SELECTION OF COLONY SITES AND NEST SITES BY COMMON TERNS STERNA HIRUNDO IN OCEAN COUNTY, NEW JERSEY

Common Terns nested on 34 of 259 saltmarsh islands along 46 miles of Ocean County coastline, New Jersey. They nested on low islands of Spartina with less than 12%, windrow ranging in size from 0.6 to 108 acres. All islands selected by terns faced at least two miles of open water from at least one direction. Selection of islands seemed a response to vegetation, size, distance to the nearest island, distance to the nearest shore and exposure to open water. Of the 225 islands without nesting terns, only three fulfilled appropriate criteria. Eighty per cent of nests were situated on windrow. Terns laid larger clutches on windrow compated to those nesting in Spartina. Nearest neighbour distance on islands with low predation varied from 85 to 485 cm and was a function of space, vegetation, and the size of the island. Terns nested closer together on windrow compared with Spartina. Considering all colonies, the mean nearest neighbour distance negatively correlated with the number of nests. Skimmers, Oystercatchers, Laughing Gulls, and Herring Gulls nested in some of the tern colonies. All tern colonies on islands also occupied by nesting Herring Gulls suffered over 10% egg-loss by predation. Proportionally more nests were preyed upon in windrow than in Spartina. Clutch sizes in nests in windrow on islands with predation were significantly lower than those in windrow on islands without predation, even though clutch sizes in Spartina were similar on islands with and without predation. Flooding by exceptional high tides destroyed significantly more nests in Spartina than in windrow. The nests that survived in Spartina were built deeper, and their rim heights were higher than nests destroyed by tides. Choice of colony and nest sites is discussed in terms of the balance of two selection pressures: predation and tidal flooding. Tern nests on windrow are more exposed to predators, but safer from flooding, whereas those nests in Spartina are more susceptible to flooding and less vulnerable to predators. The recent invasion of Herring Gulls into Ocean County has significantly increased the rate of nest predation among affected colonies of Common Terns. It is possible that in future years the terns' behaviour may be modified in response to this new selective pressure.     

Wait Until Dark? Daily Activity Patterns and Nest Predation by Snakes

Predation involves costs and benefits, so predators should employ tactics that reduce their risk of injury or death and that increase their success at capturing prey. One potential way that predators could decrease risk and increase benefits is by attacking prey at night when risks may be reduced and prey more vulnerable. Because some snakes are facultatively nocturnal and prey on bird nests during the day and night, they are ideal for assessing the costs and benefits of diurnal vs. nocturnal predation. We used automated radiotelemetry and cameras to investigate predation on nesting birds by two species of snakes, one diurnal and the other facultatively nocturnal. We predicted that snakes preying on nests at night should experience less parental nest defence and capture more adults and nestlings. Rat snakes (Pantherophis obsoletus) were relatively inactive at night (23–36% activity) but nearly always preyed on nests after dark (80% of nest predations). Conversely, racers (Coluber constrictor) were exclusively diurnal and preyed on nests during the times of day they were most active. These results are consistent with rat snakes strategically using their capacity for facultative nocturnal activity to prey on nests at night. The likely benefit is reduced nest defence because birds defended their nests less vigourously at night. Consistent with nocturnal predation being safer, rat snake predation events lasted three times longer at night than during the day (26 vs. 8 min). Nocturnal nest predation did not make nests more profitable by increasing the likelihood of capturing adults or removing premature fledging of nestlings. The disconnect between rat snake activity and timing of nest predation seems most consistent with rat snakes locating prey during the day using visual cues but waiting until dark to prey on nests when predation is safer, although designing a direct test of this hypothesis will be challenging.     

Nocturnal nest predation: a potential obstacle to recovery of a Florida Scrub-Jay population

ABSTRACT.   Population declines among birds are often linked to habitat change and associated increases in nest predation rates. In species of conservation concern identifying nest predators is an important first step in developing management strategies to mitigate low nesting success caused by depredation. Because predator composition varies geographically and with landscape factors habitat restoration may need to be tailored to reduce locally important predators. We used miniature video cameras to identify nest predators in a population of Florida Scrub-Jays ( Aphelocoma coerulescens ) significant to conservation. At 22 nests we observed 25 predation events; 22 (88%) of these events were nocturnal. Yellow rat snakes ( Elaphe obsoleta ) had the highest daily predation rate and accounted for 76% of egg and nestling losses. Florida Scrub-Jays are vulnerable to nocturnal nest predation because their vigilance behavior is ineffective against nocturnal predators, breeders cannot defend against nocturnal predators, and brooding females are at risk of being killed by nocturnal predators. If current habitat restoration efforts do not reduce numbers of yellow rat snakes and improve scrub-jay nesting success, management actions to reduce populations of nocturnal snakes may need to be considered.     

Validating the use of temperature data loggers to measure survival of songbird nests

ABSTRACT.   Accurate determination of nest fates and nest predators is possible through continuous video monitoring, but such monitoring is relatively expensive and labor intensive. If documenting of the timing of nest termination events is sufficient, then data loggers (DL) may allow more extensive sampling and may represent a viable alternative. I validated temperature DL records of nest survival time by simultaneous videotaping and compared results derived from DL records with those obtained by regular nest visits by an observer. I estimated the fate of 937 nests of nine species of open cup-nesting songbirds, including 673 nests monitored using DL, 165 monitored using video cameras, 33 validation nests monitored simultaneously using both DL and video cameras, and 132 control nests monitored only by observer visits. Deployment of DL did not negatively influence nest survival rate. DL reliably recorded survival time and allowed classification of nest fates based on the potential fledging age, regardless of the frequency of nest visits by an observer. The true fate of nests that survived beyond the potential fledging age can not be safely determined from time of failure, except for nocturnal events that suggest partial predation. Video revealed frequent partial or complete predation on nests with old nestlings that would have been categorized as successful by other methods. I conclude that temperature DL are efficient, reliable, and relatively inexpensive tools for recording exact nest survival times and classification of nest fates, with implications for nest survival modeling and discriminating between diurnal and nocturnal predation.     

Nest predators of woodland open-nesting songbirds in central Europe

I used time-lapse videotaping to identify predators of open songbird nests in fragmented deciduous woodland (nine plots, 2–10 ha each) in the Czech Republic from 2002 to 2006. I documented 22 species of predators at 171 nests of 13 species (mainly Blackcap Sylvia atricapilla , Song Thrush Turdus philomelos , Common Blackbird Turdus merula , Yellowhammer Emberiza citrinella and Chaffinch Fringilla coelebs ). The main predators were Pine Marten Martes martes (37% of 178 predation events), Jay Garrulus glandarius (29%), Buzzard Buteo buteo (7%) and Great Spotted Woodpecker Dendrocopos major (7%); mammals accounted for 48% of total predation. At least 3% of nests were depredated by multiple predators. In spite of their local abundance, Hooded Crows Corvus cornix did not present a serious threat for shrub nesting songbirds (< 1% of total predation). No predation by mice was recorded, suggesting that their importance has been overestimated in artificial nest studies. The proportional species composition of predators depended on which species occupied the monitored nest and location (study plot), but not on the year or the time of season. Corvids and raptors accounted for a relatively larger percentage of total predation of small ('warblers') and large ('thrushes') prey species, respectively, whereas carnivores were important predators of all prey species. Active nests of thrushes were only rarely robbed by Jays (< 4% of 52 events), presumably due to parental nest defence. Predation by woodpeckers was spatially clumped, probably due to individual foraging specialization. Predation by the other major predators was documented on most/all study plots.     

Nest predators of Lance-tailed Manakins on Isla Boca Brava, Panamá

ABSTRACT.   Nest predation is often the primary cause of nest failure for passerines. Despite this, little is known about predation rates and the nest predators of birds in the tropics. I used video cameras to monitor seven Lance-tailed Manakin ( Chiroxiphia lanceolata ) nests on Isla Boca Brava, Panamá. One nest fledged young and six nests failed due to predation. I recorded five predation events involving four avian predators and one mammalian predator. Crested Oropendolas ( Psarocolius decumanus ) predated two nests and a Roadside Hawk ( Buteo magnirostris ) and a Black-chested Jay ( Cyanocorax affinis ) each predated one. The mammalian predator was a common opossum ( Didelphis marsupialis ). All avian predation was diurnal; the mammalian predation was nocturnal. My results suggest that tropical birds are subject to a diverse suite of nest predators, and that avian predators may be an important cause of nest failure at my study site.     

Nest desertion by a cowbird host: an antiparasite behavior or a response to egg loss?

Natural selection can favor songbirds that desert nests containingeggs of the parasitic brown-headed cowbird (Molothrus ater).However, the high variability in desertion of parasitized nestswithin species is perplexing in light of the typically highcosts of parasitism. Because nest desertion can also be a responseto partial clutch predation, we first asked if Bell's vireos(Vireo bellii) deserted nests in response to the presence ofcowbird eggs (antiparasite response hypothesis) or to egg removalby predators and female cowbirds (egg predation hypothesis).Second, we asked whether variation in nest desertion was dueto intrinsic differences among individuals or to variation innest contents. We monitored a large number of nests (n = 494)and performed a clutch manipulation experiment to test thesehypotheses. The number of vireo eggs that remained in a nestwas a strong predictor of desertion both within and among pairs.Neither the presence of a single cowbird egg, which leads tonest failure for this host, nor the number of cowbird eggs receivedin a vireo nest influenced nest desertion. Furthermore, vireosdid not desert experimental nests when we immediately exchangedcowbird eggs for vireo eggs but deserted if we removed vireoeggs and replaced them with cowbird eggs the following morning.Desertion of parasitized nests by Bell's vireos can be almostentirely explained as a response to partial or complete clutchloss and does not appear to have been altered by selection frombrood parasitism.     

Absence from the nest due to human disturbance induces higher nest predation risk than natural recesses in Common Eiders Somateria mollissima

Human disturbance of nesting birds may cause reduced breeding success. It is therefore necessary to assess the impact of disturbance to identify steps that minimize negative impacts. We carried out a study of nesting success at two adjacent colonies of Common Eider Somateria mollissima on the islands of Grindøya and Håkøya in northern Norway between 2006 and 2011. Over the study period, nesting success was consistently higher on Håkøya (69–82%) than on Grindøya (35–60%). Between 2009 and 2011 we used camera monitoring of individual nests to identify determinants of nest survival and predation, focusing in particular on the effect of departures from the nest due to human disturbance, which differed between the colonies due to a long‐term research project on Grindøya. Overall, absence of Common Eiders from nests due to disturbance increased the predation risk by a factor of 6.42 for an increase of one additional daily disturbance. In contrast, absence due to natural recesses did not increase nest losses. Under high levels of human disturbance, camera monitoring indicated that the main cause of breeding failure was predation, primarily by Hooded Crows Corvus cornix, but also to some extent Great Black‐backed Gulls Larus marinus. The presence of cameras did not increase the predation risk. Both the presence of researchers and the sight of Common Eider females conspicuously departing from nests are likely to have provided cues to these predators. We suggest management trials to reduce nesting disturbance through the guarding of unoccupied nests to mitigate the effects of human disturbance on reproductive success.     

Coal tits increase evening body mass in response to tawny owl calls

Current theory predicts small birds should have a reduced body mass when daytime predation risk is high. However, the influence that nighttime predators might have on changes in body mass or daytime foraging behaviour has not been addressed. We therefore studied the effect of changes in perceived nocturnal predation risk on the body mass of captive coal tits. In a soundproof room, eight coal tits were housed in individual cages and an experiment was performed in which the birds were subjected to two treatments. First, morning and evening body mass was monitored following nights that were quiet. Second, these parameters were measured following nights when the call of a tawny owl had been played once per hour. Evening body mass was 3% greater on days following owl-disturbed nights, but morning body masses did not differ between treatments. To ensure this result was a response to the owl calls per se, and not a general response to increased disturbance, a second experiment was necessary. Here the coal tits were exposed hourly to the calls of a nightjar, a non-predatory nocturnal bird, but no increases in body mass were observed compared to quiet nights. We suggest the coal tits increased body mass in response to owl calls to offset increased nighttime energy expenditure in attentive behaviour. Received: 26 July 1999 / Received in revised form: 30 October 1999 / Accepted: 29 November 1999     

Nocturnal courtship,copulation, and egg-laying in the western grebe (<Emphasis Type="Italic">Aechmophorus occidentalis</Emphasis>) and Clark’s grebe (<Emphasis Type="Italic">Aechmophorus clarkii</Emphasis>)

Grebes (Podicipedidae) are primarily diurnal although migration occurs at night and some species forage opportunistically at night. We used motion-activated cameras to study nocturnal reproductive activities of the western grebe, Aechmophorus occidentalis, and Clark’s grebe, Aechmophorus clarkii, at Clear Lake, California, USA, during 2014–2016. During 9283 h of monitoring, 19.4% of rushing displays (n = 75) and 8.4% of copulations (n = 435), plus two weed dancing displays and four instances of egg-laying, occurred at night. Nocturnal copulation and egg-laying often occurred on empty, recently abandoned nests, but some incubating pairs of grebes also copulated at night. Nocturnal reproductive activities occurred more frequently at nests attached to submergent vegetation in open water far from shore when water levels were low than on nests attached to emergent vegetation close to shore when water levels were high, probably due to a reduced risk of predation by nocturnal mammals farther from shore. Nocturnal reproductive activities were not in response to elevated light levels at night, daylight disturbances, diurnal predation, high temperatures on hot days, or sexual interference during daylight. Instead, grebes attempted to increase mating investment and minimize parental investment by exploiting recently abandoned nests at night, and perhaps by undertaking extrapair copulations under the cover of darkness, but some pairs of grebes may simply extended routine reproductive activities into the night. Reproductive activities are probably limited at night by the need to feed during daylight and sleep at night, and by the increased risk of predation by mammals at night. Given the high costs of construction and maintenance of floating nests and the obvious benefit of quickly exploiting abandoned nests, nocturnal reproductive activities may occur more frequently in grebes and other waterbirds using floating nests than in other groups of birds whose reproductive activities occur mostly during daylight.     

Long-term changes in breeding phenology at two seabird colonies in the western North Sea

There is compelling evidence that the breeding phenology of many species has changed substantially in recent decades. However, taxonomic and spatial variation in the direction and rate of change is still not well understood. We explored these issues by analysing a dataset containing information on first egg dates of 10 species of seabird at two major breeding colonies (86 km apart) in the western North Sea over a period of 35 years. Within a species, timing of breeding was positively correlated between the two colonies, suggesting that factors affecting the phenology of these species operated at a regional rather than a colony scale. Comparison of time trends among the species revealed contrasting patterns, with some showing no systematic change, others becoming earlier and others later. The clearest species groupings appeared to be among the terns with arrival and/or first egg dates becoming earlier in Arctic Terns Sterna paradisaea , Common Terns Sterna hirundo and Sandwich Terns Sterna sandvicensis , and among the auks (Common Guillemot Uria aalge , Razorbill Alca torda and Atlantic Puffin Fratercula arctica ) and Black-legged Kittiwake Rissa tridactyla where the trend was in the opposite direction towards later breeding. This general trend towards later breeding in the latter group of species contrasts with correlational evidence from many other organisms indicating that breeding phenology is advancing in response to climate change.     

Non-additivity among multiple cues of predation risk: a behaviorally-driven trophic cascade between owls and songbirds

Non-lethal effects of predators on prey are initiated in the form of responses to direct and indirect cues of predation risk. Like their lethal equivalents, non-lethal effects may affect species further down the food web initiating a behaviorally-driven trophic cascade. I presented a direct cue of predation risk, owl vocalizations, to white-footed mice ( Peromyscus leucopus ) during either a new or full moon (indirect cue). Mice reduced their activity in space by nearly two-thirds in response to playbacks of owl vocalizations during a full moon. However, neither moonlight (full vs new) nor the presence/absence of owl calls had an effect on space use when each cue varied singly. Previous studies have demonstrated a tight correlation between spatial activity in mice as used in the current experiment and nest predation rates on ground-nesting birds. Because moonlight is a ubiquitous deterrent of activity in nocturnal rodents I used of long-term nesting records the veery ( Catharus fuscescens ) to test whether nest predation rates were correlated negatively with moonlight. For half the lunar cycle (∼full moon to new moon) predation rates decreased with moonlight as predicted. During the second half of the lunar cycle predation and moonlight did not correlate as expected, but this was likely due to the depletion of vulnerable nests after a period of in which predation rates were at their maximum near the full moon. These studies suggest that the non-lethal effects of predatory risk on mice (i.e. changes in space use) cascade to affect their prey. Through the mechanism of reduced space use by rodents, perceived predation risk has the potential to significantly and indirectly affect songbird nest predation rates.     

Cats and seabirds: effects of feral Domestic Cat Felis silvestris catus eradication on the population of Sooty Terns Onychoprion fuscata on Ascension Island, South Atlantic

The population of Sooty Terns Onychoprion fuscata breeding on Ascension Island in the Atlantic Ocean was monitored over 17 years (1990–2007). This period spanned the programme of feral Domestic Cat Felis silvestris catus eradication from the island, which commenced in 2001 with the last Cat recorded in 2004. We report on the abundance of Sooty Terns and Black Rats Rattus rattus before and after Cat eradication. The Sooty Tern breeding population in the 1990s averaged 368 000 and Cats were killing Terns at an average rate of 33 adults per night. Following Cat eradication, adult Terns are no longer predated. However, egg predation by both Rats and Common Mynas Acridotheres tristis has continued with Mynas destroying more eggs than Rats. Unexpectedly, we observed a change in Rat predatory behaviour. Following Cat eradication, Rats have become a major predator of Sooty Tern chicks. Despite this change, the Tern population has shown a season-on-season increase since Cat eradication, 48.8% in 2005, 8.2% in 2006 and 6.1% in 2007, and the breeding population increased to 420 000 birds in 2007. Incubation success improved from 66.0 to 84.4% during Cat eradication, before dropping down again to 67.9% after Cats were eradicated and Rat control measures were introduced. Index traplines were set for Rats and Rat numbers fluctuated widely immediately after Cats were eradicated but there were no significant differences that could be attributed to changes in Cat numbers. Ascension Island Sooty Terns breed every 9.6 months and juveniles defer breeding for seven seasons. Hence 2008 is the first year in which an increase in the breeding Sooty Tern population directly attributable to Cat eradication is likely to be detected. We conclude that long-term monitoring is essential to guide conservation practice even in this relatively simple predator–prey system.     

Visual tracking from a rigid‐hulled inflatable boat to determine foraging movements of breeding terns

ABSTRACT Defining the at‐sea foraging movements of seabirds is fundamental to understanding their ecology and can also be important in assessing the potential impact of marine developments such as offshore wind farms (OWFs). Surveys of predefined areas using aerial or boat‐based transect surveys may not allow adequate assessment of the relative importance of different areas to birds. Individual‐based satellite or radio‐telemetry can be effective in identifying foraging ranges and preferred areas, but may not be suitable for some species. We developed a method to determine the foraging movements of breeding terns (Sterna spp.) by visually tracking individuals using a rigid‐hulled inflatable boat (RHIB). Sandwich Terns (S. sandvicensis), Common Terns (S. hirundo), and Arctic Terns (S. paradisaea) were tracked from colonies in Norfolk and Anglesey, United Kingdom, from 2006 to 2008. The proportion of complete (from and to colony) trips varied from 29–60% among species, years, and colonies. Individual Sandwich Terns were tracked for periods up to 126 min over distances up to 72 km and as far as 54 km from the breeding colony, further than Arctic (up to 57 km and 29 km from the colony) and Common (to 29 km and <9 km from the colony) terns. Mean values were much smaller. Multivariate modeling of Sandwich Tern foraging trips indicated that flight speeds >50 km/hr coupled with greater distances from shore (>25 km) significantly reduced the likelihood of tracking a bird for an entire foraging trip. Use of different boats that differ in speed and performance may alleviate such issues. Visual tracking allowed us to collect data on foraging behavior, flight height, and prey capture rates, and also permitted comparisons between species. Our results indicate that visual tracking may be an effective means of determining the foraging movements and at‐sea behavior of a variety of short‐ranging, day‐active seabirds.     

Offspring desertion and parental care in the Whiskered Tern Chlidonias hybrida

In species with biparental care, a conflict of interest can arise if one mate tries to maximize its own reproductive success at the expense of the other's. One of the mates can desert the brood to accrue a number of benefits to enhance its own fitness, leaving parental care to the remaining parent. This study is the first to describe the desertion pattern in a tern species (Sternidae). We investigated offspring desertion in the Whiskered Tern Chlidonias hybrida, a species with semi‐precocial chicks. Offspring desertion was recorded in 52% of nests prior to fledging (n = 131 nests). Females also deserted during the post‐fledging period. Of the deserters, 97% were females. Desertions started when chicks were 5 days old and no longer required intense brooding. Desertions before fledging did not affect fledging success. Provisioning rates between pair members differed, and females supplied much less food than males. Female provisioning rate affected the chances of nest desertion significantly: daily desertion rates were lower when females supplied more food. After females had deserted, males increased their provisioning rates but compensated for the loss of female care only partly in two‐ and three‐chick broods. Only in small (one‐chick) broods was compensation full. We conclude that male and female Whiskered Terns adopt different reproductive strategies in the population studied here. Females invest much less in parental care than males, providing less food and deserting more frequently. Given the ready availability of food and low predation pressure, benefits appear to accrue to females that desert; selection forces may therefore not be acting against female desertion.     

Higher nest predation risk in association with a top predator: mesopredator attraction?

Breeding close to top predators is a widespread reproductive strategy. Breeding animals may gain indirect benefits if proximity to top predators results in a reduction of predation due to suppression of mesopredators. We tested if passerine birds gain protection from mesopredators by nesting within territories of a top predator, the Ural owl (Strix uralensis). We placed nest boxes for pied flycatchers (Ficedula hypoleuca) in Ural owl nest sites and in control sites (currently unoccupied by owls). The nest boxes were designed so that nest predation risk could be altered (experimentally increased) after flycatcher settlement; we considered predation rate as a proxy of mesopredator abundance. Overall, we found higher nest predation rates in treatment than in control sites. Flycatcher laying date did not differ between sites, but smaller clutches were laid in treatment sites compared to controls, suggesting a response to perceived predation risk. Relative nest predation rate varied between years, being higher in owl nest sites in 2 years but similar in another; this variation might be indirectly influenced by vole abundance. Proximity to Ural owl nests might represent a risky habitat for passerines. High predation rates within owl territories could be because small mesopredators that do not directly threaten owl nests are attracted to owl nest sites. This could be explained if some mesopredators use owl territories to gain protection from their own predators, or if top predators and mesopredators independently seek similar habitats.     

Predators at bird nests in a northern hardwood forest in New Hampshire

ABSTRACT.   Nest predation is the primary cause of nest failure in most passerine birds, and increases in nest predation associated with anthropogenic habitat disturbance are invoked as explanations for population declines of some bird species. In most cases, however, the identity of the nest predators is not known with certainty. We monitored active bird nests with infrared time-lapse video cameras to determine which nest predators were responsible for depredating bird nests in northern New Hampshire. We monitored 64 nests of 11 bird species during three breeding seasons, and identified seven species of predators during 14 predation events. In addition, we recorded two instances of birds defending nests from predators and, in both cases, these nests were ultimately lost to predation. These results contrast with other studies in terms of the relatively high proportion of nests depredated by raptors and mice, as well as the absence of any predation by snakes. The diverse suite of predators in this and other studies is likely to confound our understanding of patterns of nest predation relative to fragmentation and habitat structure.     

Feeding ecology of wintering terns in Guinea-Bissau

We studied the feeding ecology of Little Terns Sterna albifrons , Sandwich Terns S. sandvicensis and Royal Terns S. maxima in the Archipélago dos Bijagós (11°40'N, 15°45'W) in Guinea-Bissau (West Africa) during the winter of 1992/1993. More than 95% of all prey taken by these terns were roundfish, ranging in weight from 0.3 to 40 g. Birds usually fed alone, but sometimes they were observed feeding in mixed-species flocks consisting of 15–200 individuals. Capture rate ( n fish per hour foraging) in these flocks was higher than that of solitary birds. However, smaller fish were caught by birds foraging in flocks, so food intake rate (g/h) did not differ between solitary and flock-feeding birds. The relationships between foraging behaviour of the three tern species and abiotic factors, such as time, tide and water clarity, have been investigated. Capture rate of Royal Terns increased with water clarity. For Little Terns and Sandwich Terns, food intake rate was lower in the most turbid waters compared to clearer waters. There was very little foraging activity during high tide. For Little Terns and Royal Terns, food intake rate was about twice as high during receding and low tides as during an incoming tide. Food intake rate averaged 8 g/h in Little Terns, 60 g/h in Sandwich Terns and 45 g/h in Royal Terns. With a rough model, we estimate the maximum rate of daily energy expenditure of terns wintering in the tropics at 3 × BMR (defined as energy expenditure of inactive bird at thermoneutrality in a post-absorptive state during the resting phase of the daily cycle). From an energetic viewpoint, wintering Sandwich Terns in Guinea-Bissau seem to have an easy living.     

Diel activity patterns of juvenile Atlantic salmon in rivers with summer water temperature near the temperature‐dependent suppression of diurnal activity

Direct day and night underwater observations of juvenile Atlantic salmon Salmo salar during summer and autumn showed a duality in response to temperature between 7 and 11° C for young‐of‐the‐year (YOY) Atlantic salmon. They were predominantly diurnal in early summer and nocturnal in late summer although water temperatures were similar. Post‐YOY Atlantic salmon did not show a strong response to temperature as they were mostly nocturnal during the study period. It is suggested that the difference in activity patterns between YOY and post‐YOY Atlantic salmon can be explained by size‐dependent trade‐off between growth and predation risk.     

Strike Fast,Strike Hard: The Red-Throated Caracara Exploits Absconding Behavior of Social Wasps during Nest Predation

Red-throated Caracaras Ibycter americanus (Falconidae) are specialist predators of social wasps in the Neotropics. It had been proposed that these caracaras possess chemical repellents that allow them to take the brood of wasp nests without being attacked by worker wasps. To determine how caracaras exploit nests of social wasps and whether chemical repellents facilitate predation, we: (1) video recorded the birds attacking wasp nests; (2) analyzed surface extracts of the birds'' faces, feet, and feathers for potential chemical repellents; and (3) inflicted mechanical damage on wasp nests to determine the defensive behavior of wasps in response to varying levels of disturbance. During caracara predation events, two species of large-bodied wasps mounted stinging attacks on caracaras, whereas three smaller-bodied wasp species did not. The “hit-and-run” predation tactic of caracaras when they attacked nests of large and aggressive wasps reduced the risk of getting stung. Our data reveal that the predation strategy of caracaras is based on mechanical disturbance of, and damage to, target wasp nests. Caracara attacks and severe experimental disturbance of nests invariably caused wasps to abscond (abandon their nests). Two compounds in caracara foot extracts [sulcatone and iridodial] elicited electrophysiological responses from wasp antennae, and were also present in defensive secretions of sympatric arboreal-nesting Azteca ants. These compounds appear not to be wasp repellents but to be acquired coincidentally by caracaras when they perch on trees inhabited with Azteca ants. We conclude that caracara predation success does not depend on wasp repellents but relies on the absconding response that is typical of swarm-founding polistine wasps. Our study highlights the potential importance of vertebrate predators in the ecology and evolution of social wasps.