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T.A. McConnaughey

Publications and source records attributed to T.A. McConnaughey.

3 recordsLinked to original sources

Estimating lake-atmosphere CO2 exchange

Lake‐atmosphere CO 2 flux was directly measured above a small, woodland lake using the eddy covariance technique and compared with fluxes deduced from changes in measured lake‐water CO 2 storage and with flux predictions from boundary‐layer and surface‐renewal models. Over a 3‐yr period, lake‐atmosphere exchanges of CO 2 were measured over 5 weeks in spring, summer, and fall. Observed springtime CO 2 efflux was large (2.3–2.7 umol m ‐2 s ‐1 ) immediately after lake‐thaw. That efflux decreased exponentially with time to less than 0.2 umol m ‐2 s −1 within 2 weeks. Substantial interannual variability was found in the magnitudes of springtime efflux, surface water CO 2 concentrations, lake CO 2 storage, and meteorological conditions. Summertime measurements show a weak diurnal trend with a small average downward flux (−0.17 μmol m ‐2 s 1 ) to the lake's surface, while late fall flux was trendless and smaller (−0.0021 μmol m ‐2 s −1 ). Large springtime efflux afforded an opportunity to make direct measurement of lake‐atmosphere fluxes well above the detection limits of eddy covariance instruments, facilitating the testing of different gas flux methodologies and air‐water gas‐transfer models. Although there was an overall agreement in fluxes determined by eddy covariance and those calculated from lake‐water storage change in CO 2 , agreement was inconsistent between eddy covariance flux measurements and fluxes predicted by boundary‐layer and surface‐renewal models. Comparison of measured and modeled transfer velocities for CO 2 , along with measured and modeled cumulative CO 2 flux, indicates that in most instances the surface‐renewal model underpredicts actual flux. Greater underestimates were found with comparisons involving homogeneous boundary‐layer models. No physical mechanism responsible for the inconsistencies was identified by analyzing coincidentally measured environmental variables.

Limnology and Oceanography

Carbon isotopes in biological carbonates: Respiration and photosynthesis

Respired carbon dioxide is an important constituent in the carbonates of most air breathing animals but is much less important in the carbonates of most aquatic animals. This difference is illustrated using carbon isotope data from freshwater and terrestrial snails, ahermatypic corals, and chemoautotrophic and methanotrophic pelecypods. Literature data from fish otoliths and bird and mammal shell and bone carbonates are also considered. Environmental CO 2 /O 2 ratios appear to be the major controlling variable. Atmospheric CO 2 /O 2 ratios are about thirty times lower than in most natural waters, hence air breathing animals absorb less environmental CO 2 in the course of obtaining 0 2 . Tissue CO 2 therefore, does not isotopically equilibrate with environmental CO 2 as thoroughly in air breathers as in aquatic animals, and this is reflected in skeletal carbonates. Animals having efficient oxygen transport systems, such as vertebrates, also accumulate more respired CO 2 in their tissues. Photosynthetic corals calcify mainly during the daytime when photosynthetic CO 2 uptake is several times faster than respiratory CO 2 release. Photosynthesis, therefore, affects skeletal δ 13 C more strongly than does respiration. Corals also illustrate how “metabolic” effects on skeletal isotopic composition can be estimated, despite the presence of much larger “kinetic” isotope effects.

Nevada

Consumption of atmospheric methane by desert soils

Atmospheric concentrations of methane, a greenhouse gas, are increasing at a rate of about 1% yr -1 (refs 1–4). Oxidation by methylotrophic bacteria in soil is the largest terrestrial sink for atmospheric CH 4 , and is estimated to consume about 30 x 10 12 g CH 4 yr -1 (refs 4–6). Spatial and temporal variability in the rate of soil CH 4 consumption are incompletely understood 6–19 , as are the apparent inhibitory 12,13,18 or enhancing 20 effects of changes in land use. Dry deserts, which constitute 20% of total land surface, are not currently included in global soil uptake estimates. Here we describe measurements of the rate of uptake of atmospheric CH 4 by undisturbed desert soils. We observed rates as great as 4.38 mg CH 4 m -2 day -1 ; 50% of the measured rates were between 0.24 and 0.92 mg CH 4 m -2 d -1 . Uptake of CH 4 by desert soil is enhanced by rainfall after an initial soil-drainage period—opposite to the response of temperate forest soils 12 . Methane is consumed to a depth of about 2 m, allowing for deep removal of atmospheric CH 4 if near-surface conditions are unfavourable for consumption. On the basis of an annual average CH 4 consumption rate of 0.66 mg CH 4 m -2 d -1 , we estimate that the global CH 4 sink term needs to be increased by about 7 x 10 12 g yr -1 to account for the contribution of desert soils.

Nevada