scholarly journals Effect of Thinning and Harvest Type on Storage and Losses of Phosphorous inPinus taedaL. Plantations in Subtropical Argentina

2011 ◽  
Vol 2011 ◽  
pp. 1-10 ◽  
Author(s):  
Rodolfo Andrés Martiarena ◽  
Jorge Luis Frangi ◽  
Martín Alcides Pinazo ◽  
Alejandra Von Wallis ◽  
Roberto Antonio Fernández

The aim of this study was to evaluate the effect of thinning intensity and different harvest types on ecosystem P conservation in 20-year-oldPinus taedaplantation ecosystems at Misiones province, Argentina. The plantation was established in 1985, thinned at three intensities—0, 33, and 66% of basal area of control plots removed by thinning—and harvested in 2005. The nutrient content at harvest was determined for tree, shrub, and herb layers, the forest floor and upper mineral soil. Two harvest types were simulated: stem only and whole tree. Total P content was 56.8, 46.8, and 38.6 kg· ha−1for 0, 33, and 66% thinning, respectively. Total P exported by harvest was different among treatments, the highest at 0% thinning treatment. Phosphorus stability index values indicated that the P most conservative management option is 66% thinning, harvest of stem only and retention of forest floor, understory, and harvest residues.

2013 ◽  
Vol 10 (6) ◽  
pp. 3691-3703 ◽  
Author(s):  
D. Zhou ◽  
S. Q. Zhao ◽  
S. Liu ◽  
J. Oeding

Abstract. Partial cutting, which removes some individual trees from a forest, is one of the major and widespread forest management practices that can significantly alter both forest structure and carbon (C) storage. Using 748 observations from 81 studies published between 1973 and 2011, we synthesized the impacts of partial cutting on three variables associated with forest structure (mean annual growth of diameter at breast height (DBH), stand basal area, and volume) and four variables related to various C stock components (aboveground biomass C (AGBC), understory C, forest floor C, and mineral soil C). Results show that the growth of DBH increased by 111.9% after partial cutting, compared to the uncut control, with a 95% bootstrapped confidence interval ranging from 92.2 to 135.9%, while stand basal area and volume decreased immediately by 34.2% ([−37.4%, −31.2%]) and 28.4% ([−32.0%, −25.1%]), respectively. On average, partial cutting reduced AGBC by 43.4% ([−47.7%, −39.3%]), increased understory C storage by 391.5% ([220.0%, 603.8%]), but did not show significant effects on C stocks on forest floor and in mineral soil. All the effects, if significant (i.e., on DBH growth, stand basal area, volume, and AGBC), intensified linearly with cutting intensity and decreased linearly over time. Overall, cutting intensity had more strong impacts than the length of recovery time on the responses of those variables to partial cutting. Besides the significant influence of cutting intensity and recovery time, other factors such as climate zone and forest type also affected forest responses to partial cutting. For example, a large fraction of the changes in DBH growth remains unexplained, suggesting the factors not included in the analysis may play a major role. The data assembled in this synthesis were not sufficient to determine how long it would take for a complete recovery after cutting because long-term experiments were scarce. Future efforts should be tailored to increase the duration of the experiments and balance geographic locations of field studies.


1984 ◽  
Vol 14 (2) ◽  
pp. 155-162 ◽  
Author(s):  
M. A. Radwan ◽  
D. S. DeBell ◽  
S. R. Webster ◽  
S. P. Gessel

Effects of different sources of fertilizer N on selected chemical characteristics of soils and foliage, and on growth of western hemlock (Tsugaheterophylla (Raf.) Sarg.) were compared at three different sites in western Washington. Treatments were the following: untreated control (O), ammonium nitrate (AN), ammonium sulfate (AS), calcium nitrate (CN), urea (U), and urea – ammonium sulfate (US). Fertilizers were applied in the spring (April–May) at 224 kg N/ha. Forest floor and mineral soil, to a depth of 5 cm, and foliage were sampled periodically for 2 years. Height and diameter of selected trees were measured periodically for 4 years. Results are reported mostly for two sites, one in the Cascade Range and one in the coastal zone in western Washington. The pH of forest floor and mineral soil varied by treatment, and the two urea fertilizers caused substantial initial rise. Effects on soil and foliar nutrients varied by fertilizer, sampling date, and location. In general, all fertilizers increased NH4 N, N03 N, and total N in the forest floor and mineral soil, and total N in the foliage. Also, with some exceptions, especially with foliar P in the Cascade site, fertilization reduced foliar content of important nutrients. At the Cascade site, 4-year growth responses in height, basal area, and volume averaged over all fertilizers were 30, 34, and 32%, respectively. AN, AS, CN, and urea resulted in height growth significantly (P < 0.20) higher than that of the control. Significant basal area growth and volume-growth responses were produced by AN, CN, and US. No significant height-growth response to any fertilizer occurred in the coastal stand; basal area growth and volume-growth responses averaged 27 and 21%, respectively, and best response occurred with urea. These results suggest that the low and inconsistent response of hemlock to N fertilization cannot be improved by applying some N fertilizer other than urea. Factors limiting response to N fertilization may be associated with availability of native N and other nutrients or other characteristics of hemlock sites and stands.


1992 ◽  
Vol 22 (10) ◽  
pp. 1536-1546 ◽  
Author(s):  
Joseph E. Means ◽  
Paul C. MacMillan ◽  
Kermit Cromack Jr.

Logs, forest floor, and mineral soil were sampled and measured, and snags were measured, in a 450-year-old Douglas-fir (Pseudotsugamenziesii (Mirb.) Franco) stand on the H.J. Andrews Experimental Forest, Oregon. Logs, some still identifiable after 300 years on the forest floor, contained large amounts of organic matter (222 Mg/ha), C (100 Mg/ha), water (559–10 700 L/log), N (183 kg/ha), and Ca (141 kg/ha), and smaller amounts of P (5.5 kg/ha), K (22 kg/ha), Mg (14 kg/ha), and Na (3.7 kg/ha). Logs and snags covered about 17% of the forest floor and had an all-sided area index of 0.69 m2/m2. Through mineralization, C, N, and K were lost through time; Ca and Mg increased; and P and Na increased then decreased, showing no net change. Also through mineralization, cellulose and hot acid detergent soluble fraction decreased more rapidly than lignin. Lignin was apparently not lost until the later stages of decay, when N was also lost in significant amounts. This parallels the shift from initial dominance by white rots that degraded cellulose and lignin to later dominance by brown rots that preferentially degraded cellulose. Lignin and cellulose were eventually lost at more similar rates in later decay stages. This may have been due in part to a close association between the remaining cellulose and lignin in later decay stages. Lignin was a better predictor of the onset of N release than was the C:N ratio.


2013 ◽  
Vol 10 (1) ◽  
pp. 787-813 ◽  
Author(s):  
D. Zhou ◽  
S. Q. Zhao ◽  
S. Liu ◽  
J. Oeding

Abstract. Partial cutting, which removes some individual trees from a forest, is one of the major and widespread forest management practices that can significantly alter both forest structure and carbon (C) storage. Using 746 observations from 82 publications, we synthesized the impacts of partial cutting on three variables associated with forest structure (i.e. mean annual growth of diameter at breast height (DBH), basal area (BA), and volume) and four variables related to various C stock components (i.e. aboveground biomass C (AGBC), understory C, forest floor C, and mineral soil C). Results shows that the growth of DBH elevated by 112% after partial cutting, compared to the uncut control, while stand BA and volume reduced immediately by 34% and 29%, respectively. On average, partial cutting reduced AGBC by 43%, increased understory C storage by 392%, but did not show significant effects on C storages on forest floor and in mineral soil. All the effects on DBH growth, stand BA, volume, and AGBC intensified linearly with cutting intensity (CI) and decreased linearly with the number of recovery years (RY). In addition to the strong impacts of CI and RY, other factors such as climate zone and forest type also affected forest responses to partial cutting. The data assembled in this synthesis were not sufficient to determine how long it would take for a complete recovery after cutting because long-term experiments were rare. Future efforts should be tailored to increase the duration of the experiments and balance geographic locations of field studies.


1992 ◽  
Vol 57 ◽  
Author(s):  
D. Maddelein ◽  
N. Lust

In  Flanders, important drift sand areas were afforestated with Scots pine (Pinus sylvestris L.) during the last  century. Drought stress and limited nutrient availability are two major  factors limiting tree growth on these sites. Nevertheless, afforestation  succeeded extremely well and tree growth can be considered as satisfactory.      Chemical soil analysis stresses the very poor quality of the mineral soil.  Nutrient content of the mineral soil is even poorer than that of neighbouring  heathland soils.     The formation of a well developed forest floor is the most important  feature of soil evolution during the last century. A seventy year old stand  has built up a thick forest floor, with a biomass of over 10 kg/m2. This  layer functions as a main nutrient source in the ecosystem.     Annually, 4000 to 5000 kg of tree litter per hectare return to the forest  soil. Sixty percent of this fraction consists of shed needles. Needles also  have a dominant share in the nutrient amounts returned with tree litter.  Annually, about 42 kg of N, 8 kg of K, 15 kg of Ca and 2 kg of P and Mg are  returned to the soil with tree litter. These values are, with exception of N,  very low compared to other forest ecosystems.    The herbaceous layer, poor in species and dominated by wavy-hair grass (Deschampsia flexuosa (L.) Trin.),  also produces over 2500 kg of litter per year and per hectare, and plays an  equally important role in the nutrient supply of the growing vegetation.          Key words: Scots pine, drift sand, forest floor, litter


1990 ◽  
Vol 20 (3) ◽  
pp. 259-266 ◽  
Author(s):  
Jeremy S. Fried ◽  
James R. Boyle ◽  
John C. Tappeiner II ◽  
Kermit Cromack Jr.

Soil chemical and physical properties, forest floor weights, nutrient content and turnover rates, and litter fall weights and nutrient content under bigleaf maple (Acermacrophyllum Pursh) and Douglas-fir (Pseudotsugamenziesii (Mirb.) Franco var. menziesii) were compared on five sites on the eastern margin of the Oregon Coast Range. Litter fall weight and nutrient content were significantly greater under maple on every site for every macronutrient and for most micronutrients. Forest floor biomass and nutrient content were extremely variable, much more so than litter fall, and there were no consistent differences between the two species. However, turnover rates for forest floor biomass and nutrients were significantly faster under maple for every nutrient at every site. Bulk density of mineral soil was also highly variable with significant differences at only two sites. Soil under maple was consistently higher in nitrogen, and less consistently, in potassium. There were no consistent trends in amounts of calcium, magnesium, or phosphorus. Soil organic carbon content under maple was significantly greater than under Douglas-fir on four of five sites. These differences may result from the more rapid turnover of forest floors under maple trees.


1983 ◽  
Vol 13 (5) ◽  
pp. 879-893 ◽  
Author(s):  
C. T. Dyrness ◽  
Rodney A. Norum

Seven units (about 2 ha each) of black spruce – feather moss forest were experimentally burned over a range of fuel moisture conditions during the summer of 1978. Surface woody fuels were sparse and the principal carrier fuel was the forest floor (largely mosses and their decomposition products). Forest floors after burning comprised a small-scale mosaic of unburned, scorched, lightly burned, moderately burned, and heavily burned (organic materials entirely consumed) conditions. Percentage of the unit area in the moderately and heavily burned condition ranged from 11.2 to 77.2% and percent decrease in forest-floor thickness varied from 27.4 to 63.1% in the seven units. Forest-floor consumption was most closely correlated with the moisture content of lower moss (01 horizon) and lower duff layers (022 horizon) at the time of burning. For the first 3 years after fire, biomass production was greater on heavily burned than on lightly burned sites (58 vs. 37 g/m2 on an annual basis). Heavily burned sites were completely dominated by the invading species Epilobiumangustifolium L., Ceratodonpurpureus (Hedw.) Brid., and Marchantiapolymorpha L., whereas lightly burned plots were occupied by sprouting species such as Calamagrostiscanadensis (Michx.) Beauv., Vacciniumuliginosum L., and Ledumgroenlandicum Oeder. Soil pH and amounts of total P and available P in the forest floor increased significantly as a result of burning; and in all cases, increases reached a maximum in moderately and heavily burned areas. Total N in the forest floor increased significantly in moderately burned, but decreased slightly in heavily burned areas. Total N and total P showed smaller increases in the surface mineral soil as a result of burning. Supplies of available P in the mineral soil increased almost 4-fold in moderately burned and over 16-fold in heavily burned areas.


1995 ◽  
Vol 25 (8) ◽  
pp. 1278-1291 ◽  
Author(s):  
J. Clive Carlyle

The effects of thinning and residues on nutrient distribution, N fluxes, and extractable P were studied for 3 years after the first thinning of a 10-year-old Pinusradiata D. Don plantation. Treatments were (i) unthinned, (ii) thinned to 52% of basal area with all residues removed (zero residue; ZR), (iii) thinned with all residues retained and spread uniformly (normal residue; NR), and (iv) thinned with all residues retained plus the addition of those removed from the ZR treatment, approximately doubling the amount of residue in treatment NR (high residue; HR). The total nutrient contents of trees (above ground), residues, forest floor, and the top 0.30 m of mineral soil were 1206 kg N•ha−1, 126 kg P•ha−1, 828 kg K•ha−1, and 1272 kg Ca•ha−1 after thinning. Residues contained 11, 10, 10, and 7% of site N, P, K, and Ca, respectively. Thinning without residue retention (unthinned cf. ZR) elevated mean monthly maximum soil temperatures at a depth of 50 mm by up to 5.3 °C in summer and 1 °C in winter. Thinning had no effect on forest floor or mineral soil (0–0.30 m) moisture content. In the unthinned treatment an average of 25 kg N•ha−1•year−1 was mineralized, all of which was taken up by the trees, and there was no leaching. Thinning caused a 10% increase in rates of N mineralization and uptake and a small transient increase in soil mineral N concentrations, but had no effect on leaching. Maintenance of prethinning levels of N uptake by the remaining trees (after a 48% reduction in basal area) suggests that uptake per tree was approximately doubled. Maintenance of N uptake after thinning was consistent with maintenance of basal area growth (m2•ha−1) and an increase in foliar N concentrations. Thinning had no effect on extractable P in the forest floor or mineral soil. The retention of residues (NR and HR) decreased mean monthly maximum and elevated mean monthly minimum soil temperatures relative to the ZR treatment, and the effect increased with the amount of residue. Forest floor moisture content increased with the amount of residue, but residue retention had no effect on mineral soil moisture. Rates of mineralization were higher in the presence of residue and annual averages were 28, 33, and 42 kg N•ha−1•year−1 for ZR, NR, and HR treatments, respectively. Despite increased N mineralization in the presence of residue there was no leaching and all the additional N was taken up by the trees. Basal area increment increased in the presence of residue (P = 0.235) and was 10.7 (ZR), 11.1 (NR), and 11.8 (HR) m2•ha−1 over 4 years of measurement.


2020 ◽  
Vol 17 (5) ◽  
pp. 1247-1260
Author(s):  
John Marty Kranabetter ◽  
Ariana Sholinder ◽  
Louise de Montigny

Abstract. Temperate rainforest soils of the Pacific Northwest are often carbon (C) rich and encompass a wide range of fertility, reflecting varying nitrogen (N) and phosphorus (P) availability. Soil resource stoichiometry (C : N : P) may provide an effective measure of site nutrient status and help refine species-dependent patterns in forest productivity across edaphic gradients. We determined mineral soil and forest floor nutrient concentrations across very wet (perhumid) rainforest sites of southwestern Vancouver Island (Canada) and employed soil element ratios as covariates in a long-term planting density trial to test their utility in defining basal area growth response of four conifer species. There were strong positive correlations in mineral soil C, N, and organic P (Po) concentrations and close alignment in C : N and C : Po both among and between substrates. Stand basal area after 5 decades was best reflected by mineral soil and forest floor C : N, but in either case included a significant species–soil interaction. The conifers with ectomycorrhizal fungi had diverging growth responses displaying either competitive (Picea sitchensis) or stress-tolerant (Tsuga heterophylla, Pseudotsuga menziesii) attributes, in contrast to a more generalist response by an arbuscular mycorrhizal tree (Thuja plicata). Despite the consistent patterns in organic matter quality, we found no evidence for increased foliar P concentrations with declining element ratios (C : Po or C : Ptotal) as we did for N. The often high C : Po ratios (as much as 3000) of these soils may reflect a stronger immobilization sink for P than N, which, along with ongoing sorption of PO4-, could limit the utility of C : Po or N : Po to adequately reflect P supply. The dynamics and availability of soil P to trees, particularly as Po, deserves greater attention, as many perhumid rainforests were co-limited by N and P, or, in some stands, possibly P alone.


1994 ◽  
Vol 21 (1) ◽  
pp. 62-66 ◽  
Author(s):  
Richard J. Reader ◽  
Bradlay D. Bricker

A field experiment was conducted to define minimum values of irradiance (i.e. light reaching the forest floor) and exposed mineral soil required for non-forest species to become established in deciduous forest in Southern Canada. Three logging intensities (0%, 33%, and 66%, of tree basal-area removed) were combined with three plot sizes (0.01, 0.05, and 0.20 ha) to create a range of values of irradiance and exposed mineral soil. The total number of non-forest species that became established during the first three years after logging was recorded.Non-forest species invaded experimental plots only when irradiance was at least 8% of incident light. There was no single minimum area of exposed mineral soil required for invasion. A few non-forest species became established even in the absence of exposed mineral soil where penetrating irradiance was 8% or greater. More non-forest species became established as irradiance and the amount of exposed mineral soil increased.Logging increased both irradiance and the amount of exposed mineral soil. Only a small amount of logging (e.g. 33% removal of tree basal-area from a 0.01 ha plot) would be compatible with the conservation objective of preventing invasion by undesirable non-forest species.


Sign in / Sign up

Export Citation Format

Share Document