Mass Balance Calculations (mass + balance_calculation)

Distribution by Scientific Domains


Selected Abstracts


The micro-topography of the wetlands of the Okavango Delta, Botswana

EARTH SURFACE PROCESSES AND LANDFORMS, Issue 1 2005
T. Gumbricht
Abstract The surface of the 40 000 km2 Okavango alluvial fan is remarkably smooth, and almost everywhere lies within two to three metres of a perfectly smooth theoretical surface. Deviations from this perfect surface give rise to islands in the Okavango wetlands. This micro-topography was mapped by assigning empirical elevations to remotely sensed vegetation community classes, based on the observation that vegetation is very sensitive to small, local differences in elevation. Even though empirical, the method produces fairly accurate results. The technique allows estimation of depths of inundation and therefore will be applicable even when high resolution radar altimetry becomes available. The micro-topography has arisen as a result of clastic sedimentation in distributary channels, which produces local relief of less than two metres, and more importantly as a result of chemical precipitation in island soils, which produces similar local relief. The micro-topography is, therefore, an expression of the non-random sedimentation taking place on the fan. Volume calculations of islands extracted from the micro-topography, combined with estimates of current sediment in,ux, suggest that the land surface of the wetland may only be a few tens of thousands of years old. Constant switching of water distribution, driven by local aggradation, has distributed sediment widely. Mass balance calculations suggest that over a period of c. 150 000 years all of the fan would at one time or other have been inundated, and thus subject to sedimentation. Coalescing of islands over time results in net aggradation of the fan surface. The amount of vertical aggradation on islands and in channels is restricted by the water depth. Restricted vertical relief, in turn, maximizes the distribution of water, limiting its average depth. Aggradation in the permanent swamps occurs predominantly by clastic sedimentation. Rates of aggradation here are very similar to those in the seasonal swamps, maintaining the overall gradient, possibly because of the operation of a feedback loop between the two. The limited amount of local aggradation arising from both clastic and chemical sedimentation, combined with constant changes in water distribution, has resulted in a near-perfect conical surface over the fan. In addition to providing information on sedimentary processes, the micro-topography has several useful hydrological applications. Copyright © 2004 John Wiley & Sons, Ltd. [source]


Iron limits primary productivity during spring bloom development in the central North Atlantic

GLOBAL CHANGE BIOLOGY, Issue 4 2006
C. MARK MOORE
Abstract We present in situ biophysical measurements and bioassay experiments that demonstrate iron limitation of primary productivity during the spring bloom in the central North Atlantic. Mass balance calculations indicate that nitrate drawdown is iron (Fe)-limited and that aeolian Fe supply to this region cannot support maximal phytoplankton growth during the bloom. Using a simple simulation model, we show that relief of Fe limitation during the spring bloom can increase nitrate drawdown and, hence, new primary production, by 70%. We conclude that the episodic nature of iron supplied by dust deposition is an important factor controlling the dynamics of the spring bloom. From this, we hypothesize that variability in the timing and magnitude of the spring bloom in response to aeolian Fe supply will affect carbon drawdown and food web dynamics in the central North Atlantic. [source]


Nucleation and growth of myrmekite during ductile shear deformation in metagranites

JOURNAL OF METAMORPHIC GEOLOGY, Issue 7 2006
L. MENEGON
Abstract Myrmekite is extensively developed along strain gradients of continuous, lower amphibolite facies shear zones in metagranites of the Gran Paradiso unit (Western Alps). To evaluate the role of stress, strain energy and fluid phase in the formation of myrmekite, we studied a sample suite consisting of weakly deformed porphyric granites (WDGs), foliated granites (FGs) representative of intermediate strains, and mylonitic granites (MGs). In the protolith, most K-feldspar is microcline with different sets of perthite lamellae and fractures. In the WDGs, abundant quartz-oligoclase myrmekite developed inside K-feldspar only along preexisting perthite lamellae and fractures oriented at a high angle to the incremental shortening direction. In the WDGs, stress played a direct role in the nucleation of myrmekites along interfaces already characterized by high stored elastic strain because of lattice mismatch between K-feldspar and albite. In the FGs and MGs, K-feldspar was progressively dismembered along the growing network of microshear zones exploiting the fine-grained recrystallized myrmekite and perthite aggregates. This was accompanied by a more pervasive fluid influx into the reaction surfaces, and myrmekite occurs more or less pervasively along all the differently oriented internal perthites and fractures independently of the kinematic framework of the shear zone. In the MGs, myrmekite forms complete rims along the outer boundary of the small K-feldspar porphyroclasts, which are almost completely free of internal reaction interfaces. Therefore, we infer that the role of fluid in the nucleation of myrmekite became increasingly important as deformation progressed and outweighed that of stress. Mass balance calculations indicate that, in Al,Si-conservative conditions, myrmekite growth was associated with a volume loss of 8.5%. This resulted in microporosity within myrmekite that enhanced the diffusion of chemical components to the reaction sites and hence the further development of myrmekite. [source]


Carbon and nitrogen dynamics in zero-water exchange shrimp culture as indicated by stable isotope tracers

AQUACULTURE RESEARCH, Issue 11 2002
M A Epp
Abstract The uptake and assimilation of nitrogen and carbon by shrimp were measured in 1200 L mesocosms using stable isotope enrichments. Labels were added via 15N-, 13C-glycine and amino acid mixtures in feeds or as 15NH4+ to pond water. Label was incorporated into shrimp via algal growth indicating that up to 31% of nitrogen requirements were derived from pond ecosystem dynamics. This value is low in comparison with other shrimp aquaculture isotopic tracer studies but is probably due to differences in shrimp-rearing conditions. Direct incorporation of the enriched feed label was low in shrimp muscle tissue (3.3% for 13C-glycine, 5.9% for 15N-glycine and 7.8% for 15N-amino acid mixture). Mass balance calculations indicate the remaining shrimp biomass was derived from feed, but loss of label into solution during feeding led to underestimation based on tracers. Incorporation of isotopic labels into feed as large molecular weight proteinaceous or microencapsulated/fat-coated compounds is recommended to prevent dissolution and loss. [source]


Petrology of the Miller Range 03346 nakhlite in comparison with the Yamato-000593 nakhlite

METEORITICS & PLANETARY SCIENCE, Issue 2 2007
N. IMAE
The main-phase modal abundances are 67.7 vol% augite, 0.8 vol% olivine, and 31.5 vol% mesostasis. Among all known nakhlites, MIL 03346's modal abundance of olivine is the smallest and of mesostasis is the largest. Augite occurs as cumulus phenocrysts having a homogeneous core composition (En36,38Fs24,22Wo40), which is identical with other nakhlites. They accompany thin ferroan rims divided into inner and outer rims with a compositional gap at the boundary between the two rims. Olivine grains have magnesian cores (Fa , 55) and show normal zoning toward ferroan rims (Fa , 84). Mesostasis consists mostly of glass (26.0 vol%) with minor skeletal fayalites, skeletal titanomagnetites, acicular phosphate, massive cristobalite, and sulfides. We conclude that MIL 03346 is the most rapidly cooled nakhlite among all known nakhlites based on the petrography. We obtain the intercumulus melt composition for MIL 03346 from the mass balance calculation using the modal abundances and discuss the crystallization sequence of MIL 03346 in comparison with that of Yamato (Y-) 000593. Although magnesian olivines of Y-000593 are phenocrystic, magnesian olivine grains of MIL 03346 seem to have texturally crystallized from the intercumulus melt. After the MIL 03346 magma intruded upward to the Martian surficial zone, the magnesian olivine crystallized, and then the ferroan inner rim formed on phenocrystic core augite. The outer rim of phenocrystic augites formed after the crystallization of skeletal fayalites and skeletal titanomagnetites, resulting in a compositional gap between the inner and outer rims. Finally, glassy mesostasis formed from the residual melt. This crystallization sequence of MIL 03346 is different from those of other nakhlites, including Y-000593. [source]


Mineralogy, Lithogeochemistry and Elemental Mass Balance of the Hydrothermal Alteration Associated with the Gold-rich Batu Hijau Porphyry Copper Deposit, Sumbawa Island, Indonesia

RESOURCE GEOLOGY, Issue 3 2009
Arifudin Idrus
Abstract This paper discusses the mineralogy, whole-rock geochemistry and elemental mass balance of the hydrothermal alteration zones within the Batu Hijau porphyry copper-gold deposit, Sumbawa Island, Indonesia. The hydrothermal alteration and mineralisation developed in four stages, namely (i) the early stage consisting of a central copper-gold-bearing biotite (potassic), proximal actinolite (inner propylitic) and the distal chlorite-epidote (outer propylitic) zones; (ii) the transitional stage represented by the chlorite-sericite (intermediate argillic) zone; (iii) the late stages distinguished into the sericite-paragonite (argillic) and pyrophyllite-andalusite (advanced argillic) zones; and (iv) the very late stage typified by the illite-sericite zone. In general, major elements (particularly Ca, Mg, Na and K) and some minor and rare earth elements decrease from the least altered rocks towards the late alteration zones as a consequence of the breakdown of Ca-bearing hornblende, biotite and plagioclase. Chemical discrimination by means of millicationic R1 -R2 diagram indicates that R1 [4Si , 11(Na + K) , 2(Fe + Ti)] increases while R2[6Ca + 2Mg + Al] decreases with increasing alteration intensity, from least-altered, through early, transitional, to late alteration zones. Rare earth elements-chondrite (C1) normalised patterns also exhibit the depletion of the elements through the subsequent alteration zones. These results are consistent with the elemental mass balance calculation using the isocon method which shows that the degree of mass and volume depletion systematically increases during alteration. A decrease of the elements as well as mass and volume from early, through transitional to late alteration stages may imply a general decrease of the element activities in hydrothermal fluids during the formation of the alteration zones. [source]


Exposure assessment of 17,-ethinylestradiol in surface waters of the United States and Europe,

ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 12 2009
Robert Hannah
Abstract An evaluation of measured and predicted concentrations of 17,-ethinylestradiol in surface waters of the United States and Europe was conducted to develop expected long-term exposure concentrations for this compound. Measured environmental concentrations (MECs) in surface waters were identified from the literature. Predicted environmental concentrations (PECs) were generated for European and U.S. watersheds using the GREAT-ER and PhATEÔ models, respectively. The majority of MECs are nondetect and generally consistent with model PECs and conservative mass balance calculations. However, the highest MECs are not consistent with concentrations derived from conservative (worst-case) mass balance estimates or model PECs. A review of analytical methods suggests that tandem or high-resolution mass spectrometry methods with extract cleanup result in lower detection limits and lower reported concentrations consistent with model predictions and bounding estimates. Based on model results using PhATE and GREAT-ER, the 90th-percentile low-flow PECs in surface water are approximately 0.2 and 0.3 ng/L for the United States and Europe, respectively. These levels represent conservative estimates of long-term exposure that can be used for risk assessment purposes. Our analysis also indicates that average concentrations are one to two orders of magnitude lower than these 90th-percentile estimates. Higher reported concentrations (e.g., greater than the 99th-percentile PEC of ,1 ng/L) could result from methodological problems or unusual environmental circumstances; however, such concentrations are not representative of levels generally found in the environment, warrant special scrutiny, and are not appropriate for use in risk assessments of long-term exposures. [source]


Structure, reactivity and spectroscopic properties of minerals from lateritic soils: insights from ab initio calculations

EUROPEAN JOURNAL OF SOIL SCIENCE, Issue 4 2007
E. Balan
Summary We review here some recent applications of ab initio calculations to the modelling of spectroscopic and energetic properties of minerals, which are key components of lateritic soils or govern their geochemical properties. Quantum mechanical ab initio calculations are based on density functional theory and density functional perturbation theory. Among the minerals investigated, zircon is a typical resistant primary mineral. Its resistance to weathering is at the origin of the peculiar geochemical behaviour of Zr, an element often used in mass balance calculations of continental weathering. Numerical modelling gives a unique picture of the origin of the chemical durability and radiation-induced amorphization of zircon. We also present several applications of ab initio calculations to the description of properties of secondary minerals, such as kaolinite-group minerals and gibbsite. Special attention is given to the calculation of infrared and Raman spectra. Surface properties and particle shape are major properties of finely-divided materials such as clay minerals. We show how theoretical modelling of infrared spectroscopic data provides information on natural samples at both the microscopic (atomic structure) and macroscopic (particle shape) length-scale. The systematic comparison of experimental and theoretical data significantly improves our understanding of mineral transformations during soil formation and evolution in lateritic environments. [source]


Combined Treatment of Perchlorate and RDX in Ground Water Using a Fluidized Bed Reactor

GROUND WATER MONITORING & REMEDIATION, Issue 3 2007
Mark E. Fuller
A bench-scale study was conducted to assess the effectiveness of biological treatment of comingled perchlorate and hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) in ground water using fluidized bed reactors (FBRs). In addition, the ability of FBRs to treat low concentrations of perchlorate was examined. Pilot-scale FBRs were fed either acetic acid or molasses as an electron donor to facilitate simultaneous perchlorate and RDX reduction. The acetic acid-fed FBR consistently removed perchlorate from an influent level of 100 ,g/L to below 6 ,g/L, and values below the method detection limit of 1 ,g/L occurred approximately 70% of the time. RDX breakthrough from all FBRs was minimal due to sorption of the explosive on the granulated activated carbon media, but mass balance calculations indicated that more than 99.5% of the total RDX entering the acetic acid-fed FBR was biologically degraded. Approximately 80% of the RDX fed to the control FBR (i.e., no substrate addition) was accounted for at the end of the study; the remainder was assumed to have been degraded. Molasses was much less effective than acetic acid as an electron donor for treatment of perchlorate and RDX. This work demonstrates that combined treatment of perchlorate and RDX is feasible using FBR technology, and that very low levels of perchlorate (less than 100 ,g/L) can be effectively treated in an FBR. [source]


Fractionation of Caseins by Anion-exchange Chromatography Using Food-grade Buffers

JOURNAL OF FOOD SCIENCE, Issue 5 2003
K.N. Turhan
ABSTRACT : Caseins prepared by microfiltration of bovine skim milk were fractionated using anion-exchange chromatography. Laser densitometry of electrophoresis gels was shown to be sufficiently quantitative to perform accurate mass balance calculations detailing the fate of each casein fraction. L-cysteine was successfully used as a reducing agent instead of traditional toxic agents, such as dithiothreitol or ,-mercaptoethanol, enabling development of the first food-grade buffer system for casein fractionation. More salt was required for elution of the casein fractions having a greater charge: ,s -casein > ,-casein > ,-casein. Increasing flow rate decreased the extent of separation. Use of smaller beads was suggested as a method to maintain separation at increased flow rate. [source]


Prograde metamorphic sequence of REE minerals in pelitic rocks of the Central Alps: implications for allanite,monazite,xenotime phase relations from 250 to 610 °C

JOURNAL OF METAMORPHIC GEOLOGY, Issue 5 2008
E. JANOTS
Abstract The distribution of REE minerals in metasedimentary rocks was investigated to gain insight into the stability of allanite, monazite and xenotime in metapelites. Samples were collected in the central Swiss Alps, along a well-established metamorphic field gradient that record conditions from very low grade metamorphism (250 °C) to the lower amphibolite facies (,600 °C). In the Alpine metapelites investigated, mass balance calculations show that LREE are mainly transferred between monazite and allanite during the course of prograde metamorphism. At very low grade metamorphism, detrital monazite grains (mostly Variscan in age) have two distinct populations in terms of LREE and MREE compositions. Newly formed monazite crystallized during low-grade metamorphism (<440 °C); these are enriched in La, but depleted in Th and Y, compared with inherited grains. Upon the appearance of chloritoid (,440,450 °C, thermometry based on chlorite,choritoid and carbonaceous material), monazite is consumed, and MREE and LREE are taken up preferentially in two distinct zones of allanite distinguishable by EMPA and X-ray mapping. Prior to garnet growth, allanite acquires two growth zones of clinozoisite: a first one rich in HREE + Y and a second one containing low REE contents. Following garnet growth, close to the chloritoid,out zone boundary (,556,580 °C, based on phase equilibrium calculations), allanite and its rims are partially to totally replaced by monazite and xenotime, both associated with plagioclase (± biotite ± staurolite ± kyanite ± quartz). In these samples, epidote relics are located in the matrix or as inclusions in garnet, and these preserve their characteristic chemical and textural growth zoning, indicating that they did not experience re-equilibration following their prograde formation. Hence, the partial breakdown of allanite to monazite offers the attractive possibility to obtain in situ ages, representing two distinct crystallization stages. In addition, the complex REE + Y and Th zoning pattern of allanite and monazite are essential monitors of crystallization conditions at relatively low metamorphic grade. [source]


Analysis of ordinary chondrites using powder X-ray diffraction: 2.

METEORITICS & PLANETARY SCIENCE, Issue 1 2010
Applications to ordinary chondrite parent-body processes
Several observations indicate that oxidation may have occurred during progressive metamorphism of equilibrated chondrites, including systematic changes with petrologic type in XRD-derived olivine and low-Ca pyroxene abundances, increasing ratios of MgO/(MgO+FeO) in olivine and pyroxene, mean Ni/Fe and Co/Fe ratios in bulk metal with increasing metamorphic grade, and linear Fe addition trends in molar Fe/Mn and Fe/Mg plots. An aqueous fluid, likely incorporated as hydrous silicates and distributed homogeneously throughout the parent body, was responsible for oxidation. Based on mass balance calculations, a minimum of 0.3,0.4 wt% H2O reacted with metal to produce oxidized Fe. Prior to oxidation the parent body underwent a period of reduction, as evidenced by the unequilibrated chondrites. Unlike olivine and pyroxene, average plagioclase abundances do not show any systematic changes with increasing petrologic type. Based on this observation and a comparison of modal and normative plagioclase abundances, we suggest that plagioclase completely crystallized from glass by type 4 temperature conditions in the H and L chondrites and by type 5 in the LL chondrites. Because the validity of using the plagioclase thermometer to determine peak temperatures rests on the assumption that plagioclase continued to crystallize through type 6 conditions, we suggest that temperatures calculated using pyroxene goethermometry provide more accurate estimates of the peak temperatures reached in ordinary chondrite parent bodies. [source]


Alteration Patterns Related to Hydrothermal Gold Mineralizaition in Meta-andesites at Dungash Area, Eastern Desert, Egypt

RESOURCE GEOLOGY, Issue 1 2001
Hossam A. Helba
Abstract: The hydrothermal alteration patterns associating with the gold prospect hosted by metavolcanics in the Dungash area, Eastern Desert of Egypt, were investigated in order to assign their relationship to mineralization. The metavolcanics of andesitic composition are generated by regional metamorphism of greenschist facies superimposed by hydrothermal activity. Epidote and chlorite are metamorphic minerals, whereas sericite, carbonates, and chlorite are hydrothermal alteration minerals. The auriferous quartz vein is of NEE-SWW trend and cuts mainly the andesitic metavolcanics, but sometimes extends to the neighbouring metapyroclastics and metasediments. Quartz-sericite, sericite, carbonate-sericite, and chlorite-sericite constitute four distinctive alteration zones which extend outwards from the mineralized quartz vein. The quartz-sericite and sericite zones are characterized by high contents of SiO2, K2O, Rb, and As, the carbonate-sericite zone is by high contents of CaO, Au, Cu, Cr, Ni, and Y, and the chlorite-sericite zone is by high contents of MgO, Na2O, Zn, Ba, and Co. Gold and sulphide minerals are relatively more abundant in the carbonate-sericite zone followed by the sericite one. The geochemistry of the alteration system was investigated using volume-composition and mass balance calculations. The volume factors obtained for the different alteration zones, mentioned above (being 1.64, 1.19, 1.17, and 1.07, respectively), indicate that replacement had taken place with a volume gain. The mass balance calculations revealed addition of SiO2, K2O, As, Cu, Rb, Ba, Ni, and Y to the system as a whole and subtraction of Fe2O3 from the system. Initial high aK+ and aH+ for the invading fluids is suggested. As the fluids migrated into wallrocks, they became more concentrated in Mg, Ca, and Na with increasing activities of CO2 and S. The calculated loss-gain data are in agreement with the microscopic observations. Breakdown of ferromagnesian minerals and feldspars in the quartz-sericite, sericite, and chlorite-sericite zones accompanied by loss in Mg, Fe, Ca, and Na under acidic conditions and low CO2/H2O ratio may obstruct the formation of carbonates and sulphides, and the precipitation of gold in these zones. The role of metamorphic fluids in the area is expected to be restricted to the liberation of Au and some associated elements from their hosts. [source]


Weathering processes and Quaternary origin of an alpine blockfield in Arctic Sweden

BOREAS, Issue 2 2009
BRADLEY W. GOODFELLOW
The weathering and origin of an autochthonous blockfield in the northern Swedish mountains were investigated through an examination of fine matrix and clasts from two pits excavated across ridge-top sorted circles; one on a summit, the other in a saddle. At the summit, fine matrix chemical weathering is limited to the production of poorly crystallized Al- and Fe-oxyhydroxides, whereas some additional vermiculitization and gibbsite crystallization occurs in the saddle. In both locations, volumes of clay-sized matrix are low, mass balance calculations indicate only minor elemental losses and no chemically etched grains are visible under a scanning electron microscope (SEM). In addition, soil horizons are absent and chemical weathering intensity is uniformly low across both excavated sorted circles. Minor clast chemical weathering consists of Fe oxidation, which dominates in the matrix-rich circle centres, and some rind development, which increases in frequency in the clast-rich rings. The dominance of physical weathering processes and the presence of only minor chemical weathering, in both fine matrix and clasts, indicate that the blockfield is not a Neogene weathering remnant. Rather, the blockfield has a Quaternary origin, developing during interglacials, interstadials and the Holocene, primarily through subsurface weathering processes. [source]