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1.
Emissions of N2O, CH4, and CO2 from soils at two sites in the tropical savanna of central Venezuela were determined during the dry season in February 1987. Measured arithmetic mean fluxes of N2O, CH4, and CO2 from undisturbed soil plots to the atmosphere were 2.5×109, 4.3×1010, and 3.0×1013 molecules cm-2 s-1, respectively. These fluxes were not significantly affected by burning the grass layer. Emissions of N2O increased fourfold after simulated rainfall, suggesting that production of N2O in savanna soils during the rainy season may be an important source for atmospheric N2O. The CH4 flux measurements indicate that these savanna soils were not a sink, but a small source, for atmospheric methane. Fluxes of CO2 from savanna soils increased ninefold two hours after simulated rainfall, and remained three times higher than normal after 16 hours. More research is needed to clarify the significance of savannas in the global cycles of N2O, CH4, CO2, and other trace gases, especially during the rainy season. 相似文献
2.
We show that photochemical processes in the lower half of the troposphere are strongly affected by the presence of liquid water clouds. Especially CH2O, an important intermediate of CH4 (and of other hydrocarbon) oxidation, is subject to enhanced breakdown in the aqueous phase. This reduces the formation of HO
x
-radicals via photodissociation of CH2O in the gas phase. In the droplets, the hydrated form of CH2O, its oxidation product HCO2
–, and H2O2 recycle O2
– radicals which, in turn, react with ozone. We show that the latter reaction is a significant sink for O3. Further O3 concentrations are reduced as a result of decreased formation of O3 during periods with clouds. Additionally, NO
x
, which acts as a catalyst in the photochemical formation of O3, is depleted by clouds during the night via scavenging of N2O5. This significantly reduces NO
x
-concentrations during subsequent daylight hours, so that less NO
x
is available for O3 production. Clouds thus directly reduce the concentrations of O3, CH2O, NO
x
, and HO
x
. Indirectly, this also affects the budgets of other trace gases, such as H2O2, CO, and H2. 相似文献
3.
During a large nuclear war, the atmosphere would be loaded with huge quantities of pollutants, which are produced by fires in urban and industrial centers, cultivated lands, forests and grasslands. Especially detrimental are the effects of light absorbing airborne particles. An analysis of the amounts of the various types of fuels which could burn in a nuclear war indicates that more than 1014 g of black smoke could be produced by fires started by the nuclear explosions. Due to this, the penetration of sunlight to the earth's surface would be reduced greatly over extended areas of the northern hemisphere, maybe even globally. This could temporarily cause extreme darkness in large areas in midlatitudes and reduce crop growth and biospheric productivity.This situation would last for several weeks and cause very anomalous meteorological conditions. Much solar radiation would be absorbed in the atmosphere instead of at the earth's surface. The land areas and lower atmosphere would, therefore, cool and the overlying atmosphere warm, creating strong vertical thermal stability in a highly polluted atmosphere. For extended periods and in large parts of the world, weather conditions would be abnormal. The resulting cold, probably freezing, temperatures at the ground would interfere severely with crop production during the growing season and cause extreme conditions for large sections of the biosphere. The combination of lack of sunlight, frost and other adverse meteorological conditions would add enormously to the already huge problems of the survivors. 相似文献
4.
We measured the emissions of volatile aliphatic amines and ammonia produced by the manure of beef cattle, dairy cows, swine, laying hens and horses in livestock buildings. The amine emissions consisted almost exclusively of the three methylamines and correlated with those of ammonia. The molar emission ratios of the methylamines to ammonia, and data on NH3 emissions from animal husbandry in Europe, together with global statistics on domestic animals, were used to estimate the global emissions of amines. Annual global methylamine-N input to the atmosphere from animal husbandry in 1988 was 0.15±0.06 TgN (Tg=1012 g). Almost 3/4 of these emissions consisted of trimethylamine-N. This represents about half of all methylamine emissions to the atmosphere. Other sources are marine coastal waters and biomass burning.Possible reaction pathways for atmospheric methylamines are shown. Among various speculative but possible products N2O and HCN are of interest because the emission of methylamines could contribute to the global budgets of these compounds. Maximum atmospheric N2O production from methylamines are below 0.4 Tg N/year, which is less than 10% of the annual N2O growth rate. Although we do not expect the methylamine emissions to contribute in a major way to the atmospheric N2O budget, more studies are needed to establish this conclusion beyond doubt. Similar conclusions hold for HCN. 相似文献
5.
R. Müller J.-U. Grooß D. S. McKenna P. J. Crutzen C. Brühl J. M. Russell III L. L. Gordley J. P. Burrows A. F. Tuck 《Annales Geophysicae》1998,17(1):101-114
Severe chemical ozone loss has been detected in the Arctic in the winter and spring of 1995–96 by a variety of methods. Extreme reductions in column ozone due to halogen catalysed chemistry were derived from measurements of the Halogen Occultation Experiment (HALOE) on board the Upper Atmosphere Research Satellite in the Arctic vortex. Here, we discuss further aspects of the HALOE observations in the Arctic over this period. Potential problems, both in the data themselves and in the methodology of the data analysis are considered and the reason for the differences between the Arctic ozone losses deduced from HALOE data version 17 and 18 is analysed. Moreover, it is shown that HALOE measurements in the Arctic in winter and spring 1995–96 compare well with observations by other ground-based and satellite instruments. 相似文献
6.
Estimates of gross and net fluxes of carbon between the biosphere and the atmosphere from biomass burning 总被引:26,自引:0,他引:26
In order to estimate the production of charcoal and the atmospheric emissions of trace gases volatilized by burning we have estimated the global amounts of biomass which are affected by fires. We have roughly calculated annual gross burning rates ranging between about 5 Pg and 9 Pg (1 Pg = 1015 g) of dry matter (2–4 Pg C). In comparison, about 9–17 Pg of above-ground dry matter (4–8 Pg C) is exposed to fires, indicating a worldwide average burning efficiency of about 50%. The production of dead below-ground dry matter varies between 6–9 Pg per year. We have tentatively indicated the possibility of a large production of elemental carbon (0.5–1.7 Pg C/yr) due to the incomplete combustion of biomass to charcoal. This provides a sink for atmospheric CO2, which would have been particularly important during the past centuries. From meager statistical information and often ill-documented statements in the literature, it is extremely difficult to calculate the net carbon release rates to the atmosphere from the biomass changes which take place, especially in the tropics. All together, we calculate an overall effect lof the biosphere on the atmospheric carbon dioxide budget which may range between the possibilities of a net uptake or a net release of about 2 Pg C/yr. The release of CO2 to the atmosphere by deforestation projects may well be balanced by reforestation and by the production of charcoal. Better information is needed, however, to make these estimates more reliable.Now at the Max-Planck-Institute for Chemistry, Mainz, FRG.The National Center for Atmospheric Research is sponsored by the National Science Foundation. 相似文献
7.
A Nel BI Pletschke CLW Jones J Kemp G Robinson PJ Britz 《African Journal of Marine Science》2017,39(2):183-192
The effect of kelp Ecklonia maxima inclusion in formulated feeds on abalone growth and gut bacterial communities has not been previously investigated in South Africa. An eight-month on-farm growth trial was conducted with sub-adult Haliotis midae (~43 mm shell length) fed graded levels of kelp in formulated feeds. Kelp inclusion (0.44–3.54% of pellet dry mass) promoted faster growth (65.7–74.5% total mass gain), with better feed and protein conversions (apparent feed conversion ratio [FCR] 1.4–1.8, apparent protein efficiency ratio [PER] 2.3–2.7), as compared with the non-supplemented feed (52.3% total mass gain, FCR 2.1, PER 1.9; p < 0.001). Abalone-gut bacterial DNA was sequenced using 16S rRNA gene pyrosequencing and the sequences were clustered into operational taxonomic units (OTUs) at a 97% similarity level. A supplementary 16S rRNA gene denaturing gradient gel electrophoresis (DGGE) analysis was employed. The dominant OTUs differed in terms of their relative abundances, with an autochthonous Mycoplasma strain being significantly more abundant (p = 0.03) in the gut of abalone fed a kelp-supplemented feed. The DGGE band patterns displayed higher within-group variability for abalone fed the control diet, suggesting that dietary kelp inclusion promotes gut-bacteria homeostasis. This may contribute to better feed utilisation and growth in abalone fed kelp-supplemented feeds. 相似文献
8.
Age verification of rubyfish (Plagiogeneion rubiginosum) was sought using the bomb radiocarbon chronometer procedure. Stable isotopes were investigated for life history characteristics. Radiocarbon (14C) and stable isotope (δ18O and δ13C) levels were measured in micro-samples from five otoliths that had been aged using a zone count method. All the core 14C measurements were ‘pre-bomb’ indicating ages of at least 45 years, and the 14C measurements across the otolith sections suggested that the zone-count ageing method described herein is not biased. Maximum estimated age was 100 years. There was no significant between-sex difference in the von Bertalanffy growth curves. The δ18O values indicated that rubyfish are near-surface as juveniles, and move deeper with age. Adults appear to reside in 600–1000 m; this is deeper than most trawl-capture data suggest, but not implausible, and has stock assessment implications. The δ13C values reflect fish metabolic rates, trophic feeding levels and oceanographic conditions. The stable isotopes record the environmental life history of each fish, and have value in distinguishing stocks and/or indicating vertical and latitudinal migratory patterns. 相似文献
9.
C. Warneke R. Holzinger A. Hansel A. Jordan W. Lindinger U. Pöschl J. Williams P. Hoor H. Fischer P. J. Crutzen H. A. Scheeren J. Lelieveld 《Journal of Atmospheric Chemistry》2001,38(2):167-185
Airborne measurements of volatile organic compounds (VOC) were performed overthe tropical rainforest in Surinam (0–12 km altitude,2°–7° N, 54°–58° W) using the proton transferreaction mass spectrometry (PTR-MS) technique, which allows online monitoringof compounds like isoprene, its oxidation products methyl vinyl ketone,methacrolein, tentatively identified hydroxy-isoprene-hydroperoxides, andseveral other organic compounds. Isoprene volume mixing ratios (VMR) variedfrom below the detection limit at the highest altitudes to about 7 nmol/molin the planetary boundary layer shortly before sunset. Correlations betweenisoprene and its product compounds were made for different times of day andaltitudes, with the isoprene-hydroperoxides showing the highest correlation.Model calculated mixing ratios of the isoprene oxidation products using adetailed hydrocarbon oxidation mechanism, as well as the intercomparisonmeasurement with air samples collected during the flights in canisters andlater analysed with a GC-FID, showed good agreement with the PTR-MSmeasurements, in particular at the higher mixing ratios.Low OH concentrations in the range of 1–3 × 105molecules cm-3 averaged over 24 hours were calculated due to lossof OH and HO2 in the isoprene oxidation chain, thereby stronglyenhancing the lifetime of gases in the forest boundary layer. 相似文献
10.
Joanne H. Shorter J. Barry Mcmanus Charles E. Kolb Eugene J. Allwine Brian K. Lamb Byard W. Mosher Robert C. Harriss Uwe Partchatka Horst Fischer Geoffrey W. Harris Paul J. Crutzen Hans-Josef Karbach 《Journal of Atmospheric Chemistry》1996,24(2):121-140
We have investigated methane emissions from urban sources in the former East Germany using innovative measurement techniques including a mobile real-time methane instrument and tracer release experiments. Anthropogenic and biogenic sources were studied with the emphasis on methane emissions from gas system sources, including urban distribution facilities and a production plant. Methane fluxes from pressure regulating stations ranged from 0.006 to 24. l/min. Emissions from diffuse sources in urban areas were also measured with concentration maps and whole city flux experiments. The area fluxes of the two towns studied were 0.37 and 1.9 g/m2/s. The emissions from individual gas system stations and total town emissions of this study are comparable to results of similar sites examined in the United States. 相似文献