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1.
Atomic layer deposition (ALD) thin film coating was applied to improve the hydrophilia of biochar derived from black willow. 2 (2Al, 0.82 wt% Al2O3), 5 (5Al, 1.40 wt% Al2O3), and 10 (10Al, 2.36 wt% Al2O3) cycles of alumina ALD were applied. The biochars were characterized by inductively coupled plasma–atomic emission spectroscopy, nitrogen adsorption and desorption, scanning electron microscopy, and Fourier transform infrared spectroscopy. The adsorbents were utilized for the removal of methylene blue (MB) from an aqueous solution to evaluate their adsorption capacities. The 5Al biochar showed the highest adsorption capacity, compared to the uncoated biochar and other Al2O3 coated biochars, due to its improved hydrophilia. The amount of MB adsorbed onto the 5Al biochar was almost three times that adsorbed onto the uncoated biochar during the first hour of adsorption experiments. Adsorption isotherms were modeled with the Langmuir and Freundlich isotherms. The data fit well with the Langmuir isotherm, and the maximum adsorption capacities were found to be 26.8 and 35.0 mg/g at 25 °C for the uncoated biochar and 5Al biochar, respectively. The adsorbed MB amount per square meter achieved 1.3 mg/m2 onto the 5Al biochar, and it was twice the amount on the uncoated biochar. The experimental data were analyzed by pseudo-first-order and pseudo-second-order kinetics models of adsorption. The pseudo-second-order model better describes adsorption kinetic data for the uncoated biochar and 5Al biochar than the pseudo-first-order model does.  相似文献   

2.
Biochar is considered a promising amendment for the reduction of metal concentration in plants; however, the effects of biochar in terms of dose and feedstock on metal uptake by plants remain widely unclear. In the current study, three individual biochars were prepared at 450 °C from different feedstocks (wheat straw, sukh chain (Pongamia pinnata), and cotton sticks). The main aim was to evaluate their ability to remediate cadmium (Cd)-spiked soil in terms of growth response and Cd uptake by wheat (Triticum aestivum) tissues. Biochars were separately applied at 0, 1, and 2% (w/w) in Cd-spiked soil and wheat was grown until maturity in pots and then morphological and physiological parameters and Cd concentrations in grains, roots, and shoots were determined. The post-harvest soil was analyzed for extractable Cd concentrations. Plants grown in Cd-spiked soil treated with biochars had higher seed germination, lengths of roots, shoots, and spikes, grains per spike and leaf relative water contents, chlorophyll contents, and dry weight of roots, shoots, and grains as compared to the untreated control. Biochar treatments significantly decreased the Cd concentrations in shoots, roots, and grains as well as total Cd uptake by grains. Soil extractable Cd concentrations were significantly decreased with biochar treatments. The application of 2.0% wheat straw biochar was the most efficient treatment in increasing grain yield and decreasing Cd in grains as well as soil extractable Cd than the other two biochars and doses applied.  相似文献   

3.
Biochars generated at various temperatures might show significant differences in sorption for organic contaminants. In this study, a series of biochars, generated from pyrolyzing maize straws at different temperatures, were systematically characterized. The characterization results showed that with increasing pyrolysis temperature, the surface areas, micropore areas and aromaticity of biochars were enhanced. Batch experiments were conducted to study methyl tert-butyl ether (MTBE) and benzene sorption to biochars. The results indicated that the sorption capacity of benzene to biochars was higher than that of MTBE. The higher pyrolyzed temperature of biochars resulted in a stronger sorption affinity for target compounds, and the dominant sorption mechanisms varied for biochars pyrolyzed at different temperatures. The sorption to biochars pyrolyzed at 700 and 800 °C performed a high adsorption capacity, which indicated that they might be a promising sorbent to remove MTBE and benzene from water. Biochar pyrolyzed at 400 °C showed transitional sorption mechanisms from partition to adsorption for MTBE and benzene. Pore-filling was a possible sorption mechanism to biochars pyrolyzed at high temperature.  相似文献   

4.
Methane is one of the potential greenhouse gases contributing to global climate change, with a global warming potential of about 25 times than that of carbon dioxide. Aerobic methane oxidation (methanotrophy) is the key process that counteracts emission of methane to atmosphere. In this study, methane oxidation capacity of different methane-oxidizing bacteria (methanotrophs) isolated from six different ecosystems was investigated. Methanotrophic consortium isolated from dumpsite proved to be most effective in oxidizing methane. Initially, methane oxidation rate was found to be 0.72 ± 0.036 mM/day; in course of the study consortium M5 showed an increase in methane oxidation rate up to 1.7 ± 0.016 mM/day. A maximum of 0.78 mol of CO2 production was found during methane oxidation in methanotrophs from dumpsite (M5). While varying temperatures, methane oxidation rate was in the range of 1.3–1.7 mM/day which has been found in the temperature range of 30–40 °C. Even at higher temperature (50 °C), 0.076 ± 0.14 mM of the methane was utilized per day. Methane oxidation was assessed by Michaelis–Menten kinetics. By varying the methane concentration, methane oxidation was studied and kinetic parameters such as V max and K m were derived using Lineweaver–Burk plot and found to be 1.497 mM/day and 2.23 mM, respectively. In methane mitigation approach, Methane soil sink is very essential because a balance between methane production by methanogens and consumption by methanotrophs plays an important role in methane emission reduction. Enhancing the methane soil sink will be a cost-effective method to cut down methane emission.  相似文献   

5.
To increase soil productivity, ameliorate nutrient scarcity, and reduce metal toxicity in highly weathered acidic soils usually requires fertilizer and lime application. Effects of three biochars on soil acidity, Olsen-phosphorus (P), phosphatase activities, and heavy metal availability were investigated to test potential of these biochars as soil amendments in highly weathered acidic soils. Incubation experiments were conducted for 6 weeks with three acidic soils: Alfisol, Ultisol, and Oxisol. Three biochars were derived from chicken manure (CMB), pig manure (PMB), and peat moss (PB) at 400 °C and applied at 1 or 2% (wt/wt). The addition of the three biochars increased Olsen-P in the three acidic soils in the following order: CMB?>?PMB?>?PB. Application of 2% CMB increased Olsen-P contents by 2.41-, 7.4-, and 1.78-fold in the Ultisol, Oxisol, and Alfisol compared with controls, respectively. Moreover, CMB increased the soil pH, electrical conductivity (EC), cation exchange capacity (CEC), and alkaline phosphatase activity, but reduced exchangeable acidity, acid phosphatase activity, and the availability of heavy metals—more effectively than PMB and PB. Addition of CMB increased soil pH by 0.90, 0.90, and 0.92 units for the Alfisol, Ultisol, and Oxisol, respectively, correspondingly followed by 0.80, 0.84, and 0.87 units for PMB and 0.15, 0.28, and 0.25 for PM. Changes in EC, CEC, and exchangeable acidity followed the same order for the three soils: CMB?>?PMB?>?PB. The results suggested that the magnitude of changes in soil properties and Olsen-P contents depended on biochar type and application rate. Application of CMB increased nutrient availability and reduced the availability of heavy metals more than other amendments. Due to higher pH, EC, and CEC, and greater concentrations of carbon, nitrogen, and exchangeable calcium and potassium, incorporation of CMB should be a better cost-effective method to correct soil acidity and improve fertility and Olsen-P contents in Ultisols and Oxisols from tropical and subtropical regions of the world.  相似文献   

6.
Biochars have received increasing attention in recent years because of their significant properties such as carbon sequestration, soil fertility, and contaminant immobilization. In this work, the adsorptive removal of paraquat (1,1′-dimethyl-4,4′-dipyridinium chloride, one of the most widely used herbicides) from aqueous solution onto the swine-manure-derived biochar has been studied at 25 °C in a batch adsorption system. The adsorption rate has been investigated under the controlled process parameters including initial pH (i.e., 4.5, 6.0, 7.5, and 9.0), paraquat concentration (i.e., 0.5, 1.0, 2.0, 4.0, and 6.0 mg/L), and biochar dosage (i.e., 0.10, 0.15, 0.20, 0.25, and 0.30 g/L). Based on the adsorption affinity between cationic paraquat and carbon-like adsorbent, a pseudo-second order model has been developed using experimental data to predict the adsorption kinetic constant and equilibrium adsorption capacity. The results showed that the adsorption process could be satisfactorily described with the reaction model and were reasonably explained by assuming an adsorption mechanism in the ion exchange process. Overall, the results from this study demonstrated that the biomass-derived char can be used as a low-cost adsorbent for the removal of environmental cationic organic pollutants from the water environment.  相似文献   

7.
Soil CO2 efflux from an ecosystem responds to the active layer thawing depth (H) significantly. A Li-8100 system was used to monitor the CO2 exchange from a wet meadow ecosystem during a freeze–thaw cycle of the active layer in a permafrost region on the Qinghai-Tibet Plateau. An exponential regression equation ( $ F_{\text{soil\, flux}} = 1.84e^{0.023H} + 5.06\,R^{2} = 0.96 $ ) has been established on the basis of observed soil CO2 efflux versus the thawed soil thickness. Using this equation, the total soil CO2 efflux during an annual freeze–thaw cycle has been calculated to be approximately 8.18 × 1010 mg C. The results suggest that freeze–thaw cycles in the active layer play an important role in soil CO2 emissions and that thawed soil thickness is the major factor controlling CO2 fluxes from the wet meadow ecosystem in permafrost regions on the Qinghai-Tibet Plateau. It can be concluded that with active layer thickening due to permafrost degradation, massive amounts of soil carbon would be emitted as greenhouse gases, and the permafrost region would become a carbon source with a positive feedback effect on climate warming. Hence, more attention should be paid to the influences of the active layer changes on soil carbon emission from these permafrost regions.  相似文献   

8.
The history of life on Earth is critically dependent on the carbon, sulfur and oxygen cycles of the lithosphere – hydrosphere – atmosphere – biosphere system. An Archean oxygen-poor greenhouse atmosphere developed through: (i) accumulation of CO2 and CH4 from episodic injections of CO2 from volcanic activity, volatilised crust impacted by asteroids and comets, metamorphic devolatilisation processes and release of methane from sediments; and (ii) little CO2 weathering-capture due to both high temperatures of the hydrosphere (low CO2 solubility) and a low ratio of exposed continents to oceans. In the wake of the Sturtian glaciation, enrichment in oxygen and appearance of multicellular eukaryotes heralded the onset of the Phanerozoic where greenhouse conditions were interrupted by periods of strong CO2-sequestration through intensified capture of CO2 by marine plants, onset of land plants and burial of carbonaceous shale and coal (Late Ordovician; Carboniferous – Permian; Late Jurassic; Late Tertiary – Quaternary). The progression from Late Mesozoic and Early Tertiary greenhouse conditions to Late Tertiary – Quaternary ice ages was related to the sequestration of CO2 by rapid weathering of the emerging Alpine and Himalayan mountain chains. A number of peak warming and sea-level-rise events include the Late Oligocene, mid-Miocene, mid-Pliocene and Pleistocene glacial terminations. The Late Tertiary – Quaternary ice ages were dominated by cyclic orbital-forcing-triggered terminations which involved CO2-feedback effects from warming seas and the biosphere and albedo flips due to ice-sheet melting. Since ca AD 1750 human emissions were ～305 Gt of carbon, as compared with ～750 Gt C in the atmosphere. The emissions constitute ～12% of the terrestrial biosphere and ～10% of the known global fossil fuel reserve of ～4000 Gt C, whose combustion would compare to the ～ 4600 Gt C released to the atmosphere during the K – T impact event 65 million years ago, with associated ～65% mass extinction of species. The current growth rate of atmospheric greenhouse gases and global mean temperatures exceed those of Pleistocene glacial terminations by one to two orders of magnitude. The relationship between temperatures and sea-levels for the last few million years project future sea-level rises toward time-averaged values of at least 5 m per 1°C. The instability of ice sheets suggested by the Dansgaard – Oeschinger glacial cycles during 50 – 20 ka, observed ice melt lag effects of glacial terminations, spring ice collapse dynamics and the doubling per-decade of Greenland and west Antarctic ice melt suggest that the Intergovernmental Panel on Climate Change's projected sea-level rises (<59 cm) for the 21st century may be exceeded. The biological and philosophical rationale underlying climate change and mass extinction perpetrated by an intelligent carbon-emitting mammal species may never be known.  相似文献   

9.
The sorption of ionizable benzotriazole (BTA) to corncob biochars pyrolyzed at different temperature (i.e., 300 oC, 500 oC and 800 oC) was investigated in this study. Biochars produced at higher temperature showed higher surface area, micropore volume and aromaticity. Consequently, the sorption of BTA changed from absorption to adsorption for biochars pyrolyzed at 300 oC and 800 oC, respectively. Solution pH affected speciation of BTA and surface charge properties of biochars. For BTA0, H-bond, partition and micropore filling are dominant sorption mechanisms. For BTA-, it is suggested that negative charge-assisted H-bond plays an important role in sorption. Corncob biochar pyrolyzed at high temperature (e.g., 800 oC) showed the highest sorption affinity for BTA. Ca2+ in solution enhanced BTA- and BTA0 sorption through cation-bridge and surface complexation.  相似文献   

10.
We determined the melting phase relations, melt compositions, and melting reactions of carbonated peridotite on two carbonate-bearing peridotite compositions (ACP: alkali-rich peridotite + 5.0 wt % CO2 and PERC: fertile peridotite + 2.5 wt % CO2) at 10–20 GPa and 1,500–2,100 °C and constrain isopleths of the CO2 contents in the silicate melts in the deep mantle. At 10–20 GPa, near-solidus (ACP: 1,400–1,630 °C) carbonatitic melts with < 10 wt % SiO2 and > 40 wt % CO2 gradually change to carbonated silicate melts with > 25 wt % SiO2 and < 25 wt % CO2 between 1,480 and 1,670 °C in the presence of residual majorite garnet, olivine/wadsleyite, and clinoenstatite/clinopyroxene. With increasing degrees of melting, the melt composition changes to an alkali- and CO2-rich silicate melt (Mg# = 83.7–91.6; ~ 26–36 wt % MgO; ~ 24–43 wt % SiO2; ~ 4–13 wt % CaO; ~ 0.6–3.1 wt % Na2O; and ~ 0.5–3.2 wt % K2O; ~ 6.4–38.4 wt % CO2). The temperature of the first appearance of CO2-rich silicate melt at 10–20 GPa is ~ 440–470 °C lower than the solidus of volatile-free peridotite. Garnet + wadsleyite + clinoenstatite + carbonatitic melt controls initial carbonated silicate melting at a pressure < 15 GPa, whereas garnet + wadsleyite/ringwoodite + carbonatitic melt dominates at pressure > 15 GPa. Similar to hydrous peridotite, majorite garnet is a liquidus phase in carbonated peridotites (ACP and PERC) at 10–20 GPa. The liquidus is likely to be at ~ 2,050 °C or higher at pressures of the present study, which gives a melting interval of more than 670 °C in carbonated peridotite systems. Alkali-rich carbonated silicate melts may thus be produced through partial melting of carbonated peridotite to 20 GPa at near mantle adiabat or even at plume temperature. These alkali- and CO2-rich silicate melts can percolate upward and may react with volatile-rich materials accumulate at the top of transition zone near 410-km depth. If these refertilized domains migrate upward and convect out of the zone of metal saturation, CO2 and H2O flux melting can take place and kimberlite parental magmas can be generated. These mechanisms might be important for mantle dynamics and are potentially effective metasomatic processes in the deep mantle.  相似文献   

11.
While the Intergovernmental Panel on Climate Change classifies coal as anthracite, bituminous coal, and sub-bituminous coal, Korea only distinguishes coal as anthracite and bituminous coal while sub-bituminous coal is considered bituminous coal. As a result, Korea conducted research in the CO2 emission factors of anthracite and bituminous coal, but largely ignored sub-bituminous coal. Therefore, the purpose of this research is to develop the CO2 emission factor of sub-bituminous coal by classifying sub-bituminous coal from resources of bituminous coal activities collected in Korea between 2007 and 2011. The 2007–2011 average carbon content of sub-bituminous coal was analyzed to be 69.63 ± 3.11 %, the average hydrogen content 4.97 ± 0.37 %, the inherent moisture 12.60 ± 4.33 %, the total moisture 21.91 ± 5.45 %, and the dry-based gross calorific value was analyzed to be 5,914 ± 391 kcal/kg; using these analyzed values, the as-received net calorific value was found to be 20.75 ± 7.59 TJ/Gg and the CO2 emission factor was found to be 96,241 ± 4,064 kg/TJ. In addition, the 62.7 million ton amount for the 2009 greenhouse gas emission from sub-bituminous coal as estimated with the analyzed value of this study is an amount that is equivalent to 11.1 % of the 2009 total greenhouse gas emission amount of 564.7 million tons, and this amount is larger than the 9.3 % for the industrial processes sector, 3.3 % for the agricultural sector and 2.5 % for the waste sector. Therefore, it is important to reflect the realities of Korea when estimating the greenhouse gas emission from such sub-bituminous coals.  相似文献   

12.
Biological soil crusts (BSCs) are an important cover in arid desert landscapes, and have a profound effect on the CO2 exchange in the desert system. Although a large number of studies have focused on the CO2 flux at the soil–air interface, relatively few studies have examined the soil CO2 concentration in individual layers of the soil profile. In this study, the spatiotemporal dynamics of CO2 concentration throughout the soil profile under two typical BSCs (algae crusts and moss crusts) and its driving factors were examined in a revegetated sandy area of the Tengger Desert from Mar 2010 to Oct 2012. Our results showed that the mean values of the vertical soil CO2 concentrations under algal crusts and moss crusts were 600–1,200 μmol/mol at the 0–40 cm soil profiles and increased linearly with soil depth. Daily CO2 concentrations showed a single-peak curve and often had a 1–2 h time delay after the maximum soil temperature. During the rainy season, the mean soil CO2 concentration profile was 1,200–2,000 μmol/mol, which was 2–5 times higher as compared to the dry season (400–800 μmol/mol). Annually, soil moisture content was the key limiting factor of the soil CO2 concentration, but at the daily time scale, soil temperature was the main limiting factor. Combined with infiltration depth of crusted soils, we predicted that precipitation of 10–15 mm was the most effective driving factor in arid desert regions.  相似文献   

13.
Soil aggregation is one of the key properties affecting the productivity of soils and the environmental side effects of agricultural soils. In this study, we aimed to identify whether biochar could be used to improve aggregate stability. A 2-year field experiment was conducted to investigate the effect of biochar application (0, 2.5, 5, 10, 20, 30 and 40 t ha?1) on aggregate characteristics of upland red soil under a rapeseed–sweet potato rotation in subtropical China. Percentage of aggregate destruction (PAD0.25), mean weight diameter (MWD), geometric mean diameter (GMD) and fractal characteristics of soil aggregates were measured using both wet and dry sieving methods. Results showed that applying biochar significantly decreased the percentage of aggregate destruction and soil fractal dimension and increased the MWD and GMD. The optimal amelioration was observed when biochar was applied at a rate of 40 t ha?1. The decline of the fractal dimension of dry aggregates was 2–9 times as much as that of water-stable aggregates in the 0–15 soil layer and 1–4 times in the 15–30 cm soil layer. These results suggested that biochar could improve the resistance of aggregates to stresses and provide scientific strategies for the agricultural production.  相似文献   

14.
Biochar is charcoal made from waste biomass and intended to be added to soil to improve soil function and reduce emissions from the biomass caused by natural degradation to CO2. Nitrogen (N) forms in biochar can be complex and their lability likely to be influenced by pyrolysis temperature which, together with the nature of carbon (C), will influence N mineralisation or immobilisation. These complex relationships are poorly understood, yet impact strongly on the potential agronomic value of biochar. In this study, N in different biochar samples produced from human and animal waste streams (biosolids and cow manure; each mixed with eucalyptus wood chips in a 1:1 dry wt. ratio) at different pyrolysis conditions (highest heating temperature 250, 350, 450 and 550 °C) was extracted with 6 M HCl. The acid hydrolysable, extractable N (THN) was fractionated into ammonia N (AN), amino acid N (AAN), amino sugar N (ASN) and uncharacterisable hydrolysable N (UHN). Biochar samples were also treated with 0.167 M K2Cr2O7 acid to determine N potentially available in the long term. An incubation study of the different biochar samples mixed with acid washed sand was conducted at 32 °C for 81 days to study both C and N turnover. During incubation, the CO2 released was trapped in NaOH and quantified. Hydrolysable N decreased as pyrolysis temperature increased from 250 to 550 °C. Fractionation into AN, AAN, ASN and UHN revealed progressive structural rearrangement of N with pyrolysis temperature. Based on HCl hydrolysis and dichromate oxidation results, C and N in biochar became more stable as pyrolysis temperature increased. The ratio of volatile C to THN was a useful indicator of whether net N mineralisation or immobilisation of N in biochar occurred. THN thus seems a sound estimate of the labile N fraction in biochar in the short term; however, dichromate-oxidisable N is probably more meaningful in the long run. Further studies using different types of biochar need to be conducted under more realistic conditions to obtain more information on N availability in biochar once in soil.  相似文献   

15.
This study investigates the occurrence of greenhouse gases (GHGs) and the role of groundwater as an indirect pathway of GHG emissions into surface waters in a gaining stretch of the Triffoy River agricultural catchment (Belgium). To this end, nitrous oxide (N2O), methane (CH4) and carbon dioxide (CO2) concentrations, the stable isotopes of nitrate, and major ions were monitored in river and groundwater over 8 months. Results indicated that groundwater was strongly oversaturated in N2O and CO2 with respect to atmospheric equilibrium (50.1 vs. 0.55 μg L?1 for N2O and 14,569 vs. 400 ppm for CO2), but only marginally for CH4 (0.45 vs. 0.056 μg L?1), suggesting that groundwater can be a source of these GHGs to the atmosphere. Nitrification seemed to be the main process for the accumulation of N2O in groundwater. Oxic conditions prevailing in the aquifer were not prone for the accumulation of CH4. In fact, the emissions of CH4 from the river were one to two orders of magnitude higher than the inputs from groundwater, meaning that CH4 emissions from the river were due to CH4 in-situ production in riverbed or riparian zone sediments. For CO2 and N2O, average emissions from groundwater were 1.5?×?105 kg CO2 ha?1 year?1 and 207 kg N2O ha?1 year?1, respectively. Groundwater is probably an important source of N2O and CO2 in gaining streams but when the measures are scaled at catchment scale, these fluxes are probably relatively modest. Nevertheless, their quantification would better constrain nitrogen and carbon budgets in natural systems.  相似文献   

16.
Biochar has been considered a safe soil additive to enhance soil fertility and agronomic traits of different crops. This study was conducted to explore the impacts of sugarcane waste straw biochar on soil characteristics and some agronomic traits of okra. The experiment was carried out with four treatments, i.e., control, sugarcane waste straw biochar (10 ton ha?1), farmyard manure (FYM, 10 ton ha?1), and chemical fertilizers (NPK; 120:100:80 kg ha?1) having three replications of each treatment. Soil samples were tested for texture, bulk density, particle density, pH, electrical conductivity (EC), organic matter content, nitrate nitrogen (NO3-N), and extractable-P. The sugarcane waste straw biochar was characterized for plant major nutrient elements. The impact of various treatments was observed on soils and agronomic traits of okra like plant height, fruit size, fruit length, and yield of okra. Results revealed that sugarcane waste straw biochar expressed higher EC value and noticeable amounts of nitrogen (N), phosphorus (P), potassium (K), sulfur (S), and magnesium (Mg). The sugarcane waste straw biochar, in comparison with FYM and NPK, significantly improved the NO3-N, extractable-P, OM and EC of the calcareous soil, and reduced the soil bulk density. Furthermore, plant growth and yield parameters were significantly improved under biochar application over the control, FYM and NPK. Overall, sugarcane waste straw biochar proved to be a good alternative to conventional organic and inorganic fertilizers under calcareous soil conditions.  相似文献   

17.
We present new equilibrium mixed-volatile (H2O–CO2) solubility data for a phonotephrite from Erebus volcano, Antarctica. H2O–CO2-saturated experiments were conducted at 400–700 MPa, 1,190 °C, and ~NNO + 1 in non-end-loaded piston cylinders. Equilibrium H2O–CO2 fluid compositions were determined using low-temperature vacuum manometry, and the volatile and major element compositions of the glassy run products were determined by Fourier transform infrared spectroscopy and electron microprobe. Results show that the phonotephrite used in this study will dissolve ~0.8 wt% CO2 at 700 MPa and a fluid composition of $ X_{{{\text{H}}_{ 2} {\text{O}}}} $ ~0.4, in agreement with previous experimental studies on mafic alkaline rocks. Furthermore, the dissolution of CO2 at moderate to high $ X_{{{\text{H}}_{ 2} {\text{O}}}}^{\text{fluid}} $ in our experiments exceeds that predicted using lower-pressure experiments on similar melts from the literature, suggesting a departure from Henrian behavior of volatiles in the melt at pressures above 400 MPa. With these data, we place new constraints on the modeling of Erebus melt inclusion and gas emission data and thus the interpretation of its magma plumbing system and the contributions of primitive magmas to passive and explosive degassing from the Erebus phonolite lava lake.  相似文献   

18.
A field control experiment was carried out to determine the influence of water table changes on soil CO2, CH4, and N2O emissions in Calamagrostis angustifolia freshwater marsh in Northeast of China. The results showed that the water depth of 5 cm below the ground surface increased soil CO2 emission, but there was no significant influence of deeper water table on gas emission. CH4 emission was accelerated by deep standing water and approached the peak in the plant booming time. This suggests that root activity has influence on CH4 production. The result also demonstrated that both low water table level and inundated environment would inhibit N2O emission. Comparing the total global warming potential of three gases under different conditions, it can be concluded that maintaining a comparatively steady water table near the soil surface can benefit soil carbon sequestration in the C. angustifolia marsh, and decrease of the greenhouse gases emissions to the atmosphere.  相似文献   

19.
Because of their physicochemical properties, biochars can be used as sorption materials for removal of toxic substances. The purpose of the present study was to determine whether biochar obtained from cones of larch (Larix decidua Mill. subsp. decidua) and spruce (Picea abies L. H. Karst) could be used as a sorbent for Cd2+, Pb2+ and Co2+ in aqueous solutions. So far, this feedstock had not been tested in this respect. The material was subjected to pyrolysis at 500 and 600 °C for the duration of 5, 10 and 15 min. The obtained pyrolysates were found to differ in terms of pH and the contents of the essential macroelements. The different values of these parameters were determined for varying temperature, duration of the pyrolysis process and type of feedstock. Sorption capacities of the biochars for removal of Cd2+, Pb2+ and Co2+ were examined using simulated contamination of aqueous solutions with salts of these metals. The findings showed the highest, nearly complete, removal for Pb2+ were maximum 99.7%, and almost three times lower value for Cd2+ and Co2+ (respectively, 35.7 and 24.8%). It was demonstrated that pyrolysis of conifer cones produced optimum sorption capacities when the process was conducted at a temperature of 500 °C for the duration of 5 min. It was shown that products of spruce cone pyrolysis were characterized by better sorption capacity in comparison with products of larch cone pyrolysis. The properties of conifer cone biochar create the possibility of using it as an adsorbent in water and wastewater treatment as well as in production of filters and activated carbon.  相似文献   

20.
Measuring fluxes of greenhouse gases (GHGs) is fundamental to estimating their impact on global warming. We examined diurnal variations of carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) vertical fluxes in a tidal marsh ecosystem. Measurements were recorded on neap and spring tide days in April and September 2010 in the Shanyutan wetland of the Min River estuary, southeast China. Here, we define a positive flux as directing into the atmosphere. CH4 fluxes on the diurnal scale were positive throughout, and CH4 emissions into the atmosphere on neap tide days were higher than on spring tide days. CH4 releases from the marsh ecosystem on neap tide days were higher in the daytime; however, on spring tide days, daily variations of CH4 emissions were more complex. The marsh ecosystem plays a twofold role in both releasing and assimilating CO2 and N2O gases on the diurnal scale. Average CO2 fluxes were positive on the daily scale both on neap and spring days and were greater on the neap tide days than on spring tide days. Diurnal variations of N2O fluxes fluctuated more. Over the diurnal period, soil temperature markedly controlled variations of CH4 emissions compared to other soil factors, such as salinity and redox potential. Tidal water height was a key factor influencing GHGs fluxes at the water–air interface. Compared with N2O, the diurnal course of CO2 and CH4 fluxes in the marsh ecosystem appeared to be directly controlled by marsh plants. These results have implications for sampling and scaling strategies for estimating GHGs fluxes in tidal marsh ecosystems.  相似文献   

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