76 research outputs found

    Seed Release in Lodgepole Pine Forests After Mountain Pine Beetle Outbreak

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    Serotinous lodgepole pine (Pinus contorta var. latifolia) usually regenerates after fire or harvesting provided conditions that are warm enough to open the cones. There are concerns that large-scale stand mortality due to mountain pine beetle (MPB) outbreak could greatly reduce natural regeneration of lodgepole pine because the closed cones are held in place in the tree canopy without any seed release. We selected 15 stands (five gray-attacked, five red-attacked, and five green) in the Sub-Boreal Spruce biogeoclimatic zone of British Columbia to determine loss of canopy seed via breakage of twig-bearing cones and cone opening (i.e., loss of serotiny) throughout the 2008 growing season. We also quantified seed loss of fallen cones via predation and cone opening. Red-attacked stands lost an estimated 175 000 seed-bearing canopy cones ha-1 yr -1 due to crown friction resulting in twig breakage, representing an over three-fold increase compared to green stands. This result was considered ecologically important since it equated to over 25 % of canopy cones lost to the forest floor. Red- and gray-attacked stands also had 15 % of canopy seed lost due to cone weathering resulting in cone opening. Additional seed losses occurred in the gray-attacked stands due to additional cone opening (58 % yr-1) on the forest floor and predation (12 000 fallen seed-bearing cones ha-1 yr-1). MPB-killed stands released some canopy seed through breakage of twig-bearing cones, partial loss of serotiny, and forest floor cone opening. The implications are: i) seed supply is gradually lost in the first years after attack; ii) if adequate levels of regeneration are to occur, either anthropogenic or fire disturbances must happen shortly after tree mortality. We conclude that lodgepole pine is poorly-adapted to disturbances such as MPB because seed is slowly released onto an unfavorable seed bed

    Suckering response of aspen to traffic-induced-root wounding and the barrier-effect of log storage

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    In a growth chamber, we tested how the seasonal timing of placing a physical barrier (simulating a possible effect of log storage) and inflicting root damage impacted aspen (Populus tremuloides Michx.) root systems and their suckering capability. Roots from 4-year-old saplings were used, and one half of these root systems had the above-ground portion cut in the winter (dormant) while the other half was cut during the growing season in the summer. Damage was inflicted to the roots by driving a large farm tractor over them, and a covering treatment was applied using a polystyrene board to prevent suckers from emerging from the soil. Soil temperatures for the winter-cut root systems were kept at 5 8C over the growing season, using a water bath, while for the summer-cut root systems soil temperatures were maintained at 17 8C over the growing season. In the winter-cut root systems, both log storage and root wounding caused a 40% reduction in living root mass and carbohydrate reserves, as well as reducing sucker numbers and their growth performance. In the summer-cut root systems log storage and root wounding reduced living root mass by approximately 35% as well as sucker growth, but had less of an impact on the number of suckers produced

    Aspen regeneration on log decking areas as influenced by season and duration of log storage

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    This study assessed aspen regeneration on decking areas as affected by season of log deck building and duration of log storage; as well as root wounding, soil com- paction, and slash depth. On former decking areas that were built after a summer harvest, aspen regeneration was 50% lower and root death 35% greater compared to former decking areas of a fall harvest. Duration of log storage after a fall harvest had little effect on aspen regeneration; short (1.5–3 months) or long (11 months) storage resulted in similar regeneration. Slash load was greatly increased on decking areas while root wounding and soil bulk density were only slightly increased compared to controls. For best management practices, log storage after summer harvest should be avoided especially when logs are kept over the growing period when suckering occurs. Additionally, removing the inter- woven mat of slash covering decking areas and limiting machine traffic to frozen soil will ensure vigorous suckering

    N-transfer through aspen litter and feather moss layers after fertilization with ammonium nitrate and urea

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    When fertilizer is broadcast in boreal forest stands, the applied nutrients must pass through a thick layer of either feather moss or leaf litter which covers the forest floor. In a growth chamber experiment we tested the transfer of N through living feather moss or aspen litter when fertilized with urea ((NH2)2CO) or NH4NO3 at a rate of 100 kg ha−1 and under different watering regimes. When these organic substrates were frequently watered to excess they allowed the highest transfer of nutrients through, although 72% of the applied fertilizer was captured in the substrates. In a field experiment we also fertilized moss and aspen litter with urea ((NH2)2CO) or NH4NO3 at a more operationally relevant rate of 330 kg ha−1. We captured the NO3− or NH4+ by ion exchange resin at the substrate–mineral soil interface. In contrast to the growth chamber experiment, this fertilizer rate killed the moss and there was no detectable increase in nutrient levels in the aspen litter or feather moss layers. Instead, the urea was more likely transferred into the mineral soil; mineral soil of the urea treatment had 1.6 times as much extractable N compared to the NH4NO3 treatment. This difference between the growth chamber and field studies was attributed to observed fertilizer- damage to the living moss and possibly damage to the litter microflora due to the higher rate of fertilization in the field. In addition, the early and substantial rainfall after fertilization in the field experiment produced conditions for rapid leaching of N through the organic layers into the mineral soil. In the field, only 8% of the urea-N that was applied was captured by the ion exchange resin, while 34% was captured in for the NH4NO3 fertilization. Thus, the conditions for rapid leaching in the field moved much of the N in the form of urea through the organic layers and into the mineral soil before it was hydrolyzed

    A Functional Framework for Improved Management of Western North American Aspen (Populus tremuloides Michx.)

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    Quaking or trembling aspen (Populus tremuloides Michx.) forests occur in highly diverse setting across North America. However, management of distinct communities has long relied on a single aspen to-conifer successional model. We examine a variety of aspen dominated stand types in the western portion of its range as ecological systems; avoiding an exclusive focus on seral dynamics or single species management. We build a case for a large-scale functional aspen typology based on existing literature. Aspen functional types are defined as aspen communities that differ markedly in their physical and biological processes. The framework presented here describes two “functional types” and seven embedded “subtypes”: Seral (boreal, montane), Stable (parkland, Colorado Plateau, elevation and aspect limited, terrain isolated), and a Crossover Seral-Stable subtype (riparian). The assessment hinges on a matrix comparing proposed functional types across a suite of environmental characteristics. Differences among functional groups based on physiological and climatic conditions, stand structures and dynamics, and disturbance types and periodicity are described herein. We further examine management implications and challenges, such as human alterations, ungulate herbivory, and climate futures, that impact the functionality of these aspen systems. The functional framework lends itself well to stewardship and research that seeks to understand and emulate ecological processes rather than combat them. We see advantages of applying this approach to other widespread forest communities that engender diverse functional adaptations

    Carbon isotope discrimination and water stress in trembling aspen following variable retention harvesting

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    Variable retention harvesting (VRH) has been proposed as a silvicultural practice to maintain biodiversity and ecosystem integrity. No previous study has examined tree carbon isotope discrimination to provide insights into water stress that could lead to dieback and mortality of trees following VRH. We measured and compared the carbon isotope ratios (ÎŽ13C) in stem wood of trembling aspen (Populus tremuloides Michx.) before and after VRH. Eight trees were sampled from isolated residual, edge and control (interior of unharvested stand) positions from each of seven plots in three regions (Calling Lake and Drayton Valley, Alberta and Lac Duparquet, Qu

    Photosynthetic adaptation and acclimation to exploit seasonal periods of direct irradiance in three temperate, deciduous-forest herbs

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    1.  We evaluated the potential for three species of deciduous-forest herbs to exploit seasonal periods of direct irradiance. In particular, we investigated the importance of photosynthetic acclimation as a mechanism for shade-tolerant herbs to utilize direct light reaching the forest floor before canopy expansion in the spring and after canopy leaf drop in the autumn. 2.  We measured the photosynthetic and growth characteristics of three co-occurring herbs of a northern hardwood forest: the spring ephemeral Allium tricoccum Ait., the summer-green Viola pubescens Ait., and the semi-evergreen Tiarella cordifolia L. 3.  Leaf CO 2 exchange, leaf mass per area, and leaf biochemistry differed among species and seasonally within species to match the changing light environment below the forest canopy. From spring to summer, as irradiance dropped with the expansion of the overstorey canopy, Viola leaves exhibited reduction of both photosynthetic capacity and light compensation point. Weaker acclimation of less magnitude occurred in Tiarella leaves over the spring–summer light transition; this was followed by further acclimation to the stronger autumn irradiance. 4.   Viola ’s greater range of photosynthetic acclimation was associated with shifts in allocation between Rubisco and chlorophyll, as well as changes in total leaf nitrogen (N) concentration and leaf mass per area (LMA). In contrast, Tiarella ’s narrow range of acclimation was associated solely with changes in allocation to Rubisco versus chlorophyll, with no changes in total leaf N or LMA. 5.  Seasonal changes in leaf chemistry and structure in Viola suggest a stepwise ontogeny whereby individual leaves are able to function as ‘sun leaves’ for 3–5 weeks in the spring, and then as ‘shade leaves’ for up to 3 months in the summer. 6.  Whole-plant biomass accumulation showed that all three species accumulated most of their annual biomass increment during periods of direct irradiance. These results demonstrate the importance of brief seasonal periods of strong irradiance to the growth of deciduous forest herbs, even shade-tolerant, summer and evergreen species.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/75494/1/j.0269-8463.2001.00584.x.pd

    The handbook for standardized field and laboratory measurements in terrestrial climate change experiments and observational studies (ClimEx)

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    1. Climate change is a world‐wide threat to biodiversity and ecosystem structure, functioning and services. To understand the underlying drivers and mechanisms, and to predict the consequences for nature and people, we urgently need better understanding of the direction and magnitude of climate change impacts across the soil–plant–atmosphere continuum. An increasing number of climate change studies are creating new opportunities for meaningful and high‐quality generalizations and improved process understanding. However, significant challenges exist related to data availability and/or compatibility across studies, compromising opportunities for data re‐use, synthesis and upscaling. Many of these challenges relate to a lack of an established ‘best practice’ for measuring key impacts and responses. This restrains our current understanding of complex processes and mechanisms in terrestrial ecosystems related to climate change. 2. To overcome these challenges, we collected best‐practice methods emerging from major ecological research networks and experiments, as synthesized by 115 experts from across a wide range of scientific disciplines. Our handbook contains guidance on the selection of response variables for different purposes, protocols for standardized measurements of 66 such response variables and advice on data management. Specifically, we recommend a minimum subset of variables that should be collected in all climate change studies to allow data re‐use and synthesis, and give guidance on additional variables critical for different types of synthesis and upscaling. The goal of this community effort is to facilitate awareness of the importance and broader application of standardized methods to promote data re‐use, availability, compatibility and transparency. We envision improved research practices that will increase returns on investments in individual research projects, facilitate second‐order research outputs and create opportunities for collaboration across scientific communities. Ultimately, this should significantly improve the quality and impact of the science, which is required to fulfil society's needs in a changing world
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