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151 results for “Nest site”
Data from: Does the history of option quality affect nest site choice in the acorn ant?
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Data from: An invasive insect, hemlock woolly adelgid, indirectly impacts Louisiana Waterthrush nest site selection and nest survival in the southern Appalachians
<p>Eastern hemlock (<i>Tsuga canadensis</i>) is declining throughout the eastern United States due to hemlock woolly adelgid (<i>Adelges tsugae</i> Annand), an invasive insect from Asia. In the southern Appalachians, hemlock is concentrated in moist ravines and its decline threatens riparian ecosystems. Previous research on this invasion has focused on adelgid control and how hemlock decline affects community composition or forest processes; few studies have evaluated the consequences for demography of obligate riparian species. The Louisiana Waterthrush (<i>Parkesia motacilla</i>) is an obligate riparian species that could be sensitive to hemlock condition in this region, but how individuals respond to decline is currently unknown. To address this knowledge gap, we leveraged recent adelgid treatment efforts in Great Smoky Mountains National Park to evaluate the relationship(s) between hemlock decline and waterthrush habitat selection (foraging and nest site) and vital rates (nest and adult survival). We found that hemlock decline was unrelated to foraging habitat selection and apparent adult survival, but was related to nest site selection through an interaction with percent ground cover of exposed live tree roots: birds selected for nest sites in areas with more exposed live roots but only when hemlock were in poor condition. Nest survival was lower in areas where deciduous species (vs. evergreen species) dominated the understory, suggesting that adelgid invasion could indirectly impact waterthrush fitness depending on how vegetative succession proceeds following hemlock decline. Our results suggest that the short-term consequences of adelgid invasion on this riparian avian species are minimal in this area, but these relationships are likely dynamic and dependent on local habitat features and the predator community response to hemlock decline.Eastern hemlock (<i>Tsuga canadensis</i>) is declining throughout the eastern United States due to hemlock woolly adelgid (<i>Adelges tsugae</i> Annand), an invasive insect from Asia. In the southern Appalachians, hemlock is concentrated in moist ravines and its decline threatens riparian ecosystems. Previous research on this invasion has focused on adelgid control and how hemlock decline affects community composition or forest processes; few studies have evaluated the consequences for demography of obligate riparian species. The Louisiana Waterthrush (<i>Parkesia motacilla</i>) is an obligate riparian species that could be sensitive to hemlock condition in this region, but how individuals respond to decline is currently unknown. To address this knowledge gap, we leveraged recent adelgid treatment efforts in Great Smoky Mountains National Park to evaluate the relationship(s) between hemlock decline and waterthrush habitat selection (foraging and nest site) and vital rates (nest and adult survival). We found that hemlock decline was unrelated to foraging habitat selection and apparent adult survival, but was related to nest site selection through an interaction with percent ground cover of exposed live tree roots: birds selected for nest sites in areas with more exposed live roots but only when hemlock were in poor condition. Nest survival was lower in areas where deciduous species (vs. evergreen species) dominated the understory, suggesting that adelgid invasion could indirectly impact waterthrush fitness depending on how vegetative succession proceeds following hemlock decline. Our results suggest that the short-term consequences of adelgid invasion on this riparian avian species are minimal in this area, but these relationships are likely dynamic and dependent on local habitat features and the predator community response to hemlock decline.</p>
Data from: A description of nesting behaviors, including factors impacting nest site selection, in black-and-white ruffed lemurs (Varecia variegata)
Nest site selection is at once fundamental to reproduction and a poorly understood component of many organisms' reproductive investment. This study investigates the nesting behaviors of black-and-white ruffed lemurs, Varecia variegata, a litter-bearing primate from the southeastern rainforests of Madagascar. Using a combination of behavioral, geospatial, and demographic data, I test the hypotheses that environmental and social cues influence nest site selection, and that these decisions ultimately impact maternal reproductive success. Gestating females built multiple large nests throughout their territories. Of these, females used only a fraction of the originally constructed nests, as well as several parking locations as infants aged. Nest construction was best predicted by environmental cues, including the size of the nesting tree and density of feeding trees within a 75 m radius of the nest, whereas nest use depended largely on the size and average distance to feeding trees within that same area. Microhabitat characteristics were unrelated to whether females built or used nests. Although unrelated to nest site selection, social cues, specifically the average distance to conspecifics' nest and park sites, were related to maternal reproductive success; mothers whose litters were parked in closer proximity to others' nests experienced higher infant survival than those whose nests were more isolated. This is likely because nesting proximity facilitated communal crèche use by neighboring females. Together, these results suggest a complex pattern of nesting behaviors that involves females strategically building nests in areas with high potential resource abundance, using nests in areas according to their realized productivity, and communally rearing infants within a network of nests distributed throughout the larger communal territory.
Figure 4. - Nest defending postures of Xylocopanasalis; Defending posture tactics performed by females Xylocopanasalis to repel other conspecifics in the aggregated nesting site. The bee blocking the entrance via protruding her head out from the nest entrance (4a). Guarding the entrance by using the dorsal side of her metasoma to block the invaders (4b).
Figure 4. - Nest defending postures of Xylocopanasalis; Defending posture tactics performed by females Xylocopanasalis to repel other conspecifics in the aggregated nesting site. The bee blocking the entrance via protruding her head out from the nest entrance (4a). Guarding the entrance by using the dorsal side of her metasoma to block the invaders (4b).
Figure 1. - Location of sites where records of caterpillars of Phengarisalcon (triangles) and Phengarisnausithous (circles) in ant nests are known in the Czech Republic.
Figure 1. - Location of sites where records of caterpillars of Phengarisalcon (triangles) and Phengarisnausithous (circles) in ant nests are known in the Czech Republic.
Figure 1. - Location of sites where records of caterpillars of Phengarisalcon (triangles) and Phengarisnausithous (circles) in ant nests are known in the Czech Republic.
Figure 1. - Location of sites where records of caterpillars of Phengarisalcon (triangles) and Phengarisnausithous (circles) in ant nests are known in the Czech Republic.
Fig. 2 in Black Tern Nest-Site Fidelity In An Unstable Habitat: A Preliminary Study
Fig. 2. The distance resighted / recaptured nesting Black Terns moved
Fig. 1 in Black Tern Nest-Site Fidelity In An Unstable Habitat: A Preliminary Study
Fig. 1. The number of birds returning in different periods of time from 2012 till 2019.
Effects of nest-site availability on male-male competition and the foraging costs associated with paternal care in a resource-defense species
<p><strong>Effects of nest-site availability on male-male competition and associated costs of nest site maintenance and paternal care in a resource-defense species</strong></p> <p>This repository contains the .csv files used for the statistical analyses of the study "Effects of nest-site availability on male-male competition and associated costs of nest site maintenance and paternal care in a resource-defense species". In case of questions, please email Laís A. Grossel: <a href="mailto:laisgrossel@gmail.com">laisgrossel@gmail.com</a></p> <p><strong>Data files and structure</strong></p> <p>We have files for the analysis with field and experimental data.</p> <p>With the file <strong>field.csv</strong> we tested the probability of males obtaining a nest and receiving eggs from females. In this file, we have the headers:</p> <ul> <li><strong>maleID:</strong> identity of males in the field</li> <li><strong>DSW:</strong> dorsal scute width, in mm</li> <li><strong>mass:</strong> to the nearest 0.001 g</li> <li><strong>nest_possession:</strong> with 2 levels: 0 if the male did not possess a nest and 1 if the male possessed a nest</li> <li><strong>nest_opening:</strong> in cm</li> <li><strong>parental_status:</strong> with 3 levels: 0 if the male did not have a nest, 1: if the male had a nest but no eggs, and 2: if the male had a nest and eggs</li> </ul> <p>With the file <strong>experiment_nests.csv</strong> we tested predictions related with the nest possession. In this file, we have the headers:</p> <ul> <li><strong>terrariaID:</strong> identity of the 14 terraria (containing 4 or 8 nests)</li> <li><strong>exp_group:</strong> experimental group, with 2 levels of nests availability: low (4 nests per terraria) and high (8 nests per terraria)</li> <li><strong>nestID:</strong> identity of the nests</li> <li><strong>occupation:</strong> if the nest was once occupied during the experiment, with 2 levels: 0 if it was never occupied and 1 if it was occupied at least once</li> <li><strong>occupied_scans:</strong> number of scans with any male inside the nest</li> <li><strong>vacant_scans:</strong> number of scans without any male inside the nest</li> <li><strong>total_scans:</strong> total number of observation scans </li> <li><strong>owners:</strong> number of different owners of the nest (at least 6 consecutive scans)</li> <li><strong>turnover:</strong> if there was at least a substitution of the nest owner without figths, with 2 levels: 0 if there was not any substitution and 1 if there was a substitution</li> <li><strong>turnovers_number:</strong> number of substitutions of the nest owner without figths</li> <li><strong>takeover:</strong> if there was at least a takeover attempt of the nest after figths, with 2 levels: 0 if there was not any attempt and 1 if there was an attempt</li> <li><strong>takeovers_number:</strong> number of takeover attempts of the nest after figths</li> <li><strong>fight:</strong> if there was at least a figth inside or close to the nest, with 2 levels: 0 if there was not any figth and 1 if there was a figth</li> <li><strong>fights_number:</strong> number of figths inside or close to the nest</li> <li><strong>canibalism:</strong> if there was at least a cannibalism event inside the nest, 2 levels: 0 if there was not any cannibalism event and 1 if there was a cannibalism event</li> <li><strong>canibalism_number:</strong> number of cannibalism events inside the nest</li> </ul> <p>With the file <strong>experiment_males.csv</strong> we tested predictions related to the males owners. In this file, we have the headers:</p> <ul> <li><strong>terrariaID:</strong> identity of the 14 terraria (containing 4 or 8 nests)</li> <li><strong>exp_group:</strong> experimental group, with 2 levels of nests availability: low (4 nests per terraria) and high (8 nests per terraria)</li> <li><strong>maleID:</strong> identitity of the males</li> <li><strong>DSW:</strong> dorsal scute width, in mm</li> <li><strong>nest_possession:</strong> with 2 levels: 0 if the male never possessed a nest during the experiment and 1 if the male possessed a nest at least once (6 consecutive scans)</li> <li><strong>nestID:</strong> identity of the nest possessed by the male</li> <li><strong>inside_scans:</strong> number of scans with the male inside his nest</li> <li><strong>outside_scans:</strong> number of scans with the male outside his nest</li> <li><strong>total_scans:</strong> total number of scans in which the male was the owner of the nest</li> <li><strong>takeover:</strong> if the male suffered a takeover attempt of his nest, with 2 levels: 0 if the male did not suffer any attempt and 1 if the male suffered an attempt</li> <li><strong>eggs:</strong> if the male received eggs from a female, with 2 levels: 0 if the male did not receive eggs and 1 if the male received eggs</li> <li><strong>eggs_number:</strong> number of eggs received </li> <li><strong>cannibalism:</strong> if the owner male cannibalized the eggs inside the nest, 2 levels: 0 if the male did not cannibalize eggs and 1 if the male cannibalized eggs</li> <li><strong>cannibalism_number:</strong> number of cannibalism events by the owner male </li> </ul> <p>With the file <strong>fights-takeovers.csv</strong> we tested predictions related with nest takeovers. In this file, we have the headers:</p> <ul> <li><strong>terrariaID:</strong> identity of the 14 terraria (containing 4 or 8 nests)</li> <li><strong>exp_group:</strong> experimental group, with 2 levels of nests availability: low (4 nests per terraria) and high (8 nests per terraria)</li> <li><strong>nestID:</strong> identity of the nest possessed by the male</li> <li><strong>focalID:</strong> identitity of the focal males (the owner nest)</li> <li><strong>DSW:</strong> dorsal scute width, in mm</li> <li><strong>fight:</strong> if the male was involved in at least a figth, with 2 levels: 0 if the male was not involved in any figth and 1 if the male was involved in a figth</li> <li><strong>takeover:</strong> if the male suffered a takeover attempt of his nest, with 2 levels: 0 if the male did not suffer any attempt and 1 if the male suffered an attempt. Obs: the nest takeover always happens after a fight. If there was a takeover, then there was a fight too.</li> <li><strong>res_focal: </strong>result of the figth or takeover for the focal male, with 2 levels: 0 if the focal male did not lose the figth or the nest and 1 if the focal male lost the figth or the nest</li> <li><strong>intruderID:</strong> identity of the intruder male involved in the figth or the takeover with the owner male</li> <li><strong>intruder_DSL: </strong>dorsal scute width of the intruder male, in mm</li> <li><strong>dyad:</strong> identity of the two individuals involved in the figth or takeover (owner male and intruder male)</li> <li><strong>DSW_difference:</strong> difference between the dorsal scute width of the dyad (focal male minus intruder male)</li> </ul> <p>With the file <strong>foraging.csv</strong> we tested a prediction related with males foraging. In this file, we have the headers:</p> <ul> <li><strong>terrariaID:</strong> identity of the 14 terraria (containing 4 or 8 nests)</li> <li><strong>exp_group:</strong> experimental group, with 2 levels of nests availability: low (4 nests per terraria) and high (8 nests per terraria)</li> <li><strong>nestID:</strong> identity of the nest possessed by the male</li> <li><strong>maleID:</strong> identitity of the males</li> <li><strong>parental_status:</strong> with 2 levels: 0 if the male did not have eggs in the nest and 1: if the male had eggs</li> <li><strong>inside_scans:</strong> number of scans with the male inside his nest</li> <li><strong>outside_scans:</strong> number of scans with the male outside his nest</li> <li><strong>total_scans:</strong> total number of scans in which the male was the owner of the nest</li> </ul>
Figure 2 in The nest-site characteristics of the forest population of common blackbird (Turdus merula) in Eskişehir, Turkey
Figure 2. The dispersion of Nh, TW, and Nx ratios on a 3-dimensional (x–y–z) plane.
Figure 1 in The nest-site characteristics of the forest population of common blackbird (Turdus merula) in Eskişehir, Turkey
Figure 1. Nest-site characteristics diagram.
Consistent apparent adult survival and nest-site fidelity of Whimbrel (Numenius phaeopus) near Churchill, Manitoba, Canada over a 40-year period
<p>Reliable estimates of adult survival for many shorebird species are lacking. We used Cormack-Jolly-Seber (CJS) methods to provide an estimate of apparent, or local, survival (φ) of a population of Whimbrels, <em>Numenius phaeopus</em>, breeding in the subarctic Churchill, Manitoba region. We used data collected in two time periods: 1973–1976 and 2010–2014. We also quantified nest-site fidelity in 2010–2014 to provide context to our apparent survival estimates because mark-recapture analyses cannot distinguish between mortality and permanent emigration. The most parsimonious CJS model did not include effects of sex or time on apparent adult survival in either period (φ = 0.76 ± 0.13 SE; φ = 0.75 ± 0.04 SE, 1973 – 1976 and 2010 – 2014, respectively). Additionally, observations of marked Whimbrels between 2010 and 2019 (n = 124) showed that 61 of the 105 marked individuals (58.1%) were resighted. These estimates of return rates are, as expected, much lower than estimates of apparent survival. The median year-to-year distance between nests (n = 139) from 2010 to 2014 was 198 ± 88 m SE and did not differ significantly (<em>p</em> = 0.84) between females (<em>x</em> ̅ = 721.9 ± 119.8 m SE) and males (<em>x</em> ̅ = 720.3 ± 83.1 m SE). If our apparent survival estimate is indicative of true survivorship, then adult mortality during the nonbreeding season has remained constant over the last five decades, implying that the recent decline in Whimbrel populations may stem largely from reduced fecundity, including egg or juvenile survival, rather than primarily from reduced adult survival.</p>
Vulnerability of sea turtle nesting sites to erosion and inundation: a decision support framework to maximize conservation
<p>Sandy beaches provide essential nesting habitat for sea turtles but are threatened globally by a rapidly changing climate. Identifying which nesting sites are at greatest risk from erosion and inundation remains an important goal of sea turtle conservation globally. Yet, efforts to identify at-risk sites have been hindered by the ability to model complex processes and incomplete information on nesting distribution and abundance. To assess the erosion and inundation risk to the reproductive success of a discrete genetic stock of flatback turtles (<em>Natator</em> <em>depressus</em>) across its nesting range in the Pilbara region of Western Australia, we used the Integrated Valuation of Ecosystem Services and Trade-offs (InVEST) Coastal Vulnerability Model. A relative exposure index was calculated for 402 nesting beaches in terms of six geophysical variables: wind and wave exposure, surge potential, relief, observed sea level rise and coastal geomorphology, and coupled with published information on the distribution and abundance of turtle tracks in the region. </p> <p>The majority of beaches (74%) had an intermediate to high exposure. In particular, 36% of beaches with a high abundance of flatback tracks (the top 25% of the frequency distribution) had a high exposure (the top 25% of the frequency distribution). This suggests that coastal exposure is a key vulnerability to the reproductive success of sea turtles that nest in this region. Promisingly, five beaches with a high abundance of turtle tracks also had a low exposure (bottom 25% of the frequency distribution) and these beaches may be critical for the long-term resilience of the stock against sea level rise and severe storms. Exposure varied across nesting sites and the approach presented here allows for a rapid and broadscale assessment of relative erosion and inundation risks at a scale most relevant to management. </p>
Data and analysis code for Norton and DuVal - Causes and consequences of nest site fidelity in a tropical lekking bird: win-stay-lose-shift tactics are unrelated to subsequent success, but site-faithful females nest earlier
<p>Nest site selection influences the survival of care-giving parents and their offspring, but search costs and site availability may limit site choices. Returning to previous nest sites may reduce costs and allow parents to better avoid local predators or access familiar resources. We investigated nest site fidelity in the Lance-tailed Manakin (Chiroxiphia lanceolata), in which long-lived females raise offspring without male assistance, and found that site choices are responsive to past success but do not predict future outcomes. We compared georeferenced nest locations for the same females detected in consecutive years (245 comparisons for 138 females) and females nesting repeatedly within a year (137 comparisons for 97 females). Females were faithful to nesting sites in 13.9% of comparisons across years and 10.2% within years, and were more likely to nest again in the same site if their offspring fledged. When switching sites, females moved farther if their previous nest failed. Nest-site fidelity was unrelated to mate fidelity or female age. We then assessed whether site choice related to subsequent female survival, nest timing, or nest survival. Contrary to the hypothesis that win-stay-lose-shift tactics improve subsequent nesting outcomes, we found females were no more likely to fledge chicks or survive to a later year after they reused nest-sites. However, across years, site-faithful females nested earlier on average than females that switched sites. Early nests were more likely to fledge chicks, and early-nesting females were more likely to renest when their first nesting effort was complete. Win-stay-lose-shift tactics may allow females to avoid areas where predation is likely, but new nest sites are not safer. Females that reuse nest sites benefit from early nest initiation, which both correlates with immediate success and creates potential for longer-term benefits of fidelity through increased opportunities to renest throughout the breeding season.</p>
Data from: Mother knows best: Nest-site choice homogenizes embryo thermal environments among populations in a widespread ectotherm
<p><span>Species with large geographic ranges provide an excellent model of how different populations respond to dissimilar local conditions, particularly variation in climate. Maternal effects, such as oviposition-site choice greatly affect offspring phenotypes and survival. Thus, maternal behavior has the potential to mitigate the effects of divergent climatic conditions across a species' range. We delineated natural nesting areas of six populations of painted turtles (<em>Chrysemys picta</em>) that span a broad latitudinal range and quantified spatial and temporal variation in nest characteristics. To quantify microhabitats available for females to choose, we also identified sites within the nesting area of each location that were representative of available thermal microhabitats. Across the range females nested non-randomly and targeted microhabitats that generally had less canopy cover and thus higher nest temperatures. Nest microhabitats differed among locations but did not predictably vary with latitude or historic mean air temperature during embryonic development. In conjunction with other studies of these populations, nest-site choice appears to be homogenizing nest environments, buffering embryos from thermally-induced selection, which could stymie evolution of embryonic traits. Thus, although effective at a macroclimatic scale, nest-site choice may be unable to compensate for novel stressors that rapidly increase local temperatures.</span></p>
Nesting activity of Olive ridley and effect of artificial shade at Cascajilloso Beach, a new inhabited nesting site in Pacific Panama
<p><span>Sea turtle nesting activity on newly monitored beaches yields important data to support future regional and global conservation assessments. Here we report on nesting activity of Olive Ridley (<em>Lepidochelys</em> <em>olivacea</em>) at Cascajilloso Beach in Pacific Panama based on data from a new hatchery during seasons 2019, 2020 and 2021. Besides, we conducted a field experiment analyzing the effects of artificial shading on </span><span>hatchlings' biometric characteristics, hatching success and the incubation period. Nesting activity based on number of egg clutches transferred to the hatchery reached a peak between September (33%) and October (25%). Curved carapace length (CCL) of nesting females (64.3–66.2 cm) was similar to other populations of the Eastern Tropical Pacific (ETP). The number of egg clutches was 80 in 2019, 74 in 2020 and 108 in 2021, however, the clutch size was slightly smaller (91.5 to 94.5 eggs) compared with other populations of the ETP. This could be a phenotypic variation of nesting females at this beach. The ability to move egg clutches to the hatchery was affected during 2020 season due to COVID-19 restrictions. Heavy rainfall during the incubation period influenced the nest temperatures registered under artificial shade and unshaded treatments (maximum average 29.9 °C), potentially resulting in males. The warmer temperatures in our experimental nests produced heavier hatchlings contrary to general assumptions, but this was also related to straight carapace length only after a threshold value of 40 mm. Hatchlings under the artificial shade were able to grow to a certain size but potentially at the cost of storing less mass (trade-off). The ongoing beach patrolling and hatchery management techniques with long-term baseline data collection are needed to secure the nesting population of <em>L. olivacea</em> at this recently surveyed beach.</span></p>
An experimental test of information use by North American wood ducks (Aix sponsa): external habitat cues, not social visual cues, influence initial nest-site selection
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Data from: Solar panels as novel nest sites for the European paper wasp Polistes dominula
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Data from: Wood hardness drives nest site selection in woodpeckers of the humid Chaco
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Data from: Factors influencing nest site selection in a rapidly declining shorebird, the Eurasian curlew
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