Nitrogen uptake in light versus darkness of the seagrass Zostera noltei: integration with carbon metabolism

We conducted a study that shows that light and dark conditions do not affect the uptake rates of ammonium and nitrate by the seagrass Zostera noltei. This is an important advantage over some seaweed species in which these rates are severely reduced at night. In the light, the ammonium uptake rates were initially higher (15 and 20 μmol·g^?1·h^?1) and stabilized at a rate of 5 μmol·g^?1·h^?1 after 1 h, whereas in the dark the rates remained constant at a rate of 10 μmol·g^?1·h^?1 over the first 180 min of incubation. The rates of nitrate uptake in the light were high within the first 120 min of incubation (7.2–11.1 μmol·g^?1·h^?1) and decreased afterwards to lower values (0.8–3.9 μmol·g^?1·h^?1), whereas in the dark the rates fluctuated around 0.0–11.1 μmol·g^?1·h^?1 throughout the whole incubation time (7 h). The soluble sugar content of Z. noltei leaves increased significantly with both ammonium and nitrate incubations in the light, indicating the metabolic outcome of photosynthesis. In the dark, there was no significant variation in either the soluble sugar or in the starch content of leaves, rhizomes or roots in either the ammonium or nitrate incubations. However, the total starch content of plants decreased at night whereas the total soluble sugars increased, suggesting a process of starch catabolism to generate energy with the consequent production of smaller monosaccharide products. The starch content of rhizomes decreased significantly during the light incubations with nitrate but not with ammonium. These results suggest that carbohydrate mobilization is necessary for Z. noltei to account for extra energetic costs needed for the uptake and assimilation of nitrate. Furthermore, our results suggest that nitrate uptake, at least during the day, requires the mobilization of starch whereas the uptake of ammonium does not.     

Sensitivity Analysis of Time Dependent Settlements in Hydraulic Fills

This paper reports some numerical investigation carried out on hydraulic fills. A methodology based on the numerical solution of the governing equation via the finite volume method is introduced and tested, and proven to be very efficient. Typical dimensional performance curves are obtained and the influence of governing parameters is discussed. A sensitivity analysis is carried out in order to characterize the influence of the numerous parameters used to simulate the time dependent settlement in hydraulic fills on the outputs of the model.     

Origin and evolution of a salty gypsum/anhydrite karst spring: the case of Poiano (Northern Apennines, Italy)

Poiano is the largest karst spring of the Emilia Romagna region (northern Italy). It drains an aquifer of unique properties composed of anhydrite with halite lenses at depth and gypsum at the surface (both with high NaCl content). Hydrogeological research has been undertaken using automatically recorded hourly data on temperature, electrical conductivity, and water level. Water feeding the Poiano spring is restricted within the gypsum/anhydrite outcrop between the Lucola, Sologno and Secchia rivers. Karstification in the Upper Secchia Valley only concerns the gypsum rocks mainly present along the border and in the shallower parts of the sulfate outcrop and does not appear to occur at depth. Data strongly support the hypothesis that the salt content in the spring water derives from active halokinetic movements. For the first time, the fundamental hydrogeological importance of the anhydrite part inside the sulfate rocks is demonstrated. If gypsum prevails over anhydrite the karst drainage network can extend deep into the rocks following a network of fractures and fissures. Instead, if in the deep parts of the aquifer anhydrite prevails over gypsum, the karst evolution cannot take place at depth and the structure of the underground drainage paths only follows near-surface paths in gypsum.     

Emission estimates of methyl chloride from industrial sources in China based on high frequency atmospheric observations

Methyl Chloride (CH₃Cl) is a chlorine-containing trace gas in the atmosphere contributing significantly to stratospheric ozone depletion (Carpenter et al. 2014). In the global CH₃Cl budget, the atmospheric CH₃Cl emissions is predominantly maintained by natural sources, of which magnitudes have been relatively well-constrained. However, significant uncertainties still remain in the CH₃Cl emission strengths from anthropogenic sources. High-frequency and high-precision in situ measurements of atmospheric CH₃Cl concentrations obtained since 2008 at Gosan station (a remote background site in the East Asia) reveal significant pollution events superimposed on the seasonally varying regional background levels. Back trajectory statistics showed that air masses corresponding to the observed CH₃Cl enhancement largely originated from regions of intensive industrial activities in China. Based on an inter-species correlation method, estimates of CH₃Cl emissions from manufacturing industries including coal combustion, use of feedstocks, or process agents in chemical production for China (2008–2012) are 297 ± 71 Gg yr.^?1 in 2008 to 480 ± 99 Gg yr.^?1 in 2009, followed by a gradual decrease of about 25% between 2009 and 2012 (398 ± 92 Gg yr.^?1 for 2010; 286 ± 68 Gg yr.^?1 for 2011; 358 ± 92 Gg yr.^?1 for 2012). The annual average of industrial CH₃Cl emissions for 2008–2012 (363 ± 85 Gg yr.^?1) in China is comparable to the known total global anthropogenic CH₃Cl emissions accounting only for coal combustion and indoor biofuel use. This may suggest that unless emissions from the chemical industry are accounted for, global anthropogenic emissions of CH₃Cl have been substantially underestimated. In particular, since industrial production and use of CH₃Cl have not been regulated under the Montreal Protocol (MP) or its successor amendments, continuous monitoring of Chinese CH₃Cl outflow is important to properly evaluate its anthropogenic emissions.     

Damage evaluation and conservation treatment of the tenth century Korean rock-carved Buddha statues

This study focuses on the lithological characterization, quantitative deterioration assessment and conservation treatment of the tenth century rock-carved Buddha statues in Korea. The Buddha statues were carved on light gray macrocrystalline biotite granite, and features microcline phenocrysts and pegmatite patches. The rock-forming minerals are quartz, plagioclase, microcline and biotite showing micrographic and porphyritic textures. Feldspars and biotite in the host rock have been partly altered into sericite and chlorite by weathering. The surface of the Buddha statues is remarkably irregular due to granular disintegration and the differential weathering of the quartz and microcline. In addition, horizontal and vertical cracks in the host rock have promoted mechanical weathering. Biological colonization of the statues was serious, and featured dark gray and yellowish green lichen, dark green bryophyte and some plants. The Buddha statues were evaluated as the highly weathered rock by ultrasonic survey. The lower parts under the influence of water and areas with severely broken surfaces showed a much more advanced weathering grade. Therefore, scientific conservation treatment was carried out for the long-term maintenance and conservation of the Buddha statues. After pretests, dry, wet and chemical cleanings were applied to the statues. Next, joining of cracked parts and surface consolidating were executed. Finally, the site environment was improved by installation of drain and trimming trees around the statues to ensure more stable long-term conservation.     

Chemical and isotopic compositions of groundwater and stream water in a heavy agricultural basin of Korea

The chemical and isotopic compositions of groundwater and stream water in the Haean basin, Korea, which have been intensively used for agricultural irrigation, were examined. The field parameters and chemical compositions were typical of relatively uncontaminated waters, except for the agricultural impact. The low EC levels indicated that the waters had not experienced any significant geochemical processes such as water-rock interaction and evaporation. The very similar chemical compositions and ionic ratios were also indicative of fast circulation and good hydraulic connection. The oxygen and hydrogen isotopic compositions of most of the samples in wet and dry seasons showed very similar range which indicated a single source for both waters without any significant geochemical alteration. However, in the wet season, evaporation trends were observed in some groundwaters because of inflow of irrigation return flow from a rice paddy field. The isotopes of both waters were affected by the altitude and amount of precipitation.     

29Si and 27Al magic-angle-spinning NMR studies of the thermal transformation of kaolinite

Thermal transformations of kaolinite of different degree of crystallinity have been monitored by ²⁷Al and ²⁹Si high-resolution NMR with magic-angle spinning (MAS NMR), X-ray diffraction, Fourier transform infrared, atomic absorption spectrophotometry and thermogravimetric analysis. NMR shows differences in the dehydroxylation process of kaolinites with different degree of crystallinity and reveals the presence of short-range order in metakaolinite. ²⁹Si NMR spectra acquired with a 30 s recycle delay of poorly and highly crystalline samples heated at 480 and 500° C, respectively, contain three distinct signals; we discuss their assignment in the light of experiments involving leaching of the samples with aqueous KOH. Ca. 40% of Si sites retain their original Q ³ symmetry just above the onset of dehydroxylation and the Q ⁴ environment is present showing that a small amount of amorphous silica has already segregated. The spectrum of samples treated at 1000° C contains a signal at -110ppm (from Q ⁴ silicons) and a faint resonance, from mullite, at ca. -87 ppm. ²⁹Si NMR also shows that cristobalite germs are already present at 950–1000° C. The ²⁷Al MAS NMR spectra of metakaolinite reveal the presence of 4-, 5-and 6-coordinated Al. Changes in the three Al populations as a function of temperature have been monitored quantitatively. Below 800° C, 4-and 5-coordinated Al appears at the expense of 6-coordinated Al, but above 800° C the amount of 6-coordinated Al increases again. We suggest a dehydroxylation scheme which accounts for the presence of 4-and 5 coordinated Al. Above 900–950° C the latter signal is no longer present in the ²⁷Al NMR spectra and new 4-and 6-coordinated Al species (mullite and γ-alumina) appear. We propose new ideas for the structure of metakaolinite.