A Look at Amazon Basin Seasonal Dynamics with the Biophysical ...
A Look at Amazon Basin Seasonal Dynamics with the Biophysical ... A Look at Amazon Basin Seasonal Dynamics with the Biophysical ...
Soil-Atmosphere Flux of Nitrous Oxide and Methane Measured Over Two Years onSand and Clay Soils in Undisturbed Forest at the FLONA Tapajos, BrazilJadson Dias 1 , Eraclito Sousa 1 , Hudson Silva 2 , Michael Keller 2 , Patrick M. Crill 2 ;Raimundo Cosme de Oliveira Junior 3.1Fundação Floresta Tropical, Santarem, Para, Brazil,2University of New Hampshire3 EMBRAPA Amazonia Oriental, Santarem, Para, BrazilEmail addresses: hj@tap.com.br, eraclito@tap.com.br, hsilva@kaos.sr.unh.edu,michael.keller@unh.edu, patrick.crill@unh.edu, cosme@cpatu.embrapa.brNitrous oxide (N 2 O) and methane (CH 4 ) are important greenhouse gases.Tropical forest soils account for the largest natural source of N 2 O. Most upland tropicalforest soils studied so far consume CH 4 . We measured soil-atmosphere flux of N 2 O andCH 4 using static chambers during 30 minute long emplacements. Four samples wereremoved at equal time intervals in nylon syringes and transported to our laboratory inSantarem for analysis within about 24 hours of collection. We analyzed N 2 O and CH 4using gas electron capture and flame ionization gas chromatography. To determineconcentrations, integrated sample peak areas were compared to peak areas forcommercially prepared standards that had been calibrated against the LBA-ECOstandards. We calculated fluxes by linear regression of 3-4 concentration-time pairs.Our sampling points were randomly selected at intervals of 2-4 weeks at matureundisturbed forest sites near the km 83 IBAMA base in the Tapajos National Forest(FLONA Tapajos). Approximately 8 chamber measurements were made during eachsampling period on both sandy Ultisols and clayey Oxisols. Soil and air temperature andsoil moisture were measured at the same time as gas fluxes.N 2 O emissions from clay greatly exceeded the emissions from sand. During 2years of measurement, N 2 O emissions from clay soils averaged 7 ng-N cm -2 h -1 whileemissions from sand soils averaged only 2 ng-N cm -2 h -1 . Sand soils generally consumedmore CH 4 than clay soils -1 mg-CH4 m -2 d -1 vs.0 mg-CH4 m -2 d -1 ). Seasonal variationof both N 2 O and CH 4 fluxes appeared to be controlled primarily by soil moisture. ForN 2 O, wet season (January-June) emissions greatly exceeded dry season (July –December) emissions. In the case of CH 4 , fluxes were near zero or positive during thewet season but notably negative (indicating consumption of methane in the soil) duringthe dry season.
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Soil-Atmosphere Flux of Nitrous Oxide and Methane Measured Over Two Years onSand and Clay Soils in Undisturbed Forest <strong>at</strong> <strong>the</strong> FLONA Tapajos, BrazilJadson Dias 1 , Eraclito Sousa 1 , Hudson Silva 2 , Michael Keller 2 , P<strong>at</strong>rick M. Crill 2 ;Raimundo Cosme de Oliveira Junior 3.1Fundação Floresta Tropical, Santarem, Para, Brazil,2University of New Hampshire3 EMBRAPA <strong>Amazon</strong>ia Oriental, Santarem, Para, BrazilEmail addresses: hj@tap.com.br, eraclito@tap.com.br, hsilva@kaos.sr.unh.edu,michael.keller@unh.edu, p<strong>at</strong>rick.crill@unh.edu, cosme@cp<strong>at</strong>u.embrapa.brNitrous oxide (N 2 O) and methane (CH 4 ) are important greenhouse gases.Tropical forest soils account for <strong>the</strong> largest n<strong>at</strong>ural source of N 2 O. Most upland tropicalforest soils studied so far consume CH 4 . We measured soil-<strong>at</strong>mosphere flux of N 2 O andCH 4 using st<strong>at</strong>ic chambers during 30 minute long emplacements. Four samples wereremoved <strong>at</strong> equal time intervals in nylon syringes and transported to our labor<strong>at</strong>ory inSantarem for analysis <strong>with</strong>in about 24 hours of collection. We analyzed N 2 O and CH 4using gas electron capture and flame ioniz<strong>at</strong>ion gas chrom<strong>at</strong>ography. To determineconcentr<strong>at</strong>ions, integr<strong>at</strong>ed sample peak areas were compared to peak areas forcommercially prepared standards th<strong>at</strong> had been calibr<strong>at</strong>ed against <strong>the</strong> LBA-ECOstandards. We calcul<strong>at</strong>ed fluxes by linear regression of 3-4 concentr<strong>at</strong>ion-time pairs.Our sampling points were randomly selected <strong>at</strong> intervals of 2-4 weeks <strong>at</strong> m<strong>at</strong>ureundisturbed forest sites near <strong>the</strong> km 83 IBAMA base in <strong>the</strong> Tapajos N<strong>at</strong>ional Forest(FLONA Tapajos). Approxim<strong>at</strong>ely 8 chamber measurements were made during eachsampling period on both sandy Ultisols and clayey Oxisols. Soil and air temper<strong>at</strong>ure andsoil moisture were measured <strong>at</strong> <strong>the</strong> same time as gas fluxes.N 2 O emissions from clay gre<strong>at</strong>ly exceeded <strong>the</strong> emissions from sand. During 2years of measurement, N 2 O emissions from clay soils averaged 7 ng-N cm -2 h -1 whileemissions from sand soils averaged only 2 ng-N cm -2 h -1 . Sand soils generally consumedmore CH 4 than clay soils -1 mg-CH4 m -2 d -1 vs.0 mg-CH4 m -2 d -1 ). <strong>Seasonal</strong> vari<strong>at</strong>ionof both N 2 O and CH 4 fluxes appeared to be controlled primarily by soil moisture. ForN 2 O, wet season (January-June) emissions gre<strong>at</strong>ly exceeded dry season (July –December) emissions. In <strong>the</strong> case of CH 4 , fluxes were near zero or positive during <strong>the</strong>wet season but notably neg<strong>at</strong>ive (indic<strong>at</strong>ing consumption of methane in <strong>the</strong> soil) during<strong>the</strong> dry season.