Continuation of Lecture 3 on parental care, focusing on brood parasitism.
Core theme: the co-evolutionary “arms race” between cuckoos (obligate brood parasites) and their host bird species.
Lecture segment picks up after coverage of:
Pre-laying host defence behaviours.
Manipulation of clutch size.
Egg mimicry and pattern complexity.
Host rejection thresholds.
Arms race = reciprocal, escalating adaptations and counter-adaptations.
Key selective pressures:
Cuckoos must successfully exploit host parental care.
Hosts must avoid wastage of limited resources on unrelated young.
Brood parasitism costs host parents in terms of energy, time, and lost genetic fitness.
Conflict occurs before laying, at egg stage, and throughout chick development.
Hosts evolve highly variable, intricate eggshell patterns → harder for cuckoos to replicate.
Common cuckoo (Europe):
Parasitises 8 distinct host species.
Exhibits plastic egg mimicry: changes colour/pattern expression to match the current host clutch.
Host-specific examples:
Brambling → excellent at detecting foreign eggs; strong selection on cuckoo egg accuracy.
Dunnock → poor at detection; weak selection on egg mimicry so cuckoo eggs may look un-matched.
Prediction: If host detection improves, cuckoo egg morphology should evolve toward finer mimicry (future arms-race steps).
Some cuckoo nestlings mimic host begging calls to trigger adult feeding.
Superb fairy-wren study (Australia):
Species parasitised by bronze cuckoo.
Female wrens sing a unique “password” call to embryos while still in the egg.
True offspring match the password post-hatch; cuckoo chicks fail → parents reduce/cease provisioning.
Trade-off: Increased calling raises risk of nest predation but enhances chick recognition accuracy.
Demonstrates learning pre-hatching and cross-generational information transfer.
Bronze cuckoo complex (shining, Horsfield’s, etc.):
Adults look nearly identical across species → minimal selection on adult phenotype.
Chicks show dramatic divergence mirroring respective host nestlings.
Mimicked traits: skin pigmentation, distribution of natal down tufts, gape colour/pattern, feather tracts.
Host-specificity vs mimicry precision:
Horsfield’s bronze cuckoo: least accurate chick mimicry but least host-specific (multi-host strategy requires phenotypic plasticity rather than perfect fidelity).
Illustration of developmental plasticity and selective pressure targeted at life-history stage with highest detection risk.
Shining cuckoo (NZ name = pīpī wharauroa; AUS name = shining bronze cuckoo):
Migrates to Pacific islands during non-breeding season.
Primary NZ host: grey warbler (riroriro).
Long-tailed cuckoo (NZ):
Hosts: whitehead, yellowhead, brown creeper.
Highlights geographic variation in host–parasite networks.
Parents possess finite resources (R_{total}), allocated among:
Current offspring (\sum R_{current})
Future reproductive opportunities (R_{future})
Parent–offspring conflict:
Present within broods (sibling rivalry) and across generations (current vs future broods).
Brood parasitism amplifies conflict by adding unrelated competitor.
Coevolutionary dynamics are frequency-dependent and may oscillate through time (Red Queen scenario).
Raises questions of genetic vs social parenthood: who “owns” parental investment?
Demonstrates natural examples of deception, adoption, and selective discrimination.
Practical relevance to conservation:
Understanding host vigilance can inform management where endangered hosts suffer high parasitism.
Predicting outcomes as species distributions shift with climate change.
Links to sexual selection (next lecture) via mate choice costs and reproductive strategies.
Complements earlier discussions on life-history theory (resource allocation, trade-offs).
Illustrates principles of signal evolution, sensory biases, and learning.
Textbook: Rubenstein & Alcock, Parental Care chapter (Chs. 11 or 12 depending on edition).
Video resource: David Attenborough’s documentary segment on cuckoos (link in Moodle).
Upcoming Moodle quiz “Cuckoo vs Host” to consolidate recognition of adaptations.
Limited resources force strategic allocation; raising non-kin is costly.
Brood parasitism produces a multi-level arms race (egg, call, morphology).
Evolution acts on whichever life stage offers most leverage for success or defence.
Studying these systems illuminates conflict resolution mechanisms across taxa and generations.