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Technical Note

Information Needs of Next-Generation Forest Carbon Models: Opportunities for Remote Sensing Science

Canadian Forest Service (Pacific Forestry Centre), Natural Resources Canada, 506 West Burnside Road, Victoria, BC V8Z 1M5, Canada
*
Author to whom correspondence should be addressed.
Remote Sens. 2019, 11(4), 463; https://doi.org/10.3390/rs11040463
Submission received: 11 January 2019 / Revised: 19 February 2019 / Accepted: 20 February 2019 / Published: 23 February 2019
(This article belongs to the Section Forest Remote Sensing)

Abstract

:
Forests are integral to the global carbon cycle, and as a result, the accurate estimation of forest structure, biomass, and carbon are key research priorities for remote sensing science. However, estimating and understanding forest carbon and its spatiotemporal variations requires diverse knowledge from multiple research domains, none of which currently offer a complete understanding of forest carbon dynamics. New large-area forest information products derived from remotely sensed data provide unprecedented spatial and temporal information about our forests, which is information that is currently underutilized in forest carbon models. Our goal in this communication is to articulate the information needs of next-generation forest carbon models in order to enable the remote sensing community to realize the best and most useful application of its science, and perhaps also inspire increased collaboration across these research fields. While remote sensing science currently provides important contributions to large-scale forest carbon models, more coordinated efforts to integrate remotely sensed data into carbon models can aid in alleviating some of the main limitations of these models; namely, low sample sizes and poor spatial representation of field data, incomplete population sampling (i.e., managed forests exclusively), and an inadequate understanding of the processes that influence forest carbon accumulation and fluxes across spatiotemporal scales. By articulating the information needs of next-generation forest carbon models, we hope to bridge the knowledge gap between remote sensing experts and forest carbon modelers, and enable advances in large-area forest carbon modeling that will ultimately improve estimates of carbon stocks and fluxes.

Graphical Abstract

1. Introduction

Multiple research domains contribute to the scientific understanding of forest carbon accumulation and fluctuations, including: plant and tree physiology and genetics; plant, tree, and landscape dynamics; and atmospheric interactions between plants, landscape, and soil. Forests establish themselves through interacting with pedospheric and atmospheric conditions as well as other on-site vegetation. Trees and other vegetation in forests grow, die, and decompose, influencing their environment and their interrelationships. Forests are also disturbed. When combined, these processes and interactions define forest dynamics, and determine how much carbon accumulates at a site. None of the research domains related to forest dynamics has a complete understanding of forest carbon accumulation and variability [1,2,3,4]. Moreover, some processes and interactions are not yet understood or well described [5]. The very complexity of the forest carbon cycle is challenging for measuring, monitoring, and projecting changes to forest carbon. In addition, the geographic extent and spatiotemporal variability in the system prohibits a complete census of forest carbon [6]. As a result, no single forest carbon model, or modeling approach, currently provides a complete assessment of carbon stocks and fluxes, at any scale. Instead, multiple modeling approaches exist to quantify and understand the different processes that contribute to forest carbon accumulation and fluxes at various spatiotemporal scales. New imperatives to commodify and account for carbon highlight the need to improve these models [7].
Regional to large-area forest carbon models range from models based on tree measurements and forest inventory data, to representations of known processes at scales varying from the leaf level to the global level. All of these models have limitations, chief among them being the need for the improved sampling of forest systems. Remote sensing can aid in alleviating some of these limitations by providing data that is spatially exhaustive, spatially explicit, and that captures change at a resolution that is commensurate with the human impact on the landscape [8]. Our objectives herein are to summarize the current state of scientific knowledge regarding forest carbon and dynamics, describe current forest carbon models and their limitations, and articulate where contributions from remote sensing science can inform next-generation forest carbon models. Our overarching goal is to expand understanding in the remote sensing community regarding the information needs that are associated with carbon modeling in general, and next-generation forest carbon models more specifically, thereby encouraging collaborative contributions to estimates of forest carbon dynamics and forest carbon modeling science.

2. Background: Forest Carbon Science

Forests are the largest plant community on the Earth’s land surface [9], and therefore the most important terrestrial primary producers; they absorb the most carbon from the atmosphere [10]. Trees and plants convert light energy into chemical energy via photosynthesis. Stomata allow CO2 into the plant, as well as water exchanges with the atmosphere, and are a central link between plants and their environment [11]. Carbon, which is stored as carbohydrate molecules, is the currency for processes such as respiration, growth, defense, and reproduction. Much plant physiology research relies on tracking carbohydrates [12]. Carbon accumulation and flux depend on the fine balance between two large central processes: photosynthesis and respiration. For example, the estimated carbon sink for the managed forests of Canada between 1990–2008, despite the large fluxes from major disturbances, was due to small differences between respiration and net primary productivity [13]. Respiration releases CO2 and water back to the atmosphere at the same spatiotemporal scales as photosynthesis, making the two central processes to ecosystem structure and function [14] difficult to estimate.
Atmospheric CO2 levels are rarely a limiting factor to carbon absorption; rather, temperature, radiation, and water interact to impose complex and varying limitations on vegetation productivity in different areas of the globe [15]. Figure 1 depicts the global distribution of the limiting abiotic factors to primary production in terms of water, sunlight, and temperature on a global scale. Temperature (heat) controls the rate of plant metabolism (processes), which in turn determines the amount of photosynthesis and respiration that take place. Where temperatures are between 0–50 °C [16] and water and solar radiation are available for photosynthesis, productivity is influenced by species and stand structure [17], age and site nutrients [18], the physiological adaptation of plants [19], disturbance [20], and sometimes forest management practices [21]. The level of productivity is further refined by forest phenology [22], biodiversity [23], forest stand and landscape dynamics [24], and by feedback between the changes occurring in forests and the global environment [25,26,27,28].
The overriding processes of carbon fixation (photosynthesis, respiration, and heat/water exchanges) are present at the leaf-level. Knowledge of these driving processes of carbon cycle science are relatively well established:
  • Photosynthesis is a light-dependent process. It was described to the level of the physics of molecules in the 1980s [30], but despite this detailed description, our understanding of photosynthesis is still expanding with the advancement of quantum physics [31];
  • Respiration is not as well defined with model choice dependent on the spatiotemporal scale under scrutiny [32,33,34]; and
  • Latent heat and water interact at the leaf level via evapotranspiration and hydrological processes in forests [35,36], with research still advancing our knowledge of this complex interaction [37,38].
Moving from leaf-level processes to tree-level and forest-level processes is not additive or multiplicative [39]. The cumulative effect of fast and locally controlled processes, such as photosynthesis and respiration, combine with new processes as the spatiotemporal scale changes; trees distribute resources for the reproduction, defense, and production of fine roots, and allocate nitrogen following sometimes-undefined patterns; trees and plants change their facilitation and competition processes as they grow; forests have microbial and fungal communities that contribute to decomposition and respiration, and interact with the climate system [40,41]. Even well-defined processes can exhibit different behaviours at different scales [42,43], while other processes are still under debate [1,5,44,45,46,47]. Process interactions are extensively being studied [48,49,50,51], and entire fields of research that are determinant in forest carbon content and fluxes are evolving rapidly [1,52,53]. Research is also showing that under changing climatic conditions, species are adapting, changing our knowledge of the plasticity of tree species traits [54]. Collectively, these unknowns explain why there are currently no precise whole tree or whole forests carbon balances: we do not currently understand all the processes and their interactions [3]. Furthermore, as species are adapting to a changing environment [55], process and interactions are also changing. In short, forest carbon science is still elucidating processes and their relationships across spatial scales. In contrast to other research fields such as physics, forest ecology does not have rules or laws that transcend scales and provide consistent parameters for modeling.

3. Forest Carbon Models

3.1. The Current Carbon Modeling Continuum

The continuum of large-area forest carbon models ranges from empirical models to models of known processes that drive forest carbon balances, with all the possible combinations of these two approaches in between. While empirical models focus on describing the statistical relationships between data, process models focus on accounting for the mechanisms or processes that determine carbon accumulation in forest ecosystems. Unlike empirical models, process models are sufficiently generalized so that they remain relevant when faced with new conditions, making them suitable for future projections. Modeling approaches along this continuum vary in their level of detail (spatial, temporal, and attributional) depending on the purpose for which they were generated, the data available, and the composition and expertise of the model development team. Here, we give an overview of the different model types.
International obligations require signatory countries to report and monitor greenhouse gas balances from forests [56]. Many carbon models use the same data that is used by forest management agencies and the forest industry to estimate forest carbon for reporting purposes [57]. This includes forest inventory, land cover, land use, and ownership data, change and disturbance information, growth and yield estimates, biodiversity and wildlife management data, etc. These models have varying levels and types of ecological processes represented, with some also including simplified soil processes [58]. These carbon models range from simple statistical relationships, such as emission factors used in systems where few data are available [59,60], to complex combinations of empirical models (equations), process models (deterministic equations), and assumptions that enable these models to be executed in a timely manner [57]. It is common practice to use tree or stand-level measurements to estimate biomass using allometric equations in sampled locations, and then expand these estimates via statistical or machine learning methods to the region of interest. To obtain carbon estimates, the total biomass is then divided by a factor of two, regardless of the species or growing conditions [60,61].
Most process-based models support scientific understanding, and are often used for exploring potential responses under changing environmental conditions [62,63,64,65,66]. Basic sampling theory tells us that models based on observational data, such as statistical or machine learning models, are not suitable for the projection of future conditions, since the relationships and conditions that these observations represent are from the past, and these relationships and conditions are changing [67]. Hence, process-based models are a more appropriate tool for projections of future conditions. Some efforts have attempted to bridge both empirical models and process-based models [68,69,70,71]; however, these approaches are often too onerous for carbon reporting and management applications. The current limits of process understanding, including their scale-dependent behavior as well as their complicated and cumulative interactions, are the main limits of our ability to model forest carbon via process-based models. Hence, current process-based models usually represent a limited suite of well-understood processes [72].
Forests interact and influence global conditions, representing a potentially important feedback to changing climatic conditions [73,74]. However, forests are but one terrestrial biome contributing to global carbon balance estimates [75,76,77,78]. In large-area carbon models based on biogeochemical measurements [3,64,79,80,81], forest contributions are often calculated as the remaining balance from atmospheric and oceanic models instead of being modeled independently [82]. Atmospheric and oceanic models need to be constrained by estimates of forest carbon stock and fluxes [3,83], because forest are an integral part of the hydrological, energy, and carbon budgets in regional models [37].

3.2. Limitations of Current Carbon Models

Three ubiquitous limitations challenge current large-area forest carbon models: limited sample size, the population sampled relative to the population contributing to carbon storage and fluxes, and system understanding, particularly across spatial scales.
Large-area forest carbon models suffer from data paucity [84,85]. Managed forests are often the best-sampled land base in carbon modeling, wherein carbon estimates are derived from the height and diameter measurements of commercial tree species. However, those sub-populations also suffer from low sample sizes [86]. Even if we assumed that sample sizes were adequate in managed forests, these measurements are applied to allometric equations (which are also a significant source of uncertainty [87,88]) to estimate aboveground biomass [89,90,91,92,93], and are then divided by a factor of two to estimate carbon. Since biomass measurements are very labor-intensive, the biomass equations themselves suffer from low sample sizes, with equations developed using limited samples (i.e., in the order of hundreds of trees) and applied to species distributed across a vast geographical extent [88,92,94]. Moreover, the selection of the allometric models themselves can affect estimation [87]. Further, the 0.5 ratio to estimate carbon content from biomass estimates [60,95] also introduces another source of unaccounted error, since the carbon content of biomass, even when considering dry weight, varies much more than the 0.5 ratio that is widely used [96,97]. Process-based models, which rely on long-term measurements from sophisticated scientific equipment, typically have even lower observation data ratios, with data from a limited number of sites used to represent entire biomes [79].
Models that rely on forest inventory data for carbon estimates, such as the forest carbon balance models that are used for reporting, are generally built on a sample of a sub-population that is relevant to managed forests, such as specific commercial tree species in the productive forests that are managed for forest product extraction. Given the complexity of forest dynamics, it is unlikely that reliable carbon content and flux estimates can result from a poor sample in one strata of the forested landscape that targets specific tree species above a given diameter, even if those trees are the dominant feature of the forest biomass. Boreal forests alone, which are an ecosystem that is largely classified as unmanaged [98] and hence lacking detailed forest inventory data, are estimated to account for ~50% or more of world forest ecosystem carbon stocks, much of which is in their soils [58]. Furthermore, most allometric equations do not include biomass from other vegetation such as small diameter trees, non-commercial species, shrubs, or bryophytes, despite these components’ demonstrated contributions to forest productivity [99,100,101,102]. Very few studies have quantified the carbon in non-commercial species, small-sized commercial species [103], shrubs and lichens [53,104,105], or mosses [106]. The functional and dynamic nature of all these components add to the aforementioned incomplete understanding of forests dynamics and to the challenge of modeling or predicting the productivity and carbon levels of forested ecosystems [107,108,109].

4. Potential Remote Sensing Contributions to Carbon Modeling

Remotely sensed data can aid in alleviating several of these aforementioned limitations and contribute to the next-generation of carbon modeling. Current research efforts in the remote sensing community in support of carbon modeling often assume that resulting products can be readily integrated into carbon balance assessments. However, current forest carbon models are not able to easily adapt to new data types or inputs. For example, much of the carbon-supporting research in the remote sensing community has focused on biomass estimates [110]. However, given the complexity of forest carbon estimates, their spatiotemporal variation, and the current state of forest carbon science modeling, a static estimate of biomass at a single point in time alone is inadequate information for estimating the carbon balances of large forest areas. Given our current understanding of forest carbon cycles, existing models do not provide sufficiently accurate or consistent carbon estimates across spatiotemporal scales [111]. Remote sensing science has already contributed to important improvements to large-area forest carbon modeling. However, developing the next generation of carbon models—models that are spatially explicit, that account for changes in situ, and that afford more consistent estimates of carbon over space and time—will require a closer integration of remote sensing and carbon science in models. Research advances in remote sensing science, combined with advances in both empirical and process modeling of large-area forest carbon, can lead to improved forest carbon estimates [111]. There is an urgent need for more detailed observations to support the empirical modeling of forest carbon. Remotely sensed data can currently provide many useful inputs to both empirical and process-based forest carbon models: land cover, disturbance, leaf area index (LAI), biomass, phenology, age, height, and estimates of gross and net primary production, among others [112]. These inputs come from a myriad of sensor types: optical, radar, lidar, hyperspectral [112,113]; however, the operational readiness of these sensors to support large-area, spatially explicit modeling is not uniform [84]. The current proliferation of remote sensing missions and operational sensors at various spatiotemporal scales is poised to aid in addressing the sampling paucity and cross-scale issues that currently limit carbon modeling and system understanding. Remote sensing also seems like a logical avenue to improve the estimation and understanding of the light-driven processes at the core of carbon fixation, such as photosynthesis [114]. Better sampling supported by the remote sensing expertise to explore empirical relationships will create the opportunity to improve understanding of forest carbon cycles and their role in the large global carbon cycle and build better models. Here, we identify those limitations where remote sensing science is poised to make the greatest contribution to improving large-area carbon modeling science and application.

4.1. Increased Sampling in Space and Time

Remote sensing, despite not directly measuring most of the variables that are traditionally used across the spectrum of present-day carbon models, can now provide a census of forest systems [115], which is something unprecedented in forest modeling. This is the primary reason why products derived from remotely sensed data will be at the core of the next generation of forest carbon models. The variability resulting from the fast, locally controlled processes of carbon exchange (photosynthesis and respiration), layered with the increasing complexity of added processes with scale, demands that we acquire more information for modeling purposes. Remotely sensed information permits spatially-explicit modeling, capturing some of the spatial variability of these processes, which is becoming the minimum requirement for the next-generation models.
Remote sensing gives different observations than those that carbon modelers are used to: for example, energy from either the Sun or the sensor itself interacts with forest targets, and can be further interpreted to infer forest attributes [116]. These observations and their derived inferences are neither better nor worse than field data; both are surrogate measures for forest attributes, and both require due diligence and preferably cross-validation to increase confidence in their inference [117]. In both cases, forest attributes are themselves surrogates to biomass, which is a surrogate to carbon, adding two layers of modeling and their associated errors and uncertainties to the estimation of carbon. Carbon estimates from both field-based and remotely sensed observations often ignore these additional sources of uncertainty. A notable advantage of the remotely sensed information is that they can be extracted over different spatiotemporal scales and frequencies [118]. Repeated measures provide the opportunity for change measurement [116], which has been notoriously difficult to measure in forest systems, but is essential for change monitoring, system understanding, and projections of carbon fluxes.
There are vast forested landscapes that have no forest inventory, such as the northern forests of Canada [13]. Carbon estimates in these forests must rely on remotely sensed information with field validation. The few existing estimates for these areas have also combined with process modeling [119]. In these northern systems, additional challenges exist in the ambiguity of ecotones between wetlands, peatlands, and forests [120], which is another level of variability that remote sensing can help alleviate by better defining these ecotones and/or identifying their distinguishing components. To date, unmanaged forest carbon estimates are for scientific purposes, but since these northern forests are thought to contain large amounts of stored carbon [58,121], potentially released under changing environmental conditions, it follows that complete carbon stocks and flux estimates for these areas will eventually be required for climate change policy development.

4.2. Upscaling of Estimates and Improved System Understanding across Spatial Scales

Increasing the frequency and extent of observations and developing inferences about forest attributes will in itself contribute to advancing our understanding of processes and their cross-scale interactions. Never before have so many observations about forests been available. Of particular usefulness is the potential that remotely sensed information offer for the scaling of various processes across spatiotemporal scales [116]. Information about forest composition, structure, productivity, and disturbances are useful for the more practical applications of carbon modeling, and are also useful for tracking changes in forests, and therefore for studying and understanding the forest system. With a proliferation of remote sensing satellites offering an increasing number and variety of observations [122], the potential for virtual constellations expands [123], further increasing the observation capacity for forests.
The rapid evolution of remotely sensed data products and methods provides at least two further opportunities: the use of machine learning algorithms, and the advancement of the cross-scale tracking of processes. In the previous state of data paucity, machine learning techniques were of little use in forest modeling. However, remote sensing provides an increasingly overwhelming observational capacity, permitting the use of these powerful tools [124], and with them, possibilities of increasing the available information and associated understanding of our forested landscapes. Although these tools do not replace statistical inference, they do increase the amount of information that is available, and can be the basis for further research that can lead to statistical inference, and eventually to more complete process modeling. The expertise for exploring the potential of these tools and their application to the plethora of remotely sensed data available lies in the remote sensing community, outside the realm of forest carbon expertise but that is essential for modeling and carbon science improvements.
One example of the process scaling that is brought by remotely sensed observations is with newly available observations of solar-induced fluorescence, which is a detectable measurement of light released during photosynthesis [125]. Photosynthesis is driven by light and is the central carbon accumulation process; it follows that observations of energy via remote sensors may have a much closer link to this driving process than tree or localized gas exchange measurements, and may possibly be even more trackable across spatial scales. This may be instrumental in our scientific understanding of the global carbon cycle, and in parallel, of forest carbon [126], since this level of productivity tracking has never been possible before.
Remotely sensed data also offer the capacity to improve the linkages between measurements acquired at different spatial scales [127,128]. Terrestrial laser scanning provides data that can improve sample sizes for allometry [129] or provide direct estimates of plot-level biomass [130]. Airborne laser scanning can provide additional data to augment ground plots [104] and link to Landsat-scale time series observations [115]. Moreover, the recent launch of two spaceborne lidars, the Advanced Topographic Laser Altimeter System (ATLAS) instrument onboard IceSat-2 [131,132] and the Global Ecosystem Dynamics Investigations (GEDI) full waveform light detection and ranging (lidar) onboard the International Space Station [133,134], provide further data for the spatial scaling of forest attributes, which is essential for carbon models [135,136]. In turn, insights enabled by cross-scale comparisons may provide further insights to modelers [137]. Exploring the potential of measuring forest or tree traits with remote sensing and modeling forest productivity also shows promise [64,138,139,140]. In addition to the aforementioned sensors and platforms, numerous hyperspectral satellite missions are currently in various stages of development [141], and small satellites—microsats and cubesats—have now demonstrated viability and affordability as platforms for Earth observation [142].

5. Discussion

Forest are complex. Our understanding of the forest system is not yet complete, and therefore, our models are likewise deficient, and our estimates are consequently variable with unknown accuracy and large uncertainties. Models, by default, push forward assumptions that are—as of yet—not supported by carbon-science findings [143]. Models often ignore scale issues for practicality, and this applies equally to those models that use remotely sensed data and those that do not.
Field data do not provide “true” carbon estimates any more than remotely sensed data do. Biases and errors need to be estimated with both data types and preferably cross validated. Declaring any exactitude in carbon estimates ignores the efforts of scientists in remote sensing science, carbon science, and the field of forest biometrics that strive to improve data products and refine models, and does not enable movement toward better science. Moreover, sensors vary in their usefulness depending on biomes [144]; biomass equations have large errors [88], tree-level biomass estimation presents many challenges [145], and errors need to be explicitly explored for different sensors [113,117,146].
There is likely no universal approach to forest carbon modeling; rather, different modeling solutions may be required in different environments, depending on the information needs, the purpose of the modeling, and the data that is available. Next-generation large-area forest carbon models will require cross-disciplinary teams to provide the appropriate specialized knowledge that is required from all of the involved disciplines. Such knowledge will enable the generation of useful remotely sensed outputs that can be incorporated into next-generation carbon models in a meaningful way [117,144]. The cross-pollination of carbon modeling and remote sensing can lead to improved model inputs, informed bias corrections [147], and more accurate estimates that account for scaling and uncertainty. Data sharing and open science is also a vital component of next-generation forest carbon models (e.g., http://forest-observation-system.net/), and indeed of all science [148].
To fully characterize the contribution of forest ecosystems to the global carbon balance, all forests need to be modeled, rather than just productive forest areas that are managed for forest products. Remote sensing science will be essential in providing data for these unproductive and unmanaged forestlands. Moreover, those components of productive forests that are not currently modeled also present particular challenges for carbon modeling, and require the support of remotely sensed observations. Further exploration of the link between the energy observations from remote sensing and the energy-based processes that drive forest productivity (light and heat) will move both fields toward better understanding and better science.

6. Conclusions

Carbon is the “end-product” of forest dynamics, and remote sensing is well poised for quantifying present and changing conditions in forests and therefore in carbon. The next generation of forest carbon models will include remotely sensed information, and evolve with it as well. Field data needs will remain a strong component of forest carbon modeling, since neither field nor remotely sensed observations are direct measures of carbon or carbon fluxes. However, the methods by which that field information is acquired are also evolving as a function of changing technologies. Repeated measures, both in situ and remotely sensed, are essential in this changing environment if our goal is to develop reliable models. All data is necessary to further the representation and understanding of the forest system. Models are needed that can use all levels of information, are flexible, and can adapt to new data types. That requires open science, open data, and broader collaborations. Examples of such approaches are already emerging [149]. Although forest carbon modelers are typically not prescriptive in the data sources or methods by which their model inputs are generated, they can more clearly articulate their information needs to the remote sensing community. By better understanding the information needs, the remote sensing community in turn can respond with innovative solutions and information products that are rigorously and transparently generated. Herein, we have offered some context on current forest carbon models and their challenges and limitations, highlighting the information needs of next-generation forest carbon models. From a remote sensing perspective, opportunities to acquire observations of the globe’s forests at increasingly refined spatial, spectral, and temporal resolutions have never been greater. The challenge for both remote sensing and forest carbon scientists and modelers is how to best integrate and manage these large and diverse data flows in the interest of defining and enhancing the next-generation forest carbon models, while also advancing scientific understanding of the underlying mechanisms and processes that regulate forest carbon dynamics.

Author Contributions

Both authors jointly conceived, researched and wrote this Technical Note in equal parts.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Sokol, N.W.; Bradford, M.A. Microbial formation of stable soil carbon is more efficient from belowground than aboveground input. Nat. Geosci. 2019, 12, 46–53. [Google Scholar] [CrossRef]
  2. Fernández-Martínez, M.; Sardans, J.; Chevallier, F.; Ciais, P.; Obersteiner, M.; Vicca, S.; Canadell, J.G.; Bastos, A.; Friedlingstein, P.; Sitch, S.; et al. Global trends in carbon sinks and their relationships with CO2 and temperature. Nat. Clim. Chang. 2019, 9, 73–79. [Google Scholar] [CrossRef]
  3. Anav, A.; Friedlingstein, P.; Beer, C.; Ciais, P.; Harper, A.; Jones, C.; Murray-Tortarolo, G.; Papale, D.; Parazoo, N.C.; Peylin, P.; et al. Spatiotemporal patterns of terrestrial gross primary production: A review. Rev. Geophys. 2015, 53, 785–818. [Google Scholar] [CrossRef] [Green Version]
  4. Beerling, D.J. Gas valves, forests and global change: A commentary on Jarvis (1976) ‘The interpretation of the variations in leaf water potential and stomatal conductance found in canopies in the field’. Phil. Trans. R. Soc. B Biol. Sci. 2015, 370. [Google Scholar] [CrossRef] [PubMed]
  5. Sala, A.; Piper, F.; Hoch, G. Physiological mechanisms of drought-induced tree mortality are far from being resolved. New Phytol. 2010, 186, 274–281. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. FAO. State of the World’s Forests. Available online: http://www.fao.org/publications/sofo/2016/en/ (accessed on 23 February 2019).
  7. Fahey, T.J.; Woodbury, P.B.; Battles, J.J.; Goodale, C.L.; Hamburg, S.P.; Ollinger, S.V.; Woodall, C.W. Forest carbon storage: Ecology, management, and policy. Front. Ecol. Environ. 2010, 8, 245–252. [Google Scholar] [CrossRef]
  8. Wulder, M.A.; Masek, J.G.; Cohen, W.B.; Loveland, T.R.; Woodcock, C.E. Opening the archive: How free data has enabled the science and monitoring promise of Landsat. Remote Sens. Environ. 2012, 122, 2–10. [Google Scholar] [CrossRef]
  9. Kindermann, G.E.; McCallum, I.; Fritz, S.; Obersteiner, M. A global forest growing stock, biomass and carbon map based on FAO statistics. Silva Fenn. 2008, 42, 387–396. [Google Scholar] [CrossRef]
  10. Federici, S.; Tubiello, F.N.; Salvatore, M.; Jacobs, H.; Schmidhuber, J. New estimates of CO2 forest emissions and removals: 1990–2015. For. Ecol. Manag. 2015, 352, 89–98. [Google Scholar] [CrossRef]
  11. Berner, L.T.; Law, B.E.; Hudiburg, T.W. Water availability limits tree productivity, carbon stocks, and carbon residence time in mature forests across the western US. Biogeosciences 2017, 14, 365–378. [Google Scholar] [CrossRef] [Green Version]
  12. Martínez-Vilalta, J.; Sala, A.; Asensio, D.; Galiano, L.; Hoch, G.; Palacio, S.; Piper, F.I.; Lloret, F. Dynamics of non-structural carbohydrates in terrestrial plants: A global synthesis. Ecol. Monogr. 2016, 86, 495–516. [Google Scholar] [CrossRef]
  13. Stinson, G.; Kurz, W.A.; Smyth, C.E.; Neilson, E.T.; Dymond, C.C.; Metsaranta, J.M.; Boisvenue, C.; Rampley, G.J.; Li, Q.; White, T.M.; et al. An inventory-based analysis of Canada’s managed forest carbon dynamics, 1990 to 2008. Glob. Chang. Biol. 2011, 17, 2227–2244. [Google Scholar] [CrossRef]
  14. Boisvenue, C.; Running, S.W. 4.12—Controls on provisioning services and forest productivity: Responses and risk under changing environmental conditions. In Climate Vulnerability; Pielke, R.A., Ed.; Academic Press: Oxford, UK, 2013; pp. 129–149. [Google Scholar]
  15. Boisvenue, C.; Running, S.W. Impacts of climate change on natural forest productivity—Evidence since the middle of the 20th century. Glob. Chang. Biol. 2006, 12, 862–882. [Google Scholar] [CrossRef]
  16. Hopkins, W.G.; Hüner, N.P.A. Introduction to Plant Physiology, 3rd ed.; Wiley: Hoboken, NJ, USA, 2004; p. 560. [Google Scholar]
  17. Liang, J.; Crowther, T.W.; Picard, N.; Wiser, S.; Zhou, M.; Alberti, G.; Schulze, E.-D.; McGuire, A.D.; Bozzato, F.; Pretzsch, H.; et al. Positive biodiversity-productivity relationship predominant in global forests. Science 2016, 354. [Google Scholar] [CrossRef] [PubMed]
  18. Yu, Y.; Chen, J.M.; Yang, X.; Fan, W.; Li, M.; He, L. Influence of site index on the relationship between forest net primary productivity and stand age. PLoS ONE 2017, 12, e0177084. [Google Scholar] [CrossRef] [PubMed]
  19. Law, B.E. Regional analysis of drought and heat impacts on forests: Current and future science directions. Glob. Chang. Biol. 2014, 20, 3595–3599. [Google Scholar] [CrossRef] [PubMed]
  20. Zhang, F.; Chen, J.M.; Pan, Y.; Birdsey, R.A.; Shen, S.; Ju, W.; Dugan, A.J. Impacts of inadequate historical disturbance data in the early 20th century on modeling recent carbon dynamics (1951–2010) in conterminous US forests. J. Geophys. Res. Biogeosci. 2015. [Google Scholar] [CrossRef]
  21. Montoro Girona, M.; Rossi, S.; Lussier, J.-M.; Walsh, D.; Morin, H. Understanding tree growth responses after partial cuttings: A new approach. PLoS ONE 2017, 12, e0172653. [Google Scholar] [CrossRef] [PubMed]
  22. Richardson, A.D.; Anderson, R.S.; Arain, M.A.; Barr, A.G.; Bohrer, G.; Chen, G.; Chen, J.M.; Ciais, P.; Davis, K.J.; Desai, A.R.; et al. Terrestrial biosphere models need better representation of vegetation phenology: Results from the North American Carbon Program Site Synthesis. Glob. Chang. Biol. 2011, 18, 566–584. [Google Scholar] [CrossRef]
  23. Gross, K. Ecology: Biodiversity and productivity entwined. Nature 2016, 529, 293–294. [Google Scholar] [CrossRef] [PubMed]
  24. Sharma, T.; Kurz, W.A.; Stinson, G.; Pellatt, M.G.; Li, Q. A 100-year conservation experiment: Impacts on forest carbon stocks and fluxes. For. Ecol. Manag. 2013, 310, 242–255. [Google Scholar] [CrossRef]
  25. Seidl, R.; Thom, D.; Kautz, M.; Martin-Benito, D.; Peltoniemi, M.; Vacchiano, G.; Wild, J.; Ascoli, D.; Petr, M.; Honkaniemi, J.; et al. Forest disturbances under climate change. Nat. Clim. Chang. 2017, 7, 395–402. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Meigs, G.W.; Zald, H.S.J.; Campbell, J.L.; Keeton, W.S.; Kennedy, R.E. Do insect outbreaks reduce the severity of subsequent forest fires? Environ. Res. Lett. 2016, 11, 045008. [Google Scholar] [CrossRef] [Green Version]
  27. Anderegg, W.R.L.; Hicke, J.A.; Fisher, R.A.; Allen, C.D.; Aukema, J.; Bentz, B.; Hood, S.; Lichstein, J.W.; Macalady, A.K.; McDowell, N.; et al. Tree mortality from drought, insects, and their interactions in a changing climate. New Phytol. 2015. [Google Scholar] [CrossRef] [PubMed]
  28. Schimel, D.; Stephens, B.B.; Fisher, J.B. Effect of increasing CO2 on the terrestrial carbon cycle. Proc. Natl. Acad. Sci. USA 2015, 112, 436–441. [Google Scholar] [CrossRef] [PubMed]
  29. IPCC. IPCC Meeting on Current Scientific Understanding of the Processes Affecting Terrestrial Carbon Stocks and Human Influences Upon Them. In Proceedings of the Intergovernmental Panel on Climate Change (IPCC) Working Group I Technical Support Unit—National Oceanic & Atmospheric Administration (NOAA), Geneve, Switzerland, 21–23 July 2003. [Google Scholar]
  30. Farquhar, G.D.; Caemmerer, S.V.; Berry, J.A. A biochemical model of photosynthetic CO2 assimilation in leaves of C3 plants. Planta 1980, 149, 78–90. [Google Scholar] [CrossRef] [PubMed]
  31. Jacobs, M.; Lopez-Garcia, M.; Phrathep, O.P.; Lawson, T.; Oulton, R.; Whitney, H.M. Photonic multilayer structure of Begonia chloroplasts enhances photosynthetic efficiency. Nat. Plants 2016, 2. [Google Scholar] [CrossRef] [PubMed]
  32. Amthor, J.S. A Functional model of respiration. In Respiration and Crop Productivity; Amthor, J.S., Ed.; Springer: New York, NY, USA, 1989. [Google Scholar]
  33. Thornley, J.H.M.; Cannell, M.G.R. Modelling the components of plant respiration. Ann. Bot. 2000, 68, 211–226. [Google Scholar] [CrossRef]
  34. Tjoelker, M.G.; Oleksyn, J.; Reich, P.B. Modelling respiration of vegetation: Evidence for a general temperature-dependent Q10. Glob. Chang. Biol. 2001, 7, 223–230. [Google Scholar] [CrossRef]
  35. Kuchment, L.S.; Demidov, V.N. Modeling of influence of hydrological processes on the carbon cycle of a forest ecosystem. Environ. Model. Softw. 2006, 21, 111–114. [Google Scholar] [CrossRef]
  36. Fisher, J.B.; DeBiase, T.A.; Qi, Y.; Xu, M.; Goldstein, A.H. Evapotranspiration models compared on a Sierra Nevada forest ecosystem. Environ. Model. Softw. 2005, 20, 783–796. [Google Scholar] [CrossRef] [Green Version]
  37. Ellison, D.; Morris, C.E.; Locatelli, B.; Sheil, D.; Cohen, J.; Murdiyarso, D.; Gutierrez, V.; Noordwijk, M.V.; Creed, I.F.; Pokorny, J.; et al. Trees, forests and water: Cool insights for a hot world. Glob. Environ. Chang. 2017, 43, 51–61. [Google Scholar] [CrossRef] [Green Version]
  38. Peters, W.; van der Velde, I.R.; van Schaik, E.; Miller, J.B.; Ciais, P.; Duarte, H.F.; van der Laan-Luijkx, I.T.; van der Molen, M.K.; Scholze, M.; Schaefer, K.; et al. Increased water-use efficiency and reduced CO2 uptake by plants during droughts at a continental scale. Nat. Geosci. 2018, 11, 744–748. [Google Scholar] [CrossRef] [PubMed]
  39. Dieleman, W.I.J.; Vicca, S.; Dijkstra, F.A.; Hagedorn, F.; Hovenden, M.J.; Larsen, K.S.; Morgan, J.A.; Volder, A.; Beier, C.; Dukes, J.S.; et al. Simple additive effects are rare: A quantitative review of plant biomass and soil process responses to combined manipulations of CO2 and temperature. Glob. Chang. Biol. 2012, 18, 2681–2693. [Google Scholar] [CrossRef] [PubMed]
  40. Khaine, I.; Woo, S.Y. An overview of interrelationship between climate change and forests. For. Sci. Technol. 2014, 11, 11–18. [Google Scholar] [CrossRef]
  41. Magnabosco, C.; Lin, L.H.; Dong, H.; Bomberg, M.; Ghiorse, W.; Stan-Lotter, H.; Pedersen, K.; Kieft, T.L.; van Heerden, E.; Onstott, T.C. The biomass and biodiversity of the continental subsurface. Nat. Geosci. 2018, 11, 707–717. [Google Scholar] [CrossRef]
  42. Binkley, D.; Campoe, O.C.; Gspaltl, M.; Forrester, D.I. Light absorption and use efficiency in forests: Why patterns differ for trees and stands. For. Ecol. Manag. 2013, 288, 5–13. [Google Scholar] [CrossRef]
  43. Leuzinger, S.; Luo, Y.; Beier, C.; Dieleman, W.; Vicca, S.; Körner, C. Do global change experiments overestimate impacts on terrestrial ecosystems? Trends Ecol. Evol. 2011, 26, 236–241. [Google Scholar] [CrossRef] [PubMed]
  44. Garcia-Forner, N.; Sala, A.; Biel, C.; Savé, R.; Martínez-Vilalta, J. Individual traits as determinants of time to death under extreme drought in Pinus sylvestris L. Tree Physiol. 2016, 36, 1196–1209. [Google Scholar] [CrossRef] [PubMed]
  45. Swann, A.L.S.; Hoffman, F.M.; Koven, C.D.; Randerson, J.T. Plant responses to increasing CO2 reduce estimates of climate impacts on drought severity. Proc. Natl. Acad. Sci. USA 2016, 113, 10019–10024. [Google Scholar] [CrossRef] [PubMed]
  46. Miller, A.D.; Dietze, M.C.; Delucia, E.H.; Anderson-Teixeira, K.J. Alteration of forest succession and carbon cycling under elevated CO2. Glob. Chang. Biol. 2016, 22, 351–363. [Google Scholar] [CrossRef] [PubMed]
  47. Jones, A.G.; Scullion, J.; Ostle, N.; Levy, P.E.; Gwynn-Jones, D. Completing the FACE of elevated CO2 research. Environ. Int. 2014, 73, 252–258. [Google Scholar] [CrossRef] [PubMed]
  48. Asner, G.P.; Knapp, D.E.; Anderson, C.B.; Martin, R.E.; Vaughn, N. Large-scale climatic and geophysical controls on the leaf economics spectrum. Proc. Natl. Acad. Sci. USA 2016, 113, E4043–E4051. [Google Scholar] [CrossRef] [PubMed]
  49. Leys, B.A.; Likens, G.E.; Johnson, C.E.; Craine, J.M.; Lacroix, B.; McLauchlan, K.K. Natural and anthropogenic drivers of calcium depletion in a northern forest during the last millennium. Proc. Natl. Acad. Sci. USA 2016, 113, 6934–6938. [Google Scholar] [CrossRef] [PubMed]
  50. Booth, B.B.B.; Jones, C.D.; Collins, M.; Totterdell, I.J.; Cox, P.M.; Sitch, S.; Huntingford, C.; Betts, R.A.; Harris, G.R.; Lloyd, J. High sensitivity of future global warming to land carbon cycle processes. Environ. Res. Lett. 2012, 7, 024002. [Google Scholar] [CrossRef] [Green Version]
  51. Mol Dijkstra, J.P.; Reinds, G.J.; Kros, H.; Berg, B.; de Vries, W. Modelling Soil Carbon Sequestration of Intensively Monitored Forest Plots in Europe by Three Different Approaches; Elsevier: Kidlington, UK, 2009; p. 14. [Google Scholar]
  52. Van Looy, K.; Bouma, J.; Herbst, M.; Koestel, J.; Minasny, B.; Mishra, U.; Montzka, C.; Nemes, A.; Pachepsky, Y.A.; Padarian, J.; et al. Pedotransfer Functions in Earth System Science: Challenges and Perspectives. Rev. Geophys. 2017, 55, 1199–1256. [Google Scholar] [CrossRef] [Green Version]
  53. Bjorkman, A.D.; Myers-Smith, I.H.; Elmendorf, S.C.; Normand, S.; Rüger, N.; Beck, P.S.A.; Blach-Overgaard, A.; Blok, D.; Cornelissen, J.H.C.; Forbes, B.C.; et al. Plant functional trait change across a warming tundra biome. Nature 2018. [Google Scholar] [CrossRef] [PubMed]
  54. McCulloh, K.A.; Petitmermet, J.; Stefanski, A.; Rice, K.E.; Rich, R.L.; Montgomery, R.A.; Reich, P.B. Is it getting hot in here? Adjustment of hydraulic parameters in six boreal and temperate tree species after 5 years of warming. Glob. Chang. Biol. 2016, 22, 4124–4133. [Google Scholar] [CrossRef] [PubMed]
  55. Ballantyne, A.; Smith, W.; Anderegg, W.; Kauppi, P.; Sarmiento, J.; Tans, P.; Shevliakova, E.; Pan, Y.; Poulter, B.; Anav, A.; et al. Accelerating net terrestrial carbon uptake during the warming hiatus due to reduced respiration. Nat. Clim. Chang. 2017, 562, 57–62. [Google Scholar] [CrossRef]
  56. Baker, D.J.; Richards, G.; Grainger, A.; Gonzalez, P.; Brown, S.; DeFries, R.; Held, A.; Kellndorfer, J.; Ndunda, P.; Ojima, D.; et al. Achieving forest carbon information with higher certainty: A five-part plan. Environ. Sci. Policy 2010, 13, 249–260. [Google Scholar] [CrossRef]
  57. Kim, H.; Kim, Y.H.; Kim, R.; Park, H. Reviews of forest carbon dynamics models that use empirical yield curves: CBM-CFS3, CO2FIX, CASMOFOR, EFISCEN. For. Sci. Technol. 2015, 11, 212–222. [Google Scholar] [CrossRef]
  58. DeLuca, T.H.; Boisvenue, C. Boreal forest soil carbon: Distribution, function and modelling. Forestry 2012, 85, 161–184. [Google Scholar] [CrossRef]
  59. Ward, D.E.; Hao, W.M.; Susott, R.A.; Babbitt, R.E.; Shea, R.W.; Kauffman, J.B.; Justice, C.O. Effect of fuel composition on combustion efficiency and emission factors for African savanna ecosystems. J. Geophys. Res. 1996, 101, 23569–23576. [Google Scholar] [CrossRef]
  60. Smith, J.E.; Heath, L.S.; Woodbury, P.B. How to estimate forest carbon for large areas from inventory data. J. For. 2004, 102, 25–31. [Google Scholar]
  61. Pilli, R.; Grassi, G.; Kurz, W.A.; Smyth, C.E.; Blujdea, V. Application of the CBM-CFS3 model to estimate Italy’s forest carbon budget, 1995–2020. Ecol. Model. 2013, 266, 144–171. [Google Scholar] [CrossRef]
  62. Shugart, H.H.; Wang, B.; Fischer, R.; Ma, J.; Fang, J.; Yan, X.; Huth, A.; Armstrong, A.H. Gap models and their individual-based relatives in the assessment of the consequences of global change. Environ. Res. Lett. 2018, 13, 033001. [Google Scholar] [CrossRef] [Green Version]
  63. Peterson, D.W.; Kerns, B.K.; Dodson, E.K. Climate Change Effects on Vegetation in the Pacific Northwest: A Review and Synthesis of the Scientific Literature and Simulation Model Projections; Pacific Northwest Research Station: Fort Collins, CO, USA, 2014; pp. 1–183. [Google Scholar]
  64. Wullschleger, S.D.; Epstein, H.E.; Box, E.O.; Euskirchen, E.S.; Goswami, S.; Iversen, C.M.; Kattge, J.; Norby, R.J.; Van Bodegom, P.M.; Xu, X. Plant functional types in Earth system models: Past experiences and future directions for application of dynamic vegetation models in high-latitude ecosystems. Ann. Bot. 2014, 114, 1–16. [Google Scholar] [CrossRef] [PubMed]
  65. Aaheim, A.; Chaturvedi, R.; Sagadevan, A. Integrated modelling approaches to analysis of climate change impacts on forests and forest management. Mitig. Adapt. Strateg. Glob. Chang. 2010, 16, 247–266. [Google Scholar] [CrossRef] [Green Version]
  66. Boisvenue, C.; Running, S. Simulations show decreasing carbon stocks and potential for carbon emissions in Rocky Mountain forests over the next century. Ecol. Appl. 2010, 20, 1302–1319. [Google Scholar] [CrossRef] [PubMed]
  67. Keenan, T.F.; Davidson, E.; Moffat, A.M.; Munger, W.; Richardson, A.D. Using model-data fusion to interpret past trends, and quantify uncertainties in future projections, of terrestrial ecosystem carbon cycling. Glob. Chang. Biol. 2012, 18, 2555–2569. [Google Scholar] [CrossRef] [Green Version]
  68. Lonsdale, J.; Xenakis, G.; Mencuccini, M.; Perks, M. A comparison of models for quantifying growth and standing carbon in UK Scots pine forests. iForest 2015, 8, 596–605. [Google Scholar] [CrossRef] [Green Version]
  69. Battaglia, M.; Sands, P.J. Process-based forest productivity models and their application in forest management. For. Ecol. Manag. 1998, 102, 13–32. [Google Scholar] [CrossRef]
  70. Mäkelä, A.; Landsberg, J.; Ek, A.R.; Burk, T.E.; Ter-Mikaelian, M.; Ågren, G.I.; Oliver, C.D.; Puttonen, P. Process-based models for forest ecosystem management: Current state of the art and challenges. Tree Physiol. 2000, 20, 289–298. [Google Scholar] [CrossRef] [PubMed]
  71. Peng, C.; Liu, J.; Dang, Q.; Apps, M.J.; Jiang, H. TRIPLEX: A generic hybrid model for predicting forest growth and carbon and nitrogen dynamics. Ecol. Model. 2002, 153, 109–130. [Google Scholar] [CrossRef]
  72. Norby, R.J.; Luo, Y. Evaluating ecosystem responses to rising atmospheric CO2 and global warming in a multi-factor world. New Phytol. 2004, 162, 281–293. [Google Scholar] [CrossRef]
  73. Birdsey, R.A.; Bridgham, S.D.; Conant, R.T.; Davis, K.; Hales, B.; Richard, A.; Houghton, G.M.; Jenkins, J.C.; Johnston, M.; Marland, G.; et al. Appendix A—Historical Overview of the Development of United States, Canadian, and Mexican Ecosystem Sources and Sinks for Atmospheric Carbon; US Government: Climate Change Science Program (U.S.). In The First State of the Carbon Cycle Report (SOCCR): The North American Carbon Budget and Implications for the Global Carbon Cycle; Synthesis and Assessment Products U.S. Global Change Research Program: Washington, DC, USA, 2007; pp. 117–126. [Google Scholar]
  74. Piao, S.; Huang, M.; Liu, Z.; Wang, X.; Ciais, P.; Canadell, J.G.; Wang, K.; Bastos, A.; Friedlingstein, P.; Houghton, R.A.; et al. Lower land-use emissions responsible for increased net land carbon sink during the slow warming period. Nat. Geosci. 2018, 11, 739–743. [Google Scholar] [CrossRef]
  75. Matthew, C.; Shijie, S.; Atul, K.J.; Almut, A.; Josep, C.; Pierre, F.; Richard, A.H.; Etsushi, K.; Charles, K.; Prabir, P.; et al. The terrestrial carbon budget of South and Southeast Asia. Environ. Res. Lett. 2016, 11, 105006. [Google Scholar] [Green Version]
  76. Franklin, J.; Serra-Diaz, J.M.; Syphard, A.D.; Regan, H.M. Global change and terrestrial plant community dynamics. Proc. Natl. Acad. Sci. USA 2016, 113, 3725–3734. [Google Scholar] [CrossRef] [PubMed]
  77. Ito, A. A historical meta-analysis of global terrestrial net primary productivity: Are estimates converging? Glob. Chang. Biol. 2011, 17, 3161–3175. [Google Scholar] [CrossRef]
  78. Luo, Y.; Weng, E. Dynamic disequilibrium of the terrestrial carbon cycle under global change. Trends Ecol. Evol. 2011, 26, 96–104. [Google Scholar] [CrossRef] [PubMed]
  79. Baldocchi, D. Breathing of the terrestrial biosphere: Lessons learned from a global network of carbon dioxide flux measurement systems. Aust. J. Bot. 2008, 56, 1–26. [Google Scholar] [CrossRef]
  80. Dolman, A.; van der Werf, G.; van der Molen, M.; Ganssen, G.; Erisman, J.W.; Strengers, B. A Carbon Cycle Science Update Since IPCC AR-4. AMBIO J. Hum. Environ. 2010, 39, 402–412. [Google Scholar] [CrossRef] [Green Version]
  81. Friend, A.D.; Arneth, A.; Kiang, N.Y.; Lomas, M.; Ogee, J.; Rodenbeck, C.; Running, S.W.; Santaren, J.-D.; Sitch, S.; Viovy, N.; et al. FLUXNET and modelling the global carbon cycle. Glob. Chang. Biol. 2007, 13, 610–633. [Google Scholar] [CrossRef]
  82. Pan, Y.; Birdsey, R.A.; Fang, J.; Houghton, R.; Kauppi, P.E.; Kurz, W.A.; Phillips, O.L.; Shvidenko, A.; Lewis, S.L.; Canadell, J.G.; et al. A Large and Persistent Carbon Sink in the World’s Forests. Science 2011, 333, 988–993. [Google Scholar] [CrossRef] [PubMed]
  83. Gonsamo, A.; Chen, J.M.; Lombardozzi, D. Global vegetation productivity response to climatic oscillations during the satellite era. Glob. Chang. Biol. 2016, 22, 3414–3426. [Google Scholar] [CrossRef] [PubMed]
  84. Goetz, S.; Dubayah, R. Advances in remote sensing technology and implications for measuring and monitoring forest carbon stocks and change. Carbon Manag. 2011, 2, 231–244. [Google Scholar] [CrossRef] [Green Version]
  85. Joshua, B.F.; Daniel, J.H.; Christopher, R.S.; Deborah, N.H.; Eric, S.; Kevin, S.; Yiqi, L.; Stan, D.W.; Scott, G.; Charles, E.M.; et al. Missing pieces to modeling the Arctic-Boreal puzzle. Environ. Res. Lett. 2018, 13, 020202. [Google Scholar] [Green Version]
  86. Boisvenue, C.; Smiley, B.P.; White, J.C.; Kurz, W.A.; Wulder, M.A. Integration of Landsat time series and field plots for forest productivity estimates in decision support models. For. Ecol. Manag. 2016, 376, 284–297. [Google Scholar] [CrossRef]
  87. Duncanson, L.; Huang, W.; Johnson, K.; Swatantran, A.; McRoberts, R.E.; Dubayah, R. Implications of allometric model selection for county-level biomass mapping. Carbon Balance Manag. 2017, 12–18. [Google Scholar] [CrossRef] [PubMed]
  88. Duncanson, L.; Rourke, O.; Dubayah, R. Small Sample Sizes Yield Biased Allometric Equations in Temperate Forests. Sci. Rep. 2015, 5, 17153. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  89. Muukkonen, P. Generalized allometric volume and biomass equations for some tree species in Europe. Eur. J. For. Res. 2007, 126, 157–166. [Google Scholar] [CrossRef]
  90. Heath, L.S.; Hansen, M.; Smith, J.E.; Miles, P.D.; Smith, B.W. Investigation into Calculating Tree Biomass and Carbon in the FIADB Using a Biomass Expansion Factor Approach. In Proceedings of the Forest Inventory and Analysis (FIA) Symposium 2008, Park City, UT, USA, 21–23 October 2008; p. 26. [Google Scholar]
  91. Ung, C.-H.; Bernier, P.; Guo, X.-J. Canadian national biomass equations: New parameter estimates that include British Columbia data. Can. J. For. Res. 2008, 38, 1123–1132. [Google Scholar] [CrossRef]
  92. Lambert, M.C.; Ung, C.H.; Raulier, F. Canadian national tree aboveground biomass equations. Can. J. For. Res. 2005, 35, 1996–2018. [Google Scholar] [CrossRef]
  93. Jenkins, J.C.; Chojnacky, D.C.; Heath, L.S.; Birdsey, R.A. National-Scale Biomass Estimators for United States Tree Species. For. Sci. 2003, 49, 12–35. [Google Scholar]
  94. Boudewyn, P.; Song, X.; Magnussen, S.; Gillis, M.D. Model-Based, Volume-to-Biomass Conversion for Forested and Vegetated Land in Canada; Information Report BC-X-411; Natural Resources Canada: Victoria, BC, Canada, 2007.
  95. Kurz, W.A.; Dymond, C.C.; White, T.M.; Stinson, G.; Shaw, C.H.; Rampley, G.J.; Smyth, C.; Simpson, B.N.; Neilson, E.T.; Trofymow, J.A.; et al. CBM-CFS3: A model of carbon-dynamics in forestry and land-use change implementing IPCC standards. Ecol. Model. 2009, 220, 480–504. [Google Scholar] [CrossRef]
  96. Thomas, S.C.; Martin, A.R. Carbon Content of Tree Tissues: A Synthesis. Forests 2012, 3, 332–352. [Google Scholar] [CrossRef] [Green Version]
  97. Martin, A.R.; Doraisami, M.; Thomas, S.C. Global patterns in wood carbon concentration across the world’s trees and forests. Nat. Geosci. 2018, 11, 915–920. [Google Scholar] [CrossRef]
  98. Astrup, R.; Bernier, P.Y.; Genet, H.; Lutz, D.A.; Bright, R.M. A sensible climate solution for the boreal forest. Nat. Clim. Chang. 2018, 8, 11–12. [Google Scholar] [CrossRef]
  99. Gundale, M.J.; Deluca, T.H.; Nordin, A. Bryophytes attenuate anthropogenic nitrogen inputs in boreal forests. Glob. Chang. Biol. 2011, 17, 2743–2753. [Google Scholar] [CrossRef]
  100. Hagemann, U.; Moroni, M.T.; Shaw, C.H.; Kurz, W.A.; Makeschin, F. Comparing measured and modelled forest carbon stocks in high-boreal forests of harvest and natural-disturbance origin in Labrador, Canada. Ecol. Model. 2010, 221, 825–839. [Google Scholar] [CrossRef]
  101. Bond-Lamberty, B.; Gower, S.T.; Ahl, D.E. Improved simulation of poorly drained forests using Biome-BGC. Tree Physiol. 2007, 27, 703–715. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  102. Ingerpuu, N.; Kupper, T.; Vellak, K.; Kupper, P.; Sõber, J.; Tullus, A.; Zobel, M.; Liira, J. Response of bryophytes to afforestation, increase of air humidity, and enrichment of soil diaspore bank. For. Ecol. Manag. 2019, 432, 64–72. [Google Scholar] [CrossRef]
  103. Annighöfer, P.; Ameztegui, A.; Ammer, C.; Balandier, P.; Bartsch, N.; Bolte, A.; Coll, L.; Collet, C.; Ewald, J.; Frischbier, N.; et al. Species-specific and generic biomass equations for seedlings and saplings of European tree species. Eur. J. For. Res. 2016, 135, 313–329. [Google Scholar] [CrossRef]
  104. Daniel, E.A.; Daniel, G.; Sarah, E.H.; Kelly, P.; Erin, J.; Jacques, C.F. Uniform shrub growth response to June temperature across the North Slope of Alaska. Environ. Res. Lett. 2018, 13, 044013. [Google Scholar] [Green Version]
  105. Fraser, R.H.; Lantz, T.C.; Olthof, I.; Kokelj, S.V.; Sims, R.A. Warming-Induced Shrub Expansion and Lichen Decline in the Western Canadian Arctic. Ecosystems 2014, 17, 1151–1168. [Google Scholar] [CrossRef]
  106. Turetsky, M.R.; Bond-Lamberty, B.; Euskirchen, E.; Talbot, J.; Frolking, S.; McGuire, A.D.; Tuittila, E.S. The resilience and functional role of moss in boreal and arctic ecosystems. New Phytol. 2012, 196, 49–67. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  107. Hararuk, O.; Shaw, C.; Kurz, W.A. Constraining the organic matter decay parameters in the CBM-CFS3 using Canadian National Forest Inventory data and a Bayesian inversion technique. Ecol. Model. 2017, 364, 1–12. [Google Scholar] [CrossRef]
  108. Denny, C.; Nielsen, S. Spatial Heterogeneity of the Forest Canopy Scales with the Heterogeneity of an Understory Shrub Based on Fractal Analysis. Forests 2017, 8, 146. [Google Scholar] [CrossRef]
  109. Fenton, N.; Lecomte, N.; Légaré, S.; Bergeron, Y. Paludification in black spruce (Picea mariana) forests of eastern Canada: Potential factors and management implications. For. Ecol. Manag. 2005, 213, 151–159. [Google Scholar] [CrossRef]
  110. Lu, D.; Chen, Q.; Wang, G.; Liu, L.; Li, G.; Moran, E. A survey of remote sensing-based aboveground biomass estimation methods in forest ecosystems. Int. J. Digit. Earth 2016, 9, 63–105. [Google Scholar] [CrossRef]
  111. Popkin, G. The hunt for the world’s missing carbon. Nature 2015, 523, 20–22. [Google Scholar] [CrossRef] [PubMed]
  112. Turner, D.P.; Ollinger, S.V.; Kimball, J.S. Integrating Remote Sensing and Ecosystem Process Models for Landscape- to Regional-Scale Analysis of the Carbon Cycle. BioScience 2004, 54, 573–584. [Google Scholar] [CrossRef] [Green Version]
  113. Gregoire, T.G.; Næsset, E.; McRoberts, R.E.; Ståhl, G.; Andersen, H.-E.; Gobakken, T.; Ene, L.; Nelson, R. Statistical rigor in LiDAR-assisted estimation of aboveground forest biomass. Remote Sens. Environ. 2016, 173, 98–108. [Google Scholar] [CrossRef]
  114. Ryu, Y.; Berry, J.A.; Baldocchi, D.D. What is global photosynthesis? History, uncertainties and opportunities. Remote Sens. Environ. 2019, 223, 95–114. [Google Scholar] [CrossRef]
  115. Matasci, G.; Hermosilla, T.; Wulder, M.A.; White, J.C.; Coops, N.C.; Hobart, G.W.; Bolton, D.K.; Tompalski, P.; Bater, C.W. Three decades of forest structural dynamics over Canada’s forested ecosystems using Landsat time-series and lidar plots. Remote Sens. Environ. 2018, 216, 697–714. [Google Scholar] [CrossRef]
  116. Masek, J.G.; Hayes, D.J.; Joseph Hughes, M.; Healey, S.P.; Turner, D.P. The role of remote sensing in process-scaling studies of managed forest ecosystems. For. Ecol. Manag. 2015, 355, 109–123. [Google Scholar] [CrossRef] [Green Version]
  117. Fassnacht, F.E.; Hartig, F.; Latifi, H.; Berger, C.; Hernández, J.; Corvalán, P.; Koch, B. Importance of sample size, data type and prediction method for remote sensing-based estimations of aboveground forest biomass. Remote Sens. Environ. 2014, 154, 102–114. [Google Scholar] [CrossRef]
  118. Wulder, M.A.; White, J.C.; Bater, C.W.; Coops, N.C.; Hopkinson, C.; Chen, G. Lidar plots—A new large-area data collection option: Context, concepts, and case study. Can. J. Remote Sens. 2012, 38, 600–618. [Google Scholar] [CrossRef]
  119. Gonsamo, A.; Chen, J.M.; Colombo, S.J.; Ter-Mikaelian, M.T.; Chen, J. Global change induced biomass growth offsets carbon released via increased forest fire and respiration of the central Canadian boreal forest. J. Geophys. Res. Biogeosci. 2017, 122, 1275–1293. [Google Scholar] [CrossRef]
  120. Lees, K.J.; Quaife, T.; Artz, R.R.E.; Khomik, M.; Clark, J.M. Potential for using remote sensing to estimate carbon fluxes across northern peatlands—A review. Sci. Total Environ. 2018, 615, 857–874. [Google Scholar] [CrossRef] [PubMed]
  121. Underwood, E. Major uncertainties in estimates of carbon trapped in soil. EOS 2018. [Google Scholar] [CrossRef]
  122. Belward, A.S.; Skøien, J.O. Who launched what, when and why; trends in global land-cover observation capacity from civilian earth observation satellites. ISPRS J. Photogramm. Remote Sens. 2015, 103, 115–128. [Google Scholar] [CrossRef] [Green Version]
  123. Wulder, M.A.; Hilker, T.; White, J.C.; Coops, N.C.; Masek, J.G.; Pflugmacher, D.; Crevier, Y. Virtual constellations for global terrestrial monitoring. Remote Sens. Environ. 2015, 170, 62–76. [Google Scholar] [CrossRef] [Green Version]
  124. Belgiu, M.; Drăguţ, L. Random forest in remote sensing: A review of applications and future directions. ISPRS J. Photogramm. Remote Sens. 2016, 114, 24–31. [Google Scholar] [CrossRef]
  125. Brown, A. Mapping photosynthesis. Nat. Clim. Chang. 2018, 8, 559. [Google Scholar] [CrossRef]
  126. MacBean, N.; Maignan, F.; Bacour, C.; Lewis, P.; Peylin, P.; Guanter, L.; Köhler, P.; Gómez-Dans, J.; Disney, M. Strong constraint on modelled global carbon uptake using solar-induced chlorophyll fluorescence data. Sci. Rep. 2018. [Google Scholar] [CrossRef]
  127. Duncanson, L.I.; Dubayah, R.O.; Cook, B.D.; Rosette, J.; Parker, G. The importance of spatial detail: Assessing the utility of individual crown information and scaling approaches for lidar-based biomass density estimation. Remote Sens. Environ. 2015, 168, 102–112. [Google Scholar] [CrossRef]
  128. Wilson, A.M.; Silander, J.A.; Gelfand, A.; Glenn, J.H. Scaling up: Linking field data and remote sensing with a hierarchical model. Int. J. Geogr. Inf. Sci. 2011, 25, 509–521. [Google Scholar] [CrossRef]
  129. Stovall, A.E.L.; Anderson-Teixeira, K.J.; Shugart, H.H. Assessing terrestrial laser scanning for developing non-destructive biomass allometry. For. Ecol. Manag. 2018, 427, 217–229. [Google Scholar] [CrossRef]
  130. Calders, K.; Newnham, G.; Burt, A.; Murphy, S.; Raumonen, P.; Herold, M.; Culvenor, D.; Avitabile, V.; Disney, M.; Armston, J.; et al. Nondestructive estimates of above-ground biomass using terrestrial laser scanning. Methods Ecol. Evol. 2014, 6, 198–208. [Google Scholar] [CrossRef] [Green Version]
  131. Popescu, S.C.; Zhou, T.; Nelson, R.; Neuenschwander, A.; Sheridan, R.; Narine, L.; Walsh, K.M. Photon counting LiDAR: An adaptive ground and canopy height retrieval algorithm for ICESat-2 data. Remote Sens. Environ. 2018, 208, 154–170. [Google Scholar] [CrossRef]
  132. Neuenschwander, A.; Pitts, K. The ATL08 land and vegetation product for the ICESat-2 Mission. Remote Sens. Environ. 2019, 221, 247–259. [Google Scholar] [CrossRef]
  133. Qi, W.; Lee, S.-K.; Hancock, S.; Luthcke, S.; Tang, H.; Armston, J.; Dubayah, R. Improved forest height estimation by fusion of simulated GEDI Lidar data and TanDEM-X InSAR data. Remote Sens. Environ. 2019, 221, 621–634. [Google Scholar] [CrossRef]
  134. Qi, W.; Dubayah, R.O. Combining Tandem-X InSAR and simulated GEDI lidar observations for forest structure mapping. Remote Sens. Environ. 2016, 187, 253–266. [Google Scholar] [CrossRef]
  135. Nelson, R.; Margolis, H.; Montesano, P.; Sun, G.; Cook, B.; Corp, L.; Andersen, H.-E.; de Jong, B.; Pellat, F.P.; Fickel, T.; et al. Lidar-based estimates of aboveground biomass in the continental US and Mexico using ground, airborne, and satellite observations. Remote Sens. Environ. 2017, 188, 127–140. [Google Scholar] [CrossRef] [Green Version]
  136. Margolis, H.A.; Nelson, R.F.; Montesano, P.M.; Beaudoin, A.; Sun, G.; Andersen, H.-E.; Wulder, M. Combining Satellite Lidar, Airborne Lidar and Ground Plots to Estimate the Amount and Distribution of Aboveground Biomass in the Boreal Forest of North America. Can. J. For. Res. 2015, 45, 838–855. [Google Scholar] [CrossRef]
  137. Bell, D.M.; Gregory, M.J.; Kane, V.; Kane, J.; Kennedy, R.E.; Roberts, H.M.; Yang, Z. Multiscale divergence between Landsat- and lidar-based biomass mapping is related to regional variation in canopy cover and composition. Carbon Balance Manag. 2018, 13–15. [Google Scholar] [CrossRef] [PubMed]
  138. Asner, G.P.; Martin, R.E.; Knapp, D.E.; Tupayachi, R.; Anderson, C.B.; Sinca, F.; Vaughn, N.R.; Llactayo, W. Airborne laser-guided imaging spectroscopy to map forest trait diversity and guide conservation. Science 2017, 355, 385–389. [Google Scholar] [CrossRef] [PubMed]
  139. Russell, M.B.; Woodall, C.W.; D’Amato, A.W.; Domke, G.M.; Saatchi, S.S. Beyond mean functional traits: Influence of functional trait profiles on forest structure, production, and mortality across the eastern US. For. Ecol. Manag. 2014, 328, 1–9. [Google Scholar] [CrossRef]
  140. Reich, P.B. Key canopy traits drive forest productivity. Proc. R. Soc. B Biol. Sci. 2012, 279, 2128–2134. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  141. Veraverbeke, S.; Dennison, P.; Gitas, I.; Hulley, G.; Kalashnikova, O.; Katagis, T.; Kuai, L.; Meng, R.; Roberts, D.; Stavros, N. Hyperspectral remote sensing of fire: State-of-the-art and future perspectives. Remote Sens. Environ. 2018, 216, 105–121. [Google Scholar] [CrossRef]
  142. Houborg, R.; McCabe, M.F. A Cubesat enabled Spatio-Temporal Enhancement Method (CESTEM) utilizing Planet, Landsat and MODIS data. Remote Sens. Environ. 2018, 209, 211–226. [Google Scholar] [CrossRef]
  143. Vance, E.D. Conclusions and caveats from studies of managed forest carbon budgets. For. Ecol. Manag. 2018, 427, 350–354. [Google Scholar] [CrossRef]
  144. Zolkos, S.G.; Goetz, S.J.; Dubayah, R. A meta-analysis of terrestrial aboveground biomass estimation using lidar remote sensing. Remote Sens. Environ. 2013, 128, 289–298. [Google Scholar] [CrossRef]
  145. Temesgen, H.; Affleck, D.; Poudel, K.; Gray, A.; Sessions, J. A review of the challenges and opportunities in estimating above ground forest biomass using tree-level models. Scand. J. For. Res. 2015, 30, 326–335. [Google Scholar] [CrossRef]
  146. Hansen, M.C.; Potapov, P.; Tyukavina, A. Comment on “Tropical forests are a net carbon source based on aboveground measurements of gain and loss”. Science 2019, 363, eaar3629. [Google Scholar] [CrossRef] [PubMed]
  147. Maraun, D.; Shepherd, T.G.; Widmann, M.; Zappa, G.; Walton, D.; Gutiérrez, J.M.; Hagemann, S.; Richter, I.; Soares, P.M.M.; Hall, A.; et al. Towards process-informed bias correction of climate change simulations. Nat. Clim. Chang. 2017, 7, 764–773. [Google Scholar] [CrossRef]
  148. Schimel, D. Open data. Front. Ecol. Environ. 2017, 15, 175. [Google Scholar] [CrossRef]
  149. Kennedy, R.E.; Ohmann, J.; Gregory, M.; Roberts, H.; Yang, Z.; Bell, D.M.; Kane, V.; Hughes, M.J.; Cohen, W.B.; Powell, S.; et al. An empirical, integrated forest biomass monitoring system. Environ. Res. Lett. 2018, 13, 025004. [Google Scholar] [CrossRef] [Green Version]
Figure 1. Potential limits to vegetation net primary production (NPP) based on the fundamental physiological limits of vapor pressure deficit, water balance, light, and temperature [15]. NPP is the rate of carbon accumulation in plants after losses from plant respiration and other metabolic processes (which are necessary to maintain the plant’s living systems) are taken into account [29].
Figure 1. Potential limits to vegetation net primary production (NPP) based on the fundamental physiological limits of vapor pressure deficit, water balance, light, and temperature [15]. NPP is the rate of carbon accumulation in plants after losses from plant respiration and other metabolic processes (which are necessary to maintain the plant’s living systems) are taken into account [29].
Remotesensing 11 00463 g001

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Boisvenue, C.; White, J.C. Information Needs of Next-Generation Forest Carbon Models: Opportunities for Remote Sensing Science. Remote Sens. 2019, 11, 463. https://doi.org/10.3390/rs11040463

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Boisvenue C, White JC. Information Needs of Next-Generation Forest Carbon Models: Opportunities for Remote Sensing Science. Remote Sensing. 2019; 11(4):463. https://doi.org/10.3390/rs11040463

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Boisvenue, Céline, and Joanne C. White. 2019. "Information Needs of Next-Generation Forest Carbon Models: Opportunities for Remote Sensing Science" Remote Sensing 11, no. 4: 463. https://doi.org/10.3390/rs11040463

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