Titration of Photophosphorylation, Oxidative Phosphorylation and Glycolysis in Scenedesmus with Desaspidin: Regulation between Pathways and Sites for Photophosphorylation

Narrow concentration intervals were used, covering 10^?6– 10^?4M desaspidin. The interaction with glycolysis involves three steps, the inhibitor constants (K_i:s) being in turn 2.7 × 10^?5M, 1.3 × 10^?4M, and high. About 18% of total glycolysis is inhibited in each of the two first steps, and 65% left for the third reaction. After compensation for glycolysis, oxidative phosphorylation may show a sudden jump to about 10% inhibition at 1.5 × 10^?5M desaspidin, the possible K_i of the reaction starting here being very high. Correcting for glycolysis, desaspidin affects total Photophosphorylation in two steps, with the K_i values of 7.8 × 10^?5M and 4.6 × 10^?4M respectively. Inhibition in the first step is about 27% of the total photophosphorylation. By applying 10^?6M DCMU[/3-(3, 4-dichlorophenyl)-l, l-dimethy lurea], one can abolish non-cyclic photophosphorylation. Desaspidin then reacts in a single step with a K_i of 1.4 × 10^?4M. At 5 × 10^?5M DCMU, also the pseudocyclic photophosphorylation is abolished. The remaining, true cyclic photophosphorylation has a single K_i of 2.3 × 10^?5M for desaspidin. Under non-cyclic conditions, the true cyclic process contributes about 25% to total Photophosphorylation. Under pseudocyclic conditions, no cyclic photophosphorylation occurs. Under true cyclic conditions, the non-cyclic and pseudocyclic processes are inoperative. This indicates a regulative system, so that either (1) the (non-cyclic + true cyclic), (2) only the pseudocyclic, or (3) only the true cyclic systems can be traced, dependent on the level of DCMU applied. There are two sites for non-cyclic Photophosphorylation, one of them common to the pseudocyclic pathway. Cyclic photophosphorylation has a third site, different from the other two.     

Immune function, parasitization and extended phenotypes in colour polymorphic pygmy grasshoppers

Ecological and evolutionary consequences of host–parasite interactions have attracted considerable attention from evolutionary biologists. Previous studies have suggested that immune responsiveness may be genetically or developmentally linked with colour pattern, such that the evolution of animal colour patterns may be influenced by correlated responses to selection for parasite resistance. We studied interactions between the endoparasitic fly Leiophora innoxia (Meigen) (Diptera: Tachinidae) and its colour polymorphic pygmy grasshopper host Tetrix undulata (Sow.) (Orthoptera: Tetrigidae) to test for morph‐specific differences in parasitization and immune defence, and host‐induced variation in parasite phenotypes. Our results revealed that c. 2 and 30% of adult grasshoppers collected from the same natural population in two subsequent years, respectively were parasitized. Parasite prevalence was independent of host sex and colour morph. Pupae were larger if the parasite had developed in a female than in a male host, possibly reflecting host resource value or a physical constraint on larval growth imposed by host body size. Pupal size was also associated with host colour morph, with individuals that had developed in dark morphs being smaller at pupation compared to those that developed in paler morphs. However, immune defence, measured as the encapsulation response to a novel antigen, did not differ among individuals belonging to alternative colour morphs or sexes. Darker morphs warm up more quickly and prefer higher body temperatures than paler ones. Encapsulation was not influenced by maintenance temperature (15 vs. 30 °C), however, suggesting that indirect effects of coloration on parasite resistance mediated via differential body temperature are unlikely. The dependence of parasite body size on host colour morph may thus reflect plasticity of growth and development of the larvae in response to differential host body temperature, rather than variable host immune defence. © 2005 The Linnean Society of London, Biological Journal of the Linnean Society, 2005, 85 , 373–383.     

Contemporary carbon accumulation in a boreal oligotrophic minerogenic mire – a significant sink after accounting for all C-fluxes

Based on theories of mire development and responses to a changing climate, the current role of mires as a net carbon sink has been questioned. A rigorous evaluation of the current net C-exchange in mires requires measurements of all relevant fluxes. Estimates of annual total carbon budgets in mires are still very limited. Here, we present a full carbon budget over 2 years for a boreal minerogenic oligotrophic mire in northern Sweden (64°11′N, 19°33′E). Data on the following fluxes were collected: land–atmosphere CO₂ exchange (continuous Eddy covariance measurements) and CH₄ exchange (static chambers during the snow free period); TOC (total organic carbon) in precipitation; loss of TOC, dissolved inorganic carbon (DIC) and CH₄ through stream water runoff (continuous discharge measurements and regular C-concentration measurements). The mire constituted a net sink of 27±3.4 (±SD) g C m⁻² yr⁻¹ during 2004 and 20±3.4 g C m⁻² yr⁻¹ during 2005. This could be partitioned into an annual surface–atmosphere CO₂ net uptake of 55±1.9 g C m⁻² yr⁻¹ during 2004 and 48±1.6 g C m⁻² yr⁻¹ during 2005. The annual NEE was further separated into a net uptake season, with an uptake of 92 g C m⁻² yr⁻¹ during 2004 and 86 g C m⁻² yr⁻¹ during 2005, and a net loss season with a loss of 37 g C m⁻² yr⁻¹ during 2004 and 38 g C m⁻² yr⁻¹ during 2005. Of the annual net CO₂-C uptake, 37% and 31% was lost through runoff (with runoff TOC>DIC≫CH₄) and 16% and 29% through methane emission during 2004 and 2005, respectively. This mire is still a significant C-sink, with carbon accumulation rates comparable to the long-term Holocene C-accumulation, and higher than the C-accumulation during the late Holocene in the region.     

New gastropods from East Pacific hydrothermal vents

The following new prosobranch species are described: Cyuthermia (gen.n.) naticoides, Lucunoidc (gen.n.) exquisitus (Neomphalidae); Peltospira Iamellifera, Pachydermia (gen.n.) laevis, Depressigyra (gen. n.) g1obulus. D. plunispira, Solutigyra (gen. n.) reticulata, Lirapex (gen. n.) humata, L. granularis (Peltospiridae); Bathymargarites (gen.n.) symplector (Trochidae) and Provanna mucleani (Littorinoidea). Shells and soft parts of the species are described and figured. One species each of Sinezona (Scissurellidae), Moel1rriopsis (Seguenzoidea) and Phymorrhynchus (Turridae) is recorded from East Pacific hydrothermal vents, but not identified to species. Information about feeding biology and type of larval development is given for most of these species. The systematic position of the new species of Neomphalidae and Peltospiridae is considered uncertain, but further anatomical investigations are in progress. The gastropod fauna of East Pacific sulphide-rich environments is summarized and composition, endemism, age. dispersal, predation, adaptations and feeding biology are discussed.     

Using Fecal Glucocorticoids to Assess Stress Levels in Captive River Otters

Abstract Reintroduction projects often expose animals to a series of acute stressors that may cause chronic stress and lead to the stress response. The stress response results in the release of glucocorticoids that, when excessive, can cause detrimental effects to the animal. Glucocorticoids can be extracted from feces and quantified as an effective method for assessing stress levels. We collected scats from 10 river otters (Lontra canadensis; 3 from MD and 7 from NY, USA) held captive for the Pennsylvania River Otter Reintroduction Project (PRORP). We used these scats to verify the use of the Correlate-EIA^TM Corticosterone Enzyme Immunoassay Kit (Assay Designs, Inc., Ann Arbor, MI) to evaluate stress levels in otters. We also determined trends in stress levels during the initial 10–12 days otters were in PRORP captivity, and compared glucocorticoid levels for 5 of the New York otters the morning before, the morning of, and the morning after veterinary examinations to determine if associated procedures (e.g., physical and chemical restraint) caused increased stress levels. Glucocorticoid concentrations declined from time 1 to time 2 for the 3 otters from Maryland (an average decline of about 6-fold) and for 5 of 7 otters from New York. Among otters evaluated for stress associated with veterinary examinations, average glucocorticoid concentrations were increased the morning of and the morning after veterinary examinations from the day before the veterinary examinations. We demonstrated that fecal glucocorticoids are an effective method for assessing stress levels in otters and that PRORP's captive management program did not contribute to increasing stress during the 10–12-day evaluation period. Fecal glucocorticoid assays could be used to evaluate stress levels of zoo or permanently captive otters, determine the most effective husbandry techniques for housing otters, and evaluate effects of both management practices and environmental conditions in the wild and in captivity.     

Net primary production and light use efficiency in a mixed coniferous forest in Sweden

Simple light use efficiency (ɛ) models of net primary production (NPP) have recently been given great attention (NPP = ɛ × absorbed photosynthetically active radiation). The underlying relationships have, however, not been much studied on a time step less than a month. In this study daily NPP was estimated as the sum of net ecosystem exchange (NEE) and heterotrophic respiration (R_h) of a mixed pine and spruce forest in Sweden. NEE was measured by eddy correlation technique and R_h was estimated from measurements of forest floor respiration (R_f) and the root share of R_f. The total yearly NPP was on average 810 g C m⁻² year⁻¹ for 3 years and yearly ɛ was between 0.58 and 0.71 g C MJ⁻¹, which is high in comparison with other studies. There was a seasonal trend in ɛ with a relatively constant level of approximately 0.90 g C MJ⁻¹ from April to September Daily NPP did not increase for daily intercepted radiation above 6 MJ m⁻² d⁻¹, indicating that between-years variation in NPP is not directly dependent on total Q_i. The light was most efficiently used at an average daytime temperature of around 15 °C. At daytime vapour pressure deficit above 1400 Pa ɛ was reduced by approximately 50%.     

Toward better scientific presentation

Day, Robert A. 1979: How to Write and Publish a Scientific-Paper. 160 pp. ISI Press, Philadelphia. ISBN 0 894950088 (cloth), ISBN 0894950061 (paperback). Price USD 15.00 and 8.95, respectively.
Cremmins, Edward T. 1982: The Art of Abstracting. 145 pp. ISI Press, Philadelphia. ISBN 0894950150. Price USD 13.95 (paperback).
Barnes, Gregory A. 1982: Communication Skills for the Foreign-Born Professional. ISI Press, Philadelphia. ISBN 0894950134 (cloth). ISBN 0894950142 (paperback). Price USD 18.95 and 13.95, respectively.