Seasonal changes of arsenic speciation in lake waters in relation to eutrophication

金沢大学理工研究域物質化学系In this study, the influence of eutrophication on arsenic speciation in lake waters was investigated. Surface water samples (n = 1-10) were collected from 18 lakes in Japan during July 2007 and February 2008. The lakes were classified into mesotrophic (7 lakes) and eutrophic (11 lakes) based on the total phosphate (T-P) and chlorophyll-a (Chl-a) concentrations in water column. Inorganic, methylated and ultraviolet-labile fractions of arsenic species were determined by combining hydride generation atomic absorption spectrometry with ultraviolet irradiation. Organoarsenicals (mainly methylated and ultraviolet-labile fractions) comprised 30-60% of the total arsenic in most lakes during summer. On the other hand, inorganic arsenic species (As(III + V)) dominates (about 60-85%) during winter. The occurrence of ultraviolet-labile fractions of arsenic was higher in eutrophic lakes than those in mesotrophic lakes in both seasons. The concentration of dimethyl arsenic (DMAA) was high in eutrophic lakes during winter; and in mesotrophic lakes during summer. The results suggest that the conversion of As(III + V) to more complicated organoarsenicals occurred frequently in eutrophic lakes compared to that in mesotrophic lakes, which is thought to be the influence of biological activity in the water column. The distribution of arsenic species were well correlated with phosphate concentrations than those of Chl-a. This might be due to the competitive uptake of As(V) and phosphate by phytoplankton. The organoarsenicals (OrgAs)/As(V) ratio was higher at low phosphate concentration indicating that conversion of As(V) to OrgAs species was more active in phosphate-exhausted lakes with high phytoplankton density. © 2009 Elsevier B.V. All rights reserved

Seasonal changes of arsenic speciation in lake waters in relation to eutrophication.

金沢大学理工研究域物質化学系In this study, the influence of eutrophication on arsenic speciation in lake waters was investigated. Surface water samples (n=1-10) were collected from 18 lakes in Japan during July 2007 and February 2008. The lakes were classified into mesotrophic (7 lakes) and eutrophic (11 lakes) based on the total phosphate (T-P) and chlorophyll-a (Chl-a) concentrations in water column. Inorganic, methylated and ultraviolet-labile fractions of arsenic species were determined by combining hydride generation atomic absorption spectrometry with ultraviolet irradiation. Organoarsenicals (mainly methylated and ultraviolet-labile fractions) comprised 30-60% of the total arsenic in most lakes during summer. On the other hand, inorganic arsenic species (As(III+V)) dominates (about 60-85%) during winter. The occurrence of ultraviolet-labile fractions of arsenic was higher in eutrophic lakes than those in mesotrophic lakes in both seasons. The concentration of dimethyl arsenic (DMAA) was high in eutrophic lakes during winter; and in mesotrophic lakes during summer. The results suggest that the conversion of As(III+V) to more complicated organoarsenicals occurred frequently in eutrophic lakes compared to that in mesotrophic lakes, which is thought to be the influence of biological activity in the water column. The distribution of arsenic species were well correlated with phosphate concentrations than those of Chl-a. This might be due to the competitive uptake of As(V) and phosphate by phytoplankton. The organoarsenicals (OrgAs)/As(V) ratio was higher at low phosphate concentration indicating that conversion of As(V) to OrgAs species was more active in phosphate-exhausted lakes with high phytoplankton density

On intermediate subfactors of Goodman-de la Harpe-Jones subfactors

In this paper we present a conjecture on intermediate subfactors which is a generalization of Wall's conjecture from the theory of finite groups. Motivated by this conjecture, we determine all intermediate subfactors of Goodman-Harpe-Jones subfactors, and as a result we verify that Goodman-Harpe-Jones subfactors verify our conjecture. Our result also gives a negative answer to a question motivated by a conjecture of Aschbacher-Guralnick.Comment: To appear in Comm. Math. Phy

Magnetic properties of the itinerant A-type antiferromagnet CaCo2P2 studied by Co-59 and P-31 nuclear magnetic resonance

Co-59 and P-31 nuclear magnetic resonance (NMR) measurements in external magnetic and zero magnetic fields have been performed to investigate themagnetic properties of the A-type antiferromagnetic (AFM) CaCo2P2. NMR data, especially the nuclear spin lattice relaxation rates 1/T-1 exhibiting a clear peak, provide clear evidence for the AFM transition at a Ned temperature of T-N similar to 110 K. The magnetic fluctuations in the paramagnetic state were found to be three-dimensional ferromagnetic, suggesting ferromagnetic interaction between Co spins in the ab plane characterizes the spin correlations in the paramagnetic state. In the AFM state below T-N, we have observed Co-59 and P-31 NMR signals under zero magnetic field. From Co-59 NMR data, theordered magnetic moments of Co are found to be in ab plane and are estimated to be 0.35 mu(B) at 4.2 K. Furthermore, the external field dependence of Co-59 NMR spectrum in the AFM state suggests a very weak magnetic anisotropy of the Co ions and also provides microscopic evidence of canting the Co-ordered moments along the external magnetic field directions. The magnetic state of the Co ions in CaCo2P2 is well explained by the local-moment picture in the AFM state, although the system is metallic, as seen by 1/T1T = constant behavior

Three-Dimensional Radiofrequency Tissue Tightening: A Proposed Mechanism and Applications for Body Contouring

The use of radiofrequency energy to produce collagen matrix contraction is presented. Controlling the depth of energy delivery, the power applied, the target skin temperature, and the duration of application of energy at various soft tissue levels produces soft tissue contraction, which is measurable. This technology allows precise soft tissue modeling at multiple levels to enhance the result achieved over traditional suction-assisted lipectomy as well as other forms of energy such as ultrasonic and laser-generated lipolysis

Learning strikes again: The case of the DRS signature scheme

Lattice signature schemes generally require particular care when it comes to preventing secret information from leaking through signature transcript. For example, the Goldreich-Goldwasser-Halevi (GGH) signature scheme and the NTRUSign scheme were completely broken by the parallelepiped-learning attack of Nguyen and Regev (Eurocrypt 2006). Several heuristic countermeasures were also shown vulnerable to similar statistical attacks.At PKC 2008, Plantard, Susilo and Win proposed a new variant of GGH, informally arguing resistance to such attacks. Based on this variant, Plantard, Sipasseuth, Dumondelle and Susilo proposed a concrete signature scheme, called DRS, that has been accepted in the round 1 of the NIST post-quantum cryptography project.In this work, we propose yet another statistical attack and demonstrate a weakness of the DRS scheme: one can recover some partial information of the secret key from sufficiently many signatures. One difficulty is that, due to the DRS reduction algorithm, the relation between the statistical leak and the secret seems more intricate. We work around this difficulty by training a statistical model, using a few features that we designed according to a simple heuristic analysis.While we only recover partial information on the secret key, this information is easily exploited by lattice attacks, significantly decreasing their complexity. Concretely, we claim that, provided that signatures are available, the secret key may be recovered using BKZ-138 for the first set of DRS parameters submitted to the NIST. This puts the security level of this parameter set below 80-bits (maybe even 70-bits), to be compared to an original claim of 128-bits.</p

Dnmt3a regulates myeloproliferation and liver-specific expansion of hematopoietic stem and progenitor cells

DNMT3A mutations are observed in myeloid malignancies, including myeloproliferative neoplasms (MPN), myelodysplastic syndromes (MDS), and acute myeloid leukemia (AML). Transplantation studies have elucidated an important role for Dnmt3a in stem cell self-renewal and in myeloid differentiation. Here we investigated the impact of conditional hematopoietic Dnmt3a loss on disease phenotype in primary mice. Mx1-Cre-mediated Dnmt3a ablation led to the development of a lethal, fully penetrant myeloproliferative neoplasm with myelodysplasia (MDS/MPN) characterized by peripheral cytopenias and by marked, progressive hepatomegaly. We detected expanded stem/progenitor populations in the liver of Dnmt3a-ablated mice. The MDS/MPN induced by Dnmt3a ablation was transplantable, including the marked hepatomegaly. Homing studies showed that Dnmt3a-deleted bone marrow cells preferentially migrated to the liver. Gene expression and DNA methylation analyses of progenitor cell populations identified differential regulation of hematopoietic regulatory pathways, including fetal liver hematopoiesis transcriptional programs. These data demonstrate that Dnmt3a ablation in the hematopoietic system leads to myeloid transformation in vivo, with cell autonomous aberrant tissue tropism and marked extramedullary hematopoiesis (EMH) with liver involvement. Hence, in addition to the established role of Dnmt3a in regulating self-renewal, Dnmt3a regulates tissue tropism and limits myeloid progenitor expansion in vivo

Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutation

<p>Abstract</p> <p>Background</p> <p>Variants of mitochondrial DNA (mtDNA) have been evaluated for their association with hearing loss. Although ethnic background affects the spectrum of mtDNA variants, systematic mutational analysis of mtDNA in Japanese patients with hearing loss has not been reported.</p> <p>Methods</p> <p>Using denaturing high-performance liquid chromatography combined with direct sequencing and cloning-sequencing, Japanese patients with prelingual (N = 54) or postlingual (N = 80) sensorineural hearing loss not having pathogenic mutations of m.1555A > G and m.3243A > G nor <it>GJB2 </it>were subjected to mutational analysis of mtDNA genes (<it>12S rRNA</it>, <it>tRNA</it>^{<it>Leu(UUR)</it>}, <it>tRNA</it>^{<it>Ser(UCN)</it>}, <it>tRNA</it>^<it>Lys</it>, <it>tRNA</it>^<it>His</it>, <it>tRNA</it>^{<it>Ser(AGY)</it>}, and <it>tRNA</it>^<it>Glu</it>).</p> <p>Results</p> <p>We discovered 15 variants in <it>12S rRNA </it>and one homoplasmic m.7501A > G variant in <it>tRNA</it>^{<it>Ser(UCN)</it>}; no variants were detected in the other genes. Two criteria, namely the low frequency in the controls and the high conservation among animals, selected the m.904C > T and the m.1105T > C variants in <it>12S rRNA </it>as candidate pathogenic mutations. Alterations in the secondary structures of the two variant transcripts as well as that of m.7501A > G in <it>tRNA</it>^{<it>Ser(UCN) </it>}were predicted.</p> <p>Conclusions</p> <p>The m.904C > T variant was found to be a new candidate mutation associated with hearing loss. The m.1105T > C variant is unlikely to be pathogenic. The pathogenicity of the homoplasmic m.7501T > A variant awaits further study.</p