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At least 739 records · Page 41Linked to original sources

A sulfur-based survival strategy for putative phototrophic life in the venusian atmosphere.

Several observations indicate that the cloud deck of the venusian atmosphere may provide a plausible refuge for microbial life. Having originated in a hot proto-ocean or been brought in by meteorites from Earth (or Mars), early life on Venus could have adapted to a dry, acidic atmospheric niche as the warming planet lost its oceans. The greatest obstacle for the survival of any organism in this niche may be high doses of ultraviolet (UV) radiation. Here we make the argument that such an organism may utilize sulfur allotropes present in the venusian atmosphere, particularly S(8), as a UV sunscreen, as an energy-converting pigment, or as a means for converting UV light to lower frequencies that can be used for photosynthesis. Thus, life could exist today in the clouds of Venus.

Atmosphere↗

Haze aerosols in the atmosphere of early Earth: manna from heaven.

An organic haze layer in the upper atmosphere of Titan plays a crucial role in the atmospheric composition and climate of that moon. Such a haze layer may also have existed on the early Earth, providing an ultraviolet shield for greenhouse gases needed to warm the planet enough for life to arise and evolve. Despite the implications of such a haze layer, little is known about the organic material produced under early Earth conditions when both CO(2) and CH(4) may have been abundant in the atmosphere. For the first time, we experimentally demonstrate that organic haze can be generated in different CH(4)/CO(2) ratios. Here, we show that haze aerosols are able to form at CH(4) mixing ratios of 1,000 ppmv, a level likely to be present on early Earth. In addition, we find that organic hazes will form at C/O ratios as low as 0.6, which is lower than the predicted value of unity. We also show that as the C/O ratio decreases, the organic particles produced are more oxidized and contain biologically labile compounds. After life arose, the haze may thus have provided food for biota.

Aerosols↗

Evaluation of the growth response of six invasive species to past, present and future atmospheric carbon dioxide.

The response of plant species to future atmospheric carbon dioxide concentrations [CO(2)] has been determined for hundreds of crop and tree species. However, no data are currently available regarding the response of invasive weedy species to past or future atmospheric [CO(2)]. In the current study, the growth of six species which are widely recognized as among the most invasive weeds in the continental United States, Canada thistle (Cirsium arvense (L.) Scop.), field bindweed (Convolvulus arvensis L.), leafy spurge (Euphorbia esula L.), perennial sowthistle (Sonchus arvensis L.), spotted knapweed (Centaurea maculosa Lam.), and yellow star thistle (Centaurea solstitialis L.) were grown from seed at either 284, 380 or 719 micromol mol(-1) [CO(2)] until the onset of sexual reproduction (i.e. the vegetative period). The CO(2) concentrations corresponded roughly to the CO(2) concentrations which existed at the beginning of the 20th century, the current [CO(2)], and the future [CO(2)] projected for the end of the 21st century, respectively. The average stimulation of plant biomass among invasive species from current to future [CO(2)] averaged 46%, with the largest response (+72%) observed for Canada thistle. However, the growth response among these species to the recent [CO(2)] increase during the 20th century was significantly higher, averaging 110%, with Canada thistle again (+180%) showing the largest response. Overall, the CO(2)-induced stimulation of growth for these species during the 20th century (285-382 micromol mol(-1)) was about 3x greater than for any species examined previously. Although additional data are needed, the current study suggests the possibility that recent increases in atmospheric CO(2) during the 20th century may have been a factor in the selection of these species.

Atmosphere↗

Impact of pedospheric and atmospheric sulphur nutrition on sulphur metabolism of Allium cepa L., a species with a potential sink capacity for secondary sulphur compounds.

Onion (Allium cepa L.) was able to use atmospheric H(2)S as sole sulphur source for growth. The foliarly absorbed H(2)S was rapidly metabolized into water-soluble, non-protein thiol compounds, including cysteine, and subsequently into other sulphur compounds in the shoots. In H(2)S-exposed plants, the accumulation of sulphur compounds in the shoots was nearly linear with the concentration (0.15-0.6 microl l(-1)) and duration of the exposure. Exposure of onion to H(2)S for up to 1 week did not affect the sulphur content of the roots. Secondary sulphur compounds formed a sink for the foliarly absorbed sulphide, and the sulphur accumulation upon H(2)S exposure could, for a great part, be ascribed to enhancement of the content of gamma-glutamyl peptides and/or alliins. Furthermore, there was a substantial increase in the sulphate content in the shoots upon H(2)S exposure. The accumulation of sulphate originated both from the pedosphere and from the oxidation of absorbed atmospheric sulphide, and/or from the degradation of accumulated secondary sulphur compounds. From studies on the interaction between atmospheric and pedospheric sulphur nutrition it was evident that H(2)S exposure did not result in a down-regulation of the sulphate uptake by the roots.

Atmosphere↗

A probabilistic estimation of atmospheric tritium dose.

A radiation dose distribution has been calculated for an individual exposed to tritium oxide (tritiated water vapor) in the atmosphere. A specific activity model was used that is similar to that detailed in the Nuclear Regulatory Commission's Regulatory Guide 1.109. The values of 19 parameters are sampled consistent with assigned probability distributions using a Latin Hypercube approach. Dose was estimated assuming a concentration of tritium in atmospheric moisture of 0.13 +/- 0.16 Bq mL-1. Conventional dosimetric methods for tritium that were consistent with the Regulatory Guide result in an estimate of 0.63 microSv for annual exposures to airborne tritiated water. For the same atmospheric tritium concentration, the estimated dose distribution is lognormal and ranges from 0.08-3.2 microSv (at 95% confidence) with a median value of 0.59 microSv and a 95th percentile of 2.6 microSv.

Air Pollution, Radioactive↗

Meteorological benefits from atmospheric nuclear tests.

The presence in the atmosphere of radioactive debris from nuclear tests provided a unique opportunity to study atmospheric motions and transfers of trace substances. Measurements of the concentrations in air of radionuclides were used to verify trajectories derived solely from weather data. The profiles of radioactive concentration along the aircraft tracks were non-Gaussian. High-flying aircraft and balloons collected air and particulate samples to approximately 30,000 m from Alaska to South America. The measurements from these samples were used in verifying stratospheric motions on a hemispheric and global scale. Other benefits to the atmospheric sciences gained during the nuclear testing era are briefly described.

Atmosphere↗

The future of the carbon cycle: review, calcification response, ballast and feedback on atmospheric CO2.

The operation of the carbon cycle forms an important part of the processes relevant to future changes in atmospheric carbon dioxide. The balance of carbon between terrestrial and oceanic reservoirs is an important factor and here we focus in particular on the oceans. Future changes in the carbon cycle that may affect air-sea partitioning of CO(2) are difficult to quantify but the palaeoceanographic record and modern observational studies provide important evidence of what variations might occur. These include changes in surface nutrient use, the oceanic inventory of nutrients, and the elemental composition and rain-rate ratio of marine particles. Recent work has identified two inter-linked processes of potential importance that we consider in some detail: the response of marine calcification to changes in surface water CO(2) and the association of particulate organic carbon with ballast minerals, in particular biogenic calcite. We review evidence from corals, coccolithophores and foraminifera, which suggests that the response of reduced calcification provides a negative feedback on rising atmospheric CO(2). We then use a box model to demonstrate how the calcification response may affect the organic carbon rain rate through the ballast effect. The ballast effect on export fluxes of organic and inorganic carbon acts to counteract the negative calcification response to increased CO(2). Thus, two oceanic buffers exert a significant control on ocean-atmosphere carbonate chemistry: the thermodynamic CO(2) buffer; and the ballast/calcification buffer. Just how tightly coupled the rain-rate ratio of CaCO(3)/C(org) is to fluxes of ballast minerals is an important question for future research.

Atmosphere↗

Trace elements in the atmosphere.

The distribution and behaviour of particulate trace elements in the atmosphere have been studied by continuous measurements for 5 years at seven non-urban sites in the United Kingdom. Samples have been taken regularly of airborne dust, rainwater and dry deposition: these have been analysed for up to 36 elements. Concentrations of trace elements vary considerably between sites but the relative concentrations are among uniform: this suggests similarity of origin or good atmospheric mixing. By comparing the relative concentrations with those in soil it is possible to differentiate between trace elements that are derived from soil and those that may be attributed to industrial activity. This classification is supported by estimates of the particle sizes in air. The deposition of trace elements can be related to the concentrations presnet in soil and to the annual removal by crops. Retrospective analyses of stored samples from one site describe the history of trace element concentrations in air since 1957. The sea surface is considered as a possible source of atmospheric trace elements.

Aerosols↗

Contrasting simulated past and future responses of the Amazonian forest to atmospheric change.

Modelling simulations of palaeoclimate and past vegetation form and function can contribute to global change research by constraining predictions of potential earth system responses to future warming, and by providing useful insights into the ecophysiological tolerances and threshold responses of plants to varying degrees of atmospheric change. We contrasted HadCM3LC simulations of Amazonian forest at the last glacial maximum (LGM; 21 kyr ago) and a Younger Dryas-like period (13-12 kyr ago) with predicted responses of future warming to provide estimates of the climatic limits under which the Amazon forest remains relatively stable. Our simulations indicate that despite lower atmospheric CO2 concentrations and increased aridity during the LGM, Amazonia remains mostly forested, and that the cooling climate of the Younger Dryas-like period in fact causes a trend toward increased above-ground carbon balance relative to today. The vegetation feedbacks responsible for maintaining forest integrity in past climates (i.e. decreased evapotranspiration and reduced plant respiration) cannot be maintained into the future. Although elevated atmospheric CO2 contributes to a positive enhancement of plant carbon and water balance, decreased stomatal conductance and increased plant and soil respiration cause a positive feedback that amplifies localized drying and climate warming. We speculate that the Amazonian forest is currently near its critical resiliency threshold, and that even minor climate warming may be sufficient to promote deleterious feedbacks on forest integrity.

Atmosphere↗

An approach to balancing the positive and negative effects of elevated nitrogen oxides in the lower atmosphere on terrestrial plants.

Elevated NOx in the lower atmosphere has three major effects on terrestrial plants. On the one hand, it causes an increase in surface ozone concentration. This reduces plant growth rate. On the other hand, elevated NOx causes an increase in the flux of oxidized N compounds from the atmosphere to the land surface. This plays a dual role in the life of terrestrial plants. Additional N in soils stimulates plant growth (N-fertilization effect), whereas soil acidification may negatively affect plants. A simple empirical model for calculating the overall effect of anthropogenic increase in NOx level has been developed. The model is based on experimental "cause-response" data presented in world scientific literature. Calculations showed that at the large scale, among the above-mentioned changes, elevated O3 plays a major and negative role in plant life. Its negative effect on plants is partly compensated by N fertilization in unmanaged ecosystems. Such compensation appears to be negligible in agricultural lands. There are vast territories in Euro--Asia--for instance, a territory of Russia--in which acid atmospheric deposition has no significant effect on terrestrial plants.

Acid Rain↗

Legume species identity and soil nitrogen supply determine symbiotic nitrogen-fixation responses to elevated atmospheric [CO2].

In nitrogen (N)-limited systems, the response of symbiotic N fixation to elevated atmospheric [CO2] may be an important determinant of ecosystem responses to this global change. Experimental tests of the effects of elevated [CO2] have not been consistent. Although rarely tested, differences among legume species and N supply may be important. In a field free-air CO2 enrichment (FACE) experiment, we determined, for four legume species, whether the effects of elevated atmospheric [CO2] on symbiotic N fixation depended on soil N availability or species identity. Natural abundance and pool-dilution 15N methods were used to estimate N fixation. Although N addition did, in general, decrease N fixation, contrary to theoretical predictions, elevated [CO2] did not universally increase N fixation. Rather, the effect of elevated [CO2] on N fixation was positive, neutral or negative, depending on the species and N addition. Our results suggest that legume species identity and N supply are critical factors in determining symbiotic N-fixation responses to increased atmospheric [CO2].

Atmosphere↗

Acoustic propagation and atmosphere characteristics derived from infrasonic waves generated by the Concorde.

Infrasonic signals generated by daily supersonic Concorde flights between North America and Europe have been consistently recorded by an array of microbarographs in France. These signals are used to investigate the effects of atmospheric variability on long-range sound propagation. Statistical analysis of wave parameters shows seasonal and daily variations associated with changes in the wind structure of the atmosphere. The measurements are compared to the predictions obtained by tracing rays through realistic atmospheric models. Theoretical ray paths allow a consistent interpretation of the observed wave parameters. Variations in the reflection level, travel time, azimuth deviation and propagation range are explained by the source and propagation models. The angular deviation of a ray's azimuth direction, due to the seasonal and diurnal fluctuations of the transverse wind component, is found to be approximately 5 degrees from the initial launch direction. One application of the seasonal and diurnal variations of the observed phase parameters is the use of ground measurements to estimate fluctuations in the wind velocity at the reflection heights. The simulations point out that care must be taken when ascribing a phase velocity to a turning height. Ray path simulations which allow the correct computation of reflection heights are essential for accurate phase identifications.

Acoustics↗

Measurements of atmospheric attenuation at ultrasonic frequencies and the significance for echolocation by bats.

The absorption of sound propagating through the atmosphere under laboratory conditions of 25 degrees C and 50% relative humidity was measured at frequencies from 30 to 200 kHz. The attenuating effect on the passage of ultrasonic sounds through air ranged from 0.7 dB/m at 30 kHz. These measurements confirm theoretical expectations and earlier observations that atmospheric attenuation is progressively more severe at higher frequencies and that the atmosphere acts as a low-pass filter for conducting sounds in the frequency range used for echolocation by bats. Different species of bats use different portions of this range of frequencies, and bats emitting sonar signals predominantly above 100 kHz encounter especially severe attenuation of over 3 dB/m. With the greatly restricted operating distances for echolocation at such high frequencies, bats using these higher frequencies must be under compelling ecological pressures of a higher priority than long-range detection of targets.

Animals↗

Influence of carbonic anhydrase activity in terrestrial vegetation on the 18O content of atmospheric CO2.

The oxygen-18 (18O) content of atmospheric carbon dioxide (CO2) is an important indicator of CO2 uptake on land. It has generally been assumed that during photosynthesis, oxygen in CO2 reaches isotopic equilibrium with oxygen in 18O-enriched water in leaves. We show, however, large differences in the activity of carbonic anhydrase (which catalyzes CO2 hydration and 18O exchange in leaves) among major plant groups that cause variations in the extent of 18O equilibrium (theta(eq)). A clear distinction in theta(eq) between C3 trees and shrubs, and C4 grasses makes atmospheric C18OO a potentially sensitive indicator to changes in C3 and C4 productivity. We estimate a global mean theta(eq) value of approximately 0.8, which reasonably reconciles inconsistencies between 18O budgets of atmospheric O2 (Dole effect) and CO2.

Atmosphere↗

Life and the evolution of Earth's atmosphere.

Harvesting light to produce energy and oxygen (photosynthesis) is the signature of all land plants. This ability was co-opted from a precocious and ancient form of life known as cyanobacteria. Today these bacteria, as well as microscopic algae, supply oxygen to the atmosphere and churn out fixed nitrogen in Earth's vast oceans. Microorganisms may also have played a major role in atmosphere evolution before the rise of oxygen. Under the more dim light of a young sun cooler than today's, certain groups of anaerobic bacteria may have been pumping out large amounts of methane, thereby keeping the early climate warm and inviting. The evolution of Earth's atmosphere is linked tightly to the evolution of its biota.

Atmosphere↗

Abundance of cellular material and proteins in the atmosphere.

Suspended atmospheric particles play a crucial role in any global climate scenario: They can both enforce and suppress radiative forcing. In developing climate modeling further, a deeper understanding of atmospheric aerosol is needed. Because of extreme local and temporal variations, proper incorporation of aerosols into models requires modeling of the aerosol itself. It turns out that cellular material and proteins compose up to 25% of the atmospheric aerosol. Consequently, the source strength of the biogenic aerosol in general must be corrected and should be estimated on the order of other major aerosol sources.

Aerosols↗

REPLACEMENT RATES FOR HUMAN TISSUE FROM ATMOSPHERIC RADIOCARBON.

Carbon-14, derived from the testing of thermonuclear weapons in the atmosphere of the Northern Hemisphere during 1961-62, has been found in human tissues including the brain in amounts which reflect the atmospheric concentration of carbon-14 as of several months earlier. In collagen of cartilage, the rate of uptake of carbon-14 is much slower than in other tissues; essentially no radioactive carbon was found in the collagen of 70-year-old adults that had been exposed to the comparatively high concentrations of carbon-14 in the atmosphere during the years 1954 to 1964. Individuals from the Southern Hemisphere show little increase in the carbon-14 content of their tissues at present, and detailed tests with individuals traveling to the Northern Hemisphere from the Southern allow closer scrutiny of the tissue replacement rates.

Adult↗

The oxidizing capacity of the earth's atmosphere: probable past and future changes.

The principal oxidants in the lower atmosphere are ozone (O3) and two by-products of O3 photodissociation, the hydroxyl radical (OH) and hydrogen peroxide (H2O2). A number of critical atmospheric chemical problems depend on the earth's "oxidizing capacity," which is essentially the global burden of these oxidants. There is limited direct evidence for changes in the earth's oxidizing capacity since recent preindustrial times when, because of industrial and population growth, increasing amounts of O3 precursor trace gases (carbon monoxide, nitrogen oxides, and hydrocarbons) have been released into the atmosphere. The concentrations of O3 and possibly H2O2 have increased over large regions. Models predict that tropospheric O3 will increase approximately 0.3 to 1% per year over the next 50 years with both positive and negative trends possible for OH and H2O2. Models and the observational network for oxidants are improving, but validation of global models is still at an early stage.

Atmosphere↗