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J.E. Hines

Publications and source records attributed to J.E. Hines.

At least 55 records · Page 3Linked to original sources

On the use of capture-recapture models in mist-net studies

Capture-recapture models provide a statistical framework for estimating population parameters from mist-net data. Although Cormack-Jolly-Seber and related models have recently been used to estimate survival rates of birds sampled with mist nets, we believe that the full potential for use of capture-recapture models has not been realized by many researchers involved in mist-net studies. We present a brief discussion of the overall framework for estimation using capture-recapture methods, and review several areas in which recent statistical methods can be, but generally have not yet been, applied to mist-net studies. These areas include estimation of (I) rates of movement among areas; (2) survival rates in the presence of transients: (3) population sizes or migrating birds: (4) proportion of birds alive but not present at a breeding site (one definition of proportion of nonbreeding birds in a population): (5) population change and recruitment: and (6) species richness. Using these models will avoid the possible bias associated with use of indices. and provide statistically valid variance estimates and inference.

Book chapter

Computing and software

The reality is that the statistical methods used for analysis of data depend upon the availability of software. Analysis of marked animal data is no different than the rest of the statistical field. The methods used for analysis are those that are available in reliable software packages. Thus, the critical importance of having reliable, up–to–date software available to biologists is obvious. Statisticians have continued to develop more robust models, ever expanding the suite of potential analysis methods available. But without software to implement these newer methods, they will languish in the abstract, and not be applied to the problems deserving them. In the Computers and Software Session, two new software packages are described, a comparison of implementation of methods for the estimation of nest survival is provided, and a more speculative paper about how the next generation of software might be structured is presented. Rotella et al. (2004) compare nest survival estimation with different software packages: SAS logistic regression, SAS non–linear mixed models, and Program MARK. Nests are assumed to be visited at various, possibly infrequent, intervals. All of the approaches described compute nest survival with the same likelihood, and require that the age of the nest is known to account for nests that eventually hatch. However, each approach offers advantages and disadvantages, explored by Rotella et al. (2004). Efford et al. (2004) present a new software package called DENSITY. The package computes population abundance and density from trapping arrays and other detection methods with a new and unique approach. DENSITY represents the first major addition to the analysis of trapping arrays in 20 years. Barker & White (2004) discuss how existing software such as Program MARK require that each new model’s likelihood must be programmed specifically for that model. They wishfully think that future software might allow the user to combine pieces of likelihood functions together to generate estimates. The idea is interesting, and maybe some bright young statistician can work out the specifics to implement the procedure. Choquet et al. (2004) describe MSURGE, a software package that implements the multistate capture–recapture models. The unique feature of MSURGE is that the design matrix is constructed with an interpreted language called GEMACO. Because MSURGE is limited to just multistate models, the special requirements of these likelihoods can be provided. The software and methods presented in these papers gives biologists and wildlife managers an expanding range of possibilities for data analysis. Although ease–of–use is generally getting better, it does not replace the need for understanding of the requirements and structure of the models being computed. The internet provides access to many free software packages as well as user–discussion groups to share knowledge and ideas. (A starting point for wildlife–related applications is (http://www.phidot.org).

Animal Biodiversity and Conservation

Detecting warning signs of trouble within population fluctuations: using capture-recapture modeling to uncover changes in population dynamics leading to declines

An intensive mark-recapture/resighting program has been carried out on the Roseate Terns nesting at Falkner Island, Connecticut, since the late 1980s as part of a regional study of the metapopulation dynamics and ecology of the endangered Northwest Atlantic breeding population of this species. Substantial losses of tern eggs and chicks to predation at this colony site began in 1996 when at least five Black-crowned Night-Herons started nocturnal raids. This depredation has been a major factor in the reduction of productivity from an average of about 1.0 chicks/pair for the 10 years before night-heron predation began to as low as about 0.2 chicks/pair in 2002. Recent capture-recapture modelling analyses have detected other important impacts on the population dynamics of the Roseate Terns at this site including a reduction by about half in the 'development-of-residency' rates of first-time breeders, and a substantial decline in the local 'survival-and-fidelity' rates of experienced breeders believed due mostly to increased immigration rates to other colony sites.

Annual Meeting of the Association of Field Ornitho

Estimating natal dispersal movement rates of female European ducks with multistate modelling

1. We used up to 34 years of capture-recapture data from about 22 100 new releases of day-old female ducklings and multistate modelling to test predictions about the influence of environmental, habitat and management factors on natal dispersal probability of three species of ducks within the Engure Marsh, Latvia. 2. The mean natal dispersal distances were very similar (c. 0.6-0.7 km) for all three species and were on average 2.7 times greater than breeding dispersal distances recorded within the same study system. 3. We were unable to confirm the kinship hypothesis and found no evidence that young first-nesting females nested closer to their relatives (either mother or sister) than to the natal nest. 4. Young female northern shovelers, like adults, moved from small islands to the large island when water level was high and vice versa when water level was low before the construction of elevated small islands. Movement probabilities between the two strata were much higher for young shovelers than adults, suggesting that young birds had not yet developed strong fidelity to the natal site. Movements of young female tufted ducks , unlike those of shovelers, were not dependent on water level fluctuations and reflected substantial flexibility in choice of first nesting sites. 5. Data for young birds supported our earlier conclusion that common pochard nesting habitats in black-headed gull colonies were saturated during the entire study period. Young females, like the two adult age groups, moved into and out of colonies with similar probability. Fidelity probability of female pochards to each stratum increased with age, being the lowest (0.62) for young (DK) females, intermediate (0.78) for yearlings (SY) and the highest (0.84) for adult (ASY) females. 6. Young female tufted ducks , like adults, showed higher probabilities of moving from islands to emergent marshes when water levels were higher both before and after habitat management. The relationship between the spring water levels and movement was much weaker for young females than for adults. 7. Young female diving ducks exhibited much stronger (compared to adults) asymmetric movement with respect to proximity to water, with higher movement probabilities to near-water locations than away from these locations. 8. Local survival of day-old ducklings during the first year of life was time-specific and very low (means for different strata/states 0.01-0.08) because of high rates of emigration and prefledging mortality.

Journal of Animal Ecology

On the use of the robust design with transient capture-recapture models

Capture-mark-recapture studies provide a useful mechanism for estimating the components of the population dynamics of birds, especially survival. In such studies, it is important that the population being captured matches the population of interest. In many studies, transients are captured along with the population of interest (e.g. resident breeders). Ignoring that phenomenon produces negatively biased survival estimates, because transients do not return. Although transients cannot be distinguished from residents in the hand, previous methods have adjusted for transience by relying on those captured in more than one year to provide direct estimates of survival rate for residents. Here, we extend that approach by supplementing that cohort of known residents with those previously unmarked birds captured twice or more, at least d days apart, within a season. We provide an ad hoc approach to that extension in detail and outline two more formal approaches. That extension increases the precision of survival estimates.

The Auk

Spring hunting changes the regional movements of migrating greater snow geese

1. Human-induced disturbance such as hunting may influence the migratory behaviour of long-distance migrants. In 1999 and 2000 a spring hunt of greater snow geese Anser caerulescens atlanticus occurred for the first time in North America since 1916, aimed at stopping population growth to protect natural habitats. 2. We evaluated the impact of this hunt on the staging movements of geese along a 600-km stretch of the St Lawrence River in southern Quebec, Canada. 3. We tracked radio-tagged female geese in three contiguous regions of the staging area from the south-west to the north-east: Lake St Pierre, Upper Estuary and Lower Estuary, in spring 1997 (n = 37) and 1998 (n = 70) before the establishment of hunting , and in 1999 (n = 60) and 2000 (n = 59) during hunting . 4. We used multi-state capture-recapture models to estimate the movement probabilities of radio-tagged females among these regions. To assess disturbance level, we tracked geese during their feeding trips and estimated the probability of completing a foraging bout without being disturbed. 5. In the 2 years without hunting , migration was strongly unidirectional from the south-west to the north-east, with very low westward movement probabilities. Geese gradually moved from Lake St Pierre to Upper Estuary and then from Upper Estuary to Lower Estuary. 6. In contrast, during the 2 years with hunting westward movement was more than four times more likely than in preceding years. Most of these backward movements occurred shortly after the beginning of the hunt, indicating that geese moved back to regions where they had not previously experienced hunting . 7. Overall disturbance level increased in all regions in years with hunting relative to years without hunting . 8. Synthesis and applications. We conclude that spring hunting changed the stopover scheduling of this long-distance migrant and might further impact population dynamics by reducing prenuptial fattening. The spring hunt may also have increased crop damage. We propose that staggered hunt opening dates could attenuate secondary effects of such management actions.

Quebec

Estimation by capture-recapture of recruitment and dispersal over several sites

Dispersal in animal populations is intimately linked with accession to reproduction, i.e. recruitment, and population regulation. Dispersal processes are thus a key component of population dynamics to the same extent as reproduction or mortality processes. Despite the growing interest in spatial aspects of population dynamics, the methodology for estimating dispersal, in particular in relation with recruitment, is limited. In many animal populations, in particular vertebrates, the impossibility of following individuals over space and time in an exhaustive way leads to the need to frame the estimation of dispersal in the context of capture-recapture methodology. We present here a class of age-dependent multistate capture-recapture models for the simultaneous estimation of natal dispersal, breeding dispersal, and age-dependent recruitment. These models are suitable for populations in which individuals are marked at birth and then recaptured over several sites. Under simple constraints, they can be used in populations where non-breeders are not observed, as is often the case with colonial waterbirds monitored on their breeding grounds. Biological questions can be addressed by comparing models differing in structure, according to the generalized linear model philosophy broadly used in capture-recapture methodology. We illustrate the potential of this approach by an analysis of recruitment and dispersal in the roseate tern Sterna dougallii .

Oikos

Estimating rates of local extinction and colonization in colonial species and an extension to the metapopulation and community levels

Coloniality has mainly been studied from an evolutionary perspective, but relatively few studies have developed methods for modelling colony dynamics. Changes in number of colonies over time provide a useful tool for predicting and evaluating the responses of colonial species to management and to environmental disturbance. Probabilistic Markov process models have been recently used to estimate colony site dynamics using presence–absence data when all colonies are detected in sampling efforts. Here, we define and develop two general approaches for the modelling and analysis of colony dynamics for sampling situations in which all colonies are, and are not, detected. For both approaches, we develop a general probabilistic model for the data and then constrain model parameters based on various hypotheses about colony dynamics. We use Akaike's Information Criterion (AIC) to assess the adequacy of the constrained models. The models are parameterised with conditional probabilities of local colony site extinction and colonization. Presence–absence data arising from Pollock's robust capture–recapture design provide the basis for obtaining unbiased estimates of extinction, colonization, and detection probabilities when not all colonies are detected. This second approach should be particularly useful in situations where detection probabilities are heterogeneous among colony sites. The general methodology is illustrated using presence–absence data on two species of herons. Estimates of the extinction and colonization rates showed interspecific differences and strong temporal and spatial variations. We were also able to test specific predictions about colony dynamics based on ideas about habitat change and metapopulation dynamics. We recommend estimators based on probabilistic modelling for future work on colony dynamics. We also believe that this methodological framework has wide application to problems in animal ecology concerning metapopulation and community dynamics.

Oikos

Long-term fitness consequences of early conditions in the kittiwake

1. The long - term fitness consequences of conditions during development are receiving growing attention: they are at the interface between ecological and evolutionary processes. We addressed the influence of the length of the rearing period and 'rank' on fitness components in a long -lived seabird species with deferred breeding: the kittiwake (Rissa tridactyla). Rank, which depends on hatching order, was used as a surrogate for dominance status in the brood. Rank could be viewed as a random factor affecting individuals regardless of their possible 'intrinsic quality' at birth. The length of the rearing period was used as a surrogate for parental effort. It reflects the interaction between numerous factors such as environmental conditions , parental quality, reproductive decisions and effort, and also offspring decisions and intrinsic quality at birth. 2. There was evidence of an influence of the length of the rearing period on local survival before recruitment. Individuals with shorter rearing periods had lower local survival during the first winter (e.g. the relationship was positive). They may incur higher mortality. In rank 1 prebreeders, this relationship was negative in older age-classes. Longer rearing periods and better condition at independence may be associated with stronger migrating ability, and prebreeders that have not yet made settlement decisions may emigrate permanently to distant locations. Such a complex pattern may reflect age-related changes in the relative contribution of mortality and permanent emigration to local survival. 3. The length of the rearing period had long - term consequences on reproductive performance. The relationship was positive but the rate of increase decreased slightly at higher values of the covariate. 4. There was an unambiguously negative influence of rank on survival before recruitment and recruitment probability, but not on demographic parameters specific to the reproductive stage. Juniors recruited later than elder siblings. The disadvantage of juniors may be expressed mainly in terms of higher mortality and disappearance from the population before recruitment.

Journal of Animal Ecology

Inferences about nested subsets structure when not all species are detected

Comparisons of species composition among ecological communities of different size have often provided evidence that the species in communities with lower species richness form nested subsets of the species in larger communities. In the vast majority of studies, the question of nested subsets has been addressed using information on presence-absence, where a '0' is interpreted as the absence of a given species from a given location. Most of the methodological discussion in earlier studies investigating nestedness concerns the approach to generation of model-based matrices. However, it is most likely that in many situations investigators cannot detect all the species present in the location sampled. The possibility that zeros in incidence matrices reflect nondetection rather than absence of species has not been considered in studies addressing nested subsets, even though the position of zeros in these matrices forms the basis of earlier inference methods. These sampling artifacts are likely to lead to erroneous conclusions about both variation over space in species richness and the degree of similarity of the various locations. Here we propose an approach to investigation of nestedness, based on statistical inference methods explicitly incorporating species detection probability, that take into account the probabilistic nature of the sampling process. We use presence-absence data collected under Pollock?s robust capture-recapture design, and resort to an estimator of species richness originally developed for closed populations to assess the proportion of species shared by different locations. We develop testable predictions corresponding to the null hypothesis of a nonnested pattern, and an alternative hypothesis of perfect nestedness. We also present an index for assessing the degree of nestedness of a system of ecological communities. We illustrate our approach using avian data from the North American Breeding Bird Survey collected in Florida Keys.

Florida

Sexual selection affects local extinction and turnover in bird communities

Predicting extinction risks has become a central goal for conservation and evolutionary biologists interested in population and community dynamics. Several factors have been put forward to explain risks of extinction, including ecological and life history characteristics of individuals. For instance, factors that affect the balance between natality and mortality can have profound effects on population persistence. Sexual selection has been identified as one such factor. Populations under strong sexual selection experience a number of costs ranging from increased predation and parasitism to enhanced sensitivity to environmental and demographic stochasticity. These findings have led to the prediction that local extinction rates should be higher for species/populations with intense sexual selection. We tested this prediction by analyzing the dynamics of natural bird communities at a continental scale over a period of 21 years (1975-1996), using relevant statistical tools. In agreement with the theoretical prediction, we found that sexual selection increased risks of local extinction (dichromatic birds had on average a 23% higher local extinction rate than monochromatic species). However, despite higher local extinction probabilities, the number of dichromatic species did not decrease over the period considered in this study. This pattern was caused by higher local turnover rates of dichromatic species, resulting in relatively stable communities for both groups of species. Our results suggest that these communities function as metacommunities, with frequent local extinctions followed by colonization. Anthropogenic factors impeding dispersal might therefore have a significant impact on the global persistence of sexually selected species.

Proceedings of the National Academy of Sciences

Factors affecting breeding dispersal of European ducks on Engure Marsh, Latvia

1. We used up to 35 years of capture-recapture data from nearly 3300 individual female ducks nesting on Engure Marsh , Latvia , and multistate modelling to test predictions about the influence of environmental, habitat and management factors on breeding dispersal probability within the marsh . 2. Analyses based on observed dispersal distances of common pochards and tufted ducks provided no evidence that breeding success in year t influenced dispersal distance between t and t + 1. 3. Breeding dispersal distances (year t to t + 1) of pochards and tufted ducks were associated with a delay in relative nest initiation dates in year t + 1. The delay was greater for pochards (c. 4 days) than for tufted ducks (c. 2 days) when females dispersed > 0.8 km. 4. Northern shovelers and tufted ducks moved from a large island to small islands at low water levels and from small islands to the large island at high water levels before the construction of elevated small islands (1960-82). Following this habitat management (1983-94), breeding fidelity was extremely high and not influenced by water level in the marsh for either species. 5. Because pochard nesting habitats in black-headed gull colonies were saturated during the entire study period, nesting females moved into and out of colonies with similar probabilities. Local survival probabilities and incubation body masses were higher for both yearlings (SY) and adults (ASY) nesting within gull colonies, suggesting that these females were of better quality than females nesting outside of the colonies. 6. Tufted ducks showed higher probabilities of moving from islands to emergent marshes when water levels were higher both before and after habitat management. However, rates of movement for a given water level were higher during the period before management than after. 7. Both pochards and tufted ducks exhibited asymmetric movement with respect to proximity to water, with higher movement probabilities to near-water nesting locations than away from these locations. 8. Multistate capture-recapture models provided analyses that were useful in investigating sources of variation in breeding dispersal probabilities.

Journal of Animal Ecology

Estimating site occupancy, colonization, and local extinction when a species is detected imperfectly

Few species are likely to be so evident that they will always be detected when present. Failing to allow for the possibility that a target species was present, but undetected, at a site will lead to biased estimates of site occupancy, colonization, and local extinction probabilities. These population vital rates are often of interest in long-term monitoring programs and metapopulation studies. We present a model that enables direct estimation of these parameters when the probability of detecting the species is less than 1. The model does not require any assumptions of process stationarity, as do some previous methods, but does require detection/nondetection data to be collected in a manner similar to Pollock's robust design as used in mark?recapture studies. Via simulation, we show that the model provides good estimates of parameters for most scenarios considered. We illustrate the method with data from monitoring programs of Northern Spotted Owls (Strix occidentalis caurina) in northern California and tiger salamanders (Ambystoma tigrinum) in Minnesota, USA.

Ecology

Adjusting multistate capture-recapture models for misclassification bias: manatee breeding proportions

Matrix population models are important tools for research and management of populations. Estimating the parameters of these models is an important step in applying them to real populations. Multistate capture-recapture methods have provided a useful means for estimating survival and parameters of transition between locations or life history states but have mostly relied on the assumption that the state occupied by each detected animal is known with certainty. Nevertheless, in some cases animals can be misclassified. Using multiple capture sessions within each period of interest, we developed a method that adjusts estimates of transition probabilities for bias due to misclassification. We applied this method to 10 years of sighting data for a population of Florida manatees (Trichechus manatus latirostris) in order to estimate the annual probability of transition from nonbreeding to breeding status. Some sighted females were unequivocally classified as breeders because they were clearly accompanied by a first-year calf. The remainder were classified, sometimes erroneously, as nonbreeders because an attendant first-year calf was not observed or was classified as more than one year old. We estimated a conditional breeding probability of 0.31 + 0.04 (estimate + 1 SE) when we ignored misclassification bias, and 0.61 + 0.09 when we accounted for misclassification.

Ecology

Spatio-temporal dynamics of species richness in coastal fish communities

Determining patterns of change in species richness and the processes underlying the dynamics of biodiversity are of key interest within the field of ecology, but few studies have investigated the dynamics of vertebrate communities at a decadal temporal scale. Here, we report findings on the spado-temporal variability in the richness and composition of fish communities along the Norwegian Skagerrak coast having been surveyed for more than half a century. Using statistical models incorporating non-detection and associated sampling variance, we estimate local species richness and changes in species composition allowing us to compute temporal variability in species richness. We tested whether temporal variation could be related to distance to the open sea and to local levels of pollution. Clear differences in mean species richness and temporal variability are observed between fjords that were and were not exposed to the effects of pollution. Altogether this indicates that the fjord is an appropriate scale for studying changes in coastal fish communities in space and time. The year-to-year rates of local extinction and turnover were found to be smaller than spatial differences in community composition. At the regional level, exposure to the open sea plays a homogenizing role, possibly due to coastal currents and advection.

Proceedings of the Royal Society B: Biological Sci

Sources of variation in survival and breeding site fidelity in three species of European ducks

1. We used long-term capture-recapture-recovery data and a modelling approach developed by Burnham (1993) to test a priori predictions about sources of variation in annual survival rates and fidelity within a population of individually marked females in three species of European ducks from a breeding ground study site in Latvia. 2. True annual survival was higher for diving ducks (tufted duck 0-72, common pochard 0-65) and lower for northern shoveler (0-52). Survival of female diving ducks was positively correlated with mean winter temperatures at Western European wintering areas, the relationship being much stronger for pochard. 3. We present the first unbiased estimates of breeding fidelity and permanent emigration in European ducks. Estimated fidelity rates were high (0'88-1-0) and emigration rates low (0-0-12) for all three species, and we found strong evidence for age-specific differences in fidelity of pochards. Unusual long-distance (up to 2500 km) breeding dispersal movements that we found in female tufted ducks have not been documented in any other European waterfowl and are most probably a result of saturated nesting habitats. 4. Fidelity was a function of patch reproductive success in the previous year for all three species providing support for the idea that patch success is an important cue influencing fidelity. 5. Fidelity probability increased to 1.0 for shovelers during the last 12 years of study following provision of critical improvements in nesting habitats and suggested that habitat conditions and reproductive success determined site fidelity and settling patterns for shoveler and probably also influenced fidelity of the two other species. In predictable habitats, fidelity is a parameter that reflects the integration of fitness components and is thus a good quantity for assessing the effectiveness of habitat management actions.

Journal of Animal Ecology

On the estimation of species richness based on the accumulation of previously unrecorded species

Estimation of species richness of local communities has become an important topic in community ecology and monitoring. Investigators can seldom enumerate all the species present in the area of interest during sampling sessions. If the location of interest is sampled repeatedly within a short time period, the number of new species recorded is typically largest in the initial sample and decreases as sampling proceeds, but new species may be detected if sampling sessions are added. The question is how to estimate the total number of species. The data collected by sampling the area of interest repeatedly can be used to build species-accumulation curves: the cumulative number of species recorded as a function of the number of sampling sessions (which we refer to as ?species-accumulation data?). A classic approach used to compute total species richness is to fit curves to the data on species accumulation with sampling effort. This approach does not rest on direct estimation of the probability of detecting species during sampling sessions and has no underlying basis regarding the sampling process that gave rise to the data. Here we recommend a probabilistic, nonparametric estimator for species richness for use with species-accumulation data. We use estimators of population size that were developed for capture-recapture data, but that can be used to estimate the size of species assemblages using species-accumulation data. Models of detection probability account for the underlying sampling process. They permit variation in detection probability among species. We illustrate this approach using data from the North American Breeding Bird Survey (BBS). We describe other situations where species accumulation data are collected under different designs (e.g., over longer periods of time, or over spatial replicates) and that lend themselves to use of capture-recapture models for estimating the size of the community of interest. We discuss the assumptions and interpretations corresponding to each situation.

Alabama, Louisiana, Maine, Maryland, New Hampshire

A removal model for estimating detection probabilities from point-count surveys

Use of point-count surveys is a popular method for collecting data on abundance and distribution of birds. However, analyses of such data often ignore potential differences in detection probability. We adapted a removal model to directly estimate detection probability during point-count surveys. The model assumes that singing frequency is a major factor influencing probability of detection when birds are surveyed using point counts. This may be appropriate for surveys in which most detections are by sound. The model requires counts to be divided into several time intervals. Point counts are often conducted for 10 min, where the number of birds recorded is divided into those first observed in the first 3 min, the subsequent 2 min, and the last 5 min. We developed a maximum-likelihood estimator for the detectability of birds recorded during counts divided into those intervals. This technique can easily be adapted to point counts divided into intervals of any length. We applied this method to unlimited-radius counts conducted in Great Smoky Mountains National Park. We used model selection criteria to identify whether detection probabilities varied among species, throughout the morning, throughout the season, and among different observers. We found differences in detection probability among species. Species that sing frequently such as Winter Wren ( Troglodytes troglodytes ) and Acadian Flycatcher ( Empidonax virescens ) had high detection probabilities (∼90%) and species that call infrequently such as Pileated Woodpecker ( Dryocopus pileatus ) had low detection probability (36%). We also found detection probabilities varied with the time of day for some species (e.g. thrushes) and between observers for other species. We used the same approach to estimate detection probability and density for a subset of the observations with limited-radius point counts.

The Auk