Increasing annual runoff—broadleaf or coniferous forests?

According to widely held belief, annual evapotranspiration (ET) for broadleaf forests is less than that for coniferous forests, resulting in higher annual runoff for broadleaf forests. We processed 82 catchment runoff and 126 interception loss data from temperate regions and found that although the belief is valid under conditions of broadleaf deciduous forests and high winter precipitation (e.g. the United States), it is invalid under conditions of broadleaf evergreen forests (e.g. New Zealand) or low winter precipitation (e.g. Japan). Thus, forest management policies based on this belief should be reconsidered on the basis of our results for regions with broadleaf evergreen forests or low winter precipitation. Copyright © 2010 John Wiley & Sons, Ltd.     

Are measurements from excised leaves suitable for modeling diurnal patterns of gas exchange of intact leaves?

To examine the feasibility of using ecophysiological data from excised leaves for a meteorological simulation model of gas exchange, we compared the obtained gas exchange rates and the modelled ones using excised leaves and those using intact leaves. Instantaneous gas exchange rates of excised leaves and stomatal control in response to environmental conditions were not significantly different from those of attached leaves. Modelled gas exchange rates based on excised leaf data showed a good fit to the diurnal patterns of in situ measurements. This suggests that use of excised leaf data to predict gas exchange of intact leaves is permissible as long as the effects of excision are pre‐screened as described in this paper. Copyright © 2011 John Wiley & Sons, Ltd.     

Magnetometer survey of the proposed Sirente meteorite crater field,central Italy: Evidence for uplifted crater rims and buried meteorites

Abstract— The Sirente crater field consists of a 120 m wide, rimmed main depression flanked to the northwest by about 30 smaller depressions. It has been dated to the first centuries A.D. An impact origin is suggested, but not confirmed. The small size combined with the properties of the target material (carbonate mud) would neither allow shock features diagnostic of impact, nor projectile vaporization. Consequently, a meteoritic component in the sediments would be very localized. At impacts of this size the projectile most likely is an iron meteorite. Any iron meteorites on the ground surface would, in Iron Age Europe, have been removed shortly after the event. However, if the depressions are of impact origin they should contain meteorites at great depth in analogy with known craters. The magnetic properties of iron meteorites differ distinctly from the very low magnetic sediments and sedimentary rocks of the Sirente area. We have used a proton precession magnetometer/gradiometer to produce magnetic anomaly maps over four of the smaller depressions (～8 m diameter), as well as two crossing profiles over a fifth depression (～22 m diameter). All show distinct magnetic anomalies of about 20 nT, the larger depression up to 100 nT. Magnetic modeling shows a best fit for structures with upturned strata below their rims, excluding a karstic origin but supporting an explosive formation. The 100 nT anomaly can only be explained by highly‐magnetic objects at a few meters depth. All together, the magnetic data provides a strong indication for an impact origin of the crater field.     

The insoluble carbonaceous material of CM chondrites: A possible source of discrete organic compounds under hydrothermal conditions

Abstract— We report on the molecular analyses of the water‐ and solvent‐soluble organic compounds released from the insoluble organic material (IOM) of the Murray meteorite upon treatment with weight‐equivalent amounts of water and under conditions of elevated temperature and pressure. A varied suite of compounds was identified by gas chromatography‐mass spectrometry (GC‐MS). C₃‐C₁₇ alkyl dicarboxylic acids and N‐ and O‐containing hydroaromatic and aromatic compounds were found in the water extracts. The solvent extracts contained N‐, O‐, and S‐containing aromatic compounds, a large number of their isomers and homologs, and a series of polycyclic aromatic hydrocarbons (PAHs) of up to five rings, together with noncondensed aromatic species such as substituted benzenes, biphenyl, and terphenyls as well as their substituted homologs, and hydrated PAHs. Isotopic analyses showed that residue IOMs after hydrothermal treatment had lower deuterium and ¹⁵N content than the untreated material (ΔD = ?833‰ and Δ¹⁵N = ?24.1) but did not differ from it in ¹³C composition. The effect of the hydrothermolytic release was recorded in significant differences between the NMR spectra of untreated and residue IOM. A possible relation to common precursors for the dicarboxylic acids found in the IOM and bulk extracts is discussed.     

Estimation of vertical profiles of leaf drying times after daytime rainfall within a Bornean tropical rainforest

South‐east Asian Bornean tropical rainforests have large and complex canopy structures. To clarify how forest structure affects wet‐canopy evaporation, it is necessary to consider wet‐canopy evaporation processes within the forest canopy, such as vertical profiles of canopy drying time. In a previous study a method was proposed that utilizes sap flow measurements to estimate canopy drying time after rainfall (CDTobs) during daytime. In this present study, the method was applied to estimations of the vertical variations in CDTobs in 11 individual trees of various heights, ranging from 2·7 m to 53 m. The study derived vertical profiles and showed that the lengths of CDTobs in lower canopy trees were 2–4 h longer than those in the upper canopy trees. The new method for CDTobs profiles presented in this study, which is available for validation of multi‐layer biosphere‐atmospheric models, is a useful illustration for clarifying wet‐canopy evaporation processes in tropical rainforests. Copyright © 2008 John Wiley & Sons, Ltd.     

Hydrogen isotopes in volcanic plumes: Tracers for remote temperature sensing of fumaroles

In high-temperature volcanic fumaroles (>400 °C), the isotopic composition of molecular hydrogen (H₂) reaches equilibrium with that of the fumarolic H₂O. In this study, we used this hydrogen isotope exchange equilibrium of fumarolic H₂ as a tracer for the remote temperature at volcanic fumaroles. In this remote sensing, we deduced the hydrogen isotopic composition (δD value) of fumarolic H₂ from those in the volcanic plume. To ascertain that we can estimate the δD value of fumarolic H₂ from those in a volcanic plume, we estimated the values in three fumaroles with outlet temperatures of 630 °C (Tarumae), 203 °C (Kuju), and 107 °C (E-san). For this we measured the concentration and δD value of H₂ in each volcanic plume, along with those determined directly at each fumarole. The average and maximum mixing ratios of fumarolic H₂ within a plume’s total H₂ were 97% and 99% (at Tarumae), 89% and 96% (at Kuju), and 97% and 99% (at E-san). We found a linear relationship between the depletion in the δD values of H₂, with the reciprocal of H₂ concentration. Furthermore, the estimated end-member δD value for each H₂-enriched component (−260 ± 30‰ vs. VSMOW in Tarumae, −509 ± 23‰ in Kuju, and −437 ± 14‰ in E-san) coincided well with those observed at each fumarole (−247.0 ± 0.6‰ in Tarumae, −527.7 ± 10.1‰ in Kuju, and −432.1 ± 2.5‰ in E-san). Moreover, the calculated isotopic temperatures at the fumaroles agreed to within 20 °C with the observed outlet temperature at Tarumae and Kuju. We deduced that the δD value of the fumarolic H₂ was quenched within the volcanic plume. This enabled us to remotely estimate these in the fumarole, and thus the outlet temperature of fumaroles, at least for those having the outlet temperatures more than 400 °C. By applying this methodology to the volcanic plume emitted from the Crater 1 of Mt. Naka-dake (the volcano Aso) where direct measurement on fumaroles was impractical, we estimated that the δD value of the fumarolic H₂ to be −172 ± 16‰ and the outlet temperature to be 868 ± 97 °C. The remote temperature sensing using hydrogen isotopes developed in this study is widely applicable to many volcanic systems.     

Pressure responses of portlandite and H–D isotope effects on pressure-induced phase transitions

The pressure responses of portlandite and the isotope effect on the phase transition were investigated at room temperature from single-crystal Raman and IR spectra and from powder X-ray diffraction using diamond anvil cells under quasi-hydrostatic conditions in a helium pressure-transmitting medium. Phase transformation and subsequent peak broadening (partial amorphization) observed from the Raman and IR spectra of Ca(OH)₂ occurred at lower pressures than those of Ca(OD)₂. In contrast, no isotope effect was found on the volume and axial compressions observed from powder X-ray diffraction patterns. X-ray diffraction lines attributable to the high-pressure phase remained up to 28.5 GPa, suggesting no total amorphization in a helium pressure medium within the examined pressure region. These results suggest that the H–D isotope effect is engendered in the local environment surrounding H(D) atoms. Moreover, the ratio of sample-to-methanol–ethanol pressure medium (i.e., packing density) in the sample chamber had a significant effect on the increase in the half widths of the diffraction lines, even at pressures below the hydrostatic limit of the pressure medium.     

Generation of adakites in a cold subduction zone due to double subducting plates

Adakites have been found in various tectonic settings, since the first report for the distinct lavas as a product of slab melting in Adak Island by Kay (J Volcanol Geotherm Res 4:117–132, 1978). In this study, we present geochemical data for an ‘adakite’ and ‘adakitic rock’ suite in central Japan with a cold subduction environment due to the two overlapping subducting plates: the Pacific plate and the Philippine sea plate. Based on the major, trace and isotopic compositions of the rocks, elemental transport from initial slab inventory at the trench to the volcanic rocks as a final product is quantitatively analyzed, considering the thermal structure, slab dehydration, elemental mobility, slab-fluid migration and melting of fluid-added mantle. The analysis demonstrates a large compositional impact of slab-fluid in the arc magma generation in central Japan. The melting conditions have been also estimated inversely by optimizing the predicted magma composition to the observed composition of volcanic rock, with the two parameters: the degree of melting and the proportion of spinel and garnet lherzolites involved in melting. Consequently, a moderately low degree of near-solidus melting of dominantly garnet lherzolite with a high fluid flux from the two overlapping slabs beneath the region has been argued to be responsible for the compositional characteristics, including the adakitic signatures, of the studied rocks. These results imply that the geochemical approach may provide useful constraints on the P–T condition of melting in the mantle wedge and the thermal structure in subduction zones, being complementary to the geophysical approach.