24 research outputs found

    Considerations for management strategy evaluation for small pelagic fishes

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    Management strategy evaluation (MSE) is the state-of-the-art approach for testing and comparing management strategies in a way that accounts for multiple sources of uncertainty (e.g. monitoring, estimation, and implementation). Management strategy evaluation can help identify management strategies that are robust to uncertainty about the life history of the target species and its relationship to other species in the food web. Small pelagic fish (e.g. anchovy, herring and sardine) fulfil an important ecological role in marine food webs and present challenges to the use of MSE and other simulation-based evaluation approaches. This is due to considerable stochastic variation in their ecology and life history, which leads to substantial observation and process uncertainty. Here, we summarize the current state of MSE for small pelagic fishes worldwide. We leverage expert input from ecologists and modellers to draw attention to sources of process and observation uncertainty for small pelagic species, providing examples from geographical regions where these species are ecologically, economically and culturally important. Temporal variation in recruitment and other life-history rates, spatial structure and movement, and species interactions are key considerations for small pelagic fishes. We discuss tools for building these into the MSE process, with examples from existing fisheries. We argue that model complexity should be informed by management priorities and whether ecosystem information will be used to generate dynamics or to inform reference points. We recommend that our list of considerations be used in the initial phases of the MSE process for small pelagic fishes or to build complexity on existing single-species models.publishedVersio

    Regulation of the renal Na +

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    Demographic Parameters of Tetranychus urticae (Acari: Tetranychidae) on Four Rosa sp. Cultivars

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    The goal of this work was to determine the life parameters of Tetranychus urticae Koch on leaves of 4 rose (Rosa sp.) cultivars. To conduct this experiment a colony of T. urticae collected from ornamentals grown at Saltillo, Coahuila, Mexico, was established on bean (Phaseouls vulgaris L.) seedlings inside a Biotronette chamber at 25 ± 2 °C, 60-70 RH and 12:12 h L:D. According to the experimental design, 100 one-day old recently mated and fertilized females were transferred to 2.5 cm diam rose (Rosa sp. L.) leaf discs from ‘Emma', ‘Luna', ‘Gran Gala’ and ‘Virginia' cultivars in such a way that every experimental unit included 1 female per disc. The latter were maintained at the above temperature, RH and photoperiod conditions. Demographic parameters in this experiment showed greater growth potential of this pest on the ‘Luna' and ‘Gran Gala’ cultivars than on ‘Virginia’ and ‘Emma’.Se determinaron parámetros de vida de Tetranychus urticae Koch en hojas de las variedades de rosal Luna, Gran Gala, Virginia y Emma. Se estableció una colonia de T. urticae en recolectas de cultivos ornamentales de Saltillo, Coahuila, México, en plántulas de frijol (Phaseolus vulgaris L.) en una cámara ambiental Biotronette® con condiciones de 25 ± 2 °C, 60–70 HR y fotoperiodo 12:12 horas luz oscuridad. Para el desarrollo del experimento se seleccionaron 100 hembras de un día de edad recién apareadas y fecundadas, se colocaron en forma individual en discos de hojas de 2.5 cm de diámetro de rosal, de tal forma que cada unidad experimental consistió en una hembra por disco y se mantuvieron a las mismas condiciones de temperatura, humedad y fotoperiodo. Los parámetros poblacionales muestran de manera general un mayor potencial de crecimiento en las variedades ‘Luna’, ‘Gran Gala’ seguidas de ‘Virginia’ y ‘Emma’

    A mouse model of pseudohypoaldosteronism type II reveals a novel mechanism of renal tubular acidosis

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    Pseudohypoaldosteronism type II (PHAII) is a genetic disease characterized by association of hyperkalemia, hyperchloremic metabolic acidosis, hypertension, low renin, and high sensitivity to thiazide diuretics. It is caused by mutations in the WNK1, WNK4, KLHL3 or CUL3 gene. There is strong evidence that excessive sodium chloride reabsorption by the sodium chloride cotransporter NCC in the distal convoluted tubule is involved. WNK4 is expressed not only in distal convoluted tubule cells but also in β-intercalated cells of the cortical collecting duct. These latter cells exchange intracellular bicarbonate for external chloride through pendrin, and therefore, account for renal base excretion. However, these cells can also mediate thiazide-sensitive sodium chloride absorption when the pendrin-dependent apical chloride influx is coupled to apical sodium influx by the sodium-driven chloride/bicarbonate exchanger. Here we determine whether this system is involved in the pathogenesis of PHAII. Renal pendrin activity was markedly increased in a mouse model carrying a WNK4 missense mutation (Q562E) previously identified in patients with PHAII. The upregulation of pendrin led to an increase in thiazide-sensitive sodium chloride absorption by the cortical collecting duct, and it caused metabolic acidosis. The function of apical potassium channels was altered in this model, and hyperkalemia was fully corrected by pendrin genetic ablation. Thus, we demonstrate an important contribution of pendrin in renal regulation of sodium chloride, potassium and acid-base homeostasis and in the pathophysiology of PHAII. Furthermore, we identify renal distal bicarbonate secretion as a novel mechanism of renal tubular acidosis.Pseudohypoaldosteronism type II (PHAII) is a genetic disease characterized by association of hyperkalemia, hyperchloremic metabolic acidosis, hypertension, low renin, and high sensitivity to thiazide diuretics. It is caused by mutations in the WNK1, WNK4, KLHL3 or CUL3 gene. There is strong evidence that excessive sodium chloride reabsorption by the sodium chloride cotransporter NCC in the distal convoluted tubule is involved. WNK4 is expressed not only in distal convoluted tubule cells but also in beta-intercalated cells of the cortical collecting duct. These latter cells exchange intracellular bicarbonate for external chloride through pendrin, and therefore, account for renal base excretion. However, these cells can also mediate thiazide-sensitive sodium chloride absorption when the pendrin-dependent apical chloride influx is coupled to apical sodium influx by the sodium-driven chloride/bicarbonate exchanger. Here we determine whether this system is involved in the pathogenesis of PHAII. Renal pendrin activity was markedly increased in a mouse model carrying a WNK4 missense mutation (Q562E) previously identified in patients with PHAII. The upregulation of pendrin led to an increase in thiazide-sensitive sodium chloride absorption by the cortical collecting duct, and it caused metabolic acidosis. The function of apical potassium channels was altered in this model, and hyperkalemia was fully corrected by pendrin genetic ablation. Thus, we demonstrate an important contribution of pendrin in renal regulation of sodium chloride, potassium and acid-base homeostasis and in the pathophysiology of PHAII. Furthermore, we identify renal distal bicarbonate secretion as a novel mechanism of renal tubular acidosis

    The sodium chloride cotransporter SLC12A3: new roles in sodium, potassium, and blood pressure regulation

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    SLC12A3 encodes the thiazide-sensitive sodium chloride cotransporter (NCC), which is primarily expressed in the kidney, but also in intestine and bone. In the kidney, NCC is located in the apical plasma membrane of epithelial cells in the distal convoluted tubule. Although NCC reabsorbs only 5 to 10 % of filtered sodium, it is important for the fine-tuning of renal sodium excretion in response to various hormonal and non-hormonal stimuli. Several new roles for NCC in the regulation of sodium, potassium, and blood pressure have been unraveled recently. For example, the recent discoveries that NCC is activated by angiotensin II but inhibited by dietary potassium shed light on how the kidney handles sodium during hypovolemia (high angiotensin II) and hyperkalemia. The additive effect of angiotensin II and aldosterone maximizes sodium reabsorption during hypovolemia, whereas the inhibitory effect of potassium on NCC increases delivery of sodium to the potassium-secreting portion of the nephron. In addition, great steps have been made in unraveling the molecular machinery that controls NCC. This complex network consists of kinases and ubiquitinases, including WNKs, SGK1, SPAK, Nedd4-2, Cullin-3, and Kelch-like 3. The pathophysiological significance of this network is illustrated by the fact that modification of each individual protein in the network changes NCC activity and results in salt-dependent hypotension or hypertension. This review aims to summarize these new insights in an integrated manner while identifying unanswered questions

    Efect of antiseptic gels in the microbiologic colonization of the suture threads after oral surgery

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    Te work was supported by the Oral Medicine, Oral surgery and Implantology Unit. School of Medicine and Dentistry, University of Santiago de Compostela, Santiago de Compostela, Spain.Three diferent bioadhesive gels were evaluated in a double-blind randomized clinical trial in which microbial growth in the suture thread was assessed following post-surgical application of the aforementioned gels. Also assessed in this trial were, the intensity of post-surgical pain as well as the degree of healing of the patients’ surgical wounds. A total of 21 patients (with 42 wisdom teeth) participated in this trial. Chlorhexidine gel, chlorhexidine-chitosan gel, and hyaluronic acid gel were evaluated, with a neutral water-based gel serving as the control agent. The aerobic and facultative anaerobic bacterial recovery on blood agar was lower in the placebo group than in the experimental groups. The most signifcant diference (p=0.04) was observed in the chlorhexidine-chitosan group. in which the growth of Blood Agar and Mitis Salivarius Agar was signifcantly higher than in the placebo group. The intensity of post-surgical pain was very similar among all the groups. Signifcantly better healing rates were observed in the patients treated with chlorhexidine-chitosan gel when compared with those who used the placebo gel (p=0.03), and in particular when compared with those patients who used hyaluronic acid gel (p=0.01). Through our microbiological analyses, we were able to conclude that none of the bioadhesive gels tested resulted in benefcial reductions in the bacterial/fungal populations. However, the healing rates of patients who were treated with chlorhexidine-chitosan were better than those of the patients who used either the placebo gel or the hyaluronic acid gel
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