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<br />STATUS OF ENDANGERED COLORADO SQUAWFISH <br /> <br />959 <br /> <br />population abundance. Because comprehensive lit- <br />erature exists on CJS models, data analysis based <br />on these models, and analysis strategy including <br />model selection (e.g., Buckland 1980; Pollock <br />1982; Burnham et al. 1987; Pollock et al. 1990; <br />Burnham and Anderson 1992; Lebreton et al. <br />1992; Anderson et al. 1994; Burnham et al. 1995), <br />only minimal information is provided here. <br />The analysis strategy was to use the program <br />RELEASE (Burnham et al. 1987) to compute the <br />goodness of fit of the general time-specific CJS <br />model for the capture data. With an acceptable fit, <br />program SURGE (Lebreton et al. 1992) was used <br />to find the best model out of a set of models con- <br />sidered. Akaike's Information Criterion (AIC) was <br />used for model selection (Akaike 1973; Burnham <br />and Anderson 1992; Lebreton et al. 1992; Ander- <br />son et al. 1994; Burnham et al. 1995). The AIC is <br />a relative measure of how appropriate a model is <br />for a given set of data, with the "best" model <br />having the smallest AIC (AICmin). The difference <br />in AIC value between a given model and the best <br />model is defined as ~AIC. Models within about <br />~AIC = 2 of the best model were considered plau- <br />sible alternative models for the data. <br />The CJS model is based on two types of param- <br />eters: survival rate (<I>) and capture probability (p), <br />the probability of an individual being caught (see <br />Lebreton et al. 1992), which may vary by capture <br />occasion and time interval between occasions. A <br />circumflex n over a parameter indicates it is es- <br />timated (e.g., fJ). Models considered were the fully <br />time-specific CJS model and simpler models based <br />on a mixture of features: constant per-unit time <br />survival rates, year-specific survival rates, season- <br />specific survival rates, and capture rates that could <br />be year- or season-specific or constant, or that <br />could show a linear trend on either occasion or <br />year. Models with full time variation parameters <br />were denoted by { <1>" p,} and with no time variation <br />by {<I>, p}. Intermediate models included {<I>" p} <br />and {<I>, p,}. The notation Pyeor was used to denote <br />different capture rates between years with constant <br />capture rates for the three within-year capture oc- <br />casions. Survival rates differing in the intervals <br />between sampling (three intervals for the upper <br />reach) were denoted by <l>seasons. Models with sim- <br />ilar survival rates in short intervals (t = 3 weeks <br />or roughly 0.06 year) between spring samples but <br />different rates in the time interval over the rest of <br />the year (t = roughly 0.88 year in the upper reach) <br />were denoted <l>short; long' A model was also con- <br />sidered where no mortality was assumed during <br /> <br />the short time intervals, and the survival parameter <br />was denoted <l>short ~ I: long' <br />The CIS models were also used to ascertain ev- <br />idence of time trends in capture rates, which would <br />affect the interpretation of time trends in abun- <br />dance. These analyses were based on fitting CJS <br />models with capture probabilities (pJ having a lin- <br />ear trend over time. Denoted PT, these models used <br />logit (pJ = loge [pJ(1 - pJ] (see e.g., Burnham <br />et al. 1996; Franklin et al. 1996). A plausible al- <br />ternative model sets capture probabilities equal <br />within a year, but with a trend over the four years <br />(denoted py). By using Yi as a year code, the year- <br />specific time trend on capture probabilities was of <br />the form logit (Pi) = a + b. Yi. <br />Survival rates in capture-recapture models are <br />apparent survival probabilities, and <I> = S(F)(1 - <br />L), where F (fidelity) is the probability that a fish <br />returns to (or stays in) the river reach being sam- <br />pled and L is the probability of tag loss. Because <br />PIT tag loss or failure is minimal (Burdick and <br />Hamman 1993), L is likely to be close to zero. <br />Thus, if F is near 1, then <I> is an estimator of <br />physical survival rate (S), and 1 - S is the total <br />mortality rate. <br />Abundance and recruitment estimation.-Data <br />were too sparse to get useful occasion-specific es- <br />timates of population size based on open-model <br />methods (such as with program JOLLY; Pollock <br />et al. 1990). However, by grouping sampling pe- <br />riods into sets of three passes within a year, the <br />design corresponded closely enough to the robust <br />design (Pollock 1982) that closed-model capture- <br />recapture methods could be used to estimate pop- <br />ulation abundance each sample year. This analysis <br />assumes population closure over a time period of <br />about 6 weeks. The simplest model (the null mod- <br />el) of program CAPTURE (White et al. 1982) was <br />used to get an abundance estimate (N) by year. <br />This model assumes the same P applies at each <br />capture occasion within year, but p can vary by <br />year since the estimates were done separately. The <br />choice of this model was partly based on analyses <br />with SURGE that supported constant within-year <br />p, partly motivated by the sparseness of the data, <br />and supported by the model selection algorithm in <br />CAPTURE that suggested the use of this simplest <br />model for each year. <br />A modified open population analysis method <br />(program RECAP; Buckland et al. 1980) was used <br />as a consistency check for average population <br />abundance over the four years, for average annual <br />survival rate, and to obtain some information about <br />average annual recruitment rate (B) into the sam- <br />