Early life history of the sheepnose (Plethobasus cyphyus) (Mollusca: Bivalvia: Unionoida)

Managing a rare species can be improved with knowledge of its natural history. The sheepnose (Plethobasus cyphyus) is a freshwater mussel recently listed by the US as federally endangered. We used standard methods to study P. cyphyus brooding behaviour, host fishes in the laboratory and under natural conditions, and glochidial morphology. We monitored a population of P. cyphyus in the Chippewa River, WI during spring and summer 2007–2009 and 2011 and found brooding animals between mid-May and early August. Gravid individuals ranged between 5 and 27 yr (mean age ± 1 s.d. = 13 ± 4 yr). Plethobasus cyphyus brooded glochidia in outer gills, which varied in colour from red, orange, pink, cream, or white. We observed mature glochidia more commonly in individuals with cream or white gills and these glochidia were released in a clear, adhesive, mucus matrix. In laboratory trials we found several minnow and topminnow species (29 spp.) served as productive suitable native hosts. The mean number of juvenile mussels released per cyprinid per day was significantly higher for trials conducted at 22–25°C compared with those at 18–20°C, and 83% of trials conducted at 18–20°C using suitable host species produced no juveniles. Glochidia had a unique outline and shell morphometrics that distinguished P. cyphyus from seven other Chippewa River mussel species that produce similar sized glochidia. Using morphometrics we determined that mimic shiners (Notropis volucellus) were natural hosts for P. cyphyus, round pigtoe (Pleurobema sintoxia), and Wabash pigtoe (Fusconaia flava). Releasing mucus-bound glochidia has evolved in a variety of mussel species and may be more common than is currently realized. Our data show that P. cyphyus is a cyprinid host specialist, and propagation efforts for this species can be strengthened through improved access to mature glochidia by using females with cream-coloured gills and increased juvenile production through warmer fish holding temperatures.     

温度和pH值对羊毛织物尺寸稳定性的影响

通过一系列实验分析了温度和pH值对羊毛纤维的膨胀和羊毛织物尺寸变化的影响．在pH2．1的溶液中，羊毛织物的尺寸随温度的升高而下降，变化的幅度取决于织物组织和织物的定型率．在羊毛等电点pH4．8时，纤维的膨胀达到最小值，而织物的尺寸则随着溶液酸性的增加而减小．     

The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X

We constructed maps for eight chromosomes (1, 6, 9, 10, 13, 20, X and (previously) 22), representing one-third of the genome, by building landmark maps, isolating bacterial clones and assembling contigs. By this approach, we could establish the long-range organization of the maps early in the project, and all contig extension, gap closure and problem-solving was simplified by containment within local regions. The maps currently represent more than 94% of the euchromatic (gene-containing) regions of these chromosomes in 176 contigs, and contain 96% of the chromosome-specific markers in the human gene map. By measuring the remaining gaps, we can assess chromosome length and coverage in sequenced clones.     

Dispersal and extraterritorial movements of swift foxes ( Vulpes velox ) in northwestern Texas

Dispersal plays an important role in the population dynamics of many carnivores, yet little information exists about the dispersal and movement patterns of swift foxes ( Vulpes velox ). We radio-collared and monitored 68 swift foxes for dispersal at 2 study sites in northwestern Texas from January 2002 to April 2004. Dispersal distance for juveniles (13.1 ± 0.3 km, s ), adults (10 ± 4.7 km) and transients (25.4 ± 9.1 km) did not differ by age class ( F = 1.49, df = 2, P = 0.24) or sex ( F = 0.23, df = 1, P = 0.63) but differed by study site ( F = 4.72, df = 1, P = 0.04). Mean dispersal distance from private ranches (PR) was greater than from National Grasslands (NG). Peak dispersal occurred during October– November (13 individuals) and January–February (7 individuals). Dispersal direction was influenced by land-use practices (i.e., toward rangelands and away from anthropogenic features). Direction of dispersal among foxes that occupied the NG was uniform ( n = 16, P = 0.08), whereas foxes from PR dispersed in a northwesterly direction ( n = 18, P ≤ 0.001) away from a town and croplands. Three resident adult foxes made extraterritorial movements. Distances of these movements ranged from 0.2 km to 11.4 km. Distance of extraterritorial movements did not differ by sex ( F = 0.05, P = 0.83), nor by duration of movement ( F = 1.11, P = 0.32). Knowledge of movement distances and patterns is important for conservation and protection of swift foxes and their habitats.     

Holography in artificial neural networks

The dense interconnections that characterize neural networks are most readily implemented using optical signal processing. Optoelectronic 'neurons' fabricated from semiconducting materials can be connected by holographic images recorded in photorefractive crystals. Processes such as learning can be demonstrated using holographic optical neural networks.     

A novel brain ATPase with properties expected for the fast axonal transport motor

Identification of the ATPase involved in fast axonal transport of membranous organelles has proven difficult. Myosin and dynein, other ATPases known to be involved in cell motility, have properties that are inconsistent with the established properties of fast axonal transport, an essential component of which is readily solubilized in physiological buffer conditions rather than being stably associated with either membranous organelles or cytoskeletal elements. Adenylyl imidodiphosphate (AMP-PNP), a nonhydrolysable analogue of ATP, is a potent inhibitor of fast axonal transport that results in a stable interaction of membranous organelles with microtubules. Here we report the identification and partial characterization of an ATPase activity from brain whose binding to microtubules is stabilized by AMP-PNP. This ATPase activity seems to be associated with a polypeptide of relative molecular mass (Mr) 130,000 that is highly enriched in microtubule pellets after incubation with AMP-PNP and a soluble fraction from chick brain. This novel ATPase fraction has the predicted characteristics of the motor involved in fast axonal transport. Common features between the ATPase and fast axonal transport include interaction with the cytoskeleton in the presence of AMP-PNP, ready extractability, no Ca2+ dependence and inhibition by EDTA.     

Attachment of transported vesicles to microtubules in axoplasm is facilitated by AMP-PNP

Axoplasm extruded from the squid giant axon has been used to analyse the molecular mechanisms of intracellular vesicle transport. Using video-enhanced light microscopy, vesicle transport can be observed directly on individual microtubules at the edge of the axoplasm. Here we report that AMP-PNP (adenyl-5'-yl imidodiphosphate), a non-hydrolysable analogue of ATP, reversibly inhibited vesicle transport. Moreover, vesicles in solution attach to the microtubules and form relatively stable complexes. AMP-PNP may produce this effect by binding to an ATP-binding site on the transport machinery, thereby stabilizing the motility complex that is normally formed by a transported vesicle, an ATPase and a microtubule. The effects of AMP-PNP on the vesicle transport system indicate that the enzymatic machinery of this system differs significantly from that of the actomyosin system or the dynein-microtubule system.     

Gelsolin inhibition of fast axonal transport indicates a requirement for actin microfilaments

The actions of actin-based microfilaments in cell motility suggest a possible role in the mechanism of fast axonal transport, but the pharmacological data evaluating their role in this process are equivocal. Moreover, microfilaments are difficult to preserve and identify in ultrastructural studies, so the organization and function of axonal actin has remained uncertain. We have now evaluated the role of actin microfilaments in intracellular transport of membranous organelles using video-enhanced contrast microscopy and gelsolin to analyse fast axonal transport directly in isolated axoplasm from the squid giant axon. With this preparation it is possible to perfuse axoplasm with large molecules that do not cross the plasmalemma, while controlling cation levels. The 90,000-molecular weight protein gelsolin depolymerizes actin microfilaments in micromolar Ca2+, but not in the absence of Ca2+. Axonal transport of membranous organelles has previously been shown to be unaffected by levels of Ca2+ up to 10 microM. In the presence of EGTA, gelsolin has no effect on the movement of membranous organelles, but in the presence of 10 microM Ca2+ it completely blocks transport of all membranous organelles. No changes in the organization of the axoplasm were detected. These results and results using other probes for actin are consistent with the hypothesis that actin-based microfilaments are involved in the movement of membranous organelles in the axon.