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  1. Free, publicly-accessible full text available June 1, 2024
  2. Urbanization affects vegetation within city administrative boundary and nearby rural areas. Gross primary production (GPP) of vegetation in global urban areas is one of important metrics for assessing the impacts of urbanization on terrestrial ecosystems. To date, very limited data and information on the spatial-temporal dynamics of GPP in the global urban areas are available. In this study, we reported the spatial distribution and temporal dynamics of annual GPP during 2000–2016 from 8,182 gridcells (0.5° by 0.5° latitude and longitude) that have various proportion of urban areas. Approximately 79.3% of these urban gridcells had increasing trends of annual GPP during 2000-2016. As urban area proportion (%) within individual urban gridcells increased, the means of annual GPP trends also increased. Our results suggested that for those urban gridcells, the negative effect of urban expansion (often measured by impervious surfaces) on GPP was to large degree compensated by increased vegetation within the gridcells, mostly driven by urban management and local climate and environment. Our findings on the continued increases of annual GPP in most of urban gridcells shed new insight on the importance of urban areas on terrestrial carbon cycle and the potential of urban management and local climate and environment on improving vegetation in urban areas. 
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  3. Abstract

    Solar‐induced chlorophyll fluorescence (SIF) shows enormous promise as a proxy for photosynthesis and as a tool for modeling variability in gross primary productivity and net biosphere exchange (NBE). In this study, we explore the skill of SIF and other vegetation indicators in predicting variability in global atmospheric CO2observations, and thus global variability in NBE. We do so using a 4‐year record of CO2observations from NASA's Orbiting Carbon Observatory 2 satellite and using a geostatistical inverse model. We find that existing SIF products closely correlate with space‐time variability in atmospheric CO2observations, particularly in the extratropics. In the extratropics, all SIF products exhibit greater skill in explaining variability in atmospheric CO2observations compared to an ensemble of process‐based CO2flux models and other vegetation indicators. With that said, other vegetation indicators, when multiplied by photosynthetically active radiation, yield similar results as SIF and may therefore be an effective structural SIF proxy at regional to global spatial scales. Furthermore, we find that using SIF as a predictor variable in the geostatistical inverse model shifts the seasonal cycle of estimated NBE and yields an earlier end to the growing season relative to other vegetation indicators. These results highlight how SIF can help constrain global‐scale variability in NBE.

     
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    Abstract. At the leaf level, stomata control the exchange of water and carbon across the air–leaf interface. Stomatal conductance is typically modeledempirically, based on environmental conditions at the leaf surface. Recently developed stomatal optimization models show great skills at predictingcarbon and water fluxes at both the leaf and tree levels. However, how well the optimization models perform atlarger scales has not been extensively evaluated. Furthermore, stomatal models are often used with simple single-leaf representations of canopy radiative transfer (RT), such asbig-leaf models. Nevertheless, the single-leaf canopy RT schemes do not have the capability to model optical properties of the leaves nor the entirecanopy. As a result, they are unable to directly link canopy optical properties with light distribution within the canopy to remote sensing dataobserved from afar. Here, we incorporated one optimization-based and two empirical stomatal models with a comprehensive RT model in the landcomponent of a new Earth system model within CliMA, the Climate Modelling Alliance. The model allowed us to simultaneously simulate carbon and waterfluxes as well as leaf and canopy reflectance and fluorescence spectra. We tested our model by comparing our modeled carbon and water fluxes andsolar-induced chlorophyll fluorescence (SIF) to two flux tower observations (a gymnosperm forest and an angiosperm forest) and satellite SIFretrievals, respectively. All three stomatal models quantitatively predicted the carbon and water fluxes for both forests. The optimization model,in particular, showed increased skill in predicting the water flux given the lower error (ca. 14.2 % and 21.8 % improvement for thegymnosperm and angiosperm forests, respectively) and better 1:1 comparison (slope increases from ca. 0.34 to 0.91 for the gymnosperm forest andfrom ca. 0.38 to 0.62 for the angiosperm forest). Our model also predicted the SIF yield, quantitatively reproducing seasonal cycles for bothforests. We found that using stomatal optimization with a comprehensive RT model showed high accuracy in simulating land surface processes. Theever-increasing number of regional and global datasets of terrestrial plants, such as leaf area index and chlorophyll contents, will helpparameterize the land model and improve future Earth system modeling in general. 
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