{"dp_type": "Dataset", "free_text": "Albatross"}
[{"awards": "1951500 Jenouvrier, Stephanie", "bounds_geometry": ["POLYGON((-180 -60,-144 -60,-108 -60,-72 -60,-36 -60,0 -60,36 -60,72 -60,108 -60,144 -60,180 -60,180 -63,180 -66,180 -69,180 -72,180 -75,180 -78,180 -81,180 -84,180 -87,180 -90,144 -90,108 -90,72 -90,36 -90,0 -90,-36 -90,-72 -90,-108 -90,-144 -90,-180 -90,-180 -87,-180 -84,-180 -81,-180 -78,-180 -75,-180 -72,-180 -69,-180 -66,-180 -63,-180 -60))"], "date_created": "Tue, 27 Feb 2024 00:00:00 GMT", "description": "1. Differences among individuals within a population are ubiquitous. Those differences are known to affect the entire life cycle with important consequences for all demographic rates and outcomes. One source of among-individual phenotypic variation that has received little attention from a demographic perspective is animal personality, which is defined as consistent and heritable behavioral differences between individuals. While many studies have shown that individual variation in individual personality can generate individual differences in survival and reproductive rates, the impact of personality on all demographic rates and outcomes remains to be assessed empirically.\r\n\r\n\t2. Here, we used a unique, long-term, dataset coupling demography and personality of wandering albatross (Diomedea exulans) in the Crozet Archipelago and a comprehensive analysis based on a suite of approaches (capture-mark-recapture statistical models, Markov chains models and structured matrix population models). We assessed the effect of boldness on annual demographic rates (survival, breeding probability, breeding success), life-history out-comes (life expectancy, lifetime reproductive outcome, occupancy times), and an integrative demographic outcome (population growth rate).\r\n\r\n\t3. We found that boldness had little impact on female demographic rates, but was very likely associated with lower breeding probabilities in males. By integrating the effects of boldness over the entire life cycle, we found that bolder males had slightly lower lifetime reproductive success compared to shyer males. Indeed, bolder males spent a greater proportion of their lifetime as non-breeders, which suggests longer inter-breeding intervals due to higher reproductive allocation.\r\n\r\n\t4. Our results reveal that the link between boldness and demography is more complex than anticipated by the pace-of-life literature and highlight the importance of considering the entire life cycle with a comprehensive approach when assessing the role of personality on individual performance and demography.\r\n", "east": 180.0, "geometry": ["POINT(0 -89.999)"], "keywords": "Antarctica; Cryosphere; Demography; Sub-Antarctic", "locations": "Sub-Antarctic; Antarctica", "north": -60.0, "nsf_funding_programs": "Antarctic Integrated System Science", "persons": "Joanie, Van de Walle; Jenouvrier, Stephanie", "project_titles": "NSFGEO-NERC: Integrating Individual Personality Differences in the Evolutionary Ecology of a Seabird in the Rapidly Changing Polar Environment", "projects": [{"proj_uid": "p0010283", "repository": "USAP-DC", "title": "NSFGEO-NERC: Integrating Individual Personality Differences in the Evolutionary Ecology of a Seabird in the Rapidly Changing Polar Environment"}], "repo": "USAP-DC", "repositories": "USAP-DC", "science_programs": null, "south": -90.0, "title": "The impact of boldness on demographic rates and lifehistory outcomes in the wandering albatross", "uid": "601770", "west": -180.0}, {"awards": "1246407 Jenouvrier, Stephanie; 1840058 Jenouvrier, Stephanie", "bounds_geometry": ["POLYGON((-180 -60,-144 -60,-108 -60,-72 -60,-36 -60,0 -60,36 -60,72 -60,108 -60,144 -60,180 -60,180 -63,180 -66,180 -69,180 -72,180 -75,180 -78,180 -81,180 -84,180 -87,180 -90,144 -90,108 -90,72 -90,36 -90,0 -90,-36 -90,-72 -90,-108 -90,-144 -90,-180 -90,-180 -87,-180 -84,-180 -81,-180 -78,-180 -75,-180 -72,-180 -69,-180 -66,-180 -63,-180 -60))"], "date_created": "Mon, 27 Jun 2022 00:00:00 GMT", "description": "Individuals differ in many ways. Most produce few offspring; a handful produce many. Some\r\ndie early; others live to old age. It is tempting to attribute these differences in outcomes to differences in individual traits, and thus in the demographic rates experienced. However, there is\r\nmore to individual variation than meets the eye of the biologist. Even among individuals sharing identical traits, life history outcomes (life expectancy and lifetime reproduction) will vary due\r\nto individual stochasticity, i.e., to chance. Quantifying the contributions of heterogeneity and\r\nchance is essential to understanding natural variability. Inter-individual differences vary across environmental conditions, hence heterogeneity and stochasticity depend on environmental conditions. We show that favorable conditions increase the contributions of individual stochasticity, and reduce the contributions of heterogeneity, to variance in demographic outcomes in a seabird population. The opposite is true under poor conditions. This result has important consequence for understanding the ecology and evolution of life history strategies.\r\n\r\nSpecifically, three life-history complexes exist in a population of southern fulmar (defined as sets of life-history characteristics that occur together through the lifetime of an individual). They are reminiscent of the gradient of life- history strategy observed among species:\r\n\r\n1. Group 1 (14% of offspring at fledging) is a slow-paced life history where individuals tend to delay recruitment, recruit successfully, and extend their reproductive lifespan.\r\n2. Group 2 (67% of offspring at fledging) consists of individuals that are less likely to recruit, have high adult survival, and skip breeding often.\r\n3. Group 3 (19% of offspring at fledging) is a fast-paced life history where individuals recruit early and attempt to breed often but have a short lifespan.\r\n\r\nIndividuals in groups 1 and 3 are considered \u201chigh-quality\u201d individuals because they produce, on average, more offspring over their lives than do individuals in group 2. But group 2 is made-up of individuals that experience the highest levels of adult survival.\r\n \r\nDifferences between these groups, i.e. individual heterogeneity, only explains a small fraction of variance in life expectancy (5.9%) and lifetime reproduction (22%) when environmental conditions are ordinary. We expect that the environmental context experienced, especially when environmental conditions get extreme, is key to characterizing individual heterogeneity and its contribution to life history outcomes. Here, we build on previous studies to quantify the impact of extreme environmental conditions on the relative contributions of individual heterogeneity and stochasticity to variance in life history outcomes.\r\nWe found that the differences in vital rates and demographic outcomes among complexes depend on the sea ice conditions individuals experience. Importantly, differences across life history complexes are amplified when sea ice concentration get extremely low. Sea ice conditions did not only affect patterns of life history traits, but also the variance of life history outcomes and the relative proportion of individual unobserved heterogeneity to the total variance. These new results advance the current debate on the relative importance heterogeneity (i.e. potentially adaptive) and stochasticity (i.e. enhances genetic drift) in shaping potentially neutral vs. adaptive changes in life histories.\r\n", "east": 180.0, "geometry": ["POINT(0 -89.999)"], "keywords": "Antarctica; Biota; Birds; East Antarctica; Southern Fulmar", "locations": "Antarctica; East Antarctica", "north": -60.0, "nsf_funding_programs": "Antarctic Organisms and Ecosystems", "persons": "Jenouvrier, Stephanie", "project_titles": "Linking Foraging Behaviors to Demography to understand Albatrosses Population Responses to Climate Change; Polar Seabirds with Long-term Pair Bonds: Effects of Mating on Individual Fitness and Population Dynamics", "projects": [{"proj_uid": "p0010002", "repository": "USAP-DC", "title": "Linking Foraging Behaviors to Demography to understand Albatrosses Population Responses to Climate Change"}, {"proj_uid": "p0010090", "repository": "USAP-DC", "title": "Polar Seabirds with Long-term Pair Bonds: Effects of Mating on Individual Fitness and Population Dynamics"}], "repo": "USAP-DC", "repositories": "USAP-DC", "science_programs": null, "south": -90.0, "title": "Demographic outputs and their variances for three life history complexes for the Southern Fulmar across contrasted sea ice conditions.", "uid": "601585", "west": -180.0}, {"awards": "1840058 Jenouvrier, Stephanie", "bounds_geometry": null, "date_created": "Fri, 04 Feb 2022 00:00:00 GMT", "description": "Many animals form long-term monogamous pair-bonds, and the disruption of a pair-bond (through either divorce or widowhood) can have significant consequences for individual vital rates (survival, breeding, and breeding success probabilities) and life-history outcomes (lifetime reproductive success, life expectancy). Here, we investigated the causes and consequences of pair-bond disruption in wandering albatross (Diomedea exulans). State-of-the-art statistical and mathematical approaches were developed to estimate divorce and widowhood rates and their impacts on vital rates and life-history outcomes. In this population, females incur a higher mortality rate due to incidental fishery bycatch, hence the population is male-skewed. Therefore, we first posited that males show higher widowhood rates negatively correlated with fishing effort, and females have higher divorce rates because they have more mating opportunities. Furthermore, we expected that divorce can be an adaptive strategy, whereby individuals improve breeding success by breeding with a new partner of better quality. Finally, we posited that pair-bond disruptions can reduce survival and breeding probabilities due to the cost of remating processes, with important consequences for life-history outcomes. As expected, we show that males have higher widowhood rates than females and females have higher divorce rates in this male-skewed population. However, no correlation was found between fishing effort and male widowhood. Secondly, contrary to our expectation, we found that divorce is likely non-adaptive in this population. We propose that divorce in this population is caused by an intruder who outcompetes the original partner in line with the \"forced divorce\" hypothesis. Furthermore, we found a 16.7% and 18.0% reduction in lifetime reproductive success (LRS) only for divorced and widowed males, respectively, due to missing breeding seasons after a pair-bond disruption. Finally, we found that divorced individuals are more likely to divorce again, but whether this is related to specific individual characteristics remains an important area of investigation. \r\n\r\nDescription of data processing:\r\nThis file includes: (1) observation events data; (2) E-surge GEPAT (Generator of pattern of elementary matrices) code for fitting MULTIEVENT-CAPTURE-MARK-RECAPTURE (MECMR) models; and (3) pair-bond status and breeding success data to perform all the analysis described in Sun et al. (2022, Ecological Monographs) ", "east": null, "geometry": null, "keywords": "Antarctica; Biota; Wandering Albatross", "locations": "Antarctica", "north": null, "nsf_funding_programs": "Antarctic Organisms and Ecosystems", "persons": "Jenouvrier, Stephanie; Sun, Ruijiao; Barbraud, Christophe; Delord, Karine", "project_titles": "Polar Seabirds with Long-term Pair Bonds: Effects of Mating on Individual Fitness and Population Dynamics", "projects": [{"proj_uid": "p0010090", "repository": "USAP-DC", "title": "Polar Seabirds with Long-term Pair Bonds: Effects of Mating on Individual Fitness and Population Dynamics"}], "repo": "USAP-DC", "repositories": "USAP-DC", "science_programs": null, "south": null, "title": "Causes and consequences of pair-bond disruption in a sex-skewed population of a long-lived monogamous seabird: the wandering Albatross", "uid": "601518", "west": null}, {"awards": "1246407 Jenouvrier, Stephanie", "bounds_geometry": ["POLYGON((68.5 -48.5,68.725 -48.5,68.95 -48.5,69.175 -48.5,69.4 -48.5,69.625 -48.5,69.85 -48.5,70.075 -48.5,70.3 -48.5,70.525 -48.5,70.75 -48.5,70.75 -48.65,70.75 -48.8,70.75 -48.95,70.75 -49.1,70.75 -49.25,70.75 -49.4,70.75 -49.55,70.75 -49.7,70.75 -49.85,70.75 -50,70.525 -50,70.3 -50,70.075 -50,69.85 -50,69.625 -50,69.4 -50,69.175 -50,68.95 -50,68.725 -50,68.5 -50,68.5 -49.85,68.5 -49.7,68.5 -49.55,68.5 -49.4,68.5 -49.25,68.5 -49.1,68.5 -48.95,68.5 -48.8,68.5 -48.65,68.5 -48.5))"], "date_created": "Mon, 03 Dec 2018 00:00:00 GMT", "description": "1. Studies of the mechanisms underlying climate-induced population changes are critically needed to better understand and accurately predict population responses to climate change. Long-lived migratory species might be particularly vulnerable to climate change as they are constrained by different climate conditions and energetic requirements during the breeding and non-breeding seasons. Yet, most studies primarily focus on the breeding season of these species life cycle. Environmental conditions experienced in the non-breeding season may have downstream effects on the other stages of the annual life cycle. Not investigating such effects may potentially lead to erroneous inferences about population dynamics.\r\n2. Combining demographic and tracking data collected between 2006 and 2013 at Kerguelen Island on a long-lived migratory seabird, the Black-Browed Albatross (Thalassarche melanophris), we investigated the links between sea surface temperature during the non-breeding season and behavioural and phenological traits (at-sea behaviour and migratory schedules) while accounting for different responses between birds of different sex and reproductive status (previously failed or successful breeders). We then explored whether variation in the foraging behaviour and timing of spring migration influenced subsequent reproductive performance.\r\n3. Our results showed that foraging activity and migratory schedules varied by both sex and reproductive status suggesting different energetic requirements and constraints among individuals. Higher sea surface temperatures during late winter, assumed to reflect poor winter conditions, were associated with an earlier departure from the wintering grounds and an extended pre-breeding period. However, an earlier spring migration and an earlier return to Kerguelen grounds were associated with a lower breeding success.\r\n4. Our results highlighted that behaviour during some periods of the non-breeding season, particularly towards the end of the wintering period and the pre-breeding period, had a significant effect on the subsequent reproductive success. Therefore caution needs to be given to all stages of the annual cycle when predicting the influence of climate on population dynamics.", "east": 70.75, "geometry": ["POINT(69.625 -49.25)"], "keywords": "Albatross; Animal Behavior Observation; Antarctica; Biota; Birds; Black-Browed Albatross (thalassarche Melanophris); Field Investigations; Foraging; Kerguelen Island; Ocean Island/plateau; Ocean Island/Plateau; Southern Ocean", "locations": "Antarctica; Kerguelen Island; Southern Ocean", "north": -48.5, "nsf_funding_programs": "Antarctic Organisms and Ecosystems", "persons": "Jenouvrier, Stephanie", "project_titles": "Linking Foraging Behaviors to Demography to understand Albatrosses Population Responses to Climate Change", "projects": [{"proj_uid": "p0010002", "repository": "USAP-DC", "title": "Linking Foraging Behaviors to Demography to understand Albatrosses Population Responses to Climate Change"}], "repo": "USAP-DC", "repositories": "USAP-DC", "science_programs": null, "south": -50.0, "title": "Linking oceanographic conditions, migratory schedules and foraging behaviour during the non-breeding season to reproductive performance in a long-lived seabird", "uid": "601140", "west": 68.5}, {"awards": "1142084 Nevitt, Gabrielle", "bounds_geometry": ["POLYGON((40 -25,46 -25,52 -25,58 -25,64 -25,70 -25,76 -25,82 -25,88 -25,94 -25,100 -25,100 -29,100 -33,100 -37,100 -41,100 -45,100 -49,100 -53,100 -57,100 -61,100 -65,94 -65,88 -65,82 -65,76 -65,70 -65,64 -65,58 -65,52 -65,46 -65,40 -65,40 -61,40 -57,40 -53,40 -49,40 -45,40 -41,40 -37,40 -33,40 -29,40 -25))"], "date_created": "Wed, 11 Apr 2018 00:00:00 GMT", "description": "This dataset was recorded from tags fitted to Black-browed Albatross from the breeding colony called \"Canon des Sourcils Noirs\", on Kerguelen Island, located at 70.2433E, -49.6875S. The dataset contains the following items: \r\n1. GPS locations (lat,lon) and timestamps at local time (GMT-5)\r\n2. Timestamped stomach temperature measurements.", "east": 100.0, "geometry": ["POINT(70 -45)"], "keywords": "Albatross; Antarctica; Biota; Birds; Foraging; GPS Data; Southern Ocean; Stomach Temperature", "locations": "Antarctica; Southern Ocean", "north": -25.0, "nsf_funding_programs": "Antarctic Organisms and Ecosystems", "persons": "Losekoot, Marcel; Nevitt, Gabrielle", "project_titles": "Applying High-resolution GPS Tracking to Characterize Sensory Foraging Strategies of the Black-browed Albatross, a Top Predator of the Southern Ocean Ecosystem", "projects": [{"proj_uid": "p0000420", "repository": "USAP-DC", "title": "Applying High-resolution GPS Tracking to Characterize Sensory Foraging Strategies of the Black-browed Albatross, a Top Predator of the Southern Ocean Ecosystem"}], "repo": "USAP-DC", "repositories": "USAP-DC", "science_programs": null, "south": -65.0, "title": "Satellite tracks of Black-browed Albatross in the Southern Indian Ocean", "uid": "601093", "west": 40.0}]
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Dataset Title/Abstract/Map | NSF Award(s) | Date Created | PIs / Scientists | Project Links | Abstract | Bounds Geometry | Geometry | Selected | Visible |
---|---|---|---|---|---|---|---|---|---|
The impact of boldness on demographic rates and lifehistory outcomes in the wandering albatross
|
1951500 |
2024-02-27 | Joanie, Van de Walle; Jenouvrier, Stephanie |
NSFGEO-NERC: Integrating Individual Personality Differences in the Evolutionary Ecology of a Seabird in the Rapidly Changing Polar Environment |
1. Differences among individuals within a population are ubiquitous. Those differences are known to affect the entire life cycle with important consequences for all demographic rates and outcomes. One source of among-individual phenotypic variation that has received little attention from a demographic perspective is animal personality, which is defined as consistent and heritable behavioral differences between individuals. While many studies have shown that individual variation in individual personality can generate individual differences in survival and reproductive rates, the impact of personality on all demographic rates and outcomes remains to be assessed empirically. 2. Here, we used a unique, long-term, dataset coupling demography and personality of wandering albatross (Diomedea exulans) in the Crozet Archipelago and a comprehensive analysis based on a suite of approaches (capture-mark-recapture statistical models, Markov chains models and structured matrix population models). We assessed the effect of boldness on annual demographic rates (survival, breeding probability, breeding success), life-history out-comes (life expectancy, lifetime reproductive outcome, occupancy times), and an integrative demographic outcome (population growth rate). 3. We found that boldness had little impact on female demographic rates, but was very likely associated with lower breeding probabilities in males. By integrating the effects of boldness over the entire life cycle, we found that bolder males had slightly lower lifetime reproductive success compared to shyer males. Indeed, bolder males spent a greater proportion of their lifetime as non-breeders, which suggests longer inter-breeding intervals due to higher reproductive allocation. 4. Our results reveal that the link between boldness and demography is more complex than anticipated by the pace-of-life literature and highlight the importance of considering the entire life cycle with a comprehensive approach when assessing the role of personality on individual performance and demography. | ["POLYGON((-180 -60,-144 -60,-108 -60,-72 -60,-36 -60,0 -60,36 -60,72 -60,108 -60,144 -60,180 -60,180 -63,180 -66,180 -69,180 -72,180 -75,180 -78,180 -81,180 -84,180 -87,180 -90,144 -90,108 -90,72 -90,36 -90,0 -90,-36 -90,-72 -90,-108 -90,-144 -90,-180 -90,-180 -87,-180 -84,-180 -81,-180 -78,-180 -75,-180 -72,-180 -69,-180 -66,-180 -63,-180 -60))"] | ["POINT(0 -89.999)"] | false | false |
Demographic outputs and their variances for three life history complexes for the Southern Fulmar across contrasted sea ice conditions.
|
1246407 1840058 |
2022-06-27 | Jenouvrier, Stephanie |
Linking Foraging Behaviors to Demography to understand Albatrosses Population Responses to Climate Change Polar Seabirds with Long-term Pair Bonds: Effects of Mating on Individual Fitness and Population Dynamics |
Individuals differ in many ways. Most produce few offspring; a handful produce many. Some die early; others live to old age. It is tempting to attribute these differences in outcomes to differences in individual traits, and thus in the demographic rates experienced. However, there is more to individual variation than meets the eye of the biologist. Even among individuals sharing identical traits, life history outcomes (life expectancy and lifetime reproduction) will vary due to individual stochasticity, i.e., to chance. Quantifying the contributions of heterogeneity and chance is essential to understanding natural variability. Inter-individual differences vary across environmental conditions, hence heterogeneity and stochasticity depend on environmental conditions. We show that favorable conditions increase the contributions of individual stochasticity, and reduce the contributions of heterogeneity, to variance in demographic outcomes in a seabird population. The opposite is true under poor conditions. This result has important consequence for understanding the ecology and evolution of life history strategies. Specifically, three life-history complexes exist in a population of southern fulmar (defined as sets of life-history characteristics that occur together through the lifetime of an individual). They are reminiscent of the gradient of life- history strategy observed among species: 1. Group 1 (14% of offspring at fledging) is a slow-paced life history where individuals tend to delay recruitment, recruit successfully, and extend their reproductive lifespan. 2. Group 2 (67% of offspring at fledging) consists of individuals that are less likely to recruit, have high adult survival, and skip breeding often. 3. Group 3 (19% of offspring at fledging) is a fast-paced life history where individuals recruit early and attempt to breed often but have a short lifespan. Individuals in groups 1 and 3 are considered “high-quality” individuals because they produce, on average, more offspring over their lives than do individuals in group 2. But group 2 is made-up of individuals that experience the highest levels of adult survival. Differences between these groups, i.e. individual heterogeneity, only explains a small fraction of variance in life expectancy (5.9%) and lifetime reproduction (22%) when environmental conditions are ordinary. We expect that the environmental context experienced, especially when environmental conditions get extreme, is key to characterizing individual heterogeneity and its contribution to life history outcomes. Here, we build on previous studies to quantify the impact of extreme environmental conditions on the relative contributions of individual heterogeneity and stochasticity to variance in life history outcomes. We found that the differences in vital rates and demographic outcomes among complexes depend on the sea ice conditions individuals experience. Importantly, differences across life history complexes are amplified when sea ice concentration get extremely low. Sea ice conditions did not only affect patterns of life history traits, but also the variance of life history outcomes and the relative proportion of individual unobserved heterogeneity to the total variance. These new results advance the current debate on the relative importance heterogeneity (i.e. potentially adaptive) and stochasticity (i.e. enhances genetic drift) in shaping potentially neutral vs. adaptive changes in life histories. | ["POLYGON((-180 -60,-144 -60,-108 -60,-72 -60,-36 -60,0 -60,36 -60,72 -60,108 -60,144 -60,180 -60,180 -63,180 -66,180 -69,180 -72,180 -75,180 -78,180 -81,180 -84,180 -87,180 -90,144 -90,108 -90,72 -90,36 -90,0 -90,-36 -90,-72 -90,-108 -90,-144 -90,-180 -90,-180 -87,-180 -84,-180 -81,-180 -78,-180 -75,-180 -72,-180 -69,-180 -66,-180 -63,-180 -60))"] | ["POINT(0 -89.999)"] | false | false |
Causes and consequences of pair-bond disruption in a sex-skewed population of a long-lived monogamous seabird: the wandering Albatross
|
1840058 |
2022-02-04 | Jenouvrier, Stephanie; Sun, Ruijiao; Barbraud, Christophe; Delord, Karine |
Polar Seabirds with Long-term Pair Bonds: Effects of Mating on Individual Fitness and Population Dynamics |
Many animals form long-term monogamous pair-bonds, and the disruption of a pair-bond (through either divorce or widowhood) can have significant consequences for individual vital rates (survival, breeding, and breeding success probabilities) and life-history outcomes (lifetime reproductive success, life expectancy). Here, we investigated the causes and consequences of pair-bond disruption in wandering albatross (Diomedea exulans). State-of-the-art statistical and mathematical approaches were developed to estimate divorce and widowhood rates and their impacts on vital rates and life-history outcomes. In this population, females incur a higher mortality rate due to incidental fishery bycatch, hence the population is male-skewed. Therefore, we first posited that males show higher widowhood rates negatively correlated with fishing effort, and females have higher divorce rates because they have more mating opportunities. Furthermore, we expected that divorce can be an adaptive strategy, whereby individuals improve breeding success by breeding with a new partner of better quality. Finally, we posited that pair-bond disruptions can reduce survival and breeding probabilities due to the cost of remating processes, with important consequences for life-history outcomes. As expected, we show that males have higher widowhood rates than females and females have higher divorce rates in this male-skewed population. However, no correlation was found between fishing effort and male widowhood. Secondly, contrary to our expectation, we found that divorce is likely non-adaptive in this population. We propose that divorce in this population is caused by an intruder who outcompetes the original partner in line with the "forced divorce" hypothesis. Furthermore, we found a 16.7% and 18.0% reduction in lifetime reproductive success (LRS) only for divorced and widowed males, respectively, due to missing breeding seasons after a pair-bond disruption. Finally, we found that divorced individuals are more likely to divorce again, but whether this is related to specific individual characteristics remains an important area of investigation. Description of data processing: This file includes: (1) observation events data; (2) E-surge GEPAT (Generator of pattern of elementary matrices) code for fitting MULTIEVENT-CAPTURE-MARK-RECAPTURE (MECMR) models; and (3) pair-bond status and breeding success data to perform all the analysis described in Sun et al. (2022, Ecological Monographs) | [] | [] | false | false |
Linking oceanographic conditions, migratory schedules and foraging behaviour during the non-breeding season to reproductive performance in a long-lived seabird
|
1246407 |
2018-12-03 | Jenouvrier, Stephanie |
Linking Foraging Behaviors to Demography to understand Albatrosses Population Responses to Climate Change |
1. Studies of the mechanisms underlying climate-induced population changes are critically needed to better understand and accurately predict population responses to climate change. Long-lived migratory species might be particularly vulnerable to climate change as they are constrained by different climate conditions and energetic requirements during the breeding and non-breeding seasons. Yet, most studies primarily focus on the breeding season of these species life cycle. Environmental conditions experienced in the non-breeding season may have downstream effects on the other stages of the annual life cycle. Not investigating such effects may potentially lead to erroneous inferences about population dynamics. 2. Combining demographic and tracking data collected between 2006 and 2013 at Kerguelen Island on a long-lived migratory seabird, the Black-Browed Albatross (Thalassarche melanophris), we investigated the links between sea surface temperature during the non-breeding season and behavioural and phenological traits (at-sea behaviour and migratory schedules) while accounting for different responses between birds of different sex and reproductive status (previously failed or successful breeders). We then explored whether variation in the foraging behaviour and timing of spring migration influenced subsequent reproductive performance. 3. Our results showed that foraging activity and migratory schedules varied by both sex and reproductive status suggesting different energetic requirements and constraints among individuals. Higher sea surface temperatures during late winter, assumed to reflect poor winter conditions, were associated with an earlier departure from the wintering grounds and an extended pre-breeding period. However, an earlier spring migration and an earlier return to Kerguelen grounds were associated with a lower breeding success. 4. Our results highlighted that behaviour during some periods of the non-breeding season, particularly towards the end of the wintering period and the pre-breeding period, had a significant effect on the subsequent reproductive success. Therefore caution needs to be given to all stages of the annual cycle when predicting the influence of climate on population dynamics. | ["POLYGON((68.5 -48.5,68.725 -48.5,68.95 -48.5,69.175 -48.5,69.4 -48.5,69.625 -48.5,69.85 -48.5,70.075 -48.5,70.3 -48.5,70.525 -48.5,70.75 -48.5,70.75 -48.65,70.75 -48.8,70.75 -48.95,70.75 -49.1,70.75 -49.25,70.75 -49.4,70.75 -49.55,70.75 -49.7,70.75 -49.85,70.75 -50,70.525 -50,70.3 -50,70.075 -50,69.85 -50,69.625 -50,69.4 -50,69.175 -50,68.95 -50,68.725 -50,68.5 -50,68.5 -49.85,68.5 -49.7,68.5 -49.55,68.5 -49.4,68.5 -49.25,68.5 -49.1,68.5 -48.95,68.5 -48.8,68.5 -48.65,68.5 -48.5))"] | ["POINT(69.625 -49.25)"] | false | false |
Satellite tracks of Black-browed Albatross in the Southern Indian Ocean
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1142084 |
2018-04-11 | Losekoot, Marcel; Nevitt, Gabrielle |
Applying High-resolution GPS Tracking to Characterize Sensory Foraging Strategies of the Black-browed Albatross, a Top Predator of the Southern Ocean Ecosystem |
This dataset was recorded from tags fitted to Black-browed Albatross from the breeding colony called "Canon des Sourcils Noirs", on Kerguelen Island, located at 70.2433E, -49.6875S. The dataset contains the following items: 1. GPS locations (lat,lon) and timestamps at local time (GMT-5) 2. Timestamped stomach temperature measurements. | ["POLYGON((40 -25,46 -25,52 -25,58 -25,64 -25,70 -25,76 -25,82 -25,88 -25,94 -25,100 -25,100 -29,100 -33,100 -37,100 -41,100 -45,100 -49,100 -53,100 -57,100 -61,100 -65,94 -65,88 -65,82 -65,76 -65,70 -65,64 -65,58 -65,52 -65,46 -65,40 -65,40 -61,40 -57,40 -53,40 -49,40 -45,40 -41,40 -37,40 -33,40 -29,40 -25))"] | ["POINT(70 -45)"] | false | false |