Search USGSSearch

Geology topics

James S. Sedinger

Publications and source records attributed to James S. Sedinger.

46 records · Page 3Linked to original sources

Allocation of limited reserves to a clutch: A model explaining the lack of a relationship between clutch size and egg size

Lack (1967, 1968) proposed that clutch size in waterfowl is limited by the nutrients available to females when producing eggs. He suggested that if nutrients available for clutch formation are limited, then species producing small eggs would, on average, lay more eggs than species with large eggs. Rohwer (1988) argues that this model should also apply within species. Thus, the nutrition-limitation hypothesis predicts a tradeoff among females between clutch size and egg size (Rohwer 1988). Field studies of single species consistently have failed to detect a negative relationship between clutch size and egg size (Rohwer 1988, Lessells et al. 1992, Rohwer and Eisenhauer 1989, Flint and Sedinger 1992, Flint and Grand 1996). The absence of such a relationship within species has been regarded as evidence against the hypothesis that nutrient availability limits clutch size (Rohwer 1988, 1991, 1992; Rohwer and Eisenhauer 1989).

The Auk

Survival estimation and the effects of dependency among animals

Survival models assume that fates of individuals are independent, yet the robustness of this assumption has been poorly quantified. We examine how empirically derived estimates of the variance of survival rates are affected by dependency in survival probability among individuals. We used Monte Carlo simulations to generate known amounts of dependency among pairs of individuals and analyzed these data with Kaplan-Meier and Cormack-Jolly-Seber models. Dependency significantly increased these empirical variances as compared to theoretically derived estimates of variance from the same populations. Using resighting data from 168 pairs of black brant, we used a resampling procedure and program RELEASE to estimate empirical and mean theoretical variances. We estimated that the relationship between paired individuals caused the empirical variance of the survival rate to be 155% larger than the empirical variance for unpaired individuals. Monte Carlo simulations and use of this resampling strategy can provide investigators with information on how robust their data are to this common assumption of independent survival probabilities.

Journal of Applied Statistics

Variation in brood behavior of Black Brant

We studied behavior of broods of Black Brant ( Branta bernicla nigricans ) during five summers between 1987 and 1993, a period in which the local breeding population increased >3-fold. Goslings spent more time foraging than adults of either sex, while adult males spent more time alert and less time foraging than adult females. Percentage of time spent alert was positively correlated with brood size for adult males but not adult females. Foraging time for all age and sex classes increased with date following hatch within years. Foraging time increased and time spent alert decreased between 1987 and 1993 for both adult males and adult females. The trend in foraging behavior for adults is consistent with an hypothesis of declining food availability at higher brood densities and declining alert behavior by adults has implications for prefledging survival of young.

Alaska

Metabolizability and partitioning of energy and protein in green plants by yearling lesser snow geese

We measured apparent metabolizability of organic matter, gross energy, nitrogen and cell wall constituents of pelleted alfalfa by Lesser Snow Geese ( Chen caerulescens caerulescens . We also used simultaneous measurements of energy expenditure and apparent metabolizable energy intake to estimate heat increment of feeding and net energy for production and maintenance. Apparent metabolizability of energy was 46% as a result of substantial retention of dietary cellulose (45%). Mean slope of the relationship between energy expenditure and apparent metabolizable energy intake, which estimates heat increment at feeding, was 0.33. One minus the slope, 0.67, was our estimate of the proportion of apparent metabolizable energy available for maintenance and production. Resting metabolic rate at zero apparent metabolizable energy intake ranged from 361 kJ· kg -1 · day -1 to 432 kJ· kg -1 · da y-1 , while apparent metabolizable energy intake required for energy balance ranged from 455 kJ· kg -1 · day -1 to 871 kJ· kg -1 · day -1 . Lesser Snow Geese (>2 kg mass) were more efficient at retaining dietary energy but possibly lost more of this energy as heat than smaller Black Brant ( Branta bernicla nigricans )(∼1 kg mass), suggesting a possible relationship between body size and processing of energy in herbivorous birds.

Alaska, Northwest Territories

Environmental influence on life-history traits: Growth, survival, and fecundity in Black Brant ( Branta bernicla )

We studied relationships between body size of female Black Brant goslings ( Branta bernicla nigricans ) late in their growth period and first year survival, eventual adult body size, breeding propensity, and size and volume of clutches they eventually produced to examine the relationship between growth and fitness in this population. We indexed body size by calculating PC1 scores based on either culmen and tarsus, or culmen, tarsus, and mass. Gosling (PC scores based on culmen and tarsus) size was positively correlated with resighting rate (P = 0.005), indicating that larger goslings survived at a higher rate than did smaller goslings. Gosling size was correlated with adult size of the same individuals (P = 0.0004). Larger goslings were more likely to breed as 2- or 3-yr-olds than were medium or small goslings (P = 0.008). Larger adult brant laid more eggs (P = 0.03) and produced clutches with greater total volume (P = 0.03) than did smaller brant. Given the important role of foraging environment in growth of goslings, these data suggest an important role of early environment in determining life-history traits.

Alaska

Survival of juvenile black brant during brood rearing

Survival of young is an important and poorly understood component of waterfowl productivity. We estimated survival of black brant ( Branta bernicla nigricans ) goslings during summers 1987-89 on the Yukon-Kuskokwim Delta, Alaska, to determine timing and magnitude of gosling mortality and to compare methods of estimating gosling survival. Eighty-two percent of radio-tagged adult females (n = 61) fledged ≥1 gosling (brood success). We estimated survival of goslings within broods by 3 methods: (1) changes in mean brood size through time, (2) observation of goslings associated with marked adults, and (3) age ratios of brant captured in banding drives. Estimates of gosling survival within successful broods averaged 81% and ranged from 66 to 92%. Combining brood success and gosling survival within successful broods yielded estimates of overall gosling survival that averaged 68%, ranging from 79% in 1987 to 56% in 1989. Eighty-two percent of gosling mortality occurred in the first 15 days. Estimates of survival on the basis of age ratios of birds captured in banding drives are biased low. Our estimates of average gosling survival are higher than reported for other species of geese.

Alaska

Current status and recent dynamics of the Black Brant Branta bernicla breeding population

We summarize current knowledge about the distribution of Pacific Black Brant and recent dynamics of colonies, particularly on the Yukon-Kuskokwim (Y-K) Delta, Alaska. About 20,000 nests are required to produce the number of young in the autumn flight using estimates of clutch size, hatching success and gosling survival based on colonies on the Y-K Delta. More than 80% of the nests in the population can be accounted for currently on the Y-K Delta. Most moulting individuals that did not breed, or were unsuccessful, are unaccounted for in late summer. Numbers of Black Brant nesting in major colonies on the Y-K Delta declined >60% in the early 1980s, most likely as a result of local subsistence harvest combined with predation by arctic foxes. Effective management of this population requires a better understanding of the distribution of breeding and moulting birds, the importance of breeding habitat to colony dynamics and the role of both sport and subsistence harvest in population dynamics.

Wildfowl

Growth rate is negatively correlated with hatch date in Black Brant

Arctic geese nest in a highly seasonal environment in which ungrazed plants reach peak nitrogen concentrations when goslings hatch (Sedinger and Raveling 1986). Grazing by geese prolongs peak nutrient concentrations but reduces food availability. This should cause nutrient availability to decline seasonally. Here, we test the hypothesis that late-hatching goslings of Black Brant ( Branta bernicla nigricans ) grow more slowly than those hatching early. We substracted the sizes of wild goslings from those of captive-reared goslings of the same age and regressed the differences against hatch date. Differences between wild- and captive-reared goslings for body mass, tarsus length, and culmen length were significantly negatively related to hatch date; i.e., late-hatching wild goslings were smaller than those hatching early, after accounting for age. We detected no between-year difference in gosling size, but male goslings were larger than females of the same age for all measures. Egg size was only weakly associated with size of goslings 1 mo after hatching, but we detected no effect of other brood characteristics on growth. Seasonal variation in gosling growth rate may favor early nesting in arctic geese.

Alaska

Effects of visiting black brant nests on egg and nest survival

I used 2 methods to evaluate the effect of visiting black brant (Branta bernicla nigricans) nests on survival of whole nests and eggs in a single colony on the Yukon-Kuskokwim Delta, Alaska. The first technique regressed survival of nests or eggs during a time interval against interval length. Departure of the y-intercept from 1.0 estimated the short-term effect of the visit at the beginning of the interval. The y-intercepts (±95% CI) for whole nests and eggs during the egg laying period were 1.11 ± 0.31 and 1.06 ± 0.31, respectively. During incubation the same 2 parameters were 0.66 ± 0.31 and 0.66 ± 0.33. The regression method was, thus, imprecise and failed to discriminate among widely varying potential impacts of visitors. The second method involved visiting nests and then immediately revisiting them after pairs had returned to their territories. This method estimated loss of eggs as a result of displacement of territorial pairs during the first visit. Only 1 of 50 eggs was lost (n = 27 nests) as a result of visits during egg laying, whereas no eggs were lost (n = 225 eggs and 55 nests) owing to visits during the incubation period. I conclude that the regression approach is an imprecise tool for estimating visitor impact, but results from both methods indicate little effect of nest visitation under conditions existing on the colony I studied.

Alaska

Autumn staging of cackling Canada geese on the Alaska Peninsula

Cackling Canada Geese Branta canadensis minima undergo a long (2,800 km) migration between their autumn staging areas on the Alaska Peninsula and wintering areas in Oregon and California. Adults and young lost an average of 543 g during this migratory flight. Weight gains between fledging and autumn migration are essential for the successful completion of the flight. Autumn staging is important for the acquisition or maintenance of energy stores, particularly for young of the year, as evidenced by the intense feeding of this age class at Ugashik Bay. Factors associated with the arrival and departure of Cackling Geese at Ugashik Bay are presently unknown.

Alaska