Comparative Space Use and Habitat Selection of Moose Around Feeding Stations

ABSTRACT The practice of feeding cervids in winter, either as a supplement to enhance nutritional status or to divert animals away from roads, railways, or vulnerable habitats, is rising noticeably. Moose (Alces alces) densities in Scandinavia are currently at historically high levels, resulting in amplified damage to economically important young Scots pine (Pinus sylvestris) forest stands. Nevertheless, there is limited information as to how diversionary feeding affects herbivore space use and habitat selection. We followed 32 female moose marked with Global Positioning System collars to evaluate 1) if feeding stations serve as attraction points to the extent that habitat-selection patterns resemble those of central-place foragers (i.e., high usage and more uniform selection close to the attraction point), and 2) if moose using feeding sites select young pine stands less than those not using feeding sites. Moose that used diversionary forage concentrated their space use around feeding stations and selected habitats as predicted for a central-place forager with a decreasing probability of using areas away from feeding sites and a low degree of habitat selectivity close to feeding sites. However, moose that used feeding sites continued to select young pine stands to the same extent as moose that did not use feeding sites. Feeding sites were, therefore, not successful in diverting moose away from valuable natural browse, so we recommend wildlife managers establish feeding sites in sacrifice areas where moose browsing is permissible and, if possible, >1 km from young pine plantations.     

Survival of Tetrahymena thermophila at Low Initial Cell Densities. Effects of Lipids and Long-Chain Alcohols

ABSTRACT. Cells of the ciliate Tetrahymena thermophila failed to establish cultures in lipid-free standard synthetic nutrient medium if the initial population density was 250 cells per ml or less. These cells died within 10 h, but were saved and formed dense cultures if their medium was supplemented with 10 μg per ml of either certain phospholipids, 1,2-di-, 1-monoglycerides, fatty acids, long-chain alcohols, or sterols. Cell multiplication was followed in cultures in which the standard synthetic medium was supplemented with a selection of the compounds listed above. It was observed that the cells in the supplemented cultures in their exponential phases of growth had about the same average doubling times as control cells starting multiplication at 10-fold higher initial cell densities in lipid-free medium. These cells have been grown for decades in lipid-free synthetic nutrient media at short (ca. two-three h) doubling times. Therefore lipids have been considered nutritionally non-essential for growth and multiplication of these cells. We propose that those compounds that rescue the cells at low cell densities act as "proliferation signals," sensu lato . This effect of lipids and long-chain alcohols has so far remained unnoticed.     

Phytogenic biosynthesis and emission of methyl acetate

Acetylation of plant metabolites fundamentally changes their volatility, solubility and activity as semiochemicals. Here we present a new technique termed dynamic ¹³C‐pulse chasing to track the fate of C_1–3 carbon atoms of pyruvate into the biosynthesis and emission of methyl acetate (MA) and CO₂. ¹³C‐labelling of MA and CO₂ branch emissions respond within minutes to changes in ¹³C‐positionally labelled pyruvate solutions fed through the transpiration stream. Strong ¹³C‐labelling of MA emissions occurred only under pyruvate‐2‐¹³C and pyruvate‐2,3‐¹³C feeding, but not pyruvate‐1‐¹³C feeding. In contrast, strong ¹³CO₂ emissions were only observed under pyruvate‐1‐¹³C feeding. These results demonstrate that MA (and other volatile and non‐volatile metabolites) derive from the C_2,3 atoms of pyruvate while the C₁ atom undergoes decarboxylation. The latter is a non‐mitochondrial source of CO₂ in the light generally not considered in studies of CO₂ sources and sinks. Within a tropical rainforest mesocosm, we also observed atmospheric concentrations of MA up to 0.6 ppbv that tracked light and temperature conditions. Moreover, signals partially attributed to MA were observed in ambient air within and above a tropical rainforest in the Amazon. Our study highlights the potential importance of acetyl coenzyme A (CoA) biosynthesis as a source of acetate esters and CO₂ to the atmosphere.     

Constitutive Secretion of Acid Hydrolases in Tetrahymena thermophila

THE role of lysosomal enzymes in intracellular digestion is now well established [11]. Most often we think of lysosomal hydrolases in catabolism of endogenous or foreign material taken up by endocytosis. There is however, a number of reports dealing with the release of acid hydrolases into the extracellular fluid in a variety of eukaryote cells. These cells range from Saccharomyces cerevisiae [15], Dictyostelium discoideum [10], Leishmania donovani [20], Acanthamoeba castellani [22], Entamoeba histolytica [12, 31], and species of Tetrahymena [1–3, 6] to mammalian cells in culture [49]. Concerning the latter, fibroblasts and hepatocytes in culture release acid hydrolases to the extracellular medium, but only if the synthesis of a specific recognition marker is impaired in the cells. This marker (man-nose-6-phosphate) is used for receptor mediated segregation of lysosomal enzymes into the lysosomal compartments. If the receptor or the marker are lacking, the hydrolases fail to enter the lysosomal compartment, and are secreted in immature form together with molecules belonging to the constitutive secretory pathway of the cells [8, 49]. Such a release of acid hydrolases seems to occur spontaneously from mammalian osteoclasts [4]. Macrophages, on the other hand, need a specific stimulation for their release process [40]. In lower eukaryotes the release may     

Effects of Azide on Photophosphorylation in Isolated Spinach Chloroplasts

The influence of sodium azide on open-chain and flavine mononucleotide mediated cyclic photophosphorylation in isolated spinach chloroplasts was investigated under anaerobic conditions. Open chain phosphorylation was completely inhibited with DCMU both in the presence and absence of sodium azide in the experimental medium. Flavine mononucleotide mediated photophosphorylation was only slightly inhibited by DCMU in the absence of sodium azide but inhibited in two steps by increasing amounts of DCMU when sodium azide was present in the medium. The first step can be explained as being mainly an effect of DCMU on an open chain electron transport, with water and H₂O₂ as electron donors and with flavine mononucleotide — kept in an oxidized state by sodium azide — as the electron acceptor. The second step, as well as the comparatively insensitivity to DCMU in the absence of sodium azide, depends on cyclic photophosphorylation mediated by flavine mononucleotide.