A field study on serum vitellogenin levels in male Reeves' pond turtles (Chinemys reevesii) from estrogen-contaminated sites and a reference site

To ascertain whether wild male turtles were influenced by environmental estrogens, we examined serum vitellogenin (VTG) levels of male Reeves' pond turtles (Chinemys reevesii) collected from four study sites (A-D) in Kyoto, Japan. Sites A-C, which were impacted by domestic or industrial wastewater and effluents from sewage treatment plants, were chosen as contaminated sites, and site D was intended as a reference site. This contaminated/reference site characterization was confirmed by measuring estrogenic activities of the water samples collected at each site for over a year. Serum VTG levels in the turtles were quantified by an enzyme-linked immunosorbent assay established previously. Estrogenic activities of the water samples were measured using a previously validated yeast two-hybrid assay and expressed as the estradiol-17beta equivalent. Estrogenic activity was observed at high levels at sites A-C, but was almost undetected at site D throughout the sampling period: the mean and range were 0.74 (<0.07-2.1), 0.52 (0.17-1.6), 1.7 (<0.07-7.3), and 0.07 (<0.07-0.62) ng/l at sites A-D, respectively. Significant differences were found only in site D versus sites A, B, and C. Therefore, site D and sites A-C were confirmed to be a reference site and contaminated ones, respectively. Overall, 320 male turtles were captured and examined. The majority of the turtles showed normal VTG values (0.10-0.74 microg/ml). Although only five turtles from sites A-C showed unusually high VTG values (1.1-5.9 microg/ml, nearly one order of magnitude higher than normal values but much lower than values in adult females), there was no significant difference in the incidence of these high values between sites A-C and site D. Moreover, among the five turtles, one turtle was captured again 2 months later, but its VTG value dropped to the normal level. The unusually high VTG values may therefore be transient elevation caused by incidental and/or individually specific agents. Excluding the unusually high values, the mean serum VTG (accompanied with the range) was 0.22 (0.10-0.74), 0.27 (0.11-0.62), 0.27 (0.17-0.68), and 0.23 (0.10-0.57) microg/ml at sites A-D, respectively. There were no significant differences in the mean VTG values among sites A-D. Although it should be clarified how and why the unusually high VTG values occurred at sites A-C, our results suggested that wild male C. reevesii turtles would not be significantly affected by xenobiotic estrogens at environmentally relevant levels in terms of serum VTG elevation.     

Activated carbon nanofiber produced from electrospun polyacrylonitrile nanofiber as a highly efficient formaldehyde adsorbent

Electrospun polyacrylonitrile (PAN)-based nanofiber with a uniform diameter of ca. 800 nm was carbonized and steam-activated to produce activated carbon nanofiber with tailored microporosity and abundant nitrogen-containing functional groups as highly efficient adsorption sites. A remarkable amount of formaldehyde, a typical indoor pollutant, was adsorbed onto the pore surface of the PAN-based activated carbon nanofibers even at a low concentration (ca. 11 ppm), demonstrating more than twice as long as breakthrough time of formaldehyde adsorption as compared to conventional activated carbon fibers of larger fiber diameter. The tailored shallow microporosity was considered to afford the preferential adsorption of formaldehyde also in a humid environment.     

Nanoscale Membrane Strips for Benign Sensing of HgII Ions: A Route to Commercial Waste Treatments

The integration of actively‐functional receptors into nanoscale networks outperformed competent detection devices and other ion‐sensing designs. Synthesis of azo chromophores with long hydrophobic tails showed an ecofriendly sensing and an extreme selectivity for divalent mercury analytes. In order to tailor the tip to Hg^II ion‐sensing functionality, we manipulated the chromophores into nanoscale membrane discs, which led to small, easy‐to‐use optical sensor strips. The design of these hydrophobic probes into ordered pore‐based membranes transformed the ion‐sensing systems into smart, stable assemblies and portable laboratory assays. The nanosensor membrane strips with chemical and mechanical stability allowed for reversible, stable and reusable detectors without any structural damage, even under rigorous chemical treatment for several numbers of repeated cycles. The optical membrane strips provided Hg^II ion‐sensing recognition for both cost‐ and energy‐saving systems. Indeed, the synthetic strips proved to have an efficient ability for various analytical applications, targeting especially for on‐site and in situ chemical analyses, and for continuous monitoring of toxic Hg^II ions. On the proximity‐sensing front, these miniaturized nanomembrane strips can revolutionize the consumer and industrial market with the introduction of the probe surface‐mount naked‐eye ion‐sensor strips.     

Optical Nanoscale Pool‐on‐Surface Design for Control Sensing Recognition of Multiple Cations

General design of optical chemical nanosensors is needed to develop efficient sensing systems with high flexibility, and low capital cost for control recognition of toxic analytes. Here, we designed optical chemical nanosensors for simple, high‐speed detection of multiple toxic metal ions. The systematic design of the nanosensors was based on densely patterned chromophores with intrinsic mobility, namely, “building‐blocks” onto three‐dimensional (3D) nanoscale structures. The ability to precisely modify the nanoscale pore surfaces by using a broad range of chromophores that have different molecular sizes and characteristics enables detection of multiple toxic ions. A key feature of this building‐blocks design strategy is that the surface functionality and good adsorption characteristics of the fabricated nanosensor arrays enabled the development of “pool‐on‐surface” sensing systems in which high flux of the metal analytes across the probe molecules was achieved without significant kinetic hindrance. Such a sensing design enabled sensitive recognition of metal ions up to sub‐picomolar detection limits (～10^?11 mol dm^?3), for first time, with rapid response time within few seconds. Moreover, because these sensing pools exhibited long‐term stability, reversibility and selectivity in detecting most pollutant cations, for example, Cr(VI), Pb(II), Co(II), and Pd(II) ions, they are practical and inexpensive. The key result in our study is that the pool‐on‐surface design for optical nanosensors exhibited significant ion‐selective ability of these target ions from environmental samples and waste disposals.     

Pore Structure Evolution of Lanthana–Alumina Systems Prepared through Coprecipitation

Pure Al₂O₃ and different compositions of La₂O₃–Al₂O₃ samples have been prepared through coprecipitation. Even after heating at 1300°C, the compositions La₂O₃·11Al₂O₃ and La₂O₃·13Al₂O₃ had higher surface area compared to the pure Al₂O₃ and the La₂O₃·Al₂O₃ composition. Ethanol washing is an effective way for improving the textural stability of pure Al₂O₃ and La₂O₃–Al₂O₃ samples. The effect of steam on the thermal stability of La₂O₃·11Al₂O₃ has also been studied. La₂O₃·11Al₂O₃ sample is found to be stable in steam.     

Effect of molecular weight distribution of mineral oils on their boiling heat transfer behaviour

The range of molecular weight distribution of mineral oils has a significant effect on lubrication because it affects the thermal behaviour of the mineral oils.In view of the fact that boiling heat transfer is one of the most typical problems relevant to thermal phenomena, an investigation of boiling heat transfer from a horizontal platinum wire to mineral oils was carried out using (i) base oils characterized by narrow-range molecular weight distributions and (ii) blended oils characterized by wide-range distributions.The objective of the present study is to clarify the relationship between the range of molecular weight distribution and the boiling heat transfer behaviour of such oils.The results obtained show marked differences between base and blended oils in their boiling heat transfer behaviour, especially with respect to the heat transfer coefficients.An explanation of these differences was attempted in terms of correlation with the results of the present authors' previous investigations of the evaporation and spreading behaviour of droplets of these oils on a horizontal heating surface, both of which showed the essential differences between the base and blended oils in the heat and mass transfer properties.     

A 160-kDa Protein Is Essential for Hemocyanin-derived Melanosis of Prawn

ABSTRACT A purified 160-kDa protein, isolated from the cuticle of kurama prawn and named melanosis collaborating factor (MCF), was a key factor in promoting melanosis by a cooperative reaction with hemocyanin-derived phenoloxidase but hemocyanin itself was incapable of producing black pigment. The enzymatic activity of MCF in the body of the prawn was very stable against the process of freezing and thawing; the enzyme maintained more than 80% of its activity after 3 mo of storage at −2 5 °C. These results indicated that MCF, acting in conjunction with hemocyanin-derived phenoloxidase, played a crucial role in postharvest melanogenesis in prawn.