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Groups, competition, aggressive communication

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Title: Groups, competition, aggressive communication


1
Groups, competition, aggressive communication
  • MSc ACSB 2005/06
  • Session 14 Understanding
  • by modelling?

2
Benefits from group-living
  • Food
  • Food-finding, e.g. colony information exchange
  • Lower variance of feeding success
  • Co-operative hunting, - lions, hunting dogs
  • Safety
  • Increased vigilance - pigeon flocks
  • Dilution of risk from predators - pelagic fish
  • Co-operative defence- buffalo
  • Breeding
  • Co-operative territorial defence
  • Helpers at nest/den - scrub jay, dwarf mongoose
  • Eusocial societies - naked mole rat

3
Trade offs in group life
  • Benefits must be traded off against costs
  • cooperation increases size of prey that can be
    killed BUT low rank big group limits food
    gained
  • larger groups reduce predation risk, BUT
    increase competition at food sources
  • What currency to use for this trade-off?
  • Mean intake per hour, or per day
  • Variance in intake rates across time

4
Mean or Variance?
  • Group can reduce variance in food intake
  • High variance gt a greater risk of going bust,
    even if mean return is quite good
  • Thompson, Vertinsky Krebs (1974) JAE 43,
    785-820 Realistically-simulated flocking in
    titmice - flocking had much greater impact on
    variance than on mean return (MODEL 1)
  • Safety (low variance) may be more valuable than a
    high rate of intake

5
Badges of status
  • Access to resources in a group often depends on
    status
  • Larger, darker bib below bill on dominant Harris
    sparrows (studlies) - Rohwer
  • Birds take note of the size of the bib in their
    interactions so this badge of status allows a
    dispute about rank to be resolved without
    fighting
  • Why is the dark bib an honest signal of status?
  • If wearing a large badge gives victory at minimum
    cost, why dont subordinates pretend to be
    dominant by growing larger badges?

6
Rohwers experiments
  • Experiments in which badge size was increased or
    reduced experimentally
  • Dominants with bleached-out badges had to fight
    hard for access to food etc - badge works
  • DO win eventually - so really are better fighters
  • Subordinates with enlarged badge dont win
  • UNLESS also injected with testosterone at the
    time that the badge is enlarged

7
Møller House sparrows
  • Møller (1987) Anim. Behav., 35, 1637-1644
  • High-ranked birds had larger badges
  • Attack most common between males with equal badge
    sizes (in field, not lab flocks)
  • Attacks on birds with a similar-size badge more
    frequent among high-ranking birds so a
    subordinate with a deceptively large badge will
    face more attacks than if honest

8
Control of cheating
  • So larger badge imposes a greater cost from other
    birds attacks limits cheating
  • Møller showed elsewhere that a large badge also
    gt lower survival in autumn limits cheating
  • In many contests, differences between the
    individuals (in size, weight, prowess RHP,
    value of the resource) are likely to be used to
    decide the outcome

9
Skew in animal groups
  • Siblys model group is stable (assuming free
    entry/exit) at point where a subordinate fares as
    badly living in the group as it does when living
    independently
  • Group size reflects entryexits, or fission
  • Dominants get more of the benefits from the
    group, subordinates bear more of the costs. Skew
    within the group

10
Kinship affects skew in groups
  • Vehrencamp, 1983, Anim. Behav. 31, 667-682 (MODEL
    2)
  • In kin-groups, lowest-ranking members incur
    direct costs to benefit dominants but if
    dominants are related, subordinates get indirect
    benefits
  • Subordinates inclusive fitness is increased if
    the breeding success of these dominants is
    enhanced
  • The closer the relationship, the greater the skew
    that can be imposed on subordinates
  • So a family group may be exploitative, not wholly
    co-operative, especially if very close kin are
    involved

11
Vehrencamps model
12
Helping vs. breeding
  • Harassment in W. Fronted Bee-Eaters
  • Nest in tunnels in sandy banks
  • Shortage of food many young die
  • Eggs hatch asynchronously always stronger and
    weaker chicks weakest starve quickly if food is
    scarce while rest remain well-fed
  • Harassment halts many breeding attempts

13
Harassment (2)
  • Who causes the trouble?
  • Incidence Success
  • Parents 36-45 75-84
  • Brothers 16-19 33
  • Other kin 16-17 0
  • What is pay-off?
  • Young per pair 0.51 (unassisted)
  • 0.98 (helper)

14
Harassment (3)
  • Harasser gains 0.47 young (at r0.5) 0.235
  • loses 0.51 young at r0.25 0.1275
  • Benefit to harasser (rounded) 0.11
  • Victim Loses 0.51 at r0.5 0.2550
  • gains 0.47 sibs at r0.5 0.2350
  • Cost of harassment to victim (rounded) 0.02
  • Victim (son) has less leverage than harasser
    (dad), and so is constrained to help, not breed

15
Threat can resolve contests
  • Combat involves energy costs, and risk of injury
  • Threat displays allow animals to resolve disputes
    without physical combat
  • But if A gains victory more cheaply by giving an
    intimidating display, why does B not give an
    equally- or more-intimidating display and win
    instead?
  • The problem of honest signalling in animal
    contests

16
Phased contests have escalating costs
  • DeCarvalho et al, 2004, Anim. Behav., 68,
    473-482, measured energy of 3-phase Sierra Dome
    spider contests
  • Phases have expenditure of 3.5x, 7.4x, 11.5x BMR
  • Costs are substantial, and later phases are more
    costly, explaining why it pays a
    potentially-losing rival to quit early rather
    than to persist through phase 1 to phases 2 or 3.

17
Why do weaker rivals quit?
  • Huntingford et al. (2000) data on shore crabs
    and cichlid fish
  • Show glycogen reserves depleted, and increase in
    lactate in muscle, as contests progress so
    these contests impose costs
  • Partial energetic Wars of Attrition - where
    opponents fight until one has reached the
    critical value of (lactate accumulationglycogen
    depletion) for giving up. Fight is equivalent
    to vigorous exercise (5 min of being chased)

18
Bowl doily spider contests
  • Austad, 1983, Anim. Behav., 31, 59-73
  • Weight/size affects probability of injury
  • When males introduced together, weight -gt result
    (larger won 82 contests longer where weights
    nearly equal) (K)
  • When weight equal, fights settled by female
    value. Owner fought for longer if has
    information that makes female more valuable (V)
  • Most serious escalations when V/K equal for both
    contestants, e.g. smaller owner vs. larger
    intruder

19
Assessment-based models
  • Many think that differences in size/weight/etc.
    are assessed during contest
  • Larger/heavier rival wins in fish, spiders, etc.
  • Later phases of contest likely to provide more
    information about weight-difference than earlier
    phases
  • BUT see Taylor Elwood 2003, covered later in
    session
  • Leimar, Austad Enquist, 1991, Evolution 45,
    862-874

20
Enquists honest-signals model MODEL 3
  • Several alternative display actions can be ranked
    in terms of effectiveness and cost the most
    effective acts also the most costly
  • When high-V contest, most costly act has the
    greater payoff (P3VH is high so gt C3)
  • When low-V contest, least costly act gives
    greater payoff (P1VL gt C1 but P3VL lt C3)

21
Fulmar Contests
  • Fulmars feeding on fish scraps behaviour
    includes some (but not many) ritualised displays
  • Cost P(pecks, breast-to-breast, physical
    combat)
  • Effectiveness P(opponent gives up)
  • E.g. full wing display more costly and more
    effective than half/no wing display
  • More effective/costly acts used for higher V
    resource
  • Typically high positive rank correlations between
    cost and effectiveness of options used at each of
    successive decision points

22
But will information transfer evolve?
  • Contests longest when opponents are equal gt pick
    up info about size difference from interaction
  • Taylor Elwood (2003) show that same pattern can
    occur if each rival persists for a time related
    to its size, with no assessment need to tease
    apart effects of largers size, smallers size,
    and difference in size, to test assessment models
  • Noble no information transfer evolved in two
    A-life models designed to allow info pickup
  • http//www.comp.leeds.ac.uk/jasonn/Research/Aggres
    sion/index.html

23
Nobles simulations MODELs 4-5
  • (1998) Tough guys dont dance
  • Animats in contest change their position on the
    attack-flee continuum (? ) over time
  • Being aggressive carries cost being attacked
    carries cost. Animats differ in fighting ability
    (f)
  • Neural network implementation
  • Animats know own fighting ability, their place on
    the attack-flee dimension ?, and what they are
    doing and can see what opponent is doing

24
Tough guys (2)
  • Blind get zero info about opponents ?
  • Exptal can evolve to make use of input that
    gives info about opponents ?
  • Unfakable full info - given opponents fighting
    ability, f, so dont really need ?
  • Did not evolve to use this info about ?, although
    over time fewer contests were settled by fights,
    and 41 of fights were between opponents with
    well-matched f-values

25
Nobles next attempt
  • (2000) Talk is cheap
  • a production system implementation of Enquists
    strong/weak signal honest-signalling model (1985)
  • Strategies that evolved from a random starting
    point rarely employ information about opponents
    signal
  • Enquists honest strategy was vulnerable
    displaced by mutants that didnt use information
    about signal
  • If Noble increased the cost of just being
    attacked to unrealistic levels, information
    about opponents signal WAS now employed in some
    simulations

26
Understand behaviour through modelling?
  • Models of various types
  • Grounded simulations using time-steps
  • Algebraic analysis of costs and payoffs
  • Algebraic ESS models
  • Evolutionary A-life simulations

27
References
  • Pulliam Caraco (1984) Chapter 5 in Krebs
    Davies (Eds) Behavioural Ecology (2nd Ed only
    this edition). Blackwell, Oxford.
  • Krebs Davies (1993) An introduction to
    behavioural ecology (3rd Edn) Chapter 6, 7
  • Bradbury, JW and Vehrencamp, SL (1998) Principles
    of animal communication. Chapter 21 (and parts
    at least of Chapter 20, esp. pp. 649-658,
    662-665, 668-676)
  • Enquist et al. (1985) Anim. Behav., 33, 1007-1020
  • Nobles papers and additional info at
    http//www.comp.leeds.ac.uk/jasonn/Research/Aggres
    sion/index.html
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