275 research outputs found

    Visions of a more precise soil biology

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    Includes bibliographical references (pages 389-390).Soils have often been viewed as a black box. Soil biology is difficult to study with the precision we would wish, due to the presence of considerable soil heterogeneity, a huge diversity of organisms, and a plethora of interacting processes taking place in a complex physical-chemical environment. We have isolated a tiny fraction of the known organisms, and the possible interactions of soil parent materials, landscape, land use, depth and time with the biota mean that we are to some extent still fumbling in the dark. There have been great advances, but we argue that the pace of advance could be faster. To progress, science needs new theory and concepts but also acceptable methodologies. Coherent and generally accepted theoretical knowledge exists in many areas, but there is a shortage of valid and exact methods to test new and sometimes even old hypotheses. New methods add knowledge, but they also can add to the confusion if they are not tied to the existing knowledge base. We speculate on how to improve soil biology through improving the way we perform and interpret research. Can we deal with soil variability? Can we measure the critical variables with adequate precision to test our hypotheses? Can we avoid reinventing the wheel? Can we find a balance between the freedom to test new and maybe even controversial ideas and the control and direction of research required by society?

    Biochar addition persistently increased soil fertility and yields in maizesoybean rotations over 10 years in sub-humid regions of Kenya

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    Open Access ArticleApplication of biochar has been shown to increase soil fertility and enable soil carbon sequestration, indicating potential for agricultural and environmental benefits from using locally produced biochar on African smallholder farms. However, previous studies have been rather short-term and little is known about the longer-term effects of biochar application on crop yields. Biochar contains ash, but the potential liming effect and nutrient release from ash may be short-lasting. To investigate long-term effects, we set up a series of field trials replicated at three sites in Kenya in 2006. The trials are still on-going and are possibly the longest biochar trials in sub-Saharan Africa. Here, we report effects on crop yield and soil properties over 10 years after applying biochar, produced mainly from Acacia spp., at a rate of 50 + 50 Mg ha−1 during the first two seasons. Maize (Zea mays) and soybean (Glycine max) were grown in rotation, with or without inorganic fertiliser, and crop yield was monitored. For comparison of soil properties, additional plots were kept in bare fallow. Biochar addition slightly increased soil porosity, pH, plant-available phosphorus and soil water-holding capacity. Crop yield responded positively to biochar at all sites and yield responses were similar with and without mineral fertiliser, i.e., the effects of biochar and mineral fertiliser were additive. The seasonal yield increase due to biochar application was in average around 1.2 Mg ha−1 for maize and 0.4 Mg for soybean, independently of fertilisation, over seasons and sites. Application of mineral fertiliser to maize increased maize yield by 1.6 Mg ha−1 and the subsequent, unfertilized soybean yield by 0.6 Mg ha−1, illustrating a carry-over effect. Most importantly, the effect on maize and soybean yield of adding biochar to soil persisted over the whole 10-year period. Analysis of the carbon (C) balance in topsoil indicated that about 40% of biochar C was apparently lost through mineralization, erosion or vertical translocation. Moreover, changes in soil carbon/nitrogen ratios indicated that biochar application increased nitrogen mineralization from native soil organic matter

    On the Potts model partition function in an external field

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    We study the partition function of Potts model in an external (magnetic) field, and its connections with the zero-field Potts model partition function. Using a deletion-contraction formulation for the partition function Z for this model, we show that it can be expanded in terms of the zero-field partition function. We also show that Z can be written as a sum over the spanning trees, and the spanning forests, of a graph G. Our results extend to Z the well-known spanning tree expansion for the zero-field partition function that arises though its connections with the Tutte polynomial

    The Role of Bile in the Regulation of Exocrine Pancreatic Secretion

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    As early as 1926 Mellanby (1) was able to show that introduction of bile into the duodenum of anesthetized cats produces a copious flow of pancreatic juice. In conscious dogs, Ivy & Lueth (2) reported, bile is only a weak stimulant of pancreatic secretion. Diversion of bile from the duodenum, however, did not influence pancreatic volume secretion stimulated by a meal (3,4). Moreover, Thomas & Crider (5) observed that bile not only failed to stimulate the secretion of pancreatic juice but also abolished the pancreatic response to intraduodenally administered peptone or soap

    Selection for Heterozygosity Gives Hope to a Wild Population of Inbred Wolves

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    Recent analyses have questioned the usefulness of heterozygosity estimates as measures of the inbreeding coefficient (f), a finding that may have dramatic consequences for the management of endangered populations. We confirm that f and heterozygosity is poorly correlated in a wild and highly inbred wolf population. Yet, our data show that for each level of f, it was the most heterozygous wolves that established themselves as breeders, a selection process that seems to have decelerated the loss of heterozygosity in the population despite a steady increase of f. The markers contributing to the positive relationship between heterozygosity and breeding success were found to be located on different chromosomes, but there was a substantial amount of linkage disequilibrium in the population, indicating that the markers are reflecting heterozygosity over relatively wide genomic regions. Following our results we recommend that management programs of endangered populations include estimates of both f and heterozygosity, as they may contribute with complementary information about population viability

    An integrated pan-European research infrastructure for validating smart grid systems

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    A driving force for the realization of a sustainable energy supply in Europe is the integration of distributed, renewable energy resources. Due to their dynamic and stochastic generation behaviour, utilities and network operators are confronted with a more complex operation of the underlying distribution grids. Additionally, due to the higher flexibility on the consumer side through partly controllable loads, ongoing changes of regulatory rules, technology developments, and the liberalization of energy markets, the system’s operation needs adaptation. Sophisticated design approaches together with proper operational concepts and intelligent automation provide the basis to turn the existing power system into an intelligent entity, a so-called smart grid. While reaping the benefits that come along with those intelligent behaviours, it is expected that the system-level testing will play a significantly larger role in the development of future solutions and technologies. Proper validation approaches, concepts, and corresponding tools are partly missing until now. This paper addresses these issues by discussing the progress in the integrated Pan-European research infrastructure project ERIGrid where proper validation methods and tools are currently being developed for validating smart grid systems and solutions.This work is supported by the European Community’s Horizon 2020 Program (H2020/2014-2020) under project “ERIGrid” (Grant Agreement No. 654113). Further information is available at the corresponding website www.erigrid.eu

    Marine resource abundance drove pre-agricultural population increase in Stone Age Scandinavia

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    How climate and ecology affect key cultural transformations remains debated in the context of long-term socio-cultural development because of spatially and temporally disjunct climate and archaeological records. The introduction of agriculture triggered a major population increase across Europe. However, in Southern Scandinavia it was preceded by ~500 years of sustained population growth. Here we show that this growth was driven by long-term enhanced marine production conditioned by the Holocene Thermal Maximum, a time of elevated temperature, sea level and salinity across coastal waters. We identify two periods of increased marine production across trophic levels (P1 7600–7100 and P2 6400–5900 cal. yr BP) that coincide with markedly increased mollusc collection and accumulation of shell middens, indicating greater marine resource availability. Between ~7600–5900 BP, intense exploitation of a warmer, more productive marine environment by Mesolithic hunter-gatherers drove cultural development, including maritime technological innovation, and from ca. 6400–5900 BP, underpinned a ~four-fold human population growth

    Understory Bird Communities in Amazonian Rainforest Fragments: Species Turnover through 25 Years Post-Isolation in Recovering Landscapes

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    Inferences about species loss following habitat conversion are typically drawn from short-term surveys, which cannot reconstruct long-term temporal dynamics of extinction and colonization. A long-term view can be critical, however, to determine the stability of communities within fragments. Likewise, landscape dynamics must be considered, as second growth structure and overall forest cover contribute to processes in fragments. Here we examine bird communities in 11 Amazonian rainforest fragments of 1–100 ha, beginning before the fragments were isolated in the 1980s, and continuing through 2007. Using a method that accounts for imperfect detection, we estimated extinction and colonization based on standardized mist-net surveys within discreet time intervals (1–2 preisolation samples and 4–5 post-isolation samples). Between preisolation and 2007, all fragments lost species in an area-dependent fashion, with loss of as few as <10% of preisolation species from 100-ha fragments, but up to 70% in 1-ha fragments. Analysis of individual time intervals revealed that the 2007 result was not due to gradual species loss beginning at isolation; both extinction and colonization occurred in every time interval. In the last two samples, 2000 and 2007, extinction and colonization were approximately balanced. Further, 97 of 101 species netted before isolation were detected in at least one fragment in 2007. Although a small subset of species is extremely vulnerable to fragmentation, and predictably goes extinct in fragments, developing second growth in the matrix around fragments encourages recolonization in our landscapes. Species richness in these fragments now reflects local turnover, not long-term attrition of species. We expect that similar processes could be operating in other fragmented systems that show unexpectedly low extinction
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