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The Community Land Model (CLM) is the land component of the Community Earth System Model (CESM) and is used in several global and regional modeling systems. In this paper, we introduce model developments included in CLM version 5 (CLM5), which is the default land component for CESM2. We assess an ensemble of simulations, including prescribed and prognostic vegetation state, multiple forcing data sets, and CLM4, CLM4.5, and CLM5, against a range of metrics including from the International Land Model Benchmarking (ILAMBv2) package. CLM5 includes new and updated processes and Key Points: • Updated Community Land Model has more hydrological and ecological process fidelity and more comprehensive representation of land management. • The model is systematically evaluated using International Land Model Benchmarking system and shows marked improvement over prior versions. parameterizations: (1) dynamic land units, (2) updated parameterizations and structure for hydrology and snow (spatially explicit soil depth, dry surface layer, revised groundwater scheme, revised canopy interception and canopy snow processes, updated fresh snow density, simple firn model, and Model for Scale Adaptive River Transport), (3) plant hydraulics and hydraulic redistribution, (4) revised nitrogen cycling (flexible leaf stoichiometry, leaf N optimization for photosynthesis, and carbon costs for plant nitrogen uptake), (5) global crop model with six crop types and time-evolving irrigated areas and fertilization rates, (6) updated urban building energy, (7) carbon isotopes, and (8) updated stomatal physiology. New optional features include demographically structured dynamic vegetation model (Functionally Assembled Terrestrial Ecosystem Simulator), ozone damage to plants, and fire trace gas emissions coupling to the atmosphere. Conclusive establishment of improvement or degradation of individual variables or metrics is challenged by forcing uncertainty, parametric uncertainty, and model structural complexity, but the multivariate metrics presented here suggest a general broad improvement from CLM4 to CLM5. Plain Language Summary The Community Land Model (CLM) is the land component of the widely used Community Earth System Model (CESM). Here, we introduce model developments included in CLM version 5 (CLM5), the default land component for CESM2 which will be used for the Coupled Model Intercomparison Project (CMIP6). CLM5 includes many new and updated processes including (1) hydrology and snow features such as spatially explicit soil depth, canopy snow processes, a simple firn model, and a more mechanistic river model, (2) plant hydraulics and hydraulic redistribution, (3) revised nitrogen cycling with flexible leaf stoichiometry, leaf N optimization for photosynthesis, and carbon costs for plant nitrogen uptake, (4) expansion to six crop types (global) and time-evolving irrigated areas and fertilization rates, (5) improved urban building energy model, and (6) carbon isotopes. New optional features include a demographically structured dynamic vegetat...

Land-cover characterization of large heterogeneous landscapes is challenging because of the confusion caused by high intra-class variability and heterogeneous landscape artefacts. Neighbourhood context can be used to supplement spectral information, and a novel way of incorporating spatial dependence in a heterogeneous region is tested here using an ensemble learning technique called random forests and a measure of local spatial dependence called the Getis statistic. The overall Kappa accuracy of the random forest classifier that used a combination of spectral and local spatial (Getis) variables at three different neighbourhood sizes (3 Â 3, 7 Â 7, and 11 Â 11) ranged from 0.85 to 0.92. This accuracy was higher than that of a non-spatial random forest classifier having an overall Kappa accuracy of 0.78, which was run using the spectral variables only. This study demonstrated that the use of the Getis statistic with different neighbourhood sizes leads to substantial increase in per class classification accuracy of heterogeneous land-cover categories.

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[1] The forest area in the western United States that burns annually is increasing with warmer temperatures, more frequent droughts, and higher fuel densities. Studies that examine fire effects for regional carbon balances have tended to either focus on individual fires as examples or adopt generalizations without considering how forest type, fire severity, and regional climate influence carbon legacies. This study provides a more detailed characterization of fire effects and quantifies the full carbon impacts in relation to direct emissions, slow release of fire-killed biomass, and net carbon uptake from forest regrowth. We find important variations in fire-induced mortality and combustion across carbon pools (leaf, live wood, dead wood, litter, and duff) and across low-to high-severity classes. This corresponds to fire-induced direct emissions from 1984 to 2008 averaging 4 TgC yr À1 and biomass killed averaging 10.5 TgC yr À1, with average burn area of 2723 km 2 yr À1 across the western United States. These direct emission and biomass killed rates were 1.4 and 3.7 times higher, respectively, for high-severity fires than those for low-severity fires. The results show that forest regrowth varies greatly by forest type and with severity and that these factors impose a sustained carbon uptake legacy. The western U.S. fires between 1984 and 2008 imposed a net source of 12.3 TgC yr

In many ecosystems, nitrogen is the most limiting nutrient for plant growth and productivity.However, current Earth System Models (ESMs) do not mechanistically represent functional nitrogen allocation for photosynthesis or the linkage between nitrogen uptake and root traits. The current version of CLM (4.5) links nitrogen availability and plant productivity via (1) an instantaneous downregulation of potential photosynthesis rates based on soil mineral nitrogen availability, and (2) apportionment of soil nitrogen between plants and competing nitrogen consumers assumed to be proportional to their relative N demands. However, plants do not photosynthesize at potential rates and then downregulate; instead photosynthesis rates are governed by nitrogen that has been allocated to the physiological processes underpinning photosynthesis. Furthermore, the role of plant roots in nutrient acquisition has also been largely ignored in ESMs. We therefore present a new plant nitrogen model for CLM4.5 with (1) improved representations of linkages between leaf nitrogen and plant productivity based on observed relationships in a global plant trait database and (2) plant nitrogen uptake based on root-scale Michaelis-Menten uptake kinetics. Our model improvements led to a global bias reduction in GPP, LAI, and biomass of 70%, 11%, and 49%, respectively. Furthermore, water use efficiency predictions were improved conceptually, qualitatively, and in magnitude. The new model's GPP responses to nitrogen deposition, CO 2 fertilization, and climate also differed from the baseline model. The mechanistic representation of leaf-level nitrogen allocation and a theoretically consistent treatment of competition with belowground consumers led to overall improvements in global carbon cycling predictions.

Widespread anthropogenic land cover change over the last five centuries has influenced the global climate system through both biogeochemical and biophysical processes. Models indicate that warming from carbon emissions associated with land cover conversion has been partially offset by cooling from elevated albedo, but considerable uncertainty remains partly because of uncertainty in model treatments of albedo. This study incorporates a new spatially and temporally explicit, land cover specific albedo product derived from Moderate Resolution Imaging Spectroradiometer with a historical land use data set (Land Use Harmonization product) to provide more precise, observationally derived estimates of albedo impacts from anthropogenic land cover change with a complete range of data set specific uncertainty. The mean annual global albedo increase due to land cover change during 1700-2005 was estimated as 0.00106 ± 0.00008 (mean ± standard deviation), mainly driven by snow exposure due to land cover transitions from natural vegetation to agriculture. This translates to a top-of-atmosphere radiative cooling of À0.15 ± 0.1 W m À2 (mean ± standard deviation).Our estimate was in the middle of the Intergovernmental Panel on Climate Change Fifth Assessment Report range of À0.05 to À0.25 W m À2 and incorporates variability in albedo within land cover classes.

Nitrogen is one of the most important nutrients for plant growth and a major constituent of proteins that regulate photosynthetic and respiratory processes. However, a comprehensive global analysis of nitrogen allocation in leaves for major processes with respect to different plant functional types (PFTs) is currently lacking. This study integrated observations from global databases with photosynthesis and respiration models to determine plant-functional-type-specific allocation patterns of leaf nitrogen for photosynthesis (Rubisco, electron transport, light absorption) and respiration (growth and maintenance), and by difference from observed total leaf nitrogen, an unexplained "residual" nitrogen pool. Based on our analysis, crops partition the largest fraction of nitrogen to photosynthesis (57%) and respiration (5%) followed by herbaceous plants (44% and 4%). Tropical broadleaf evergreen trees partition the least to photosynthesis (25%) and respiration (2%) followed by needle-leaved evergreen trees (28% and 3%). In trees (especially needle-leaved evergreen and tropical broadleaf evergreen trees) a large fraction (70% and 73%, respectively) of nitrogen was not explained by photosynthetic or respiratory functions. Compared to crops and herbaceous plants, this large residual pool is hypothesized to emerge from larger investments in cell wall proteins, lipids, amino acids, nucleic acid, CO fixation proteins (other than Rubisco), secondary compounds, and other proteins. Our estimates are different from previous studies due to differences in methodology and assumptions used in deriving nitrogen allocation estimates. Unlike previous studies, we integrate and infer nitrogen allocation estimates across multiple PFTs, and report substantial differences in nitrogen allocation across different PFTs. The resulting pattern of nitrogen allocation provides insights on mechanisms that operate at a cellular scale within leaves, and can be integrated with ecosystem models to derive emergent properties of ecosystem productivity at local, regional, and global scales.