Relationships among personal,indoor and outdoor NO2 measurements

Using integrating NO₂ diffusion dosimeters, personal, indoor and outdoor exposures were measured for nine families in Topeka, Kansas. NO₂ exposures in homes that used gas for cooking were clearly different from those in homes that used electricity. The gas-cooking homes had indoor levels three times the outdoor levels. Members of the gas-cooking households had levels twice those of electric-cooking families and twice the outdoor levels. A linear model that includes outdoor concentrations and stove types explains 77% of the variance in observed NO₂ exposure. The differential NO₂ exposures in homes with and without gas stoves should be considered in epidemiologic studies of the health effects of air pollution.     

Effective Population Size in Red-Cockaded Woodpeckers: Population and Model Differences

Loss of genetic variability in isolated populations is an important issue for conservation biology. Most studies involve only a single population of a given species and a single method of estimating rate of loss. Here we present analyses for three different Red-cockaded Woodpecker ( Picoides borealis ) populations from different geographic regions. We compare two different models for estimating the expected rate of loss of genetic variability, and test their sensitivity to model parameters. We found that the simpler model (Reed et al. 1988) consistently estimated a greater rate of loss of genetic variability from a population than did the Emigh and Pollak (1979) model. The ratio of effective population size (which describes the expected rate of loss of genetic variability) to breeder population size varied widely among Red-cockaded Woodpecker populations due to geographic variation in demography. For this species, estimates of effective size were extremely sensitive to survival parameters, but not to the probability of breeding or reproductive success. Sensitivity was sufficient that error in estimating survival rates in the field could easily mask true population differences in effective size. Our results indicate that accurate and precise demographic data are prerequisites to determining effective population size for this species using genetic models, and that a single estimate of rate of loss of genetic variability is not valid across populations.     

Method for determination of turgor pressure in macroalgae,with particular reference to the Phaeophyta

A procedure is described for the determination of the internal osmotic pressure and turgor pressure of marine macroalgae, for use in the laboratory and on the shore. A volume-related parameter (either thallus fresh weight, or area) is measured before and after transfer of plant material to a range of hyperosmotic solutions. Plotting the final fresh weight/area as a percentage of the initial value gives a biphasic curve, with an initial component of negative slope due to the change in thallus volume in less extreme hyperosmotic solutions, where the non-rigid thallus contracts in response to decreasing cell turgor pressure. The second component has a shallower slope and represents plasmolysis in more extreme hyperosmotic solutions, i.e., where turgor pressure is reduced to zero and the protoplast shrinks away from the cell wall; the extraprotoplast space created by plasmolysis will be filled with the external solution and thus no further changes in weight occur. These two components intersect at the lowest osmotic pressure at which cell turgor is zero. By correcting for any effects of the cell wall on thallus volume, the relationship can be used to calculate internal osmotic pressure and hence turgor pressure, assuming that the remaining change in thallus volume of the initial component is due entirely to variation in the intraprotoplast volume (approximately equivalent to the intraprotoplast water content, determined by subtraction of the extraprotoplast water and dry weight from the thallus fresh weight). Using this procedure, the turgor pressures of Fucus spiralis L., Ectocarpus siliculosus, (Dillw.) Lyngb. and Laminaria digitata (Huds.) Lamour. (from Fife Ness, Scotland, May–August 1987) in a seawater-based medium were 0.82, 0.58 and 1.34 Osmol kg^–1, respectively. The turgor pressure of F. spiralis on the shore at Fife Ness (June 1987) was 0.74 Osmol kg^–1.     

Simulation of interactions between migrating whales and potential oil spills

A numerical model system was developed to quantify the probability of endangered bowhead and gray whales encountering spilled oil in Alaskan waters. Migration and diving-surfacing models for bowhead and gray whales, and an oil spill trajectory model comprise the system. The migration models were developed from conceptual considerations, then calibrated with and tested against observations. The distribution of whales is represented in space and time by discrete points, each of which may represent one or more whales. The movement of a whale point is governed by a random walk algorithm which stochastically follows a migratory pathway. Stochastic diving-surfacing models are used to stimulate surfacing behavior sequences for each species. The oil spill model accounts for oil transport and spreading in open water and in the presence of sea ice. Historical wind records and ice cover data sets provide the environmental conditions to generate stochastic oil spill scenarios. The oil spill, whale migration and diving-surfacing models are linked to provide quantitative estimates of whale-oil interactions. The model system was applied to the Alaskan Beaufort Sea to investigate the probability that bowhead whales would encounter oil spilled in this region.     

Behavioral strategies of American kestrels during mate replacement

Summary To determine the influence of mate replacement on the behavior and reproductive success of wild American kestrels (Falco sparverius) we removed 4 female and 16 male members of breeding pairs during incubation in 1983 and 1984. Eight males and 1 female were replaced within a mean time of 43 h. Widowed females that received a replacement spent less time hunting, but incubated and performed aerial displays more frequently than females that did not receive a replacement. After replacement, widowed females continued to incubate the original clutch, yet copulated and performed other courtship behaviors with the incoming male. Overlapping of normal temporally separate behavioral cues may be a female strategy to gain assistance from a replacement mate. However, none of the original clutches was successfully hatched. Of 8 pairs with replacement males, 2 pairs abandoned their territory, two remained on territory but did not renest, and 4 renested within a mean interval of 18 days. The lone female replacement and her mate copulated and performed nest inspections but then abandoned the territory. Incubation behavior was similar between replacement and control pairs; however, replacement males fed more invertebrate prey to nestling and made many more nest visits. All 3 replacement nests that hatched young failed within 8 days.     

Optimal escapement levels in stochastic and deterministic harvesting models

A constant-escapement feedback policy is shown to be optimal in maximizing expected discounted net revenue from an animal resource whose dynamics are described by a stochastic stock-recruitment model, provided that unit harvesting costs satisfy certain conditions. The optimal escapement in this model is compared with that in the corresponding deterministic model and it is shown how the way in which unit harvesting costs vary with population abundance can be important in determining the relative sizes of the optimal escapements. In most cases, the optimal stochastic escapement is no less than the optimal deterministic escapement.