HS

Mating Systems in Animal Reproduction - Key Concepts (Lecture 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