This file was created by scanning the printed publication. Errors identified by the software have been corrected; however, some errors may remain. Commercial Fuelwood Harvesting Affects on Small Mammal Habitats in Central Arizona William H. Kruse Abstract-In a central Arizona fuelwood harvest area, 75 percent of the overstory was cut in a commercial harvest, resulting in large quantities of residual logging debris that altered habitat for many wildlife species. Small mammals have intricate roles in ecosystem function, and current fuelwood management practices have paradoxical affects on small mammal habitats. In a small mammal study, no differences in total animals capt,ured were detected among treatment plots. Immediately following overs tory reduction or removal in 1992 and 1993, differences among species ca ptures, s pecifically deer mouse, increased significantly. The increased capture rate remained significant throughout the remainder of the study. Pinyon mouse captures declined significantly immediately following treatments, but were not detectablydifferent from pretreatment levels a year later. Commercial fuelwood harvesting generates greater and more concentrated slash and has more affect on microsite conditions than noncommercial fuelwood cutting. This has prompted some central Arizona USDA Forest Service Ranger Districts to assess the effects of commercial fuelwood removal and slash disposal, particularly by burning. Specifically, removal of slash habitat through burning is a concern. Fortunately, commercial harvest permits, however, can provide detailed slash management directions to meet specific management objectives. Burning is usually not performed by the fuelwood permit holder but instead is included in Forest Service management plans. Fuelwood removal and slash management also affects microsite nutrient cycling, miderstory production (specifically protecting forages from large ungulate grazing), and regeneration of overstory species. Small mammal populations are also affected by removal of overstory, understory composition and structure change, and slash accumulation and subsequent manipulation. Basic ecological information is needed to support current harvesting plans (Gottfried 1987). The least understood management option has been slash disposition (Severson 1986, Baker and Frischknecht 1973). Retention or removal of slash provides or eliminates specific habitat characteristics for certain small mammals. In addition, retention or removal of slash affects the potential protective cover for emerging new plants. Slash removal In: Monsen, Stephen B.; Stevens, Richard, comps. 1999. Proceedings: ecology and management of pinyon-juniper communities within the Interior West; 1997 September 15-18; Provo, UT. Proc. RMRS-P-9. Ogden, UT: U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station. William H. Kruse is Range Scientist (retired) USDA Forest Service, Rocky Mountain Research Station. The Southwest Forest Sciences Complex, 2500 S. Pine Knoll Dr. Flagstaff, AZ 86001. USDA Forest Service Proceedings RMRS-P-9. 1999 by burning affects the newly formed slash habitat for small mammals and plants and also reorganizes the nutrient base stored in the slash (Harrington 1989, Covington and DeBano 1988). Natural decomposition of residual slash provides a slower and more complete return of nutrients to the system, while providing the protective effects of slash. J uni per slash, unlike pine slash, decomposes at a slower rate. Small mammal populations are impacted by overstory disturbances (Turkowski and Reynolds 1970) while on-theground slash causes an increase in abundance of some rodent species regardless of overstory condition (Severson 1986). Kruse and others (1979) found that when the overstory was removed or reduced, rodents that preferred the woodland condition were fewer in number than those on the treated areas. This small mammal research was part of an effort to study the effect of nutrient cycling, other wildlife, and wood product management on soil, water, tree, and range resources in pinyon-juniper woodlands. This paper discusses the effects of commercial fuelwood harvesting in an old-growth or late seral pinyon-juniper woodland on small mammal populations in central Arizona. Study Area _ _ _ _ _ _ _ __ The Heber Ranger District, Apache-Sitgreaves National Forest in central Arizona was the study-site area. Average tree basal area (diameter measured at root crown) was 23.2 ± 5.4 m 2/ha, which produced 35.3 ± 12.7 m 3/ha of fuelwood (Kruse and Perry 1995). One-seed juniper (Juniperus monosperma) was the dominant species (54 percent). The second most dominant tree (25 percent) was Colorado pinyon (Pinus edulis), followed by alligator j uni per (J. deppeana) (13 percent). Ponderosa pine (Pinus ponderosa) occasionally occurred on moist sites (8 percent). Mean pretreatment canopy cover was approximately 40 percent, while the mean annual herbaceous and woody plant potential productivity was approximately 562 kg/ha. The study area is relatively flat, dissected by several small ephemeral drainages. Elevations are between 2,000 and 2,060 m. The primary soil subgroups, derived from limestone, are Lithic Ustochrepts, Udic Haplustalfs, and Typic Eutroboralfs. The mean annual precipitation is between 34 and 46 cm. Methods Field Methods The study area consisted of 33 units, 4 ha in size. Three units were treated with silvicultural prescriptions. Thirty 4 ha study units were grouped into five blocks representing 215 Figure 1-Typical overstory, preharvest conditions of late seral old-growth pinyon- juniper woodland at Heber/ Mud Tank small mammal study area. Figure 3-Type conversion. Slash accumulation but not burned following harvest of commercial fuelwood. Noncommercial stems cut and also remain. six overstory/slash treatments. Sixteen of the 30 were randomly selected for the small mammal study. Four of the 6 overstory/slash treatments were replicated in the 16 units (Kruse 1995). Trapping occurred on 4 overstory treatments: (1) controls, where the units were untreated (fig. 1); (2) burned, to simulate a forest fire (fig. 2); (3) type conversion, where fuelwood was harvested, the non-commercial residual trees cut, but slash was not burned (fig. 3); (4) type conversion, where fuelwood was harvested, residual trees cut, and slash burned (fig. 4). Type conversion is clearcutting to convert a woodland to grassland. The two overstory treatments not included were the silvicultural treatments and the commercial harvest where the noncommercial stems were left uncut as advanced regeneration. Small mammal trapping was conducted during July and August from 1990 through 1996. Before harvest, downed woody fuel was estimated at 3.15 mtJha (Kruse and Perry 1995). Post harvest slash accumulation was estimated at 55.71 mtlha (fig. 3). Treatments were assigned randomly and were not necessarily contiguous; roads or drainage channels could separate units within a given block. Harvesting began during fall! winter of 1991 and continued for 24 months. Burning commenced when the slash was at least 2 years old. Treatment schedules are in Kruse (1995). A 100 m 2 trapping grid was located in the center of each unit. 8 x 10 x 25 cm Sherman live trap was placed at each grid point, 10 m x 10 m apart. At alternate points, a 10 x 12 x 40 cm Sherman live trap was placed near the smaller one. The bait was a mixture of chicken scratch and rolled oats. Each unit was sampled yearly with 150 traps for 3 nights and 2 days. Physical measurements were taken and recorded for each animal, then they were toe clipped Figure 2-Burned standing green woodland to simulated wildfire for type conversion (clearcutting to convert a woodland to grassland). 216 Figure 4-Type conversion. All overstory harvested or cut, and slash burned. USDA Forest Service Proceedings RMRS-P-9. 1999 Table 1-Species captured and percent of composition. Species Common name Peromyscus truei Peromyscus maniculatus Eutamias dorsalis Neotoma albigula Neotoma mexicana Peromyscus boylei Sylvi/agus auduboni Spermophilus variegatus Neotoma stephensi Dipodomys ordi Microtus mexicanus 20 Composition pinyon mouse common deer mouse cliff chipmunk white-throated wood rat Mexican wood rat brush mouse desert cottontail rock squirrel Stephens wood rat Ord kangaroo rat Mexican vole Percent 42 37 9 7 2 2 <1 <1 <1 <1 and released. Recaptures were noted. Relative abundance and species composition of small mammals live trapped and released on the study area are in table 1. Analysis Methods Replicated study units among 4 blocks were selected randomly as the experimental design layout (Ludwig and Reynolds 1988). Blocks were based on similarity of pretreatment overs tory conditions and characteristics. The treatment units included combinations of no burning or cutting, burning standing green, cutting and no cutting (fig. 1-4). The small mammal study replicated these 4 treatments in each of 4 blocks. The null hypotheses was that small mammal capture rates did not differ among treatments. Capture differences 80r-------------------------------~ _ Untreated ............... '1iiiiii"'T~~~t~d" ............. '" 60 12 8 4 0 93 94 95 96 91 90 90 vs 91 P = 1.0 mean 90,91 vs.93 P = < 0.001 mean 90,91 vs.94 P = < 0.001 mean 90,91 vs.95 P = < 0.001 mean 90,91 vs.96 P = 0.004 Figure 6-The deer mouse captures. Captures were significantly increased immediately following treatments in 1992-93 (p < .001). and remained higher through the remainder of the study (p < .004) while the slash habitat was on the ground aging. Some of the units were burned before the 95 and 96 trapping periods but it is unclear whether the burning impacted the deer mouse captures. among treatments were tested by analysis of variance with years used as a repeated measure. Significance oftreatment effects was assessed based on temporal interaction (pre vs. post treatment) in treatment responses. Comparisons among treatments, for individual post treatment years were adjusted by Bonferoni correction to maintain Type I error at 0.05. Tests were performed on total captures, deer mouse captures, and pinyon mouse captures only. The 1992 data was also omitted from the analyses due to conflicting treatment effects and application. Results _ _ _ _ _ _ _ _ _ __ 40 20 o 16 90 91 93 94 95 90 vs 91 P = 1.0 mean 90,91 vs. 93 P = < 0.001 mean 90,91 vs. 94 P = 0.537 mean 90,91 vs.95 P = 1.0 mean 90,91 vs. 96 P = 1.0 Figure 5-There were no differences in captures between unharvested and to-be- harvested units during the pre-treatment period (p > .5). Total captures of all species significantly increased immediately following treatment in 1992-1993 (p < .001). but were not detected again (p > .5). USDA Forest Service Proceedings RMRS-P-9. 1999 96 Before 1992 harvest treatments, there were no differences among the unharvested and the to-be-harvested units for total captures (fig. 5). Although year-to-year differences occurred, these data demonstrated the homogeneous nature (p = 1.0) of all units in 1990 and 1991. Analysis of post treatment responses, however, indicated significant treatment effect (F= 7.17, p < 0.001). Following treatment, a significant difference among treatments in 1993 was demonstrated (F = 5.79, SE 5.47, p < 0.001). Total captures treatment effects were not significant for 1994 (p = 0.536), 1995 (p = 1.0), and 1996 (p = 1.0). Deer mouse captures on the harvested and the unharvested units (fig. 6) also showed the similarity among all units before treatment (p = 1.0), and the significant difference between treatments in 1993 (p < 0.001). Unlike total captures, differences for deer mouse captures were significant for 1994 (p < 0.001), 1995 (p < 0.001), and 1996 (p = 0.004). Half of the harvested units were burned in 1995 and 1996. Pretreatment tests on pinyon mouse captures among all study units were again similar (p = 1.0). Converse to the deer 217 mouse, pinyon mouse captures (fig. 7) significantly reflected a negative effect following treatment in 1993 (p =0.052). This negative effect for the pinyon mouse between the harvested and non-harvested units was not evident in 1994 (p = 0.322) but was evident in 1995 (p =0.017) and 1996 (p = 0.040). The 1995 and 1996 harvest unit data included some units that were burned in 1994 and 1996; 1996 was before sampling. Discussion --------------------------------This study was designed to evaluate fuel wood harvesting affects on small mammal capture rates following the harvest of old-growth or late-seral pinyon-juniper woodland overstory. The treatments were 1) overstory removal; 2) creation of large quantities of slash that was generally lopped and scattered, although some piling was _done to allow cutting, loading, and hauling, and 3) eventual slash burning. Data were insufficient to determine which treatment activity had the greater affect on the small mammal capture rates. Therefore, the "treatment" units included overstory removal, slash deposition, and some were burned. These "treatment" units were tested against the uncut units. Although not tested, it appeared that: 1) woodrat (Neotoma spp.) middens burned; 2) numbers of captures of all species may have decreased following burning; and 3) captures of brush mice (Peromyscus boylii) appeared to be greater on unburned slash units. Initially, both Peromyscus species responded positively or negatively to the harvest treatment and some differences continued for the following 3 years. Half of the harvested units were burned in 1994 and 1995. Burning standing green, during a wildfire simulation, occurred in 1994 and 1996. The study suggests that overstory removal and slash accumulation probably had more beneficial effects for the deer mouse, specifically, and to other species as well. These 2 effects were detrimental to the pinyon mouse, however, particularly in the year following cutting. This study corroborates earlier work showing that overstory is important to the pinyon mouse (Severson 1986). Burning, which would not have correctea the lack of overstory condition, was of further detriment to the pinyon mouse. Fewer captures of all species were evident in the latter 3 years that included the burning portion of the study. Tests between treated and untreated units suggest little significant difference, while treatment effects to the deer mouse still appear beneficial. Field observations suggest that unburned units still contained viable woodrat middens and higher capture numbers for other species such as the cliff chipmunk (Eutamias dorsalis). Baker and Frischknecht (1973) found no effect from slash on mice populations, except where it was windrowed, while Severson (1986) found that treatments leaving slash benefited woodrats and brush mice following canopy removal. Therefore, the detrimental burning effects in this study could have off-set the beneficial effects of the slash. In addition, slash provided improved site protective characteristics for plant regeneration and development. Population densities of small mammals are related to overstory adjustments and/or slash composition in assessing site productivity and quality. This study contributes to small mammal and basic ecological information to improve guidelines for harvesting fuel wood in pinyon -j uni per ecosystems in the Southwestern United States. 218 35 30 ............... IMJ ..l)n~~~?:t.~9; ...... . _ Treated 25 20 15 10 5 o 93 94 90 91 95 96 90 vs 91 P = 1.0 mean 90,91 vs.93 P = 0.052 mean 90,91 vs.94 P = 0.322 mean 90,91 vs.95 P = 0.017 mean 90,91 vs.96 P = 0.040 Figure 7-Pinyon mouse captures. Captures were significantly decreased immediately after treatments were implemented in 1992-93 (p = .05), but not detectably lower a year later (p = .32). Lower captures on the treated units were again apparent in 1995-96 (p < .04). References __________ Baker, Maurice F. and Neil C. Frischknecht. 1973. Small mammals increase on recently cleared and seeded juniper rangeland. J. Range Manage. 26: 101-103. Covington, W. Wallace and Leonard F. DeBano. 1988. Effects of fire on pinyon-juniper soils. pp 78-85. In Proceedings: Effects of Fire in Management of Southwestern Natural Resources. Tucson, Arizona. Nov. 14-17, 1988. Gottfried, Gerald J. 1987. Regeneration of pinyon. In: Proceedings-pinyon-juniper conference; 1986 January 13-16; Reno, NV. Ogden, UT: U.S. Department of Agriculture, Forest Service, Intermountain Research Station: 249-254. Harrington, M.G. 1989. Soil nutrient and pinyon seedling response to fire severity, p.143-147. In: Proceedings of the 10th conference on fire and forest meteorology, Maciver, D.C., ed. and others Chalk River, Ont.: Forestry, Canada, 1989,469 p. Kruse, W. H. 1995. Effects offuelwood harvesting on small mammal populations in a pinyon-juniper woodland, p91. In; Douglas W. Shaw; Earl F. Aldon; Carol LoSapio, tech. Coords. Desired future conditions for pinyon-juniper ecosystems; proceedings of the symposium; 1994 August 8-12; Flagstaff, Arizona. GTR-RM-258. Fort Collins, CO. USDA-For. Serv., Rocky Mtn. For. & Range Exp. Stn, 226 p. Kruse, W. H. and H. M. Perry, 1995. Ecosystem management and fuelwood harvesting in an "old growth" pinyon-juniper woodland, p219.In; Douglas W. Shaw; Earl F. Aldon; Carol LoSapio, tech. Coords. Desired future conditions for pinyon-juniper ecosystems; proceedings of the symposium; 1994 August 8-12; Flagstaff, Arizona. GTR-RM-258. Fort Collins, CO. USDA-For. Serv., Rocky Mtn. For. & Range Exp. Stn, 226 p. Kruse, W. H., R. P. Balda, M. J. Simono, A. M. Macrander, and C. D. Johnson. 1979. Community development in two adjacent pinyonjuniper eradication areas twenty-five years after treatment. J. Environ. Manage. 8: 237-247. Ludwig, John A. and James F. Reynolds. 1988. Statistical ecology. New York: John Wiley and Sons. 337 p. Severson, K. E. 1986. Small mammals in modified pinyon-juniper woodlands, New Mexico. Journal of Range Management. 39: 31-34. Turkowski, F. J. and H. G. Reynolds. 1970. Response of some rodent populations to pinyon-juniper reductions on the Kiabab Plateau, Arizona. Southwest. Natur. 15:23-27. USDA Forest Service Proceedings RMRS-P-9. 1999