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using a combination of field experiments and numerical simulations. Specifically, Large Eddy Simulations (LES) were used to resolve emissions of isoprene and monoterpenes, turbulent transport, and air chemistry. The coupled chemistry-transport LES included the effects of isoprene and monoterpenes reactivity due to reactions with hydroxyl radical and ozone. The LES results are used to compute vertically resolved budgets of isoprene and monoterpenes in the rainforest canopy in response to emissions, turbulent transport, surface deposition, and air chemistry. Results indicated that emission and dispersion dominated the isoprene budget as the gases were transported out of the canopy space. In a region limited by nitrogen oxides (with prevailing nitric oxide levels of < 0.5 parts per billion), the in-canopy chemical destruction removed approximately 10% of locally emitted monoterpenes. Hydroxyl radical production rates from the ozonolysis of monoterpenes amounted to ≈ 2 × 106 radicals cm􀀀 3 s􀀀 1 and had similar magnitude to the light-dependent hydroxyl radical formation. One key conclusion was that the Amazonia rainforest abundantly emitted monoterpenes whose in-canopy ozonolysis yielded hydroxyl radicals in amounts similar to the magnitude of light-dependent formation. Reactions of monoterpenes and isoprene with hydroxyl radical and ozone were necessary for the maintenance of the Amazon rainforest canopy as a photochemically active environment suitable to generate oxidants and secondary organic aerosols. 

Abstract. American bison (Bison bison L.) have recovered from the brink ofextinction over the past century. Bison reintroduction creates multipleenvironmental benefits, but impacts on greenhouse gas emissions are poorlyunderstood. Bison are thought to have produced some 2 Tg yr−1 of theestimated 9–15 Tg yr−1 of pre-industrial enteric methane emissions,but few measurements have been made due to their mobile grazing habits andsafety issues associated with measuring non-domesticated animals. Here, wemeasure methane and carbon dioxide fluxes from a bison herd on an enclosedpasture during daytime periods in winter using eddy covariance. Methaneemissions from the study area were negligible in the absence of bison(mean ± standard deviation = −0.0009 ± 0.008 µmol m−2 s−1) and were significantly greater than zero,0.048 ± 0.082 µmol m−2 s−1, with a positively skeweddistribution, when bison were present. We coupled bison location estimatesfrom automated camera images with two independent flux footprint models tocalculate a mean per-animal methane efflux of 58.5 µmol s−1 per bison, similar to eddy covariance measurements ofmethane efflux from a cattle feedlot during winter. When we sum theobservations over time with conservative uncertainty estimates we arrive at81 g CH4 per bison d−1 with 95 % confidence intervalsbetween 54 and 109 g CH4 per bison d−1. Uncertainty wasdominated by bison location estimates (46 % of the total uncertainty),then the flux footprint model (33 %) and the eddy covariance measurements(21 %), suggesting that making higher-resolution animal location estimatesis a logical starting point for decreasing total uncertainty. Annualmeasurements are ultimately necessary to determine the full greenhouse gasburden of bison grazing systems. Our observations highlight the need tocompare greenhouse gas emissions from different ruminant grazing systems anddemonstrate the potential for using eddy covariance to measure methaneefflux from non-domesticated animals. 

Feedbacks between atmospheric processes like precipitation and land surface fluxes including evapotranspiration are difficult to observe, but critical for understanding the role of the land surface in the Earth System. To quantify global surface-atmosphere feedbacks we use results of a process network (PN) applied to 251 eddy covariance sites from the LaThuile database to train a neural network across the global terrestrial surface. There is a strong land–atmosphere coupling between latent (LE) and sensible heat flux (H) and precipitation (P) during summer months in temperate regions, and betweenHandPduring winter, whereas tropical rainforests show little coupling seasonality. Savanna, shrubland, and other semi-arid ecosystems exhibit strong responses in their coupling behavior based on water availability. Feedback couplings from surface fluxes toPpeaks at aridity (P/potential evapotranspiration ET_p) values near unity, whereas coupling with respect to clouds, inferred from reduced global radiation, increases asP/ET_papproaches zero. Spatial patterns in feedback coupling strength are related to climatic zone and biome type. Information flow statistics highlight hotspots of (1) persistent land–atmosphere coupling in sub-Saharan Africa, (2) boreal summer coupling in the central and southwestern US, Brazil, and the Congo basin and (3) in the southern Andes, South Africa and Australia during austral summer. Our data-driven approach to quantifying land atmosphere coupling strength that leverages the global FLUXNET database and information flow statistics provides a basis for verification of feedback interactions in general circulation models and for predicting locations where land cover change will feedback to climate or weather.

 

Abstract. Flash droughts tend to be disproportionately destructive because theyintensify rapidly and are difficult to prepare for. We demonstrate that the2017 US Northern Great Plains (NGP) flash drought was preceded by abreakdown of land–atmosphere coupling. Severe drought conditions in the NGPwere first identified by drought monitors in late May 2017 and rapidlyprogressed to exceptional drought in July. The likelihood of convectiveprecipitation in May 2017 in northeastern Montana, however, resembled that ofa typical August when rain is unlikely. Based on the lower tropospherichumidity index (HI_low), convective rain was suppressed by theatmosphere on nearly 50% of days during March in NE Montana and centralNorth Dakota, compared to 30% during a normal year. Micrometeorologicalvariables, including potential evapotranspiration (ET_p), were neither anomalouslyhigh nor low before the onset of drought. Incorporating convective likelihoodto drought forecasts would have noted that convective precipitation in theNGP was anomalously unlikely during the early growing season of 2017. It maytherefore be useful to do so in regions that rely on convectiveprecipitation.

 

Abstract. Evaporation (E) and transpiration (T) respond differentlyto ongoing changes in climate, atmospheric composition, and land use. It isdifficult to partition ecosystem-scale evapotranspiration (ET) measurementsinto E and T, which makes it difficult to validate satellite data and landsurface models. Here, we review current progress in partitioning E and T andprovide a prospectus for how to improve theory and observations goingforward. Recent advancements in analytical techniques create newopportunities for partitioning E and T at the ecosystem scale, but theirassumptions have yet to be fully tested. For example, many approaches topartition E and T rely on the notion that plant canopy conductance andecosystem water use efficiency exhibit optimal responses to atmosphericvapor pressure deficit (D). We use observations from 240 eddy covariance fluxtowers to demonstrate that optimal ecosystem response to D is a reasonableassumption, in agreement with recent studies, but more analysis is necessaryto determine the conditions for which this assumption holds. Anothercritical assumption for many partitioning approaches is that ET can beapproximated as T during ideal transpiring conditions, which has beenchallenged by observational studies. We demonstrate that T can exceed 95 %of ET from certain ecosystems, but other ecosystems do not appear to reachthis value, which suggests that this assumption is ecosystem-dependent withimplications for partitioning. It is important to further improve approachesfor partitioning E and T, yet few multi-method comparisons have beenundertaken to date. Advances in our understanding of carbon–water couplingat the stomatal, leaf, and canopy level open new perspectives on how toquantify T via its strong coupling with photosynthesis. Photosynthesis can beconstrained at the ecosystem and global scales with emerging data sourcesincluding solar-induced fluorescence, carbonyl sulfide flux measurements,thermography, and more. Such comparisons would improve our mechanisticunderstanding of ecosystem water fluxes and provide the observationsnecessary to validate remote sensing algorithms and land surface models tounderstand the changing global water cycle.