skip to main content


Search for: All records

Creators/Authors contains: "Vourlitis, George L."

Note: When clicking on a Digital Object Identifier (DOI) number, you will be taken to an external site maintained by the publisher. Some full text articles may not yet be available without a charge during the embargo (administrative interval).
What is a DOI Number?

Some links on this page may take you to non-federal websites. Their policies may differ from this site.

  1. Urban landscaping conversions can alter decomposition processes and soil respiration, making it difficult to forecast regional CO2 emissions. Here we explore rates of initial mass loss and net nitrogen (N) mineralization in natural and four common urban land covers (waterwise, waterwise with mulch, shrub, and lawn) from sites across seven colleges in southern California. We found that rates of decomposition and net N mineralization were faster for high-N leaf substrates, and natural habitats exhibited slower rates of decomposition and mineralization than managed urban landcovers, especially lawns and areas with added mulch. These results were consistent across college campuses, suggesting that our findings are robust and can predict decomposition rates across southern California. While mechanisms driving differences in decomposition rates among habitats in the cool-wet spring were difficult to identify, elevated decomposition in urban habitats highlights that conversion of natural areas to urban landscapes enhances greenhouse gas emissions. While perceived as sustainable, elevated decomposition rates in areas with added mulch mean that while these transformations may reduce water inputs, they increase soil carbon (C) flux. Mimicking natural landscapes by reducing water and nutrient (mulch) inputs and planting drought-tolerant native vegetation with recalcitrant litter can slow decomposition and reduce regional C emissions. 
    more » « less
  2. null (Ed.)
  3. null (Ed.)
  4. Abstract

    Wetlands are important sources of methane (CH4) and sinks of carbon dioxide (CO2). However, little is known about CH4and CO2fluxes and dynamics of seasonally flooded tropical forests of South America in relation to local carbon (C) balances and atmospheric exchange. We measured net ecosystem fluxes of CH4and CO2in the Pantanal over 2014–2017 using tower‐based eddy covariance along with C measurements in soil, biomass and water. Our data indicate that seasonally flooded tropical forests are potentially large sinks for CO2but strong sources of CH4, particularly during inundation when reducing conditions in soils increase CH4production and limit CO2release. During inundation when soils were anaerobic, the flooded forest emitted 0.11 ± 0.002 g CH4‐C m−2 d−1and absorbed 1.6 ± 0.2 g CO2‐C m−2 d−1(mean ± 95% confidence interval for the entire study period). Following the recession of floodwaters, soils rapidly became aerobic and CH4emissions decreased significantly (0.002 ± 0.001 g CH4‐C m−2 d−1) but remained a net source, while the net CO2flux flipped from being a net sink during anaerobic periods to acting as a source during aerobic periods. CH4fluxes were 50 times higher in the wet season; DOC was a minor component in the net ecosystem carbon balance. Daily fluxes of CO2and CH4were similar in all years for each season, but annual net fluxes varied primarily in relation to flood duration. While the ecosystem was a net C sink on an annual basis (absorbing 218 g C m−2(as CH4‐C + CO2‐C) in anaerobic phases and emitting 76 g C m−2in aerobic phases), high CH4effluxes during the anaerobic flooded phase and modest CH4effluxes during the aerobic phase indicate that seasonally flooded tropical forests can be a net source of radiative forcings on an annual basis, thus acting as an amplifying feedback on global warming.

     
    more » « less
  5. null (Ed.)
    Abstract. Methane (CH4) emissions from natural landscapes constituteroughly half of global CH4 contributions to the atmosphere, yet largeuncertainties remain in the absolute magnitude and the seasonality ofemission quantities and drivers. Eddy covariance (EC) measurements ofCH4 flux are ideal for constraining ecosystem-scale CH4emissions due to quasi-continuous and high-temporal-resolution CH4flux measurements, coincident carbon dioxide, water, and energy fluxmeasurements, lack of ecosystem disturbance, and increased availability ofdatasets over the last decade. Here, we (1) describe the newly publisheddataset, FLUXNET-CH4 Version 1.0, the first open-source global dataset ofCH4 EC measurements (available athttps://fluxnet.org/data/fluxnet-ch4-community-product/, last access: 7 April 2021). FLUXNET-CH4includes half-hourly and daily gap-filled and non-gap-filled aggregatedCH4 fluxes and meteorological data from 79 sites globally: 42freshwater wetlands, 6 brackish and saline wetlands, 7 formerly drainedecosystems, 7 rice paddy sites, 2 lakes, and 15 uplands. Then, we (2) evaluate FLUXNET-CH4 representativeness for freshwater wetland coverageglobally because the majority of sites in FLUXNET-CH4 Version 1.0 arefreshwater wetlands which are a substantial source of total atmosphericCH4 emissions; and (3) we provide the first global estimates of theseasonal variability and seasonality predictors of freshwater wetlandCH4 fluxes. Our representativeness analysis suggests that thefreshwater wetland sites in the dataset cover global wetland bioclimaticattributes (encompassing energy, moisture, and vegetation-relatedparameters) in arctic, boreal, and temperate regions but only sparselycover humid tropical regions. Seasonality metrics of wetland CH4emissions vary considerably across latitudinal bands. In freshwater wetlands(except those between 20∘ S to 20∘ N) the spring onsetof elevated CH4 emissions starts 3 d earlier, and the CH4emission season lasts 4 d longer, for each degree Celsius increase in meanannual air temperature. On average, the spring onset of increasing CH4emissions lags behind soil warming by 1 month, with very few sites experiencingincreased CH4 emissions prior to the onset of soil warming. Incontrast, roughly half of these sites experience the spring onset of risingCH4 emissions prior to the spring increase in gross primaryproductivity (GPP). The timing of peak summer CH4 emissions does notcorrelate with the timing for either peak summer temperature or peak GPP.Our results provide seasonality parameters for CH4 modeling andhighlight seasonality metrics that cannot be predicted by temperature or GPP(i.e., seasonality of CH4 peak). FLUXNET-CH4 is a powerful new resourcefor diagnosing and understanding the role of terrestrial ecosystems andclimate drivers in the global CH4 cycle, and future additions of sitesin tropical ecosystems and site years of data collection will provide addedvalue to this database. All seasonality parameters are available athttps://doi.org/10.5281/zenodo.4672601 (Delwiche et al., 2021).Additionally, raw FLUXNET-CH4 data used to extract seasonality parameterscan be downloaded from https://fluxnet.org/data/fluxnet-ch4-community-product/ (last access: 7 April 2021), and a completelist of the 79 individual site data DOIs is provided in Table 2 of this paper. 
    more » « less