2003
DOI: 10.1111/j.0006-341x.2003.00091.x
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Demographic Analysis from Summaries of an Age‐Structured Population

Abstract: Demographic analyses of age-structured populations typically rely on life history data for individuals, or when individual animals are not identified, on information about the numbers of individuals in each age class through time. While it is usually difficult to determine the age class of a randomly encountered individual, it is often the case that the individual can be readily and reliably assigned to one of a set of age classes. For example, it is often possible to distinguish first-year from older birds. I… Show more

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Cited by 38 publications
(28 citation statements)
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“…Although it is theoretically possible to obtain parameter estimates with only one survey replicate per time period, our simulations suggest that these values could be imprecise even for relatively large sampling efforts. As such, we caution against the use of a single sampling event unless prior information on detection probabilities is available (Link et al 2003). We presented the median parameter values of 100 simulated data sets for several levels of data collection intensity.…”
Section: Discussionmentioning
confidence: 99%
“…Although it is theoretically possible to obtain parameter estimates with only one survey replicate per time period, our simulations suggest that these values could be imprecise even for relatively large sampling efforts. As such, we caution against the use of a single sampling event unless prior information on detection probabilities is available (Link et al 2003). We presented the median parameter values of 100 simulated data sets for several levels of data collection intensity.…”
Section: Discussionmentioning
confidence: 99%
“…Through May of 2008, there were relatively few breeders in the population, but with continued data collection, closer analysis of breeding state transitions may reveal important patterns. First, it may be that breeding behavior is a more important indicator of population success than survival, as survival in the EMP has been fairly good to date (based on comparisons with survival in the AWBP; Link et al 2003) while breeding has not been very successful (only 1 individual fledged from 24 nests through May of 2008); thus reproduction appears to be the limiting factor in establishment of the EMP. In addition, given that our measure of genotype quality was dam productivity, there is a stronger argument for an expectation of correlation between a dam's productivity in captivity and her offspring's productivity in the wild (an analysis that will be possible in the near future), rather than with her offspring's survival in the wild.…”
Section: S570mentioning
confidence: 99%
“…Thus, estimated rates for that population (Link et al 2003) were applied to simulated WF birds. We applied the estimated overall survival rate from their work (0.91; model CAAE) to all age and breeding classes of WF birds in place of survival rates estimated from CR females (0.66-0.82 for unpaired birds, 0.79-0.94 for birds in breeding classes).…”
Section: Alternatives To the Baseline Modelmentioning
confidence: 99%
“…We applied the estimated overall survival rate from their work (0.91; model CAAE) to all age and breeding classes of WF birds in place of survival rates estimated from CR females (0.66-0.82 for unpaired birds, 0.79-0.94 for birds in breeding classes). Link et al (2003) also provided information on year-to-year variability in survival rate as well as estimation uncertainty; therefore, the survival rate applied to WF birds varied from year to year and among simulation runs (to account for estimation uncertainty). For productivity, we assumed that CR and WF birds shared a common rate of transition into the breeder classes (i.e., probability that an unpaired female forms her first pair bond).…”
Section: Alternatives To the Baseline Modelmentioning
confidence: 99%
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