499 research outputs found

    The Pex3–Inp1 complex tethers yeast peroxisomes to the plasma membrane

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    A subset of peroxisomes is retained at the mother cell cortex by the Pex3–Inp1 complex. We identify Inp1 as the first known plasma membrane–peroxisome (PM-PER) tether by demonstrating that Inp1 meets the predefined criteria that a contact site tether protein must adhere to. We show that Inp1 is present in the correct subcellular location to interact with both the plasma membrane and peroxisomal membrane and has the structural and functional capacity to be a PM-PER tether. Additionally, expression of artificial PM-PER tethers is sufficient to restore retention in inp1Δ cells. We show that Inp1 mediates peroxisome retention via an N-terminal domain that binds PI(4,5)P2 and a C-terminal Pex3-binding domain, forming a bridge between the peroxisomal membrane and the plasma membrane. We provide the first molecular characterization of the PM-PER tether and show it anchors peroxisomes at the mother cell cortex, suggesting a new model for peroxisome retention

    Algal nutrient competition in continuous culture

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    Natural phytoplankton from Lake Constance was exposed to competition experiments in continuous culture at 6 different molar rations of PratioSi as potentially limiting nutrients. As predicted by theory there was competitive exclusion of all species but one at single nutrient limitation, and coexistence of two species in steady state when P was limiting for one and Si for the other species. In one case coexistence of three species occurred. Equilibrium species composition, which stabilized after 3 to 6 weeks of cultivation, was independent of the species composition of the inoculum and only controlled by the nutrient regime. Comparability of experimental results and field observations is discussed

    Estimates of hypolimnetic oxygen deficits in ponds

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    Shallow tropical integrated culture ponds in the Pearl River Delta, China, have been found to stratify almost daily, with high organic loadings and dense algal growth. The dissolved oxygen (DO) concentration is super-saturated in the epilimnion and is under 2 mg/l in the hypolimnion (>1m). The compensation depth corresponds to twice the Secchi disk depth ranging from 50 to 80cm. As a result, little or no net oxygen is produced in the hypolimnion (>1m). The low DO concentration in the hypolimnion causes organic materials, such as unused organic wastes and senescent algae cells, to be incompletely oxidized, since the rate of oxygen consumption by oxidable matter in water is dependent on the dissolved oxygen concentration in water. This material becomes the source of hypolimnetic oxygen deficits (HOD) which can drive whole pond DO to a dangerously low level, should sudden destratification occur. An improved estimate of hypolimnetic oxygen deficits is introduced in this article, and the advantages of this method are discussed.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/72126/1/j.1365-2109.1989.tb00341.x.pd

    Natural Orbitals and BEC in traps, a diffusion Monte Carlo analysis

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    We investigate the properties of hard core Bosons in harmonic traps over a wide range of densities. Bose-Einstein condensation is formulated using the one-body Density Matrix (OBDM) which is equally valid at low and high densities. The OBDM is calculated using diffusion Monte Carlo methods and it is diagonalized to obtain the "natural" single particle orbitals and their occupation, including the condensate fraction. At low Boson density, na3<105na^3 < 10^{-5}, where n=N/Vn = N/V and aa is the hard core diameter, the condensate is localized at the center of the trap. As na3na^3 increases, the condensate moves to the edges of the trap. At high density it is localized at the edges of the trap. At na3104na^3 \leq 10^{-4} the Gross-Pitaevskii theory of the condensate describes the whole system within 1%. At na3103na^3 \approx 10^{-3} corrections are 3% to the GP energy but 30% to the Bogoliubov prediction of the condensate depletion. At na3102na^3 \gtrsim 10^{-2}, mean field theory fails. At na30.1na^3 \gtrsim 0.1, the Bosons behave more like a liquid 4^4He droplet than a trapped Boson gas.Comment: 13 pages, 14 figures, submitted Phys. Rev.

    Eco-evolutionary dynamics on deformable fitness landscapes

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    Conventional approaches to modelling ecological dynamics often do not include evolutionary changes in the genetic makeup of component species and, conversely, conventional approaches to modelling evolutionary changes in the genetic makeup of a population often do not include ecological dynamics. But recently there has been considerable interest in understanding the interaction of evolutionary and ecological dynamics as coupled processes. However, in the context of complex multi-species ecosytems, especially where ecological and evolutionary timescales are similar, it is difficult to identify general organising principles that help us understand the structure and behaviour of complex ecosystems. Here we introduce a simple abstraction of coevolutionary interactions in a multi-species ecosystem. We model non-trophic ecological interactions based on a continuous but low-dimensional trait/niche space, where the location of each species in trait space affects the overlap of its resource utilisation with that of other species. The local depletion of available resources creates, in effect, a deformable fitness landscape that governs how the evolution of one species affects the selective pressures on other species. This enables us to study the coevolution of ecological interactions in an intuitive and easily visualisable manner. We observe that this model can exhibit either of the two behavioural modes discussed in the literature; namely, evolutionary stasis or Red Queen dynamics, i.e., continued evolutionary change. We find that which of these modes is observed depends on the lag or latency between the movement of a species in trait space and its effect on available resources. Specifically, if ecological change is nearly instantaneous compared to evolutionary change, stasis results; but conversely, if evolutionary timescales are closer to ecological timescales, such that resource depletion is not instantaneous on evolutionary timescales, then Red Queen dynamics result. We also observe that in the stasis mode, the overall utilisation of resources by the ecosystem is relatively efficient, with diverse species utilising different niches, whereas in the Red Queen mode the organisation of the ecosystem is such that species tend to clump together competing for overlapping resources. These models thereby suggest some basic conditions that influence the organisation of inter-species interactions and the balance of individual and collective adaptation in ecosystems, and likewise they also suggest factors that might be useful in engineering artificial coevolution

    Diet of two syntopic species of Crenuchidae (Ostariophysi: Characiformes) in an Amazonian rocky stream

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    Abstract This study assessed the diet of two poorly known syntopic fish species of the family Crenuchidae, Characidium aff. declivirostre and Leptocharacidium omospilus, in a Presidente Figueiredo´ rocky stream, Amazonas, Brazil. The stomach contents were analyzed and their Frequency of Occurrence (FO %) and Relative Volume (Vol %) were combined in a Feeding Index (IAi). We examined 20 individuals of C. aff. declivirostre and 23 of L. omospilus. The Morisita-Horn Index was used to estimate the overlap between the diets of these species. Immature insects were the most valuable items consumed by both fish species. The diet of C. aff. declivirostre was mainly composed of larvae and pupae of Chironomidae, while L. omospilus predominantly consumed larvae of Hydroptilidae, Hydropyschidae and Pyralidae. Thus, both species were classified as autochthonous insectivorous. Characidium aff. declivirostre was considered a more specialized species, probably reflecting lower feeding plasticity or the use of more restricted microhabitats compared to L. omospilus. When the food items were analyzed at the family taxonomic level, the diet overlap between these species was considered moderate (Morisita-Horn Index = 0.4). However, a more thorough analysis, at the genus level, indicates a very low diet overlap. Therefore, we conclude that the feeding segregation between C. aff. declivirostre and L. omospilus may favor their co-existence, despite their high phylogenetic closeness

    Colourful coexistence of red and green picocyanobacteria in lakes and seas

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    Hutchinson's paradox of the plankton inspired many studies on the mechanisms of species coexistence. Recent laboratory experiments showed that partitioning of white light allows stable coexistence of red and green picocyanobacteria. Here, we investigate to what extent these laboratory findings can be extrapolated to natural waters. We predict from a parameterized competition model that the underwater light colour of lakes and seas provides ample opportunities for coexistence of red and green phytoplankton species. To test this prediction, we sampled picocyanobacteria of 70 aquatic ecosystems, ranging from clear blue oceans to turbid brown peat lakes. As predicted, red picocyanobacteria dominated in clear waters, whereas green picocyanobacteria dominated in turbid waters. We found widespread coexistence of red and green picocyanobacteria in waters of intermediate turbidity. These field data support the hypothesis that niche differentiation along the light spectrum promotes phytoplankton biodiversity, thus providing a colourful solution to the paradox of the plankton
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