I)

Consensus tree

Fig. 2. Bayesian divergence dating analysis. NW, New World; OW, Old World. Divergence dates were estimated on the ML phylogeny derived from COI, 18S rDNA, 28S rDNA, and wingless genes (-ln L = ). Clades marked with asterisks had a posterior probability of >95% after independent Bayesian phylogenetic analysis. Lowercase letters at nodes indicate minimum age constraints obtained from the fossil record: a– c, 20 Mya (34, 35); d, 25 Mya (36, 37); e–f, 42 Mya (38); g, 50 Mya (39); h, 65 Mya (40); i, 92 Mya (32). Army ant taxa are shown in thick type. Branch lengths are drawn scaled to estimated mean values of absolute time. The origin of army ants is estimated at 105 Mya (±11 SD). Separation of Africa from S. America ~100 mya

Evolution of Eusociality Remember: independently evolved in Hymenoptera (multiple times), Isoptera, Hemiptera, Thysanoptera, Coleoptera Hymenoptera: What selective advantages favor eusociality? Solitary -> subsocial/semisocial -> eusocial – Advantages from: shared cost of nest construction Shared cost of offspring defense

Evolution or eusociality in Hymenoptera Increased longevity of female – Remains in association with offspring (subsocial) Unrelated females of the same generation associate – Cooperative rearing (Quasisociality) – Division of reproductive labor evolves Related females of the same generation associate – Cooperative rearing; mulitple queens (Quasisociality)

But what selects for reproductive division of labor? What would select for altruistic abandonment of reproduction? – Group selection – Kin selection – Maternal manipulation – Mutualism

Group selection Selection favors colonies that produce most offspring, and that happens with nonreproductive workers – Problem: presumes nonreproductive caste already exists – Problem: what could select for loss of reproduction? May contribute to maintenance of eusociality after it arises, but likely cannot account for origin of eusociality

Kin selection Historically favored, now deemed inadequate Fitness of an individual depends on its reproductive success and on reprodutive success of relatives – Relatives success discounted by degree of relatedness – Inclusive fitness Haplodiploidy makes kin selection of altruism toward relatives very likely

Kin selection Hamilton’s rule Altruism toward a relative can be favored by selection if: – rB > C – Where r = relatedness coefficient (see previous) of relative – B = benefit to the relative – C = cost to the altruist What’s the problem?

Kin selection and inclusive fitness Nowak, Tarnita, Wilson Nature 466: Eusociality and altruism rare even in animals that reproduce clonally (r even greater) Haplodiploidy universal in Hymenoptera; eusociality is rare. Termites: Haplodiploidy is not necessary For inclusive fitness and kin selection to favor altruism, interactions of altruists and recipients must be Additive and pairwise. – If not, inclusive fitness irrelevant or uncalculable

Nowak, Tarnita, Wilson Model for evolution of eusociality via natural selection Constructed expensive nests Sequential provisioning of young Eusocial allele (recessive; remain in nest) Individual simple natural selection can favor eusocial allele over noneusocial allele Once colonies form, kin selection maintains it and contributes to division of labor

Maternal manipulation It isn’t altruism, it is forced by mother Manipulation of feeding -> reproductive development Selfish maternal behavior is the primary agent selecting for eusociality

Mutualism Mutual defense of brood creates individual selective advantage to cooperation Reproductive competition within the nest Inclusive fitness and kin selection can maintain cooperation and push toward altruism

Eusociality in termites XX/XY sex determination Endosymbiotic protozoa for digestion of cellulose predispose offspring remaining with parents – Requires overlapping generations – longevity

Keep in mind… Biomass of ants: – ½ of all insect biomass – Exceeds that of non-human terrestrial vertebrates Social insects are the other dominant group on planet earth Nowak, Tarnita, Wilson Nature 466: