Agonistic relationships between female mountain gorillas (Gorilla gorilla beringei)

Females in some mountain gorilla groups can be ranked on the basis of decided, non-aggressive approach-retreat interactions. However, data on four gorilla groups show that females do not form clear agonistic dominance hierarchies. Most aggressive interactions between females were undecided, and most dyads had undecided dominance relationships (Fig. 2). Females ignored aggression or responded to it aggressively more often than they responded submissively (Fig. 3). Moreover, directional inconsistency in aggression (including escalated contests) was high, and in some groups females showed significant bidirectionality in initiation of aggression (i.e., the more often they received aggression from partners, the more often they directed aggression at those partners; Fig. 4). Assigning ranks on the basis of aggressive interactions has limited power to explain variation in rates of initiating aggression and in responses and outcomes to aggression. Aggression was most common during feeding, but usually did not interrupt feeding bouts. It was proportionately more common in contexts that seem to involve competition for access to males (Figs 5, 6). This is consistent with the argument that females depend crucially on male services. As predicted by current models of female primate social relationships, agonistic relationships between gorilla females are unlike those typical in cercopithecine primates. They resemble those of some other primates and some equids in which contest competition for food is relatively unimportant and ecological costs of female transfer are low.     

Mate retention and male polyterritoriality in the pied flycatcher Ficedula hypoleuca

Summary We studied pair bond maintenance in the pied flycatcher in an experiment on nest predation at the incubation stage. Males defending one or more additional nestboxes (i.e. polyterritorial) on the day of nest predation were significantly more successful in retaining their mate than were the monoterritorial males (54% and 13% succeed, respectively). We manipulated the number of nest sites available for renesting, and found that the females remained preferentially with those males that had access to a new site, regardless of the previous territorial status of the male. Thus, the success of the polyterritorial males in mate retention was related primarily to the resource defended (a new nest site) rather than to some quality of the particular males per se. When the females could choose between alternative nestboxes for renesting, they selected the one located at the greatest distance from the initial site (Fig. 1). Male polyterritorial behaviour has previously been interpreted as a means of achieving polygyny. Our results show that this behaviour may be advantageous even in the absence of polygyny, especially at high levels of nest predation.     

Physical variability among nest foundresses in the polygynous social wasp,Polistes annularis

Summary An individual's rank in a dominance hierarchy is often based on size or weight, especially in insects. Foundresses of the social wasp, Polistes annularis, vary greatly in size as measured by wing length, dry weight, fat weight, and residue weight after fat has been extracted. Females that emerged from the same nest are much more similar in size to each other than they are to females that emerged from other nests. Within nests however queens are usually larger than their subordinates. Queens that emerged from one nest may be smaller than subordinates that emerged from another nest. We found no evidence of a group of females that are forced into being subordinates because of inadequate feeding as larvae. Females are also probably not attempting to begin new nests with females as different in size as possible from themselves since means and variances of winglength of females on new nests do not differ from those of all females emerging from that natal nest.     

Recruitment of mates and deceptive behavior by male Tengmalm's owls

Summary Tengmalm's owl Aegolius funereus is a hole-nesting polygynous species in which female nomadism is a reaction to cyclic lows of staple prey. For 2 years during a peak in vole abundance, I examined recruitment of mates and male singing behavior in a local population. Females and about half of the breeding males seemed to arrive successively throughout the breeding period of the first year. In contrast, a majority of the breeding males and likely also females were already on the breeding grounds at the beginning of the breeding season in the second year. Before breeding in the first peak year, males were singing at up to five different nest holes. All early breeding males (67% of total number) continued to sing at secondary nest holes after attracting and installing primary females. Secondary singing locations were never closer than 300 m from primary females' nest holes, although closer locations were used for singing before mating. All bigynous males with nests within the study area were also singing at tertiary nest holes, but none successfully attracted a third female. Polyterritoriality was confirmed by a late male settling between primary and secondary nest holes of a bigynous male. Polyterritorial behavior and reduced breeding success of secondary females are in line with the deception model. Females apparently could not discriminate between paired and unpaired singing males. Females made short visits to different males before mating. During courtship, the number and quality of nest holes defended by males may have been of particular importance to female choice.     

Sexual selection and variation in reproductive strategy in male yellow warblers (Dendroica petechia)

Summary Male yellow warblers (Dendroica petechia) exhibit extensive variation in the amount and conspicuousness of the sexually distinctive brown streaking on the breast. We investigated this intraspecific variation in degree of sexual dichromatism to see if male plumage rank (essentially the amount of brown streaking) is correlated with the amount of reproductive effort allocated to parental investment, as sexual selection theory would predict. As predicted, the average rate of feeding visits to the nest by males was negatively correlated with the plumage rank of the male in 1982 (Fig. 1) and 1983 (Fig. 2), and varied little between years or among study areas. Within one study area, the higher nest visit rate of dull (low plumage rank) males was correlated with higher nestling growth rates. But in the other two study areas, where bright (high plumage rank) males predominated, nestlings of bright males tended to have the highest growth rates despite minimal nest visit rates. Thus, overall there was no correlation between male plumage rank and nestling growth rate, a potential index of relative reproductive success, in either year (Figs. 3 and 4). This overall equal nest success likely helps to maintain the behavioral and plumage polymorphism. Since we could find no evidence that the high nestling growth rates of bright males were due to an adjustment of female parental effort to compensate for low male parental effort, there must be some other benefit of being bright which contributes to nest success. To address this, we used the relationship between parental feeding rates and nestling growth rates for each nest as an index of relative territory quality. This analysis suggests that bright males generally occupy the best territories available, possibly because they are more aggressive in obtaining and defending them than dull males. Dull males appear to be relegated to poorer territories, where an increase in male parental contribution would be necessary to achieve high nestling growth rates. We propose that different males are using alternative but evolutionarily stable reproductive strategies, in a way that is consistent with the predictions of sexual selection theory. Allocation of limited reproductive effort to parental investment decreases as sexual dichromatism increases, which probably reflects an increased investment in intermale competition for the best territories.     

Parental investment in two solitary wasps Ancistrocerus adiabatus and Euodynerus foraminatus (Eumenidae: Hymenoptera)

Summary Females of the solitary eumenid wasps Ancistrocerus adiabatus and Euodynerus foraminatus control the adult size of their offspring by the amount of food provded to the larvae. For both species, larger females provision more offspring and collect more food than smaller females. Males of E. foraminatus, upon emergence as adults, fight for control of the nest area. The winning brother remains at the nest and mates with his sisters as they emerge several days later. Males of A. adiabatus are not as agonistic as males of E. foraminatus so that a number of males may remain near the natal nest. When females nest near each other, male-male interactions increase, and the likelihood of sibling mating decreases. Under conditions of clumped nesting, females make larger offspring and invest more in males than when nesting in isolation.     

Behavioral tactics of subadult female floaters in the tree swallow

Summary There are large numbers of reproductively mature female tree swallows (Tachycineta bicolor) which do not breed due to limits of suitable nesting cavities. Many of these floaters are one-year-old females that have a distinctive subadult plumage. This study examines the behavioral tactics that these subadult female floaters use to obtain breeding opportunities. Early in the season, subadult floaters tended to intrude briefly (Fig. 4) on many nest sites in succession (Figs. 2, 3), although they rarely gained close access to nest sites (Fig. 5). Subadults responded very quickly to vacant nest sites, where the resident female had been experimentally removed, by entering the nest cavity and defending it from conspecifics. We argue that the early season exploratory behavior increases a subadult's chances of discovering a vacant nest site, rather than increasing its success in evicting resident females or laying eggs in other females' nests. During the nestling period, subadult females intruded on fewer nest sites for longer periods, and often gained close access to the nest site. Late in the season, subadult floaters may be gathering information on the quality of nest sites for the next breeding season, rather than searching for current breeding opportunities. The reproductive tactics of subadult female tree swallows are consistent with the breeding threshold model for the evolution of delayed plumage maturation in passerines.     

Reproductive allocation in female house wrens is not influenced by experimentally altered male attractiveness

The differential allocation hypothesis proposes that females mated to attractive males should invest more resources in their offspring than those mated to less-attractive males, whereas the compensation hypothesis posits that females mated to less-attractive males should invest more resources in their offspring to compensate for lower-quality young. We tested these hypotheses by manipulating attractiveness of male house wrens (Troglodytes aedon) prior to female arrival by adding extra nest sites to territories of some males while leaving control males with only a single nest site. Females laid their eggs sooner in the nests of attractive males, and attractive males were more likely to retain their territory over successive broods and were marginally more likely to obtain a mate for a second brood later in the season than were control males, thereby confirming the effect of our manipulation on male attractiveness. Experimentally enhanced attractiveness also led to increased hematocrit in males. However, there were no consistent differences in the number, size, or quality of eggs laid by females mated to attractive and control males, nor were there any differences in the size, health state, or immune function of nestlings produced from these eggs. There was also no effect of treatment on the number of nestlings surviving to fledging. Collectively, these results are inconsistent with both the differential allocation hypothesis and the compensation hypothesis. Future studies should consider the possibility that the criteria used by females in selecting a mate may vary temporally and be more flexible than generally thought.     

How western meadowlarks respond to simulated intrusions by unmated females

Summary Western meadowlarks (Sturnella neglecta) were played back female calls at various stages of their breeding cycles, to examine how residents might respond to unmated females. Females reacted to intruders with aggressive displays and other responses that varied in intensity (Table 1). Males reacted not only to playback, but also to their mates' responses, often intervening in them. The responses of both males and females, however, were strongly affected by the stage of the breeding cycle at which an intrusion was simulated (Table 3). Females responded to playback most strongly before they began incubating eggs; thereafter, the strength of their responses declined rapidly. Males' also responded less strongly at later stages of their mate's nesting cycle, but the strength of their responses declined less rapidly than did the females'. When the reactions evoked from mated individuals were compared, females responded at least as strongly as their mates, until after their young had fledged (Fig. 3). These seasonal changes in the intensity of females' responses suggest that decisions about how strongly to respond take account of the costs of responding to an intruder, as well as its benefits. Our results suggest that interactions among mated and unmated females may affect the timing of bigamy and, in some cases, its incidence as well.     

Food and the deceptive acquisition of mates by polygynous male harriers

Summary Female northern harriers Circus cyaneus are polygynous, marsh-nesting raptors, whose mate choices are enigmatic. I determined the mate choice cues employed by females by correlating the order in which males were chosen with characters that 1) significantly influenced reproductive success; 2) were assessable prior to settlement; and 3) varied between breeding situations. Only nest sites and male provisioning performance met all these conditions: wet nest sites significantly (P<0.05) increased nest survival and high provisioning rates significantly (P<0.01) enhanced brood survival. The order in which females settled was strongly correlated with provisioning performance in both years (r _s -0.65, and r _s -0.84), but not with nest site quality. Females thus apperared to choose males principally on provisioning performance. Despite using the same cue, however, females choosing mated males reared only 0.28 young for every nestling raised by concurrently settling monogamous females (the lowest ratio recorded for any avian species). Extrapolation of male courtship provisioning patterns from clutch sizes and laying date indicated that females received similar proportions prior to and during egg-laying, but that males later preferentially fed females. Secondary females therefore chose mated males on the basis of a temporally changing and unreliable cue. The polyterritoriality, cooperative harems, skewed sex ratio, and sexy-son hypotheses were all inadequate in explaining polygyny in harriers. Female choice of mated males among harriers is best explained by the deceitful provisioning of food by males.     

Infanticidal and anti-infanticidal strategies in the swallow Hirundo rustica

Summary Five definite and nine suspected cases of infanticide were documented in the swallow Hirundo rustica. Unmated males visited neighbouring nests and removed entire broods during the first days of the nestling period, preferentially from nests owned by young late-breeding individuals. Infanticide followed the disappearance of the male nest owner in 11 of the 14 cases. The unmated infanticidal male later mated with the female victim although renesting during the same season only took place in 12 of the 14 cases. The fraction of unmated males increased with colony size, and infanticide was relatively more common if unmated males were abundant. Females did not engage in extra-pair copulations in order to avoid infanticide. Intense guarding of the nest and its contents prevented infanticide. Nest guarding intensity was higher in colonial compared with solitarily breeding swallows, and guarding intensity increased with colony size. Experimental removal of male swallows during the early nestling period reduced the nest guarding intensity and increased frequency of visits from unmated males in colonies, but not among solitarily breeding swallows. Colonial nests from which the male was removed suffered from infanticide more often than solitary nests, and nests where infanticide was recorded were guarded significantly less intensely than other nests before the infanticidal incidents.     

Dispersion of displaying male sage grouse

Summary The degree to which male sage grouse select lek sites and females select nesting sites to maximize proximity to the other sex was examined by contrasting male dispersions with the dispersions and movements of females in the months preceeding incubation. Wintering females exhibit highly overlapping ranges due to shared use of central refuging areas. In late winter and early spring, females move an average 9 km from wintering areas to select nest sites and males begin occupying leks. Pooled evidence suggests that females select nest sites independently of male dispersion whereas males adjust lek occupation so as to maximize proximity to females. Relevant observations include females visiting nest sites before leks, moving further to select a nest site than to select a lek, and increasing their distance to leks as a result of selecting nest sites. In addition, males avoid leks until females have moved to within 5 km of the arenas, abandon early season leks as local female densities drop, and exhibit dispersions in which mean ratios of females/male are similar across leks. Contrasts between predicted and observed dispersions of males showed that hotspot settlement models are adequate to explain male dispersions on very coarse scales (2 km or greater); on finer scales, habitat preferences of males and tendencies for males to cluster tightly must be invoked in addition to hotspots to explain specific lek sitings.     

Discrimination between nestmate and non-nestmate kin by social wasps (Polistes fuscatus,Hymenoptera: Vespidae)

Summary The threespine stickleback,Gasterosteus aculeatus is a voracious cannibal of both its own eggs and those of conspecific neighbours. Females, but not males, can distinguish their progeny from those of other fish and attacked alien eggs more frequently. In experiments to examine nest raiding, females that initiated raids on nests resulting in cannibalism were the first females to spawn in the reconstructed nest. These results support the hypothesis that cannibalism by females may be adaptive in situations where intense female competition for male guardians occurs.     

Provisioning of nestlings by dunnocks,Prunella modularis,in pairs and trios compensation reactions by males and females

Summary The mating systems in a population of dunnocks included monogamy, polygyny, polyandry and polygynandry. Broods were provisioned by lone females, by females with the part-time help of one male, by females with the full-time help of one male (pairs) or by females with the part-time or full-time help of two males (trios). We compared provisioning of nestlings in these different systems and used the results of natural and experimental removals to examine how individuals reacted to the provisioning by others. In pairs, males and females provisioned at similar rates (Fig. 2a). In trios, females and alpha males fed chicks at the same rate, and at a higher rate than beta males (Fig. 2b). Females attained maximum male help when two males shared provisioning equally (Fig. 6). Females were more likely to achieve this when they were able to escape alpha male guarding during the mating period and exercise some control over mating access by the two males (Fig. 7). Female provisioning did not increase when their help was reduced from two males to one (Fig. 4 a), but it did increase when male help was further reduced to either one male's part-time help (Fig. 5 a) or no male help (Fig. 3 a). Beta males increased their provisioning rate when alpha males were removed from a trio (Fig. 4b). Alpha males may have increased their rate when beta males were removed but any reaction was small. When one male was removed from a trio, the remaining male's provisioning rate was as expected for a male in a monogamous pair. When reactions occurred, they were not sufficient to compensate for the loss of the removed adult and nestling weight was reduced. We discuss the relevance of these results to the maintenance of parental care by pairs and trios.     

The costs of male parental care and its evolution in a neotropical frog

Summary Parental care is practiced exclusively by males of the Puerto Rican frog, Eleutherodactylus coqui. Males brood clutches of direct-developing eggs in non-aquatic nest sites and defend eggs against cannibalistic nest intruders. Here, I report on energetic and mating costs incurred by males that provide parental care, and suggest how these proximate costs affect male fitness and the evolution of male parental care in this species. Energetic costs are small for brooding males in comparison to non-brooding, calling males. Brooding males had a higher frequency of empty stomachs and lost small, but significant, fractions of their initial body mass during parental care. Abdominal fat bodies of brooding males during the middle third of parental care were significantly smaller than those of calling males; those of males brooding eggs in earlier or later stages were not different. The mating cost of parental care is greater. Most brooding males cease calling during parental care. However, gravid females are available (i.e., known to mate) on most nights during the principal breeding season; hence non-calling males miss potential opportunities to mate. A mating cost was estimated by calculating nightly mating probabilities for calling males in a plot where nightly calling male densities and daily oviposition schedules were known. On average, a male exhibiting normal calling behavior would be expected to obtain a new mate once every 35.7 days. Hence a brooding male that ceased calling for a 20-day parental care period would miss, on average, 0.56 additional mates. Males that were more successful than average in attracting mates could miss up to 1.63 matings. A marginal value model (Fig. 1) is used to analyze the net effect on male fitness of parental care benefits and costs in E. coqui (Fig. 3). The model indicates that males garner the highest reproductive success by providing care from oviposition through hatching. There is no stage during the pre-hatching period at which a desertion strategy would yield higher reproductive success. In fact, the model suggests that males should provide full parental care even in the face of much higher mating costs than currently obtain in the system.     

Female choice for complex song in the European starling: a field experiment

Male European starlings Sturnus vulgaris sing long complex songs that appear to be important in the courtship of females but which also influence competitive interactions between males. We tested the hypothesis that females choose mates on the basis of the complexity of their songs, rather than on the quality of the territories the males defended. In order to determine whether certain territories were preferred over others, the first set of birds to settle in the experimental nest-boxes was removed and a second set allowed to settle. Consistent preferences for certain nest-boxes were indicated by correlations between the settlement patterns of the first and second sets of birds. However, males with the most complex song did not necessarily occupy the most preferred nest sites. Males with more complex song acquired mates faster. This relationship remained significant when nest-site preference was statistically controlled, indicating that female starlings chose males with complex song rather than those that defended preferred nest sites. A number of morphological variables were also found to be uncorrelated with female choice. Song complexity in European starlings increases with age, and the evolution of song complexity in this species is consistent with an age-indicator model of sexual selection. Males with larger repertoires were also in better condition, indicating that females obtain high-quality mates by choosing on the basis of male song. Received: 29 April 1995/Accepted after revision: 9 September 1995     

Choice and utilization of oviposition sites by female Calopteryx maculata (Odonata: Calopterygidae)

Summary Females of the damselfly Calopteryx maculata (de Beauvois) initially choose the larger of a pair of adjacent oviposition sites, about 70% of the time (Table 1), or whichever of two equal sized sites had other ovipositing females on it (about 88% of the time-Table 2). These criteria for initial choice between a pair of sites also interact. Incoming females generally (57 to 74% of the time-Table 3) joined others on the small site rather than ovipositing alone at the adjacent, bigger site. When pairs of large and small sites were replicated across eight locations, there were nonsignificant trends towards greater utilization (eggs laid) of the larger of a pair of oviposition sites within locations (Table 4). The lack of agreement between initial choice and utilization shows that other factors besides size are important in the choice and use of oviposition sites. These include disturbance by males, the presence of other females and choice criteria that can only be assessed during oviposition. When all sites at the eight locations were equal in size, there was considerable day to day and location to location variation in eggs laid (Fig. 1). Viewed over periods of several days, some sites are obviously less attractive than others in terms of cumulative numbers of eggs laid at them. When the amount of vegetation was varied among locations, those with the bigger oviposition sites were used more often, somtimes significantly so, but there were also significant reversals (small sites used more often) (Table 5, Fig. 1). Thus, there is no simple effect of size on the utilization of oviposition sites by Calopteryx maculata females, despite a clear tendency for females to make initial choices based on this criterion. The considerable among and within location variation in number of eggs laid may reflect additional choice criteria or the interaction of size, the presence of other females, disturbance, and location.     

Polygyny and male parental care in Savannah sparrows: effects on female fitness

Summary To determine the effects of male mating status on female fitness, we compared the reproductive success, survival, and future fecundity of female Savannah sparrows (Passerculus sandwichensis) mated to monogamous vs. polygynous males in a 5-year study on Kent Island, New Brunswick, Canada. The proportion of males with more than one mate varied from 15 to 43% between years and sites. Polygynous and monogamous males fledged young of equal size in every year of the study. Females who shared paternal care with other females laid as many eggs per clutch and clutches per season as monogamously mated females. In most years polygynously mated females showed no delay in laying a second clutch, and they suffered no reduction in fecundity the following year. Recruitment of a female's offspring into the breeding population was generally independent of her mating status. Fitness costs of being mated to a polygynous male were only apparent in one year of the study, during which females mated to polygynous males had higher over-winter mortality than those mated to monogamous males. That same year, young raised by polygynous males were only one-third as likely to survive to reproductive maturity (as inferred by returns) as those raised by monogamous males. A male's mating status had no effect on his own survivorship. A male's mating status did not necessarily reflect his contributions to raising nestlings, which may partially explain why monogamously and polygynously mated females had equal fitness. At 35 nests the proportion of food deliveries brought by individual males varied from 0 to 75%; on average, males brought fewer than 30% of all food deliveries. Yet parental care by polygynous males was no less than that of monogamous males, at least at the nests of their primary females. Secondary females tended to receive less male assistance during the nestling stage, but their reproductive success was indistinguishable from that of primary females. Females feeding young without male assistance made as many food deliveries/h as did pairs in which males brought at least 30% of all food deliveries. Unassisted females did not suffer diminished fledging success or produce smaller fledglings. The benefits of polygyny for male Savannah sparrows are clear: polygynous males recruit more surviving offspring into the breeding population than monogamous males. The fitness of females, on the other hand, appears to be unaffected by whether their mate was monogamous or polygynous except in occasional years. Polygyny may be maintained in this population by the constraints of a female-biased sex ratio, the inability of females to predict a male's paternal care based on his morphology or behavior, the poor correlation between a male's mating status and his assistance at the nest, and inconsistent natural selection against mating with a polygynous male. Correspondence to: N.T. Wheelwright     

Advertisement-call modification,male competition,and female preference in the bird-voiced treefrog <Emphasis Type="Italic">Hyla avivoca</Emphasis>

Senders and receivers influence dynamic characteristics of the signals used for mate attraction over different time scales. On a moment-to-moment basis, interactions among senders competing for a mate influence dynamic characteristics, whereas the preferences of receivers of the opposite gender exert an influence over evolutionary time. We observed and recorded the calling patterns of the bird-voiced treefrog Hyla avivoca to assess how the dynamic characters of calls vary during interactions among groups of males in a chorus. This question was also addressed using playback experiments with males. Playback experiments with females showed how changes in dynamic call properties are likely to affect male mating success. Frogs calling in pairs, groups, or in response to playbacks produced longer calls than did isolated males. During call overlap, males often increased the duration of the silent interval (gaps) between the pulses of their calls so that the pulses of the calls of two neighbors interdigitated. This change resulted in increased variability of pulse rate, a traditionally static acoustic property; however, males also produced high proportions of non-overlapped calls in which variability in pulse rate was low and had species-typical values. Females preferred long calls to short- and average-duration calls, and non-overlapped calls to overlapped calls. Given a choice between pairs of overlapped calls, females preferred pairs in which the proportion of overlap was low and pairs in which the pulses of such calls interdigitated completely. The observed patterns of vocal competition thus reflect the preferences of conspecific females, which have influenced the evolution of the calling behavior of H. avivoca. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Determinants of parental effort: a behavioural study in the Eurasian kestrel,Falco tinnunculus

We recorded behaviour of kestrels (Falco tinnunculus) in western Finland during the courtship (1988–1992), incubation (1989–1991), early nestling (age of young 1–2 weeks, 1989–1992) and late nestling stages (3–4 weeks, 1989–1991) to examine determinants of their parental effort (PE). In males, PE was estimated as the hunting effort (the proportion of budget time spent in flight-hunting) and in females as the food provisioning rate (number of prey items delivered to the nest per hour). The following predictions derived from the parental investment theory were examined. (1) Parents rearing large clutches and broods should invest more in breeding than do parents rearing small clutches and broods. The hunting effort of parents did not increase with clutch or brood size, but males tending large broods had a higher prey delivery rate than males tending small broods (Figs 1–2). (2) PE of parents should increase in the course of the breeding season. In males, this was true only between the incubation and early nestling phases (Fig. 3). (3) The early pairs should invest more in breeding than late ones. This tended to be true during the early (for males) and late nestling phases (for females) (Fig. 4). (4) There should be a negative correlation between PE of mates within pairs, but no evidence for such adjustment was found (Fig. 5). (5) Females mated with bright-coloured attractive males should show higher PE than females mated with dull-coloured males but our results were inconsistent with this prediction. We conclude that PE decisions of kestrels are mainly based on cost-benefit estimates of residual reproductive value, rather than on current investment indicators, like clutch or brood size. This might be beneficial in environments with highly variable survival prospects of offspring caused by pronounced among-year variation in abundance of the main food (microtine rodents). The results also show that hypotheses explaining variation in PE in the short term are not necessarily valid for long-term PE, e.g. tending clutches or broods, which also reflects the demands of female and young.