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Global Change Abstracts The Swiss Contribution - SCNAT

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154 <strong>Global</strong> <strong>Change</strong> <strong>Abstracts</strong> – <strong>The</strong> <strong>Swiss</strong> <strong>Contribution</strong> | Coupled Systems and Cycles<br />

08.1-303<br />

Effects of increased soil water availability on<br />

grassland ecosystem carbon dioxide fluxes<br />

Risch A C, Frank D A<br />

USA, Switzerland<br />

Agriculture, Soil Sciences , Ecology , Plant Sciences<br />

<strong>The</strong>re is considerable interest in how ecosystems<br />

will respond to changes in precipitation. Alterations<br />

in rain and snowfall are expected to influence<br />

the spatio-temporal patterns of plant and soil<br />

processes that are controlled by soil moisture, and<br />

potentially, the amount of carbon (C) exchanged<br />

between the atmosphere and ecosystems. Because<br />

grasslands cover over one third of the terrestrial<br />

landscape, understanding controls on grassland<br />

C processes will be important to forecast how<br />

changes in precipitation regimes will influence<br />

the global C cycle. In this study we examined how<br />

irrigation affects carbon dioxide (CO 2) fluxes in<br />

five widely variable grasslands of Yellowstone National<br />

Park during a year of approximately average<br />

growing season precipitation. We irrigated plots<br />

every 2 weeks with 25% of the monthly 30-year average<br />

of precipitation resulting in plots receiving<br />

approximately 150% of the usual growing season<br />

water in the form of rain and supplemented irrigation.<br />

Ecosystem CO 2 fluxes were measured with<br />

a closed chamber-system once a month from May-<br />

September on irrigated and unirrigated plots in<br />

each grassland. Soil moisture was closely associated<br />

with CO 2 fluxes and shoot biomass, and was<br />

between 1.6% and 11.5% higher at the irrigated<br />

plots (values from wettest to driest grassland) during<br />

times of measurements. When examining the<br />

effect of irrigation throughout the growing season<br />

(May-September) across sites, we found that<br />

water additions increased ecosystem CO 2 fluxes<br />

at the two driest and the wettest sites, suggesting<br />

that these sites were water-limited during the<br />

climatically average precipitation conditions of<br />

the 2005 growing season. In contrast, no consistent<br />

responses to irrigation were detected at the<br />

two sites with intermediate soil moisture. Thus,<br />

the ecosystem CO 2 fluxes at those sites were not<br />

water-limited, when considering their responses<br />

to supplemental water throughout the whole season.<br />

In contrast, when we explored how the effect<br />

of irrigation varied temporally, we found that irrigation<br />

increased ecosystem CO 2 fluxes at all the<br />

sites late in the growing season (September). <strong>The</strong><br />

spatial differences in the response of ecosystem<br />

CO 2 fluxes to irrigation likely can be explained<br />

by site specific differences in soil and vegetation<br />

properties. <strong>The</strong> temporal effects likely were due to<br />

delayed plant senescence that promoted plant and<br />

soil activity later into the year. Our results suggest<br />

that in Yellowstone National Park, above-normal<br />

amounts of soil moisture will only stimulate CO 2<br />

fluxes across a portion of the ecosystem. Thus, depending<br />

on the topographic location, grassland<br />

CO 2 fluxes can be water-limited or not. Such information<br />

is important to accurately predict how<br />

changes in precipitation/soil moisture will affect<br />

CO 2 dynamics and how they may feed back to the<br />

global C cycle.<br />

Biogeochemistry, 2007, V86, N1, OCT, pp 91-103.<br />

08.1-304<br />

Chemistry, transport and dry deposition of<br />

trace gases in the boundary layer over the<br />

tropical Atlantic Ocean and the Guyanas during<br />

the GABRIEL field campaign<br />

Stickler A, Fischer H, Bozem H, Gurk C, Schiller C,<br />

Martinez Harder M, Kubistin D, Harder H, Williams<br />

J, Eerdekens G, Yassaa N, Ganzeveld L, Sander R,<br />

Lelieveld J<br />

Switzerland, Germany, Canada<br />

Meteorology & Atmospheric Sciences , Modelling<br />

We present a comparison of different Lagrangian<br />

and chemical box model calculations with measurement<br />

data obtained during the GABRIEL campaign<br />

over the tropical Atlantic Ocean and the<br />

Amazon rainforest in the Guyanas, October 2005.<br />

Lagrangian modelling of boundary layer (BL) air<br />

constrained by measurements is used to derive a<br />

horizontal gradient (approximate to 5.6 pmol/mol<br />

km(-1)) of CO from the ocean to the rainforest (east<br />

to west). This is significantly smaller than that derived<br />

from the measurements (16-48 pmol/mol<br />

km(-1)), indicating that photochemical production<br />

from organic precursors alone cannot explain the<br />

observed strong gradient. It appears that HCHO<br />

is overestimated by the Lagrangian and chemical<br />

box models, which include dry deposition but not<br />

exchange with the free troposphere (FT). <strong>The</strong> relatively<br />

short lifetime of HCHO implies substantial<br />

BL-FT exchange. <strong>The</strong> mixing-in of FT air affected<br />

by African and South American biomass burning<br />

at an estimated rate of 0.12 h(-1) increases the CO<br />

and decreases the HCHO mixing ratios, improving<br />

agreement with measurements. A mean deposition<br />

velocity of 1.35 cm/s for H 2O 2 over the ocean<br />

as well as over the rainforest is deduced assuming<br />

BL-FT exchange adequate to the results for CO.<br />

<strong>The</strong> measured increase of the organic peroxides<br />

from the ocean to the rainforest (approximate to<br />

0.66 nmol/mol d(-1)) is significantly overestimated<br />

by the Lagrangian model, even when using high<br />

values for the deposition velocity and the entrainment<br />

rate. Our results point at either heterogeneous<br />

loss of organic peroxides and/or their radical<br />

precursors, underestimated photodissociation

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