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1.
The long-term success of forest management depends primarily on the sustainability of timber production. In this study we analyse the population structure, tree age and wood increment of Malouetia tamaquarina (Aubl.) (Apocynaceae) to define a species-specific minimum logging diameter (MLD) and felling cycle by modelling volume growth. Contrary to other timber species in the nutrient-rich white-water floodplains forests (várzea), M. tamaquarina grows in the subcanopy of old-growth várzea forests. The wood of this species is utilized by local inhabitants in the floodplains for handicraft. In 35 plots of 25 m × 50 m we measured diameter at breast height (DBH) and tree height of all trees taller than 150 cm height. From 37 individuals with DBH > 15 cm we sampled two cores by increment borers to determine the wood density, tree age and diameter increment rates. In the management area of a várzea settlement with about 150 ha recently harvested trees of M. tamaquarina have been recorded and DBH was measured. The species presents an inverse J-shaped diameter distribution indicating that the species is obviously regenerating in the old-growth forests. Tree-ring analysis indicates a mean age of 74.5 years for a DBH of 22.7 cm for a studied population comprising 37 trees with maximum ages of up to 141 years for an individual with a DBH of 45.7 cm. The tree species has low annual diameter increment rates (3.16 ± 0.6 mm) despite a low wood density (0.36 ± 0.05 g cm−3). The volume growth model indicates a MLD of 25 cm and a felling cycle of 32.4 years. In the management area 35 trees with a mean DBH of 24 cm were recorded, similar to the defined MLD. The abundance of trees above the MLD is 2.7 trees ha−1, or 405 trees, when extrapolated to the whole management area. Considering a felling cycle of 32.4 years (annual production unit of 4.63 ha) this results in total of 12.5 harvestable trees, almost three times less than actually harvested. The actual practice of harvesting M. tamaquarina risks the overexploitation of this slow-growing species.  相似文献   

2.
主要对长白山北坡溪流大木质物残体现存量进行了调查和研究,包括两段河道内所有大木质物残体的基径、顶径、长度、腐烂级,并在其中一段对树种尽可能进行了鉴别,以分析河岸带植被与溪流大木质物残体的关系。在调查的红松阔叶林植被带内4500 m长河道内,共发现溪流倒木425株,分属于17个树种;其中III、IV级腐烂占相当大的比重,与林地倒木II、III级腐烂占优有所不同,其原因可能与分解环境的不同有关。两段河道溪流大木质物残体的现存量为1.733 m3/100m、 10.83m3/hm2和1.709 m3/100m、 21.36 m3/hm2。处于III、IV级腐烂的溪流大木质物残体所占比重较大,与在森林中情况有所差异,可能与分解环境的不同有关。溪流大木质物残体和林地活立木的个体数量的径级分布基本上为反J型,而它们材积的径级分布均为典型的J型。溪流大木质物残体的树种组成和不同树种的材积与河岸带植被密切相关,但存在差异,分析这种差异可以深入了解河岸带植被动态。图1表4参18。  相似文献   

3.
Wild pistachio (Pistacia atlantica Desf.) is the most economically important tree species in many rural areas in the west of Iran. The species produces resin used for a wide variety of traditional uses. Because the resin can be harvested non-destructively, the trees are maintained until mortality occurs from natural causes. The result is that natural, managed stands include a variety of age classes. In recent years, a lack of smaller size classes has been observed in the Qalajeh forest, which is located in the Zagros Mountain region of western Iran. We established a series of plots in an area typical of Qalajeh forest to characterize the diameter distribution of the wild pistachio component. We confirmed a deficit of stems <30 cm dbh, based in the expectation that the landscape-level diameter distribution should be characterized by a negative exponential curve. For trees ≥30 cm dbh, de Liocourt's equation closely fit the diameter distribution (r2 = 0.93), translating to a q-factor of 1.34. We used this curve to estimate the deficit number of stems in diameter classes <30 cm. We estimate that this forest should have 19–24 wild pistachio trees/ha in the 5–25 cm classes, as compared to about 5 trees/ha found currently. Based on local conditions, we recommend that at least 30 seedlings/ha should be planted to allow 6–8 trees to reach to the 5 cm class.  相似文献   

4.
We studied the carbon density and accumulation in trees at five sites in a tropical dry forest (TDF) to address the questions: how is the TDF structured in terms of tree and carbon density in different DBH (diameter at breast height) classes? What are the levels of carbon density and accumulation in the woody species of TDF? Is the vegetation carbon density evenly distributed across the forest? Does carbon stored in the soil reflect the pattern of aboveground vegetation carbon density? Which species in the forest have a high potential for carbon accumulation? The WSG among species ranged from 0.39 to 0.78 g cm−3. Our study indicated that most of the carbon resides in the old-growth (high DBH) trees; 88-97% carbon occurred in individuals ?19.1 cm DBH, and therefore extra care is required to protect such trees in the dry forest. Acacia catechu, Buchanania lanzan, Hardwickia binata, Shorea robusta and Terminalia tomentosa accounted for more than 10 t ha−1 carbon density, warranting extra efforts for their protection. Species also differed in their capacity to accumulate carbon indicating variable suitability for afforestation. Annually, the forest accumulated 5.3 t-C ha−1 yr−1 on the most productive, wettest Hathinala site to 0.05 t-C ha−1 yr−1 on the least productive, driest Kotwa site. This study indicated a marked patchy distribution of carbon density (151 t-C ha−1 on the Hathinala site to 15.6 t-C ha−1 on the Kotwa site); the maximum value was more than nine times the minimum value. These findings suggest that there is a substantial scope to increase the carbon density and accumulation in this forest through management strategies focused on the protection, from deforestation and fire, of the high carbon density sites and the old-growth trees, and increasing the stocking density of the forest by planting species with high potential for carbon accumulation.  相似文献   

5.
We investigated the temporal dynamics of large woody debris (LWD) in five headwater streams before and after the 2001 Dogrib fire in the foothills of Alberta. The density of LWD varied from 5 to 41 logs per 50 m of stream reach and accounted for 19.4 ± 5.1 m3 ha−1 (mean ± standard error) of wood in the riparian zones and 114.1 ± 30.1 m3 ha−1 of wood in the bankfull margins of the stream channel. Individual logs averaged 18.9 ± 1.15 cm in diameter, 5.5 ± 0.7 m in length, and 0.2 ± 0.02 m3 in volume. Logs became significantly shorter in decay classes II–IV. Bridges were longer than partial bridges, which were longer than loose and buried LWD. Individual log volume was greatest for bridges, but not significantly different among other position classes. Bridges and loose LWD contributed little to stream morphology and function; however, 55% of partial bridges and all buried logs contributed to sediment storage, channel armouring, or riffles and pools in the stream channel.  相似文献   

6.
Many ecosystems are now dominated by introduced species, and because dominant species drive ecosystem properties, these changes lead to increased uncertainty in estimates of carbon storage and cycling. We examined aboveground biomass in forests dominated by the introduced tree Rhamnus cathartica (common buckthorn) relative to forests dominated by native species, and measured aboveground biomass increment over a three-year period (2005-2008). Three of the four lowest biomass levels occurred in R. cathartica-dominated forests, and biomass in these forest types was stored primarily in trees 10-20 cm DBH. By contrast, forests dominated by native trees (including those with R. cathartica understories) had the six highest biomass levels, and biomass was stored primarily in trees >50 cm DBH. On average, forests dominated by R. cathartica stored half as much aboveground biomass (14.6 ± 3.3 kg/m2) as forests dominated by native tree species (28.9 ± 8.3 kg/m2). R. cathartica-dominated forests also had half the aboveground biomass increment of native-dominated forests (0.28 vs. 0.60 kg/m2/year). Although known anecdotally as a fast-growing species, R. cathartica growth rates declined with increasing size. Between 2005 and 2008, R. cathartica individuals <10 cm DBH grew faster than native species; however, R. cathartica individuals >10 cm DBH grew consistently slower than native species. Overall, our findings indicate that intrinsic size limitations on R. cathartica will lead to lower biomass stocks in forests where it acts as a canopy dominant relative to forests dominated by native tree species.  相似文献   

7.
Since 2000, the Chinese government has implemented emergency water diversion measures to restore the damaged riparian forest ecosystem with dominant tree species Euphrat poplar(Populus euphratica Oliv.)at the lower reaches of the Tarim River. In the present study, comparative analysis of variations in the vitality of P. euphratica trees were made using 2005 and 2010 data to illustrate the revitalization process of riparian forest. Poplar trees within 300 m of the riverbed were positively revitalized, while the vitality of trees farther than 300 m from the river decreased. Population structure was studied to demonstrate the development of poplar community. In the first belt, the class structure for the diameter at breast height(DBH) of P. euphratica fit a logistic model, and the 2nd, 3rd and 4th belt curve fittings were close to a Gaussian model; in other plots they were bimodal. Cluster analysis of the composition of the DBH class of poplar trees demonstrated that those within 16–36 cm DBH were the most abundant(58.49% of total) in study area, under 16 cm of DBH were second(31.36%), and trees 40 cm DBH were the least abundant(10.15%). More than 80% of the trees were young and medium-sized, which means that the poplar forest community in the vicinity of the lower Tarim River is at a stable developmental stage. The abundance of juvenile trees of P. euphratica in the first and second measuring belts was 12.13% in 2005 and increased to 25.52% in 2010, which means that the emergency water transfer had a positive impact on the generation of young P. euphratica trees in the vicinity of the river.  相似文献   

8.
Large tree species have a disproportional influence on the structure and functioning of tropical forests, but the forces affecting their long-term persistence in human-dominated landscapes remain poorly understood. Here we test the hypothesis that aging forest edges and small fragments (3.4–295.7 ha) are greatly impoverished in terms of species richness and abundance of large trees in comparison to core areas of forest interior. The study was conducted in a hyper-fragmented landscape of the Atlantic forest, northeast Brazil. Large tree species were quantified by recording all trees (DBH ≥ 10 cm) within fifty-eight 0.1-ha plots distributed in three forest habitats: small forest fragments (n = 28), forest edges (n = 10), and primary forest interior areas within an exceptional large forest remnant (n = 20). Large tree species and their stems ≥10 cm DBH were reduced by half in forest edges and fragments. Moreover, these edge-affected habitats almost lacked large-stemmed trees altogether (0.24 ± 0.27% of all stems sampled), and very tall trees were completely absent from forest edges. In contrast, large trees contributed to over 1.5% of the whole stand in forest interior plots (2.9 ± 2.8%). Habitats also differed in terms of tree architecture: relative to their DBH trees were on average 30% shorter in small fragments and forest edges. Finally, an indicator species analysis yielded an ecological group of 12 large tree species that were significantly associated with forest interior plots, but were completely missing from edge-affected habitats. Our results suggest a persistent and substantial impoverishment of the large-tree stand, including the structural collapse of forest emergent layer, in aging, hyper-fragmented landscapes.  相似文献   

9.
Little is known about how past forest management in Sweden influenced the quantity and quality of large woody debris (LWD) in streams. The present study provides information of the long-term dynamics of LWD in a reach of a boreal stream intersecting a managed forest. Dendrochronological methods were used to reconstruct mortality years of the pieces of LWD and the general history of fire and cuttings of the surrounding riparian forest. Today, spruce dominates among the living trees, whereas the LWD is dominated by birch in the forest and by pine in the stream. Fire frequency prior to active fire suppression was similar to values reported from boreal forests. Pine trees were more abundant in the riparian forest before selective logging operations and active fire suppression began in the 1800s. Many of the pieces of LWD found in the stream today died more than 200 years ago and derived from a cohort of pines that generated in the early 1600s. Pine LWD in stream channels is highly resistant to decomposition and can reside for more than 300 years. A substantial amount of the LWD found today in managed forest streams in boreal Sweden most likely derives from the time before extensive human influence and is likely to decrease further in the future. Management of riparian forests to ascertain future supply of long-lived LWD in streams should target to increase the proportion of pine trees.  相似文献   

10.
Long-term tree and seedling growth and survivorship data from permanent sample plots established in a neotropical dry forest in Jamaica from 1998 to 2008 were used to (1) model growth (periodic annual increment) and survivorship dynamics, (2) cluster structural and functional types, and (3) estimate the age of selected tropical dry forest tree species. A statistical comparison of parameter estimates derived from a generalized linear model (GLM) of each species to a reference species was used to group individuals based on size (DBH and height), and demographic dynamics (periodic annual increment and survivorship). We identified two groups of species based on structural types (canopy and sub-canopy species), three groups of species based on periodic annual increment (fast, intermediate, and slow growing) and four groups of species based on the probability of survivorship of seedlings and trees (very low probability of seedling survivorship but high tree survivorship (two groups); high survivorship throughout the DBH classes; very low survivorship, regardless of stem size). The composition of the groups was mixed, and included individuals of both structural types, and with different periodic annual increment and survival probabilities. The dichotomy of guilds found in tropical rainforests (pioneer and climax species) was not found in this forest. Individual and group GLMs incorporating empirical relationships between periodic annual increment and survivorship, across a spectrum of ontogenies and DBH’s, were also generated. The periodic annual increment models were then used to estimate the time taken by a newly germinated seedling to reach the largest recorded DBH. The fastest growing species was the hemi-cryptophyte Clusia flava which was estimated to take 74 years to reach its maximum recorded size (12.1 cm DBH), whereas the slowest growing species, Ziziphus sarcomphalus, was estimated to take 399 years to reach its maximum size (24.4 cm DBH). These dry forest trees were estimated to reach their maximum size (which was one-half or one-third of the largest DBH recorded for tropical rainforests) in a time similar to tropical rainforest trees. Some of the tree species are ubiquitous to other neotropical dry forests; therefore, our equations for periodic annual increment and survivorship can be applied elsewhere in the region.  相似文献   

11.
12.
Forest management practices which may represent various forms of disturbance regimes could influence liana species richness, abundance and relationship with their hosts. The study sought to determine the impacts of three management systems, namely, the Selection, Tropical Shelterwood and Post Exploitation Systems (SS, TSS and PES respectively) on liana species richness, abundance and relationship with trees in the Bobiri forest reserve, Ghana. Lianas with dbh ≥ 2 cm found on trees with dbh ≥ 10 cm were enumerated in 1 ha plot each in the SS, TSS and PES. All trees (dbh ≥ 10 cm) within the plots that did not carry lianas were also enumerated. A total of 640 liana individuals belonging to 27 species, 22 genera and 13 families were identified in the management systems. Griffonia simplicifolia (Vahl ex DC.) Baill., Motandra guineensis (Thonn.) A.DC. and Calycobolus africanus (G.Don) Heine were the abundant species in all the management systems. Unlike in SS, lianas in the TSS and PES were dominated by a few species. Larger diameter lianas were more abundant in the PES (32%) compared with the SS (18.3%) and the PES (13.1%). Liana diversity (H′) (species richness and abundance) was quantitatively higher in the SS (2.8) than the TSS (2.2) and the PES (2.0). The numbers of lianas carried by tree species differed significantly in the management systems (p < 0.001 each). Liana infestation in the forest was high. The level of liana infestation did not reflect the extent of liana load per tree in the management systems. Larger trees carried significantly more liana individuals than smaller trees in the PES (p = 0.019, r2 = 0.15). There was a positive significant relationship between host dbh and liana dbh in the PES (p < 0.001, r2 = 0.23) and TSS (p = 0.024, r2 = 0.11). Tree diversity appeared to have influenced liana species richness and abundance.  相似文献   

13.
As part of an assessment of sustainability for the strip clear-cutting system (or Palcazú Forest Management System), we determined whether commercial tree species regenerating in two strips (30 m × 150 m) clear-cut in the Peruvian Amazon in 1989 would reach commercial size (≥30 cm diameter at breast height (dbh)) 40 years after the initial cutting, the expected harvesting cycle. We projected the growth of six common commercial species (Eschweilera bracteosa, Guarea cinnamomea, Micropholis guyanensis, Pouteria guianensis, Qualea paraensis, and Cedrelinga catenaeformis) and two pioneer species (Alchornea triplinervia and Miconia phaeophylla) using bootstrapping techniques (the Lieberman model), based on 2-year diameter increments (2004–2006) and mortality rates obtained from 1630 trees growing in secondary forest sites including the regenerating strips. These demographic data were further used to project the growth of all trees ≥6.5 cm dbh of commercial (sawnwood value) species from each strip, and from a deferment-cut treatment applied to half of one of the strips. Three models were used for growth projections: (1) using all diameter increments to simulate average growing conditions, (2) using diameter increments of trees exposed to high light to simulate growing conditions under intensive forest management with low mortality rates and (3) using diameter increments of the fastest growing individuals. Roundwood volume was calculated using allometric equations for emergent, canopy, and subcanopy species.  相似文献   

14.
Biomass and carbon sequestration rate of a young (four year old) mixed plantation of Dalbergia sissoo Roxb., Acacia catechu Willd., and Albizia lebbeck Benth. growing in Terai region (a level area of superabundant water) of central Himalaya was estimated. The plantation is seed sown in the rainy season of year 2004 and spread over an area of 44 ha. Allometric equations for both above and below ground components were developed for three tree species. The density of trees in the plantation was 1322 trees ha−1 The diameters of trees were below 10 cm. Five diameter classes were defined for D. sissoo and A. catechu and 3 for A. lebbeck. 5 trees were harvested in each diameter class. Individual tree allometry was exercised for developing the allometric equations relating tree component (low and above ground) biomass to d.b.h. Post analysis equations were highly significant (P > 0.001) for each component of all species. In the plantation Holoptelia integrifolia Roxb. (Family Ulmaceae) has been reduced to shrub form because of frost. Only the aboveground biomass of H. integrifolia and other shrubs were estimated by destructive harvesting method. Herbaceous forest floor biomass and leaf litter fall were also estimated. The total forest vegetation biomass was 10.86 Mg ha−1 in 2008 which increased to 19.49 Mg ha−1 in 2009. The forest is sequestering carbon at the rate of 4.32 Mg ha−1 yr−1.  相似文献   

15.
An accurate characterization of tree carbon (TC), forest floor carbon (FFC) and soil organic carbon (SOC) in tropical forest plantations is important to estimate their contribution to global carbon stocks. This information, however, is poor and fragmented. Carbon contents were assessed in patula pine (Pinus patula) and teak (Tectona grandis) stands in tropical forest plantations of different development stages in combination with inventory assessments and soil survey information. Growth models were used to associate TOC to tree normal diameter (D) with average basal area and total tree height (HT), with D and HT parameters that can be used in 6–26 years old patula pine and teak in commercial tropical forests as indicators of carbon stocks. The information was obtained from individual trees in different development stages in 54 patula pine plots and 42 teak plots. The obtained TC was 99.6 Mg ha−1 in patula pine and 85.7 Mg ha−1 in teak forests. FFC was 2.3 and 1.2 Mg ha−1, SOC in the surface layer (0–25 cm) was 92.6 and 35.8 Mg ha−1, 76.1 and 19 Mg ha−1 in deep layers (25–50 cm) in patula pine and teak, respectively. Carbon storage in trees was similar between patula pine and teak plantations, but patula pine had higher levels of forest floor carbon and soil organic carbon. Carbon storage in trees represents 37 and 60% of the total carbon content in patula pine and teak plantations, respectively. Even so, the remaining percentage corresponds to SOC, whereas FFC content is less than 1%. In summary, differences in carbon stocks between patula pine and teak trees were not significant, but the distribution of carbon differed between the plantation types. The low FFC does not explain the SOC stocks; however, current variability of SOC stocks could be related to variation in land use history.  相似文献   

16.
Wood is an important component of forested stream ecosystems, and stream restoration efforts often incorporate large wood. In most cases, however, stream restoration projects are implemented without information regarding the amount of wood that historically occurred or the natural rates of wood recruitment. This study uses a space-for-time analysis to quantify large wood loading to 28 streams in the northeastern US with a range of in-stream and riparian forest characteristics. We document the current volume and frequency of occurrence of large wood in streams with riparian forests varying in their stage of stand development as well as stream size and gradient. Linear models relating stream wood characteristics to stream geomorphic and forest characteristics were compared using Akaike's Information Criterion (AIC) model selection. The AIC analysis indicated that the volume and frequency of large wood and wood accumulations (wood jams) in streams was most closely associated with the age of the dominant canopy trees in the riparian forest (best models: log10(large wood volume (m3 100 m−1)) = (0.0036 × stand age) − 0.2281, p < 0.001, r2 = 0.80; and large wood frequency (number per 100 m) = (0.1326 × stand age) + 7.3952, p < 001, r2 = 0.63). Bankfull width was an important factor accounting for wood volume per unit area (m3 ha−1) but not the volume of wood per length of stream (100 m−1). The empirical models developed in this study were unsuccessful in predicting wood loading in other regions, most likely due to difference in forest characteristics and the legacy of forest disturbance. However, these models may be applicable in other streams in the northeastern US or in streams with comparable riparian forests, underlying geology, and disturbance regimes—factors that could alter long-term wood loading dynamics. Our results highlight the importance of understanding region-specific processes when planning stream restoration and stream management projects.  相似文献   

17.
Liana-dominated forest patches constitute 15–20% of old-growth forests in the Eastern Amazon but are generally excluded from management for timber production. Here we ask if liana-dominated patches may be brought into production by clearing lianas and conducting enrichment planting (EP) of native timber species. We present growth results from 8 years of such EP trials. Rapid growth and low mortality of all species in this study suggest that EP in cleared liana patches can contribute to timber stocks in second and third harvests of managed forests. The most vigorous individuals of Parkiagigantocarpa and Schizolobium amazonicum in each enrichment site grew more than 1 cm diameter per year (rates were initially >2 cm yr−1), and attained dominant canopy positions and diameters equal to those of small canopy trees in the surrounding forest within 8 years of planting (mean dbh ∼18 cm and ∼20 cm, respectively, at year 8). Limited data on Ceiba pentandra plantings indicate a similar trajectory for this species (dbh ∼40 cm in 8 years). The most vigorous Swietenia macrophylla grew at least 1 cm per year in enrichment plots (mean dbh ∼10 cm in 8 years), but take longer to attain dominant positions. Tabebuia serratifolia may take much longer to reach the canopy than other species tested (rates <1 m yr−1). We attribute the excellent performance to light availability; planting in intact soil with minimal compaction and abundant organic material; and low competition rates maintained by periodic thinning of competing vegetation.  相似文献   

18.
Treelines are advancing on a global scale and encroaching upon alpine ecosystems. Browsing by vertebrate herbivores could affect treeline dynamics and forest expansion by limiting growth of trees. However, this has not been experimentally investigated, and due to a combination of herbivore behaviour and plant responses to herbivory, is unlikely to be a simple relationship. A long term (8 years of manipulation), large scale (0.3 km2) sheep enclosure experiment, in the Scandes of Norway, was used to investigate the effect of three densities of sheep (no sheep, low and high densities with respectively 0, 25 and 80 sheep km−2) on tree growth within a mountain birch (Betula pubescens tortuosa) treeline ecotone. Birch trees were most likely to be browsed at intermediate heights of around 100-130 cm and the likelihood of an individual being browsed did not differ between low and high sheep densities. However, when browsed, the intensity of browsing increased with sheep density. High densities of sheep reduced the net annual shoot growth of young mountain birch in comparison to growth in the absence of sheep. The long-term height growth of smaller mountain birch (stem diameter < 15 mm) was also reduced at high densities of sheep, but the height growth of larger birch was resistant to browsing, even though these trees were on average still within browsing height. This study shows that susceptibility to browsing in birch decreases with size, but by restraining the height growth of trees high densities of sheep can keep trees at heights at which they remain susceptible to browsing. Reductions in livestock density over a period as short as 8 years can thus facilitate altitudinal forest expansion.  相似文献   

19.
Current management practices encourage conversion of red alder (Alnus rubra) riparian forests to conifers in the Pacific Northwest U.S. Patches of young naturally regenerated conifers are commonly present in alder dominated riparian areas and an understanding of the soil processes in these patches will be helpful in guiding future riparian management. Study objectives were to: (1) determine decomposition rates of red alder leaves in riparian alder and conifer patches, (2) relate decomposition rates to environmental factors and litter chemistry, and (3) determine nutrient release from decomposing alder leaves in these patches. Study sites were riparian areas adjacent to Brown and Le Bar creeks in the Skokomish River basin, Olympic National Forest, Washington. Red alder leaves were placed in litterbags in red alder and conifer riparian patches along each stream in November 2000 and collected after 1 and 3 years. There was rapid mass loss of alder leaves in the first year in both patch types, but decomposition was significantly faster (p < 0.05) in alder patches (43.2% mass remaining, k = 0.855 year−1) than in conifer patches (48.4% mass remaining, k = 0.734 year−1). There was little mass loss after the first year and no significant difference in decomposition rates. After 3 years mass remaining was 44.2% (k = 0.283 year−1) and 47.8% (k = 0.48 year−1) in alder and conifer patches, respectively. Decomposition rate differences were attributed more to the effects of the different litters in each patch and the influence on soil microbial and faunal communities than differences in soil temperature and moisture. The forest floor was deeper in conifer patches (3.7 cm) than alder (1.8 cm) patches. This was ascribed to slower decomposition rates in conifer patches, greater litterfall in conifer patches, and/or removal of alder surface litter by flooding. Alder patches were lower in elevation (0.8 m above bankfull width) than conifer patches (2.2 m). Forest floor and soil C and N concentrations and pHs were not significantly different in alder and conifer patches. Nutrient release from decomposing alder leaves was not significantly different in conifer and alder patches, although there was a trend for C, N, P, K, and Ca to be lost faster from leaves in alder patches than conifer patches in the first year. Red alder litter input to riparian conifer patches will initially decompose rapidly and provide nutrients, particularly N and P to conifers, as well as enhancing soil C since long-term decomposition rates are slow.  相似文献   

20.
Large cavity-nesting birds depend on large-diameter trees for suitable nest sites. The increased spatial extent of commercial timber harvesting is modifying forest structure across the land base and may thus compromise the availability of large trees at the landscape scale. In this study, our objectives were to (1) characterize the availability of large living and dead trees in old-growth stands dominated by different tree species and surficial deposits that encompass the range of natural cover types of eastern Québec's boreal forest; (2) analyze the distribution of trees among decay-classes; and (3) compare the availability of large trees in unharvested, remnant, and harvested stands for the entire range of decay-classes. A total of 116 line transects were distributed across unharvested forests, remnant linear forests, and cutblocks in cutover areas. Unharvested forest stands (black spruce [Picea mariana], balsam fir [Abies balsamea]–black spruce, balsam fir–white spruce [Picea glauca] and balsam fir) reflected a gradient of balsam fir dominance. The remnant forests selected were isolated for 5–15 years. Analyses were performed at two diameter cut-off values. Trees with DBH ≥20 cm were considered for availability of total trees whereas trees with DBH ≥30 cm were considered for availability of large trees. Forest stands comprised high proportions of standing dead trees (33% of all stems, 8% were large dead stems). Availability of total and large standing trees increased with the dominance of balsam fir in stands. Forest stands located on thick surficial deposits showed higher densities of large dead trees for every stand type suggesting a higher productivity on those sites. Availability of stems according to decay-classes showed a dome-shaped distribution with higher densities of snags in intermediate decay stages. However, for large stems, black spruce stands showed a significantly lower availability that was consistent across all decay-classes. In linear remnant forests, pure balsam fir stands were absent. Remnant stands thus showed a much lower availability in large trees when compared with unharvested balsam fir stands. Clearcuts had the lowest densities of dead trees across sampled stands. Current even-aged management practices clearly affect availability and recruitment of large trees, therefore forest-dwelling wildlife relying on these structures for breeding is likely to be affected by large-scale harvesting in coniferous boreal forests.  相似文献   

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