Precise estimation of hourly global solar radiation for micrometeorological analysis by using data classification and hourly sunshine

We have developed a method for estimating hourly global solar radiation (GSR) from hourly sunshine duration data. This procedure requires only hourly sunshine duration as the input data and utilizes hourly precipitation and daily snow cover as auxiliary data to classify time intervals into six cases according to weather conditions. To obtain hourly GSR using a simple algebraic form, a quadratic function of the solar elevation angle and the sunshine duration ratio is used. Daily GSR is given by a sum of hourly GSRs. We evaluated the performance of the newly developed method using data obtained at 67 meteorological stations and found that the estimated GSR is highly consistent with that observed. Hourly and daily root-mean-square misfits are approximately 0.2 MJ/m²/h (~55 W/m²) and 1.4 to 1.5 MJ/m²/day (~16 to 17 W/m²), respectively. Our classification of weather conditions is effective for reducing estimation errors, especially under cloudy skies. Since the sunshine duration is observed at more meteorological stations than GSR, the proposed new method is a powerful tool for obtaining solar radiation with hourly resolution and a dense geographical distribution. One of the proposed methods, GSRgrn, can be applicable to hourly GSR estimations at different observation sites by setting local parameters (the precipitable water, surface albedo, and atmospheric turbidity) suitable to the sites. The hourly GSR can be applied for various micrometeorological studies, such as the heat budget of crop fields.     

Flushing rate and salinity may control the blooms of the toxic dinoflagellate Alexandrium tamarense in a river/estuary in Osaka Bay, Japan

The first observation of a red tide of the toxic dinoflagellate Alexandrium tamarense in the Yodo River estuary, Osaka Bay, Japan was in the spring of 2007. To clarify which environmental factors controlled the abundance of A. tamarense, field surveys were conducted in 2008 and 2009. In 2008, the increase of A. tamarense occurred from early to mid-March and temperatures ranged from 9 to 13 °C. In contrast, in 2009, the increase was 1 month later, from early to mid-April and therefore temperatures were higher. In both years, A. tamarense was most abundant when salinities were relatively high (15–25), river discharge was low, and the water column was stable. There were no cells during periods of low salinity (<10), high discharge. In 2008, possibly silicate and phosphate were limiting during the simultaneous diatom and A. tamarense bloom in early March with silicate restricting the further growth of diatoms. In this estuarine basin, freshwater discharge from the weir increased the flow rate at stations downstream of the weir and deterred bloom formation by A. tamarense. Conversely, the lack of discharge increased the salinity and stability of the water column and decreased in the flow rate in the river/estuary. This process promoted the initiation of the bloom of A. tamarense and the subsequent accumulation of paralytic shellfish toxin in the brackish water clam Corbicula japonica. It is recommended that a constant discharge from the weir is maintained in order to prevent blooms of A. tamarense and subsequent paralytic shellfish poisoning (PSP) incidents in this area.     

Calorimetric measurements of fusion enthalpies for Ni2SiO4 and Co2SiO4 olivines and application to olivine-liquid partitioning

Calorimetric measurements of fusion enthalpies for Ni₂SiO₄ and Co₂SiO₄ olivines were carried out using a high-temperature calorimeter, and Ni and Co partitioning between olivine and silicate liquid was analyzed using the measured heats of fusion. The fusion enthalpy of Co₂SiO₄ olivine measured by transposed-temperature drop calorimetry was 103 ± 15 kJ/mol at melting point (1688 K). The fusion enthalpy of Ni₂SiO₄ olivine was calculated based on the enthalpies of liquids in the system An₅₀Di₅₀-Ni₂SiO₄ measured by transposed-temperature drop calorimetry at 1773 K, and was 221 ± 26 kJ/mol at its metastable melting point (1923 K). The fusion enthalpy of Ni₂SiO₄ is the largest among those of olivine group, this is caused by the large crystal field stabilization energy of six-coordinated Ni²⁺ in olivine. The larger fusion enthalpy of Ni₂SiO₄ can account for the large and variable partition coefficient of Ni between olivine and silicate liquid. Based on the comparison between partition coefficients calculated from thermodynamic data and those observed in partition experiments, it is considered that the magnitude of partition coefficients is primarily dependent on the heats of fusion of the components. Furthermore, the activity coefficients for Ni-, Co- and Mn-bearing components in magmatic liquid are nearly of the same magnitude.     

Results from Nobeyama Radio Observatory (NRO) —A progress report

The title telescope — in operation since 1982 — gives a surface accuracy of better than 0.2 mm (r.m.s.), with an aperture efficiency of about 25% at 115 GHz. A 5-element interferometer is at final adjustment stage. Observations of proto-stellar objects, extragalactic objects, and spectral lines are briefly described.Paper presented at the IAU Third Asian-Pacific Regional Meeting, held in Kyoto, Japan, between 30 September–6 October, 1984.     

Effects of ground water exchange on the hydrology and ecology of surface water

Ground water exchange affects the ecology of surface water by sustaining stream base flow and moderating water-level fluctuations of ground water-fed lakes. It also provides stable-temperature habitats and supplies nutrients and inorganic ions. Ground water input of nutrients can even determine the trophic status of lakes and the distribution of macrophytes. In streams the mixing of ground water and surface water in shallow channel and bankside sediments creates a unique environment called the hyporheic zone, an important component of the lotic ecosystem. Localized areas of high ground water discharge in streams provide thermal refugia for fish. Ground water also provides moisture to riparian vegetation, which in turn supplies organic matter to streams and enhances bank resistance to erosion. As hydrologists and ecologists interact to understand the impact of ground water on aquatic ecology, a new research field called "ecohydrology" is emerging.     

Element partitioning between olivine and silicate melt under high pressure

Element partitioning between olivine and silicate melt has been investigated at pressures 1–14 GPa, by using a 6–8 type multi-anvil high pressure apparatus. In order to observe systematics in the partitioning of trivalent ions, Li was added to the starting materials in order to increase the concentration of trivalent ions in olivine. With increasing pressure, it was found that partition coefficients of most of the elements gradually decreased. Trivalent ions generally showed parabolic pattern on partition coefficient — ionic radius diagram. When pyrolite-like material was used as the starting material, partition coefficient of Al, D_Al, gradually increased with increase in pressure while the partition coefficients of the other elements decreased, and the D_Al deviated from the parabolic pattern of other trivalent ions. The deviation of D_Al from the D pattern of the other trivalent ions was also found when olivine was employed as main component of the starting material. This result may be ascribed to the compositional change of coexisting silicate melt with increase in pressure.     

Calorimetric study of high-pressure polymorphs of MnSiO3

With increasing pressure, MnSiO₃ rhodonite stable at atmospheric pressure transforms to pyroxmangite, then to clinopyroxene and further to tetragonal garnet, which finally decomposes into MnO (rocksalt) plus SiO₂ (stishovite). High temperature solution calorimetry of synthetic rhodonite, clinopyroxene and garnet forms of MnSiO₃ was used to measure the enthalpies of these transitions. ΔH ₉₇₄ ⁰ for the rhodonite-clinopyroxene and ΔH ₂₉₈ ⁰ for the clinopyroxene-garnet transition are 520±490 and 8,270±590 cal/mol, respectively. The published data on the enthalpy of the rhodonite-pyroxmangite transition, phase equilibrium boundaries, compressibility and thermal expansion data are used to calculate entropy changes for the transitions. The enthalpy, entropy and volume changes are very small for all the transitions among rhodonite, pyroxmangite and clinopyroxene. The calculated boundary for the clinopyroxene-garnet transition is consistent with the published experimental results. The pyroxene-garnet transition in several materials, including MnSiO₃, is characterized by a relatively small negative entropy change and large volume decrease, resulting in a small positiveP – T slope. The disproportionation of MnSiO₃ garnet to MnO plus stishovite and of Mn₂SiO₄ olivine to garnet plus MnO are calculated to occur at about 17–18 and 14–15 GPa, respectively, at 1,000–1,500 K.     

Prograde pressure-temperature path of jadeite-bearing eclogites and associated high-pressure/low-temperature rocks from western Tianshan, northwest China

Abstract Jadeite‐bearing eclogites and associated blueschists locally crop out in a greenschist facies area at Kuldkourla, near the Akeyazhi River in the western Chinese Tianshan region, northwestern China. Garnet in these metamorphic rocks shows prograde zoning with increasing Mg and decreasing Mn from the crystal center towards the rim, and is divided into Ca‐poor/Fe‐rich core and Ca‐rich/Fe‐poor mantle parts. The garnet cores include the assemblages of (i) jadeite/omphacite (X_jd = 0.34–0.96) + barroisite/taramite; and (ii) omphacite + barroisite/pargasite, with paragonite, epidote, rutile and quartz as major phases with rare albite. The garnet mantles rarely contain inclusions of omphacite, glaucophane, epidote, rutile and quartz. Major matrix phases of the pre‐exhumation stage are omphacite, glaucophane, paragonite, rutile and quartz. These mineral parageneses give pressure (P)‐temperature (T) conditions of 0.9 GPa/390°C?1.4 GPa/560°C for the stage of the garnet core formation, 1.8 GPa/520°C for the stage of the garnet mantle formation, and 2.2 GPa/495°C‐2.4 GPa/535°C for the peak eclogite facies assemblage in the matrix. The estimated P‐T conditions and continuous changes of mineral parageneses imply a counterclockwise P‐T path which is a combination of (i) an early prograde stage of high‐pressure/low‐temperature (HP/LT) blueschist facies and/or LP/LT eclogite facies; (ii) a later prograde stage involving compression with minimal heating; and (iii) a climax‐of‐subduction stage characterized by a slight decrease of temperature with increasing pressure. The negative dP/dT of the latest subduction stage is possibly a record of the following events after a continuous subduction and ridge approach: (i) material migration within the upper part of the subducting slab, which has an inverse thermal gradient caused by ductile flow and/or slab break during subduction; and/or (ii) temporary cooling of the wedge mantle–slab interface by continuous subduction of a relatively cold slab following subduction of a hotter ridge.