Global Change Abstracts The Swiss Contribution - SCNAT
Global Change Abstracts The Swiss Contribution - SCNAT
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