Influence of Woody Debris on Channel Structure in Old Growth and Managed Forest Streams in Central Sweden

Anecdotal information suggests that woody debris have had an important channel-forming role in Swedish streams and rivers, but there are few data to support this view. We identified 10 streams within near-natural and 10 streams within managed forest landscapes in central Sweden, and quantified their channel characteristics and content of woody debris. All pieces of woody debris greater than 0.5 m in length and greater than 0.05 m in base diameter were included. The near-natural forests were situated in reserves protected from forest cutting, whereas the managed forests had previously faced intensive logging in the area adjacent to the stream. The two sets of streams did not differ in general abiotic characteristics such as width, slope, or boulder cover, but the number of wood pieces was twice as high and the wood volume almost four times as high in the near-natural streams. This difference resulted in a higher frequency of debris dams in the near-natural streams. Although the total pool area did not differ between the two sets of streams, the wood-formed pools were larger and deeper, and potentially ecologically more important than other pools. In contrast to what has been believed so far, woody debris can be a channel-forming agent also in steeper streams with boulder beds. In a stepwise multiple regression analysis, pool area was positively and most strongly related to the quantity of woody debris, whereas channel gradient and wood volume were negatively related. The frequency of debris dams increased with the number of pieces of woody debris, but was not affected by other variables. The management implications of this study are that the wood quantity in streams in managed forests would need to be increased if management of streams will target more pristine conditions.     

PERIVITELLINE pH OF SALMONIDE EGGS IN RELATION TO AMBIENT pH1

ABSTRACT: Eggs from salmon and brown trout were reared at 6 pH levels in the pH range 4.1–7.5. By micropuncture, the pH of the perivitelline fluid (PVF) was measured at different stages of development with an antimony microelectrode system. The pH of the PVF falls with decreased pH of the ambient media, although no point of equilibrium was found at the lower pH levels. When eggs were reared at pH levels 4.1–4.7, the pH of the PVF in salmon eggs was 0.4 units above the ambient media, while that in trout eggs was 1.0 pH units above. Decreased pH of the PVF during the later, actively ion accumulation, embryonic stages will subject the embryos to ion regulating stresses similar to those registered for adult fishes.     

Polycyclic aromatic hydrocarbons (PAH) in different forest humus types

The behavior of 20 PAH in the organic layers of a L mull, an Of mull and a mor was assessed by a combined approach of a soil profile study, and the analysis of particle-size separates. Increasing PAH concentrations with depth in the mor profile (L, 866 μg kg⁻³; Of, 2902 μg kg⁻¹; Oh, 10489 ug kg⁻¹) were assigned to selective enrichment during organic matter decomposition. PAH were further highly enriched within the finer separates. For the L horizons, significant positive correlations were established between the enrichment of individual PAH (as observed from the decomposition gradient between the >2-mm fraction and the < 0.05-mm fraction), and the K_OW for each compound. The slope of the regression line, m, described the degree of differentiation between low- and high-molecular PAH during litter decomposition. Since m was greatest in the most biologically active humus type (L mull, 0.33) and smallest in the most inactive (mor, 0.20), microbial breakdown was assumed as the dominating process for this differentiation. The results also indicated that decomposition processes had already taken place in the L horizons, leading to morphological and chemical changes of organic matter, and to an enrichment of high molecular PAH.     

Amphimixis and the individual in evolving populations: does Weismann’s Doctrine apply to all,most or a few organisms?

The German biologist August Weismann (1834–1914) proposed that amphimixis (sexual reproduction) creates variability for natural selection to act upon, and hence he became one of the founders of the Neo-Darwinian theory of biological evolution. He is perhaps best known for what is called “Weismann’s Doctrine” or “Weismann’s Barrier” (i.e. the irreversible separation of somatic and germ cell functionalities early during ontogeny in multicellular organisms). This concept provided an unassailable argument against “soft inheritance” sensu Lamarck and informed subsequent theorists that the only “individual” in the context of evolution is the mature, reproductive organism. Herein, we review representative model organisms whose embryology conforms to Weismann’s Doctrine (e.g. flies and mammals) and those that do not (e.g. freshwater hydroids and plants) based on this survey and the Five Kingdoms of Life scheme; we point out that most species (notably bacteria, fungi, protists and plants) are “non-Weismannian” in ways that make a canonical definition of the “individual” problematic if not impossible. We also review critical life history functional traits that allow us to create a matrix of all theoretically conceivable life cycles (for eukaryotic algae, embryophytes, fungi and animals), which permits us to establish where this scheme Weismann’s Doctrine holds true and where it does not. In addition, we argue that bacteria, the dominant organisms of the biosphere, exist in super-cellular biofilms but rarely as single (planktonic) microbes. Our analysis attempts to show that competition among genomic variants in cell lineages played a critical part in the evolution of multicellularity and life cycle diversity. This feature was largely ignored during the formulation of the synthetic theory of biological evolution and its subsequent elaborations.     

Sharing developed countries’ post-2012 greenhouse gas emission reductions based on comparable efforts

The Bali Action Plan as adopted under the United Nations Framework Convention on Climate Change (UNFCCC) in 2007, states that Annex I (developed) countries should reduce their greenhouse gas emissions, based on comparable efforts. Within this context, we have explored various comparable effort approaches (for example, equal marginal abatement costs for all countries) for reducing emissions by the year 2020 for individual countries and regions. In all calculations, the total reduction for Annex I countries as a group is assumed to be 30% below 1990 levels. In the analysis, we compare the reduction targets as calculated from the different approaches with the emission reductions as pledged by these countries as part of the Copenhagen Accord, as drafted under the UNFCCC in 2009. Our analysis indicates that the different elements in these calculations may cause a diversity in outcomes and that, therefore, individual countries may favour certain elements over others. These elements include (a) the choice of the approach itself (the same approach may produce very different outcomes for countries with diverging national circumstances, such as Canada and Russia); (b) the reference year (such as 1990 or 2006 emissions, is very important for countries with an increase in emissions since 1990 (e.g. the United States, Canada) or for those that have lower emission levels (e.g. Russia, the Ukraine)); and (c) rules on land use (these are important for countries with large forest areas). It should be noted that the stringency of the individual countries’ reductions as pledged, differs substantially from the stringency of the reduction targets calculated from the effort-sharing approaches. The current pledges by both the European Union and the United States, are lower than the reductions that would be obtained in the effort-sharing approaches for a 30% overall reduction in Annex I countries.