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A fuzzy logic decision support model for climate-driven biomass loss risk in western Oregon and Washington


Authors: T. Sheehan aff001;  D. Bachelet aff003
Authors place of work: Conservation Biology Institute, Corvallis, Oregon, United States of America aff001;  Environmental Sciences Program, Oregon State University, Corvallis, Oregon, United States of America aff002;  Department of Biological and Ecological Engineering, Oregon State University, Corvallis, Oregon, United States of America aff003
Published in the journal: PLoS ONE 14(10)
Category: Research Article
doi: https://doi.org/10.1371/journal.pone.0222051

Summary

Dynamic global vegetation model (DGVM) projections are often put forth to aid resource managers in climate change-related decision making. However, interpreting model results and understanding their uncertainty can be difficult. Sources of uncertainty include embedded assumptions about atmospheric CO2 levels, uncertain climate projections driving DGVMs, and DGVM algorithm selection. For western Oregon and Washington, we implemented an Environmental Evaluation Modeling System (EEMS) decision support model using MC2 DGVM results to characterize biomass loss risk. MC2 results were driven by climate projections from 20 General Circulation Models (GCMs) and Earth System Models (ESMs), under Representative Concentration Pathways (RCPs) 4.5 and 8.5, with and without assumed fire suppression, for three different time periods. We produced maps of mean, minimum, and maximum biomass loss risk and uncertainty for each RCP / +/- fire suppression / time period. We characterized the uncertainty due to RCP, fire suppression, and climate projection choice. Finally, we evaluated whether fire or climate maladaptation mortality was the dominant driver of risk for each model run. The risk of biomass loss generally increases in current high biomass areas within the study region through time. The pattern of increased risk is generally south to north and upslope into the Coast and Cascade mountain ranges and along the coast. Uncertainty from climate future choice is greater than that attributable to RCP or +/- fire suppression. Fire dominates as the driving factor for biomass loss risk in more model runs than mortality. This method of interpreting DGVM results and the associated uncertainty provides managers with data in a form directly applicable to their concerns and should prove helpful in adaptive management planning.

Keywords:

Carbon dioxide – Biomass – Climate change – Wildfires – Fire suppression technology – Oregon – Climate modeling – Fuzzy logic

Introduction

Anthropogenic emissions have caused oceanic and atmospheric warming, diminished snow and ice, and rising sea level [1]. The effects of climate change vary regionally [1] and have already affected crop yields [25]), biodiversity [67], and wildfire risk [810]. In the Pacific Northwest of the conterminous United States (PNW), anthropogenic influences are the leading contributor to observed warming [1112], with impacts including lower winter snowpack and increased wildfire risk [11]. Expected future warming in the PNW is projected to cause continued snowpack loss, increased risk of insect infestations [13], increased risk of wildfires, and changes in vegetation [11, 14].

Numerous studies within or including the PNW have projected climate-driven changes in vegetation, fire regime, pests, and forest productivity [1425]. These studies have used a variety of methods and models, including Dynamic Global Vegetation Models (DGVMs) [14, 20, 25], statistical models [1519], reconstruction of relationships between past climate, fire, and vegetation [23], observation and imputation [24], hybrid process and statistical models [21], and hybrid state and transition models [22]. While these studies present both spatial and regional model results, and in many cases, uncertainty associated with those results, the implications for higher level management decisions require interpretation.

Climate impacts have been a steadily growing research topic for over thirty years, and the focus on climate adaptation has seen a marked increase over the last decade [26] Uncertainty in future climate includes the unknown trend of CO2 concentrations, which in turn depend on political and economic decisions, and the wide range of future projections from GCMs and ESMs [1, 2728]. The uncertainty in vegetation modeling results is due to the range of climate futures driving them [2728], soil representation [29], parameter values based on 20th century records [2728], and model choice [28].

A common solution for resource managers faced with uncertainty is adaptive management [3031], the “flexible decision making that can be adjusted in the face of uncertainties as outcomes from management actions and other events become better understood ([32] in [30]).” Accounting for and characterizing uncertainty are important aspects of adaptive management [28, 3031].

In this study we report on a fuzzy logic model for assessing the risk of biomass loss due to climate change in western Oregon and Washington (Fig 1). We created a decision support model (DSM) to evaluate the risk of losing biomass under climate change projections. In the DSM we included results from 80 runs of the MC2 Dynamic Global Vegetation Model (DGVM) [33] as well as carbon stocks from [34]. We characterized uncertainty due to the diverse climate futures driving MC2 runs, and we tested our assumptions about fire suppression.

Study area.
Fig. 1. Study area.
Portions of Oregon and Washington west of the Cascade Mountain Range crest.

We evaluate the ability of our model to: 1) interpret vegetation modeling results and express risk over time in a useable way for managers and decision makers; 2) provide upper and lower bounds of that risk; 3) quantify uncertainty in a straightforward manner; 4) attribute uncertainty to its source; 5) attribute risk to its underlying drivers.

Methods

Study area

The study area (Fig 1) consists of the region of Oregon and Washington west of the Cascade Mountain Range crest that includes Coast Range, Klamath Mountains/California High North Coast Range, Willamette Valley, Puget Lowlands, Cascades, and North Cascades Level III Ecoregions [35]. This region is subject to strong coastal influence with mild, wet winters and warm dry summers.

MC2 results used in this study

The protocol used to generate the MC2 results presented here was designed for an earlier project [14]. In this case, MC2 did not account for historical or future land use, nor past disturbances (pest outbreaks, diseases, or windthrow). Historical results (1895–2010) were obtained using PRISM [36] data and observed atmospheric CO2 concentrations as drivers. Our baseline period was 1971–2000. The vegetation model was run twice, once with fire suppression (FS) and once without (NFS—no fire suppression).

Our future scenarios included either FS or NFS, with either Representative Concentration Pathway (RCP) 4.5 or 8.5 CO2 concentrations. For each of those scenarios, MC2 was run with 20 different climate futures from different Climate Model Intercomparison Project Phase 5 (CMIP5) [37] General Circulation Models (GCMs) or Earth System Models (ESMs; Fig 2). MC2 results were summarized over three time periods: early 21st c. (2011–2030), mid 21st c. (2036–2065), and late 21st c. (2071–2099). We refer to one set of 20 MC2 results for one scenario and one future time period as an ensemble of results.

Model scenarios.
Fig. 2. Model scenarios.
Schematic of scenario and GCM/ESM climate driver combinations used to produce MC2 results used in this study.

EEMS fuzzy logic modeling

The Environmental Evaluation Modeling System (EEMS) [38] is a fuzzy logic [3940] modeling platform designed to inform answers to management questions. A model is represented by a logic tree, with each node corresponding to a displayable spatial layer or map (e.g. Fig 3). The bottom-most nodes in the tree represent input data layers. Each input layer is first normalized (0 to 1 for this study) to produce a node representing its level of agreement with a user-defined statement. For example, a fuel load metric might be mapped to the statement Simulated Live Biomass is High using user-defined thresholds to characterize High. Normalized values are combined into higher level nodes using fuzzy logic operators that evaluate the relationship between two or more datasets to another statement. For example, data for Simulated Live Biomass is High might be combined with data for Vegetation Stress is High to create a resulting node for Mortality Risk is High. In a complete model, nodes are repeatedly combined to produce a final, top-level node that informs the original management question.

Logic tree for <i>Biomass Loss Risk</i> (formally <i>Risk of Biomass Loss is High</i>) EEMS model.
Fig. 3. Logic tree for Biomass Loss Risk (formally Risk of Biomass Loss is High) EEMS model.
Each model node (box) represents a spatial data layer (map). Unshaded nodes represent input data layers. Shaded nodes represent data layers with normalized variable values. Labels are formal fuzzy logic statements with informal index labels in parentheses.

Formally, each node in a fuzzy logic model corresponds to a factual statement, and the values for the node (the normalized values described above) are the values for the statement’s fuzzy truth. Fuzzy truths range from 0 for fully false to 1 for fully true. Values between 0.0 and 0.5 are considered partially false, 0.5 is neither true nor false, and values between 0.5 and 1.0 are partially true. Informally, values in the nodes are considered as indices for the attribute associated with the factual statement. For example, a fuzzy value for Vegetation Stress is High might be referred to simply as the level of Vegetation Stress from low (0) to high (1). We use the informal node labels hereafter.

The spatial datasets used in an EEMS model must share the same extent, projection, and reporting units (normally either polygons, or grid cells as in this study). Operations are performed using corresponding reporting units from different data layers (Fig 4A). Reporting units within layers are treated independently of one another and do not influence each other’s values.

Operations in EEMS.
Fig. 4. Operations in EEMS.
A) Reporting units (grid cells in this example) in all data layers must correspond to one another. Fuzzy logic operators use the content of matching reporting units in different layers, but not between reporting units within the same layer. B) Two methods of applying fuzzy logic operations in the extended version of EEMS. Three-dimensional variables 1 and 2 are combined by operator 1 to produce the three-dimensional variable 3. Operator 2 uses values across the Z dimension of variable 3 to produce two-dimensional variable 4. In this study, the Z dimension corresponds to the 20 members of an ensemble.

The EEMS fuzzy logic operators used in this project are And (minimum value of the inputs), Or (maximum value of the inputs), and Union (mean value of the inputs). With the And and Or operators a reporting unit’s result value comes from only of the input values (unless multiple input values yield the same minimum value (for And) or maximum value (for Or)). For example, if corresponding cells from nodes A and B have values of 0.3 and 0.5, and these nodes are inputs to the And operator to produce node C, C’s value for the corresponding cell would be 0.3 and would come from only the cell in node A. A result of this is that the values in cells of a node produced by And or Or can be attributed to their source node.

Decision support modeling

We created an EEMS decision support model (Fig 3) to evaluate the combined Biomass Loss Risk (formally, Risk of Biomass Loss is High) from fire and climate maladaptation using MC2 ensemble results and aboveground biomass simulated by [34] (hereafter, Hudiburg). For modeled risk to be considered high, the threat to a cell’s biomass–either from fire or modeled vegetation type departure from baseline vegetation type–must be high, and the biomass in the cell must also be high. High modeled biomass is insured by input variables in the MC2 Biomass Loss Risk branch of the model. Hudiburg’s biomass values are based on observed biomass measurements and their inclusion in the EEMS model serves to adjust Biomass Loss Risk down due to the legacy effects of disturbance and harvest.

Normalization of the datasets to obtain fuzzy values was done by establishing minimum (fully false) and maximum (fully true) thresholds and applying linear interpolation between thresholds, such that


where inputval < minthresh

where minthresh < = inputval < = maxthresh

where inputval > maxthresh where fuzzyval is the normalized fuzzy value, inputval is the input (raw) data value, minthresh is the minimum threshold corresponding to the formal node statement, and maxthresh is the maximum threshold.

To normalize MC2 biomass and fire frequency values, we used the distribution of each variable over the study area during the baseline period. The 10th percentile value for each variable was used as the minimum threshold and the 90th percentile was used for the maximum threshold (Table 1). Similarly, we normalized Hudiburg’s biomass values and used the 10th and 90th percentile values from that data set. We calculated MC2 vegetation departure (a shift from the original modeled vegetation type to a new type) by comparing the cell’s modal vegetation type for a future period to its vegetation type for the baseline period. A departure value quantifying the level of disparity between past and future vegetation types was obtained from a lookup table based on expert opinion (S1 Table). To normalize the departure values and produce a data layer representing the overall vegetation stress level (MC2 Vegetation Stress) we used departure values of 0 and 3 for minimum and maximum thresholds respectively.

Tab. 1. EEMS conversion thresholds.
EEMS conversion thresholds.
Conversion thresholds used in the EEMS model to evaluate Biomass Loss Risk. Threshold values are based on the distribution of each variable except for vegetation type departures.

Uncertainty Analysis

We characterized uncertainty by first calculating the variability of Biomass Loss Risk values spatially across each ensemble of results. Results from each ensemble of 20 MC2 runs were combined into 3-dimensional datasets with ensemble members comprising the third dimension (Fig 4B). Biomass Loss Risk was calculated independently for each ensemble member. An extended version of EEMS was used to produce a data layer for each of the minimum, maximum, and mean fuzzy values (Fig 4B), bracketing the variability. The fuzzy value High Variability (formally, Variability is High) was calculated for each cell in each ensemble by converting standard deviations into fuzzy space using the minimum possible standard deviation (0) as the false threshold and the maximum possible standard deviation (0.5) as the true threshold.

We characterized the non-spatial uncertainty between members of each ensemble using box and whisker plots of their area-weighted means for Biomass Loss Risk. Plots for all scenarios within a time period are displayed together for inter-scenario comparison.

To determine whether climate futures’ annual temperature and/or precipitation are tightly coupled with MC2 biomass loss risk, we evaluated the relationships between those 3 variables. First, we compared each ensemble member’s area-weighted mean change in temperature from the baseline period against its change in precipitation. Secondly, we compared each ensemble member’s contribution to an ensemble’s fraction of area matching the maximum MC2 Biomass Loss Risk vs its fraction of area matching the minimum. A visual comparison of an ensemble member’s position in the first graph to its position in the second graph illustrates the strength of relationship between these two measures.

Drivers of biomass loss risk

The Or operator in the model node MC2 Biomass Loss Risk (Fig 3) takes the maximum values of the two inputs, one corresponding to the simulated biomass lost by fire from the MC2 model, the other corresponding to the risk of mortality due to vegetation shift (not due to fire) as simulated by MC2. For each ensemble, we took the ensemble mean for each of MC2 Fire Loss Risk, MC2 Mortality Risk, and MC2 Fire Loss Risk minus MC2 Mortality Risk to show which factor most strongly drives MC2 Biomass Loss Risk. Absolute difference values are greatest where one factor produces a high risk and the other produces a low risk. These results reflect the contribution to Biomass Loss Risk from MC2 results without the contribution from Hudiburg Biomass.

We characterized the influence of fire versus that of vegetation shift over the study area. For each ensemble member, we compared the fraction of the area for which mortality due to vegetation shift was the dominant driver of the risk to lose biomass vs the fraction of area where fire was the main driver of risk. Grid cells with a zero risk value were not considered.

Results

In this manuscript, we present detailed results for the RCP 8.5 / NFS / 2071–2099 time period ensemble and summary results from other ensembles. Detailed results from other ensembles are in supplemental materials.

Decision support modeling

We used normalized biomass values from Hudiburg (Fig 5) for all our EEMS model runs. Biomass is highest in the Cascade Mountains and in the Olympic Peninsula, and lowest around Puget Sound, on the east side of the Northern Cascades, throughout the Willamette Valley, and in southern Oregon around the cities of Roseburg, Medford, and Ashland. Eleven percent of the study area is assumed to have zero biomass.

Hudiburg Biomass.
Fig. 5. Hudiburg Biomass.
11% of the area has a value of 0.

Biomass Loss Risk is low in areas where Hudiburg Biomass is low (Figs 56 and S1S3 Figs). For RCP 8.5 with or without fire suppression, mean and minimum values of Biomass Loss Risk are highest during the mid 21st c. in the southern portion of the study area (Fig 6 and S3A, S3B, S3E, S3F, S3I, S3J Fig). For RCP 4.5, the trend is similar, but less pronounced (S1S2 Figs A, B, E, F, I, J), and less apparent or absent for maximum values across all scenarios (Fig 6 and S1S3 Figs C, E, K). Overall, the risk of biomass loss is higher in the southern portion of the study area and the Coast Range than in the Cascade Range (Fig 6 and S1S3 Figs A, B, C, E, F, G, I, J, K).

Maps of <i>Biomass Loss Risk</i> from EEMS model for the RCP 8.5 NFS scenario.
Fig. 6. Maps of Biomass Loss Risk from EEMS model for the RCP 8.5 NFS scenario.
Figure rows include the mean, minimum, maximum, and uncertainty representation for one time period. (min: minimum; max: maximum; uncert: uncertainty).

The area weighted mean of Biomass Loss Risk increases with time, is lower for RCP 4.5 than for RCP 8.5, and is slightly higher for NFS scenarios than for FS (Fig 7, Table 2). The range of values increases for all scenarios through time (Fig 7, Table 2).

Distribution of area weighted mean values <i>Biomass Loss Risk</i> from EEMS model.
Fig. 7. Distribution of area weighted mean values Biomass Loss Risk from EEMS model.
Each point represents the area weighted mean of one ensemble member.
Tab. 2. Regional values for Biomass Loss Risk.
Regional values for <i>Biomass Loss Risk</i>.
Mean, minimum, maximum, and uncertainty for area weighted mean of Biomass Loss Risk EEMS model.

Uncertainty

Uncertainty is 0 where Hudiburg Biomass is 0, and is generally lower or higher corresponding to lower and higher values for Biomass Loss Risk (Fig 6 and S1S3 Figs D, H, L). In the Olympic Peninsula, uncertainty is generally higher overall except near the end of the century for the RCP 8.5 scenarios. In the southeastern portion of the study area, uncertainty is low across all scenarios. Area weighted mean uncertainty is similar overall and increases with time (Table 2).

Between RCP 4.5 and RCP 8.5, uncertainty ranges from 0.01 to 0.09, increasing through time (Table 3). Between FS and NFS, uncertainty ranges from 0.00 to 0.03, with the lowest values for the early 21st c. (Table 3).

Tab. 3. Area weighted mean of uncertainty for RCP 4.5 vs RCP 8.5 and FS vs NFS.
Area weighted mean of uncertainty for RCP 4.5 vs RCP 8.5 and FS vs NFS.

Drivers of Results

MC2 Fire Loss Risk (Fig 8 and S4S6 Figs A, D, F) is greatest in the southern portion of the study region and generally expands through time north through the Willamette Valley and Puget Trough in the center of the region, east and west from the center into the foothills of the Coast and Cascade mountain ranges, and also on the northeast edge of the study region. The expansion into the Coast and Cascade ranges is greater under NFS than FS and markedly greater under RCP 8.5 than under RCP 4.5, with expansion towards the Cascade crest in the late 21st c. (Fig 8 and S6 Fig. G). MC2 Fire Loss Risk falls in the southern and eastern portions of the study area under RCP 8.5 in the late 21st c. (Fig 8 and S6 Fig. G).

Drivers of <i>MC2 Mortality Risk</i>.
Fig. 8. Drivers of MC2 Mortality Risk.
Maps of MC2 Fire Loss Risk (A, D, G), MC2 Mortality Risk (B, E, H), and MC2 Fire Loss Risk minus MC2 Mortality Risk (C, F, I) from the EEMS model for the RCP 8.5 NFS scenario. Figure rows represent time periods.

MC2 Mortality Risk (Fig 8 and S4S6 Figs B, E, H) is greatest along the coast, somewhat high in the Olympic Peninsula of northwestern Washington, and expands into the foothills of the Cascades and the central portion of the study region through time. It is greater under RCP 8.5 than RCP 4.5, and is virtually unaffected by +/- fire suppression.

The general spatial separation of high MC2 Fire Loss Risk from high MC2 Mortality Risk (Fig 8 and S4S6 Figs A, B, D, E, G, H) is reflected in the driver difference maps (Fig 8 and S4S6 Figs C, F, I). The southern portion and northeastern corner of the study area are driven by fire whereas the coast and Olympic Peninsula are driven by mortality. Under RCP 4.5, mortality drives MC2 Biomass Loss Risk more strongly in the Cascades (S4S5 Figs C, F, I). However, under RCP 8.5, the stronger driver shifts from mortality to fire in the Cascades in the late 21st c (Fig 8 and S6 Fig. C, F, I).

The fraction of area with 0 MC2 Biomass Loss Risk is somewhat greater for RCP 4.5 scenarios than for RCP 8.5, and declines through time, with a minimum of 11% for any ensemble member (Table 4). Fire (MC2 Fire Loss Risk) contributes more to the risk of losing biomass (Biomass Loss Risk) than does vegetation shift (Mortality Risk) for all ensembles with the exception of RCP 8.5, FS, 2071–2099 (Table 5, Fig 9). The difference is generally smaller for FS scenarios than for NFS scenarios.

Drivers of <i>MC2 Biomass Loss Risk</i>.
Fig. 9. Drivers of MC2 Biomass Loss Risk.
Fraction of the study area at risk driven by vegetation shifts (MC2 Mortality Risk) versus driven by fire (MC2 Fire Loss Risk) in the EEMS node MC2 Biomass Loss Risk.
Tab. 4. Area-weighted summary of MC2 Biomass Loss Risk drivers.
Area-weighted summary of <i>MC2 Biomass Loss Risk</i> drivers.
Fraction of area with no risk of losing biomass, risk driven by either fire (MC2 Fire Loss Risk) or vegetation shift (MC2 Mortality Risk) in the EEMS MC2 Biomass Loss Risk model node.
Tab. 5. Per ensemble drivers of MC2 Biomass Loss Risk.
Per ensemble drivers of <i>MC2 Biomass Loss Risk</i>.
Driving factor of the risk of losing biomass illustrated by the number of ensemble members for which either fire (MC2 Fire Loss Risk) or simulated vegetation shifts (MC2 Mortality Risk) drive the risk of biomass loss for MC2 Biomass Loss Risk.

Ensemble members with the greatest (or least) change in annual temperature generally do not correspond to climate futures responsible for the largest area of maximum (minimum) risk of biomass loss (Fig 10 and S7 Fig.). One exception is under HadGEM2-ES365 (model 9) which drives the greatest change in temperature for 2071–2099 under both RCP 4.5 and RCP 8.5 and causes the greatest simulated area at risk in the node Maximum Biomass Loss Risk. Over time, the ratio of the number of climate models causing the largest vs the smallest areas at risk of losing biomass (Biomass Loss Risk) increases substantially (2-5/x models for 2011–2030 to 17-19/x for 2071–2099).

Relationship between climate change summary and MC2 Biomass Loss Risk.
Fig. 10. Relationship between climate change summary and MC2 Biomass Loss Risk.
Change (1971–2000 vs future time period) in average maximum temperature vs change in average annual precipitation for each of the 20 RCP 8.5 climate futures (A-C), and fraction of the simulated area with maximum and minimum values MC2 Biomass Loss Risk for the RCP 8.5 FS scenario (D-F) and the NFS scenario (G-I). In graphs D-I, a point above the 45° line indicates that the results of the MC2 run driven by that climate future showed a greater number of high vs low values of MC2 Biomass Loss Risk over more of the study area. Points below the 45° line indicate that MC2 results showed a greater number of low vs high values over more of the area. (mm: millimeters).

Discussion

Context

We compared our method of presenting uncertainty with those from seven studies covering our study area using inputs from climate models. Climate-based uncertainty was handled in a variety of ways. [15] used the average results from two GCMs, predicating their results on the correctness of those GCMs and the CO2 projections driving them. [16] used an ensemble mean of results from 17 GCMs as a means of defining a consensus future climate before using that climate in their model. Many studies presented graphs and/or tables of region-summarized values of selected drivers and results [14, 1920, 22, 25, 33]. Several presented sets of maps allowing visual comparisons of result variation [14, 1920, 25, 33], but only two presented spatial uncertainty. [19] classified risk to Douglas fir in terms of the percentage of models agreeing or disagreeing on its occurrence, and [20] mapped the number of models agreeing on the direction of change in ecosystem carbon, burn area, and vegetation type. To our knowledge, ours is the first study in this region to provide a detailed, quantified, spatial measure of climate-based uncertainty for modeled future vegetation.

Limitations

An ensemble mean provides a single measure of risk for the ensemble, however climate models driving the results may not be completely independent of one another [41]. Weighting results based on the similarities of the underlying climate models could adjust for this but understanding the provenance of many climate models can be onerous.

We did not account for the uncertainty resulting from assumed ignitions or the built-in CO2 fertilization effect in MC2. The consequences of these assumptions on MC2 fire and carbon dynamics results were found to be substantial [25], but including those uncertainties was beyond the goal of this study. Likewise, we did not incorporate the uncertainty in Hudiburg’s [34] data due to the study’s limited scope.

General implications

Our results show the risk of biomass loss generally increasing with time in current high biomass areas within the study region. The pattern of increased fire-driven risk through time is generally south to north and upslope as fires become more frequent due to increasing temperatures. Mortality-driven risk increases along the coast where vegetation becomes maladapted to warming and where coastal climate influences reduce fire risk.

Changes in biomass are directly related to ecosystem services such as timber production, carbon sequestration, wildlife habitat provision, recreational opportunities, and fresh water quality [42]. Thinning, prescribed fire, and suppression can mitigate fire risk, however each of these actions has associated economic and other costs [4344]. Thinning may increase forest resistance and resilience to drought, however, it may make forests less resistant and resilient as forests age [45]. When physiological processes cannot be buffered against environmental variability, maladaptation leads to mortality [18]. Maintaining biomass in forested areas under climate change-induced maladaptation may depend on management strategies such as sourcing seeds and species from better climatically suited sources (i.e. assisted migration) [4647]. Tools to help mangers implement such strategies have been developed (e.g. Seedlot Selection Tool, https://seedlotselectiontool.org/sst/).

Management and planning

Our results provide managers with spatial datasets representing three aspects of the Biomass Loss Risk metric. The mean value of biomass lost across all climate futures provides an overall idea of potential magnitude of loss while minimum and maximum values bracket the range, suggesting limits for management alternatives. Uncertainty quantifies the variability of the model results. Land management takes place at multiple scales, with planning and assessment at the national or regional level and implementation at more local levels [48]. Using terminology appropriate for managers such as risk and uncertainty, as well as using a spatial scale appropriate for local information makes our results appropriate for local planning.

Environmental models are often found to be insufficiently accurate to use as forecasts [31]. However, they provide insights and scenarios useful for scenario planning [31] and are useful for decreasing uncertainty rather than making predictions [28]. Our work is intended to be viewed within this context, providing one set of results with as much clarity as possible regarding uncertainty, sources of uncertainty, and drivers of risk.

Process-based models, such as MC2, are considered more limited than empirical models in quantifying uncertainty [28], thus limiting their usefulness in management planning. Our method alleviates this limitation, making it easier for managers to use process-based models in their decision making.

It has been suggested that when a range of future possibilities is needed for planning, selecting the most extreme climate projections (e.g. warmest, coolest, wettest, driest) as inputs to ecological models provides brackets for the needed answers [28]. The lack of correspondence we found between the most extreme climate futures and their influence on minimum or maximum risk indicate that simple metrics for climate extremes are not sufficient for bracketing our model results. In a process-based model such as MC2, seasonal patterns and extreme events that are not reflected in annual values or averages over multi-year time periods have the potential to strongly affect fire and vegetation trajectories. Finding climate metrics that predict the most extreme results would be challenging, if not impossible, due to complex interactions within the model. While culling input datasets from GCMs and ESMs that perform poorly in the region may be required to reduce uncertainty [49], culling less extreme climate futures may inadvertently reduce the desired range of results.

Conclusions

Fuzzy logic modeling has been used in a variety of ecological modeling applications [50], including species distribution (e.g. [51]), habitat mapping (e.g. [52]), water quality (e.g. [53]), wildfire risk (e.g. [54]), and the human valuation of natural elements (e.g. [55]). Managing forests in light of climate change requires understanding climate’s potential effects on not only forests, but also industries and communities [26].

Our model may prove useful to managers by itself, but it has the potential to provide greater utility when combined with other metrics reflecting landscape condition, status, and value. The modular nature of the EEMS framework would allow our model to be easily combined into new models. Ignition probabilities, fire spread probabilities, and fire refugia data [5658] could be added to provide greater detail for fire risk. Submodels of climate refugia related to microclimate and enduring landscape features [5960] could provide more realism for mortality-based risk. Combining our risk model with submodels for current habitat quality (e.g. [61]), connectivity corridors [62], and species presence or absence could help guide management conservation decisions. Similarly, incorporating risk with submodels for economic, social, and cultural values could help managers with biocultural approaches to conservation [63]. Stakeholder input and expert opinion can be used to parameterize these models so that they precisely reflect management concerns. It is our hope that this model and this methodology can contribute to sound decision making for a wide variety of purposes in our study region and beyond.

Supporting information

S1 Table [docx]
Lookup table for vegetation type differences.

S1 Fig [tif]
Maps of from EEMS model for the RCP 4.5 FS scenario.

S2 Fig [tif]
Maps of from EEMS model for the RCP 4.5 NFS scenario.

S3 Fig [tif]
Maps of from EEMS model for the RCP 8.5 FS scenario.

S4 Fig [tif]
Drivers of .

S5 Fig [tif]
Drivers of .

S6 Fig [tif]
Drivers of .

S7 Fig [tiff]
Relationship between climate change summary and MC2 Biomass Loss Risk.


Zdroje

1. Pachauri RK, Allen MR, Barros VR, Broome J, Cramer W, Christ R, et al. Climate Change 2014: synthesis report. Contribution of Working Groups I, II and III to the fifth assessment report of the Intergovernmental Panel on Climate Change. IPCC; 2014.

2. Urban D, Roberts MJ, Schlenker W, Lobell DB. Projected temperature changes indicate significant increase in interannual variability of US maize yields. Climatic Change. 2012 May 1;112(2):525–33.

3. Houston L, Capalbo S, Seavert C, Dalton M, Bryla D, Sagili R. Specialty fruit production in the Pacific Northwest: adaptation strategies for a changing climate. Climatic Change. 2018 Jan 1;146(1–2):159–71.

4. Leng G, Huang M. Crop yield response to climate change varies with crop spatial distribution pattern. Scientific Reports. 2017 May 3;7(1):1463. doi: 10.1038/s41598-017-01599-2 28469171

5. Tito R, Vasconcelos HL, Feeley KJ. Global climate change increases risk of crop yield losses and food insecurity in the tropical Andes. Global Change Biology. 2018 Feb;24(2):e592–602. doi: 10.1111/gcb.13959 29055170

6. Thom D, Rammer W, Dirnböck T, Müller J, Kobler J, Katzensteiner K, et al. The impacts of climate change and disturbance on spatio‐temporal trajectories of biodiversity in a temperate forest landscape. Journal of Applied Ecology. 2017 Feb 1;54(1):28–38. doi: 10.1111/1365-2664.12644 28111479

7. Fernández-Manjarrés J, Ruiz-Benito P, Zavala M, Camarero J, Pulido F, Proença V, et al. Forest adaptation to climate change along steep ecological gradients: the case of the Mediterranean-temperate transition in South-Western Europe. Sustainability. 2018 Sep;10(9):3065.

8. Jolly WM, Cochrane MA, Freeborn PH, Holden ZA, Brown TJ, Williamson GJ, et al. Climate-induced variations in global wildfire danger from 1979 to 2013. Nature Communications. 2015 Jul 14;6:7537. doi: 10.1038/ncomms8537 26172867

9. Abatzoglou JT, Williams AP. Impact of anthropogenic climate change on wildfire across western US forests. Proceedings of the National Academy of Sciences. 2016 Oct 18;113(42):11770–5.

10. Stevens‐Rumann CS, Kemp KB, Higuera PE, Harvey BJ, Rother MT, Donato DC, et al. Evidence for declining forest resilience to wildfires under climate change. Ecology Letters. 2018 Feb;21(2):243–52. doi: 10.1111/ele.12889 29230936

11. May C, Luce C, Casola J, Chang M, Cuhaciyan J, Dalton M, et al. Northwest. In Reidmiller DR, Avery CW, Easterling DR, Kunkel KE, Lewis KL, Maycock TK, et al. Impacts, Risks, and Adaptation in the United States: Fourth National Climate Assessment, Volume II. 2018.

12. Abatzoglou JT, Rupp DE, Mote PW. Seasonal climate variability and change in the Pacific Northwest of the United States. Journal of Climate. 2014 Mar;27(5):2125–42.

13. Kolb TE, Fettig CJ, Ayres MP, Bentz BJ, Hicke JA, Mathiasen R, et al. Observed and anticipated impacts of drought on forest insects and diseases in the United States. Forest Ecology and Management. 2016 Nov 15;380:321–34.

14. Sheehan T, Bachelet D, Ferschweiler K. Projected major fire and vegetation changes in the Pacific Northwest of the conterminous United States under selected CMIP5 climate futures. Ecological Modelling. 2015 Dec 10;317:16–29.

15. Rehfeldt GE, Crookston NL, Warwell MV, Evans JS. Empirical analyses of plant-climate relationships for the western United States. International Journal of Plant Sciences. 2006 Nov;167(6):1123–50.

16. Rehfeldt GE, Jaquish BC, López-Upton J, Sáenz-Romero C, St Clair JB, Leites LP, et al. Comparative genetic responses to climate for the varieties of Pinus ponderosa and Pseudotsuga menziesii: Realized climate niches. Forest Ecology and Management. 2014 Jul 15;324:126–37.

17. Rehfeldt GE, Leites LP, St Clair JB, Jaquish BC, Sáenz-Romero C, López-Upton J, et al. Comparative genetic responses to climate in the varieties of Pinus ponderosa and Pseudotsuga menziesii: Clines in growth potential. Forest Ecology and Management. 2014 Jul 15;324:138–46.

18. Rehfeldt GE, Jaquish BC, Sáenz-Romero C, Joyce DG, Leites LP, St Clair JB, et al. Comparative genetic responses to climate in the varieties of Pinus ponderosa and Pseudotsuga menziesii: reforestation. Forest Ecology and Management. 2014 Jul 15;324:147–57.

19. Littell JS, Oneil EE, McKenzie D, Hicke JA, Lutz JA, Norheim RA, et al. Forest ecosystems, disturbance, and climatic change in Washington State, USA. Climatic Change. 2010 Sep 1;102(1–2):129–58.

20. Rogers BM, Neilson RP, Drapek R, Lenihan JM, Wells JR, Bachelet D, et al. Impacts of climate change on fire regimes and carbon stocks of the US Pacific Northwest. Journal of Geophysical Research: Biogeosciences. 2011 Sep 1;116(G3). doi: 10.1029/2011jg001641

21. Coops NC, Waring RH, Beier C, Roy‐Jauvin R, Wang T. Modeling the occurrence of 15 coniferous tree species throughout the Pacific Northwest of North America using a hybrid approach of a generic process‐based growth model and decision tree analysis. Applied Vegetation Science. 2011 Aug;14(3):402–14.

22. Creutzburg MK, Halofsky JE, Halofsky JS, Christopher TA. Climate change and land management in the rangelands of central Oregon. Environmental Management. 2015 Jan 1;55(1):43–55. doi: 10.1007/s00267-014-0362-3 25216989

23. Whitlock C, Shafer SL, Marlon J. The role of climate and vegetation change in shaping past and future fire regimes in the northwestern US and the implications for ecosystem management. Forest Ecology and Management. 2003 Jun 3;178(1–2):5–21.

24. Latta G, Temesgen H, Barrett TM. Mapping and imputing potential productivity of Pacific Northwest forests using climate variables. Canadian Journal of Forest Research. 2009 Jun 17;39(6):1197–207.

25. Sheehan T, Bachelet D, Ferschweiler K. Fire, CO2, and climate effects on modeled vegetation and carbon dynamics in western Oregon and Washington. PloS One. 2019 Jan 25;14(1):e0210989. doi: 10.1371/journal.pone.0210989 30682107

26. Keenan RJ. Climate change impacts and adaptation in forest management: a review. Annals of Forest Science. 2015 Mar 1;72(2):145–67.

27. Pianosi F, Beven K, Freer J, Hall JW, Rougier J, Stephenson DB, et al. Sensitivity analysis of environmental models: A systematic review with practical workflow. Environmental Modelling & Software. 2016 May 1;79:214–32.

28. Littell JS, McKenzie D, Kerns BK, Cushman S, Shaw CG. Managing uncertainty in climate‐driven ecological models to inform adaptation to climate change. Ecosphere. 2011 Sep;2(9):1–9.

29. Luo Y, Ahlström A, Allison SD, Batjes NH, Brovkin V, Carvalhais N, et al. Toward more realistic projections of soil carbon dynamics by Earth system models. Global Biogeochemical Cycles. 2016 Jan 1;30(1):40–56.

30. Williams BK. Adaptive management of natural resources—framework and issues. Journal of Environmental Management. 2011 May 1;92(5):1346–53. doi: 10.1016/j.jenvman.2010.10.041 21075505

31. Millar CI, Stephenson NL, Stephens SL. Climate change and forests of the future: managing in the face of uncertainty. Ecological Applications. 2007 Dec 1;17(8):2145–51. doi: 10.1890/06-1715.1 18213958

32. National Research Council. Adaptive Management for Water Resources Planning. The National Academies Press, Washington, DC. 2004.

33. Bachelet D, Ferschweiler K, Sheehan TJ, Sleeter BM, Zhu Z. Projected carbon stocks in the conterminous USA with land use and variable fire regimes. Global Change Biology. 2015 Dec;21(12):4548–60. doi: 10.1111/gcb.13048 26207729

34. Hudiburg T, Law B, Turner DP, Campbell J, Donato D, Duane M. Carbon dynamics of Oregon and Northern California forests and potential land‐based carbon storage. Ecological Applications. 2009 Jan 1;19(1):163–80. doi: 10.1890/07-2006.1 19323181

35. Omernik JM, Griffith GE. Ecoregions of the conterminous United States: evolution of a hierarchical spatial framework. Environmental Management. 2014 Dec 1;54(6):1249–66. doi: 10.1007/s00267-014-0364-1 25223620

36. Daly C, Halbleib M, Smith JI, Gibson WP, Doggett MK, Taylor GH, et al. Physiographically sensitive mapping of climatological temperature and precipitation across the conterminous United States. International Journal of Climatology: a Journal of the Royal Meteorological Society. 2008 Dec;28(15):2031–64.

37. Taylor KE, Stouffer RJ, Meehl GA (2012). An overview of CMIP5 and the experiment design. Bulletin of the American Meteorological Society. 2012 April1;93(4):485–498.

38. Sheehan T, Gough M. A platform-independent fuzzy logic modeling framework for environmental decision support. Ecological Informatics. 2016 Jul 1;34:92–101.

39. Zadeh LA. Outline of a new approach to the analysis of complex systems and decision processes. IEEE Transactions on systems, Man, and Cybernetics. 1973 Jan(1):28–44.

40. Giles R. Łukasiewicz logic and fuzzy set theory. International Journal of Man-Machine Studies. 1976 May 1;8(3):313–27.

41. Masson D, Knutti R. Climate model genealogy. Geophysical Research Letters. 2011 Apr 28;38(8).

42. Neary DG, Ice GG, Jackson CR. Linkages between forest soils and water quality and quantity. Forest Ecology and Management. 2009 Oct 30;258(10):2269–81.

43. Hurteau MD, Koch GW, Hungate BA. Carbon protection and fire risk reduction: toward a full accounting of forest carbon offsets. Frontiers in Ecology and the Environment. 2008 Nov;6(9):493–8.

44. Fischer AP, Spies TA, Steelman TA, Moseley C, Johnson BR, Bailey JD, et al. Wildfire risk as a socioecological pathology. Frontiers in Ecology and the Environment. 2016 Jun;14(5):276–84.

45. D'Amato AW, Bradford JB, Fraver S, Palik BJ. Effects of thinning on drought vulnerability and climate response in north temperate forest ecosystems. Ecological Applications. 2013 Dec 1;23(8):1735–42. doi: 10.1890/13-0677.1 24555305

46. Bradley St Clair J, Howe GT. Genetic maladaptation of coastal Douglas‐fir seedlings to future climates. Global Change Biology. 2007 Jul;13(7):1441–54.

47. Chmura DJ, Anderson PD, Howe GT, Harrington CA, Halofsky JE, Peterson DL, et al. Forest responses to climate change in the northwestern United States: ecophysiological foundations for adaptive management. Forest Ecology and Management. 2011 Apr 1;261(7):1121–42.

48. Hann WJ, Bunnell DL. Fire and land management planning and implementation across multiple scales. International Journal of Wildland Fire. 2001;10(4):389–403.

49. Rupp DE, Abatzoglou JT, Hegewisch KC, Mote PW. Evaluation of CMIP5 20th century climate simulations for the Pacific Northwest USA. Journal of Geophysical Research: Atmospheres. 2013 Oct 16;118(19):10–884.

50. Adriaenssens V, De Baets B, Goethals PL, De Pauw N. Fuzzy rule-based models for decision support in ecosystem management. Science of the Total Environment. 2004 Feb 5;319(1–3):1–2. doi: 10.1016/S0048-9697(03)00433-9 14967497

51. Barbosa AM, Real R. Applying fuzzy logic to comparative distribution modelling: a case study with two sympatric amphibians. The Scientific World Journal. 2012;2012.

52. Petrou ZI, Kosmidou V, Manakos I, Stathaki T, Adamo M, Tarantino C, et al. A rule-based classification methodology to handle uncertainty in habitat mapping employing evidential reasoning and fuzzy logic. Pattern Recognition Letters. 2014 Oct 15;48:24–33.

53. Forio MA, Mouton A, Lock K, Boets P, Nguyen TH, Ambarita MN, et al. Fuzzy modelling to identify key drivers of ecological water quality to support decision and policy making. Environmental Science & Policy. 2017 Feb 1;68:58–68.

54. Soto ME. The identification and assessment of areas at risk of forest fire using fuzzy methodology. Applied Geography. 2012 Nov 1;35(1–2):199–207.

55. Smith MJ, Wagner C, Wallace KJ, Pourabdollah A, Lewis L. The contribution of nature to people: Applying concepts of values and properties to rate the management importance of natural elements. Journal of Environmental Management. 2016 Jun 15;175:76–86. doi: 10.1016/j.jenvman.2016.02.007 27056439

56. Meigs G, Krawchuk M. Composition and Structure of Forest Fire Refugia: What Are the Ecosystem Legacies across Burned Landscapes?. Forests. 2018 May;9(5):243.

57. Meddens AJ, Kolden CA, Lutz JA, Smith AM, Cansler CA, Abatzoglou JT, et al. Fire Refugia: What Are They, and Why Do They Matter for Global Change?. BioScience. 2018 Oct 3;68(12):944–54.

58. Krawchuk MA, Haire SL, Coop J, Parisien MA, Whitman E, Chong G, et al. Topographic and fire weather controls of fire refugia in forested ecosystems of northwestern North America. Ecosphere. 2016 Dec 1;7(12).

59. Morelli TL, Daly C, Dobrowski SZ, Dulen DM, Ebersole JL, Jackson ST, et al. Managing climate change refugia for climate adaptation. PLoS One. 2016 Aug 10;11(8):e0159909. doi: 10.1371/journal.pone.0159909 27509088

60. Theobald DM, Harrison-Atlas D, Monahan WB, Albano CM. Ecologically-relevant maps of landforms and physiographic diversity for climate adaptation planning. PLoS One. 2015 Dec 7;10(12):e0143619. doi: 10.1371/journal.pone.0143619 26641818

61. Zabihi K, Paige GB, Hild AL, Miller SN, Wuenschel A, Holloran MJ. A fuzzy logic approach to analyse the suitability of nesting habitat for greater sage-grouse in western Wyoming. Journal of Spatial Science. 2017 Jul 3;62(2):215–34.

62. Krosby M, Breckheimer I, Pierce DJ, Singleton PH, Hall SA, Halupka KC, et al. Focal species and landscape “naturalness” corridor models offer complementary approaches for connectivity conservation planning. Landscape Ecology. 2015 Dec 1;30(10):2121–32.

63. Gavin MC, McCarter J, Mead A, Berkes F, Stepp JR, Peterson D, Tang R. Defining biocultural approaches to conservation. Trends in Ecology & Evolution. 2015 Mar 1;30(3):140–5.


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