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1.
Behavioral data were collected during the breeding season on eight pairs of Hawaiian crows (Corvus hawaiiensis) housed at two facilities on different islands. All data were collected from videocamera time‐lapse recordings of the nesting platforms. Behaviors included frequency of nest cup manipulation, percent of time spent on nest, allopreening, play, and stereotypy. The number of breeding pairs increased from four in 1996 to six in 1997, to seven in 1998, and to eight in 1999. Five of the older birds (three males and two females) were solitary‐reared for most if not all of their first year, while the remaining 12 birds were all socially reared. Significant differences were found between isolate‐ and socially‐reared birds, with isolate‐reared birds having higher rates of solo play (P = 0.0041) and stereotypies (P = 0.0090). Pairs that were comprised of at least one isolate‐reared bird engaged in significantly less allopreening (P = <0.0001) than pairs in which both birds were socially reared. From 1996 to 1999, 87 eggs were laid, with a mean of 1.88 ± 0.24 SEM eggs per clutch. Only three females produced clutches every year, and they were responsible for 85.1% of the eggs laid. Although not significant, the mean number of clutches produced per pair decreased from 2.50 ± 0.65 in 1996 to 0.87 ± 0.99 in 1999. Age of females does not appear to be a critical factor in the decrease in clutch production. New pairing combinations are under way in an effort to improve propagation in this highly endangered species. Zoo Biol 21:59–75, 2002. © 2002 Wiley‐Liss, Inc.  相似文献   

2.
This article reports biparental mouthbrooding of the bagrid catfish Phyllonemus filinemus in Lake Tanganyika, based on analysis of specimens collected during SCUBA diving. This catfish was nocturnally active, and in the daytime it was concealed singly or in pairs beneath rocks. Within a breeding pair, the male or female alone incubated all the brood in the mouth until the offspring attained 12 mm or so in total length, but thereafter joint mouthbrooding or guarding by both parents took place. Most females of nonbrooding pairs showed high values of gonadosomatic index (GSI), whereas all females of brooding pairs and most single females showed low GSI values. This fact indicated that a pair is formed at a time near the gonadal maturation of the female and separates after the brood is reared. No significant difference in body condition among parents of different reproductive states was observed, which suggested that their condition does not deteriorate markedly as the result of foraging by an off-duty parent. Received: September 16, 2000 / Revised: November 18, 2000 / Accepted: January 23, 2001  相似文献   

3.
Pair‐living and a monogamous mating strategy are rare and theoretically unexpected among mammals. Nevertheless, about 10% of primate species exhibit such a social system, which is difficult to explain in the absence of paternal care. In this study, we investigated the two major hypotheses proposed to explain the evolution of monogamy in mammals, the female defence hypothesis (FDH) and the resource defence hypothesis (RDH), in red‐tailed sportive lemurs (Lepilemur ruficaudatus), a nocturnal primate from Madagascar. We analysed behavioural data from eight male–female pairs collected during a 24‐mo field study to illuminate the determinants of pair‐living in this species. Male and female L. ruficaudatus were found to live in dispersed pairs, which are characterised by low cohesion and low encounter rates within a common home range. Social interactions between pair partners were mainly agonistic and characterised by a complete absence of affiliative interactions – body contact was only observed during mating. During the short annual mating season, males exhibited elevated levels of aggression towards mates, as well as extensive mate guarding and increased locomotor activity. In addition, males were exclusively responsible for the maintenance of proximity between pair partners during this period, and they defended their territories against neighbouring males but not against females. Together, these results point towards the importance of female defence in explaining pair‐living in L. ruficaudatus. We discuss the spatial and temporal distribution of receptive females in relation to the female defence strategies of males and suggest possible costs that prevent male red‐tailed sportive lemurs from defending more than one female.  相似文献   

4.
Mating behaviour often increases predation risk, but the vulnerability within mating pairs differs between the sexes. Such a sex difference is expected to lead to differences in responses to predation risk between the sexes. In the two‐spotted spider mite Tetranychus urticae, males engage in pre‐copulatory mate guarding because only the first mating results in fertilisation. We investigated (i) whether pre‐copulatory pairs are more conspicuous to the predatory mite Phytoseiulus persimilis than solitary females, (ii) whether the vulnerability to the predator differs between sexes within the pre‐copulatory pair, (iii) whether each sex of T. urticae responds to predation risk during pre‐copulatory mate guarding and (iv) whether T. urticae's response to predation risk affects predator behaviour. Because T. urticae females are immobile during pre‐copulatory mate guarding, we observed male behaviour to evaluate effects of predation risk. We found that the predators detect more pre‐copulatory pairs than solitary females and that more females than males of the pre‐copulatory pairs are preyed upon by the predators. The preference of spider mite males for pre‐copulatory pairs versus solitary females was affected by whether or not the female had been exposed to predators during development. Male T. urticae exposed to predation risk did not alter their behaviour. These results suggest that only the most vulnerable sex, that is the female, responds to predation risk, which modifies male behaviour. Regardless of T. urticae females’ experience, however, P. persimilis detected more T. urticae pre‐copulatory pairs than solitary females, suggesting that pre‐copulatory mate guarding itself is dangerous for T. urticae females when these predators are present. We discuss our results in the context of sex‐dependent differences in predation risk.  相似文献   

5.
A total of 1527 specimens of poor cod, Trisopterus minutus, was collected by trawl fishing between April 2001 and March 2002 from the ?zmir Bay (Middle Aegean Sea). Fish size ranged from 10.6 cm total length (TL, minimum) in September to 24.8 cm TL in April. Of the sampled population 53% were males and 41% females (sex ratio female : male = 1 : 1.3). Length–weight relationships were determined for males, females and combined sexes as W = 0.007L3.16, W = 0.009L3.04 and W = 0.007L3.14 respectively.  相似文献   

6.
D. G. Reid    P. Abello    C. G. Warman    E. Naylor 《Journal of Zoology》1994,232(3):397-407
The relationship between the size of a given mating male Carcinus maenas (L.) (Brachyura, Portunidae) and the size of the female with which it was paired was studied for 1248 pairs of crabs collected from the shore In 764 of these pairs the female was in pre-moult and so the pair were in pre-copula. In the remaining 484 pairs the female had already moulted and the pairs were in copula. There were significant correlations between the sizes of the males and females in both pre-copula and copula pairs. It was found that male Carcinus collected in mating pairs and tested in the laboratory were unable to distinguish between females in terms of their size or stage of pre-moult. The positive correlation between the sizes of males and females in mating pairs on the shore is proposed to be, in part, a function of a mechanical constraint of the size of female that a given male can hold, defend and copulate with. In addition, encounters between solitary males and males carrying females, resulting in the formation of new pairs, appear to enhance the size-related mating pattern observed.  相似文献   

7.
Symbiotic crustaceans are expected to live solitarily with their hosts when members of their host species are small (relative to symbiont body size) and structurally simple. We tested the hypothesis of a solitary lifestyle in Ascidonia flavomaculata, a symbiotic shrimp that inhabits the branchial chamber of the relatively small and structurally simple tunicate Ascidia mentula in the subtidal zone of the Islas Baleares, Spain. We found that members of A. flavomaculata dwell as solitary individuals in the branchial chamber of ascidians at a higher frequency than expected by chance alone. Given this host use pattern of A. flavomaculata, we hypothesized that males actively move among host individuals in search of receptive females. We provide several lines of evidence consistent with that hypothesis. First, a positive correlation between shrimp and host body size was detected for females, but not for males, during one of the sampling seasons. If males as well as females spend long periods of time within their host individuals, a positive correlation between shrimp and host body size should have been found for both males and females. Second, the body sizes of individuals in the few male‐female pairs observed during this study were poorly correlated. If males of A. flavomaculata shared their host individuals with females for long periods of time, a positive correlation between the sizes of males and females in a pair should have been found. Lastly, the body sizes of paired males were larger than those of solitary males during summer, when reproduction was more intense. This difference in body size between paired and solitary males additionally suggests competition among putatively roaming males for receptive females. Manipulative experiments and behavioral observations are necessary to reveal the details of the mating system of A. flavomaculata and other symbiotic crustaceans with a solitary lifestyle.  相似文献   

8.
Reproductive behavior and mate fidelity of the gobiid fish,Valenciennea longipinnis, were studied on the coral reef at Sesoko Island, Okinawa, Japan. These fish usually live in pairs, not only foraging together for benthic animals in sandy areas, but also constructing several burrows within their home range. Before spawning, both fish, although mainly the male, constructed a mound, piling up dead-coral fragments, pebbles, shells, sand and algae onto one of the burrows. After spawning an egg mass on the ceiling of the burrow, the female stayed outside and continued the construction and maintenance of the mound for 3–5 days until hatching, while the male tended the eggs inside. Mate guarding of females seemed to prevent males from monopolizing several females. Although some pairs showed mate fidelity through several spawnings, more than half of the pairs broke up after only one spawning. The pair bond was broken by mate desertion and the disappearance of each sex. Both sexes preferred larger spawning partners; larger females spawned more eggs and larger males provided better egg care. Mate desertion occurred when larger potential mates, relative to the current partner, became available. The frequency of solitary individuals was higher in males than in females, resulting in females deserting their mates more often than males. Two factors seem to have facilitated mate desertion: (1) occurrence of size mis-matched pairing and (2) overlapping home ranges.  相似文献   

9.
Harassment on mating pairs by solitary males is usually considered an attempt by the male to (1) take over the female, (2) guard the female against further insemination (when the solitary male has previously copulated with this female), or (3) influence mating duration. Paired males of a seed bug repel harassment on mating pairs by solitary males by firmly grasping females using their legs and/or genital claspers; in this way, mating duration is prolonged. Male fertilization success increases as mating duration increases. Males of the seed bug, Togo hemipterus (Scott) (Heteroptera: Lygaeidae), use seminal substances to inhibit female remating. These substances induce protracted female refractory periods and are transferred to the females in a time‐dependent manner. Consequently, mating duration has important effects on fitness in this species. We observed harassment on T. hemipterus mating pairs by solitary males, and examined conflicts between paired and solitary males over mating duration. None of the solitary males were able to take over a mating female, and this may be due to the unique male genital structure in this species. All conflicts over mating duration resulted in wins by the paired males over the solitary males. Paired males prolonged mating durations, whereas severe harassment on mating pairs by solitary males shortened durations. We show that even though there is no immediate reward for the solitary male (i.e., it is unable to take over the mating female), this harassment behavior may be adaptive.  相似文献   

10.
A pair‐living social organisation can typically be explained by obligate biparental care. We investigated pair‐living in the absence of biparental care in the Australian sleepy lizard, Tiliqua rugosa, which forms exceptionally strong pair bonds. We fitted 10 lizards, five male–female pairs, with Global Positioning System (GPS) recorders and continuously monitored social associations and separations between active pair partners, based on location records taken every 10 min over 3 mo. Males temporarily separated and reunited the pair more frequently than females, but females also contributed to the maintenance of the pair bond. These behavioural data were consistent with the hypothesis that females successfully coerce males into associations with one female. Lower frequencies of social association between pair partners once mating had finished support this interpretation. Males that are coerced into pair associations appear to experience higher costs of pair‐living than females, because males initiated temporary separations of the pair more frequently than females. Males showed higher movement activity and remained active later each day. This sex bias in activity may be an important mechanism to mitigate the higher costs of pair‐living for males. Costs for males might include within‐pair competition for food as females appear more competitive. Our study provides detailed empirical data on a lizard pair bond and provides important insights into pair‐living in the absence of biparental care.  相似文献   

11.
The last recorded presence of the Eurasian otter (Lutra lutra) in the Netherlands dates from 1989 and concerned a dead individual. In 2002 a reintroduction programme was started, and between June 2002 and April 2008 a total of 30 individuals (10 males and 20 females) were released into a lowland peat marsh in the north of the Netherlands. Noninvasive genetic monitoring based on the genetic profiles obtained from DNA extracted from otter faeces (spraints) was chosen for the post-release monitoring of the population. To this end, the founding individuals were genotyped before release and spraints were collected in the release area each winter from 2002 to 2008. From June 2002 to April 2008 we analysed the genetic profile of 1,265 spraints on the basis of 7–15 microsatellite loci, 582 of which (46%) were successfully assigned to either released or newly identified genotypes. We identified 54 offspring (23 females and 31 males): the females started to reproduce after 2 years and the males after 4 years. The mating and reproductive success among males was strongly skewed, with a few dominant males fathering two-thirds of the offspring, but the females had a more even distribution. The effective population size (Ne) was only about 30% of the observed density (N), mainly because of the large variance in reproductive success among males. Most juvenile males dispersed to surrounding areas on maturity, whereas juvenile females stayed inside the area next to the mother’s territory. The main cause of mortality was traffic accidents. Males had a higher mortality rate (22 out of 41 males (54%) vs. 9 out of 43 females (21%)). During winter 2007/08 we identified 47 individuals, 41 of which originated from mating within the release area. This study demonstrates that noninvasive molecular methods can be used efficiently in post-release monitoring studies of elusive species to reveal a comprehensive picture of the state of the population.  相似文献   

12.
Among the factors that may contribute to the evolution of social monogamy are selection for extended mate guarding of females and selection for territorial ‘cooperation’. Many socially monogamous taxa are also territorial, with ‘partners’ sharing a single territory, suggesting that one or both partners may benefit by sharing territorial maintenance. Snapping shrimp (genus Alpheus) are socially monogamous and territorial, living in excavated burrows or with host organisms, with females performing all parental care. The territorial cooperation hypothesis predicts that male and female partners share (1) territorial defence, resulting in a reduction in the risk of eviction from the burrow, (2) burrow construction duties, such that individuals in pairs spend less time in burrow construction relative to solitary individuals, and/or (3) foraging duties, by returning food to the burrow, where it is consumed by both partners. UsingA. angulatus as a model species, a territorial defence experiment revealed that females in pairs were significantly less likely than solitary females to be evicted by female intruders, but males in pairs were not significantly less likely than solitary males to be evicted by male intruders. A subsequent experiment revealed that paired males were significantly less likely to be evicted by an intruding male if paired with sexually receptive females than if paired with nonreceptive females. Another experiment revealed that (1) paired females spent significantly more time in burrow construction than paired males, and (2) both males and females consistently returned food items to the burrow, perhaps incidentally provisioning their mates. These data suggest that social monogamy may have been selected for in part because of the advantages of territorial cooperation, as both males and females are likely to benefit by dividing the labour of territorial defence and maintenance. These tests of the territorial cooperation hypothesis are synthesized with data from tests of the extended mate-guarding hypothesis to place snapping shrimp pairing behaviour into a larger construct incorporating both the influence of ecological pressures (territoriality) and mating interactions between the sexes. Copyright 2002 The Association for the Study of Animal Behaviour. Published by Elsevier Science Ltd. All rights reserved.  相似文献   

13.
Many vertebrates form monogamous pairs to mate and care for their offspring. However, genetic tools have increasingly shown that offspring often arise from matings outside of the monogamous pair bond. Social monogamy is relatively common in coral reef fishes, but there have been few studies that have confirmed monogamy or extra‐pair reproduction, either for males or for females. Here, long‐term observations and genetic tools were applied to examine the parentage of embryos in a paternally mouth‐brooding cardinalfish, Sphaeramia nematoptera. Paternal care in fishes, such as mouth‐brooding, is thought to be associated with a high degree of confidence in paternity. Two years of observations confirmed that S. nematoptera form long‐term pair bonds within larger groups. However, genetic parentage revealed extra‐pair mating by both sexes. Of 105 broods analysed from 64 males, 30.1% were mothered by a female that was not the partner and 11.5% of broods included eggs from two females. Despite the high paternal investment associated with mouth‐brooding, 7.6% of broods were fertilized by two males. Extra‐pair matings appeared to be opportunistic encounters with individuals from outside the immediate group. We argue that while pair formation contributes to group cohesion, both males and females can maximize lifetime reproductive success by taking advantage of extra‐pair mating opportunities.  相似文献   

14.
Female‐initiated pair formation and mating were observed during long term observations of lobsters (Homarus americanus) in seminatural environments. Females left their solitary shelters and selected the company of dominant, territorial males as much as 7 days before molting. During subsequent pair formation and shelter sharing a number of new behavior patterns were observed, some previously not reported for other Crustacea. Both behavioral displays and a female sex pheromone appear to be involved in pair formation. Mating took place one half hour after the female molted. After mating, pairs remained together in the male's shelter for up to an additional 7 days. During this time males fed on the molt shell and actively defended the area. Females of 58–70 mm carapace length showed varying levels of incomplete pair formation and mating behavior, indicating that courtship and mating behavior may require a number of molts to develop. This size class forms a behavior‐ally defined transition stage. Females larger than 75 mm were behaviorally mature.

Pair formation in lobsters appears to protect mature, postmolt females against predation and cannibalism and to insure the reproductive success of dominant males. These observations provide a more natural behavioral context for the function of a sex pheromone in Homarus americanus.  相似文献   

15.
Comparison of male field crickets (Gryllus veletis and G. pennsylvanicus) collected either by themselves (solitary) or with one or more females (paired) showed that the paired males were significantly older and significantly less parasitized by gregarines (protozoan gut parasites) than were solitary males. Body size did not differ between the two groups. These results corroborate earlier experimental findings that females are preferentially attracted to older males and suggest that the ability of less parasitized males to produce more spermatophores under laboratory conditions may also be important in the field. Calculation of sexual-selection differentials and gradients for G. pennsylvanicus did not reveal any indirect selection on body size and confirmed the strong selection on male age.  相似文献   

16.
Coloration in birds can act as an important sexual signal in males, yet in many species, both sexes display bright colors. Social selection may account for this pattern, with more brightly colored individuals pairing together on the best territories. Mutual mate choice may also explain this, as males investing a great deal of parental care in the offspring should be choosy about their social mates. It is less clear whether this pattern of mate choice can apply to extra‐pair partners as well. We examined western bluebirds (Sialia mexicana) to determine whether more colorful individuals tended to pair with one another, both in social pairs and between females and their extra‐pair partners. Both male and female western bluebirds display both UV‐blue structural plumage and a melanin‐based chestnut breast patch, although females are duller than males. Social pairs mated assortatively with regard to UV‐blue brightness, but not chestnut coloration. There was no evidence that extra‐pair partners mated assortatively, but males with brighter UV‐blue coloration had fewer extra‐pair offspring in their nests. Older males were more successful at siring extra‐pair offspring, despite displaying no differences in coloration compared to younger males. Coloration did not play a role in determining extra‐pair male success. These results suggest that coloration plays a role in the formation of social pairs, but not mate choice for extra‐pair partners.  相似文献   

17.
Recently, it has been proposed that through sexual imprinting on their parents, young birds learn to discriminate between males and females. Support for this suggestion was given by a study on zebra-finch males Taniopygia guttata, which showed that males of this species develop a strong sexual preference for mother-like females over father-like females. The present study investigates whether zebra-finch females also develop a sexual preference for mates resembling the opposite-sex parent. The females used had been raised either by normal pairs, by white pairs or by pairs of both morphs. The preferences were tested by confronting these females with normal and white males, both in simultaneous two-stimulus tests and successive one-stimulus tests. In contrast to males, females raised by a pair of mixed-morph parents did not show a preference for mating partners of the opposite-sex-parent's morph. Instead, they showed a preference for males of the mother's plumage type. It is suggested that the difference in which sexual imprinting proceeds in males and females may be related to the different role each sex plays in the pair formation.  相似文献   

18.
In socially monogamous species, mate‐guarding could be a reproductive strategy that benefits both males and females, especially when males contribute to parental care. By actively guarding mates, males may reduce their chances of being cuckolded, whereas females that mate‐guard may reduce the likelihood that their mates will desert them or acquire additional mates, and hence limit or reduce paternal care of offspring. Owl monkeys (Aotus spp.) are socially monogamous with biparental care of young and, hence, potential beneficiaries of mate‐guarding. We presented mated pairs of captive owl monkeys (A. nancymaae) with unfamiliar male and female conspecifics, to determine if either member of the pair exhibits intraspecific aggression toward an intruder or stays close to its mate, behaviors indicative of mate‐guarding. Male mates were more responsible for the maintenance of close proximity between mates than females. Male mates also exhibited elevated levels of behavior that signify arousal when presented with a male conspecific. These responses by mated male owl monkeys are consistent with patterns that may help prevent cuckoldry. Am. J. Primatol. 72:942–950, 2010. © 2010 Wiley‐Liss, Inc.  相似文献   

19.
Genetic population structure of Japanese bagrid catfishes   总被引:3,自引:1,他引:2  
 The genetic population structures of four bagrid catfishes, allopatrically distributed in Japan, were investigated based on nucleotide sequence data from the mitochondrial control region (ca. 420 bp) of 296 specimens from 29 river systems. Almost no sequence variations were found within riverine populations of each species, especially Pseudobagrus ichikawai, in which no individual variations were found in any specimens from eight river systems throughout its range. In contrast, the P. nudiceps population in the Lake Biwa–Yodo River system showed relatively high polymorphism. These results imply that the riverine populations have undergone a bottleneck situation at some time. Most of the riverine populations of P. nudiceps and P. ichikawai, which are mainly distributed in areas around an inland sea or bay, were fixed into a single haplotype for each species. On the other hand, in P. tokiensis and P. aurantiacus, which are distributed in areas surrounding extensive mountainous regions, the haplotype compositions clearly differed among conspecific populations. These results suggest that some degree of gene flow existed among populations of each of the former two species during glacial regression periods. Based on the genetic variability of P. fulvidraco, widely distributed in continental East Asia, and the degree of genetic divergence between P. aurantiacus and its possible sister species, P. taeniatus, in China, the evolutionary rate of East Asian bagrids appears to be relatively low, estimated at a few percent per million years or less. Received: June 5, 2002 / Revised: December 6, 2002 / Accepted: December 26, 2002  相似文献   

20.
Data on the length–weight relationship, age, growth, sex ratio and mortality were analysed for the Mediterranean sand smelt, Atherina (Atherina) hepsetus L. (total = 2805; males = 1258; females = 1547) collected in the eastern middle Adriatic island area during the reproductive period (February to April) in 2002. The total length of sampled specimens ranged from 3.8 to 14.5 cm and the weight from 0.28 to 22.39 g. The overall sex ratio was 1.23 : 1 in favour of females, significantly different from the expected 1 : 1 ratio (χ2 = 29.76; P < 0.05). All individuals >13.4 cm were females. The oldest collected male and female specimens were 5 years old. The von Bertalanffy growth formula was estimated for females (L = 15.79 (1−e−0.43(t+0.049)) and males (L = 15.25 (1−e−0.43(t+0.018)). The power values (b) of the length–weight relationship were very similar for both sexes (b = 3.14) and indicated a slightly allometric growth. The instantaneous rates of mortality for all collected fish were Z = 1.44 year−1; M = 0.94 year−1 and F = 0.50 year−1. The exploitation ratio was E = F/Z = 0.35. The value for M is highly uncertain, however, as well as those values for F and E.  相似文献   

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