211 research outputs found
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Regeneration patterns on some modified staggered-setting clearcuts on the H.J. Andrews experimental forest
A survey of natural regeneration of Doug1as-fir and associated species was made on 15 staggered-setting cuttings four and five years after logging. These areas were on the H. J. Andrews Experimental Forest which is located in the McKenzie River area of western Oregon. Five types of cuttings were represented: (1) four north-south oriented strip clear cuts varying from 50 to 330 feet in width; (2) three east-west orientated strip clear-cut varying from 100 to 300 feet in width; (3) six patch or group clear-cuts varying from one fourth to four acres in size; (4) a shade-seed-tree cutting on which residual trees were left to provide shade and seed; and (5) a typical staggered-setting clear-cut. The modified cuttings were designed to utilize shade from the residual stand to favor regeneration by reducing high surface, soil temperatures, a major deterrent to the establishment of tree seedlings in this area. Results of the survey showed that all of the modified cutting units were better stocked than the typical staggered-setting clearcut and with two exceptions had at least 500 we11-spaced trees per acre. The east-west orientated strips regenerated best with 69 to 89 percent of milacre plots stocked. The small group clearcuts also regenerated well; stocking varied from 8 to 72 percent of milacre plots stocked. The north-south orientated strips were the most poorly stocked group of small cuttings with from 35 to 61 percent of milacre plots stocked. The shade-seed-tree cutting had 61 percent of plots stocked and the staggered-setting clearcut 28 percent of plots stocked. The statistical analysis indicated that the parameter of shade hours per plot was consistently related to regeneration of all species together and of Douglas-fir alone. The degree of this relationship varied considerably between types of units and to a lesser extent among units of a particular type. In addition there was some evidence that intermittent shading was more effective in favoring regeneration than a similar amount of shade received in a single period of time. Distance from seed source was not found to be related to stocking on the small cutting units studied. This author concludes that consideration should be given to the use of special cutting methods such as east-west orientated strip clearcuts, small patch clearcuts, and shade-seed-tree cuttings, to aid in natural regeneration of Douglas fir, especially on severe sites. These cuttings should be laid out primarily to provide shade rather than from the standpoint of seed dispersal
Managing fire-prone forests in the western United States
The management of fire-prone forests is one of the most controversial natural resource issues in the US today, particularly in the west of the country. Although vegetation and wildlife in these forests are adapted to fire, the historical range of fire frequency and severity was huge. When fire regimes are altered by human activity, major effects on biodiversity and ecosystem function are unavoidable. We review the ecological science relevant to developing and implementing fire and fuel management policies for forests before, during, and after wildfires. Fire exclusion led to major deviations from historical variability in many dry, low-elevation forests, but not in other forests, such as those characterized by high severity fires recurring at intervals longer than the period of active fire exclusion. Restoration and management of fire-prone forests should be precautionary, allow or mimic natural fire regimes as much as possible, and generally avoid intensive practices such as post-fire logging and planting
Potential Site Productivity Influences the Rate of Forest Structural Development
Development and maintenance of structurally complex forests in landscapes formerly managed for timber production is an increasingly common management objective. It has been postulated that the rate of forest structural development increases with site productivity. We tested this hypothesis for Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) forests using a network of permanent study plots established following complete timber harvest of the original old-growth forests. Forest structural development was assessed by comparing empirical measures of live tree structure to published values for Douglas-fir forests spanning a range of ages and structural conditions. The rate of forest structural development—resilience—exhibited a positive relationship with site index, a measure of potential site productivity. Density of shade-intolerant conifers declined in all study stands from an initial range of 336–4068 trees/ha to a range of 168–642 trees/ha at the most recent measurement. Angiosperm tree species declined from an initial range of 40–371 trees/ha to zero in seven of the nine plots in which they were present. Trends in shade-tolerant tree density were complex: density ranged from 0 to 575 trees/ha at the first measurement and was still highly variable (25–389 trees/ha) at the most recent measurement. Multivariate analysis identified the abundance of hardwood tree species as the strongest compositional trend apparent over the study period. However, structural variables showed a strong positive association with increasing shade-tolerant basal area and little or no association with abundance of hardwood species. Thus, while tree species succession and forest structural development occur contemporaneously, they are not equivalent processes, and their respective rates are not necessarily linearly related. The results of this study support the idea that silvicultural treatments to accelerate forest structural development should be concentrated on lower productivity sites when the management objective is reserve-wide coverage of structurally complex forests. Alternatively, high-productivity sites should be prioritized for restoration treatments when the management objective is to develop structurally complex forests on a portion of the landscape
The ICO Approach to Quantifying and Restoring Forest Spatial Pattern: Implementation Guide
This document is intended as a “How To” guide for managers and stakeholders wishing to implement the Individual, Clumps, and Openings (ICO) method for silvicultural prescriptions and/or monitoring. This guide is organized into stand-alone chapters. Managers should read and use chapters as they find useful to their own needs.https://scholarworks.umt.edu/ico/1002/thumbnail.jp
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The effects of fire on soil nitrogen associated with patches of the actinorhizal shrub Ceanothus cordulatus
Nitrogen is a limiting resource in many temperate forests and nitrogen-fixing plants are usually limited to the early
stages of post-disturbance succession. In fire-dependent Sierra Nevada forests, however, Ceanothus cordulatus is
relatively abundant even in old-growth forest conditions which are at least partly maintained by fire.We conducted
a field experiment to determine if soil beneath Ceanothus patches represent ‘resource islands’ of available N which
persist after fire. Nine plots containing discrete patches of Ceanothus, Arctostaphylos patula (manzanita; chosen
as a non N-fixing reference species), and bare forest floor were subjected to either a low-intensity (n = 3) or highintensity
(n = 3) bum treatment, or remained unburned as controls (n = 3). Soil temperatures during the bum were
monitored by a network of thermocouples placed at the surface of the mineral soil and at ca. 10 cm depths. Soil
samples were collected from the organic horizon, 0-10 cm and 15-25 cm depths within each patch type immediately
before burning and 2 days, and 6, and 11 months after. Soil moisture, total C and N, and ammonium and nitrate
concentrations were determined in the laboratory. Before the burn, Ceanothus patches were significantly enriched
in total and inorganic N in the organic horizon relative to the other patch types. A sharp increase in inorganic N was
observed in all patch types and depths immediately following burning, but by 6 months after the burn, Ceanothus
patches were significantly enriched relative to the surrounding patch types and remained so at months. Resprouting
Ceanothus patches will continue to be an important source of a limiting nutrient in this fire-prone ecosystem.Keywords: Frankia, Sierra Nevada, Fire, Ceanothus, Nitroge
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Facilitative and competitive effecs of a N-fixing shrub on white fir saplings
In Sierra Nevada forests, shrubs are considered strong soil moisture competitors with regenerating trees, reducing seedling establishment, and
slowing growth. Recent studies, however, suggest that in some circumstances shrubs can facilitate tree establishment and growth by modifying
harsh microclimate conditions; increasing acquisition of water, carbon, and/or nutrients via shared mycorrhizal connections; or enhancing soil
fertility, particularly under nitrogen-fixing shrubs such as Ceanothus spp. We examined the establishment dates and growth rates and patterns of
white fir saplings growing in greenleaf manzanita, whitethorn ceanothus, and bare patches to examine whether establishment was correlated with
past wet years, whether saplings growing in ceanothus had nitrogen-enriched foliage or faster growth rates than in the other two patches, and
whether saplings in shrub patches experienced competition for light.
Sapling establishment was not correlated with high precipitation or heavy snowpack years, suggesting shade-tolerant saplings do not need wet
years to become established. Soils under ceanothus were nitrogen enriched, but white fir sapling foliage did not have higher nitrogen concentrations
and saplings did not grow faster in ceanothus than in the other two patches. Because growth rates of saplings were comparable in all patch types
examined despite significantly different edaphic and abiotic conditions, we inferred that the various competitive and facilitative interactions
affecting tree growth are in net balance across the patch types examined. However, competition for light is important—a significant percentage of
growth release events occurred after saplings emerged above their host shrubs. Where shrubs are present, shade-tolerant species (i.e., white fir) are
favored over drought-tolerant (pine) species. Our results may help interpret changes in understory conditions that are contributing to mixed
conifer’s compositional shift toward more shade-tolerant species after a century of fire-suppression.Keywords: shade tolerance, soil fertility, forest regeneration, fire suppression, nitrogen fixation, mixed conifer, plant competitio
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Facilitative and competive effects of a N-fixing shrub on white fir saplings
In Sierra Nevada forests, shrubs are considered strong soil moisture competitors with regenerating trees, reducing seedling establishment, and
slowing growth. Recent studies, however, suggest that in some circumstances shrubs can facilitate tree establishment and growth by modifying
harsh microclimate conditions; increasing acquisition of water, carbon, and/or nutrients via shared mycorrhizal connections; or enhancing soil
fertility, particularly under nitrogen-fixing shrubs such as Ceanothus spp. We examined the establishment dates and growth rates and patterns of
white fir saplings growing in greenleaf manzanita, whitethorn ceanothus, and bare patches to examine whether establishment was correlated with
past wet years, whether saplings growing in ceanothus had nitrogen-enriched foliage or faster growth rates than in the other two patches, and
whether saplings in shrub patches experienced competition for light.
Sapling establishment was not correlated with high precipitation or heavy snowpack years, suggesting shade-tolerant saplings do not need wet
years to become established. Soils under ceanothus were nitrogen enriched, but white fir sapling foliage did not have higher nitrogen concentrations
and saplings did not grow faster in ceanothus than in the other two patches. Because growth rates of saplings were comparable in all patch types
examined despite significantly different edaphic and abiotic conditions, we inferred that the various competitive and facilitative interactions
affecting tree growth are in net balance across the patch types examined. However, competition for light is important—a significant percentage of
growth release events occurred after saplings emerged above their host shrubs. Where shrubs are present, shade-tolerant species (i.e., white fir) are
favored over drought-tolerant (pine) species. Our results may help interpret changes in understory conditions that are contributing to mixed
conifer’s compositional shift toward more shade-tolerant species after a century of fire-suppression.Keywords: Nitrogen fixation, Shade tolerance, Forest regeneration, Plant competition, Fire suppression, Soil fertility, Mixed conife
Interacting Factors Driving a Major Loss of Large Trees with Cavities in a Forest Ecosystem
Large trees with cavities provide critical ecological functions in forests worldwide, including vital nesting and denning resources for many species. However, many ecosystems are experiencing increasingly rapid loss of large trees or a failure to recruit new large trees or both. We quantify this problem in a globally iconic ecosystem in southeastern Australia--forests dominated by the world's tallest angiosperms, Mountain Ash (Eucalyptus regnans). Tree, stand and landscape-level factors influencing the death and collapse of large living cavity trees and the decay and collapse of dead trees with cavities are documented using a suite of long-term datasets gathered between 1983 and 2011. The historical rate of tree mortality on unburned sites between 1997 and 2011 was >14% with a mortality spike in the driest period (2006-2009). Following a major wildfire in 2009, 79% of large living trees with cavities died and 57-100% of large dead trees were destroyed on burned sites. Repeated measurements between 1997 and 2011 revealed no recruitment of any new large trees with cavities on any of our unburned or burned sites. Transition probability matrices of large trees with cavities through increasingly decayed condition states projects a severe shortage of large trees with cavities by 2039 that will continue until at least 2067. This large cavity tree crisis in Mountain Ash forests is a product of: (1) the prolonged time required (>120 years) for initiation of cavities; and (2) repeated past wildfires and widespread logging operations. These latter factors have resulted in all landscapes being dominated by stands ≤72 years and just 1.16% of forest being unburned and unlogged. We discuss how the features that make Mountain Ash forests vulnerable to a decline in large tree abundance are shared with many forest types worldwide.This work was supported by Australian Research Council DP1097170; Parks Victoria; and Victorian Department of Sustainability and Environment. The
funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript
Interacting factors driving a major loss of large trees with cavities in a forest ecosystem
Large trees with cavities provide critical ecological functions in forests worldwide, including vital nesting and denning resources for many species. However, many ecosystems are experiencing increasingly rapid loss of large trees or a failure to recruit new large trees or both. We quantify this problem in a globally iconic ecosystem in southeastern Australia - forests dominated by the world's tallest angiosperms, Mountain Ash (Eucalyptus regnans). Tree, stand and landscape-level factors influencing the death and collapse of large living cavity trees and the decay and collapse of dead trees with cavities are documented using a suite of long-term datasets gathered between 1983 and 2011. The historical rate of tree mortality on unburned sites between 1997 and 2011 was >14% with a mortality spike in the driest period (2006-2009). Following a major wildfire in 2009, 79% of large living trees with cavities died and 57-100% of large dead trees were destroyed on burned sites. Repeated measurements between 1997 and 2011 revealed no recruitment of any new large trees with cavities on any of our unburned or burned sites. Transition probability matrices of large trees with cavities through increasingly decayed condition states projects a severe shortage of large trees with cavities by 2039 that will continue until at least 2067. This large cavity tree crisis in Mountain Ash forests is a product of: (1) the prolonged time required (>120 years) for initiation of cavities; and (2) repeated past wildfires and widespread logging operations. These latter factors have resulted in all landscapes being dominated by stands <= 72 years and just 1.16% of forest being unburned and unlogged. We discuss how the features that make Mountain Ash forests vulnerable to a decline in large tree abundance are shared with many forest types worldwide
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