Isometric force development, isotonic shortening, and elasticity measurements from Ca(2+)-activated ventricular muscle of the guinea pig

Isometric tension and isotonic shortening were measured at constant levels of calcium activation of varying magnitude in mechanically disrupted EGTA-treated ventricular bundles from guinea pigs. The results were as follows: (a) The effect of creatine phosphate (CP) on peak tension and rate of shortening saturated at a CP concentration more than 10 mM; below that level tension was increased and shortening velocity decreased. We interpreted this to mean that CP above 10 mM was sufficient to buffer MgATP(2-) intracellularly. (b) The activated bundles exhibited an exponential stress-strain relationship and the series elastic properties did not vary appreciably with degree of activation or creatine phosphate level. (c) At a muscle length 20 percent beyond just taut, peak tension increased with Ca(2+) concentration over the range slightly below 10(-6) to slightly above 10(-4)M. (d) By releasing the muscle length-active tension curves were constructed. Force declined to 20 percent peak tension with a decrease in muscle length (after the recoil) of only 11 percent at 10(-4)M Ca(2+) and 6 percent at 4x10(-6)M Ca(2+). (e) The rate of shortening after a release was greater at lower loads. At identical loads (relative to maximum force at a given Ca(2+) level), velocity at a given time after the release was less at lower Ca(2+) concentrations; at 10 M(-5), velocity was 72 percent of that at 10(-4)M, and at 4x10(-6)M, active shortening was usually delayed and was 40 percent of the velocity at 10(-4) M. Thus, under the conditions of these experiments, both velocity and peak tension depend on the level of Ca(2+) activation over a similar range of Ca(2+) concentration.     

A PCR-Based Genetic Map for Human Chromosome 3

Oligonucleotide primers for 125 simple sequence repeat microsatellite-based genetic markers have been assayed by polymerase chain reaction (PCR) in the CEPH reference family panel. These microsatellites include 101 dinucleotide repeats as well as 24 new tetranucleotide repeats. The average heterozygosity of this marker set was 72.4%. Genetic data were analyzed with the genetic mapping package LINKAGE. A subset of these microsatellite markers define a set of 56 uniquely ordered loci (>1000:1 against local inversion) that span 271 cM. Sixty-seven additional loci were tightly linked to markers on the uniquely ordered map, but could not be ordered with such high precision. These markers were positioned by CMAP into confidence intervals. One hundred thirteen of the microsatellite markers were also tested on a chromosome 3 framework somatic cell hybrid panel that divides this chromosome into 23 cytogenetically defined regions, integrating the genetic and physical maps of this chromosome. The high density, high heterozygosity, and PCR format of this genetically and physically mapped set of markers will accelerate the mapping and positional cloning of new chromosome 3 genes.     

Sodium absorption by barley roots: its mediation by mechanism 2 of alkali cation transport

Radioactively labeled Na⁺ absorbed by barley roots was sequestered in an intracellular compartment or compartments (“inner” spaces) in which it was only very slowly exchangeable with exogenous Na⁺. Absorption of this fraction proceeded at a constant rate for at least 1 hour.     

Spatial Use and Survivorship of Translocated Wild-Caught Texas Horned Lizards

The Texas horned lizard (Phrynosoma cornutum), a state threatened species in Texas, USA, appears to be declining throughout much of its distribution. Because of popular interest in restoring lizard populations, we conducted a 3-year radio-telemetric study to evaluate the feasibility of reintroducing Texas horned lizards into previously occupied areas with suitable habitat characteristics. We translocated lizards from natural populations in western Texas to the McGillivray and Leona McKie Muse Wildlife Management Area (MWMA) in the Cross Timbers and Prairies of north-central Texas, an ecoregion that has experienced apparent local extirpations of horned lizards. We translocated lizards after partly restoring a 32.5-ha portion of the MWMA from ashe juniper (Juniperus ashei)-honey mesquite (Prosopis glandulosa) woodland to mid-grass prairie. After a 10-day acclimation period and soft release, we tracked 57 horned lizards from March 2014 to October 2016 to evaluate daily movements, spatial use, sources of mortality, reproduction, and changes in body condition. Daily movement averages (1.16–174.18 m) and area used by individuals (<0.01–6.81 ha) were similar to those recorded for natural populations, with peaks in movement occurring in May and June. Annual survivorship for individuals (1.1–47.2%) was also similar to that reported from natural populations; however, survivorship declined across the 3 active seasons. Although mortality of translocated lizards was high, body condition remained relatively stable across active seasons, and reproduction occurred each year, indicating that translocation could be a viable option for restoring horned lizard populations to previously occupied parts of their range. © 2019 The Wildlife Society.     

Active Silicon Uptake by Wheat

The absorption of Si by wheat, Triticum aestivum L. ‘Yecora Rojo,’ followed Michaelis–Menten kinetics over a concentration range of 0.004–1.0 mM. K_m and V_max were determined using linear transformations and the calculated curve fitted the data closely. The absorption resulted in accumulation ratios of 200/1 or more. In keeping with that finding, this study also demonstrated that Si uptake by wheat is under metabolic control, being severely restricted by dinitrophenol (DNP) and potassium cyanide (KCN). Silicon uptake by wheat was not significantly affected by phosphate ions, but the chemical analog Ge exerted a direct competitive effect on Si uptake, and vice versa.