scholarly journals Full life-cycle models from ring-recovery data: estimating fecundity from age ratios at capture

2018 ◽  
Author(s):  
Todd. W. Arnold

AbstractTag-recovery data from organisms captured and marked post breeding are commonly used to estimate juvenile and adult survival. If annual fecundity could also be estimated, tagging studies such as European and North American bird-ringing schemes could provide all parameters needed for building full life-cycle projection models.I modified existing tag-recovery models to allow estimation of annual fecundity using age composition and recapture probabilities obtained during routine banding operations of northern pintails (Anas acuta) and dark-eyed juncos (Junco hyemalis), and I conducted simulations to assess estimator performance in relation to sample size.For pintails, population growth rate from band-recovery data (λ = 0.929, SD 0.060) was similar but less precise than count-based estimates from the Waterfowl Breeding Pair and Habitat Survey (λ 0.945, SE 0.001). Models with temporal variation in vital rates indicated that annual population growth in pintails was driven primarily by variation in fecundity. Juncos had lower survival but greater fecundity, and their estimated population growth rate (λ 1.01, SD 0.19) was consistent with count-based surveys (λ 0.986).Simulations indicated that reliable (CV < 0.10) estimates of fecundity could be obtained with >1000 same-season live encounters. Although precision of survival estimates depended primarily on numbers of adult recoveries, estimates of population growth rate were most sensitive to total number of live encounters.Synthesis and applications: Large-scale ring-recovery programmes could be used to estimate annual fecundity in many species of birds, but the approach requires better data curation, including accurate assessment of age, better reporting of banding totals and greater emphasis on obtaining and reporting same-season live encounters.

2019 ◽  
Vol 97 (2) ◽  
pp. 112-120 ◽  
Author(s):  
Michael E. Wheeler ◽  
Jeb A. Barzen ◽  
Shawn M. Crimmins ◽  
Timothy R. Van Deelen

Population growth rate in long-lived bird species is often most sensitive to changes in adult survival. Sandhill Cranes (Antigone canadensis (Linnaeus, 1758)) have long life spans, small broods, and delayed first reproduction. Only territorial adult Sandhill Cranes participate in breeding, and territory acquisition reflects the interplay between the availability of suitable territories and the variation in mortality of adult birds occupying those territories. We estimated vital rates of a population at equilibrium using long-term resightings data (2000–2014; n = 451 marked individuals) in a multistate mark–resight model and used a stage-structured projection matrix to assess how strongly territorial adult survival affects population growth rate. Elasticity analysis indicated territorial birds surviving and retaining territories had a 2.58 times greater impact on population growth compared with the next most important transition rate (survival of nonterritorial adults remaining nonterritorial). Knowing how changes in vital rates of various stage classes will differentially impact population growth rate allows for targeted management actions including encouraging growth in recovering populations, assessing opportunity for recreational harvest, or maintaining populations at a desired level. This study also highlights the value of collecting demographic data for all population segments, from which one can derive reproductive output or growth rate.


2021 ◽  
Author(s):  
Omar Lenzi ◽  
Arpat Ozgul ◽  
Roberto Salguero-Gomez ◽  
Maria Paniw

Temporal variation in vital rates (e.g., survival, reproduction) can decrease the long-term mean performance of a population. Species are therefore expected to evolve demographic strategies that counteract the negative effects of vital rate variation on the population growth rate. One key strategy, demographic buffering, is reflected in a low temporal variation in vital rates critical to population dynamics. However, comparative studies in plants have found little evidence for demographic buffering, and little is known about the prevalence of buffering in animal populations. Here, we used vital rate estimates from 31 natural populations of 29 animal species to assess the prevalence of demographic buffering. We modeled the degree of demographic buffering using a standard measure of correlation between the standard deviation of vital rates and the sensitivity of the population growth rate to changes in such vital rates across populations. We also accounted for the effects of life-history traits, i.e., age at first reproduction and spread of reproduction across the life cycle, on these correlation measures. We found no strong or consistent evidence of demographic buffering across the study populations. Instead, key vital rates could vary substantially depending on the specific environmental context populations experience. We suggest that it is time to look beyond concepts of demographic buffering when studying natural populations towards a stronger focus on the environmental context-dependence of vital-rate variation.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Daniel Oro ◽  
Daniel F. Doak

Abstract Standard procedures for capture–mark–recapture modelling (CMR) for the study of animal demography include running goodness-of-fit tests on a general starting model. A frequent reason for poor model fit is heterogeneity in local survival among individuals captured for the first time and those already captured or seen on previous occasions. This deviation is technically termed a transience effect. In specific cases, simple, uni-state CMR modeling showing transients may allow researchers to assess the role of these transients on population dynamics. Transient individuals nearly always have a lower local survival probability, which may appear for a number of reasons. In most cases, transients arise due to permanent dispersal, higher mortality, or a combination of both. In the case of higher mortality, transients may be symptomatic of a cost of first reproduction. A few studies working at large spatial scales actually show that transients more often correspond to survival costs of first reproduction rather than to permanent dispersal, bolstering the interpretation of transience as a measure of costs of reproduction, since initial detections are often associated with first breeding attempts. Regardless of their cause, the loss of transients from a local population should lower population growth rate. We review almost 1000 papers using CMR modeling and find that almost 40% of studies fitting the searching criteria (N = 115) detected transients. Nevertheless, few researchers have considered the ecological or evolutionary meaning of the transient phenomenon. Only three studies from the reviewed papers considered transients to be a cost of first reproduction. We also analyze a long-term individual monitoring dataset (1988–2012) on a long-lived bird to quantify transients, and we use a life table response experiment (LTRE) to measure the consequences of transients at a population level. As expected, population growth rate decreased when the environment became harsher while the proportion of transients increased. LTRE analysis showed that population growth can be substantially affected by changes in traits that are variable under environmental stochasticity and deterministic perturbations, such as recruitment, fecundity of experienced individuals, and transient probabilities. This occurred even though sensitivities and elasticities of these parameters were much lower than those for adult survival. The proportion of transients also increased with the strength of density-dependence. These results have implications for ecological and evolutionary studies and may stimulate other researchers to explore the ecological processes behind the occurrence of transients in capture–recapture studies. In population models, the inclusion of a specific state for transients may help to make more reliable predictions for endangered and harvested species.


2009 ◽  
Vol 59 (1) ◽  
pp. 127-144 ◽  
Author(s):  
Lia Hemerik ◽  
Chris Klok ◽  
Maja Roodbergen

AbstractMany populations of wader species have shown a strong decline in number in Western-Europe in recent years. The use of simple population models such as matrix models can contribute to conserve these populations by identifying the most profitable management measures. Parameterization of such models is often hampered by the availability of demographic data (survival and reproduction). In particular, data on survival in the pre-adult (immature) stage of wader species that remain in wintering areas outside Europe are notoriously difficult to obtain, and are therefore virtually absent in the literature. To diagnose population decline in the wader species; Black-tailed Godwit, Curlew, Lapwing, Oystercatcher, and Redshank, we extended an existing modelling framework in which incomplete demographic data can be analysed, developed for species with a pre-adult stage of one year. The framework is based on a Leslie matrix model with three parameters: yearly reproduction (number of fledglings per pair), yearly pre-adult (immature) and yearly adult (mature) survival. The yearly population growth rate of these populations and the relative sensitivity of this rate to changes in survival and reproduction parameters (the elasticity) were calculated numerically and, if possible, analytically. The results showed a decrease in dependence on reproduction and an increase in pre-adult survival of the population growth rate with an increase in the duration of the pre-adult stage. In general, adult survival had the highest elasticity, but elasticity of pre-adult survival increased with time to first reproduction, a result not reported earlier. Model results showed that adult survival and reproduction estimates reported for populations of Redshank and Curlew were too low to maintain viable populations. Based on the elasticity patterns and the scope for increase in actual demographic parameters we inferred that conservation of the Redshank and both Curlew populations should focus on reproduction. For one Oystercatcher and the Black-tailed Godwit populations we suggested a focus on both reproduction and pre-adult survival. For the second Oystercatcher population pre-adult survival seemed the most promising target for conservation. And for the Lapwing populations all demographic parameters should be considered.


1997 ◽  
Vol 75 (12) ◽  
pp. 2027-2037 ◽  
Author(s):  
Ali El-Keblawy ◽  
K. H. Shaltout ◽  
J. Lovett-Doust ◽  
A. Ramadan

Natural populations of the evergreen shrub, Thymelaea hirsuta (L.) Endl., were studied over 6 years at five desert habitats, in terms of seedling recruitment and adult survival and as a function of plant size and gender class. Habitat and time significantly influenced mortality of both reproductive and non-reproductive plants. Plant size also significantly affected adult mortality. Seedling recruitment varied significantly with habitat and year and approached zero some years. Significant among-year and among-population variation in population growth rates were observed over the 6 years of study, and all populations declined in size (ranging from −1.7% per year at the coastal dune site to −10.9% per year at the inland plateau site). Spearman rank correlation analysis between habitats ranked according to a north–south gradient and demographic variables indicates that this gradient is associated with a pattern of lower seedling emergence and survival and a lower population growth rate and greater mortality for all size-classes of Thymelaea plants. In experimental botanic garden plots, germination of seed collected from five natural populations, and seedling survival in the following year were assessed under conditions of high, medium, and low seedling density. Seedling emergency differed significantly according to maternal habitat. With regular watering, seeding survival to one year was 72% (averaged across habitats and densities). This compares with 64% for seedlings grown at the highest density, suggesting that the intense mortality observed under field conditions is more likely to be a result of water shortage than intraspecific competition. Key words: Egyptian desert, Thymelaea hirsuta, germination and establishment, seedlings, recruitment, competition, population growth rate.


Elem Sci Anth ◽  
2014 ◽  
Vol 2 ◽  
Author(s):  
Aldo Compagnoni ◽  
Peter B. Adler

Abstract Climate change threatens to exacerbate the impacts of invasive species. In temperate ecosystems, direct effects of warming may be compounded by dramatic reductions in winter snow cover. Cheatgrass (Bromus tectorum) is arguably the most destructive biological invader in basins of the North American Intermountain West, and warming could increase its performance through direct effects on demographic rates or through indirect effects mediated by loss of snow. We conducted a two-year experimental manipulation of temperature and snow pack to test whether 1) warming increases cheatgrass population growth rate and 2) reduced snow cover contributes to cheatgrass’ positive response to warming. We used infrared heaters operating continuously to create the warming treatment, but turned heaters on only during snowfalls for the snowmelt treatment. We monitored cheatgrass population growth rate and the vital rates that determine it: emergence, survival and fecundity. Growth rate increased in both warming and snowmelt treatments. The largest increases occurred in warming plots during the wettest year, indicating that the magnitude of response to warming depends on moisture availability. Warming increased both fecundity and survival, especially in the wet year, while snowmelt contributed to the positive effects of warming by increasing survival. Our results indicate that increasing temperature will exacerbate cheatgrass impacts, especially where warming causes large reductions in the depth and duration of snow cover.


PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e10708
Author(s):  
Douglas C. Heard ◽  
Kathryn L. Zimmerman

Most woodland caribou (Rangifer tarandus caribou) populations are declining primarily because of unsustainable predation resulting from habitat-mediated apparent competition. Wolf (Canis lupus) reduction is an effective recovery option because it addresses the direct effect of predation. We considered the possibility that the indirect effects of predation might also affect caribou population dynamics by adversely affecting summer foraging behaviour. If spring and/or summer nutrition was inadequate, then supplemental feeding in fall might compensate for that limitation and contribute to population growth. Improved nutrition and therefore body condition going into winter could increase adult survival and lead to improved reproductive success the next spring. To test that hypothesis, we fed high-quality food pellets to free-ranging caribou in the Kennedy Siding caribou herd each fall for six years, starting in 2014, to see if population growth rate increased. Beginning in winter 2015–16, the Province of British Columbia began a concurrent annual program to promote caribou population increase by attempting to remove most wolves within the Kennedy Siding and the adjacent caribou herds’ ranges. To evaluate the impact of feeding, we compared lambdas before and after feeding began, and to the population trend in the adjacent Quintette herd over the subsequent four years. Supplemental feeding appeared to have an incremental effect on population growth. Population growth of the Kennedy Siding herd was higher in the year after feeding began (λ = 1.06) compared to previous years (λ = 0.91) and to the untreated Quintette herd (λ = 0.95). Average annual growth rate of the Kennedy Siding herd over the subsequent four years, where both feeding and wolf reduction occurred concurrently, was higher than in the Quintette herd where the only management action in those years was wolf reduction (λ = 1.16 vs. λ = 1.08). The higher growth rate of the Kennedy Siding herd was due to higher female survival (96.2%/yr vs. 88.9%/yr). Many caribou were in relatively poor condition in the fall. Consumption of supplemental food probably improved their nutritional status which ultimately led to population growth. Further feeding experiments on other caribou herds using an adaptive management approach would verify the effect of feeding as a population recovery tool. Our results support the recommendation that multiple management actions should be implemented to improve recovery prospects for caribou.


2002 ◽  
Vol 357 (1425) ◽  
pp. 1299-1306 ◽  
Author(s):  
Valery E. Forbes ◽  
Peter Calow

Assessing the ecological risks of toxic chemicals is most often based on individual–level responses such as survival, reproduction or growth. Such an approach raises the following questions with regard to translating these measured effects into likely impacts on natural populations. (i) To what extent do individual–level variables underestimate or overestimate population–level responses? (ii) How do toxicant–caused changes in individual–level variables translate into changes in population dynamics for species with different life cycles? (iii) To what extent are these relationships complicated by population–density effects? These issues go to the heart of the ecological relevance of ecotoxicology and we have addressed them using the population growth rate as an integrating concept. Our analysis indicates that although the most sensitive individual–level variables are likely to be equally or more sensitive to increasing concentrations of toxic chemicals than population growth rate, they are difficult to identify a priori and, even if they could be identified, integrating impacts on key life–cycle variables via population growth rate analysis is nevertheless a more robust approach for assessing the ecological risks of chemicals. Populations living under density–dependent control may respond differently to toxic chemicals than exponentially growing populations, and greater care needs to be given to incorporating realistic density conditions (either experimentally or by simulation) into ecotoxicological test designs. It is impractical to expect full life–table studies, which record changes in survival, fecundity and development at defined intervals through the life cycle of organisms under specified conditions, for all relevant species, so we argue that population growth rate analysis should be used to provide guidance for a more pragmatic and ecologically sound approach to ecological risk assessment.


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