Habitat Conditions Associated With Lynx Hunting Behavior During Winter in Northern Washington

Abstract Effectively managing habitat for threatened populations of Canada lynx (Lynx canadensis) requires knowledge of habitat conditions that provide for the ecological needs of lynx. We snow-tracked lynx to identify habitat conditions associated with hunting behavior and predation during winters of 2002–2003 and 2003–2004 in the northern Cascade Range in Washington state, USA. We recorded number and success of predation attempts, prey species killed, and trail sinuosity on 149 km of lynx trails. Lynx killed snowshoe hares (Lepus americanus), red squirrels (Tamiasciurus hudsonicus), and cricetids more than expected in Englemann spruce (Picea engelmannii) and subalpine fir (Abies lasiocarpa) forests, where snowshoe hare densities were highest. Lynx killed prey less than expected in Douglas-fir (Pseudotsuga menziesii) and ponderosa pine (Pinus ponderosa) forests and forest openings. We used the sinuosity of lynx trails as an index of quality of habitat hunted. Lynx trails that included predation attempts were more sinuous than trail segments without predation attempts. Lynx trails had greater sinuosity in forest stands with high hare densities dominated by Engelmann spruce and subalpine fir than in stands with low hare densities dominated by Douglas-fir and ponderosa pine or in forest openings. We encourage forest managers to maintain or create sufficient understory cover to support high densities of snowshoe hares as foraging habitat for lynx.     

Stomatal responses to humidity and temperature in darkness

Stomatal responses to leaf temperature (T_l) and to the mole fractions of water vapour in the ambient air (w_a) and the leaf intercellular air spaces (w_i) were determined in darkness to remove the potential effects of changes in photosynthesis and intercellular CO₂ concentration. Both the steady‐state and kinetic responses of stomatal conductance (g_s) to w_a in darkness were found to be indistinguishable from those in the light. g_s showed a steep response to the difference (Δw) between w_a and w_i when w_a was varied. The response was much less steep when w_i was varied. Although stomatal apertures responded steeply to T_l when Δw was held constant at 17 mmol mol^?1, the response was much less steep when Δw was held constant at about zero. Similar results were obtained in the light for Δw = 15 mmol mol^?1 and Δw ≈ 0 mmol mol^?1. These results are discussed in the context of mechanisms for the stomatal response to humidity.     

WHAT CAN HISTORY DO FOR BIOETHICS?

This article details the relationship between history and bioethics. I argue that historians' reluctance to engage with bioethics rests on a misreading of the field as solely reducible to applied ethics, and overlooks previous enthusiasm for historical perspectives. I claim that seeing bioethics as its practitioners see it – as an interdisciplinary meeting ground – should encourage historians to collaborate in greater numbers. I conclude by outlining how bioethics might benefit from new histories of the field, and how historians can lend a fresh perspective to bioethical debates.     

Ultrastructure and Vacuolar Movements in the Free-Living Diplomonad Trepomonas agilis Klebs*

SYNOPSIS. The structure of Trepomonas agilis communis Klebs is described from light and electron microscope observations on 2 clone isolates of the organism. The surface membrane shows marked differentiation into an extremely thick (16 nm) symmetric membrane which covers the greater part of the body, and a thinner (∼ 10–12 nm) asymmetric membrane which lines the 2 lateral oral grooves and the posterior channel connecting them; a similar asymmetric membrane covers the flagella. Thorium dioxide staining suggests a denser distribution of acidic carbohydrate groups on the asymmetric membrane. The pathways of cytoplasmic streaming observed in the living flagellate coincide with those of microtubule bands arising close to the flagellar basal bodies and it is suggested that the bands play an orienting role in the streaming of food vacuoles. The contractile vacuole undergoes diastole in the anterior (postnuclear) cytoplasm, and is formed by coalescence of smaller vesicles. At systole the entire vacuole migrates to the posterior extremity to discharge into the posterior channel; the route of exit lacks guiding structural elements. Features of the flagellate's physiology and organization are discussed in relation to the observed lack of mitochondria, microbodies and Golgi apparatus in diplomonads.     

Scale and uncertainty in modeled soil organic carbon stock changes for US croplands using a process‐based model

Process‐based model analyses are often used to estimate changes in soil organic carbon (SOC), particularly at regional to continental scales. However, uncertainties are rarely evaluated, and so it is difficult to determine how much confidence can be placed in the results. Our objective was to quantify uncertainties across multiple scales in a process‐based model analysis, and provide 95% confidence intervals for the estimates. Specifically, we used the Century ecosystem model to estimate changes in SOC stocks for US croplands during the 1990s, addressing uncertainties in model inputs, structure and scaling of results from point locations to regions and the entire country. Overall, SOC stocks increased in US croplands by 14.6 Tg C yr^?1 from 1990 to 1995 and 17.5 Tg C yr^?1 during 1995 to 2000, and uncertainties were ±22% and ±16% for the two time periods, respectively. Uncertainties were inversely related to spatial scale, with median uncertainties at the regional scale estimated at ±118% and ±114% during the early and latter part of 1990s, and even higher at the site scale with estimates at ±739% and ±674% for the time periods, respectively. This relationship appeared to be driven by the amount of the SOC stock change; changes in stocks that exceeded 200 Gg C yr^?1 represented a threshold where uncertainties were always lower than ±100%. Consequently, the amount of uncertainty in estimates derived from process‐based models will partly depend on the level of SOC accumulation or loss. In general, the majority of uncertainty was associated with model structure in this application, and so attaining higher levels of precision in the estimates will largely depend on improving the model algorithms and parameterization, as well as increasing the number of measurement sites used to evaluate the structural uncertainty.