The niche of benthic foraminifera, critical thresholds and proxies

Ecological studies of benthic foraminifera are carried out to explain patterns of distribution and the dynamics of communities. They are also used to provide data to establish proxy relationships with selected factors. According to niche theory, the patterns of distribution of benthic foraminifera are controlled by those environmental factors that have reached their critical thresholds. For each species, in variable environments, different factors may be limiting distributions both temporally and spatially. For a species or an assemblage to be useful as a proxy its abundance must show a strong correlation with the chosen factor. Since numerous factors influence each species, it is only in those environments where the majority of factors show little variation but one particular factor shows significant variation that the proxy relationship for that factor can be determined. On theoretical grounds, the reliability of using foraminiferal abundance as a proxy of a selected environmental factor should be restricted to the range close to the upper and lower thresholds. For oxygen, foraminifera are potential proxies for the lower limits but once oxygen levels rise to values of perhaps >1 or 2 ml l-1, there is no longer a relationship between oxygen levels and abundance. By contrast, the flux of organic matter over a large range shows a sufficiently close relationship with foraminiferal assemblages so that transfer functions can be derived for the deep sea. However, the relationship at species level is far less clear cut. Much more accurate estimates of primary productivity and modern organic flux rates are required to improve the determination of past flux rates

On the topological classification of binary trees using the Horton-Strahler index

The Horton-Strahler (HS) index $r=\max{(i,j)}+\delta_{i,j}$ has been shown to be relevant to a number of physical (such at diffusion limited aggregation) geological (river networks), biological (pulmonary arteries, blood vessels, various species of trees) and computational (use of registers) applications. Here we revisit the enumeration problem of the HS index on the rooted, unlabeled, plane binary set of trees, and enumerate the same index on the ambilateral set of rooted, plane binary set of trees of $n$ leaves. The ambilateral set is a set of trees whose elements cannot be obtained from each other via an arbitrary number of reflections with respect to vertical axes passing through any of the nodes on the tree. For the unlabeled set we give an alternate derivation to the existing exact solution. Extending this technique for the ambilateral set, which is described by an infinite series of non-linear functional equations, we are able to give a double-exponentially converging approximant to the generating functions in a neighborhood of their convergence circle, and derive an explicit asymptotic form for the number of such trees.Comment: 14 pages, 7 embedded postscript figures, some minor changes and typos correcte

Topological self-similarity on the random binary-tree model

Asymptotic analysis on some statistical properties of the random binary-tree model is developed. We quantify a hierarchical structure of branching patterns based on the Horton-Strahler analysis. We introduce a transformation of a binary tree, and derive a recursive equation about branch orders. As an application of the analysis, topological self-similarity and its generalization is proved in an asymptotic sense. Also, some important examples are presented

ELM triggering conditions for the integrated modeling of H-mode plasmas

Recent advances in the integrated modeling of ELMy H-mode plasmas are presented. A model for the H-mode pedestal and for the triggering of ELMs predicts the height, width, and shape of the H-mode pedestal and the frequency and width of ELMs. Formation of the pedestal and the L-H transition is the direct result of ExB flow shear suppression of anomalous transport. The periodic ELM crashes are triggered by either the ballooning or peeling MHD instabilities. The BALOO, DCON, and ELITE ideal MHD stability codes are used to derive a new parametric expression for the peeling-ballooning threshold. The new dependence for the peeling-ballooning threshold is implemented in the ASTRA transport code. Results of integrated modeling of DIII-D like discharges are presented and compared with experimental observations. The results from the ideal MHD stability codes are compared with results from the resistive MHD stability code NIMROD.Comment: 12th International Congress on Plasma Physics, 25-29 October 2004, Nice (France

Atlantic Bluefin Tuna Tagging Programme in Ireland 2016

It is important that stock origin, habitat utilisation and large-scale movement patterns of Atlantic bluefin are characterised in detail to ensure that the population models and concepts used in Atlantic bluefin tuna stock assessment and Management Strategy Evaluation (MSE) are parameterised as accurately as possible. Investigation of the distribution and movements of Atlantic bluefin tuna in Irish waters is now a priority for Ireland. The ocean waters off south Donegal are now regarded by the International Commission for the Conservation of Atlantic Tuna (ICCAT) as an important area for Atlantic bluefin tuna and indications are that significant numbers arrive in the area over the period August to November each year. The Department of Agriculture Food and the Marine (DAFM) requested that the Marine Institute carry out a bluefin tagging programme in autumn 2016 to support the International Commission for the Conservation of Atlantic Tuna (ICCAT) Grand Bluefin Year Programme (GBYP) Atlantic research programme for Bluefin tuna

A leap forward in geographic scale for forest ectomycorrhizal fungi

Published versio

Spironolactone-induced inhibition of aldosterone biosynthesis in primary aldosteronism: Morphological and functional studies

Twenty-five patients harboring aldosterone-producing adenomas were treated with spironolactone for 2-170 days immediately preoperatively. In the early period of administration of the drug (up to 27 days), plasma and urinary aldosterone decreased sharply while plasma renin activity (PRA) and serum potassium were rising. During this period of time, spironolactone bodies (SB), which form exclusively in cells actively producing aldosterone, were forming rapidly in the tumor cells but not in the inactive glomerulosa cells proper. The SB appear to be a morphological expression of a block in aldosterone biosynthesis. Since SB do not occur in normal fasciculata cells, which, like glomerulosa cells, also synthesize corticosterone, it is concluded that spironolactone inhibition of aldosterone biosynthesis occurs between corticosterone and aldosterone. Recent studies in vitro by others have suggested that the inhibition occurs at the corticosterone-methyl oxidase step, I (Ulick's nomenclature). The great diuresis of sodium and retention of potassium resulting from continued administration of the drug sharply activates aldosterone stimulatory factors. Aldosterone production may return to baseline levels in several weeks but it is inappropriately low in relation to the levels of PRA and serum potassium. With the further passage of time (average 4-6 wk), aldosterone production may increase 50%-100% above baseline levels, suggesting that the block has disappeared or is receding. At this time SB are diminishing in number and by 170 days of the drug they have virtually disappeared. We have hypothesized, among other possibilities, that recovery of the ability to convert corticosterone to aldosterone occurs by virtue of a mechanism activated by sodium deficiency, independent of angiotensin, which stimulates step 1 of the corticosterone-methyl oxidase system. As the block in the final step(s) of the biosynthetic pathway recedes, the existing elevated levels of angiotensin become much more effective in stimulating the production of aldosterone.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/22806/1/0000363.pd