Geopotential harmonics of order 15 and odd degree from analysis of resonant orbits

We have analysed the variations of inclination in 13 satellite orbits as they pass slowly, under the action of air drag, through 15th-order resonance with the geopotential, when successive equatorial crossings are 24° apart and the ground track repeats after 15 rev. The size and form of the change in inclination are determined mainly by the values of the geopotential harmonics of 15th order and odd degree, $\text{C}\text{?}{}_{\mathrm{l,15}}$ and $\text{S}\text{?}{}_{\mathrm{l,15}}$ (with l = 15, 17, 19, …) in the usual notation. Our analysis gives values of these coefficients up to l = 33 as follows:

     

742.

Variations in the atmospheric neutral density at 145km     

J.M. Forbes  H.B. Garrett 《Planetary and Space Science》1975,23(10):1399-1404

A least-squares multiple linear regression is performed on orbital decay density data obtained from precise orbital analysis of 22 low-perigee (130–160 km) Air Force satellites. Variations related to solar activity, the semi-annual effect, geomagnetic activity, and the zenith angle of the Sun are in agreement with the model of Jacchia (1971). Density variations in longitude and latitude are also deduced and compared with recent results from other investigations within this altitude regime.     

743.

Transport and emplacement of crater and basin deposits     

Verne R. Oberbeck  Robert H. Morrison  Friedrich Hörz 《Earth, Moon, and Planets》1975,13(1-3):9-26

Material is ejected from impact craters in ballastic trajectories; it impacts first near the crater rim and then at progressively greater ranges. Ejecta from craters smaller than approximately 1 km is laid predominantly on top of the surrounding surface. With increasing crater size, however, more and more surrounding surface will be penetrated by secondary cratering action and these preexisting materials will be mixed with primary crater ejecta. Ejecta from large craters and especially basin forming events not only excavate preexisting, local materials, but also are capable of moving large amounts of material away from the crater. Thus mixing and lateral transport give rise to continuous deposits that contain materials from within and outside the primary crater. As a consequence ejecta of basins and large highland craters have eroded and mixed highland materials throughout geologic time and deposited them in depressions inside and between older crater structures.Because lunar mare surfaces contain few large craters, the mare regolith is built up by successive layers of predominantly primary ejecta. In contrast, the lunar highlands are dominated by the effects of large scale craters formed early in lunar history. These effects lead to thick fragmental deposits which are a mixture of primary crater material and local components. These deposits may also properly be named regolith though the term has been traditionally applied only to the relatively thin fine grained surficial deposit on mare and highland terranes generated during the past few billion year. We believe that the surficial highland regolith - generated over long periods of time - rests on massive fragmental units that have been produced during the early lunar history.     

744.

Na depletion in modern adakites via melt / rock reaction within the sub-arc mantle     

X.L. Xiong  B. Xia  J.F. Xu  H.C. Niu  W.S. Xiao 《Chemical Geology》2006,229(4):273-292

Interaction between slab-derived melt and mantle peridotite and the role of slab melt as a metasomatizing agent in the sub-arc mantle is being increasingly recognized. Adakite, the slab melt erupted on the surface, usually exhibits anomalously high MgO, CaO, Cr and Ni contents that indicate interaction with mantle peridotitite. Here we note that Cenozoic adakites have Na₂O contents below 5.8 wt.% with ∼95% samples lower than 5.0 wt.%, and are generally depleted in this component relative to experimental basalt partial melts (mostly beyond 5.0 wt.% and up to 9.0 wt.% Na₂O) produced under 1.5-3.0 GPa conditions that are most relevant to adakite production. We interpret the adakite Na depletion to be also a consequence of the melt / rock reaction that takes place within the hot mantle wedge. During ascent and reaction with mantle peridotite, primary adakite melts gain mantle components MgO, CaO, Cr and Ni but lose Na₂O, SiO₂ and perhaps K₂O to the mantle, leading to Na-rich mantle metasomatism. Selective assimilation of predominately mantle clinopyroxene, some spinel and minor olivine at high T/P has been considered to be an important process in producing high-Mg adakites from primary low-Mg slab melts [Killian, R., Stern, C. R., 2002. Constraints on the interaction between slab melts and the mantle wedge from adakitic glass in peridotite xenoliths. Eur. J. Mineral. 14, 25-36]. In such a process, Na depletion in the assimilated melt is the result of dilution due to the increase in melt mass. Phase relationships in the reaction system siliceous melt + peridotite and quantitative calculation suggest that assimilation of mantle clinopyroxene, olivine and spinel and fractional crystallization of sodic amphibole and orthopyroxene, under conditions of moderate T/P and increasing melt mass, is also an important process that modifies the composition of adakites and causes the Na depletion.     

745.

Mantle plumes from top to bottom   总被引：5，自引：0，他引：5  

Norman H. Sleep 《Earth》2006,77(4):231-271

Hotspots include midplate features like Hawaii and on-axis features like Iceland. Mantle plumes are a well-posed hypothesis for their formation. Starting plume heads provide an explanation of brief episodes of flood basalts, mafic intrusions, and radial dike swarms. Yet the essence of the hypothesis hides deep in the mantle. Tests independent of surface geology and geochemistry to date have been at best tantalizing. It is productive to bare the current ignorance, rather than to dump the plume hypothesis. One finds potentially fruitful lines of inquiry using simple dynamics and observations. Ancient lithospheric xenoliths may reveal heating by plumes and subsequent thermal equilibration in the past. The effect at the base of the chemical layer is modest 50-100 K for transient heating by plume heads. Thinning of nonbuoyant platform lithosphere is readily observed but not directly attributable to plumes. The plume history in Antarctica is ill constrained because of poor geological exposure. This locality provides a worst case on what is known about surface evidence of hotspots. Direct detection of plume tail conduits in the mid-mantle is now at the edge of seismic resolution. Seismology does not provide adequate resolution of the deep mantle. We do not know the extent of a chemically dense dregs layer or whether superplume regions are cooler or hotter than an adiabat in equilibrium with the asthenosphere. Overall, mid-mantle seismology is most likely to give definitive results as plume conduits are the guts of the dynamic hypothesis. Finding them would bring unresolved deep and shallow processes into place.     

746.

Influence of physiology and climate on δD of leaf wax n-alkanes from C₃ and C₄ grasses     

Francesca A. Smith  Katherine H. Freeman 《Geochimica et cosmochimica acta》2006,70(5):1172-1187

We measured hydrogen isotope compositions (δD) of high-molecular-weight n-alkanes (C₂₇-C₃₃) from grasses grown in greenhouses and collected from the US Great Plains. In both cases, n-alkanes from C₄ grasses are enriched in D by more than 20‰ relative to those from C₃ grasses. The apparent enrichment factor (ε_C29-GW) between C₂₉n-alkane and greenhouse water is −165 ± 12‰ for C₃ grasses and −140 ± 15‰ for C₄ grasses. For samples from the Great Plains, δD values of C₂₉n-alkanes range from −280 to −136‰, with values for C₄ grasses ca. 21‰ more positive than those for C₃ grasses from the same site. Differences in C₃ and C₄ grass n-alkane δD values are consistent with the shorter interveinal distance in C₄ grass leaves, and greater back-diffusion of enriched water from stomata to veins, than in C₃ grass leaves. Great Plains’ grass n-alkane isotopic ratios largely reflect precipitation δD values. However, the offset or apparent fractionation between n-alkanes and precipitation is not uniform and varies with annual precipitation and relative humidity, suggesting climatic controls on lipid δD values. The dryer sites exhibit smaller absolute apparent fractionation indicative of D-enrichment of source waters through transpiration and/or soil evaporation. To explore the relationship between climate and n-alkane δD values, we develop three models. (1) The ‘direct analog’ model estimates δD_C29 values simply by applying the apparent enrichment factors, ε_C29-GW, observed in greenhouse grasses to precipitation δD values from the Great Plains. (2) The ‘leaf-water’ model uses a Craig-Gordon model to estimate transpirational D-enrichment for both greenhouse and field sites. The transpiration-corrected enrichment factors between C₂₉ and bulk leaf-water, ε_C29-GW, calculated from the greenhouse samples (−181‰ for C₃ and −157‰ for C₄) are applied to estimate δD_C29 values relative to modeled bulk leaf-water δD values. (3) The ‘soil- and leaf-water’ model estimates the combined effects of soil evaporation, modeled by analogy with a flow-through lake, and transpiration on δD_C29 values. Predictions improve with the addition of the explicit consideration of transpiration and soil evaporation, indicating that they are both important processes in determining plant lipid δD values. D-enrichment caused by these evaporative processes is controlled by relative humidity, suggesting that important climatic information is recorded in leaf wax n-alkane δD values. Calibration studies such as this one provide a baseline for future studies of plant-water-deuterium systematics and form the foundation for interpretation of plant wax hydrogen isotope ratios as a paleo-aridity proxy.     

747.

Restructuring of polygalacturonate on alumina upon hydration—Effect on phosphate sorption kinetics     

Christian Mikutta  Jaane Krüger  Friederike Lang 《Geochimica et cosmochimica acta》2006,70(12):2957-2969

Hydration of organic coatings in soils is expected to affect the sorption of oxyanions onto hydrous Fe and Al oxides. We hypothesized that the hydration of polygalacturonate (PGA) coatings on alumina (Al₂O₃) increases their permeability for phosphate. Pure and PGA-coated alumina were equilibrated in deionized water for 2 and 170 h at pH 5 and 20 °C before studying (i) their porosity with N₂ gas adsorption and ¹H NMR relaxometry, (ii) structural changes of PGA-coatings with differential scanning calorimetry (DSC), and (iii) the kinetics of phosphate sorption and PGA desorption in batch experiments. Scanning electron micrographs revealed that PGA molecules formed three-dimensional networks with pores ranging in size from <10 to several hundred nanometers. Our NMR results showed that the water content of intraparticle alumina pores decreased upon PGA sorption, indicating a displacement of pore water by PGA. The amount of water in interparticle alumina pores increased strongly after PGA addition, however, and was attributed to water in pores of PGA and/or in pores at the PGA-alumina interface. The flexibility of PGA molecules and the fraction of a PGA gel phase increased within one week of hydration, implying restructuring of PGA. Hydration of PGA coatings increased the amount of phosphate defined as instantaneously sorbed by 84%, showing that restructuring of PGA enhanced the accessibility of phosphate to external alumina surfaces. Despite the fact that the efficacy of phosphate to displace PGA was higher after 170 h than after 2 h, a higher phosphate surface loading was required after 170 h to set off PGA desorption. Our findings imply that the number of PGA chain segments directly attached to the alumina surface decreased with time. We conclude that hydration/dehydration of polymeric surface coatings affects the sorption kinetics of oxyanions, and may thus control the sorption and transport of solutes in soils.     

748.

Production of rhamnolipids by Pseudomonas aeruginosa growing on carbon sources     

H. Rashedi M. Sc.  Ph.D.  M. Mazaheri Assadi M.Sc.  Ph.D.  E. Jamshidi M.Sc.  Ph.D.  B. Bonakdarpour M.Sc.  Ph.D. 《International Journal of Environmental Science and Technology》2006,3(3):297-303

Arhamnolipid producing bacterium, Pseudomonas aeruginosa was previously isolated from Iranian oil over years. Isolated strain was identified by morphological, biochemical, physiological and 16 sr RNA (1). Glycolipid production by isolated bacterium using sugar beet molasses as a carbon and energy source was investigated. Biosurfactant production was quantified by surface tension reduction, Critical Micelle Dilution (CMD), Emulsification Capacity (EC), and Thin Layer Chromatogeraphy. biosurfactants during growth on waste Dates as the primary carbon and nitrogen sources, respectively. After 48 h of growth the culture supernatant fluid had a rhamnose concentration of 0.18 g/L and surface tension was reduced to 20 mN/m ( %).( reduced the interfacial tension against crude oil from 21 mN/m to 0,47 mN/m) Result from the study showed that the growth of the bacteria using molasses as carbon sources is growth-associated. The specific production rate of rhamnolipid with 2 %, 4 %, 6 %, 8 % and 10 % of molasses are 0.00065; 4.556; 8.94; 8.85; and 9.09. respectively The yield of rhamnolipid per biomass with 2%,4%,6%,8% and 10% molasses are 0.003;0.009;0.053;0.041 and 0.213 respectively. The production of rhamnolipid (0.0531 g rhamnolipid/g biomass) is higher compare to the culture grown in aerobic condition (0.04 g rhamnolipid/g biomass).The rhamnolipids were able to form stable emulsions with n-alkanes, aromatics, crude oil and olive oil. These studies indicate that renewable, relatively inexpensive and easily available resources can be used for important biotechnological processes.     

749.

Slow arsenic poisoning of the contaminated groundwater users     

M. M. Uddin  A. K. M. Harun-Ar-Rashid  S. M. Hossain  M. A. Hafiz  K. Nahar  S. H. Mubin 《International Journal of Environmental Science and Technology》2006,3(4):447-453

This paper gives impact of Arsenic contaminated water on human health as well as overview of the extent and severity of groundwater arsenic contamination in Bangladesh. Scalp hair is the most important part of the human body to monitor the accumulation of this type of poison. Therefore, an experiment has been carried out by Neutron Activation Analysis (NAA) at Atomic Energy Research Establishment (AERE), Savar, Dhaka, Bangladesh on human hair of corresponding tube well water users of these areas to determine the total accumulation of arsenic to their body. Hair samples collected from the region where the groundwater was found highly contaminated with arsenic. The obtained results of arsenic concentration in the lower age (Hb) categories of users (below 12 years of age users) is in the range of 0.33 to 3.29 /gmg/g (ppm) and that in the Hu categories (upper 12 years of age users) is 0.47 to 6.64 μg/g (ppm). Where as maximum permissible range is 1 ppm certified from WHO. Results show that the peoples are highly affected where the groundwater is highly contaminated with arsenic and acts as the primary source of arsenic poisoning among the peoples of those areas. The results indicate that human population is affected with arsenic locally using the contaminated water for a long time.     

750.

The removal of color and COD from wastewater containing water base color by coagulation process     

H. Asilian M.Sc.  Ph.D.  Sh. Moradian fard M.Sc.  A. Rezaei M.Sc.  Ph.D.  S. B. Mortazavi M.Sc.  Ph.D.  A. Khavanin M.Sc.  Ph.D. 《International Journal of Environmental Science and Technology》2006,3(2):153-157

In this study acrylic water base color was removed from synthetic wastewater using coagulation process. Experiments were conducted on the sample containing 100 mg/L and 400 mg/L of acrylic water base color. Destruction of color by means of coagulation/flocculation techniques using ferrous sulfate, alum, lime and polyelectrolyte (cationic, anionic and non ionic). The study was performed in a systematic approach searching optimum values of alum and FeSO₄ concentration, pH and temperature. All the experiments were run in a laboratory scale.The obtained results show that treatment with alum and ferrous sulfate alone proved to be very effective in removing the color (> 99 %) and part of COD (60–70 %) from aqueous solution. Lime alone did not significant change on COD and color removal.     

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l	109C?l,15	109S?l,15
15	?23.5 ± 0.8	?7.7 ± 0.8
17	6.3 ± 1.5	5.6 ± 1.5
19	?25.1 ± 2.5	?7.3 ± 2.3
21	27.8 ± 3.6	?0.7 ± 3.4
23	17.1 ± 4.1	13.9 ± 4.8
25	?1.1 ± 3.0	8.5 ± 4.2
27	10.0 ± 3.3	6.7 ± 2.7
29	?9.4 ± 3.5	0.1 ± 4.7
31	10.1 ± 5.4	3.8 ± 5.6
33	1.1 ± 5.7	3.1 ± 5.8

Variations in the atmospheric neutral density at 145km

A least-squares multiple linear regression is performed on orbital decay density data obtained from precise orbital analysis of 22 low-perigee (130–160 km) Air Force satellites. Variations related to solar activity, the semi-annual effect, geomagnetic activity, and the zenith angle of the Sun are in agreement with the model of Jacchia (1971). Density variations in longitude and latitude are also deduced and compared with recent results from other investigations within this altitude regime.     

Transport and emplacement of crater and basin deposits

Material is ejected from impact craters in ballastic trajectories; it impacts first near the crater rim and then at progressively greater ranges. Ejecta from craters smaller than approximately 1 km is laid predominantly on top of the surrounding surface. With increasing crater size, however, more and more surrounding surface will be penetrated by secondary cratering action and these preexisting materials will be mixed with primary crater ejecta. Ejecta from large craters and especially basin forming events not only excavate preexisting, local materials, but also are capable of moving large amounts of material away from the crater. Thus mixing and lateral transport give rise to continuous deposits that contain materials from within and outside the primary crater. As a consequence ejecta of basins and large highland craters have eroded and mixed highland materials throughout geologic time and deposited them in depressions inside and between older crater structures.Because lunar mare surfaces contain few large craters, the mare regolith is built up by successive layers of predominantly primary ejecta. In contrast, the lunar highlands are dominated by the effects of large scale craters formed early in lunar history. These effects lead to thick fragmental deposits which are a mixture of primary crater material and local components. These deposits may also properly be named regolith though the term has been traditionally applied only to the relatively thin fine grained surficial deposit on mare and highland terranes generated during the past few billion year. We believe that the surficial highland regolith - generated over long periods of time - rests on massive fragmental units that have been produced during the early lunar history.     

Na depletion in modern adakites via melt / rock reaction within the sub-arc mantle

Interaction between slab-derived melt and mantle peridotite and the role of slab melt as a metasomatizing agent in the sub-arc mantle is being increasingly recognized. Adakite, the slab melt erupted on the surface, usually exhibits anomalously high MgO, CaO, Cr and Ni contents that indicate interaction with mantle peridotitite. Here we note that Cenozoic adakites have Na₂O contents below 5.8 wt.% with ∼95% samples lower than 5.0 wt.%, and are generally depleted in this component relative to experimental basalt partial melts (mostly beyond 5.0 wt.% and up to 9.0 wt.% Na₂O) produced under 1.5-3.0 GPa conditions that are most relevant to adakite production. We interpret the adakite Na depletion to be also a consequence of the melt / rock reaction that takes place within the hot mantle wedge. During ascent and reaction with mantle peridotite, primary adakite melts gain mantle components MgO, CaO, Cr and Ni but lose Na₂O, SiO₂ and perhaps K₂O to the mantle, leading to Na-rich mantle metasomatism. Selective assimilation of predominately mantle clinopyroxene, some spinel and minor olivine at high T/P has been considered to be an important process in producing high-Mg adakites from primary low-Mg slab melts [Killian, R., Stern, C. R., 2002. Constraints on the interaction between slab melts and the mantle wedge from adakitic glass in peridotite xenoliths. Eur. J. Mineral. 14, 25-36]. In such a process, Na depletion in the assimilated melt is the result of dilution due to the increase in melt mass. Phase relationships in the reaction system siliceous melt + peridotite and quantitative calculation suggest that assimilation of mantle clinopyroxene, olivine and spinel and fractional crystallization of sodic amphibole and orthopyroxene, under conditions of moderate T/P and increasing melt mass, is also an important process that modifies the composition of adakites and causes the Na depletion.     

Mantle plumes from top to bottom

Hotspots include midplate features like Hawaii and on-axis features like Iceland. Mantle plumes are a well-posed hypothesis for their formation. Starting plume heads provide an explanation of brief episodes of flood basalts, mafic intrusions, and radial dike swarms. Yet the essence of the hypothesis hides deep in the mantle. Tests independent of surface geology and geochemistry to date have been at best tantalizing. It is productive to bare the current ignorance, rather than to dump the plume hypothesis. One finds potentially fruitful lines of inquiry using simple dynamics and observations. Ancient lithospheric xenoliths may reveal heating by plumes and subsequent thermal equilibration in the past. The effect at the base of the chemical layer is modest 50-100 K for transient heating by plume heads. Thinning of nonbuoyant platform lithosphere is readily observed but not directly attributable to plumes. The plume history in Antarctica is ill constrained because of poor geological exposure. This locality provides a worst case on what is known about surface evidence of hotspots. Direct detection of plume tail conduits in the mid-mantle is now at the edge of seismic resolution. Seismology does not provide adequate resolution of the deep mantle. We do not know the extent of a chemically dense dregs layer or whether superplume regions are cooler or hotter than an adiabat in equilibrium with the asthenosphere. Overall, mid-mantle seismology is most likely to give definitive results as plume conduits are the guts of the dynamic hypothesis. Finding them would bring unresolved deep and shallow processes into place.     

Influence of physiology and climate on δD of leaf wax n-alkanes from C3 and C4 grasses

We measured hydrogen isotope compositions (δD) of high-molecular-weight n-alkanes (C₂₇-C₃₃) from grasses grown in greenhouses and collected from the US Great Plains. In both cases, n-alkanes from C₄ grasses are enriched in D by more than 20‰ relative to those from C₃ grasses. The apparent enrichment factor (ε_C29-GW) between C₂₉n-alkane and greenhouse water is −165 ± 12‰ for C₃ grasses and −140 ± 15‰ for C₄ grasses. For samples from the Great Plains, δD values of C₂₉n-alkanes range from −280 to −136‰, with values for C₄ grasses ca. 21‰ more positive than those for C₃ grasses from the same site. Differences in C₃ and C₄ grass n-alkane δD values are consistent with the shorter interveinal distance in C₄ grass leaves, and greater back-diffusion of enriched water from stomata to veins, than in C₃ grass leaves. Great Plains’ grass n-alkane isotopic ratios largely reflect precipitation δD values. However, the offset or apparent fractionation between n-alkanes and precipitation is not uniform and varies with annual precipitation and relative humidity, suggesting climatic controls on lipid δD values. The dryer sites exhibit smaller absolute apparent fractionation indicative of D-enrichment of source waters through transpiration and/or soil evaporation. To explore the relationship between climate and n-alkane δD values, we develop three models. (1) The ‘direct analog’ model estimates δD_C29 values simply by applying the apparent enrichment factors, ε_C29-GW, observed in greenhouse grasses to precipitation δD values from the Great Plains. (2) The ‘leaf-water’ model uses a Craig-Gordon model to estimate transpirational D-enrichment for both greenhouse and field sites. The transpiration-corrected enrichment factors between C₂₉ and bulk leaf-water, ε_C29-GW, calculated from the greenhouse samples (−181‰ for C₃ and −157‰ for C₄) are applied to estimate δD_C29 values relative to modeled bulk leaf-water δD values. (3) The ‘soil- and leaf-water’ model estimates the combined effects of soil evaporation, modeled by analogy with a flow-through lake, and transpiration on δD_C29 values. Predictions improve with the addition of the explicit consideration of transpiration and soil evaporation, indicating that they are both important processes in determining plant lipid δD values. D-enrichment caused by these evaporative processes is controlled by relative humidity, suggesting that important climatic information is recorded in leaf wax n-alkane δD values. Calibration studies such as this one provide a baseline for future studies of plant-water-deuterium systematics and form the foundation for interpretation of plant wax hydrogen isotope ratios as a paleo-aridity proxy.     

Restructuring of polygalacturonate on alumina upon hydration—Effect on phosphate sorption kinetics

Hydration of organic coatings in soils is expected to affect the sorption of oxyanions onto hydrous Fe and Al oxides. We hypothesized that the hydration of polygalacturonate (PGA) coatings on alumina (Al₂O₃) increases their permeability for phosphate. Pure and PGA-coated alumina were equilibrated in deionized water for 2 and 170 h at pH 5 and 20 °C before studying (i) their porosity with N₂ gas adsorption and ¹H NMR relaxometry, (ii) structural changes of PGA-coatings with differential scanning calorimetry (DSC), and (iii) the kinetics of phosphate sorption and PGA desorption in batch experiments. Scanning electron micrographs revealed that PGA molecules formed three-dimensional networks with pores ranging in size from <10 to several hundred nanometers. Our NMR results showed that the water content of intraparticle alumina pores decreased upon PGA sorption, indicating a displacement of pore water by PGA. The amount of water in interparticle alumina pores increased strongly after PGA addition, however, and was attributed to water in pores of PGA and/or in pores at the PGA-alumina interface. The flexibility of PGA molecules and the fraction of a PGA gel phase increased within one week of hydration, implying restructuring of PGA. Hydration of PGA coatings increased the amount of phosphate defined as instantaneously sorbed by 84%, showing that restructuring of PGA enhanced the accessibility of phosphate to external alumina surfaces. Despite the fact that the efficacy of phosphate to displace PGA was higher after 170 h than after 2 h, a higher phosphate surface loading was required after 170 h to set off PGA desorption. Our findings imply that the number of PGA chain segments directly attached to the alumina surface decreased with time. We conclude that hydration/dehydration of polymeric surface coatings affects the sorption kinetics of oxyanions, and may thus control the sorption and transport of solutes in soils.     

Production of rhamnolipids by Pseudomonas aeruginosa growing on carbon sources

Arhamnolipid producing bacterium, Pseudomonas aeruginosa was previously isolated from Iranian oil over years. Isolated strain was identified by morphological, biochemical, physiological and 16 sr RNA (1). Glycolipid production by isolated bacterium using sugar beet molasses as a carbon and energy source was investigated. Biosurfactant production was quantified by surface tension reduction, Critical Micelle Dilution (CMD), Emulsification Capacity (EC), and Thin Layer Chromatogeraphy. biosurfactants during growth on waste Dates as the primary carbon and nitrogen sources, respectively. After 48 h of growth the culture supernatant fluid had a rhamnose concentration of 0.18 g/L and surface tension was reduced to 20 mN/m ( %).( reduced the interfacial tension against crude oil from 21 mN/m to 0,47 mN/m) Result from the study showed that the growth of the bacteria using molasses as carbon sources is growth-associated. The specific production rate of rhamnolipid with 2 %, 4 %, 6 %, 8 % and 10 % of molasses are 0.00065; 4.556; 8.94; 8.85; and 9.09. respectively The yield of rhamnolipid per biomass with 2%,4%,6%,8% and 10% molasses are 0.003;0.009;0.053;0.041 and 0.213 respectively. The production of rhamnolipid (0.0531 g rhamnolipid/g biomass) is higher compare to the culture grown in aerobic condition (0.04 g rhamnolipid/g biomass).The rhamnolipids were able to form stable emulsions with n-alkanes, aromatics, crude oil and olive oil. These studies indicate that renewable, relatively inexpensive and easily available resources can be used for important biotechnological processes.     

Slow arsenic poisoning of the contaminated groundwater users

This paper gives impact of Arsenic contaminated water on human health as well as overview of the extent and severity of groundwater arsenic contamination in Bangladesh. Scalp hair is the most important part of the human body to monitor the accumulation of this type of poison. Therefore, an experiment has been carried out by Neutron Activation Analysis (NAA) at Atomic Energy Research Establishment (AERE), Savar, Dhaka, Bangladesh on human hair of corresponding tube well water users of these areas to determine the total accumulation of arsenic to their body. Hair samples collected from the region where the groundwater was found highly contaminated with arsenic. The obtained results of arsenic concentration in the lower age (Hb) categories of users (below 12 years of age users) is in the range of 0.33 to 3.29 /gmg/g (ppm) and that in the Hu categories (upper 12 years of age users) is 0.47 to 6.64 μg/g (ppm). Where as maximum permissible range is 1 ppm certified from WHO. Results show that the peoples are highly affected where the groundwater is highly contaminated with arsenic and acts as the primary source of arsenic poisoning among the peoples of those areas. The results indicate that human population is affected with arsenic locally using the contaminated water for a long time.     

The removal of color and COD from wastewater containing water base color by coagulation process

In this study acrylic water base color was removed from synthetic wastewater using coagulation process. Experiments were conducted on the sample containing 100 mg/L and 400 mg/L of acrylic water base color. Destruction of color by means of coagulation/flocculation techniques using ferrous sulfate, alum, lime and polyelectrolyte (cationic, anionic and non ionic). The study was performed in a systematic approach searching optimum values of alum and FeSO₄ concentration, pH and temperature. All the experiments were run in a laboratory scale.The obtained results show that treatment with alum and ferrous sulfate alone proved to be very effective in removing the color (> 99 %) and part of COD (60–70 %) from aqueous solution. Lime alone did not significant change on COD and color removal.