Forest Ecology and Management 255 (2008) 3952–3961 Contents lists available at ScienceDirect Forest Ecology and Management journal homepage: www.elsevier.com/locate/foreco Long-term post-wildfire dynamics of coarse woody debris after salvage logging and implications for soil heating in dry forests of the eastern Cascades, Washington Philip G. Monsanto, James K. Agee * College of Forest Resources, Box 352100, University of Washington, Seattle, WA 98195-2100, USA A R T I C L E I N F O A B S T R A C T Article history: Received 19 December 2007 Received in revised form 12 March 2008 Accepted 13 March 2008 Long-term effects of salvage logging on coarse woody debris were evaluated on four stand-replacing wildfires ages 1, 11, 17, and 35 years on the Okanogan-Wenatchee National Forest in the eastern Cascades of Washington. Total biomass averaged roughly 60 Mg ha1 across all sites, although the proportion of logs to snags increased over the chronosequence. Units that had been salvage logged had lower log biomass than unsalvaged units, except for the most recently burned site, where salvaged stands had higher log biomass. Mesic aspects had higher log biomass than dry aspects. Post-fire regeneration increased in density over time. In a complementary experiment, soils heating and surrogate-root mortality caused by burning of logs were measured to assess the potential site damage if fire was reintroduced in these forests. Experimentally burned logs produced lethal surface temperatures (60 8C) extending up to 10 cm laterally beyond the logs. Logs burned in late season produced higher surface temperatures than those burned in early season. Thermocouples buried at depth showed mean maximum temperatures exponentially declined with soil depth. Large logs, decayed logs, and those burned in late season caused higher soil temperatures than small logs, sound logs, and those burned in early season. Small diameter (1.25 cm), live Douglas-fir branch dowels, buried in soil and used as surrogates for small roots, indicated that cambial tissue was damaged to 10 cm depth and to 10 cm distance adjacent to burned logs. When lethal soil temperature zones were projected out to 10 cm from each log, lethal cover ranged up to 24.7% on unsalvaged portions of the oldest fire, almost twice the lethal cover on salvaged portions. Where prescribed fire is introduced to post-wildfire stands aged 20–30 years, effects of root heating from smoldering coarse woody debris will be minimized by burning in spring, at least on mesic sites. There may be some long-term advantages for managers if excessive coarse woody debris loads are reduced early in the post-wildfire period. ß 2008 Elsevier B.V. All rights reserved. Keywords: Salvage logging Soil heating Wildfire Pinus ponderosa Coarse woody debris Washington state 1. Introduction Prior to European settlement, wildland fire was the major historical disturbance factor in seasonally dry forests of the Intermountain West. These low elevation forests, typically dominated by Pinus ponderosa (ponderosa pine), were maintained by frequent, low intensity fires (Everett et al., 2000; Wright and Agee, 2004), which consumed fuels, killed small trees, and maintained open forests in classic low-severity fire regimes (Agee, 1993, 1998; Covington and Moore, 1994; Covington et al., 1994). Early travelers described the ease with which horses could be galloped through these groves, and the ease with which wagons traversed these forests (Dutton, 1881; Agee and Maruoka, 1994). These descriptions imply that coarse woody debris was limited in * Corresponding author. Tel.: +1 425 868 6031; fax: +1 206 543 3254. E-mail address: jagee@u.washington.edu (J.K. Agee). 0378-1127/$ – see front matter ß 2008 Elsevier B.V. All rights reserved. doi:10.1016/j.foreco.2008.03.048 historical dry forests, observations consistent with the frequent recurrence of fire, which would limit the standing life of snags and consume logs due to fire recurrence on a near decadal basis (Skinner, 2002; Agee, 2002). Fire exclusion in the 20th century, together with livestock grazing and selective removal of large P. ponderosa, changed the fuel and vegetation structure of these dry forests. Tree densities increased by orders of magnitude, single canopied forests became multi-canopied forests, average tree size declined, and dead fuel loads increased (McNeil and Zobel, 1980; Covington et al., 1994). While climate has historically (Heyerdahl et al., 2001) and more recently (Westerling et al., 2006) been a driver of fire size, the type of stand-replacing fire that is now commonly observed in these forests appears to have been nearly absent in historical dry forests based on the density of fire-scarred trees that survived 20–30 fires (Heyerdahl et al., 2001; Wright and Agee, 2004). The increase in fire severity, largely due to changes in fuels and stand structure, P.G. Monsanto, J.K. Agee / Forest Ecology and Management 255 (2008) 3952–3961 was predicted as early as the 1940s (Weaver, 1943). After these higher-severity wildfires, forests that once had sustainable but limited quantities of coarse woody debris now have much to all of the large, live, above-ground biomass converted to coarse woody debris. Post-wildfire removal of the dead timber, a process known as salvage logging, has sometimes been attempted, primarily to recoup economic value. Concern has been raised about damage to ecological values (Beschta et al., 2004; Lindenmayer et al., 2004), and a review of the available literature on salvage logging (McIver and Starr, 2000) found almost all studies dealt with short-term effects, and none, as expected due to the unplanned timing of the wildfires, were experimental in nature. Modeled fire behavior was projected to increase immediately after salvage logging in the Biscuit Fire in southwest Oregon (Donato et al., 2006) due to fine fuels left after tree fall and yarding. Fuel loading projections over longer timeframes (McIver and Ottmar, 2007) after salvage logging in northeastern Oregon with fine woody debris loads almost identical to the Biscuit fire (6.2–6.7 Mg ha1 for salvaged stands and 1.3 Mg ha1 for unsalvaged stands) suggested that these fine fuel loads would converge over time as fuel mass from unsalvaged stands would differentially increase as the higher number of snags fell in those areas (McIver and Ottmar, 2007). Higher fire severity occurred in 15-year-old stands salvaged logged and planted than in unmanaged stands in areas of the Silver fire (1987) reburned by the Biscuit fire (2002) in southwest Oregon, but the relative influence of fuels and young tree density could not be separated (Thompson et al., 2007). No experimental or retrospective studies have looked at long-term effects of decisions to salvage log severely burned stands in dry forests. For example, if young post-fire stands are actively managed to avoid subsequent stand-replacing events, what is the relative influence of coarse woody debris with and without salvage logging on effects such as soil heating and root mortality from prescribed fire? As forests dominated or co-dominated by P. ponderosa recover after being burned by high-severity wildfires, the typical dry summer conditions and long fire seasons virtually ensure that future wildfire will occur and place the young post-fire forest stands at risk for another stand-replacing event. Active management, such as prescribed fire, may be desirable to reduce the potential intensity and severity of future wildfires. Yet few studies have focused on the dynamics of post-wildfire coarse woody debris in dry forests (see Passovoy and Fule, 2006), and the implications of salvage logging on the potential severity of either prescribed fires or subsequent wildfires. We saw a significant retrospective opportunity to do this in eastern Washington, where four large, stand-replacing wildfires in dry forest types had periodically occurred over the previous 35 years. We chose to evaluate the following questions: What are the patterns of coarse woody debris mass and cover up to 35 years after wildfire in the presence and absence of salvage logging? What are the patterns of soil heating and fine root mortality caused by experimentally burning logs? 2. Methods 2.1. Study area Four dry forest study units that burned with high-severity fire in the Wenatchee River and Entiat River basins of the OkanoganWenatchee National Forest (Fig. 1) were selected for study: the 2004, 6700 ha Fischer Fire (1 year); 1994, 38,000 ha Tyee Fire (11 years); 1988, 21,000 ha Dinkelman Fire (17 years); and 1970, 25,000 ha Entiat Fire (35 years). Historical (1700–1900 A.D.) fire frequency at Mud Creek within the Tyee fire area averaged 7 years 3953 Fig. 1. Location of the four wildfires analyzed in this study. Approximate center of study area is located at NAD83 478440 1500 N, 1208220 0800 W. (within 199–1697 ha sample units; Everett et al., 2000), in part due to the fire climate of the area. Climate is hot and dry during summer months, with mean maximum July temperatures over 30 8C and July precipitation less than 1 cm (Entiat Fish Hatchery, 1989–2003 NAD83 478410 5400 N, 1208190 2500 W, Western Regional Climate Center, 2003). Annual precipitation averages 34 cm, with a gradient of increasing precipitation west from the Columbia River. On the driest aspects (south and west) of all four study units, forest series are P. ponderosa and Pseudotsuga menziesii, and on the higher productivity mesic aspects (north and east), forest series are P. menziesii and a minor amount of Abies grandis (Lillybridge et al., 1995). Fire had been excluded from these areas from 60 to 90 years at the time of each of the stand-replacing wildfires, and some areas experienced selective harvest of old-growth ponderosa pine. 2.2. Coarse woody debris study design and methods Each of the four wildfires burned for weeks to months through a variety of fire weather conditions, and after each fire, timber was salvaged on a portion of each burned landscape. We did not have records to establish either the exact locations of salvage or the intensity of salvage on any of the fires except for the Fischer Fire. We could identify salvaged stands by searching for charcoal-free cut surfaces of stumps, and unsalvaged stands by the presence of either large snags or logs associated with each stub or stump. The range of salvage intensity was similar on each fire, but the average volume removed likely differed, with higher average salvage intensities on the older fires due to less attention to the retention of dead wood for wildlife purposes. Due to the difference in productivity between dry (south, west) and mesic (north, east) P.G. Monsanto, J.K. Agee / Forest Ecology and Management 255 (2008) 3952–3961 3954 Fig. 2. (A) The placement of thermocouples adjacent to and beneath logs. Thermocouples X1–X5 are located at 10 cm from log edge, log edge, center of log, log edge, and 10 cm from log edge. Thermocouples X3 and X6–X8 are located at 0, 5, 10, and 15 cm depth beneath log center. (B) The root surrogates of Douglas-fir branch dowels are located at 0, 5 and 10 cm beneath the log center and at 5 and 10 cm depth at 10 cm away from the log edge. aspects, we assumed that coarse woody debris might differ by aspect, and therefore stratified our sampling by aspect. The limited areas that reburned between any two fires were identified from mapped perimeters and avoided for sampling. The experimental design was a stratified randomized sampling design. Sample units were distributed evenly across the following factors: Fire Unit (4 wildfires of ages 1, 11, 17, and 35), Salvage (2; present or absent), and Aspect (2; dry or mesic). Each factor combination was represented by three sampling units, for a total sample size of 48 sites. While we recognized that fire unit can be considered a pseudoreplicated factor, the large size of the units and the length of time they burned (weeks to months) made each fire unit quite variable within itself. At each randomly selected sample location, a center point was established and plots and transects were used to measure coarse woody debris (snags and logs) and post-fire vegetation. Variableradius plots with a 5 BAF (English unit) prism and 10 m 10 m fixed plots were established at the sample point center and at two locations 50 m from the center, with the direction of the first line located randomly, and the second also located randomly, subject to the constraint that the angle between the two lines exceeded 908. The variable-radius plots were used to measure live and dead tree composition, structure and density. Each live ‘‘in’’ tree had the following characteristics measured: species, height, diameter at breast height (dbh), crown ratio, dominance, and whether or not it was a post-fire surviving residual. Snags had species, dbh, broken top diameter, and decay class (Maser et al., 1979) recorded. Small trees with no dbh were tallied by species on the 10 m 10 m plot. The two 50 m lines were used to measure log biomass and cover (Brown, 1974; Bate et al., 2004). Log cover was measured using model II of Bate et al. (2004): percent cover ¼ p hX 2L di i where L = length of sample line and d = diameter of log at intersection with line. Only dead fuels exceeding 7.62 cm at the point of intersection (lower threshold of 1000-h timelag fuels) were measured. 2.3. Log burning study design and methods Log segments were experimentally burned on 1.25 m 1.85 m decks constructed of cement block frames filled with local soil, which was a loamy, mixed, shallow, Vitrandic Haploxeroll (NRCS, 2007). Large rocks were removed from the mostly inorganic soil, and soil was packed to a depth of 40 cm in each deck. Forty logs, each 1.2 m in length, were burned over the 2006 fire season (early [6/21–7/21] and late [9/1–10/1]), in two diameter classes (20 cm and 40 cm) and two decay classes (sound: bark intact and wood showing little obvious decay; and rotten: little bark and evidence of cubical rot). Each log was weighed using a hanging scale before and after burning to determine consumption. The log was placed on a bed of pine needles and fine branches and ignited once from each edge of the log deck. Log decks were instrumented with eight type K thermocouples (Fig. 2a) with four directly beneath the log (0, 5, 10, and 15 cm depths), and five at the surface (center of log, one at each edge of the log, and one 10 cm from each edge of the log). Thermocouples were connected to a CR1000 datalogger (Campbell Scientific, North Logan, UT, USA) that recorded temperature every second for a per-minute average. Temperatures above 60 8C were of particular importance, as that threshold for one minute or longer has been associated with tissue death (Hare, 1961). A more direct evaluation of lethal heat was obtained by burying short dowels of live Douglas-fir branches around the logs as surrogates for fine roots. The dowels were freshly cut segments of branches, about 10 cm long, and 1.25 cm in diameter. Six dowels were used for each of 36 logs: one control, three buried directly under the log at 0, 5, and 10 cm depths, and two buried 10 cm away from the log edge at 5 and 10 cm depths (Fig. 2b). After each log was burned, the dowels were removed and refrigerated overnight with the control. The next morning an orthotolodieneurea hydroxide solution was applied to exposed cambial tissue on each dowel to assess tissue condition: if the rusty red color turned dark blue after application, the tissue remained alive (Ryan et al., 1988). Each dowel was then classified as live or dead. 2.4. Data analysis Coarse woody debris was evaluated based on changes in snag biomass, log biomass and cover, and the proportion of log biomass in rotten versus sound logs. Snag biomass (boles only, branches were ignored) was calculated using an estimate of log volume by Smalian’s rule (Bell and Dilworth, 2002). Specific gravities of 0.48 for sound logs and 0.30 for rotten logs (Lolley, 2005) were applied to the data to compute mass. Log biomass and cover were P.G. Monsanto, J.K. Agee / Forest Ecology and Management 255 (2008) 3952–3961 computed for each transect using standard methods for estimating fuel loads (Brown, 1974; Bate et al., 2004) and averaged by site. The proportion of biomass and cover in rotten logs was calculated for each line averaged by site, and transformed with an arcsine function (Zar, 1999) to normalize the distribution of model residuals. Live tree data were used to calculate post-fire stand density, but because current density is an unknown mix of planting and natural regeneration it is not quantitatively analyzed. Analysis of variance was used to evaluate the effects of time since fire, aspect, and post-fire logging history on coarse woody debris. Fire unit (time since fire) aspect, and logging history were all treated as fixed treatment effects in three-way ANOVA analyses for log biomass and cover. Analysis of total coarse woody debris biomass was done only for unsalvaged stands in order to assess natural decomposition of the entire coarse dead wood biomass over time. A two-way fixed effects ANOVA with fire unit and aspect as factors was applied to these data. The proportion of biomass and cover in rotten logs, transformed with an arcsine (Zar, 1999) was analyzed using a one-way ANOVA, with the fixed effect of fire unit. Mean maximum temperatures recorded in the log burning experiment were analyzed using two four-way fixed effects ANOVAs with treatments thermocouple location, diameter class, decay class, and season of burn. The first analysis was conducted on the surface thermocouples (Fig. 2a) and the second was conducted on the thermocouples buried at depth. An unbalanced design resulted from occasional malfunction of a thermocouple, so the results utilized a conservative Type III sums of squares. The root surrogate dowels were analyzed using three Chisquare tests. The first analysis included those dowels buried directly beneath the log (Fig. 2b), and as these data were frequencies of live or dead dowels, a Chi-square test was used on a 2 3 contingency table (live or dead, three depths). The second and third analyses consisted of 2 2 contingency tables using surrogate root condition (live or dead), and under and adjacent to the log (log center or 10 cm from edge of log) in order to test the effect of distance from log on tissue survival. Separate analyses were conducted on surrogate roots buried at 5 cm depth and 10 cm depth. Significant effects were evaluated on the basis of P-values of 0.05 or lower. 3955 Fig. 3. Total coarse woody debris on unsalvaged portions of the four sites. On the xaxis, the first letter refers to site (F = Fischer (1 year), T = Tyee (11 years), D = Dinkelman (17 years), and E = Entiat (35 years), and the second letter refers to aspect (D = Dry, M = Mesic). 3.2. Timber salvage effect on log biomass and cover Log biomass increased with time since fire (P = .000), as snags decayed and fell (Fig. 3). Salvage significantly reduced log biomass (P = .000), and all interactions were also significant (.000 < P < .039). Log biomass ranged from 0.1 Mg ha1 (SE = 0.04) on Fischer (1 year) mesic unsalvaged stands to 55.3 Mg ha1 (SE = 7.1) in Entiat (35 years) mesic unsalvaged stands (Fig. 4). The salvage unit interaction (P = .000) was due to the Fischer (1 year) fire having more log biomass on salvaged units, whereas all the other units showed a decrease in log biomass on salvaged units. There was less log biomass on dry aspects than on mesic aspects (P = .002), and again the Dinkelman (17 years) unit showed a larger effect of aspect than other units (including Fischer, as there was very little log biomass there on either aspect group). The cover of logs followed similar trends to log biomass, as the metrics are related. Cover varied from 0% on Fischer (1 year) mesic unsalvaged stands to 10.2% on the Entiat (35 years) mesic 3. Results 3.1. Total coarse woody debris In the absence of salvage logging, total coarse woody debris averaged about 60 Mg ha1 but varied by fire unit (P = .001), aspect (P = .000), and the fire unit x aspect interaction (P = .001) (Fig. 3). There was not a linear change with time, as the Dinkelman unit (17 years fire) had the lowest average mass. Mesic aspects had a higher total biomass than dry aspects, and the effect of aspect varied by unit. On two units (Tyee [11 years] and Entiat [35 years]) total biomass was similar on both aspects, but on the Dinkelman and Fischer units, total biomass on dry aspects was less than on mesic aspects. These two units are furthest east and slightly drier than the other two units, so the effect of aspect might be magnified on these units. After 35 years, the total biomass appears not to have significantly changed in a clear temporal pattern, although the proportion of standing versus down and sound versus rotten have changed. The proportion of the total biomass in snags declines with time, and the proportion of the log biomass that is rotten increases from close to zero on the 1 year (Fischer) and 11 years (Tyee) fires to 7% on the 17 years (Dinkelman) fire and 57% on the 35 years (Entiat) fire (P = .001). Fig. 4. Effect of timber salvage on log biomass. Dry and mesic aspects are averaged together on each site. The box represents the interquartile range which contains the middle 50% of records. The upper edge of boxes indicates the 75th percentile, and the lower edge indicates the 25th percentile. The line in the box indicates the median value. Whiskers indicate minimum and maximum data values. The asterisk indicates a high outlier in the dataset on a no-salvage, dry aspect sample that was close to a clump of top-snapped trees. P.G. Monsanto, J.K. Agee / Forest Ecology and Management 255 (2008) 3952–3961 3956 Table 1 Comparison of (A) mean log percent cover (standard error in parentheses) and (B) effective range of lethal cover when 20 cm are added to each log Fischer (1) Tyee (11) Dinkelman (17) Entiat (35) Table 2 Post-fire density (ha1) of live trees with measurable diameter at breast height (dbh), trees shorter than breast height, and total trees (standard error) Year (fire) A. Salvage No salvage Dry Dry unsalvage Dry salvage Mesic unsalvage Mesic salvage 0.3 0.3 0.0 2.5 (.13) (.09) (.00) (.26) 5.6 3.0 6.1 5.3 Dry unsalvage Dry salvage Mesic unsalvage Mesic salvage 0.6 0.7 0.1 6.2 (.22) (.21) (.04) (.55) 11.3 7.3 15.8 13.6 (.09) (.64) (.34) (.64) 2.9 1.2 8.4 6.4 (.20) (.26) (1.03) (.77) 6.4 4.8 10.2 4.9 (.47) (1.00) (.87) (.59) 6.4 2.9 21.1 15.8 (.51) (.37) (2.94) (1.49) 12.9 11.0 24.7 11.4 (.62) (2.12) (2.22) (1.51) B. (.09) (1.60) (.70) (1.71) unsalvaged sites (Table 1A). The only difference in the cover analysis was the absence of the salvage x aspect interaction (P = .930) in the log cover analysis. All main effects and the other two-way interactions had P = .000, and the three-way interaction was significant at P = .003. Mesic Trees with dbh 1 (Fischer) 11 (Tyee) 17 (Dinkelman) 35 (Entiat) 2.9 0.0 78.9 1069.2 Trees with no dbh 1 (Fischer) 11 (Tyee) 17 (Dinkelman) 35 (Entiat) 7 136 110 608 Total trees 1 (Fischer) 11 (Tyee) 17 (Dinkelman) 35 (Entiat) 9.9 136 188.9 1677.2 (0.1) (0.0) (2.2) (30.1) (4.6) (24.8) (54.4) (64.0) 5.7 125.9 70.7 1073.4 126 375 249 575 Dry (0.2) (3.5) (2.0) (30.2) (33.3) (49.6) (45.5) (99.5) 131.7 500.9 319.7 1648.4 Mesic 12.1 4.6 .1 478.6 53 355 10 515 (0.3) (0.1) (0.0) (13.5) (23.1) (117.0) (5.6) (117.8) 65.1 359.6 10.1 993.6 5.4 0.0 79.7 2269.5 7 359 60 1498 (0.2) (0.0) (2.2) (63.9) (6.6) (37.5) (18.1) (347.5) 12.4 359 139.7 3767.5 Year indicates age of fire referenced to 2005. 3.3. Young stand recovery The young recovering stands on all units were likely a mix of natural regeneration and planting, and the two sources of origin could not be separated. There was a low density of regeneration with measurable breast-high diameter, averaging less than 100 stems ha1, on all units except for the Entiat (35 years) fire (Table 2). Regeneration was almost exclusively P. ponderosa and P. menziesii. On the Entiat fire, Pinus contorta was a codominant species, and the average density was over 1200 stems ha1. Total tree density, including trees below breast height, suggest adequate to overstocked conditions in post-fire years 11–35 on all but the dry aspects of the Dinkelman (11 years) site. Fig. 5. Temperature profiles for small diameter logs (20 cm) (a) burned late spring/early summer and (b) burned late summer/early fall. Lines represent average of replicates for each treatment. Adjoining graphs, from left to right, represent 10 cm from left edge of log (10L), left edge of log (L), directly beneath center of log (C), right edge of log (R), and 10 cm from right edge of log (10R). P.G. Monsanto, J.K. Agee / Forest Ecology and Management 255 (2008) 3952–3961 3.4. Temperature profiles around logs Moisture content of small and large diameter logs averaged 17.7 and 14.7% in early season to 11.9 and 12.5% in late season. Log consumption increased from 52 and 59.2% consumption in early season to 70.8 and 74.3% in late season burns. Soil moisture was equivalent to air-dry conditions (<5%). Mean maximum surface temperatures spiked early in the flaming period for both small diameter (Fig. 5) and large diameter (Fig. 6) logs, and gradually decreased as more smoldering combustion occurred. In all conditions, mean maximum surface temperatures were well above lethal temperatures for cambial tissue. Mean maximum surface temperatures for diameter class (P = .504), decay class (P = .065), and thermocouple location (P = .057) did not differ. Lethal temperatures were reached out to 10 cm distance from each log edge. Logs burned in late season, however, did show higher surface temperatures than those burned in early season (P = .000). Thermocouples buried at depth under small diameter (Fig. 7) and large diameter (Fig. 8) logs showed more differences. There were differences in mean maximum temperatures due to depth (P = .000), diameter class (P = .001), decay class (P = .043), and season (P = .006), with a diameter season interaction (P = .005). Mean maximum temperature decreased with depth (Fig. 9), and lethal temperatures were reached on all early season logs to 5 cm depth but not deeper. Large logs, rotten logs, and late season burns had higher temperatures than small logs, sound logs, and early season burns. Large logs burned in late season reached lethal 3957 temperatures to 15 cm depth, but small logs, regardless of decay class, reached lethal temperatures only down to 5 cm. 3.5. Effects of soil heating on root surrogates Mean bark thickness of the Douglas-fir live branch dowels used as root surrogates was 1.2 mm (S.D. 0.4 mm). All control dowels, cut at the same time as treatment dowels and refrigerated overnight with them, showed no cambial damage when measured the next day. In most treatment combinations, a majority of the dowels showed signs of cambial damage (Table 3). Directly beneath logs, 83 of 108 surrogate roots had dead tissue (Table 4). There were no differences in the frequency of mortality with depth directly under the log (Table 3a; x2 = 3.85, x2 critical = 5.99). There were also no differences between the frequency of mortality between dowels buried at 5 cm depth and 10 cm depth between locations directly under the log and at 10 cm distance from the edge of the log(x2 values of 0.84 and 3.65 compared to x2 critical value of 3.84). 3.6. Lethal zone of cover from burning logs Given the results of the root surrogate treatment, the lethal zone for roots, even those not right at the surface, extended a minimum of 10 cm away from each edge of the burning log. Therefore, an additional 20 cm was added to each log diameter measured on the log transects on the four study units, and an estimate of lethal cover was calculated (Table 1B). The highest Fig. 6. Temperature profiles for large diameter logs (40 cm) (a) burned late spring/early summer and (b) burned late summer/early fall. Lines represent average of replicates for each treatment. Adjoining graphs, from left to right, represent 10 cm from left edge of log (10L), left edge of log (L), directly beneath center of log (C), right edge of log (R), and 10 cm from right edge of log (10R). 3958 P.G. Monsanto, J.K. Agee / Forest Ecology and Management 255 (2008) 3952–3961 Fig. 7. Temperature profiles for small diameter logs (20 cm) (a) burned late spring/early summer and (b) burned late summer/early fall. Lines represent average of replicates for each treatment. Adjoining graphs, from left to right, represent 0, 5, 10, and 15 cm in the soil. Fig. 8. Temperature profiles for large diameter logs (40 cm) (a) burned late spring/early summer and (b) burned late summer/early fall. Lines represent average of replicates for each treatment. Adjoining graphs, from left to right, represent 0, 5, 10, and 15 cm in the soil. P.G. Monsanto, J.K. Agee / Forest Ecology and Management 255 (2008) 3952–3961 3959 Table 4 Contingency tables for surrogate roots in various configurations around and beneath logs Depth (cm) 0 5 10 A. A 2 3 contingency table for surrogate roots directly beneath logs Live 5 8 12 Dead 31 28 24 Total 36 36 36 Total 25 83 108 Location at 5 cm depth Log center 10 cm from edge Total B. A 2 2 contingency table for surrogate roots buried at 5 cm depth directly under the log and at 10 cm distance from the edge of the log Live 8 5 13 Dead 28 31 59 Total Fig. 9. Maximum temperatures (8C) reached from the surface to 15 cm depth directly under burning logs. actual cover of logs was 10.2% on the 35-year-old unit (mesic unsalvaged at Entiat), and this increased to a lethal cover up to 24.7% when the additional lethal heating zone was added. Salvaged sites within the Entiat unit averaged about 12% lethal cover, with little difference between aspects. 36 36 72 10 cm from edge Total Location at 10 cm depth Log center C. A 2 2 contingency table for surrogate roots buried at 10 cm depth directly under the log and at 10 cm distance from the edge of the log Live 11 19 30 Dead 25 17 42 Total 36 36 72 4. Discussion Stand-replacing fires, while historically uncommon in dry forests of the American West, were historically the norm in wet and/or cold forests (Romme, 1982; Agee, 1993). ‘‘Boom and bust’’ patterns, beginning with large increments of coarse woody debris immediately after the fire, followed by decreases due to decomposition and lack of new input from the young, small post-fire trees, and eventual increases when the new forest produced trees large enough to persist as logs, created a U-shaped distribution of coarse woody debris over centuries (Harmon et al., 1986; Agee and Huff, 1987). Much lower and less variable coarse woody debris patterns were characteristic of historic P. ponderosa forests (Agee, 2002). With the change in fire regime from low-severity to mixedor high-severity, seasonally dry forests being burned now by intense fires have biomass and cover of coarse woody debris at many times historical levels (Agee, 2002; Skinner, 2002). For example, cover of logs in old-growth P. ponderosa stands of central Oregon and northern California was 1.7% (Youngblood et al., 2004), and a study in old growth Pinus jeffreyi forest in Mexico calculated a log cover of 1.5% (Stephens et al., 2007). Ohmann and Waddell (2002) estimated percent cover of logs between 12 and 50 cm diameter in young, mature, and old-growth forests to be 1.1, 1.3, and 1.0% for P. ponderosa forests of Oregon and Washington. Our mean percent cover of logs, by post-wildfire age 35, ranged from 4.8 to 10.2% 35 years after wildfire (Table 1), much higher than in old growth stands of dry forests and at levels higher than suggested to optimize protection of soils and wildlife habitat while mitigating fire danger (Brown et al., 2003). These fire-prone environments are dry enough that natural decomposition is slow. Using Olson’s (1963) single exponential decay model and the decay rate constant of 0.073 for P. ponderosa (>25 cm) (Harmon et al., 1986), snag bole fragmentation could take more than 40 years, and this rate appears to close to what we observed at the 35-year-old Entiat fire (Fig. 3). However, this process was nearly the same on the 11-year-old Tyee fire, so that local factors likely create substantial variability on the conversion of snags to down logs. Parminter (2002) estimated a decay rate for log boles of 0.035, and McIver and Ottmar (2007) used 0.03 and 0.02 for P. ponderosa and P. menziesii logs. These rates would result in 100–150 years for a population of logs to decompose. During that time, the stands remain at risk to wildfire. Early in succession (ages 0–30) the young trees are small enough that regardless of coarse woody debris loads, high-severity fire is likely to occur if another wildfire burns through the stand (McIver and Ottmar, 2007; Thompson et al., 2007). Table 3 Percent of P. menziesii surrogate roots showing cambium death as indicated by Orthotolidiene/urea hydroxide solution Log size, decay, and season burned Surface 5 cm depth 5 cm depth (10 cm edge) 10 cm depth 10 cm depth (10 cm edge) Large diameter logs Early rotten Early sound Late rotten Late sound 100 33 100 80 75 33 100 80 75 100 100 80 50 33 100 80 50 0 100 80 Small diameter logs Early rotten Early sound Late rotten Late sound 100 75 100 100 80 75 80 80 80 75 100 80 60 50 80 80 0 25 60 40 ‘‘10 cm edge’’ refers to dowels 10 cm from the edge of logs. 3960 P.G. Monsanto, J.K. Agee / Forest Ecology and Management 255 (2008) 3952–3961 While our results were restricted to coarse woody debris, they are consistent with what Donato et al. (2006) and McIver and Ottmar (2007) found with fine woody debris: salvage logging immediately increases the biomass of woody debris on the ground. At the Fischer fire, this biomass consisted of lopped and scattered tops left after the salvage logging. The convergence of levels of fine woody debris between salvaged and unsalvaged stands suggested by McIver and Ottmar (2007) occurred in our study with coarse woody debris. By age 10, levels of coarse woody debris in salvaged stands fell below those of unsalvaged stands, and that pattern remained through age 35. Salvage removes boles that would otherwise become coarse woody debris, so one would expect lowered coarse woody debris levels decades after salvage logging compared to unsalvaged sites. The difference in percent cover of coarse woody debris between salvaged and unsalvaged stands at the 35-year-old Entiat fire ranged from 1.6 (dry aspects) to 5.3% (mesic aspects). When the lethal cover was calculated, these differences increased to 1.9 (dry aspects) to 13.3% (mesic aspects), and almost 25% lethal cover occurred on unsalvaged mesic aspects at the Entiat fire. These values suggest that prescribed fire introduced for the purpose of lowering wildfire risk could significantly damage young stands, even if crown damage was minimal, due to root damage, as has been demonstrated for old growth pine stands (Swezy and Agee, 1991; Kolb et al., 2007). On dry aspects, which might be chosen as a higher priority for young stand fuel treatments, salvage appeared to have a less dramatic effect than on the mesic aspects. We used live Douglas-fir branches as surrogates for small roots (1.25 cm and smaller). We justified this on the basis that in situ experiments were not easily designed, and that small branches should function similarly to roots in a physiological sense. Our controls indicated that a cut branch left out for the day and refrigerated overnight showed no cambial damage the next day. We were confident that the root surrogate treatment would be a better test of root damage than temperature profiles alone, and the results suggested substantial damage could occur to roots not only beneath burning logs but also adjacent to them. Our tests were conservative, as we used a single log model. When large woody fuels burn in isolation, as in our experiments, they may burn with less intensity or less completely than when burned in close proximity to other sufficiently dry fuels of the same size or smaller (Albini and Reinhardt, 1995, 1997). Harrington (1981) observed that grouped logs burned more completely than when they burned in isolation. Therefore, the temperature profiles we measured are likely conservative, as we only burned single logs. We did not extend our measurement zone beyond 10 cm from the edge of logs, so we did not extrapolate potential damage further away from the burned logs. 4.1. Management considerations Some managers have considered breaking the cycle of stand replacement burning (e.g., Thompson et al., 2007) by intervening with treatments such as prescribed fire when the post-wildfire stand reaches age 20 or 30 (Peterson et al., 2007). By managing tree density and fuels, the intent is to ease the process of fire suppression should a wildfire occur, create adequate space for tree growth, and reduce potential wildfire severity in the young stand. Conducting prescribed fires in young stands with substantial coarse woody debris presents several challenges, including the amount of smoke from smoldering logs (Hardy et al., 2001). But one underappreciated effect is the potential root damage from consumption of coarse woody debris from prescribed fires intended to reduce fuels and make the young stand more resistant to wildfire. Busse et al. (2005) showed that burning masticated residues up to 12.5 cm deep created lethal surface temperatures that increased with soil dryness and mulch depth. Lethal temperatures were observed down to 10 cm depth in the heavier mulch treatment, and they suggested burning these residues ranked between moderate severity prescribed fires and damaging effects of heavy slash fires. The spatial distribution of wood mulch at one site showed that about 25% of the area would experience lethal temperatures to 10 cm depth, but at another site the mulch depths were less and lower soil heating would be predicted there. Whether stands have been salvaged or not, soil heating from smoldering logs will be a concern. Salvage reduces but does not eliminate coarse woody debris. Some coarse woody debris will be valuable for wildlife habitat (Brown et al., 2003), and some will be too small to be commercially useful. Spring burning may be one solution where high levels of coarse woody debris occur. Our data suggest that spring burns had less heating than fall burns, and early season burns typically cover less area. If we had used moist soil under the logs burned in late spring, the differences likely would have been even more pronounced (Frandsen and Ryan, 1986). Perrakis and Agee (2006) reported for old-growth forest a range of 19–37% area burned from spring burns with a much higher 64–86% for fall burns. Spring burns typically consume less coarse woody debris, too. Knapp et al. (2005) reported 57% of log biomass consumed in spring burns compared to 83% in fall burns, again in old-growth forest. Spring prescribed burns in the 1970 Entiat fire, under young stands, showed similar patchiness (Peterson et al., 2007). All of the forest floor was consumed over 45% of the area, between 5 and 95% was consumed on 27% of the area, and 28% of the area was unburned. It would seem prudent that for mesic aspects in unsalvaged areas, initial prescribed burns in spring would be favored to mitigate the effect of root heating from smoldering logs. Subsequent fires in such areas, and initial fires in salvaged stands, might have wider seasonal windows for burning. In the past, most concerns regarding salvage logging have dealt with short-term issues (Beschta et al., 2004). Longer-term ecological effects, such as some of the effects of excessively high levels of coarse woody debris, should be factored into the decisionmaking process. In dry forest types there may be some long-term advantages for managers if excessive coarse woody debris loads are reduced early in the post-wildfire period. Acknowledgements This research was funded under Joint Venture Agreement PNW #03-JV-11261927-534, CROP Forest Ecology, between the USDA Forest Service, Pacific Northwest Research Station and the University of Washington. 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