Photosynthetic response of loblolly pine and sweetgum seedling stands to elevated carbon dioxide, water stress, and nitrogen level

1996 ◽  
Vol 26 (1) ◽  
pp. 95-102 ◽  
Author(s):  
J.W. Groninger ◽  
J.R. Seiler ◽  
S.M. Zedaker ◽  
P.C. Berrang
Keyword(s):  
Loblolly Pine ◽  
Light Extinction ◽  
Photosynthetic Response ◽  
Mixed Stands ◽  
Photosynthetic Rates ◽  
Leaf Mass ◽  
Unit Leaf ◽  
Application Rates ◽  
Species Specific ◽  
Individual Seedling

Seedling stands of loblolly pine (Pinustaeda L.) and sweetgum (Liquidambarstyraciflua L.) were grown in monoculture or mixed stands for two growing cycles in controlled-environment chambers. Treatments consisted of ambient (408 ppm) and elevated (806 ppm) CO2, concentrations, water-stressed and well-watered conditions, and low (20 kg N/ha) and high (215 kg N/ha) nitrogen application rates. Photosynthesis rates were measured under ambient and elevated cuvette CO2 concentrations for both whole stands and individual seedlings from these stands. Significant interactions between CO2 and water suggested that elevated CO2 concentration compensated for low water availability in individually measured loblolly pine and in whole seedling stands regardless of stand type. Expressing photosynthesis on a soil area versus a leaf-mass basis influenced the photosynthetic rankings of the three stand types relative to one another. Net photosynthetic rates per unit leaf mass were 390 and 880% higher in individually measured seedlings than in whole monoculture stands for loblolly pine and sweetgum, respectively. Lower photosynthetic contributions from lower canopy leaves in whole seedling stands compared with the upper canopy leaves used in individual-seedling measurements were thought to be responsible for lower photosynthetic rates in seedling stands. These results suggest that photosynthetic response is influenced by canopy dynamics that are unaccounted for by individual-seedling measurements of photosynthesis. Differences in photosynthetic response between loblolly pine and sweetgum stands and individuals are thought to be largely due to species-specific differences in canopy light extinction characteristics.

Effects of elevated CO2, water stress, and nitrogen level on competitive interactions of simulated loblolly pine and sweetgum stands

1995 ◽  
Vol 25 (7) ◽  
pp. 1077-1083 ◽  
Author(s):  
J.W. Groninger ◽  
J.R. Seiler ◽  
S.M. Zedaker ◽  
P.C. Berrang
Keyword(s):  
Loblolly Pine ◽  
Water Availability ◽  
Nitrogen Availability ◽  
Competitive Interactions ◽  
Total Biomass ◽  
Mixed Stands ◽  
Multiple Resources ◽  
Species Response ◽  
Application Rates ◽  
Stand Type

Loblolly pine (Pinustaeda L.) and sweetgum (Liquidambarstyraciflua L.) were grown in mixed stands and in monocultures at 2.54 × 2.54 cm spacing in controlled-environment chambers. Treatments consisted of present (ambient) and projected future (ambient + 400 ppm) carbon dioxide (CO2) concentrations, drought-stressed, and well-watered conditions, and low (20 kg N/ha) and high (474 kg N/ha) nitrogen application rates. After two accelerated growing cycles, total biomass of both species was significantly greater under elevated CO2. No significant interactions between CO2 concentration and water availability, nitrogen availability, or stand type were observed. Competitive interactions between loblolly pine and sweetgum were strongly influenced by water availability, but not CO2 concentration. Assessment of species response to CO2 was dependent upon growth in monoculture or mixture. Under low water availability, data from monocultures suggested that sweetgum had a stronger growth response to elevated CO2 concentrations than loblolly pine. In contrast, results from mixed-species stands showed that the competitive status of loblolly pine and sweetgum did not change under the high CO2 concentration. These results underscore the value of growing co-occurring species in mixed stands under varying levels of multiple resources for the determination of relative performance under future environments.

Impact of Deer Browsing on Regeneration in Mixed Stands in Southern New England

1995 ◽  
Vol 12 (3) ◽  
pp. 115-120 ◽  
Author(s):  
David B. Kittredge ◽  
P. Mark S. Ashton
Keyword(s):  
New England ◽  
Tree Species ◽  
Sugar Maple ◽  
Red Maple ◽  
White Pine ◽  
Mixed Stands ◽  
Tree Species Composition ◽  
Southern New England ◽  
Pine Seedlings ◽  
Species Specific

Abstract Browsing preferences by white-tailed deer were evaluated for 6 tree species in northeastern Connecticut. Deer density averaged 23/mile². Deer exhibited no species-specific preferences for seedlings greater than 19 in. For seedlings less than 19 in., hemlock and black birch were preferred. Red maple, sugar maple, and white pine seedlings were avoided. Red oak seedlings were neither preferred nor avoided. A much higher proportion of seedlings greater than 19.7 in. in height was browsed, regardless of species. Browsing preferences for species in the smaller seedling class, combined with a lack of preference for species in the larger class may result in future stands with less diverse tree species composition. Deer densities in excess of 23/mile² may be incompatible with regeneration of diverse forests in southern New England. North. J. Appl. For. 12(3):115-120.

scholarly journals Effect of Radiation and Temperature on Cranberry Photosynthesis and Characterization of Diurnal Change in Photosynthesis

2004 ◽  
Vol 129 (1) ◽  
pp. 106-111 ◽  
Author(s):  
S. Kumudini
Keyword(s):  
Net Photosynthesis ◽  
Vaccinium Macrocarpon ◽  
Controlled Environment ◽  
Photosynthetic Response ◽  
Radiation Level ◽  
Photosynthetic Rates ◽  
Air Temperatures ◽  
Predicted Values ◽  
The Impact

Cranberry [Vaccinium macrocarpon (Ait.)] yield has been associated with photosynthate supply. However, the impact of temperature and radiation on photosynthesis of the cranberry plant is not well understood. The objective of this experiment was to characterize the photosynthetic response to radiation and temperature in order to develop a model for estimation of cranberry photosynthetic rates. Two cranberry cultivars, `Stevens' and `Ben Lear', were tested for photosynthetic response at air temperatures ranging from 15 to 35 °C and radiation intensities from 200 to 1200 μmol·m-2·s-1. Depending on temperature, maximum photosynthesis (Pmax) was ≈10 or 12 μmol CO2/m2/s (net photosynthesis) and the saturating radiation level was estimated to be 600 to 800 μmol·m-2·s-1. Cranberry quantum yield was estimated as 0.03 mol CO2/mol photon. Both models; Blackman and the nonrectangular hyperbola with a Θ (angle of curvature) of 0.99 were a good fit for measured photosynthetic rates under controlled environment conditions. The disparity between modeled predicted values, and observed values in the field around midday, indicates a reduction in potential photosynthetic rates in a diurnal cycle that is consistent with the phenomenon of midday depression.

Photosynthesis and physiological traits of evergreen broadleafed saplings during winter under different light environments in a temperate forest

2006 ◽  
Vol 84 (1) ◽  
pp. 60-69 ◽  
Author(s):  
Yoshiyuki Miyazawa ◽  
Kihachiro Kikuzawa
Keyword(s):  
Temperate Forest ◽  
Light Availability ◽  
Net Photosynthesis ◽  
Carbon Gain ◽  
Leaf Mass Per Area ◽  
Camellia Japonica ◽  
Leaf Mass ◽  
Unit Leaf ◽  
Canopy Trees ◽  
Photosynthetic Traits

Photosynthetic traits of the evergreen broadleafed species Camellia japonica L. and Quercus glauca Thunb. were continuously investigated during autumn and winter using saplings that grew in different light environments (gap, deciduous canopy understory, and evergreen canopy understory) in a temperate forest. Light-saturated rates of net photosynthesis in midwinter and spring were lower than those in autumn. Photosynthetic capacity, scaled to a common leaf temperature of 25 °C, increased or remained stable after autumn and then decreased in spring in most leaves. Photosynthetic traits per unit leaf area were different among leaves in different light environments of both Camellia and Quercus during most periods. However, photosynthetic traits per unit leaf mass did not differ among leaves in different light environments, suggesting that differences in photosynthetic traits were mainly due to different leaf mass per area among leaves. Photosynthetic rates under light availability typical in the environment were lower in winter than in autumn in leaves in the sun in a gap but were not different in leaves in the shade under evergreen canopy trees. Thus, the importance of winter carbon gain for annual carbon gain is small in leaves in a gap but is large in leaves under evergreen canopy trees.

scholarly journals Use of Species-specific Controlled-release Fertilizer Rates to Manage Growth and Quality of Container Nursery Crops

2015 ◽  
Vol 25 (3) ◽  
pp. 370-379 ◽  
Author(s):  
Mary Jane Clark ◽  
Youbin Zheng
Keyword(s):  
Controlled Release ◽  
Growth Index ◽  
Dry Weight ◽  
Temperate Climate ◽  
Controlled Release Fertilizer ◽  
Shoot Dry Weight ◽  
Application Rates ◽  
Nursery Crops ◽  
Species Specific

The objective of this study was to determine the optimal controlled-release fertilizer (CRF) application rates or ranges for the production of five 2-gal nursery crops. Plants were evaluated following fertilization with 19N–2.6P–10.8K plus minors, 8–9 month CRF incorporated at 0.15, 0.45, 0.75, 1.05, 1.35, and 1.65 kg·m−3 nitrogen (N). The five crops tested were bigleaf hydrangea (Hydrangea macrophylla), ‘Green Velvet’ boxwood (Buxus ×), ‘Magic Carpet’ spirea (Spiraea japonica), ‘Palace Purple’ coral bells (Heuchera micrantha), and rose of sharon (Hibiscus syriacus). Most plant growth characteristics (i.e., growth index, plant height, leaf area, and shoot dry weight) were greater in high vs. low CRF treatments at the final harvest. Low CRF rates negatively impacted overall appearance and marketability. The species-specific CRF range recommendations were 1.05 to 1.35 kg·m−3 N for rose of sharon, 0.75 to 1.05 kg·m−3 N for ‘Magic Carpet’ spirea, and 0.75 to 1.35 kg·m−3 N for bigleaf hydrangea and ‘Green Velvet’ boxwood, whereas the recommended CRF rate for ‘Palace Purple’ coral bells was 0.75 kg·m−3 N. Overall, species-specific CRF application rates can be used to manage growth and quality of containerized nursery crops during production in a temperate climate.

Terrestrial vegetation monitoring at Cape Hatteras National Seashore: 2019 data summary

2022 ◽  
Author(s):  
Maxwell Boyle ◽  
Elizabeth Rico
Keyword(s):  
North Carolina ◽  
Loblolly Pine ◽  
Terrestrial Vegetation ◽  
Vegetation Monitoring ◽  
The North ◽  
Cape Hatteras ◽  
Monitoring Effort ◽  
Cape Hatteras National Seashore ◽  
Species Specific ◽  
National Seashore

The Southeast Coast Network (SECN) conducts long-term terrestrial vegetation monitoring as part of the nationwide Inventory and Monitoring Program of the National Park Service (NPS). The vegetation community vital sign is one of the primary-tier resources identified by SECN park managers, and monitoring is currently conducted at 15 network parks (DeVivo et al. 2008). Monitoring plants and their associated communities over time allows for targeted understanding of ecosystems within the SECN geography, which provides managers information about the degree of change within their parks’ natural vegetation. The first year of conducting this monitoring effort at four SECN parks, including 52 plots on Cape Hatteras National Seashore (CAHA), was 2019. Twelve vegetation plots were established at Cape Hatteras NS in July and August. Data collected in each plot included species richness across multiple spatial scales, species-specific cover and constancy, species-specific woody stem seedling/sapling counts and adult tree (greater than 10 centimeters [3.9 inches {in}]) diameter at breast height (DBH), overall tree health, landform, soil, observed disturbance, and woody biomass (i.e., fuel load) estimates. This report summarizes the baseline (year 1) terrestrial vegetation data collected at Cape Hatteras National Seashore in 2019. Data were stratified across four dominant broadly defined habitats within the park (Maritime Tidal Wetlands, Maritime Nontidal Wetlands, Maritime Open Uplands, and Maritime Upland Forests and Shrublands) and four land parcels (Bodie Island, Buxton, Hatteras Island, and Ocracoke Island). Noteworthy findings include: A total of 265 vascular plant taxa (species or lower) were observed across 52 vegetation plots, including 13 species not previously documented within the park. The most frequently encountered species in each broadly defined habitat included: Maritime Tidal Wetlands: saltmeadow cordgrass Spartina patens), swallow-wort (Pattalias palustre), and marsh fimbry (Fimbristylis castanea) Maritime Nontidal Wetlands: common wax-myrtle (Morella cerifera), saltmeadow cordgrass, eastern poison ivy (Toxicodendron radicans var. radicans), and saw greenbriar (Smilax bona-nox) Maritime Open Uplands: sea oats (Uniola paniculata), dune camphorweed (Heterotheca subaxillaris), and seabeach evening-primrose (Oenothera humifusa) Maritime Upland Forests and Shrublands: : loblolly pine (Pinus taeda), southern/eastern red cedar (Juniperus silicicola + virginiana), common wax-myrtle, and live oak (Quercus virginiana). Five invasive species identified as either a Severe Threat (Rank 1) or Significant Threat (Rank 2) to native plants by the North Carolina Native Plant Society (Buchanan 2010) were found during this monitoring effort. These species (and their overall frequency of occurrence within all plots) included: alligatorweed (Alternanthera philoxeroides; 2%), Japanese honeysuckle (Lonicera japonica; 10%), Japanese stilt-grass (Microstegium vimineum; 2%), European common reed (Phragmites australis; 8%), and common chickweed (Stellaria media; 2%). Eighteen rare species tracked by the North Carolina Natural Heritage Program (Robinson 2018) were found during this monitoring effort, including two species—cypress panicgrass (Dichanthelium caerulescens) and Gulf Coast spikerush (Eleocharis cellulosa)—listed as State Endangered by the Plant Conservation Program of the North Carolina Department of Agriculture and Consumer Services (NCPCP 2010). Southern/eastern red cedar was a dominant species within the tree stratum of both Maritime Nontidal Wetland and Maritime Upland Forest and Shrubland habitat types. Other dominant tree species within CAHA forests included loblolly pine, live oak, and Darlington oak (Quercus hemisphaerica). One hundred percent of the live swamp bay (Persea palustris) trees measured in these plots were experiencing declining vigor and observed with symptoms like those caused by laurel wilt......less

scholarly journals The influence of competition and species mixture on plantation-grown white spruce: Growth and foliar nutrient response after 20 years

2014 ◽  
Vol 90 (01) ◽  
pp. 70-79 ◽  
Author(s):  
Breanne A. Neufeld ◽  
Dave M. Morris ◽  
Nancy Luckai ◽  
Douglas E.B. Reid ◽  
F. Wayne Bell ◽  
...  
Keyword(s):  
Chemical Properties ◽  
Basal Area ◽  
White Spruce ◽  
Mixed Stands ◽  
Density Control ◽  
Foliar Nutrient ◽  
Thinning Operations ◽  
Species Specific ◽  
Foliar Sampling ◽  
Physical And Chemical

A 20-year-old experimental white spruce plantation was used to identify key stand (neighbourhood competition) and soil (physical and chemical properties) factors influencing spruce growth (Periodic Basal Area Increment) and foliar nutrients. Total and species-specific competition was estimated using Hegyi’s distance-dependent index for 39 individual spruce trees. Twelve trees, covering the range of total HCI (2 to 8) and aspen competition (0% to >75%), were selected for repeated (May through October) foliar sampling. Spruce PBAI declined approximately 10% for each additional unit of total HCI; species did not significantly affect this decline. Increasing aspen presence significantly influenced spruce foliar N (1.17% to 1.31%), P (0.15% to 0.23%), and K (0.68% to 0.88%), but led to declines in Ca (0.81% to 0.48%). Multiple linear regression indicated that soil carbon (partial r2 = 0.386) and available soil moisture (partial r2 = 0.131) together explained more of the variation in spruce growth than did competition factors alone (partial r2 = 0.251). The results suggest that, at this stage of stand development, precommercial thinning operations should focus on density control and inter-tree spacing, while retaining an aspen component resulting in well-spaced, free-growing mixed stands of white spruce and aspen.

Reexamining the empirical relation between plant growth and leaf photosynthesis

2006 ◽  
Vol 33 (5) ◽  
pp. 421 ◽  
Author(s):  
Eric L. Kruger ◽  
John C. Volin
Keyword(s):  
Gas Exchange ◽  
Plant Growth ◽  
Leaf Area ◽  
Leaf Gas Exchange ◽  
Empirical Relation ◽  
Leaf Photosynthesis ◽  
Unit Leaf Area ◽  
Leaf Mass ◽  
Unit Leaf ◽  
Growth Variation

Technological advances during the past several decades have greatly enhanced our ability to measure leaf photosynthesis virtually anywhere and under any condition. Associated with the resulting proliferation of gas-exchange data is a lingering uncertainty regarding the importance of such measurements when it comes to explaining intrinsic causes of plant growth variation. Accordingly, in this paper we rely on a compilation of data to address the following questions: from both statistical and mechanistic standpoints, how closely does plant growth correlate with measures of leaf photosynthesis? Moreover, in this context, does the importance of leaf photosynthesis as an explanatory variable differ among growth light environments? Across a wide array of species and environments, relative growth rate (RGR) was positively correlated with daily integrals of photosynthesis expressed per unit leaf area (Aarea), leaf mass (Amass), and plant mass (Aplant). The amount of RGR variation explained by these relationships increased from 36% for the former to 93% for the latter. Notably, there was close agreement between observed RGR and that estimated from Aplant after adjustment for theoretical costs of tissue construction. Overall, based on an analysis of growth response coefficients (GRCs), gross assimilation rate (GAR), a photosynthesis-based estimate of biomass gain per unit leaf area, explained about as much growth variation as did leaf mass ratio (LMR) and specific leaf area (SLA). Further analysis of GRCs indicated that the importance of GAR in explaining growth variation increased with increasing light intensity. Clearly, when considered in combination with other key determinants, appropriate measures of leaf gas exchange effectively capture the fundamental role of leaf photosynthesis in plant growth variation.

Diel patterns of leaf carbohydrate concentrations differ between seedlings and mature trees of two sympatric oak species

Botany ◽  
2014 ◽  
Vol 92 (7) ◽  
pp. 535-540 ◽  
Author(s):  
Ori Baber ◽  
Martijn Slot ◽  
Gerardo Celis ◽  
Kaoru Kitajima
Keyword(s):  
Gas Exchange ◽  
Carbon Balance ◽  
Leaf Gas Exchange ◽  
Sun Exposure ◽  
Fundamental Aspect ◽  
Sink Strength ◽  
Mature Trees ◽  
Leaf Mass ◽  
Diel Patterns ◽  
Unit Leaf

A fundamental aspect of the carbon cycle is the exchange of carbon between plants and the atmosphere. It is, therefore, important to understand factors that affect differences in gas exchange and carbon balance within and among species. Concentrations of nonstructural carbohydrates are often used as a proxy for carbon balance. We determined diel patterns of leaf carbohydrate concentrations in relation to irradiance (sun vs. shade) in seedlings and mature trees of two sympatric oak species (Quercus virginiana Mill. and Quercus hemisphaerica Bartram ex Willd.). For seedlings, we also measured leaf gas exchange. Higher sun exposure significantly increased photosynthesis and carbohydrate concentrations in both species. Carbohydrate concentrations of seedling leaves showed strong diel fluctuations, whereas concentrations in mature tree leaves did not. This contrast might be attributed to faster carbohydrate export from leaves of mature trees. The difference in sink strength between seedlings and adults may be related to the decreasing ratio of leaf mass to plant mass with ontogeny, increasing the demand for carbohydrates per unit leaf mass. Seedlings and mature trees are clearly functionally different and care must be taken when extrapolating results from seedling experiments to mature trees.

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