DIEL VARIATION IN MIGRATION RATES OF EASTERN PACIFIC GRAY WHALES MEASURED WITH THERMAL IMAGING SENSORS

We recorded the blows of gray whales during their southbound migration past central California in January 1994, 1995, and 1996, using thermal imaging sensors. For our sampling purposes, we defined day (0730–1630) and night (1630–0730) to coincide with the on/off effort periods of the visual counts being conducted concurrently. We pooled data across the three years of sampling and tested for diel variation in surfacing interval, pod size, offshore distance, migration rate, and swimming speed by comparing paired day/night means for samples collected within the respective 24-h period. We performed these tests using data from the entire migration period and then repeated the tests for samples collected prior to and after the approximate median migration date (15 January). Over the entire migration period we observed larger diurnal pod sizes (x?_day= 1.75 ± 0.280, x?_night= 1.63 ± 0.232) and greater diurnal offshore distances (x?_day= 2.30 ± 0.328 km, x?_night= 2.03 ± 0.356 km) but found no diel variation in surfacing interval. For the entire migration period, the nocturnal migration rate (average number of whales passing per hour) was higher than the diurnal rate. During the first half of the migration we detected no diel variation in pod size or surfacing interval, but diurnal offshore distances were larger than at night (x?_day= 2.28 ± 0.273 km, x?_night= 1.96 ± 0.318 km). Diurnal and nocturnal migration rates prior to 15 January were not different. During the second half of the migration, there was no diel variation in surfacing interval, pod size, or distance offshore, but the nocturnal migration rate was higher (28%, SE = 11.6%) than the diurnal rate. We found no diel variation in swimming speed in any comparison. We propose that later migrants socialize more during the day, which effectively slows their diurnal rate of migration relative to nocturnal rates.     

犬蝠夜栖息地及夜栖息巢特征的初步研究

<正>大多数种类的蝙蝠不会整个晚上都进行觅食,通常在觅食期间有一段长短不一的时间停留在临时地休息,此为夜栖息行为(Hatfield,1937;Krutzsch,1954;Barbour and Davis,1969;Kunz,1973,1974;Hirshfeld et al.,1977)。蝙蝠在夜栖息地进食(Vaughan,1976;Funakoshi and Maeda,2003)、休息并消化食物(Brigham,1991;Funakoshi and Maeda,2003),甚至社会交流(Kunz,1982;Kunz and Lumsden,2003)。不同种类的蝙蝠     

Energetics of bluetongue lizards (<Emphasis Type="Italic">Tiliqua scincoides</Emphasis>) in a seasonal tropical environment

We studied the physiological ecology of bluetongue lizards (Tiliqua scincoides) on the Adelaide River floodplain in tropical Australia to determine the seasonal patterns of energy expenditure and to determine the mechanisms by which seasonal differences were achieved. Field metabolic rates (FMR) were significantly lower in the dry season (37.6 kJ kg(-1) day(-1); n=9) than in the wet (127.3 kJ kg(-1) day(-1); n=7). Water flux was also lower in the dry season (6.8 ml kg(-1) day(-1); n=9) than in the wet (39.4 ml kg(-1) day(-1); n=7). Measurements of body temperatures (T(b)) and movements of free-ranging animals, and standard metabolic rate (SMR) of recently caught animals, allowed a detailed analysis of energy budgets for wet and dry seasons. In the dry, bluetongue lizards expended 90 kJ kg(-1) day(-1) less energy than in the wet season. Unlike some other lizards of the wet-dry tropics, SMR did not differ between seasons. About 5% of the seasonal difference in FMR was due to lower night time T(b) during the dry season, and about 7% was due to lower diurnal T(b). The remaining 88% of the decrease in energy expended in the dry season was due to a substantial decrease in other costs that may include reproduction, growth, digestion and activity. If we assume the animals fed daily and the costs of digestion are taken into account, the estimates are: 14% of the savings result from lower T(b) at night, 20% from lower T(b) in the day, and 66% result from decreased activity. It is therefore apparent that, unlike some agamid and varanid lizards that use a combination of behavioural and physiological mechanisms to conserve energy when food and water are limited, bluetongue lizards primarily use behavioural mechanisms to achieve a dramatic reduction in energy expenditure in the dry season.     

Field energetics of free-living, lactating and non-lactating echidnas (Tachyglossus aculeatus)

We measured daily energy expenditure (DEE) and water turnover rates in lactating and non-lactating short beaked echidnas (Tachyglossus aculeatus) using the doubly labelled water technique during the lactation period in spring. Reproductively inactive echidnas were on average significantly heavier (median: 3354 g; range: 2929-3780 g; N=4) than lactating females (median: 2695 g; range: 2690-2715 g; N=3) during the equivalent time period. The median water flux rate of lactating echidnas (152 ml day(-1); range: 120-198 ml day(-1)) did not differ significantly from that of non-lactating females (170 ml day(-1); range: 128-227 ml day(-1)). The median DEE of echidnas that were lactating was 645 kJ day(-1) (range: 581-850 kJ day(-1)), which was not different from the median DEE of non-reproductive control females (763 kJ day(-1); range: 720-766 kJ day(-1)). Lactating females somehow compensate for the energy costs of milk production, resulting in a daily energy budget that is not different from that of non-reproductive females. At least part of their energy minimising strategy could involve the use of moderate heterothermy, allowing a greater proportion of daily energy expenditure to diverted to milk production.     

Predation risk and resource availability explain roost locations of Whimbrel Numenius phaeopus in a tropical mangrove delta

Roosts are important sites for shorebirds in non‐breeding areas at night and during high tides. How the spatial configuration of food and risk of predation and disturbance influence roost site use in tropical locations remains poorly known. We analysed the locations of nocturnal roosts of Whimbrel Numenius phaeopus in mangroves of Sanquianga National Park, Colombia, with respect to variation in spatial variables related to food resources and risk of predation and disturbance. We contrasted characteristics of all 13 known nocturnal roost locations with those of all other mangrove islands (n = 209) within the limits of the park. We estimated the distance from roosts and other mangrove islands to foraging sites, and sources of predators and human disturbance. Larger areas of feeding habitat surrounded nocturnal roosts than other mangrove islands, and the average distance to individual feeding patches was shorter. Roosts were also more isolated than other islands, but proximity to sources of human disturbance did not differ. We conclude that Whimbrel roost site use in Sanquianga was best explained by a combination of access to feeding territories and isolation from potential sources of mainland predators, but not by avoidance of human disturbance. Beyond identifying factors influencing roost site selection, the large aggregations of individuals in single locations may suggest that presence of conspecifics itself also plays a role in the formation of Whimbrel roosts. We highlight the interaction of food and risk landscapes with intraspecific attraction on the roost site selection by Whimbrels and the importance of mangroves as roosting sites in tropical regions.     

High ambient temperatures induce aggregations of chimney swifts Chaetura pelagica inside a roost

One proposed advantage of communal roosting in birds is a reduction in the costs of thermoregulation. As thermoregulatory benefits are directly linked to the distance between roosting birds, we examined whether temperature is related to inter‐bird spacing in roosting chimney swifts Chaetura pelagica. To test the hypothesis that huddling is used to reduce the costs of thermoregulation, we predicted that swifts would cluster more at colder temperatures. We mounted an all‐weather camera atop a 61 m tall industrial masonry chimney, one of the largest swift roosts in the study region. We deployed temperature loggers inside the chimney and obtained ambient air temperature from a nearby weather station. From 16 May–24 July 2013, we captured hourly images of the positions of roosting swifts at night. We used image analysis software to mark the angular positions of all roosting swifts, and calculated mean angles of orientation (preferred direction) inside the roost and the circular variance (i.e. the concentration of swifts around the mean angle). We used a Gamma regression to relate temperature inside and outside the roost to the clustering of swifts around the mean angle for 3 time periods (pre‐nesting, nesting, and post‐nesting). Converse to our prediction, swifts were closer together when ambient air temperatures were warmer in all periods (pre‐nesting (p < 0.001, n = 168), nesting (p < 0.001, n = 224), and post‐nesting (p < 0.001, n = 135)). Our findings suggest that swifts do not increase clustering intensity in response to colder temperatures, but instead they increase clustering intensity in response to the warmest ambient temperatures. This likely a metabolic response to reduced prey availability at higher temperatures and/or an attempt to reduce evaporative water loss. We suggest clustering may be used by chimney swifts as an energy saving mechanism during periods of lowered food availability.     

Directed flight and optimal airspeeds: homeward‐bound gulls react flexibly to wind yet fly slower than predicted

Birds in flight are proposed to adjust their body orientation (heading) and airspeed to wind conditions adaptively according to time and energy constraints. Airspeeds in goal‐directed flight are predicted to approach or exceed maximum‐range airspeeds, which minimize transport costs (energy expenditure per unit distance) and should increase in headwinds and crosswinds. Diagnosis of airspeed adjustment is however obscured by uncertainty regarding birds' goal‐directions, transport costs, interrelations with orientation strategy and the attainability of predicted behaviour. To address these issues, we tested whether gulls minimized transport costs through adjustment of airspeed and heading to wind conditions during extended inbound flight over water (180–360 km) to their breeding colony, and introduce a methodology to assess transport (energy) efficiency given wind conditions. Airspeeds, heading, flight mode and energy expenditure were estimated using GPS tracking, accelerometer and wind data. Predicted flight was determined by simulating each trip according to maximum‐range airspeeds and various orientation strategies. Gulls employed primarily flapping flight (93%), and negotiated crosswinds flexibly to exploit both high altitude tailwinds and coastal soaring opportunities. We demonstrate that predicted airspeeds in heavy crosswinds depend strongly on orientation strategy and presumed preferred direction. Measured airspeeds increased with headwind and crosswind similarly to maximum‐range airspeeds based on full compensation for wind drift, yet remained ～ 30% lower than predicted by all strategies, resulting in slower and 30–35% costlier flight. Interestingly, more energy could be saved through adjustment of airspeed (median 40%) than via orientation strategy (median 4%). Therefore, despite remarkably flexible reaction to wind at sea, these gulls evidently minimized neither time nor energy expenditure. However, airspeeds were possibly over‐predicted by current aerodynamic models. This study emphasizes the importance of accounting for orientation strategy when assessing airspeed adjustments to wind and indicates that either the cost or adaptive ‘currency’ of extended flight among gulls may require revision.     

Resource availability and roosting ecology shape reproductive phenology of rain forest insectivorous bats

Bats in temperate and subtropical regions typically synchronize birth of a single young with peaks in resource availability driven by local climate patterns. In tropical rain forest, insects are available throughout the year, potentially allowing departures from seasonal monoestry. However, reproductive energy budgets may be constrained by the cost of commuting to foraging grounds from distant roosts. To test these hypotheses, we simultaneously tracked female reproductive activity of 11 insectivorous bat species, insect biomass, and local weather variables for 20 months in a Malaysian rain forest. Five species roost in forest structures and hence have low commuting costs, whereas six species depend on caves, which are limited in the landscape, and are presumed to incur higher commuting costs to foraging sites. Monthly insect biomass was positively correlated with monthly rainfall, and there was a significant relationship between insect biomass and lactation in cave‐roosting but not forest‐roosting species. Cave‐roosting species were seasonally monoestrus, with parturition confined to a two‐month period, whereas in forest‐roosting species, pregnancy and lactation were recorded throughout the year. Our results suggest that the energetic costs of commuting from roosts to foraging grounds shape annual reproductive patterns in tropical rain forest insectivorous bats. Ongoing changes in forest landscapes are likely to increase these costs for cave‐roosting bats, further restricting reproductive opportunities. Climate change is projected to influence the timing of rainfall events in many tropical habitats, which may disrupt relationships between rainfall, insect biomass, and bat reproductive timing, further compromising reproductive success.     

Flight by night or day? Optimal daily timing of bird migration

Many migratory bird species fly mainly during the night (nocturnal migrants), others during daytime (diurnal migrants) and still others during both night and day. Need to forage during the day, atmospheric structure, predator avoidance and orientation conditions have been proposed as explanations for the widespread occurrence of nocturnal migration. However, the general principles that determine the basic nocturnal-diurnal variation in flight habits are poorly known. In the present study optimal timing of migratory flights, giving the minimum total duration of the migratory journey, is evaluated in a schematic way in relation to ecological conditions for energy gain in foraging and for energy costs in flight. There exists a strong and fundamental advantage of flying by night because foraging time is maximized and energy deposition can take place on days immediately after and prior to the nocturnal flights. The increase in migration speed by nocturnal compared with diurnal migration will be largest for birds with low flight costs and high energy deposition rates. Diurnal migration will be optimal if it is associated with efficient energy gain immediately after a migratory flight because suitable stopover/foraging places have been located during the flight or if energy losses during flight are substantially reduced by thermal soaring and/or by fly-and-forage migration. A strategy of combined diurnal and nocturnal migration may be optimal when birds migrate across regions with relatively poor conditions for energy deposition (not only severe but also soft barriers). Predictions about variable timing of migratory flights depending on changing foraging and environmental conditions along the migration route may be tested for individual birds by analysing satellite tracking results with respect to daily travel routines in different regions. Documenting and understanding the adaptive variability in daily travel schedules among migrating animals constitute a fascinating challenge for future research.     

Energetics of the annual cycle of Dippers Cinclus cinclus

Time-activity budgets and energy expenditure of Dippers Cinclus cinclus were studied in all months of the year and for every stage of the annual cycle. The commonest daytime activity was feeding (54%), then resting (43%) and flying (4%). On a 24-hr day basis the most marked changes in activity followed from changing daylengths. DEE (Daily Energy Expenditure), derived from time-activity budgets through the year and laboratory estimates of metabolism, averaged 201 kj d ^-1 in females and 228 kj d ^-1 in the larger males. Over a more restricted range of circumstances, direct estimates of DEE obtained from 77 Dippers using the doubly labelled water technique averaged 205 ± 43 kj d^-1 and 251 ± 55 kj d^-1 in females and males, respectively. Overall, the correspondence between these largely independent estimates of energy expenditure was reasonably close. DEE was highest during breeding (laying-females; rearing-males) and in late winter for both sexes. The lowest energy expenditures occurred during moult, amongst juveniles and in early winter. Incubating females and mate-guarding males also had low energy costs. Across all stages of the annual cycle body size, activity patterns, ambient temperature and river flow had significant effects on energy expenditure. The rate at which food was gathered to meet these changing energy demands varied widely. While some of this variation was imposed by a seasonal environment, it was also likely to reflect adaptive shifts in rates of food gathering, in some cases consequent upon the changing fitness benefits of various non-feeding activities.     

Night roosting and the nocturnal time budget of the little brown bat,Myotis lucifugus: Effects of reproductive status,prey density,and environmental conditions

Summary The insectivorous bat Myotis lucifugus typically apportions the night into two foraging periods separated by an interval of night roosting. During this interval, many bats occupy roosts that are used exclusively at night and are spatially separate from maternity roosts. The proportion of the night which bats spend roosting, and thus the proportion spent foraging, vary both daily and seasonally in relation to the reproductive condition of the bats, prey density, and ambient temperature. A single, continuous night roosting period is observed during pregnancy. During lactation, females return to maternity roosts between foraging bouts, and night roosts are used only briefly and sporadically. Maximum use of night roosts occurs in late summer after young become volant. Superimposed upon these seasonal trends is day-to-day variation in the bats' nightly time budget. Long night roosting periods and short foraging periods are associated with cool nights and low prey density. This behavioral response may minimize energetic losses during periods of food scarcity.     

Compensation in resting metabolism for experimentally increased activity

To study zebra finch allocation of energy to day and night at two different workloads, we assessed the daily energy turnover from: (1) metabolizable energy of the food, and (2) doubly-labeled water. In both experiments we imposed two levels of activity on captive zebra finches (Taeniopygia guttata), by applying different computer-controlled workload schedules. A low workload required 20 hops, and a high workload 40 hops to obtain 10 s access to food. In experiment 1, we further measured nocturnal energy expenditure by overnight oxygen consumption. From experiment 2 we derived an estimate of the costs of hopping activity, from inter-individual association of daily amount of hopping and daily energy expenditure. Surprisingly, the daily energy budget was, on average, reduced slightly when birds were subjected to a high workload. Since hopping activity was 50% higher during the high workload than during the low workload, the birds apparently compensated, even over-compensated, for the increased energetic demands of activity. Nocturnal energy expenditure was indeed reduced for the high workload, which was largely due to a reduction in resting metabolic rate. Economizing on energy was more than could have been accomplished by a reduction in mass alone, and we discuss the occurrence and potential mechanisms of physiological compensation. The amount of energy saved during the night did account for part of the total amount of energy saved. We surmise that the strategy of energetic compensation observed during the night was extended into the inactive hours of the day. Accepted: 10 July 1998     

Origins and characteristics of Nearctic landbirds in Britain and Ireland in autumn: a statistical analysis

We used data from eastern North America in regressions to explain autumn frequencies of Nearctic landbird species in Britain and Ireland (UK‐IR). The data were: day‐counts of 16 August–15 November from Nova Scotia (NS) on Sable Island 1963–2000 and Seal Island (1963–2002), combined in half‐monthly intervals to account for seasonality; published seasonal totals (10‐ to 11‐day intervals, 20 August–10 November 1955–80) of birds killed at a Florida (FL) TV tower; and published counts following a ‘Fallout’, 11 October 1998, of unseasonal species and southern vagrants in NS, believed to have originated as migrants in the southeast USA that followed a cold front offshore into strong southwest flow beyond. We also used the following species variables: body mass and wing length for size; sd of mass as a proxy for lipid capacity; a five‐level index of migratory span (1 for within North America to 5 for almost totally to South America); latitude of easternmost breeding, and distance to nearest normal range to indicate status in NS; a two‐level index for day vs. night migrants; an index, where pertinent, of significant population change (0 and 2 for a decrease and increase, respectively, 1 for no change). We also used classification and regression trees to cluster the potential transatlantic vagrants into homogeneous groups based on the explanatory variables. Standard generalized linear model regressions using counts from NS islands and FL produced highly positively skewed residuals (many species too common in UK‐IR), but robust regressions eliminated statistical problems, and strengthened effects of non‐count variables. Results using Fallout records, representing a subset of longer‐distance night migrants, were statistically acceptable. The Fallout list, when supplied with counts from the same species from the NS islands and FL, produced highly significant (R² = 0.79–0.93) and statistically acceptable regressions that were not improved by robust versions. Overall, the results indicate that October counts, especially of generally larger, longer‐distance migrants, best represented those reaching UK‐IR. The effect of geographical remoteness was negative – vagrants in NS were less likely to appear in UK‐IR. Population changes were important in predicting the 1956–2003 UK‐IR counts from 1955–80 FL counts. The seasonal characteristics, high explanatory power of the Fallout list and over‐representation of probable over‐ocean migrants in the standard regressions all support suggestions by others that many Nearctic vagrants in UK‐IR originate in flights off southeast USA and are displaced downwind across the North Atlantic.     

Diel variability in nitrogenous nutrient uptake at photic and subphotic depths

Diel patterns in nitrogen uptake were investigated at threepositions along an offshore orientated transect in the SouthernBenguela Upwelling System. Both photic and sub-photic depthswere targeted in the ¹⁵N tracer experiments. An appreciableproportion of nitrogen uptake was found to occur at sub-photicdepths during both the day and the night. The importance ofsub-photic uptake decreased offshore but remained non-trivialat all locations. Although NH₄ dominated this uptake, NO₃ removalat depth did account for an important fraction of the totalwater column NO₃ uptake, particularly over the shelf at night.For example, sub-photic NO₃ uptake at night for the inshorestations averaged 68% of the total for the water column decliningto 3% offshore. The impact of sub-photic NO₄ uptake on new productionwill depend on whether the NO₃ is incorporated into primaryassimilation pathways or is transported to the sediments ininorganic form. Whereas sub-photic/photic uptake decreased offshore,night/day uptake ratios increased with distance from the coast,approaching unity at the offshore location. This effect wasmost obvious for the photic communities This finding supportsthe belief that dark nitrogen uptake assumes increased importanceas nutrients become less available. Photic zone f-ratios weresmaller at night (mean = 0.14) than during the day (mean = 0.28)indicating a greater importance of reduced nitrogen uptake duringthe dark hours This emphasis on NH₄ utilization at night canbe explained purely in terms of energy efficiency. Such die1phasing in f-ratios needs to be accounted for in scaling totalproduction to new proifudon.     

The use of energy stores in the puerulus of the spiny lobster Jasus edwardsii across the continental shelf of New Zealand

Nektonic pueruli of the spiny lobster, Jasus edwardsii, were caught from two locations about 20 km apart across the continental shelf on the south east of the North Island, New Zealand. The pueruli were assayed for total protein, glucose, glycogen, and lipid content. Only the lipid content differed between pueruli caught onshore and offshore (mean difference=3.1 mg or 3.4% of dry mass). The average difference in lipid content measured over this distance was used to calculate the rate of energy consumption and timing for pueruli to actively swim from the continental shelf to shore. These results confirmed previous theoretical estimates and indirect measures. Furthermore, the rate of energy consumption would allow all of the pueruli caught offshore to swim to shore based on their total measured lipids. However, some individuals with low energy stores may be energetically compromised at arrival which may affect their subsequent moulting and survival. The results of this study indicate that lipid is the primary format for energy storage of the nektonic puerulus of the spiny lobster and that these lipid reserves have sufficient energetic capacity to allow the puerulus to actively swim the distance across the shelf to settle on the coast.     

VARIATION IN THE FORAGING LOCATION OF ANTARCTIC FUR SEALS (ARCTOCEPHALUS GAZELLA) AND THE EFFECTS ON DIVING BEHAVIOR

This study investigated how female Antarctic fur seals adapt their foraging behavior, over time scales of days, to spatial unpredictability in the distribution of their food. Lactating Antarctic fur seals are central-place foragers that feed on highly patchy but spatially and temporally dynamic food. We measured the foraging distribution of 28 fur seals to test whether variation in foraging trip durations was reflected in variation in the location of foraging and the diving behavior of seals at sea. Based on the maximum distance travelled from the breeding beach, three categories of foraging trips were denned: those to the continental shelf area ( n = 12, median = 71 km), to oceanic water ( n = 11, median =164 km), and to farther offshore oceanic waters ( n = 5, median = 260 km). Trip duration and mean surface speed were positively correlated with the maximum distance travelled from the breeding beach. Seals on longer trips spent proportionally less of their time submerged, but there was no significant difference in the total number of dives or the total time spent foraging by seals in relation to trip duration. Evidence from this study and previous work investigating energy gain suggests that an animal on a longer foraging trip could potentially have a higher mean energy return per dive than a similar animal on a shorter foraging trip. Evidence presented suggests that the type of foraging trip (near or far) is not predetermined by the animal but may be a simple response to the stochastic distribution of the resources available.     

Roost preferences and foraging ranges of the eastern forest bat Vespadelus pumilus under two disturbance histories in northern New South Wales,Australia

Little is known about the habitat requirements of Australian bats; however, this information is needed to make better‐informed decisions when systems are disturbed. This study contrasts the roosting and foraging ecology of the eastern forest bat Vespadelus pumilus (Vespertilionidae), one of Australia’s smallest bats, between two sites of differing disturbance history on the mid‐north coast of New South Wales. Lorne Flora Reserve (182 ha) is primarily old‐growth forest surrounded by regrowth forest and eucalypt plantations, while Swans Crossing is dominated by regrowth and eucalypt plantations established on part of an old dairy farm. A total of 38 bats were tracked during the maternity and mating seasons at the two sites. Roost preferences were determined by comparing trees used as roosts with those randomly available, while foraging bats were triangulated from fixed stations at night. Bats tracked at Lorne Flora Reserve typically roosted in hollows within large, mature trees and showed a strong preference for roosting and foraging (females only) within the Reserve. Lactating females at Swans Crossing roosted in hollows of remnant rainforest trees within a gully and dead eucalypts, while males often roosted in understorey trees (such as Acacia). Dead trees were frequently used as roosts at both sites. Under both disturbance histories, the mean distance of female maternity roosts from creeks was 20 m, indicating that riparian zones provide important roosting habitat for V. pumilus. However, roosts shifted to the mid‐slope prior to winter when bats mate. Retention of mature trees in a variety of topographic locations may allow behavioural adjustments with the seasons. Bats caught in the regrowth forest also foraged there, with foraging ranges averaging just 5.3 ha (n = 10), indicating that regrowth is used by this bat for both foraging and roosting.     

Home range and habitat use by the serotine bat, Eptesicus serotinus, in England

Serotine nursery roosts with less than 20 bats were found to have home ranges of at least 24 to 77 km² and core areas of activity from 13 to 33 km². The size of the range may have increased further if more individuals had been tracked, as three of the four colonies studied had not reached their asymptotes. The total home-range area covered by four serotine colonies was 127.36 km². Excluding non-breeding bats, a density of one bat per 120 ha was estimated. However, actual density was likely to be higher if there were additional non-breeding females and immatures that were not in nursery roosts. Colonial home ranges and core areas overlapped, with individuals from different colonies feeding at the same sites. Individual home ranges ( n = 32) varied from 0.16 to 47.58 km², but these were not used exclusively by one individual. Around the colonial core area and breeding roosts, home ranges were used by all individuals from a single colony. It is only further from the core area that ranges appeared to be used by individuals. The distance from roost to feeding areas varied by up to 7.4 km, but the bat usually commuted along lines of trees and hedges and over pastures. This resulted in greater distances being travelled than if they had flown by a direct route. On average, individuals commuted distances of 8 km each night between feeding areas, with a maximum distance of over 41 km. They visited between 0 and 10 feeding sites each night (mean = 2.89).     

Dialect use in large assemblies: a study in European starling Sturnus vulgaris roosts

Dialects may signal social or population identity and increase tolerance within communities. We hypothesized that in European starling Sturnus vulgaris communal roosts, birds coming from the same breeding area, i.e. dialectal zone, might tend to stay together within the roost. Recordings were performed in the colonies, revealed in earlier studies, multiple dialects and small sectors where birds shared the same variants at the different levels. We also performed recordings in different locations within night roosts. The dialects recorded in the roosts were the same as those recorded at nest sites during the day and they were not distributed randomly within roosts: birds from the same geographical diurnal origin would gather and stay together, either because they arrived together or were attracted to their dialect. Although our results have to be confirmed by the study of identifiable individuals, we propose original lines of thought on roost structuring and on the role of song dialects.     

Mechanisms for the formation and maintenance of traditional night roost aggregations in a territorial damselfly

Communal roosting has been studied extensively in birds, but the mechanisms and functions of this taxonomically widespread behaviour pattern remain poorly understood. We studied the roosting behaviour of rubyspot damselflies, Hetaerina americana, in relation to sex and territorial status, and conducted field experiments to test for specific mechanisms of roost formation and maintenance. Both sexes tended to return close to their previous night's roost, but only males were significantly more roost site faithful than chance expectations based on individual day ranges. Males were more roost site faithful when they held mating territories. After acquiring a territory, males usually began roosting closer to the territory after a delay of a few days. Roosts were not located at sites that reduced the daily commuting distance between hunting areas and territories; males generally hunted closer to their territories than to their roosts. In field experiments, sites 'seeded' with synthetic models of male rubyspots attracted more recruits than vacant control sites and control sites seeded with nonrubyspot (clear-winged) damselfly models. Sites seeded repeatedly with rubyspot models often remained popular for roosting after the models were removed, suggesting that the models established new traditional roosts. These results indicate that conspecific attraction and individual spatial memory together may be sufficient to explain, at a proximate level, the traditional night roost aggregations of this species. We discuss these results in relation to functional hypotheses for roost site choice and fidelity. Copyright 2000 The Association for the Study of Animal Behaviour.