HS

Animal Mating Systems – Comprehensive Study Notes

Key Definitions & Classification of Mating Systems

  • Mating system = complete suite of behaviours/strategies governing:
    • How mates locate one another
    • Frequency/number of matings
    • Nature of pair‐bonds
    • Extent/type of parental care
  • Principal axis of classification: number of mates per sex
    • Monogamy – each sex mates with only one partner
    • Often involves long-term pair bonds & biparental care
    • Polygamy (umbrella term = ≥1 sex mates with >1 partner)
    • Polygyny – 1 male, \ge 2 females
    • Polyandry – 1 female, \ge 2 males
    • Polygynandry – both sexes mate multiply but retain semi-stable pairings/coalitions (e.g.
      chimps, bonobos)
    • Promiscuity – both sexes mate multiply, no stable bonds or territories

Why Is Monogamy Paradoxical for Males?

  • Classic sexual-selection theory predicts males boost fitness by maximising number of matings
  • Yet monogamy is common (esp. birds)
  • Key ecological variables:
    • Spatial/temporal distribution of females ⇒ “economic defendability”
    • Dispersed/isolated females → hard to guard >1 ⇒ monogamy favoured
    • Clumped females/resources → polygyny easier (male defends clump)
    • Requirement for biparental care (offspring survival ↑ when both stay)

Three Main Hypotheses for the Evolution of Monogamy

  • Mate-Guarding Hypothesis

    • Male remains with single female to prevent rival insemination
    • Favoured when
    • Female receptive period short but allows re-mating (high sperm-competition risk)
    • Females scarce/hard to locate
    • Example: Hulagin shrimp – dispersed females & brief receptivity
  • Mate-Assistance (Biparental Care) Hypothesis

    • Male gains greater fitness by aiding offspring than by seeking extra matings
    • Empirical test: California mice (Peromyscus californicus)
    • Warm conditions: father presence = no significant litter‐survival gain
    • Cold conditions: litter survival jumps from \approx30\% \to 80\% when father present
    • Mechanisms: thermoregulation, joint foraging, protection
  • Female-Enforced Monogamy

    • Female behaviour prevents male from attracting/accepting extra mates
    • Burying beetles (Nicrophorus spp.)
    • Males emit pheromone atop carcass to lure more females
    • Resident female mounts & physically blocks male; experiment with tethered female ⇒ males signalled >4× longer when unrestrained

Monogamy Across Taxa

  • Birds: \approx90\% form social pairs
    • BUT genetic studies show social ≠ genetic monogamy
    • DNA fingerprinting (1980s-90s) ➔ widespread extra-pair copulations (EPCs) & extra-pair paternity (EPP)
    • Meta-analysis n=150 spp: >90\% show some EPP; strict genetic monogamy in <25\%
    • Extremes:
      • Reed bunting – >50\% offspring, 86\% broods contain EPP
      • Superb fairywren – 72\% offspring, 95\% broods with ≥1 EPP chick
    • Rare true monogamy: North Island saddleback/Tieke
  • Mammals: only 3\text{–}5\% monogamous
    • Constraints: internal gestation, lactation, often precocial young → limited male role

Costs & Benefits of EPCs / Polyandry within “Monogamy”

  • Male benefits: extra offspring; costs: time away → own mate may re-mate, paternity loss
    • Example: Bank swallows – males guard mates intensively during female fertile window, then seek EPCs themselves
  • Female benefits (parallel to polyandry lecture):
    • Good genes – increase genetic quality/viability of brood
    • Fertility insurance – guarantee fertilisation of all eggs (supported in blue tits)
      • Study: clutches of EPC females had significantly fewer unfertilised eggs
    • Material/resource gains – nuptial gifts, access to territories, etc.
  • Female costs: desertion risk, loss of male care, disease, aggression

Case Study: New Zealand Tūī (Prosthemadera novaeseelandiae)

  • Socially monogamous yet extreme EPP
    • 72\% of females mate outside pair; 57\% of offspring extra-pair
  • Males \approx50\% heavier than females (unusual for socially monogamous birds)
  • Data: negative correlation between male tarsus length (proxy for size) & proportion of EPP in his nest ⇒ larger males better at paternity defence/attraction
  • Hypotheses: aggressive singing displays monopolise mates; large size evolved via sexual selection to reduce cuckoldry

Polyandry & Sex-Role Reversal

  • Complete reversal: female competes, male provides sole care
    • Conditions: clutch transferable (eggs), high male care benefit > cost, female able to produce multiple clutches
    • Examples:
    • Spotted sandpipers (Actitis macularius)
    • Northern jacanas (Jacana spinosa)
    • Malleefowl (Leipoa ocellata)

Forms of Polygyny

  • Resource-Defence Polygyny

    • Male monopolises critical resource → females visit
    • Example: Pseudoscorpions on harlequin beetles – male defends beetle’s elytra as “taxi” to rotten logs
  • Female-Defence Polygyny

    • Direct guarding of female clusters (e.g., tree weaver birds, spear-nosed bats)
  • Lek Polygyny

    • Males defend small display arenas devoid of resources
    • Female choice drives extreme skew
    • Sage grouse: top male ≈50\% of copulations; many males get 0
    • Other examples: cock-of-the-rock, fallow deer, mosquito swarms
    • NZ example: Lesser short-tailed bat (Pekapeka tō-roa)
    • Communal day roosts; at night males occupy “singing roosts” near colony; coat selves in urine; females visit briefly to mate
  • Scramble-Competition Polygyny

    • Little/no aggression; success = speed & sensory ability
    • Two subtypes:
    • Explosive breeding assemblages – synchronised female availability (e.g.
      pond-breeding frogs)
    • Prolonged searching – females dispersed; selection for mobility
      Cook Strait giant wētā – fastest, long-legged but light males arrive first & gain matings

Interactions with Sexual Selection & Ecology

  • Economic defendability concept: costs to guard > returns = monogamy / polyandry; defendable clumps = polygyny
  • Sperm competition shapes mate-guarding & EPC behaviour
  • Parental investment theory: sex investing more in offspring (often female) becomes limiting resource, but role reversal possible under ecological/physiological constraints

Methodological & Ethical Notes

  • DNA fingerprinting revolutionised behavioural ecology; exposed hidden genetic relationships
  • Conservation implications:
    • Understanding genetic mating systems critical for managing small populations, ensuring genetic diversity
    • Example: translocations must consider true breeding structure, not assumed social pairs
  • Philosophical: challenges anthropomorphic views of “faithfulness”, highlights adaptive rather than moral basis of behaviour

Quick Numerical/Statistical Summary

  • Birds socially monogamous: \approx90\%; genetically monogamous <25\%
  • Mammals genetically/socially monogamous: 3\text{–}5\%
  • Superb fairywren EPP: 72\% offspring, 95\% broods
  • Tūī EPP: 57\% offspring, 72\% females engage EPCs
  • California mice: litter survival in cold ↑ from \approx30\% \to 80\% with male care
  • Sage grouse lek: top ranked male ≈48\% of copulations (one study)

Key Take-Home Messages

  • Mating systems are diverse, context-dependent, and often differ between social observations & genetic realities
  • Distribution of females/resources + necessity of parental care jointly determine evolutionary stable strategies
  • Monogamy persists via mate-guarding, cooperative parenting, or female enforcement, but is frequently violated via EPCs
  • Polygyny takes multiple ecological forms; polyandry and role-reversal, though rarer, underscore flexibility of sexual selection dynamics
  • Modern molecular tools are indispensable for uncovering true reproductive strategies, influencing both theory and conservation practice