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
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)
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
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
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
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
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)
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
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
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
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)
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