Collective Waves of Sleep in Gulls (Larus spp.)

How should animals sleep in groups? Because sleeping reduces the ability of an individual to detect potential threats, not all individuals should sleep at the same time. The obvious solution of taking turns to sleep is not documented in animal groups. Individuals can also organize their sleeping bouts independently of each other but this simple strategy can be dangerous if too many individuals happen to sleep at the same time. One solution to this problem is to monitor the behaviour of other group members and adjust sleeping bouts accordingly. For instance, as the number of sleeping individuals increases, companions may decide that it must be a safe time to sleep. However, when fewer group members are sleeping, an individual may benefit by curtailing sleep, given that it would be more vulnerable than vigilant group members should an attack occur. Such monitoring can therefore lead to contagious behaviour in the group, which can be detected in a group by collective waves of activities through time. Using spectral analysis, I investigated the proportion of sleeping birds in loafing gulls (Larus spp.) as a function of time over 2 yr and found that in many groups, the proportion of sleeping birds rises and decreases in a systematic and statistically significant fashion. These results add more weight to the now increasingly supported view that vigilance in general is a social phenomenon and suggest that adaptive behaviour at the level of the individual can lead to collective phenomena such as waves of sleep in animal groups.     

Sleeping gulls monitor the vigilance behaviour of their neighbours

Individuals in groups are often thought to scan their surroundings for threats independently of one another. Models, however, suggest that foragers should monitor the vigilance level of their neighbours to prevent cheating, and to gather information about incipient predation risk. Evidence for monitoring of vigilance is scant. Here, I examined changes in vigilance levels in sleeping gulls (Larus sp.) surrounded by neighbours in various states of alertness. Controlling for group size and neighbour density, gulls interrupted sleep more often to scan their surroundings, and were therefore more vigilant, when their neighbours were alert rather than sleeping or preening. The results provide evidence for copying of vigilance within groups of birds, suggesting a complex flow of information about predation risk in groups.     

Many eyes or many ewes: vigilance tactics in female bighorn sheep Ovis canadensis vary according to reproductive status

In gregarious animals, there is usually a negative relationship between individual vigilance and group size. This effect of group size is generally explained by increasing probability of predator detection (the many-eyes hypothesis) and by the dilution of risk occurring in larger groups. Few studies have attempted to examine the specific implications of either hypothesis on the expected vigilance pattern of an animal. Here we examine whether reproductive status affects vigilance patterns in bighorn sheep Ovis canadensis ewes. We also test whether the observed vigilance patterns are consistent with predictions from dilution or detection models of vigilance. Although vigilance decreased with increasing group size, vigilance tactics differed between barren and lactating females. Lactating ewes relied solely on predator detection. In contrast, barren ewes benefited from both detection and dilution effects when group size increased and adjusted vigilance effort according to the proportion of lactating ewes in their group. It is generally assumed that gregariousness increases safety. Here we further show that reproductive status influenced how animals reduce predation risk and that some individuals take advantage of the vigilance effort provided by others.     

Influence of rainfall on sleeping site choice by a group of anubis baboons (Papio anubis)

For diurnal nonhuman primates, shifting among different sleeping sites may provide multiple benefits such as better protection from predators, reduced risk of parasitic infection, and closer proximity to spatially and temporally heterogeneous food and water. This last benefit may be particularly important in sleeping site selection by primates living in savanna‐woodlands where rainfall is more limited and more seasonally pronounced than in rainforests. Here, we examined the influence of rainfall, a factor that affects food and water availability, on the use of sleeping sites by anubis baboons (Papio anubis) over two 13‐month study periods that differed in rainfall patterns. We predicted that during wet periods, when food and water availability should be higher, the study group would limit the number of sleeping sites and would stay at each one for more consecutive nights than during dry periods. Conversely, we predicted that during dry periods the group would increase the number of sleeping sites and stay at each one for fewer consecutive nights as they searched more widely for food and water. We also predicted that the group would more often choose sleeping sites closer to the center of the area used during daytime (between 07:00 and 19:00) during wet months than during dry months. Using Global Positioning System data from collared individuals, we found that our first prediction was not supported on either monthly or yearly timescales, although past monthly rainfall predicted the use of the main sleeping site in the second study period. Our second prediction was supported only on a yearly timescale. This study suggests that baboons’ choice of sleeping sites is fluid over time while being sensitive to local environmental conditions, one of which may be rainfall.     

Disturbances by dog barking increase vigilance in coots Fulica atra

Animals frequently interrupt their activity to look up and to scan their surrounding environment for potential predators (vigilance). As vigilance and other activities are often mutually exclusive, such behaviours are at the expense of feeding, sleeping or preening. Authors of many wildlife disturbance studies found that people with free-running dogs provoked the most pronounced disturbances (e.g. greater flushing distances and more birds affected). However, dogs on leash may also negatively affect wild animals, and barking dogs may lead to an increase in vigilance. In this study, I tested this hypothesis in coots (Fulica atra) using three different playback procedures: (1) dog barks, (2) conspecific coot alarm calls and (3) chaffinch song. The trials were conducted in spring and autumn 2005 at three study sites in southwestern Germany. During the dog playbacks, vigilance increased significantly from 17 to 28%. This increase in vigilance is comparable to the presence of a natural predator. As expected, vigilance also increased significantly during conspecific coot alarm calls but not during playbacks of the chaffinch song control. Two main findings result from the study: (1) coots respond to acoustic traits of dogs and may be able to acoustically recognise this predator and (2) this increase in vigilance might have implications for conservation, especially when considering buffer zones around sensitive areas.     

Dynamic species co‐occurrence networks require dynamic biodiversity surrogates

In conservation it is inevitable that surrogates be selected to represent the occurrence of hard‐to‐find species and find priority locations for management. However, species co‐occurrence can vary over time. Here we demonstrate how temporal dynamics in species co‐occurrence influence the ability of managers to choose the best surrogate species. We develop an efficient optimisation formulation that selects the optimal set of complementary surrogate species from any co‐occurrence network. We apply it to two Australian datasets on successional bird responses to disturbances of revegetation and fire. We discover that a surprisingly small number of species are required to represent the majority of species co‐occurrences at any one time. Because co‐occurrence patterns are temporally dynamic, the optimal set of surrogates, and the number of surrogates required to achieve a desired surrogacy power, depend on sampling effort and the successional state of a system. Overlap in optimal sets of surrogates for representing 70% of co‐occurring species ranges from zero to 57% depending on when the surrogacy decision is made. Surrogate sets representing early successional communities over‐estimate the power of surrogacy decisions at later times. Our results show that in dynamic systems, optimal surrogates might be selected in different ways: 1) use short‐term monitoring to choose a larger number of static less‐informative surrogates; 2) use long‐term monitoring to choose a smaller number of static high‐power surrogates that may poorly represent early successional co‐occurrence; 3) develop adaptive surrogate selection frameworks with high short‐term and long‐term surrogacy power that update surrogate sets and capture temporal dynamics in species co‐occurrence. Our results suggest vigilance is needed when selecting surrogates for other co‐occurring species in dynamic landscapes, as selected surrogates from one time may have reduced effectiveness at a different time. Ultimately, decisions that fail to acknowledge dynamic species co‐occurrence will lead to uninformative or redundant surrogates.     

Factors Affecting Sleep/vigilance Behaviour in Incubating Mallards

Vigilance is a behavioural tactic that allows individuals to control their surroundings and to assess predation risk. In contrast, sleep is unique behavioural state with widely hypothesized restorative and energy‐saving functions, but reducing attentiveness and increasing susceptibility to predation. Sleeping birds resolve this conflict by interrupting sleep with short periods of eye opening (termed ‘scans’) during vigilant sleep. Miscellaneous environmental factors and sleeping postures may affect the perception of risk and corresponding vigilance level. Here, we investigated the influence of nest vegetation concealment, time of day and sleeping postures on the sleep/vigilance trade‐off in incubating Mallards (Anas platyrhynchos). We found that incubating females increased their vigilance with increasing nest vegetation cover facing the vigilant eye during both the day and the night periods; however, mean nest vegetation concealment did not affect female vigilance. Females also reduced their total vigilance along with scan frequency during the night period, while displaying the opposite pattern during the daylight. The rest‐sleeping position was preferred more during the night compared with the daylight period, and females were more vigilant in this position at night. Our data show that the nest vegetation concealment regardless of visual abilities during different light conditions, time of day and sleeping posture play an underlying role in antipredator vigilance during sleep in this cryptic ground‐nesting bird.     

Circadian Reactions to nCPAP Treatment

To determine possible effects of apnea attacks on the spontaneous behavior of the circadian system (body temperature, sleeping behavior, vigilance), 11 patients with obstructive sleep apnea (OSA) were observed before therapy over a 24h period under a special constant routine (bed-rest study) and again during therapy with nCPAP (nasal continuous positive airway pressure). Clinical indicators (polysomnographical, subjective sleep quality, etc.) indicated successful therapy. During the bed-rest study with nCPAP therapy, the 24h amplitude of core temperature was found to be greater than the amplitude measured before therapy. Also, therapy decreased sleep disturbances at night and reduced daytime sleeping times. Consequently, the level of subjective vigilance was higher during the daytime during therapy. OSA attacks do not only impair sleep; they disturb the whole circadian system. This may also impair recuperation and sleep. Further research should test whether measurements of the spontaneous circadian system could have additional diagnostic value and whether the stabilization of the circadian system has therapeutic value.     

Multiple central place foraging by spider monkeys: travel consequences of using many sleeping sites

Summary Central place foraging models assume that animals return to a single central place such as a nest, burrow, or sleeping site. Many animals, however choose between one of a limited number of central places. Such animals can be considered Multiple Central Place Foragers (MCPF), and such a strategy could reduce overall travel costs, if the forager selected a sleeping site close to current feeding areas. We examined the selection of sleeping sites (central places) by a community of spider monkeys (Ateles geoffroyi) in Santa Rosa National Park, Costa Rica in relation to the location of their feeding areas. Spider monkeys repeatedly used 11 sleeping trees, and they tended to choose the sleeping site closest to their current feeding area. A comparison of the observed travel distances with distances predicted for a MCPF strategy, a single central place strategy, and a strategy of randomly selecting sleeping sites demonstrated (1) that the MCPF strategy entailed the lowest travel costs, and (2) that the observed travel distance was best predicted by the MCPF strategy. Deviations between the observed distance travelled and the values predicted by the MCPF model increased after a feeding site had been used for several days. This appears to result from animals sampling their home range to locate new feeding sites.     

Do Sharp-Tailed Grouse Select Loafing Sites to Avoid Visual or Olfactory Predators?

ABSTRACT Grouse should seek loafing sites hidden from predators; however, good hiding sites from predators that use vision to locate prey differ from good hiding sites from predators that use odor to locate prey. We compared characteristics of control sites to sites used for loafing by sharp-tailed grouse (Tympanuchus phasianellus) to determine whether selection of loafing sites was more influenced by the need to hide from visual or olfactory predators. Sites used for loafing were similar to control sites in characteristics that would help hide a grouse from visual predators (i.e., visual obstruction, lateral visibility, visual obstruction, cover ht, and surface roughness), but loafing sites differed from control sites in characteristics that would help hide a grouse from olfactory predators (i.e., greater updrafts, wind velocities, and atmospheric turbulence).     

Variation in predation risk and vole feeding behaviour: a field test of the risk allocation hypothesis

Many prey animals experience temporal variation in the risk of predation and therefore face the problem of allocating their time between antipredator efforts and other activities like feeding and breeding. We investigated time allocation of prey animals that balanced predation risk and feeding opportunities. The predation risk allocation hypothesis predicts that animals should forage more in low- than in high-risk situations and that this difference should increase with an increasing attack ratio (i.e. difference between low- and high-risk situations) and proportion of time spent at high risk. To test these predictions we conducted a field test using bank voles (Clethrionomys glareolus) as a prey and the least weasel (Mustela nivalis nivalis) as a predator. The temporal pattern and intensity of predation risk were manipulated in large outdoor enclosures and the foraging effort and patch use of voles were measured by recording giving-up densities. We did not observe any variation in feeding effort due to changes in the level of risk or the proportion of time spent under high-risk conditions. The only significant effect was found when the attack ratio was altered: the foraging effort of voles was higher in the treatment with a low attack ratio than in the treatment with a high attack ratio. Thus the results did not support the predation risk allocation hypothesis and we question the applicability of the hypothesis to our study system. We argue that the deviation between the observed pattern of feeding behaviour of bank voles and that predicted by the predation risk allocation hypothesis was mostly due to the inability of voles to accurately assess the changes in the level of risk. However, we also emphasise the difficulties of testing hypotheses under outdoor conditions and with mammals capable of flexible behavioural patterns.     

Contrasting patterns of wetland use by sympatric larids in winter

The population dynamics and behaviour of the larid assemblage of a Mediterranean coastal wetland, the Vourkari inlet in Greece, were studied during the winter of 2008–2009. More black-headed gulls (Larus ridibundus) were seen in the inlet in December, more Mediterranean gulls (Larus melanocephalus) were present from mid-January to mid-February, while little variation was observed in yellow-legged gull (Larus michahellis) numbers throughout winter. Bird numbers remained stable through the day for the yellow-legged gull, but fewer black-headed and Mediterranean gulls were present in the late morning than the other periods. Diurnal activity patterns showed that feeding was the primary behaviour for yellow-legged gulls and resting and sleeping for black-headed and Mediterranean gulls, with locomotion being equally important for all species. All larids were primarily feeding in the late morning period, but yellow-legged gulls were doing so in much higher proportions. These contrasting patterns suggested that the Vourkari inlet was more important as a day roost for black-headed and Mediterranean gulls and a preferred feeding ground for yellow-legged gulls. Furthermore, results suggested that resting and sleeping were interchangeable activities and all other activities had more or less the same time demands on a daily basis, and also a consistent pattern across species in sleeping proportions that might indicate cross-species synchrony in sleep patterns; however future research is needed to resolve these issues. This study provided important new information on the winter ecology of three larids and revealed patterns of wetland use by these species that could help assess the importance of certain areas and improve coastal habitat management strategies to benefit birds.     

Sleeping birds do not respond to predator odour

Background

During sleep animals are relatively unresponsive and unaware of their environment, and therefore, more exposed to predation risk than alert and awake animals. This vulnerability might influence when, where and how animals sleep depending on the risk of predation perceived before going to sleep. Less clear is whether animals remain sensitive to predation cues when already asleep.

Methodology/Principal Findings

We experimentally tested whether great tits are able to detect the chemical cues of a common nocturnal predator while sleeping. We predicted that birds exposed to the scent of a mammalian predator (mustelid) twice during the night would not go into torpor (which reduces their vigilance) and hence would not reduce their body temperature as much as control birds, exposed to the scent of another mammal that does not represent a danger for the birds (rabbit). As a consequence of the higher body temperature birds exposed to the scent of a predator are predicted to have a higher resting metabolic rate (RMR) and to lose more body mass. In the experiment, all birds decreased their body temperature during the night, but we did not find any influence of the treatment on body temperature, RMR, or body mass.

Conclusions/Significance

Our results suggest that birds are not able to detect predator chemical cues while sleeping. As a consequence, antipredatory strategies taken before sleep, such as roosting sites inspection, may be crucial to cope with the vulnerability to predation risk while sleeping.     

Effects of Habitat Degradation on Sleeping Site Choice and Use in Sahamalaza Sportive Lemurs (Lepilemur sahamalazensis)

Sleeping sites may be beneficial for animals in terms of thermoregulation, proximity to foraging sites, and protection from predators and infectious diseases. The abundance of adequate sleeping sites is thus essential for the survival of primates. We investigated microhabitats around sleeping sites, and the influence of habitat degradation on sleeping site choice and usage, in the nocturnal Sahamalaza sportive lemur, Lepilemur sahamalazensis. We used quarter point sampling (N?=?315) to describe five forest fragments and 57 sleeping sites and continuous focal animal sampling (N?=?45) to determine the diurnal activity budget, to determine whether individuals inhabiting different fragments or sleeping site types showed different levels of vigilance. Our results suggest that tall trees with large crowns, a high density of small trees, and dense canopy are particularly important for sleeping site choice. Microhabitat structure around sleeping sites did not differ between forest fragments or sleeping site types. Diameter at breast height, crown diameter, canopy cover, and bole height were similar for all sleeping trees, as were the number of lianas in trees with tree-tangle sleeping sites, and the volume of tree holes. Tree holes used as sleeping sites were most often found in dead trees of Bridelia pervilleana (50–62.5 %), whereas tree tangle sites were most often located in Sorindeia madagascariensis (20–62.5 %). Lemurs were active 5–14 % of the daytime, although they never left their sleeping sites or fed. Individuals occupying tree holes had higher levels of activity than those in tree tangles, and those in more degraded fragments were more active. Our results suggest that Sahamalaza sportive lemurs choose their sleeping sites according to specific habitat characteristics, and that factors associated with old and intact forest are likely to be crucial for their survival.     

Interactions among social monitoring,anti-predator vigilance and group size in eastern grey kangaroos

Group size is known to affect both the amount of time that prey animals spend in vigilance and the degree to which the vigilance of group members is synchronized. However, the variation in group-size effects reported in the literature is not yet understood. Prey animals exhibit vigilance both to protect themselves against predators and to monitor other group members, and both forms of vigilance presumably influence group-size effects on vigilance. However, our understanding of the patterns of individual investment underlying the time sharing between anti-predator and social vigilance is still limited. We studied patterns of variation in individual vigilance and the synchronization of vigilance with group size in a wild population of eastern grey kangaroos (Macropus giganteus) subject to predation, in particular focusing on peripheral females because we expected that they would exhibit both social and anti-predator vigilance. There was no global effect of group size on individual vigilance. The lack of group-size effect was the result of two compensating effects. The proportion of time individuals spent looking at other group members increased, whereas the proportion of time they spent scanning the environment decreased with group size; as a result, overall vigilance levels did not change with group size. Moreover, a degree of synchrony of vigilance occurred within groups and that degree increased with the proportion of vigilance time peripheral females spent in anti-predator vigilance. Our results highlight the crucial roles of both social and anti-predator components of vigilance in the understanding of the relationship between group size and vigilance, as well as in the synchronization of vigilance among group members.     

Detecting predators and locating competitors while foraging: an experimental study of a medium-sized herbivore in an African savanna

Vigilance allows individuals to escape from predators, but it also reduces time for other activities which determine fitness, in particular resource acquisition. The principles determining how prey trade time between the detection of predators and food acquisition are not fully understood, particularly in herbivores because of many potential confounding factors (such as group size), and the ability of these animals to be vigilant while handling food. We designed a fertilization experiment to manipulate the quality of resources, and compared awareness (distinguishing apprehensive foraging and vigilance) of wild impalas (Aepyceros melampus) foraging on patches of different grass height and quality in a wilderness area with a full community of predators. While handling food, these animals can allocate time to other functions. The impalas were aware of their environment less often when on good food patches and when the grass was short. The animals spent more time in apprehensive foraging when grass was tall, and no other variable affected apprehensive behavior. The probability of exhibiting a vigilance posture decreased with group size. The interaction between grass height and patch enrichment also affected the time spent in vigilance, suggesting that resource quality was the main driver when visibility is good, and the risk of predation the main driver when the risk is high. We discuss various possible mechanisms underlying the perception of predation risk: foraging strategy, opportunities for scrounging, and inter-individual interference. Overall, this experiment shows that improving patch quality modifies the trade-off between vigilance and foraging in favor of feeding, but vigilance remains ultimately driven by the visibility of predators by foragers within their feeding patches.     

THE EFFECTS OF DIURNAL AND TIDAL PERIODICITIES IN THE NUMBERS AND ACTIVITIES OF HERRING GULLS LARUS ARGENTATUS IN A COLONY

The average numbers of Herring Gulls Larus argentatus present in a breeding colony on Walney Island, Cumbria, were found to vary with the tidal cycle but to remain effectively constant with time of day through the breeding season. An activity survey, based on 50 Herring Gulls observed at half-hourly intervals during March and April 1973, showed that sleep and rest varied inversely with each other with sleep increasing to 50 per cent at midday. After a peak in the proportion of gulls asleep four hours before low tide, sleeping progressively decreased until low tide; seemingly a result of resident gulls waking and remaining more alert as others left the colony in search of food. Preening was constant throughout the day and tide cycle. Other behaviours (mostly courtship and agonistic behaviour associated with territory defence) increased slightly during low tide and were more common early and late in the day. Night observations of the gulls' activities showed that there was a peak of sleeping between midnight and 02.00 hours. It is suggested that Herring Gulls have a bimodal diel sleep pattern.     

On how risk and group size interact to influence vigilance

Vigilance allows animals to monitor their surroundings for signs of danger associated with predators or rivals. As vigilance is costly, models predict that it should increase when the risk posed by predators or rivals increases. In addition, vigilance is expected to decrease in larger groups that provide more safety against predators. Risk and group size are thus two key determinants of vigilance. Together, they could have additive or interactive effects. If risk and group size interacted, the magnitude of the group‐size effect on vigilance would vary depending on the level of risk experienced, implying that the benefits of sociality in terms of vigilance vary with risk. Depending on the model, vigilance is predicted to decrease more rapidly with group size at low risk or at high risk. Little work has focused directly on the interaction between risk and group size, making it difficult to understand under which conditions particular interactive effects arise and whether interactive effects are common in natural systems. I review the vast literature on vigilance in birds and mammals to assess whether interactive effects between risk and group size are common, and if present, which pattern occurs more frequently. In studies involving predation risk, the greatest proportion reported no statistically significant interactive effects. In other cases, vigilance decreased with group size more rapidly at low or high risk in a similar proportion of studies. In studies involving risk posed by rivals (social risk), most documented a more rapid decrease in vigilance with group size at low than at high risk, as predicted if the need to monitor rivals increases in larger groups. Low statistical power to detect interactive effects might have been an issue in several studies. The absence of interactive effects, on the other hand, might suggest constraints or limits on the ability of animals to adjust vigilance to current risk or group sizes. Interactive effects on vigilance have implications for the evolution of sociality and for our understanding of the phenotypic plasticity of predator‐ and competitor‐induced defences and deserve more attention in future studies.     

麻阳河自然保护区黑叶猴夏季的夜宿行为

因昼行性灵长类动物一天中相当一部分时间在其夜宿地度过,其夜宿行为在一定程度上影响着它们的活动方式与行为特点(Anderson,1998).对夜宿行为的观察可收集白天无法收集到的灵长类社会活动和社会关系的信息,如夜宿地分布(sleeping site)、睡眠时间(time)、睡眠抱团组成(huddling)等(Takahashhi,1997;Ogawa etal.,2007;黎大勇,2010),灵长类夜宿行为的研究对于分析了解其白昼活动方式与行为适应特点具有重要的启迪作用(Anderson,1998).