Parental effort of kestrels (Falco tinnunculus) in nest defense: effects of laying time, brood size, and varying survival prospects of offspring

We studied the nest defense behavior of Eurasian kestrels (Falcotinnunculus) towards a stuffed pine marten (Martes martes) througha 3-year vole cycle (1990–92) in western Finland. Survivalprobability of offspring decreases with a later start of breeding,and, therefore, early breeders should protect their offspringmore than late ones. We found this true for males during theincubation period, but not for females. In addition, we expectedthe nest defense intensity to increase with offspring number.During the incubation period, this was true for females, butnot for males. During the nestling phase, parents did not adjusttheir defense effort to natural or manipulated (by one to twoyoung) brood size. Survival prospects of kestrel offspring werehighest in the increasing vole year 1991 and lowest in the decreasingvole year 1992, and, therefore, we expected the defense activityof kestrels to follow the same trend. However, the oppositeresult appeared true for females with a similar tendency formales. Most hypotheses predicting avian nest defense behaviorwere not supported by our data. Temporally heterogeneous environmentand low degree of nest-site tenacity of migratory kestrels maymake them unfamiliar with environmental variation and survivalprospects of their offspring. Therefore, fitness benefits ofparental care are not predictable, and kestrels may thus adjusttheir parental effort to their own future reproductive potential(i.e., number of future breeding attempts), rather than to somecurrent investment indicator, like offspring age and number.     

Parental provisioning and predation risk in rhinoceros auklets (Cerorhinca monocerata): effects on nestling growth and fledging

We examined the effects of predation risk on the behavior ofrhinoceros auklets (Cerorhinca monocerata) breeding at PineIsland, British Columbia, in 1990. Provisioning parents in someareas of the colony risked predation by bald eagles (Haliacetusleucocephalus). Chicks in high and low predation risk areasof the colony hatched on approximately the same date, receivedsimilar amounts of food to 46 days of age, grew at the samerate, reached similar peak masses, and fledged at similar masses.However, chicks in high predation areas fledged at a youngerage than did chicks in low predation areas. These data are consistentwith the hypothesis that parents in high risk areas terminatedprovisioning several days before those in lower risk areas.Mass at fledging was inversely related to age at fledging inboth high and low risk areas. The regression line for the highrisk habitats lies below that from the low risk habitats, aspredicted by a model that examines optimal time of fledgingfrom the perspective of the parents. We conclude that risk ofpredation represents a significant cost of reproduction to somerhinoceros auklets and that individual auklets within the colonyvary their behavior according to predation risk.     

Sexual selection for large male size in a polyandrous butterfly: the effect of body size on male versus female reproductive success in Pieris napi

Sexual selection theory predicts that the larger sex shouldbe that for which fitness increases at the faster rate withsize. In butterflies, as in most invertebrates, females areusually the larger sex, but previous comparative analysis hasshown that relative male size increases with female polyandryamong butterflies. In agreement with this pattern, males arelarger than females in the strongly polyandrous green-veinedwhite butterfly, Pieris napi L., and in this article we assessthe size dependence of reproductive success in both sexes. Inan experiment where virgin males and females were released inthe field, we found no strong association between size and malemating success. However, laboratory experiments showed thatthere was a strong correlation between size and the ejaculatethat the male delivered to the female at mating and that largeejaculates delayed female remating for a longer time comparedto small ejaculates. Moreover, female P. napi utilize male-derivednutrients received at mating to increase their fecundity. Hence,large males sire more offspring both by way of donating morenutrients to female egg production and by way of delaying femaleremating (given that the last male to mate with the female willfather most of the offspring). Laboratory experiments showedthat the association between size and fecundity was low, ornonexistent, among P. napi females allowed to mate only once.However, weak size dependence was found for polyandrous females.We hypothesize that size dependence of female fecundity maybe especially weak among polyandrous butterflies because a fundamentalsource of variation in fecundity relates to their ability tofind nutrient giving males, an ability which may be unrelatedto female size. According to this hypothesis there is a causalassociation between weak size dependence of female fecundityand polyandry, and a strong size dependence of male reproductivesuccess that may underlie the comparative pattern of positivecorrelation between relative male size and polyandry.     

Conflict between sexes in the water strider, Gerris lacustris: a test of two hypotheses for male guarding behavior

We studied the effect of operational sex ratio on female reluctanceand male persistence to mate as well as on the length of copulationand postcopulatory guarding in Gerris lacustris by adding fivesurplus males or females to the basin with a pair in tandem.In the control treatment, a pair alone was tested. Accordingto the copulatory guarding hypothesis (CGH), males should prolongmating and guard females in the presence of surplus males. Accordingto the convenience polyandry hypothesis (CPH), females shouldshow lower levels of resistance to prolonged mating in the presenceof surplus males because the mating male protects the femaleagainst harassment from other males. As expected on the basisof both the CGH and CPH, mating (copulation + guarding) averagedlonger in the male-biased treatment. The behavior of males andfemales during mating suggested that both hypotheses hold true:females showed less resistance to prolonged mating (as predictedfrom CPH), and male behavior suggested stronger efforts to stayon the female when surplus males were present (as predictedfrom CGH). Comparisons of the treatment with surplus femaleswith the results from the mating pair without surplus individualssuggested that the capabilities of water striders in tandemto assess the sex of nearby nonmating striders are limited.     

Testosterone effects on the immune system and parasite infestations in the barn swallow (Hirundo rustica): an experimental test of the immunocompetence hypothesis

The immunocompetence hypothesis predicts that testosterone (T)enhances the expression of male secondary sexual characterswhile exerting a suppressive effect on the immune system therebyexposing hosts to higher intensities of parasite infestations.In a natural population of barn swallow (Hirundo rustica) males,the intensity of infestation by some ectoparasites was negativelycorrelated with tail length and was positively correlated withimmunoglobulin levels, but no clear relationship was observedbetween immune responses (leukocyte counts, immunoglobulins)and tail length. Males implanted with T had higher intensitiesof parasite infestations at the time of recapture than controlmales, and T-implanted males experienced an increase in countsof eosinophils. In T-implanted males, immunoglobulin levelsinitially decreased and then increased as time from implantationelapsed. Among T-implanted males, those with longer tails hada smaller increase in eosinophil counts, tended to experiencea smaller increase of parasite infestations, and were more likelyto survive until the following breeding season than those withshorter tails. The relationships between parasite burden, immunesystem, and exaggeration of tail length in the natural populationof males are consistent with some aspects of the immunocompetencehandicap hypothesis. The results from the manipulation of Tplasma levels are also partly consistent with the hypothesis,since T-implantation resulted in higher levels of parasite infestations,but contradict the assumption of an obligatory immunosuppressiveeffect of T. Higher activation of the immune system of T-implantedmales indicate that high T plasma levels imposed a two-foldcost because of the effects on parasites and the immune responseto parasites, and this suggests that the effect of T on parasitesmight not be mediated by the immune system of the host. Theresults of the manipulation of T plasma levels support the handicapversion of the immunocompetence hypothesis since high quality,long-tailed males paid less in terms of activation of the immunesystem, change in parasite infestations, and chances of survivalthan low-quality, short-tailed males.     

Correlates of male quality in the field cricket, Gryllus campestris L.: age, size, and symmetry determine pairing success in field populations

Sexual selection in field crickets (Gryllidae) is well documented.Several studies have identified male traits, such as age andbody size, that influence pairing success in the field. HereI show how these traits covary with male quality by examiningthe degree of fluctuating asymmetry in male Gryllus campestris.Older males were both larger and more symmetrical. Principalcomponents analysis suggests that these three variables wereessentially measures of the same trait, male quality. A comparisonof paired and calling males showed that males of high qualitywere more successful in obtaining mates; paired males were older,larger, and more symmetrical. The area of the harp covariedwith morphological traits and determined the carrier frequencyof the male's call. Information related to male quality wastherefore available for female discrimination.     

Predicting group size in primates: foraging costs and predation risks

We present a direct test of the long-standing hypothesis thatfood competition limits primate group size. Group size is acritical social variable because it constrains most other aspectsof social organization. We develop a simple population-specificindex of indirect feeding competition based on daily foragingcosts. This index explains nearly two-thirds of between-populationvariation in mean group sizes of mostly fruit-eating (but notof mostly leaf-eating) primates. Group size is also significantlyrelated to body size and terrestriality (or use of open country),which are suspected correlates of predation risk, although feedingcompetition remains an important predictor of group size evenwhen these correlates are controlled. Phylogeny also appearsto be important: the differences between observed mean populationgroup sizes and those predicted using ecological factors aremost positive for the Old World monkeys and most negative forthe lemuroids in our sample. The weak relationship between groupsize and feeding competition found for folivorous species maybe explained either by the energetic constraints of a leafydiet or by limits to group size imposed by infanticide as ahabitual male reproductive strategy.     

On the economics of sit-and-wait foraging: site selection and assessment

We present two models of optimal resource exploitation for sit-and-waitforagers. The first model assumes immediate recognition of sitequality and that site quality does not change over time. Thismodel predicts a forager's minimum acceptable site quality.We present a graphical analysis to show how (1) the distributionof site qualities, (2) the travel time between sites, (3) costof search, and (4) expected duration of the foraging processinfluence the minimum acceptable rate. Our second model allowssite qualities to change and relaxes the assumption of immediaterecognition. This model defines conditions of (1) state duration,(2) recognition time, (3) site abundance, and (4) cost of searchwhere the optimal policy is to stay put in a site regardlessof experience. We discuss the implications of these models forthe design and interpretation of field experiments of site useand habitat selection.     

Black-and-white plumage in male pied flycatchers (Ficedula hypoleuca) reduces the risk of predation from sparrowhawks (Accipiter nisus) during the breeding season

Bright colors in birds might signal that they are undesirableas prey (aposematic), an idea that has been difficult to test.When stuffed pied flycatchers Ficedula hypoleuca are exposedto migrating sparrowhawks Accipiter nisus in spring or in autumn,the hawks attack cryptic females more often than bright males.To achieve better statistical control and to assess whethermale plumage also reduces predation risk in the breeding seasonand in the nesting habitat of the pied flycatcher, I placedpairs of male and female flycatcher mounts in similar positionsnear 22 nests of sparrowhawks. The hawks attacked mainly femalemounts, verifying that the preference is real. The sparrowhawkscaught at least 19 live pied flycatchers; 12 young, 5 adultmales, 1 adult female, and 1 female or young. Hawks that caughtan adult male seemed to prefer attacking female mounts. I discussthree interpretations of these results, suggesting that black-and-whitemale flycatchers may benefit from being a novel and aberrantprey, at least early in the breeding season.     

The location of landmark leks in the small heath butterfly, Coenonympha pamphilus: evidence against the hot-spot model

Two major theories have been developed to explain the locationand evolution of leks. According to the hot-spot model leksare male initiated and occur because males aggregate at locationsof maximum female home range overlap. The alternative femalepreference model, on the other hand, assumes that leks are femaleinitiated, and that females prefer to mate with males that aggregate.Small heath butterfly leks are situated close to landmarks suchas trees and bushes in open grassland. Censuses of wild populationsand experiments with artificial landmarks showed that theirattractiveness increased with height and width measured at themiddle of tree height. Landmark width at field layer heightwas negatively correlated with attractiveness, which suggeststhat a cornet shape is preferred to a pyramid shape. Togetherthese landmark size variables explained 60% of variation inlek size. Release experiments showed that landmarks were approachedby receptive virgin females, but mated females were indifferentto them. Landmark use was correlated to microclimatic conditions.Males preferred wider landmarks during cooler weather. Theyalso competed for the lee side of landmarks. There was no correlationbetween the location of landmarks and the dispersion of matedfemales or emergence sites of females. Hence, receptive femaledispersion was largely determined by their mate-locating behavior,which in turn appeared to result from male dispersion. Leksmay initially have developed around easily detected visual cuesthat offered a more suitable microclimate for male activity.Females visiting these locations would find a suitable matemore rapidly and save valuable time for oviposition. Althoughnonadaptive evolution cannot be excluded, taken together theresults support the female preference model for lek evolution.     

The definition of eusociality

We describe more precise definitions for the term "eusociality"and other social systems. Our criterion for eusociality is thepresence of castes, which are groups of individuals that becomeirreversibly behaviorally distinct at some point prior to reproductivematurity. Eusocial societies are characterized by two traits:(1) helping by individuals of the less-reproductive caste, and(2) either behavioral totipotency of only the more reproductivecaste (facultative eusociality) or totipotency of neither caste(obligate eusociality). We define "cooperative breeding" asalloparental care without castes. Cooperatively breeding societiesmay comprise two types, semisocial (distribution of lifetimereproductive success bimodal), and quasisocial (distributionof lifetime reproductive success unimodal), but this hypothesisrequires empirical analysis. Our definitions conceptually unifystudies of arthropod and vertebrate sociality.     

Energetic constraints and foraging efficiency

Previous research considers foraging options that differ interms of their gross rate of gain b and rate of energy expenditurec. This research argues that maximizing efficiency b/c willmaximize net energetic gain when there is an upper limit onthe amount of energy that can be assimilated. This analysisdoes not include the expenditure during the time for which theanimal is unable to forage because of this constraint. Whenthis expenditure is included, maximizing efficiency is no longeroptimal. Instead the best feeding option is the one with thehighest value of b/(c – c₁), where c, is the metabolicrate when the animal is not foraging.     

Energy expenditure, nestling age, and brood size: an experimental study of parental behavior in the great tit Parus major

A brood manipulation experiment on great tits Parus major was performedto study the effects of nestling age and brood size on parentalcare and offspring survival. Daily energy expenditure (DEE)of females feeding nestlings of 6 and 12 days of age was measuredusing the doubly-labeled water technique. Females adjusted theirbrooding behavior to the age of the young. The data are consistentwith the idea that brooding behavior was determined primarilyby the thermoregulatory requirements of the brood. Female DEEdid not differ with nestling age; when differences in body masswere controlled for, it was lower during the brooding periodthan later. In enlarged broods, both parents showed significantlyhigher rates of food provisioning to the brood. Female DEE wasaffected by brood size manipulation, and it did not level offwith brood size. There was no significant effect of nestlingage on the relation between DEE and manipulation. Birds wereable to raise a larger brood than the natural brood size, althoughlarger broods suffered from increased nestling mortality ratesduring the peak demand period of the nestlings. Offspring conditionat fledging was negatively affected by brood size manipulation,but recruitment rate per brood was positively related to broodsize, suggesting that the optimal brood size exceeds the naturalbrood size in this population.     

Dynamic discarding decisions: foraging theory for high-grading in a trawl fishery

The decision by fishermen to discard or retain fish of low valueto make room for more valuable fish in the hold of a boat (high-grading)is similar to diet choice problems faced by natural foragers.In our study, we apply the rationale of diet choice theory tohigh-grading behavior in the Oregon trawl fishery by treatingfishermen as foragers who must decide how much of each net'shaul to "ingest" before searching for more prey. We derive astate-dependent, temporal model of discarding behavior withina fishing trip. This optimization considers the availabilityof differently valued fish, trip quotas set by the regulatoryagency, and the risk of premature trip termination due to lossof gear or injury. The results indicate that those parametersaffect discarding behavior through their effect on the probabilityof exceeding the allowable catch, which we consider analogousto gut capacity. High-grading (partial prey consumption) occurredthroughout many simulated trips. The predictions were consistentwith the trends in discarding observed in the Oregon trawl fleet.Behavioral models such as ours can be useful to fishery managersby providing a means to explore the potential responses of fishermento new regulations before they are implemented.     

Tail loss reduces home range size and access to females in male lizards, Psammodromus algirus

Numerous lizard species use caudal autotomy as an antipredatordevice even though there must be significant costs during theperiod of tail regeneration. Strategies used by tailless individualsto enhance survival in natural populations are still poorlyunderstood. We experimentally examine tail loss in large, dominantmales of Psammodromus algirus in the middle of the breedingseason in the field. We report data showing home range reductionof large dominant males after autotomy, reduction in the numberof females in the home ranges of manipulated males, and a potentialincrease in mating opportunities of small subordinate maleswith complete tails. We conclude that changes in home rangeuse because of desertion of areas with less cover can resultin decreased predation risk at the cost of decreased accessto females.     

Suppressed breeding in the field vole (Microtus agrestis): an adaptation to cyclically fluctuating predation risk

The densities of microtine rodents and their main predators,small mustelids, fluctuate synchronously in 3–5-year cyclesin central and northern Fennoscandia. Predation by small mustelidshas been suggested as one of the driving forces in microtinecyclicity, causing deep synchronous declines of several volespecies. We studied experimentally the effects of small mustelidson mating behavior, foraging, and breeding in nonwintered fieldvoles (Microtus agrestis) originating from a cyclic population.By using mustelid odors, we simulated a crash phase environmentwith high predation risk for breeding pairs of voles. In ourexperiments, 87% of the female field voles suppressed breedingwhen exposed to mustelid odors. Both female and male behaviorchanged, and no mating behaviors were observed under the simulatedpredation risk. Weights of both sexes decreased when exposedto mustelid odor, probably due to decreased foraging; weightsof the control females increased due to pregnancy; and no weightchanges occurred in control males. Decreased breeding and foragingpossibilities under high predation pressure may form the basisfor the ultimate explanation for breeding suppression. Thereare at least two different mechanisms for breeding suppression:either mating does not take place or malnutrition in femalesdoes not' allow breeding to occur. Delayed breeding under highrisk of predation, for whatever reason, could increase the probabilityof individuals, especially that of the females, to survive overthe crash to the next, safer breeding season when their youngwould have better possibilities to survive.     

The effect of group size manipulations on the foraging behavior of black-tailed prairie dogs

Individuals foraging in large groups are thought to benefitbecause they are better able to detect and avoid predators.As a consequence, individuals in groups can adopt more risky,but rewarding, foraging behaviors without exposing themselvesto excessive danger. I experimentally manipulated the size ofblack-tailed prairie dog (Cynomys ludovicianus) groups to determineif individuals in large groups do forage in a more risky manner.I found that prairie dogs foraged more alertly and in less riskylocations (nearer to burrows, nearer to the center of the group,and in shorter vegetation) when group size was reduced. Effectsof group-size reductions were reversed when removed individualswere replaced, and persisted for at least three weeks in experimentswhere group size was permanently reduced. My results provideevidence that the relationships between group size and bothalertness and risk-place foraging are causal.     

Toward a theory of dominance hierarchies: effects of assessment, group size, and variation in fighting ability

We introduce assessment to the analysis of dominance hierarchiesby exploring the effect of an evolutionarily stable fightingrule when there is variation in resource holding potential (RHP)and RHP is not a perfectly reliable predictor of the outcomeof a fight. With assessment, the probability of a linear hierarchydecreases with group size but can remain appreciable for groupsof up to seven or eight individuals, whereas it decreases virtuallyto zero if there is no assessment. The probability of a hierarchythat correlates perfectly with RHP is low unless group sizeis small.     

Sexual cannibalism, competition, and size dimorphism in the orb-weaving spider Nephila plumipes Latreille (Araneae: Araneoidea)

The degree and direction of sexual dimorphism varies widely,but in several taxa of orb-weaving spiders, including Nephila,males may be less than one-tenth the size of females. This differenceis commonly attributed to selection through precopulation sexualcannibalism: females may either fail to detect very small males,or ignore them as potential prey items. However, there is oftenthe potential for male-male competition in these species becauseseveral males can be found on the web of a single female. Weinvestigated experimentally the effects of sexual cannibalismand male-male competition on male body size and hence sexualdimorphism in the Australian golden orb-weaver (Nephila plumipes).Small males were less likely to be detected and cannibalizedthan larger males. However, larger males excluded small malesfrom the central hub of the web, where mating takes place. Theconflicting effects of sexual cannibalism and male-male competitionmay be responsible for the relatively large variation in malebody size in this species.     

Dynamics of female choice for parental care in a fish species where care is facultative

In the peacock wrasse (Symphodus tinca), females either placetheir eggs in a nest under the care of a male or disperse theireggs widely so that they receive no protection. The same femalecan spawn in both modes. Females appear to prefer males withnests early in the nesting cycle, and they spawn less oftenthan expected in late-cycle nests and with non-nesting males.Survival and hatching success are consistently higher for eggsplaced in early nests, particularly in mid-season when egg predationis intense and hatching times are relatively long. Nevertheless,30%-80% of females place their eggs outside nests, even whenhatching success is more than four times greater with care.A model incorporating search time for nests correctly predictedthe qualitative changes in the tendency of females to choosecare or no care over the course of the mating season. Extensionsof the model suggest that in the early part of the season, whennests are rare and the relative survival advantage of parentalcare is small, females should sample no more than one nest beforeopting for no care. In mid-season, when the advantages of careare highest and between-nest travel times are low, females areestimated to visit at least 8 nests before abandoning the effort,corresponding to a giving-up time of about 43 min of search.Later in the season, when short hatching times reduce the relativebenefit of care, females are estimated to visit between 4 and5 nests before giving up, corresponding to about 31 min of search.We suggest that the variability in parental care in this speciesarises from seasonal changes in relative costs and benefitsof care for the two sexes.