885 research outputs found

    A Holling-Tanner predator-prey model with strong Allee effect

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    We analyse a modified Holling-Tanner predator-prey model where the predation functional response is of Holling type II and we incorporate a strong Allee effect associated with the prey species production. The analysis complements results of previous articles by Saez and Gonzalez-Olivares (SIAM J. Appl. Math. 59 1867-1878, 1999) and Arancibia-Ibarra and Gonzalez-Olivares (Proc. CMMSE 2015 130-141, 2015)discussing Holling-Tanner models which incorporate a weak Allee effect. The extended model exhibits rich dynamics and we prove the existence of separatrices in the phase plane separating basins of attraction related to co-existence and extinction of the species. We also show the existence of a homoclinic curve that degenerates to form a limit cycle and discuss numerous potential bifurcations such as saddle-node, Hopf, and Bogadonov-Takens bifurcations

    Land cover and water yield: inference problems when comparing catchments with mixed land cover

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    Controlled experiments provide strong evidence that changing land cover (e.g. deforestation or afforestation) can affect mean catchment streamflow (<i>Q</i>). By contrast, a similarly strong influence has not been found in studies that interpret <i>Q</i> from multiple catchments with mixed land cover. One possible reason is that there are methodological issues with the way in which the Budyko framework was used in the latter type studies. We examined this using <i>Q</i> data observed in 278 Australian catchments and by making inferences from synthetic <i>Q</i> data simulated by a hydrological process model (the Australian Water Resources Assessment system Landscape model). The previous contrasting findings could be reproduced. In the synthetic experiment, the land cover influence was still present but not accurately detected with the Budyko- framework. Likely sources of interpretation bias demonstrated include: (i) noise in land cover, precipitation and <i>Q</i> data; (ii) additional catchment climate characteristics more important than land cover; and (iii) covariance between <i>Q</i> and catchment attributes. These methodological issues caution against the use of a Budyko framework to quantify a land cover influence in <i>Q</i> data from mixed land-cover catchments. Importantly, however, our findings do not rule out that there may also be physical processes that modify the influence of land cover in mixed land-cover catchments. Process model simulations suggested that lateral water redistribution between vegetation types and recirculation of intercepted rainfall may be important

    Evaluation of precipitation estimation accuracy in reanalyses, satellite products, and an ensemble method for regions in Australia and south and east Asia

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    Precipitation estimates from reanalyses and satellite observations are routinely used in hydrologic applications, but their accuracy is seldom systematically evaluated. This study used high-resolution gauge-only daily precipitation analyses for Australi

    The role of climatic and terrain attributes in estimating baseflow recession in tropical catchments

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    The understanding of low flows in rivers is paramount more than ever as demand for water increases on a global scale. At the same time, limited streamflow data to investigate this phenomenon, particularly in the tropics, makes the provision of accurate estimations in ungauged areas an ongoing research need. This paper analysed the potential of climatic and terrain attributes of 167 tropical and sub-tropical unregulated catchments to predict baseflow recession rates. Daily streamflow data (m<sup>3</sup> s<sup>–1</sup>) from the Global River Discharge Center (GRDC) and a linear reservoir model were used to obtain baseflow recession coefficients (<i>k</i><sub>bf</sub>) for these catchments. Climatic attributes included annual and seasonal indicators of rainfall and potential evapotranspiration. Terrain attributes included indicators of catchment shape, morphology, land cover, soils and geology. Stepwise regression was used to identify the best predictors for baseflow recession coefficients. Mean annual rainfall (MAR) and aridity index (AI) were found to explain 49% of the spatial variation of <i>k</i><sub>bf</sub>. The rest of climatic indices and the terrain indices average catchment slope (SLO) and tree cover were also good predictors, but co-correlated with MAR. Catchment elongation (CE), a measure of catchment shape, was also found to be statistically significant, although weakly correlated. An analysis of clusters of catchments of smaller size, showed that in these areas, presumably with some similarity of soils and geology due to proximity, residuals of the regression could be explained by SLO and CE. The approach used provides a potential alternative for <i>k</i><sub>bf</sub> parameterisation in ungauged catchments

    Evaluation of precipitation estimation accuracy in reanalyses, satellite products, and an ensemble method for regions in Australia and south and east Asia

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    Precipitation estimates from reanalyses and satellite observations are routinely used in hydrologic applications, but their accuracy is seldom systematically evaluated. This study used high-resolution gauge-only daily precipitation analyses for Australia (SILO) and South and East Asia [Asian Precipitation-Highly-Resolved Observational Data Integration Towards Evaluation (APHRODITE)] to calculate the daily detection and accuracy metrics for three reanalyses [ECMWF Re-Analysis Interim (ERA-Interim), Japanese 25-yr Reanalysis (JRA-25), and NCEP-Department of Energy (DOE) Global Reanalysis 2] and three satellite-based precipitation products [Tropical Rainfall Measuring Mission (TRMM) 3B42V6, Climate Prediction Center morphing technique (CMORPH), and Precipitation Estimation from Remotely Sensed Imagery Using Artificial Neural Networks (PERSIANN)]. A depthfrequency- adjusted ensemble mean of the reanalyses and satellite products was also evaluated. Reanalyses precipitation from ERA-Interim in southern Australia (SAu) and northern Australasia (NAu) showed higher detection performance. JRA-25 had a better performance in South and East Asia (SEA) except for the monsoon period, in which satellite estimates from TRMM and CMORPH outperformed the reanalyses. In terms of accuracy metrics (correlation coefficient, root-mean-square difference, and a precipitation intensity proxy, which is the ratio of monthly precipitation amount to total days with precipitation) and over the three subdomains, the depth-frequency-adjusted ensemble mean generally outperformed or was nearly as good as any of the single members. The results of the ensemble show that additional information is captured from the different precipitation products. This finding suggests that, depending on precipitation regime and location, combining (re)analysis and satellite products can lead to better precipitation estimates and, thus,more accurate hydrological applications than selecting any single product

    Pruning cuts affect wood necrosis but not the percentage of budburst or shoot development on spur pruned vines for different grapevine varieties

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    Two experimental studies were performed in this trial. In the first, the aim was to quantify wood necrosis generated by pruning cuts on aboveground permanent (arms and trunks) and non-permanent (spurs) woody structures of 'Cabernet Sauvignon' vines. In the second, the goal was to evaluate the effect of cutting distance from the basal end of the shoot in spur pruned vines on budburst and further shoot development for 'Grenache', 'Cabernet Franc' and 'Malbec' varieties. Based upon the first experiment, the area and depth of wood necrosis was highly influenced by the distance where the pruning cut was performed over the node. Furthermore, the diameter of the spur that was cut was not significantly related to either the area or the depth of the necrotic wood generated after the cut. Aboveground vine wood necrotic area ranged from 9 to 44 % of the total wood area measured in 'Cabernet Sauvignon' cordon trained spur pruned 25-year-old grapevines. For each vine a larger proportion of the necrotic wood (20 to 46 % of necrotic area) was present in the arms when compared to the trunks (1 to 28 % of necrotic area). As a result of the second experiment, spur budburst and further shoot development was not affected by the distance from the node where the pruning cut was performed for any of the cultivars considered in the study contrary to what is commonly believed

    Astrocyte Ca2+-evoked ATP release regulates myelinated axon excitability and conduction speed

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    INTRODUCTION: Astrocytes support neuronal function throughout the central nervous system. In the gray matter, they regulate synapse number during development, remove synaptically released neurotransmitters to terminate their action and prevent excitotoxicity, control the extracellular potassium concentration to prevent hyperexcitability, regulate blood flow to ensure an adequate energy supply, provide lactate to neurons for energy, and respond to rises of intracellular calcium concentration ([Ca2+]i) by releasing adenosine triphosphate (ATP) and other gliotransmitters that act on neuronal receptors to modulate information processing. However, their role is unclear in the white matter, which transmits information rapidly between gray matter areas using axons wrapped with capacitance-reducing myelin (although they have been suggested to regulate myelination during development and during normal function). RATIONALE: Recently, it has been suggested that learning and memory may reflect not only changes in synaptic function in the gray matter, but also changes in white matter function. In particular, neural circuit function might be regulated by changes in the conduction speed of myelinated axons that result in an altered arrival time of action potentials at a distant neuron. These speed changes might be brought about by alterations of the properties of the passively conducting myelinated internodes or of the intervening excitable nodes of Ranvier, where the action potential is generated. We applied immunohistochemistry to assess how astrocytes interact with myelinated axons, neuronal stimulation and light-evoked calcium uncaging in astrocytes to evoke Ca2+-dependent release of gliotransmitters, and electrophysiology and pharmacology to characterize how astrocyte-released substances might affect the axon initial segment (AIS) and nodes of Ranvier of myelinated neurons. Measurements of conduction velocity and computer modeling allowed us to interpret the results. RESULTS: Astrocytes closely approach the axons of myelinated neurons in layer V of the cerebral cortex that enter the corpus callosum. Uncaging Ca2+ within astrocytes or stimulating spike trains in neurons evoked a rise of astrocyte [Ca2+]i that triggered the release of ATP-containing vesicles from these cells. This evoked an inward current in the AIS and nodes of Ranvier of the pyramidal neurons. Pharmacology showed that this was mediated by the activation of Gs-linked adenosine A2a receptors (A2aRs), implying that the released ATP was converted to adenosine by extracellular enzymes. The A2aRs raise the intracellular concentration of cyclic AMP, which activates hyperpolarization-activated cyclic nucleotide–gated (HCN) channels mediating the inward hyperpolarization-activated current (Ih) and thus depolarizes the cell. In the AIS, the activation of A2aRs alters excitability and hence action potential generation, whereas in the nodes of Ranvier, it decreases the conduction speed of the action potential along the axon. CONCLUSION: As in the gray matter, astrocyte [Ca2+]i regulates the release of ATP into the extracellular space in the white matter. After conversion to adenosine, this regulates the excitability and conduction speed of myelinated axons. The changes in excitability at the AIS will lead to changes in the relationship between the synaptic input and action potential output of the cell. The altered conduction speed of the myelinated axon may change neural circuit function by changing the action potential arrival time at the cell’s output synapses, thus altering the integration of signals in postsynaptic neurons. Variations in astrocyte-derived adenosine level can occur between wake and sleep states, and the extracellular adenosine concentration rises during energy deprivation conditions. These changes in adenosine level could thus control white matter information flow and neural circuit function

    The evolution of Balmer jump selected galaxies in the ALHAMBRA survey

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    We present a new color-selection technique, based on the Bruzual & Charlot models convolved with the bands of the ALHAMBRA survey, and the redshifted position of the Balmer jump to select star-forming galaxies in the redshift range 0.5 < z < 1.5. These galaxies are dubbed Balmer jump Galaxies BJGs. We apply the iSEDfit Bayesian approach to fit each detailed SED and determine star-formation rate (SFR), stellar mass, age and absolute magnitudes. The mass of the haloes where these samples reside are found via a clustering analysis. Five volume-limited BJG sub-samples with different mean redshifts are found to reside in haloes of median masses ∼1012.5±0.2M⊙\sim 10^{12.5 \pm 0.2} M_\odot slightly increasing toward z=0.5. This increment is similar to numerical simulations results which suggests that we are tracing the evolution of an evolving population of haloes as they grow to reach a mass of ∼1012.7±0.1M⊙\sim 10^{12.7 \pm 0.1} M_\odot at z=0.5. The likely progenitors of our samples at z∼\sim3 are Lyman Break Galaxies, which at z∼\sim2 would evolve into star-forming BzK galaxies, and their descendants in the local Universe are elliptical galaxies.Hence, this allows us to follow the putative evolution of the SFR, stellar mass and age of these galaxies. From z∼\sim1.0 to z∼\sim0.5, the stellar mass of the volume limited BJG samples nearly does not change with redshift, suggesting that major mergers play a minor role on the evolution of these galaxies. The SFR evolution accounts for the small variations of stellar mass, suggesting that star formation and possible minor mergers are the main channels of mass assembly.Comment: 14 pages, 10 figures. Submitted to A&A. It includes first referee's comments. Abstract abridged due to arXiv requirement

    Astrocyte Ca2+-evoked ATP release regulates myelinated axon excitability and conduction speed*

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    INTRODUCTION: Astrocytes support neuronal function throughout the central nervous system. In the gray matter, they regulate synapse number during development, remove synaptically released neurotransmitters to terminate their action and prevent excitotoxicity, control the extracellular potassium concentration to prevent hyperexcitability, regulate blood flow to ensure an adequate energy supply, provide lactate to neurons for energy, and respond to rises of intracellular calcium concentration ([Ca2+]i) by releasing adenosine triphosphate (ATP) and other gliotransmitters that act on neuronal receptors to modulate information processing. However, their role is unclear in the white matter, which transmits information rapidly between gray matter areas using axons wrapped with capacitance-reducing myelin (although they have been suggested to regulate myelination during development and during normal function). RATIONALE: Recently, it has been suggested that learning and memory may reflect not only changes in synaptic function in the gray matter, but also changes in white matter function. In particular, neural circuit function might be regulated by changes in the conduction speed of myelinated axons that result in an altered arrival time of action potentials at a distant neuron. These speed changes might be brought about by alterations of the properties of the passively conducting myelinated internodes or of the intervening excitable nodes of Ranvier, where the action potential is generated. We applied immunohistochemistry to assess how astrocytes interact with myelinated axons, neuronal stimulation and light-evoked calcium uncaging in astrocytes to evoke Ca2+-dependent release of gliotransmitters, and electrophysiology and pharmacology to characterize how astrocyte-released substances might affect the axon initial segment (AIS) and nodes of Ranvier of myelinated neurons. Measurements of conduction velocity and computer modeling allowed us to interpret the results. RESULTS: Astrocytes closely approach the axons of myelinated neurons in layer V of the cerebral cortex that enter the corpus callosum. Uncaging Ca2+ within astrocytes or stimulating spike trains in neurons evoked a rise of astrocyte [Ca2+]i that triggered the release of ATP-containing vesicles from these cells. This evoked an inward current in the AIS and nodes of Ranvier of the pyramidal neurons. Pharmacology showed that this was mediated by the activation of Gs-linked adenosine A2a receptors (A2aRs), implying that the released ATP was converted to adenosine by extracellular enzymes. The A2aRs raise the intracellular concentration of cyclic AMP, which activates hyperpolarization-activated cyclic nucleotide–gated (HCN) channels mediating the inward hyperpolarization-activated current (Ih) and thus depolarizes the cell. In the AIS, the activation of A2aRs alters excitability and hence action potential generation, whereas in the nodes of Ranvier, it decreases the conduction speed of the action potential along the axon. CONCLUSION: As in the gray matter, astrocyte [Ca2+]i regulates the release of ATP into the extracellular space in the white matter. After conversion to adenosine, this regulates the excitability and conduction speed of myelinated axons. The changes in excitability at the AIS will lead to changes in the relationship between the synaptic input and action potential output of the cell. The altered conduction speed of the myelinated axon may change neural circuit function by changing the action potential arrival time at the cell’s output synapses, thus altering the integration of signals in postsynaptic neurons. Variations in astrocyte-derived adenosine level can occur between wake and sleep states, and the extracellular adenosine concentration rises during energy deprivation conditions. These changes in adenosine level could thus control white matter information flow and neural circuit function
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