Age‐specific survival and recruitment of piping plovers Charadrius melodus in the Great Lakes region

Juvenile survival and age at first breeding (i.e. recruitment) are critical parameters affecting population dynamics in birds, but high levels of natal dispersal preclude measurement of these variables in most species. We used multi‐state capture–recapture models to measure age‐specific survival and recruitment probabilities of piping plovers Charadrius melodus in the Great Lakes region during 1993–2012. This federally endangered population is thoroughly monitored throughout its entire breeding range, minimizing concerns that measures of survival and recruitment are confounded by temporary or permanent emigration. First‐year survival (± SE) averaged 0.284 ± 0.019 from mean banding age (9 d) and 0.374 ± 0.023 from fledging age (23 d). Factors that increased first‐year survival during the pre‐fledging period (9–23 d) included earlier hatching dates, older age at banding, greater number of fledglings at a given site, and better body condition at time of banding. However, when chicks that died prior to fledging were excluded from analysis, only earlier hatching dates improved first‐year survival estimates. Females had a higher probability (0.557 ± 0.066) of initiating breeding at age one than did males (0.353 ± 0.052), but virtually all plovers began breeding by age three. Adult survival was reduced by increased hurricane activity on the southeast U.S. Atlantic coast where Great Lakes piping plovers winter and by higher populations of merlins Falco columbarius. Mean annual adult survival declined from 1993 to 2012, and did not differ between males and females. Enhanced body condition led to higher survival to fledge and early breeding led to improved first‐year survival; therefore, management actions focused on ensuring access to quality feeding habitat for growing young and protecting early nests may increase recruitment in this federally endangered population.     

Sex-specific costs of reproduction on survival in a long-lived seabird

Costs of reproduction on survival have captured the attention of researchers since life history theory was formulated. Adults of long-lived species may increase survival by reducing their breeding effort or even skipping reproduction. In this study, we aimed to evaluate the costs of current reproduction on survival and whether skipping reproduction increases adult survival in a long-lived seabird. We used capture–mark–recapture data (1450 encounters) from two populations of Bulwer''s petrel (Bulweria bulwerii), breeding in the Azores and Canary Islands, North Atlantic Ocean. Using a multi-event model with two different breeding statuses (breeders versus non-breeders), we calculated probabilities of survival and of transitions between breeding statuses, evaluating potential differences between sexes. Females had lower survival probabilities than males, independent of their breeding status. When considering breeding status, breeding females had lower survival probabilities than non-breeding females, suggesting costs of reproduction on survival. Breeding males had higher survival probabilities than non-breeding males, suggesting that males do not incur costs of reproduction on survival and that only the highest quality males have access to breeding. The highest and the lowest probabilities of skipping reproduction were found in breeding males from the Azores and in breeding males from the Canary Islands, respectively. Intermediate values were observed in the females from both populations. This result is probably due to differences in the external factors affecting both populations, essentially predation pressure and competition. The existence of sex-specific costs of reproduction on survival in several populations of this long-lived species may have important implications for species population dynamics.     

Cohort and tag-site-specific tag-loss rates in mark–recapture studies: A southern elephant seal cautionary case

Marker-loss is a common feature of mark–recapture studies and important as it may bias parameter estimation. A slight alteration in tag-site of double tagged southern elephant seals (Mirounga leonina), marked at Marion Island from 1983 to 2005 in an ongoing mark–recapture program, had important consequences for tag-loss. We calculated age-specific tag-retention rates and cumulative tag-retention probabilities using a maximum likelihood model selection approach in the software application TAG_LOSS 3.2.0. Under the tag-loss independence assumption, double tag-loss of inner interdigital webbing tags (IIT; 17 cohorts) remained below 1% in the first 5 yr and increased monotonically as seals aged, with higher tag-loss in males. Lifetime cumulative IIT tag-loss was 11.9% for females and 18.4% for males, and equivalent for all cohorts. Changing the tag-site to the outer interdigital webbing (OIT; 6 cohorts) resulted in increased and cohort-dependent tag-loss, although the variation (mean ± 95% CI) in cumulative tag-loss probabilities never exceeded 5.3% between cohorts at similar age. Although different studies may homogenize techniques, we advocate the importance of data set-specific assessment of tag-loss rates to ensure greatest confidence in population parameters obtained from mark–recapture experiments. Permanent marking should be implemented where feasible.     

Survival and Cause-Specific Mortality of Mature Male White-Tailed Deer

ABSTRACT Understanding sources of male deer mortality is a prerequisite to a successful management program, especially in Texas, USA, where white-tailed deer (Odocoileus virginianus) are the most economically important game species. South Texas, USA, is one of the few areas where males reach older age classes (> 4.5 yr), in part because of intense population management. Therefore, we obtained survival rates and causes of mortality of 48 mature male deer in south Texas, USA, over 2 years. We calculated Kaplan—Meier survival estimates during 2 study years modified for a staggered-entry design and annual survival rates for one cohort of deer from 1998 to 2004 using recapture and radiotelemetry data. We documented 21 mortalities (16 harvest and 5 nonhunting mortalities). Average annual survival of the known-aged 1998 cohort was 82% with 52% of surviving to 6.5 years of age. Survival in study year 2 (0.497 ± 0.069) was less than in study year 1 (0.781 ± 0.073; P = 0.0047), largely because males had finally reached harvestable age (> 6.5 yr old). All but one non-harvest mortality occurred during the rut or postrut periods. It appears that a large percentage of males can reach mature age classes under intense population management, making them available for harvest when at peak antler size. This allows for increased economic returns on intensively managed white-tailed deer populations.     

Geographic variation and environmental correlates of apparent survival rates in adult tree swallows Tachycineta bicolor

Determining demographic rates in wild animal populations and understanding why rates vary are important challenges in population ecology and conservation. Whereas reproductive success is reported frequently for many songbird species, there are relatively few corresponding estimates of annual survival for widespread populations of the same migratory species. We incorporated mark–recapture data into Cormack–Jolly–Seber models to estimate annual apparent survival and recapture rates of adult male and female tree swallows Tachycineta bicolor in eight local breeding populations across North America for periods of 7–33 yr. We found strong site‐specific and annual variation in apparent survival rates of adult swallows, and evidence of higher survival or site fidelity among males than females. There were no strong associations between putative overwintering region and survival. Strength and patterns of winter climate‐apparent survival relationships varied across four sites monitored for >15 yr; at one site, spring pond conditions, local spring precipitation and, to a lesser extent, winter North Atlantic Oscillation Index were credible predictors of annual apparent survival. Further work is needed to evaluate how survival is related to environmental conditions throughout the annual cycle and how these factors affect population dynamics of swallows and related species of conservation concern.     

High survival rate of a critically endangered species, the Azores Bullfinch Pyrrhula murina, as a contribution to population recovery

This paper reports analyses of a capture–mark–recapture (CMR) dataset of 149 Azores Bullfinches ringed on S?o Miguel island (Azores) between 2005 and 2007, and recaptured–resighted on a monthly basis over a 4-year period (2005–2008) throughout their breeding range. We examined the effect of time, age (adults vs. juveniles), gender (adult males and females), and environmental covariates (temperature, rainfall, NAO index) on survival probabilities. The modelling found a high and constant monthly survival probability (mean ± SE) estimated at 0.96 ± 0.01, similar between both adults and juveniles and independent of environmental conditions and gender. These findings agree with expectations from island-based life-history theory where relatively mild conditions and lack of predators should favour high survival rates to compensate for the low reproductive output. The annual survival rate was estimated at 0.62, which was also consistent with this pattern when compared with survival estimates of mainland bullfinch and passerine species on other subtropical islands obtained in similar CMR studies. Based on a canonical estimator, the size of the studied population (mean ± SE) was estimated at 1608 ± 326 individuals. Given that the population size was only around 120–400 individuals in the early 1990s, we suggest that the high survival probabilities currently applying to this critically endangered species may have substantially contributed to the recent recovery of this population. Future research studies on the species’ demography should continue to monitor survival in order to measure the effect of management interventions currently taking place within the range of the Azores Bullfinch, including the restoration of the biodiversity rich laurel forest, but also focusing on nest success, which is important for understanding population dynamics.     

Variation in Survival and Harvest Rates in Florida Mottled Duck

The Florida mottled duck (Anas fulvigula fulvigula) inhabits a relatively small range of approximately 90,000 km² within peninsular Florida, USA, and is threatened by habitat loss and genetic introgression with feral mallards (Anas platyrhynchos). Moreover, the Florida mottled duck population status has not been assessed for more than a decade. We used band-recovery and recapture data from 2000–2013 to examine geographic and demographic factors that influence the survival of Florida mottled ducks and to determine whether survival and harvest probabilities have changed over time. Mean survival probabilities were higher for birds banded in the southern portion of their Florida range than for those banded in the northern portion and higher for adult males than for adult females in both areas. Harvest probabilities increased in the northern extent of its range in Florida for adults and juveniles and remained relatively constant in the southern portion of its range during the study period. Mean harvest probabilities for adult males in both areas were higher than for adult females. Mean harvest probability for juvenile females was higher than that for juvenile males in the north but was similar between the sexes in the south. Our results suggest that mortality rates are generally greater in the northern portion of the Florida mottled duck range because of regional differences in habitat distribution and permanence and in how mottled ducks and humans use wetlands in these areas. We suggest increasing conservation efforts in the north portion of the Florida mottled duck range and improving inferences from leg banding by incorporating live recapture data. © 2020 The Wildlife Society.     

Leopard density in post-conflict landscape,Cambodia: Evidence from spatially explicit capture–recapture

Effective conservation of large carnivores requires reliable estimates of population density, often obtained through capture–recapture analysis, in order to prioritize investments and assess conservation intervention effectiveness. Recent statistical advances and development of user-friendly software for spatially explicit capture–recapture (SECR) circumvent the difficulties in estimating effective survey area, and hence density, from capture–recapture data. We conducted a camera-trapping study on leopards (Panthera pardus) in Mondulkiri Protected Forest, Cambodia. We compared density estimates using SECR with those obtained from conventional approaches in which the effective survey area is estimated using a boundary strip width based on observed animal movements. Density estimates from Chao heterogeneity models (3.8 ± SE 1.9 individuals/100 km²) and Pledger heterogeneity models and models accounting for gender-specific capture and recapture rates (model-averaged density 3.9 ± SE 2.9 individuals/100 km²) were similar to those from SECR in program DENSITY (3.6 ± SE 1.0/100 km²) but higher than estimates from Jack-knife heterogeneity models (2.9 ± SE 0.9 individuals/100 km²). Capture probabilities differed between male and female leopards probably resulting from differences in the use of human-made trails between sexes. Given that there are a number of biologically plausible reasons to expect gender-specific variation in capture probabilities of large carnivores, we recommend exploratory analysis of data using models in which gender can be included as a covariate affecting capture probabilities particularly given the demographic importance of breeding females for population recovery of threatened carnivores. © 2011 The Wildlife Society.     

Nasal Discs and the Vital Rates of Lesser Scaup

Nasal discs have been used to identify ducks in studies of survival and reproduction. To date, there has not been a comprehensive assessment of nasal-disc effects on the vital rates of wild ducks. We applied nasal discs to 603 juvenile and 784 adult lesser scaup (Aythya affinis) females from a population breeding in southwest Montana, USA, and released 1,399 juvenile and 71 adult females wearing only metal leg bands between June 2005 and September 2016. Using resighting, recapture, and hunter-recovery data collected from those individuals, we estimated survival and recovery probability with multistate capture-recapture models in Program MARK. We also assessed if recovery distance from our study site and pre-breeding and brood-rearing body condition were diminished for females wearing nasal discs. Model-averaged survival probabilities were 0.231 ± 0.035 (SE) for juveniles and 0.482 ± 0.019 for adults released with nasal discs. Survival was 1.8–3.4 times higher for females released with metal leg bands when compared to those released with nasal discs; survival of these juveniles was 0.433 ± 0.049 and 0.693 ± 0.039 for adults. We did not find evidence for recovery probability or recovery distance varying between females that wore nasal discs and those that did not. During the pre-breeding and brood-rearing seasons, we did not find females wearing nasal discs to be in lower body condition when compared to unmarked females. Our comprehensive assessment of nasal discs on wild lesser scaup suggests that survival probabilities estimated from nasal-marked study populations should be cautiously interpreted as minimum estimates. © 2021 The Wildlife Society.     

Demography of Slate‐throated Redstarts (Myioborus miniatus): a non‐migratory Neotropical warbler

Most wood‐warblers (Parulidae) are non‐migratory residents of the Neotropics and subtropics, and the demographic characteristics of these species are poorly known. I examined the annual survival, reproductive output, dispersal, age of first breeding, and other demographic characteristics of a permanently territorial non‐migratory tropical warbler, the Slate‐throated Redstart (Myioborus miniatus), based on a 5‐yr study of a color‐banded population in Monteverde, Costa Rica. Territorial males showed strong site fidelity, but 26% of females engaged in short‐distance between‐year breeding dispersal. Estimated annual survival of territory holders, corrected for undetected female breeding dispersal, was 0.56 for males and 0.43 for females, values lower than expected and comparable to survival estimates for North American migrant warblers. The lower annual survival of females had two demographic consequences; unpaired territorial males were present in 3 of 5 yr, and some 1‐yr‐old males appeared to be floaters. Unpaired females or female floaters, however, were not observed. Mean natal dispersal distance was significantly greater for females (935 m) than males (485 m). Estimated first‐year survival was 0.29, but this is almost certainly an underestimate because of undetected long‐distance, female‐biased natal dispersal. Annual fecundity (fledglings per female) was 1.8, less than that of temperate warblers and attributable to small mean clutch sizes and a low incidence of double brooding. Estimated population growth rate (λ) was <1 for both males and females, suggesting that the study population was a demographic sink, most likely due to lower‐than‐expected adult survival.     

Laying date,body mass and tick infestation of nestling tropical Roseate Terns Sterna dougallii predict fledging success,first‐year survival and age at first return to the natal colony

Both intrinsic and extrinsic factors recorded at individual nests can predict offspring fitness and survival but few studies have examined these effects in the tropics. We recorded nestling survival, post‐fledging survival and age at first return of Roseate Terns breeding at Aride Island, Seychelles, over a 12‐year period (1998–2009). Nest data recorded at the egg, nestling and fledging stages were collected during six breeding seasons (1998, 2001–2005) and a capture‐mark‐recapture dataset of six cohorts of fledglings was obtained from 2001–2009. Logistic regression models were used to assess the predictive effect of reproductive variables on fledging success, while multistate capture‐mark‐recapture models were used to estimate post‐fledging survival and return–recruitment probabilities to the natal site. Nestling survival probability increased with earliness of laying and was negatively affected by tick infestation during the growth period (0–23 days). Fledging probability was also positively related to chick body condition, whereas other pre‐fledging reproductive parameters such as clutch size and egg size were not influential. A multistate modelling of age‐specific survival and return–recruitment (transition) rates found that first‐year survival differed between cohorts and was also negatively affected by tick infestation. Annual survival stabilized from age 2 onwards at 0.83 ± 0.02. Transition rates were positively related to body condition at fledging, with heavier individuals returning for the first time to the natal colony at a younger age compared with lighter individuals. These results highlight the importance of local conditions encountered by tropical seabirds during the breeding season in shaping demographic parameters.     

Life history patterns,individual heterogeneity,and density dependence in breeding common goldeneyes of the northern boreal forest

Life history patterns and their associated tradeoffs influence population dynamics, as they determine how individuals allocate resources among competing demographic traits. Here we examined life history strategies in common goldeneyes Bucephala clangula (hereafter goldeneye), a cavity‐nesting sea duck, in the northern boreal forest of interior Alaska, USA. We used multistate capture–mark–recapture models to estimate adult survival, breeding probability, first‐year survival, and recruitment probability using a long‐term nest box study (1997–2010). We detected annual variation in adult survival, which varied from 0.74 ± 0.12 (SE) to 0.93 ± 0.06. In contrast, breeding probability remained relatively high and invariant (0.84 ± 0.11) and was positively related to individual nest success the year prior. Nonbreeding individuals in one year were more likely to remain a nonbreeder, than attempt to breed the following year. First‐year survival decreased with smaller residual duckling mass and larger brood sizes. Probability of recruitment into the breeding population conditioned on survival was constant during the study (0.96 ± 0.06), and did not vary among ages 2–5 yr‐old. Overall, goldeneyes exhibited high, but somewhat variable, adult survival, and high breeding and recruitment probabilities, which is consistent with observed patterns in bet‐hedging species that breed annually in high quality breeding environments, but whose reproductive output is often influenced by stochastic events. Demographic estimates from this study are among the first for goldeneyes within Alaska. Life history patterns are known to vary geographically, therefore, we recommend further examination of life history patterns within the distribution of goldeneyes.     

Erratum to: Using multistate capture–mark–recapture models to quantify effects of predation on age-specific survival and population growth in black-tailed deer

Effective species management and conservation relies on accurate estimates of vital rates and an understanding of their link to environmental variables. We used multistate capture–mark–recapture models to directly quantify effects of predation on age-specific survival of black-tailed deer Odocoileus hemionus columbianus in California, USA. Survival probabilities were derived from individual encounter histories of 136 fawns and 57 adults monitored over 4 years. Based on results from our survival analysis we parameterized a Lefkovitch matrix and used elasticity analyses to investigate contributions of mortality due to predation to changes in population growth. We found strong evidence for age-specific survival including senescence. Survival of females >1 year old was consistently low (0.56 ± 0.18 for yearlings, 0.77 ± 0.13 for prime-aged females, and 0.55 ± 0.08 for senescent individuals), primarily due to high puma Puma concolor predation during summer. Predation from black bears Ursus americanus and coyotes Canis latrans was the primary cause for low annual survival of fawns (0.24 ± 0.16). Resulting estimates of population growth rates were indicative of a strongly declining population (λ = 0.82 ± 0.13). Despite high sensitivity to changes in adult survival, results from a lower-level elasticity analysis suggested that predation on fawns was the most significant individual mortality component affecting population decline. Our results provide a rare, direct link between predation, age-specific survival and the predicted population decline of a common ungulate species. The magnitude of predation was unexpected and suggests that ungulates in multi-predator systems struggle to cope with simultaneous reductions in survival probabilities from predators targeting different age classes.     

Sex ratio,survival, and recapture rate in a Cuban population of the damselfly <Emphasis Type="BoldItalic">Hypolestes trinitatis</Emphasis> (Odonata: Megapodagrionidae)

Male-biased sex ratios in adult odonate populations have been the subject of vigorous discussion between the students of this order of insects. The debate has centered on whether the observed male bias in many populations is real, perhaps due to unequal survival rates, or whether it is an artifact caused by differences in recapture probabilities. A mark–recapture study to assess the relative contribution of survivorship and recapture rates on male-biased sex ratio was performed in a Cuban population of the damselfly Hypolestes trinitatis. Maximum likelihood theory and Akaike information criterion were used for parameter estimation and model selection, respectively. Females in the sample were outnumbered two to one by males. Estimated recapture and survival rates were 0.188 (females) and 0.638 (males), and 0.933 (females) and 0.944 (males), respectively. Recapture rates only partially explained the bias since the population sex ratio estimated after correcting for differences in this parameter was male biased (1.5). The observed higher survival probabilities in males could have generated the male-biased population sex ratio. Therefore, we concluded that the observed male-biased population sex ratio in H. trinitatis is real.     

Population parameters and harvest risks for polar bears (<Emphasis Type="Italic">Ursus maritimus</Emphasis>) of Kane Basin,Canada and Greenland

We estimated demographic parameters and current harvest risks for a population of polar bears (Ursus maritimus Phipps) inhabiting northern Smith Sound and Kane Basin, Canada and Greenland. Our demographic analysis included a detailed assessment of age- and sex-specific survival and recruitment from 141 marked polar bears, using information contained within the standing age distribution of captures and mark-recapture analysis. Total survival rates for females were: 0.374 ± 0.180 (cubs), 0.686 ± 0.157 (ages 1–4), and 0.967 ± 0.043 (ages 5+). Mean litter size was 1.67 ± 0.08 cubs. Females did not reproduce until at least age 6, which is late compared to other populations of polar bears. The model-averaged, mark–recapture estimate of mean abundance (±1 SE) for years 1994–1997 was 164 ± 35 bears. We incorporated demographic parameters and their variances into a harvest risk analysis (i.e., a stochastic, harvested population viability analysis, PVA). Results suggest that polar bears in the region were severely over-harvested during the mark–recapture interval (1992–1997). The current status of the population is unknown.     

Demography and population viability of polar bears in the Gulf of Boothia, Nunavut

We estimated demographic parameters and harvest risks for polar bears ( Ursus maritimus ) inhabiting the Gulf of Boothia, Nunavut, from 1976 to 2000. We computed survival and abundance from capture–recapture and recovery data (630 marks) using a Burnham joint live–dead model implemented in program MARK. Annual mean total survival (including harvest) was 0.889 ± 0.179 (± 1 SE) for cubs, 0.883 ± 0.087 for subadults (ages 1–4), 0.919 ± 0.044 for adult females, and 0.917 ± 0.041 for adult males. Abundance in the last 3 yr of study was 1,592 ± 361 bears. Mean size of newborn litters was 1.648 ± 0.098 cubs. By age 7, 0.97 ± 0.30 of available females were producing litters. Harvest averaged 38.4 ± 4.2 bears/year in the last 5 yr of study; however, the 2002–2007 kill averaged 56.4 bears/yr. We used a harvested Population Viability Analysis (PVA) to examine impacts of increasing rates of harvest. We estimated the current population growth rate, λ _H , to be 1.025 ± 0.032. Although this suggests the population is growing, progressive environmental changes may require more frequent population inventory studies to maintain the same levels of harvest risk.     

Assessment of costs of reproduction in a pelagic seabird using multistate mark-recapture models

We used a long‐term population band‐resight survey database, a parallel reproduction database, and multistate mark–recapture analysis to assess the costs of reproduction, a keystone concept of life‐history evolution, in Nazca boobies (Sula granti) from Punta Cevallos, Isla Española, Galápagos, Ecuador. We used eight years of resight and breeding data to compare models that included sex‐ and state‐specific survival probabilities and probabilities of transition between reproductive states using multistate mark–recapture models. Models that included state‐specific effects were compared with models lacking such effects to evaluate costs of reproduction. The top model, optimizing the trade‐off of model simplicity and fit to the data using the Akaike Information Criterion (AIC), showed evidence of a temporally varying survival cost of reproduction: nonbreeders showed higher annual survival than breeders did in some years. Because increasing investment among breeders showed no negative association with survival and subsequent breeding success, this evidence indicates a cost to both males and females of initiating, but not of continuing, a reproductive attempt. In some cases, breeders reaching the highest reproductive state (fledging an offspring) showed higher survival or subsequent breeding success than did failed breeders, consistent with differences in overall quality that promote both survival and reproduction. Although a male‐biased adult sex ratio was observed in this population of Nazca boobies, models of state‐ and sex‐specific survival and transition probabilities were not supported, indicating that males and females do not incur different costs of reproduction, and that the observed sex ratio bias is not due to sex‐specific adult mortality.     

Assessing Compensatory Versus Additive Harvest Mortality: An Example Using Greater Sage-Grouse

ABSTRACT We used band-recovery data from 2 populations of greater sage-grouse (Centrocercus urophasianus), one in Colorado, USA, and another in Nevada, USA, to examine the relationship between harvest rates and annual survival. We used a Seber parameterization to estimate parameters for both populations. We estimated the process correlation between reporting rate and annual survival using Markov chain Monte Carlo methods implemented in Program MARK. If hunting mortality is additive to other mortality factors, then the process correlation between reporting and survival rates will be negative. Annual survival estimates for adult and juvenile greater sage-grouse in Nevada were 0.42±0.07 (x̄±SE) for both age classes, whereas estimates of reporting rate were 0.15±0.02 and 0.16±0.03 for the 2 age classes, respectively. For Colorado, average reporting rates were 0.14±0.016, 0.14±0.010, 0.19±0.014, and 0.18±0.014 for adult females, adult males, juvenile females, and juvenile males, respectively. Corresponding mean annual survival estimates were 0.59±0.01, 0.37±0.03, 0.78±0.01, and 0.64±0.03. Estimated process correlation between logit-transformed reporting and survival rates for greater sage-grouse in Colorado was ρ = 0.68±0.26, whereas that for Nevada was ρ = 0.04±0.58. We found no support for an additive effect of harvest on survival in either population, although the Nevada study likely had low power. This finding will assist mangers in establishing harvest regulations and otherwise managing greater sage-grouse populations.     

Estimating age‐dependent survival when juveniles resemble females: Invasive ring‐necked parakeets as an example

Many species only show sexual dimorphism at the age of maturity, such that juveniles typically resemble females. Under these circumstances, estimating accurate age‐specific demographic parameters is challenging. Here, we propose a multievent model parameterization able to estimate age‐dependent survival using capture–recapture data with uncertainty in age and sex assignment of individuals. We illustrate this modeling approach with capture–recapture data from the ring‐necked parakeet Psittacula krameri. We analyzed capture, recapture, and resighting data (439 recaptures/resightings) of 156 ring‐necked parakeets tagged with neck collars in Barcelona city from 2003 to 2016 to estimate the juvenile and adult survival rate. Our models successfully estimated the survival probabilities of the different age classes considered. Survival probability was similar between adults (0.83, 95% CI = 0.77–0.87) and juveniles during their second (0.79, 95% CI = 0.58–0.87) and third winter (0.83, 95% CI = 0.65–0.88). The youngest juveniles (1st winter) showed a slightly lower survival (0.57, 95% CI = 0.37–0.79). Among adults, females showed a slightly higher survival than males (0.87, 95% CI = 0.78–0.93; and 0.80, 95% CI = 0.73–0.86, respectively). These high survival figures predict high population persistence in this species and urge management policies. The analysis also stresses the usefulness of multievent models to estimate juvenile survival when age cannot be fully ascertained.     

Mixed-stock aging analysis reveals variable sea turtle maturity rates in a recovering population

Quantifying demographic parameters and variable vital rates, such as somatic growth rates, time to maturity, and reproductive longevity, is important for effective management of threatened and endangered populations such as sea turtles (Cheloniidae). To address these knowledge gaps, we applied skeletochronology to analyze and compare somatic growth rates and variation in life-history traits such as age and size at sexual maturity for 65 green turtles (Chelonia mydas) in the eastern Pacific Ocean (EP), along the west coast of the United States; turtles belonged to ≥2 nesting subpopulations that differed in body size (mean nesting size). Green turtles in the EP spend approximately 5 years in the oceanic stage before recruiting to nearshore habitats, males may be smaller and younger than females at maturation (x̅ = 17.7 ± 5.5 yr vs. 28.0 ± 8.2 yr), and younger age at sexual maturity was associated with smaller size at sexual maturity, suggesting that mean nesting body size may be reflective of maturation timing for subpopulations. Smaller body sizes for females nesting at Michoacán, Mexico (continental) rookeries, yielded a younger predicted age at sexual maturity (x̅ = ~17 yr) compared to females from Revillagigedo Islands, Mexico rookeries, which displayed larger body sizes and older age at sexual maturity (x̅ = ~30 yr). We consider possible mechanisms driving the observed divergence in life-history traits, including the possibility that earlier maturation (reduced generation length) for turtles in the Michoacán nesting subpopulation may be a response to intense harvesting in the past 50 years, and consideration of such anthropogenic impacts is warranted by population managers. Finally, our results indicate green turtles moved into nearshore neritic habitats at a young age (4–6 yr), emphasize the importance of protecting neritic habitats along the southwestern United States and northwestern Mexican coasts, and encourage the incorporation of variable maturation time in population recovery assessments.