Forest fire history of Desolation Peak, Washington

1990 ◽  
Vol 20 (3) ◽  
pp. 350-356 ◽  
Author(s):  
James K. Agee ◽  
Mark Finney ◽  
Roland De Gouvenain

Forests in the vicinity of Desolation Peak, Washington, are of special ecological interest because of their transitional nature between coastal and interior forest types. The area is west of the Cascade Mountain crest but in the rainshadow of mountains farther to the west. Fire return intervals were hypothesized to be shorter than typical for coastal forest types, such as those dominated by western hemlock and Pacific silver fir, and longer than typical for interior forest types, such as ponderosa pine, owing to the close juxtaposition of these types at Desolation Peak. Seven forest community types were defined, and a 400-year fire history was developed for this 3500-ha area. The average natural fire rotation was 100 years; this varied by a factor of two by century and by topographic aspect. Forest types typical of coastal regions, such as Douglas-fir, – western hemlock and mountain hemlock – Pacific silver fir, had mean fire return intervals (108–137 years) much lower than in other western Washington areas. The most interior forest type, ponderosa pine – Douglas-fir, had a higher mean fire return interval (52 years) than reported for similar forest types east of the Cascades. Historically, fire has created structural and landscape diversity on Desolation Peak and may be an important process in the maintenance of such diversity into the future.

1985 ◽  
Vol 15 (5) ◽  
pp. 914-921 ◽  
Author(s):  
Heather E. Erickson ◽  
R. L. Edmonds ◽  
C. E. Peterson

Logging residue decomposition rates were determined in four conifer forest ecosystems in the State of Washington, U.S.A. (coastal western hemlock, Puget lowland Douglas-fir, high-elevation Pacific silver fir, and eastern Cascade ponderosa pine), by examining wood density changes in a series of south-facing harvest areas with residues of different ages. Decomposition rates were determined for two diameter classes (1–2 and 8–12 cm) and two vertical locations (on and >20 cm above the soil surface). Pacific silver fir and ponderosa pine ecosystems had the lowest k values (0.005 and 0.010 year−1, respectively) followed by Douglas-fir (range, 0.004–0.037 year−1) and western hemlock (range, 0.010–0.030 year−1). Small-diameter residues decomposed at rates significantly slower than large-diameter residues in Douglas-fir and western hemlock ecosystems; this relationship was also implied in the other ecosystems. In all four ecosystems, dry season moisture contents were lower in smaller-diameter residues. Moisture levels associated with small-diameter residues were too low for significant decomposition to occur during the dry summer period and probably contributed to the slow annual decay rates. Residues located above the soil surface decomposed significantly slower than residues on the soil surface only in the Douglas-fir ecosystem. Dry season residue moisture, rather than initial lignin concentration, appeared to be the dominant factor determining residue decomposition rates on exposed harvested areas.


1994 ◽  
Vol 4 (2) ◽  
pp. 65 ◽  
Author(s):  
SW Barrett

A fire history investigation was conducted for three forest community types in the Absaroka Mountains of Yellowstone National Park, Wyoming. Master fire chronologies were based on fire-initiated age classes and tree fire scars. The area's major forest type, lodgepole pine (Pinus contorta Dougl. var. latifolia) ecosystems, revealed a predominant pattern of stand replacing fires with a 200 year mean interval-nearly half the length estimated in previous studies of lodgepole pine on less productive subalpine plateaus in YNP. High elevation whitebark pine (P. albicaulis Engelm.) forests had primarily stand replacing fires with >350 year mean intervals, but some stands near timberline also occasionally experienced mixed severity- or non-lethal underburns. Before nearly a century of effective fire suppression in Yellowstone's northern range, lower elevation Douglas-fir (Pseudotsuga menziesii [Mirb.] Franco.) communities adjacent to Artemesia tridentata (Nutt.) grasslands experienced primarily non-lethal underburns at 30 year mean intervals. While short interval fire regimes have been altered by longterm fire suppression, fire exclusion apparently had only limited influence on the area's infrequently burned ecosystems prior to widespread stand replacement burning in 1988.


1987 ◽  
Vol 17 (9) ◽  
pp. 1115-1123 ◽  
Author(s):  
N. J. Livingston ◽  
T. A. Black

Douglas-fir (Pseudotsugamenziesii (Mirb.) Franco), western hemlock (Tsugaheterophylla (Raf.) Sarg.), and Pacific silver fir (Abiesamabilis (Dougl.) Forbes) container-grown 1-0 seedlings were spring planted on a south-facing high elevation clear-cut located on Mount Arrowsmith, Vancouver Island, British Columbia. Treatments, which included inclining seedlings to the southwest, provision of shade cards, irrigation, and irrigation and shade cards combined, were applied to determine whether modification of seedling microclimate would increase survival. Highest survival rates, regardless of treatment, were shown by Douglas-fir. By April 1984, 72 and 82% of untreated Douglas-fir seedlings planted in 1981 and 1982, respectively, survived, whereas survival of treated seedlings ranged from 81 to 95%. The high survival rate in Douglas-fir appeared to be due to their high drought tolerance. The osmotic potential of unirrigated Douglas-fir seedlings declined by over 1.1 MPa during the course of the 1982 growing season in response to decreasing soil water potentials and consequently turgor was maintained in the foliage. Transpiration rates of these seedlings were never less than 50% of those that were irrigated. Western hemlock and Pacific silver fir seedlings exhibited very poor survival, possibly owing to the lack of stress avoidance and tolerance mechanisms. Survival rates of the two species were increased by shade cards and irrigation but never exceeded 64%.


Author(s):  
Eric S. Kasischke ◽  
David L. Verbyla

Fire is ubiquitous throughout the global boreal forest (Wein 1983, Payette 1992, Goldammer and Furyaev 1996, Kasischke and Stocks 2000). The inter- and intra-annual patterns of fire in this biome depend on several interrelated factors, including the quantity and quality of fuel, fuel moisture, and sources of ignition. Fire cycles in different boreal forest types vary between 25 and >200 years (Heinselman 1981, Yarie 1981, Payette 1992, Conard and Ivanova 1998). Although the increased presence of humans in some regions of boreal forest has undoubtedly changed the fire regime (DeWilde 2003), natural fire is still a dominant factor in ecosystem processes throughout this biome. Boreal forest fires are similar to those of other forests in that they vary between surface and crown fires, depending on forest type and climatic factors. Surface fires kill and consume most of the understory vegetation, as well as portions of the litter or duff lying on the forest floor, resulting in varying degrees of mortality of canopy and subcanopy trees. Crown fires consume large amounts of the smaller plant parts (or fuels) present as leaves, needles, twigs, and small branches and kill all trees. These fires are important in initiating secondary succession (Lutz 1956, Heinselman 1981, Van Cleve and Viereck 1981, Van Cleve et al. 1986, Viereck 1983, Viereck et al. 1986). Unlike fires in other forest types, smoldering ground fires in the boreal forest can combust a significant fraction of the deep organic (fibric and humic) soils in forests overlying permafrost (Dyrness and Norum 1983, Landhauesser and Wein 1993, Kasischke et al. 2000a, Miyanishi and Johnson 2003). During periods of drought, when water tables are low, or prior to spring thaw, organic soils in peatlands can become dry enough to burn, as well (Zoltai et al. 1998, Turetsky and Wieder 2001, Turetsky et al. 2002).


1982 ◽  
Vol 12 (3) ◽  
pp. 469-473 ◽  
Author(s):  
Randy Molina

Four isolates of the ectomycorrhizal fungus Laccarialaccata (Scop. ex Fr.) Berk and Br. were inoculated singly onto containerized Douglas-fir (Pseudotsugamenziesii (Mirb.) Franco), ponderosa pine (Pinusponderosa Dougl. ex Laws.), Sitka spruce (Piceasitchensis (Bong.) Carr.), and western hemlock (Tsugaheterophylla (Raf.) Sarg.) seedlings to detect ecotypic variation in colonization success and effects on seedling growth. All isolates formed well-developed ectomycorrhizae on all inoculated seedlings. Abundance ratings of short roots colonized did not differ between the four isolates for any conifer species; most inoculated seedlings developed ectomycorrhizae on over 80% of their short roots. There were also no differences between isolates in affecting seedling height, stem diameter, and dry weight of tops and roots for all conifer species. Inoculations did not improve seedling growth over uninoculated controls. Uninoculated controls of Douglas-fir and ponderosa pine had significantly greater dry weight than their inoculated seedlings; growth of Sitka spruce and western hemlock seedlings was not affected by any inoculation treatment. Laccarialaccata vigorously colonized the entire container rooting substrate and appears a prime candidate for artificial ectomycorrhizal inoculation of containerized western conifers.


1980 ◽  
Vol 10 (3) ◽  
pp. 327-337 ◽  
Author(s):  
Robert L. Edmonds

Decomposition rates and changes in the nutrient content of needle and leaf litter were examined in Douglas-fir (Pseudotsugamenziesii Mirb. Franco), western hemlock (Tsugaheterophylla (Raf.) Sarg.), Pacific silver fir (Abiesamabilis (Dougl.) Forbes), and red alder (Alnusrubra Bong.) ecosystems in western Washington, U.S.A. Nylon litterbags (1-mm mesh) were placed in the stands in November and December 1974. Bags were collected after 3, 6, 12, and 24 months and weighed, except in the Pacific silver fir stand when bags were collected after 6, 9, 14, and 24 months. Litter was analyzed for C, N, P, K, Ca, Mg, Mn, lignin, and cellulose. Decomposition constants (k values) were determined. Fastest decomposition after 2 years occurred in red alder leaves, followed by Douglas-fir, western hemlock, and Pacific silver fir needles. There were significant differences in weight loss among species after 1 year, but no significant differences were evident after 2 years. Red alder leaves showed rapid weight loss in the 1st year but decomposed little in the 2nd year. Decomposition constants were highly positively correlated with minimum air temperatures and negatively correlated with C:N ratios. Low litter moisture tended to reduce decomposition in summer, particularly in the Pacific silver fir stand. Decomposition proceeded under snow in this ecosystem. The pattern of loss of elements from litterbags after 2 years varied from ecosystem to ecosystem, particularly for N. The following element mobility series resulted for the four ecosystems: red alder (K > Mg > Ca > P > N > Mn), Douglas-fir (K > P > Ca > Mg > Mn > N), western hemlock (K > Ca > Mg > N > Mn > P), and Pacific silver fir (K > Mg > Ca > Mn > P > N).


2000 ◽  
Vol 129 (1-3) ◽  
pp. 207-225 ◽  
Author(s):  
Richard L Everett ◽  
Richard Schellhaas ◽  
Dave Keenum ◽  
Don Spurbeck ◽  
Pete Ohlson

2005 ◽  
Vol 35 (4) ◽  
pp. 990-1001 ◽  
Author(s):  
David C Shaw ◽  
Jiquan Chen ◽  
Elizabeth A Freeman ◽  
David M Braun

We investigated the distribution and severity of trees infected with western hemlock dwarf mistletoe (Arceuthobium tsugense (Rosendahl) G.N. Jones subsp. tsugense) in an old-growth Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) – western hemlock (Tsuga heterophylla (Raf.) Sarg.) forest. With the use of Hawksworth six-class dwarf mistletoe rating system, infection status was assessed for 3516 hemlock and true firs ≥5 cm diameter on a 12-ha stem-mapped plot located in the Cascade Mountains of southwest Washington State. Within the plot, 33% of the area had some level of infection and 25% (719) of western hemlocks, 2.2% (12) of Pacific silver fir (Abies amabilis (Dougl.) Forbes), and 29% (2) of noble fir (Abies procera Rehd.) trees were infected. Infected trees are larger than uninfected trees, on average, and within the infected tree population, the severely infected trees averaged larger than lightly infected trees. Abundant dwarf mistletoe in larger trees definitely positions the dwarf mistletoe population for future spread. Ripley's K analysis indicates a negative association between infected and uninfected hemlock trees, confirming that the infected trees form distinct dwarf mistletoe infection centers. The infection centers are actively spreading at their margins, which was confirmed by nearest neighbor analysis. Heavily infected trees had a negative association with uninfected trees, while lightly infected trees had a positive association with uninfected trees.


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