Intermittent rain events drive dynamic pulses of carbon and water exchange in many arid and semiarid ecosystems. Although soil moisture is known to control these pulses, the effect of atmospheric dryness on pulses is not well documented. Here we hypothesized that vapor pressure deficit (VPD) modulates net ecosystem production (NEP) and ecosystem‐scale water use efficiency (WUE) during pulse events due to its effects on canopy stomatal conductance and evapotranspiration. We quantified relationships between VPD and carbon and water exchange during growing season rain events and tested their generality across four semiarid flux sites with varied vegetation in the southwest United States. Across grassland, shrubland, and savanna sites, we found that high VPD during pulses suppressed ecosystem photosynthesis and surface conductance to a greater degree than respiration or evapotranspiration, particularly when soil moisture was high. Thus, periods of high VPD were associated with a 13–64% reduction in NEP and an 11–25% decrease in WUE, relative to moderate VPD conditions. Sites dominated by shrubs with the C3 photosynthetic pathway were more sensitive to VPD than sites dominated by C4 grasses. We found that a 1 kPa increase in VPD reduced the average NEP of pulse events by 13–56%, which illustrates the potential for projected increases in atmospheric demand to reduce the net productivity of semiarid ecosystems.
20 December 2013 in Atmospheric Chemistry and Physics
Stratosphere-to-troposphere transport (STT) results in air masses of stratospheric origin intruding into the free troposphere. Once in the free troposphere, ozone (O3)-rich stratospheric air can be transported and mixed with tropospheric air masses, contributing to the tropospheric O3 budget. Evidence of STT can be identified based on the differences in the trace gas composition of the two regions. Because O3 is present in such large quantities in the stratosphere compared to the troposphere, it is frequently used as a tracer for STT events. This work reports on airborne in situ measurements of O3 and other trace gases during two STT events observed over California, USA. The first, on 14 May 2012, was associated with a cutoff low, and the second, on 5 June 2012, occurred during a post-trough, building ridge event. In each STT event, airborne measurements identified high O3 within the stratospheric intrusion, which were observed as low as 3 km above sea level. During both events the stratospheric air mass was characterized by elevated O3 mixing ratios and reduced carbon dioxide (CO2) and water vapor. The reproducible observation of reduced CO2 within the stratospheric air mass supports the use of non-conventional tracers as an additional method for detecting STT. A detailed meteorological analysis of each STT event is presented, and observations are interpreted with the Realtime Air Quality Modeling System (RAQMS). The implications of the two STT events are discussed in terms of the impact on the total tropospheric O3 budget and the impact on air quality and policy-making.
In this paper, we report the vertical profiles of CO 2 and CH 4 measured with a cavity ring-down spectrometer (CRDS) on a research aircraft from near-ground level to 8 km above mean sea level. The airborne platform employed in this paper is an Alpha Jet aircraft operated from NASA's Ames Research Center. Flights were undertaken to Railroad Valley, NV, USA, to coincide with overpasses of the Greenhouse Gases Observing Satellite (GOSAT). Ground-based CO 2 and CH 4 were simultaneously measured using CRDS, at the time and location of the airborne and satellite measurements. Results of three GOSAT coordinated aircraft profiles and ground-based measurements in June 2011 are presented and discussed in this paper. The accuracy of the CO 2 and CH 4 measurements has been determined based upon laboratory calibrations (World Meteorological Organisation traceable standard) and pressure/temperature flight simulations in a test chamber. The overall uncertainty for the airborne measurements ranged from 0.31 to 0.39 ppm for CO 2 and from 3.5 to 5.6 ppb for CH 4 . Our column-averaged CO 2 and CH 4 measurements, which include about 61% of the total atmospheric mass, are extrapolated, using different techniques, to include the remainder of the tropospheric and stratospheric CO 2 and CH 4 . The CO 2 data are then analyzed using the Atmospheric CO 2 Observations from Space 2.9 and 3.3 algorithms. For methane data, the RemoTeC v2.1 algorithm was used in its full physics setup. Column-averaged CO 2 and XCO 2 , measured by GOSAT and analyzed from our data, ranged from 388.1 to 396.4 ppm, and XCH 4 ranged from 1.743 to 1.822 ppm. The agreement of the satellite and aircraft CO 2 mixing ratios, as well as ground measurements, falls within the uncertainties of the methods employed to acquire these numbers.