Correction to: Sedimentary phosphorus accumulation and distribution in the continuum of three cascade dams (Creuse River, France).

The missing Electronic Supplementary Material in the original paper is included in this paper.

Sedimentary phosphorus accumulation and distribution in the continuum of three cascade dams (Creuse River, France).

Dam construction leads to both sediment discontinuities and the creation of internal phosphorus (P) loads in reservoirs capable of supporting eutrophication. Today, majority of large rivers are dammed and numerous of these infrastructures are constructed in cascade. However, few studies focus on the cumulative effect of the presence of dam on sediment P mobility and bioavailability in downstream reservoirs and rivers parts or throughout the continuum.

Phosphorus mobility in dam reservoir affected by redox oscillations: An experimental study.

The internal sedimentary phosphorus (P) load of aquatic systems is able to support eutrophication, especially in dam-reservoir systems where sedimentary P stock is high and where temporary anaerobic conditions occur. The aim of this study therefore is to examine the response of sedimentary P exposed to redox oscillations. Surface sediments collected in the Champsanglard dam-reservoir (on the Creuse River, France) were subjected to two aerobic phases (10 and 12 days) alternated with two anaerobic periods (21 and 27 days) through batch incubations.

Self-blood pressure monitoring in an urban, ethnically diverse population: a randomized clinical trial utilizing the electronic health record.

Background: Hypertension is a leading risk factor for cardiovascular disease. Although control rates have improved over time, racial/ethnic disparities in hypertension control persist. Self-blood pressure monitoring, by itself, has been shown to be an effective tool in predominantly white populations, but less studied in minority, urban communities.

Elimination of the BK(Ca) channel's high-affinity Ca(2+) sensitivity.

We report here a combination of site-directed mutations that eliminate the high-affinity Ca(2+) response of the large-conductance Ca(2+)-activated K(+) channel (BK(Ca)), leaving only a low-affinity response blocked by high concentrations of Mg(2+). Mutations at two sites are required, the "Ca(2+) bowl," which has been implicated previously in Ca(2+) binding, and M513, at the end of the channel's seventh hydrophobic segment. Energetic analyses of mutations at these positions, alone and in combination, argue that the BK(Ca) channel contains three types of Ca(2+) binding sites, one of low affinity that is Mg(2+) sensitive (as has been suggested previously) and two of higher affinity that have similar binding characteristics and contribute approximately equally to the power of Ca(2+) to influence channel opening.