Abundance trends of American martens in Michigan based on statistical population reconstruction

Estimating the dynamics of furbearer populations is challenging because their elusive behavior and low densities make observations difficult. Statistical population reconstruction is a flexible approach to demographic assessment for harvested populations, but the technique has not been applied to furbearers. We extended this approach to furbearers and analyzed 8 yr of age-at-harvest data for American marten (Martes americana) in the Upper Peninsula of Michigan. Marten abundance estimates showed a general downward trend from an estimate of = 1,733.3 animals in 2000 to = 1,163.9 in 2007. The harvest probability of martens increased nearly 5-fold from 0.0542 in 2000 to 0.2637 in 2007, which corresponded to a 5-fold increase in trap-nights. Continued monitoring of martens in the Upper Peninsula, Michigan, and a reassessment of current harvest regulations are necessary given the estimated decreases. Moreover, we do not encourage the use of harvest indices as the sole technique to assess the status and trends of marten and fisher populations. Auxiliary studies in the Upper Peninsula, Michigan, will allow for continued use and improvement in the application of these models. © 2011 The Wildlife Society.     

Occupancy and abundance of wintering birds in a dynamic agricultural landscape

Assessing wildlife management action requires monitoring populations, and abundance often is the parameter monitored. Recent methodological advances have enabled estimation of mean abundance within a habitat using presence–absence or count data obtained via repeated visits to a sample of sites. These methods assume populations are closed and intuitively assume habitats within sites change little during a field season. However, many habitats are highly variable over short periods. We developed a variation of existing occupancy and abundance models that allows for extreme spatio-temporal differences in habitat, and resulting changes in wildlife abundance, among sites and among visits to a site within a field season. We conducted our study in sugarcane habitat within the Everglades Agricultural Area southeast of Lake Okeechobee in south Florida. We counted wintering birds, primarily passerines, within 245 sites usually 5 times at each site during December 2006–March 2007. We estimated occupancy and mean abundance of birds in 6 vegetation states during the sugarcane harvest and allowed these parameters to vary temporally or spatially within a vegetation state. Occupancy and mean abundance of the common yellowthroat (Geothlypis trichas) was affected by structure of sugarcane and uncultivated edge vegetation (occupancy = 1.00 [ = 0.96–1.00] and mean abundance = 7.9 [ = 3.2–19.5] in tall sugarcane with tall edge vegetation versus 0.20 [ = 0.04–0.71] and 0.22 [ = 0.04–1.2], respectively, in short sugarcane with short edge vegetation in one half of the study area). Occupancy and mean abundance of palm warblers (Dendroica palmarum) were constant (occupancy = 1.00, = 0.69–1.00; mean abundance = 18, = 1–270). Our model may enable wildlife managers to assess rigorously effects of future edge habitat management on avian distribution and abundance within agricultural landscapes during winter or the breeding season. The model may also help wildlife managers make similar management decisions involving other dynamic habitats such as wetlands, prairies, and even forested areas if forest management or fires occur during the field season. © 2011 The Wildlife Society.     

Estimation and correction of seed recovery bias from moist-soil cores

Scientists estimate seed abundances to calculate seasonal carrying capacities and assess wetland management actions for waterfowl and other wildlife using soil core samples. We evaluated recovery of known quantities of moist-soil seeds from whole and subsampled experimental core samples containing 12 seed taxa representing small, medium, and large size classes. We recovered 86.3% (SE = 1.8) of all seeds added to experimental cores; 8.3% (SE = 1.2) of seeds were destroyed during the sieving process and 5.4% (SE = 1.2) were not recovered by observers. Recovery rates varied by seed size, but not seed quantity or disproportionate ratios of seed-size classes. Overall seed recovery rates were similar between subsampled ( = 81.2%, SE = 3.6) and whole–processed core samples ( = 86.3%, SE = 1.8). We used recovery rates to generate size-specific, taxon-specific, and constant correction factors and applied each to actual core sample data. Size-specific correction factors increased seed mass estimates in the Mississippi Alluvial Valley ( = 10.1%, SE = 0.32), upper Midwest ( = 21.2%, SE = 0.61), and both regions combined ( = 15.7%, SE = 0.51) differently, as seed composition in core samples varied regionally. We suggest scientists consider using size-specific correction factors to account for seed recovery bias in core samples because these factors may be applied to a variety of taxa and produced similar mass estimates as taxon-specific correction factors. However, if data from core samples are unavailable at the resolution of seed size classes, we suggest increasing seed mass estimates by 16% to account for seed recovery bias. © 2011 The Wildlife Society.     

Construction of Prediction Intervals in Location-Scale Families

Let x₁ ≤x₂ ≤x₃ … ≤x_r be the r smallest observations out of n observations from a location-scale family with density $ \frac{1}{\sigma}f\left({\frac{{x - \mu}}{\sigma}} \right) $ where μ and σ are the location and the scale parameters respectively. The goal is to construct a prediction interval of the form $ \left({\hat \mu + k_1 \hat \sigma,\,\hat \mu + k_2 \hat \sigma} \right) $ for a location-scale invariant function, T(Y) = T(Y₁, …, Y_m), of m future observations from the same distribution. Given any invariant estimators $ \hat \mu $ and $ \hat \sigma $, we have developed a general procedure for how to compute the values of k₁ and k₂. The two attractive features of the procedure are that it does not require any distributional knowledge of the joint distribution of the estimators beyond their first two raw moments and $ \hat \mu $ and $ \hat \sigma $ can be any invariant estimators of μ and σ. Examples with real data have been given and extensive simulation study showing the performance of the procedure is also offered.     

Variation in demographic patterns and population structure of raccoons across an urban landscape

Raccoons (Procyon lotor) are considered synanthropic, with high densities reported from urban landscapes. However, little information is available on population density and demography within the urban matrix. To better understand how urban land-use patterns influence raccoon density and demographic patterns, we sampled raccoons at multiple, replicated sites across an urban landscape. Density differed by land-use type (F_2,17 = 4.66, P = 0.027): urbanized sites, = 4.96 ± 2.64 raccoons/km², range = 1.25–10.00 raccoons/km²; urban open sites, = 14.84 ± 6.35 raccoons/km², range = 3.00–29.25 raccoons/km²; rural open sites, = 15.50 ± 4.66 raccoons/km², range = 13.00–20.25. Although we found no clear patterns in sex ratio, reproductive condition, or body condition, we observed differences in age structure among urban open, rural open, and urbanized sites. The most striking difference was the absence of older animals at urbanized sites and relatively low numbers of young individuals at urban open sites. Raccoons were the dominant mesocarnivore in open fragments, but less so in the urban matrix. Spatial variation in density across urban landscapes is likely influenced by site level differences in abundance of anthropogenic resources and differences in habitat quality. Furthermore, the association between changes in land-use and population age structure may have reflected different mortality sources across the landscape. Our results illustrate that wildlife species considered synanthropic may have complex relationships with urban landscapes. © 2012 The Wildlife Society.     

Hibernal thermal ecology of eastern box turtles within a managed forest landscape

Box turtles are being extirpated from much of their former range and remaining populations often live in association with anthropogenically altered habitats. This is particularly evident at the northern distributional limit of eastern box turtles (Terrapene carolina carolina) and is an important factor to consider during the winter months when their ability to respond to microclimatic change is limited. Using temperature dataloggers, we studied the hibernal microclimate of box turtles and associated habitat following timber harvests. We monitored the body temperatures of 38 eastern box turtles and collected detailed air and soil profile temperatures of 12 box turtle hibernacula, 6 clearcuts, and 6 adjacent forested areas during the hibernal season (winter 2009–2010). We partitioned the hibernal season into 2 biologically significant thermal periods: hibernation and emergence. The mean hibernation body temperature averaged (3.28° C, SE = 0.09) and corresponded to an average depth of 10 cm. Clearcuts were consistently colder ( = 1.91° C) than forests ( = 2.68° C) and hibernacula ( = 2.77° C) during hibernation, but became the warmest areas during emergence ( = 9.96° C). We found that in the average clearcut, turtles could burrow to approximately 20 cm to attain the average hibernation body temperature or to approximately 15 cm to attain a body temperature no different than those overwintering on colder, northeast-facing slopes in the forest ( = 2.83° C). Alternatively, we found that southwest-facing slopes were warmer and if turtles chose to overwinter only in clearcuts on those slopes, they could remain shallower. All but 1 turtle overwintered in forested areas; however, our study suggests that some timber harvested areas offer various microhabitats exploitable by hibernating box turtles based on soil profile temperatures, slope aspect, and depth of hibernation. © 2012 The Wildlife Society.     

Disease,population viability,and recovery of endangered Sierra Nevada bighorn sheep

Sierra Nevada bighorn sheep (Ovis canadensis sierrae) experienced a severe population decline after European settlement from which they have never recovered; this subspecies was listed as endangered under the United States Endangered Species Act (ESA) in 1999. Recovery of a listed species is accomplished via federally mandated recovery plans with specific population goals. Our main objective was to evaluate the potential impact of disease on the probability of meeting specific population size and persistence goals, as outlined in the Sierra Nevada bighorn sheep recovery plan. We also sought to heuristically evaluate the efficacy of management strategies aimed at reducing disease risk to or impact on modeled bighorn populations. To do this, we constructed a stochastic population projection model incorporating disease dynamics for 3 populations (Langley, Mono, Wheeler) based on data collected from 1980 to 2007. We modeled the dynamics of female bighorns in 4 age classes (lamb, yearling, adult, senescent) under 2 disease scenarios: 5% lower survival across the latter 3 age classes and persistent 65% lower lamb survival (i.e., mild) or 65% reduced survival across all age classes followed by persistent 65% lower lamb survival (i.e., severe). We simulated management strategies designed to mitigate disease risk: reducing the probability of a disease outbreak (to represent a strategy like domestic sheep grazing management) and reducing mortality rate (to represent a strategy that improved survival in the face of introduced disease). Results from our projection model indicated that management strategies need to be population specific. The population with the highest growth rate ( ; Langley; = 1.13) was more robust to the effects of disease. By contrast, the population with the lowest growth rate (Mono; = 1.00) would require management intervention beyond disease management alone, and the population with a moderate growth rate (Wheeler; = 1.07) would require management sufficient to prevent severe disease outbreaks. Because severe outbreaks increased adult mortality, disease can directly reduce the probability of meeting recovery plan goals. Although mild disease outbreaks had minimal direct effects on the populations, they reduced recruitment and the number of individuals available for translocation to other populations, which can indirectly reduce the probability of meeting overall, range-wide minimum population size goals. Based on simulation results, we recommend reducing the probability of outbreak by continuing efforts to manage high-risk (i.e., spatially close) allotments through restricted grazing regimes and stray management to ensure recovery for Wheeler and Mono. Managing bighorn and domestic sheep for geographic separation until Sierra Nevada bighorn sheep achieve recovery objectives would enhance the likelihood of population recovery. © 2011 The Wildlife Society.     

Survival of white-tailed deer fawns in the grasslands of the northern Great Plains

Environmental factors, such as forest characteristics, have been linked to fawn survival in eastern and southern white-tailed deer (Odocoileus virginianus) populations. In the Great Plains, less is known about how intrinsic and habitat factors influence fawn survival. During 2007–2009, we captured and radiocollared 81 fawns in north-central South Dakota and recorded 23 mortalities, of which 18 died before 1 September. Predation accounted for 52.2% of mortality; remaining mortality included human (hunting, vehicle, and farm accident; 26.1%) and hypothermia (21.7%). Coyotes (Canis latrans) accounted for 83.3% of predation on fawns. We used known-fate analysis in Program MARK to estimate summer (15 May–31 Aug) survival rates and investigated the influence of intrinsic and habitat variables on survival. We developed 2 a priori model sets, including intrinsic variables and a test of annual variation in survival (model set 1) and habitat variables (model set 2). Model set 1 indicated that summer survival varied among years (2007–2009); annual survival rates were 0.94 (SE = 0.06, n = 22), 0.78 (SE = 0.09, n = 27), and 0.54 (SE = 0.10, n = 32), respectively. Model set 2 indicated that survival was further influenced by patch density of cover habitats (Conservation Reserve Program [CRP]-grasslands, forested cover, and wetlands). Mean CRP-grassland and wetland patch density (no. patches/100 ha) were greater (P < 0.001) in home-range areas of surviving fawns ( = 1.81, SE = 0.10, n = 63; = 1.75, SE = 0.14, n = 63, respectively) than in home-range areas of fawns that died ( = 0.16, SE = 0.04, n = 18; = 1.28, SE = 0.10, n = 18, respectively). Mean forested cover patch density was less (P < 0.001) in home-range areas of surviving fawns ( = 0.77, SE = 0.10, n = 63) than in home-range areas of fawns that died ( = 1.49, SE = 0.21, n = 18). Our results indicate that management activities should focus on CRP-grassland and wetland habitats in order to maintain or improve fawn survival in the northern Great Plains, rather than forested cover composed primarily of tree plantings and shelterbelts. © 2012 The Wildlife Society.     

Equi-replicated balanced block designs generated by a balanced matrix

In this paper it is shown that if N= \documentclass{article}\pagestyle{empty}\begin{document}$ \mathop \sum \limits_{i = 1}^{S_h} $\end{document} c_ihN_ih, where c_ih are some non-negative integer numbers and N_ih are such incidence matrices that A_h = \documentclass{article}\pagestyle{empty}\begin{document}$ \mathop \sum \limits_{i = 1}^{S_h} $\end{document} i N_ih is a balanced matrix defined by SHAH (1959), for h = 1, 2,…, p, then a block design with an incidence matrix Ñ = [N, N,…,N] is an equi-replicated balanced block design. Here the balance of a block design is defined in terms of the matrix M₀ introduced by CALI?SKI (1971).     

The role of predator removal,density-dependence,and environmental factors on mallard duckling survival in North Dakota

Duckling survival is an important component of mallard (Anas platyrhynchos) recruitment and population growth, yet many factors regulating duckling survival are poorly understood. We investigated factors affecting mallard duckling survival in the drift prairie of northeastern North Dakota, 2006–2007. Mammalian meso-predators were removed by trapping on 4 92.3 km² study sites and another 4 study sites served as controls. We monitored 169 broods using telemetry and periodic resighting, and we modeled cumulative survival to 30 days of age using the nest survival module in Program MARK. Duckling survival was not affected by predator removal ( , 85% CI: 0.182–0.234; , 85% CI: 0.155–0.211) and was only weakly negatively correlated with duckling density. Duckling survival was higher in 2007 ( , 85% CI: 0.193–0.355) than 2006 ( , 85% CI: 0.084–0.252) and increased with total seasonal and semipermanent wetland area and declined with perennial cover in the surrounding landscape. Broods that hatched earlier in the season (especially in 2006) and ducklings that were heavier at hatch also had higher survival. Our estimates of duckling survival are among the lowest reported for mallards and contradict previous research in Saskatchewan that found predator removal increased duckling survival. However, our results are consistent with other studies suggesting that earlier hatch date, increased wetland availability, and better duckling condition lead to increased survival. Management actions that increase wetland density, improve nest success early in the season, and potentially target brood-specific predators such as mink (Neovison vison) would likely lead to higher duckling survival. © 2011 The Wildlife Society.     

Bayesian Bootstrap Clones for Censored Markov Chains

In this article, we consider r observations from a non‐homogeneous censored Markov chain, with transition probability matrix P. For the product estimator of P proposed by Aalen and Johansen (1978) and Phelan (1988), we investigate the behavior of Bayesian bootstrap clones to approximate the sampling distribution of , and then construct approximate confidence interval. It is shown that the approximation based on the random‐weighted distribution is first‐order consistent. The performance of the Bayesian bootstrap clones (BBC) is also discussed by small sample simulation. Finally, we illustrate the BBC procedure in the application to the WHO malaria survey data (cf. Singer and Cohen 1970).     

Optical anisotropy of polypeptide chains

Optical anisotropies γ² of N-t-butylacetamide (tBA), N-Methylacetamide (MA), and N, N-dimethylacetamide (DMA) have been determined from the Rayleigh ratios for depolarzed scattering by dilute solutions of the amides in p-dioxane. Traceless optical polarizability tensors \documentclass{article}\pagestyle{empty}\begin{document}$ \widehat{\rm \alpha } $\end{document} for the amides are derived from these results in conjunction with the Kerr constant for tBA determined by LeGèvre and co-workers. It is shown that the tensor \documentclass{article}\pagestyle{empty}\begin{document}$ \widehat{\rm \alpha } $\end{document}_i for the glycyle unit in a polypeptide chain may be identified with \documentclass{article}\pagestyle{empty}\begin{document}$ \widehat{\rm \alpha } $\end{document}MA . Methods for deriving corresponding tensors for other peptide units are indicated and the traceless polarizability tensor \documentclass{article}\pagestyle{empty}\begin{document}$ \widehat{\rm \alpha } $\end{document} for a polypeptide chain in any specified configuration is formulated.     

Polarized fluorescence in an electric field. A model calculation with application to the geometry of the 2-hydroxy-4,4′-diamidinostilbene–DNA complex

Theoretical expressions are derived for the change in the polarized components of the fluorescence, resulting from the orientation of a rigid molecule bearing a chromophore with arbitrary angles for the absorption and transition moments \documentclass{article}\pagestyle{empty}\begin{document}$ \vec \mu _a $\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$ \vec \mu _e $\end{document} with respect to the molecular axis. The break in the symmetry relation H_V = V_H is related to the tilt angle between \documentclass{article}\pagestyle{empty}\begin{document}$ \vec \mu _a $\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$ \vec \mu _e $\end{document}. The theory is applied to a sonicated DNA–2-hydroxy-4,4′-diamidinostilbene complex, in the blue and red emission bands of this peculiar dye. Simultaneous measurements of linear dichroism and fluorescence lead to the determination of an angle of 47° between a fluorescent bound dye and the DNA axis, with no difference for the blue- and red-emitting species, but confirm the presence of nonfluorescent bound dye in a more perpendicular arrangement.     

A population genetic study of the Banks and Torres Islands (Vanuatu) and of the Santa Cruz Islands and polynesian outliers (Solomon Islands)

As part of a multidisciplinary survey of populations in the Banks and Torres Islands of Vanuatu and the Southern and Central Districts of the Solomon Islands, nearly 2,400 persons have been tested for ABO blood groups and a number of serum protein and red cell enzyme genetic marker systems. For the ABO system, the populations are characterized in general by high gene O and low gene B frequencies except in two of the Polynesian Outlier Islands, Rennell and Bellona, which have high frequencies of B. Among the serum proteins, several alleles have distributions indicating significant movement of people between islands. These include Albumin ^{New Guinea} and the transferrin alleles Tf, and Tf, and Tf. Similar specific alleles for red cell enzymes also show distributions reflecting interisland population movement as well as contact with persons from outside the southern Pacific region. Examples are ACP in the acid phosphatase system, PGM and PGM, PGM and PGM, PGK⁴ and also HbJ^Tongariki. The data available for 11 polymorphic systems were used to generate genetic distances. Of the four Polynesian Outlier Islands, Anuta is most remote genetically, with Rennell and Bellona also relatively isolated. The fourth Polynesian Outlier, Tikopia, occupies a position genetically close to the Melanesian populations of the Banks and Torres Islands and the southern Solomons. The history of early European contact and voyaging in the Pacific, as well as archaeological and linguistic evidence and local legends, indicate that significant movements of people occurred between islands and provided opportunities for genes to be introduced from Europeans, Africans, and Asians. The genetic marker studies give evidence for genes from all these sources, though at a low level. Despite this admixture, the Polynesian Outlier and Melanesian populations have preserved their own distinctive genetic patterns.     

Variation in spring harvest rates of male wild turkeys in New York,Ohio, and Pennsylvania

Spring harvest rates of male wild turkeys (Meleagris gallapavo) influence the number and proportion of adult males in the population and turkey population models have treated harvest as additive to other sources of mortality. Therefore, hunting regulations and their effect on spring harvest rates have direct implications for hunter satisfaction. We used tag recovery models to estimate survival rates, investigate spatial, temporal, and demographic variability in harvest rates, and assess how harvest rates may be related to management strategies and landscape characteristics. We banded 3,266 male wild turkeys throughout New York, Ohio, and Pennsylvania during 2006–2009. We found little evidence that harvest rates varied by year or management zone. The proportion of the landscape that was forested within 6.5 km of the capture location was negatively related to harvest rates; however, even though the proportion forested ranged from 0.008 to 0.96 across our study area, this corresponded to differences in harvest rates of only 2–5%. Annual survival was approximately twice as high for juveniles as adults . In turn, spring harvest rates for adult turkeys were greater for adults than juveniles . We estimated the population of male turkeys in New York and Pennsylvania ranged from 104,000 to 132,000 in all years and ranged from 63,000 to 75,000 in Ohio. Because of greater harvest rates for adult males, the proportion of adult males in the population was less than in the harvest and ranged from 0.40 to 0.81 among all states and years. The high harvest rates observed for adults may be offset by greater recruitment of juveniles into the adult age class the following year such that these states can sustain high harvest rates yet still maintain a relative high proportion of adult males in the harvest and population. © 2011 The Wildlife Society.     

The effects of predator removal on mallard production and population change in northeastern North Dakota

In 1994, Delta Waterfowl Foundation began trapping mammalian meso-predators in North Dakota during the breeding season in an attempt to increase waterfowl nest success and enhance recruitment into the fall flight and subsequent breeding population. Multiple studies on these sites demonstrated that removing predators results in near doubling of nest success, which previous simulation modeling suggests is the most influential vital rate influencing the population growth rate of mid-continent mallards (Anas platyrhynchos). We present an assessment of the impact of predator removal on mallard production using population models. We conducted this study on 9 township-sized (93.2 km²) sites (4–8 sites annually per vital rate) in northeastern North Dakota from 2006–2008. Trappers removed mammalian meso-predators on 5 sites and the other 4 served as unmanaged reference sites. To estimate recruitment, we used derived estimates and process variance of pair numbers, hen success (nest survival corrected for renesting), initial brood size, pre-fledging survival, and post-fledging survival, along with previously published estimates of breeding propensity and adult female survival rates. Trapped sites had greater hen success (H = 0.69, = 0.03) than reference sites (H = 0.53, = 0.06), but similar indicated breeding pairs, initial brood size, and pre-fledging survival. We estimated that females on trapped sites added 140 more mallards of both sexes to the fall flight than females on reference sites, at an approximate cost of $74.29 per incremental mallard. Additionally, trapping predators provided a marginal increase (0.04) in finite population growth. We found that predator removal targeted at mammalian nest predators did not produce as many incremental mallards as previously thought and may not be a viable strategy for increasing mallard productivity under conditions similar to those observed during this study. We conducted a sensitivity analysis and determined that pre-fledging survival was the most influential factor regulating mallard population growth. Although hen success increased as a result of trapping, duckling survival became a limiting factor. We suggest that waterfowl managers assess multiple vital rates to determine the likelihood that management actions focused on a single parameter, such as nest success, will yield desired population level effects. © 2012 The Wildlife Society.     

Einfluß extracellulärer Kaliuminoenkonzentrationen auf die celluläre Natriumionenkonzentration von Lodderomyces elongisporus D

It was found that the cellular Na⁺-concentration (C) of Lodderomyces elongisporus D is depended on the extracellular K⁺-concentration (C). The relationship can be described by an equation in the form The function of the natrium ion seem to be to support the utilisation rate of potassium ion at lower extracellular K⁺-concentration.     

Nest site fidelity and dispersal of Rio Grande wild turkey hens in Texas

Rio Grande wild turkey (Meleagris gallopavo intermedia) nests suffer high predation rates exceeding 65%, which may limit recruitment. We evaluated post-nesting movements of reproductively active female Rio Grande wild turkeys. We monitored 194 nesting attempts between 2005 and 2010 and documented 17% and 32% overall apparent nest success for the Edwards Plateau and Central Rio Grande Plains study regions, respectively. Rio Grande wild turkey hens move approximately 1.2 km (SD = 0.7) between nesting attempts within a nesting season and approximately 1.4 km (SD = 1.6) between initial nesting attempts among years. Rio Grande wild turkey hens selected open areas with moderate woody cover for nesting ( = 37.7%; range = 3.0–88.2%). Patchiness of vegetation in the nesting landscape also was borne out by typically low edge-to-area ratios ( = 0.20; range = 0.040–0.732). We found no clear pattern in movement distance and either landscape composition or edge-to-area ratio for within or between breeding season nest site selection for either the Edwards Plateau or Central Rio Grande Plains study region. Based on our results, movement distances post-nest failure do not seem to influence habitat selection. © 2012 The Wildlife Society.     

Effects of temperature on microbial ethanol production. II. A thermodynamic interpretation of the temperature profile curve of ethanol production

An attempt is made to give a thermodynamic interpretation of the complete temperature profile curve of ethanol formation. Taking into consideration an enhancing competition between thermal activation and thermal deactivation of ethanol formation at increasing temperatures and supposing that the ethanol production is affected by a reversible and an irreversible term of thermal deactivation of a modified ARRHENIUS equation being current for the total biokinetic sphere may be derived: . The quantities ΔH and ΔH^D_2T are identical with the temperature functions of the change of entropy caused by reversible and irreversible deactivation of ethanol formation, respectively. Accordingly for the yeast strain Saccharomyces cerevisiae Sc 5 the calculated entropy coefficients of reversible and irreversible thermal deactivation of ethanol formation amount to C = (0.245± 0.013) kJ/mol · deg.² and C = (1.657 ± 0.046) kJ/mol · deg.².     

Relationship between wildfire,salvage logging,and occupancy of nesting territories by northern spotted owls

The northern spotted owl (Strix occidentalis caurina) is one of the most intensively studied raptors in the world; however, little is known about the impacts of wildfire on the subspecies and how they use recently burned areas. Three large-scale wildfires in southwest Oregon provided an opportunity to investigate the short-term impacts of wildfire and salvage logging on site occupancy of spotted owls. We used Program MARK to develop single-species, multiple-season models of site occupancy using data collected during demographic surveys of spotted owl territories. In our first analysis, we compared occupancy dynamics of spotted owl nesting territories before (1992–2002) and after the Timbered Rock burn (2003–2006) to a reference area in the south Cascade Mountains that was not affected recently by wildfire. We found that the South Cascades had greater colonization probabilities than Timbered Rock before and after wildfire ( , 95% CI = 0.60–2.03), and colonization probabilities declined over time at both areas ( , 95% CI = −0.12 to 0.00). Extinction probabilities were greater at South Cascades than at Timbered Rock prior to the burn ( , 95% CI = 0.23–2.62); however, Timbered Rock had greater extinction probabilities following wildfire ( , 95% CI = 0.29–2.62). The Timbered Rock and South Cascades study areas had similar patterns in site occupancy prior to the Timbered Rock burn (1992–2001). Furthermore, Timbered Rock had a 64% reduction in site occupancy following wildfire (2003–2006) in contrast to a 25% reduction in site occupancy at South Cascades during the same time period. This suggested that the combined effects of habitat disturbances due to wildfire and subsequent salvage logging on private lands negatively affected site occupancy by spotted owls. In our second analysis, we investigated the relationship between wildfire, salvage logging, and occupancy of spotted owl territories at the Biscuit, Quartz, and Timbered Rock burns from 2003 to 2006. Extinction probabilities increased as the combined area of early seral forests, high severity burn, and salvage logging increased within the core nesting areas ( , 95% CI = 0.10–3.66). We were unable to identify any relationships between initial occupancy or colonization probabilities and the habitat covariates that we considered in our analysis where the β coefficient did not overlap zero. We concluded that site occupancy of spotted owl nesting territories declined in the short-term following wildfire, and habitat modification and loss due to past timber harvest, high severity fire, and salvage logging jointly contributed to declines in site occupancy. © 2013 The Wildlife Society.