Reciprocal Allogrooming in Dam-reared and Hand-reared Impala Fawns

Among adult females and males of African antelope impala are unique in their performance of reciprocal allogrooming. The occurrence of this behaviour in neonatal impala fawns was explored in a free-ranging impala herd at the San Diego Wild Animal Park where 5 dam-reared fawns were observed from birth through 10 weeks of age. One-way maternal grooming and reciprocal allogrooming with the dam and non dam partners emerged as distinct behavioural systems. Maternal grooming, directed mostly to the anogenital area, was typical of that seen in other ungulates, and sharply declined over the first two weeks. Reciprocal allogrooming, characterized by alternate exchanges of grooming bouts with a partner in the same manner as in adults, was seen as early as 3–8 d after birth. All fawns were grooming with unrelated adult females by the end of the second week. By week 2 virtually every measure of reciprocal allogrooming by fawns (grooming delivered per hour, reciprocity, and percent of encounters initiated) was as high as for adults. The appearance of this reciprocal allogrooming pattern, especially at such an early age, appears to be unique among ungulates, and possibly mammals in general. Three hand-reared impala fawns, deprived of the opportunity to interact with older herdmates, but having access to impala fawns and heterospecific fawns, were observed from 1–3 mo of age. The hand-reared impala showed no alteration in the occurrence of reciprocal allogrooming behaviour compared with the dam-reared control fawns, indicating that allogrooming experience with older animals was not required for the appearance of reciprocal allogrooming at an early age. Interestingly, hand-reared fawns persisted in grooming heterospecific fawns despite the fact that heterospecifics rarely reciprocated grooming. We postulate that the strong predisposition for impala young to groom others may be related to the threat of tick infestation in the impala's ecotone habitat.     

Parturition and perinatal behaviour in captive cotton-top tamarins (Saguinus oedipus)

Fourteen births to seven female cotton-top tamarins in a successful breeding colony were observed. All births occurred between 17:50 and 20:40. Behavioural changes indicating the onset of labour are described. Delivery was usually accomplished rapidly, with short intervals between successive infants. One suspected and one verified breech presentation occurred; these deliveries were accompanied by a marked increase in the duration of the interval between infants, and one infant apparently died during expulsion. All other presentations seen were vertex occiput posterior. Fathers, and sometimes older offspring of both sexes, frequently shared with the mother in eating the placenta. Carrying of infants by individuals other than the mother was rare in the hour after birth, and was usually confined to fathers. One primipara rejected her second-born infant, but all other parents showed competent parental behaviour from birth onwards. The results are compared to data from other primates, and their relevance to the successful breeding of this species is discussed.     

Why Do Male Tree Weta Aggressively Evict Females from Galleries After Mating?

The sexually dimorphic Wellington tree weta ( Hemideina crassidens Blanchard) (Orthoptera: Anostostomatidae) is a harem-defending polygynous insect in which males use their enormous mandibles to fight conspecifics for access to harems residing in tree cavities (gallery). Tree weta ejaculates (spermatophores) do not include a nuptial meal (spermatophylax) to delay removal by females as in some ensiferan Orthoptera. Consequently, male tree weta are predicted to remain with their mates post-copula to ensure complete sperm transfer. Contrary to prediction, however, males forcibly eject females from the mating site (gallery) soon after copulation. Results suggest that forcible ejection occurs apparently because females consume the previous spermatophore if either the resident male or a rival initiates a subsequent copulation attempt. Thus, ejection appears to reduce the resident male's risk that his ejaculate will be eaten and his mate will copulate with another male.     

Sexual behaviour of male and female tammar wallabies (Macropus eugenii) at post-partum oestrus

This study describes the sexual behaviour of the adult male and female tammar wallaby from the time a female gives birth to the end of post-partum oestrus. Eleven females were continuously observed from around the time of birth until up to 3 h after the last observed mating attempt. Males began to associate with females from around the time of birth, thus females appear to be attractive to males at, but not prior to parturition. Females subsequently allowed males to mate with them from 1.3±0.8h (mean±S.D.) post-partum, although the first ejaculation was delayed until 1.8±0.8h after birth owing to intense intermale aggression directed towards any male which attempted to mate with an oestrous female. Mating chases, in which a post-partum female was pursued by several males, were observed from 1.3±0.8h post-partum. All of this mating activity usually occurred within the first 6h after birth.     

Infanticide and expulsion of females in a cooperative mammal.

In cooperative groups of suricates (Suricata suricatta), helpers of both sexes assist breeding adults in defending and feeding pups, and survival rises in larger groups. Despite this, dominant breeding females expel subordinate females from the group in the latter half of their (own) pregnancy apparently because adult females sometimes kill their pups. Some of the females that have been expelled are allowed to rejoin the group soon after the dominant female''s pups are born and subsequently assist in rearing the pups. Female helpers initially resist expulsion and repeatedly attempt to return to their natal group, indicating that it is unlikely that dominant females need to grant them reproductive concessions to retain them in the group.     

Breed, litter and parity effects on placental weight and placentome number, and consequences for the neonatal behaviour of the lamb

Lamb survival is impaired in low birth weight lambs, and those that are slow to stand and suck. Many of the factors that influence lamb vigour, such as parity, litter size, and breed, may exert their effects, at least partially, before birth by influencing placenta development. Our hypothesis was that retarded lamb behavioural development was due to differences in placentation in these animals. Data were collected from Blackface and Suffolk lambs in the first 2 h after birth and placentas were collected when delivered. Suffolk lambs, which were behaviourally slower and had lower rectal temperatures than Blackface lambs, were associated with larger but less efficient placentas (placental efficiency defined as foetal weight supported per g placenta) with fewer foetal cotyledons than Blackface placentas. Triplet lambs were significantly slower than twin or single lambs to suck and had lower rectal temperatures. Although placenta efficiency increased with litter size, placenta and cotyledon weight, and cotyledon number increased with twinning but not thereafter. It seemed likely that triplet lambs suffered some placental insufficiency in comparison to other litter sizes. Lambs born to first parity mothers were slower to stand and reach the udder than lambs of more experienced ewes, and first parity ewes also had smaller and less efficient placentas although cotyledon number was not affected. Male lambs tended to be slower than female lambs for most behaviours, although rectal temperatures were not affected. The sire of the lamb also influenced lamb behaviour and rectal temperature. Both lamb sex and lamb sire influenced the average weight of placental cotyledons, thus some of the sire effect on the behaviour and birth weight of his progeny might be mediated through placental development. Lamb neonatal vigour was correlated with placental efficiency suggesting that lamb behaviour immediately after birth is related to placental development and function.     

Parturition in a feral baboon (Papio anubis)

During a study of feral baboons at the Gombe Stream National Park, Tanzania, the premature birth of a dead, breechborn infant was observed and photographed. The placenta was immediately eaten and the dead infant carried by the mother for two days. The birth itself attracted little attention from other troop members, but the dead infant was investigated by several baboons, especially three females who had recently become dominant to the mother in a fight.     

Parturient behaviour of a viviparous skink: evidence for maternal cannibalism when basking opportunity is low

We documented the behaviour of pregnant McCann’s skinks (Oligosoma maccanni) before, during and after parturition. Females were maintained in captivity from early pregnancy under thermal environments differing in basking opportunity (low, mid and high regimes). Thermal regime during pregnancy had little influence on maternal behaviours, including basking behaviour prior to birth and the duration of, and site selection for, labour. The majority of births (78%) occurred in the open and warm areas. Most females (61%; n?=?102 births, n?=?36 females) aided offspring post-birth by biting them free of the enclosing extra-embryonic membrane. Some females from the low regime consumed non-viable offspring, but whether this is a consistent difference among females held under different basking regimes requires further study. Many females (c. 79%) also exhibited a brief transient decrease in control of hind-limbs post-birth. Further studies on other squamates are recommended to shed light on the evolutionary history and possible conservation consequences of maternal behaviour during parturition.     

Reciprocal Allogrooming in Wild Impala Lambs

Adult impala engage in a form of reciprocal allogrooming distinguished by a high degree of reciprocity and ***lack of influence of dominance or relatedness on partner preference or distribution of grooming between partners. A previous study on reciprocal allogrooming of captive newborn impala lambs in a zoological park found that the allogrooming emerged as early as the first week after birth and was identical in structure and reciprocity to allogrooming in adults. Because these findings of apparently unique allogrooming behavior of newborn impala could have been a reflection of the effects of being born and raised in a small, stable captive herd, it was necessary to investigate reciprocal allogrooming in newborn impala in the wild. The emergence, reciprocity, rate, and partner distribution of reciprocal allogrooming in wild newborn impala were observed at two study sites: a national park in Zimbabwe and a game farm in South Africa. Maternal one-way grooming between mother and newborn emerged as distinct from reciprocal allogrooming and rapidly declined after week 1 postpartum. Reciprocal allogrooming by lambs was first seen between 5 and 8 d postpartum, and as soon as the behavior occurred it was the same basic pattern as seen in adult impala. The reciprocity index for lambs was near 0.5, indicating that lambs delivered as much grooming during an encounter as the partner. Lambs were grooming frequently with non-mother adults and other lambs by week 1 or 2; by week 3 and onward the allogrooming rate of lambs was more than twice that of their mothers, as predicted by the body size principle of the programmed grooming model. The strong predisposition of neonatal impala lambs to deliver reciprocal allogrooming as early as the first or second week postpartum would appear to reflect a genetically acquired adaptation to the threat of tick infestation in their natural habitat.     

Sexual motivation suppresses paternal behaviour of male gerbils during their mates' postpartum oestrus

Adult male Mongolian gerbils, Meriones unguiculatus, avoid contact with their young on the day that the young are born. However, on succeeding days, fathers spend nearly as much time in contact with their offspring as do mothers. We undertook a series of studies to investigate the causes of the day-to-day change in male parental behaviour. In experiment 1, we tested males' response to pups before, after and on the day of their mates' parturition, and found that males were more parental both before and after the day of birth of their young than on that day. In experiment 2, we compared the parental behaviour of males paired either with intact or with ovariectomized dams (which do not come into postpartum oestrus) and found that males that were mated to intact females were less attentive to pups on the day of their birth than were the males mated to ovariectomized females. In experiment 3, we compared the parental responses of castrated and intact males to newborn pups and found that castrated males were more parental than intact males. In experiment 4, we compared the parental responses of males that were exposed to postpartum oestrous females but prevented from mating for 24 h. Extending the period of male sexual arousal to 24 h inhibited paternal responsiveness to neonates for 24 h. We interpret these results as being consistent with the hypothesis that on the day of birth of a litter, a male's parental behaviour is inhibited by the motivation to mate during his partner's postpartum oestrus.     

Foraging behaviour of wild impala (Aepyceros melampus) and Burchell's zebra (Equus burchelli) in relation to sward height

Foraging behaviour plays a key role in the interaction between herbivores and vegetation, their predominant food source. Understanding this interaction is crucial to providing information that is useful for conservation of herbivores. The objective of this study was to determine how sward height influences functional response and movement patterns of free ranging wild impala and zebra at the Kenya Wildlife Service Training Institute. The study was conducted for 3 months. Sward height is an important parameter that indicates how intensive a sward has been grazed and it influences intake rate through its effect on bite size. Bite size, instantaneous intake rate, specific mass intake rate and feeding station interval for impala and zebra increased with sward height. Sward height in combination with an animal's sex was found to have a profound effect on specific mass intake rate in impala. Zebra had a longer feeding station interval and lower stepping rate in tall swards compared to impala. Despite differences in their specific body mass and digestive strategies, impala and zebra maximized their intake rates in tall swards as a trade‐off among the swards. Tall swards are therefore critical in the study area and should be protected from bush encroachment which is a persistent problem.     

Homosexual behaviour and female-male mounting in mammals—a first survey

Information from the literature is given on the presence or absence of homosexual behaviour and female-male mounting in 125 species of mammals, both captive and wild. Such behaviour occurs in the male and often female young of many species soon after their birth. It is more common in young, often in play, than in adults. Adult homosexual behaviour is widespread in male and female mammals (recorded in 63 and 71 species respectively), but common in few species. In males it is most likely to be correlated with dominance and thus to occur in species with hierarchies such as terrestrial monkeys and members of the sheep and goat tribe. In females it is often correlated with sexual condition; a female in heat most often mounted another female, and one in heat was next most likely to be mounted by another female. Anoestral females rarely mounted other anoestral females. Females of 43 species mounted males, which often excited them sexually. Captive mammals tended to mount animals of the same sex more often than did wild ones when comparative data were available. Domestic animals also mounted more man did wild ones, with several exceptions. Some phylogenetic groups of animals displayed similar degrees of homosexual mounting, but there was often considerable variation between closely related species. Nor could homosexual mounting be always correlated with the social structure of a group. The four reasons for, or contexts of, homosexual and female-male mountings were social play (in 34 species), aggression (19 species), sexual excitement (36 species), and physical contact—non-play (30 species). This last category included a state of tension, getting attention, greeting, grooming, caressing, reassurance and appeasement. There was some overlap between categories. Homosexual pair-bonds occur in captive mammals and have been observed throughout the year in non-captive female Japanese monkeys.     

Parturition in gilts: duration of farrowing, birth intervals and placenta expulsion in relation to maternal, piglet and placental traits

Large White x Meishan F2 crossbred gilts (n = 57) were observed continuously during farrowing while the placentae of their offspring were labeled in order to examine the duration of farrowing and placenta expulsion in relation to maternal-, piglet- and placental traits and the duration of birth interval in relation to birth weight, birth order and placental traits. Independently from each other, litter size, gestation length and offspring directed aggression significantly (P 0.05) affected duration of farrowing. An increase in litter size was associated with an increase of duration of farrowing and an increase in gestation length was associated with a decrease of duration of farrowing. Aggressive gilts took longer to farrow, compared to non-aggressive ones. After taking into account litter size, gestation length and offspring directed aggression, placental thickness (i.e., placental weight corrected for placental surface area) was significantly (P < 0.05) related to duration of farrowing, i.e., litters with on average thicker placentae took longer to farrow. The latter effect is the result of the fact that individual placental thickness significantly (P < 0.01) affected individual birth interval, independent of birth weight. The piglet has to break its own membranes to be able to start its journey through the uterus towards the birth channel. Apparently, a thicker placenta offers more resistance and thus prolongs the process of birth. Independent of placental thickness, birth interval significantly (P < 0.01) decreased with an increase in birth order (first born to last born). The high variation of birth intervals for the last born piglets, caused a slight increase in average birth interval for the latter piglets. Litters with on average more areolae per placenta took significantly (P < 0.001) less time to be born than litters with on average less areolae per placenta (independent of total number of piglets born and other placental traits), while birth intervals within litters were not affected by this trait. Thus, these results are probably due to a gilt trait rather than a piglet trait. Since the number of areolae represent the number of uterine glands present, the gilt trait might be uterine development. Duration of placenta expulsion significantly (P < 0.01) increased with an increase of duration of farrowing. Furthermore, the first placenta was expelled significantly (P < 0.01) earlier relative to last piglet when duration of farrowing was protracted, while there was no relation of the time interval between first placenta and last piglet and the duration of placenta expulsion. In conclusion, the most important finding of this study is that placental thickness rather than birth weight appears to play an important role in the duration of birth intervals and as a result, of duration of parturition in gilts.     

Photoperiod influences the development and the expression of personality traits and social behaviour in wild cavies (Cavia aperea)

Seasonality influences behaviour, physiology and life history of organisms, and photoperiod is a reliable and influential cue gearing individual adaptation to seasonal changes in the environment. Plastic phenotypic adjustments according to the prevailing season are a widespread, well-studied phenomenon. Less well known are effects on developmental trajectories of animals born into different seasons. By manipulating the photoperiod during pregnancy and lactation independent of food availability and temperature, we studied if maternal behaviour in the precocial wild cavy (Cavia aperea) responds to this seasonal cue and if maternal behaviour and photoperiod shape offspring development and behaviour. We repeatedly observed mothers before and after birth. We investigated if pups differ in risk-taking behaviours directly after birth (indicating direct prenatal effects) or only after gaining independence of the mother (indicating delayed prenatal or postnatal effects due to own cue sampling). Furthermore, we tested if different simulated seasons of birth affect social and aggressive behaviour of adult animals. While theoretical predictions according to risk-taking are quite clear, they are contradictory for social behaviours that are much less well studied. We predicted that animals born into spring photoperiods would be aggressive because of a need to gather enough resources for early reproduction and successfully establishing a territory at least in males. Spring-born males were more aggressive than autumn-borns, while females did not differ with respect to season. Spring-born females, however, lost more body mass when they had to integrate into an established group and autumn-born females initiated more aggressive interactions. Our data demonstrate flexible and long-term stable seasonal effects on behaviours that likely affect fitness outcomes under natural conditions.     

Significance of the weaning period for natality and maternal behaviour of laboratory rats.

Normally weaned females (at 30 days) displayed seasonal cyclic changes in natality and the characteristics of the young. Natality in the spring and summer was high, the litters were large, the proportion of females and males in the litter was equal and deaths among the unweaned young were very few. Natality in the autumn and winter was low and the litters were small and consisted mainly of males. The death rate among the young was higher than in the spring and summer. Prematurely weaned females (at 15 days) displayed no seasonal cycle either in natality or in the characteristics of the young. The studied parameters corresponded to the values found in the spring and summer in normally weaned females. No differences were found in maternal retrieving, but there was a marked difference in nest-building. The normally weaned female tore up paper (building material) into small fragments 24 hours before giving birth and dropped the young into a soft nest of finely shredded paper. On leaving the nest it covered the young up. The prematurely weaned female scattered the paper about the cage 24 hours before giving birth and dropped the young into a depression stamped out among whole pieces of paper. It did not cover the young up on leaving the nest. The cause of the difference in building behaviour is evidently that prematurely weaned females failed to acquire early experience of this behaviour between the 15th and 30th day of life.     

Atlantic sturgeon Acipenser oxyrinchus surfacing behaviour

Atlantic sturgeon Acipenser oxyrinchus surfacing behaviour was investigated in Minas Basin (45° 20′ N; 64° 00′ W) and the Bay of Fundy with pop‐up satellite archival tags (MiniPAT) measuring physical variables (pressure, temperature, light ) . Of six tags deployed during June and July, five provided pop‐up locations and two were recovered after c. 4 months. Analysis of recovered archival data revealed that the frequency of surfacing events was highest (78·9%) when A. oxyrinchus were in Minas Basin at depths <10 m. Surfacing frequency decreased substantially when fish migrated into greater depths of the Bay of Fundy (>40 m). The tidal cycle in Minas Basin had a significant relationship to surfacing frequency, with the most surfacing events (49·5%) occurring on the flood tide, from mid‐ to high‐tide. Surfacing events ranged from 0–12 a day and the maximum number occurred between 2300 and 0300 hours. Maximum surfacing ascent speeds ranged from 0·50 to 4·17 m s^?1 and maximum descent speeds ranged from 0·17 to 3·17 m s^?1. Buoyancy control, by gulping air to inflate the gas bladder, is proposed as the main reason for surfacing behaviour in A. oxyrinchus.     

Inhibition of mating behaviour before feeding in the tick Aponomma hydrosauri

When on their host, both male and female adults of the reptile tick Aponomma hydrosauri require at least five days of feeding before normal mating behaviour will start. In off-host trials, fed females attract significantly more male contact than do unfed females, but unfed males show normal mating behaviour. All aspects of female mating behaviour are inhibited before feeding. Male mating behaviour has two stages: one comprises detachment and searching, the other, courtship behaviour. Only the former is inhibited before male feeding. This suggests the female signal has two components: one initiating searching, and the other initiating courtship. Males will always respond to the second component, but only after feeding will they respond to the first.     

The origin of circulating 13,14-dihydro-15-keto-prostaglandin F2α during delivery

All uterine tissues as well as the fetal membranes and the placenta can form prostaglandins from endogenous precursors but it is not clear which of the tissues is the main site for the increase in PGF_2α production during human parturition. To examine this question, we measured plasma prostaglandin levels before and at intervals after expulsion of the fetus, placenta, and membranes. The concentration of PGFM at the beginning of the second stage of labor was significantly higher than before the onset of labor. Five minutes after the birth of the infant, the concentration had doubled. Thirty minutes after the expulsion of placenta and membranes, plasma PGFM had fallen to the levels at full dilatation; two hours postpartum it was still significantly raised over levels before labor. Since the halflife of PGFM in the circulation is about 7 minutes, these findings indicate that the uterine tissues are important sources of PGFM during labor. In contrast, endogenous oxytocin levels, which were significantly raised over control levels at the second stage of labor, did not change during the third stage, and decline postpartum to control levels. Oxytocin infusion did not influence PGFM levels at 5 and at 30 minutes postpartum, but raised them at 2 hours.     

Competing for last place: Mating behaviour in a pill-box crab, Halicarcinus cookii (Brachyura: Hymenosomatidae)

The mating strategy of Halicarcinus cookii was investigated to ascertain how males maximised their fitness through mate choice. An intertidal population at Kaikoura, New Zealand, was dominated by mature crabs of both sexes in summer and by immature crabs in the colder months. More than 95% of mature females were ovigerous with early stage and late stage broods found in almost every month, indicating that egg production and larval release is continuous. The operational sex ratio was less than 1 male/female in summer, but often more than 1.0 in the colder months. The gonosomatic index increased along with brood development so that as soon as zoeae were released, the next clutch of eggs was ready to be fertilised. Males searched for receptive females and began pre-copulatory mate guarding without any courtship display. They mated preferentially with late stage or non-ovigerous females: copulation duration was longest for stage 5 females as was post-copulatory guarding (mean 18.3 h). Late stage females were up to 14% of the female population. Mate attraction seems to be the result of an ovarian signal rather than from the developing brood. Manipulation of the sex ratio had effects upon copulation duration and post-copulatory guarding: presence of a rival male increased duration of guarding. Females showed precocious mating in the penultimate instar and were able to lay fertilised eggs after their pubertal moult in the absence of males. H. cookii females have many mates, but males attempt to ensure paternity by preferentially pursuing mature females close to egg laying and by guarding these females after copulation. These behaviours are all elements of a competitive strategy to ensure that a male loses (not wins) the race to copulate because females have a ventral seminal receptacle, giving sperm precedence to the last male to mate. Male mating behaviour is a consequence and evolutionary response to female morphology.