The effects of minimal tillage, contour cultivation and in-field vegetative barriers on soil erosion and phosphorus loss.

Runoff, sediment, total phosphorus and total dissolved phosphorus losses in overland flow were measured for two years on unbounded plots cropped with wheat and oats. Half of the field was cultivated with minimum tillage (shallow tillage with a tine cultivator) and half was conventionally ploughed. Within each cultivation treatment there were different treatment areas (TA). In the first year of the experiment, one TA was cultivated up and down the slope, one TA was cultivated on the contour, with a beetle bank acting as a vegetative barrier partway up the slope, and one had a mixed direction cultivation treatment, with cultivation and drilling conducted up and down the slope and all subsequent operations conducted on the contour. In the second year, this mixed treatment was replaced with contour cultivation. Results showed no significant reduction in runoff, sediment losses or total phosphorus losses from minimum tillage when compared to the conventional plough treatment, but there were increased losses of total dissolved phosphorus with minimum tillage. The mixed direction cultivation treatment increased surface runoff and losses of sediment and phosphorus. Increasing surface roughness with contour cultivation reduced surface runoff compared to up and down slope cultivation in both the plough and minimum tillage treatment areas, but this trend was not significant. Sediment and phosphorus losses in the contour cultivation treatment followed a very similar pattern to runoff. Combining contour cultivation with a vegetative barrier in the form of a beetle bank to reduce slope length resulted in a non-significant reduction in surface runoff, sediment and total phosphorus when compared to up and down-slope cultivation, but there was a clear trend towards reduced losses. However, the addition of a beetle bank did not provide a significant reduction in runoff, sediment losses or total phosphorus losses when compared to contour cultivation, suggesting only a marginal additional benefit. The economic implications for farmers of the different treatment options are investigated in order to assess their suitability for implementation at a field scale

PKA Mediates Constitutive Activation of CFTR in Human Sweat Duct

The cystic fibrosis transmembrane conductance regulator (CFTR) Cl− channels are constitutively activated in sweat ducts. Since phosphorylation-dependent and -independent mechanisms can activate CFTR, we sought to determine the actual mechanism responsible for constitutive activation of these channels in vivo. We show that the constitutively activated CFTR Cl− conductance (gCFTR) in the apical membrane is completely deactivated following α-toxin permeabilization of the basolateral membrane. We investigated whether such inhibition of gCFTR following permeabilization is due to the loss of cytoplasmic glutamate or due to dephosphorylation of CFTR by an endogenous phosphatase in the absence of kinase activity (due to the loss of kinase agonist cAMP, cGMP or GTP through α-toxin pores). In order to distinguish between these two possibilities, we examined the effect of inhibiting the endogenous phosphatase activity with okadaic acid (10−8 M) on the permeabilization-induced deactivation of gCFTR. We show that okadaic acid (1) inhibits an endogenous phosphatase responsible for dephosphorylating cAMP but not cGMP or G protein-activated CFTR and (2) prevents deactivation of CFTR following permeabilization of the basolateral membrane. These results indicate that distinctly different phosphatases may be responsible for dephosphorylating different kinase-specific sites on CFTR. We conclude that the phosphorylation by PKA alone appears to be primarily responsible for constitutive activation of gCFTR in vivo

Maturation and Reproduction of Shovelnose Sturgeon in the Middle Mississippi River

Shovelnose sturgeon Scaphirhynchus platorynchus in the middle Mississippi River provide one of the last commercially viable sturgeon fisheries in the world, yet their maturation and reproduction have not been linked. During 2005 and 2006, we sampled adult and age-0 shovelnose sturgeon to link age at maturation, the timing and periodicity of spawning, age-0 sturgeon production, and the resulting age-0 growth rates. Age at maturity was later than previous estimates, the minimum age of first maturation being 8 years for males and 9 years for females. Total egg count was slightly lower than previously reported (mean = 29,573 per female; SE = 2,472). Males and females typically spawned every 2 and 3 years, respectively. Peaks in mature fish coincided with rising river stages and water temperatures at which shovelnose sturgeon probably spawn. Peaks in spent adults followed. Age-0 shovelnose sturgeon occurred during June and July 2005 and May and June 2006, confirming successful spawning. Age-0 sturgeon grew between 0.69 and 1.69 mm total length/d; four distinct weekly cohorts occurred each year. During fall 2006, females contained ripe eggs, males were milting, and a single age-0 sturgeon (total length = 55 mm) was captured, suggesting that shovelnose sturgeon spawn during fall as well as spring. Management must consider the protracted nature of spawning within seasons as well as differences in spawning activity between seasons

Long-Term PIT and T-Bar Anchor Tag Retention Rates in Adult Muskellunge

Mark-recapture studies require knowledge of tag retention rates specific to tag types, fish species and size, and study duration. We determined the probability of tag loss for passive integrated transponder (PIT) tags implanted into dorsal musculature, T-bar anchor tags attached to dorsal pterygiophores, and loss of both tags in relation to years post-tagging for double-marked adult muskellunge Esox masquinongy over a 10 year period. We also used PIT tags as a benchmark to assess the interactive effects of fish length at tagging, sex, and years post-tagging on T-bar anchor tag loss rates. Only five instances of PIT tag loss were identified; the calculated probability of a fish losing its PIT tag was consistently \u3c 1.0% for up to 10 years post-tagging. The probability of T-bar anchor tag loss by muskellunge was related to the number of years post-tagging and total length of fish at tagging. T-bar anchor tag loss rate one year after tagging was 6.5%. Individuals \u3c 750 mm total length at tagging had anchor tag loss rates \u3c 10% for up to 6 years after tagging. However, the proportion of fish losing T-bar anchor tags steadily increased with increasing years post-tagging (~30% after 6 years) for larger muskellunge. Fish gender did not influence probability of T-bar anchor tag loss. Our results indicate that T-bar anchor tags are best suited for short-term applications (≤ 1 year duration) involving adult muskellunge. We recommend use of PIT tags for longer-term tagging studies, particularly for muskellunge \u3e 750 mm total length