Leaf Area Index Distribution Research Articles

Sensitivity of a general circulation model to global changes in leaf area index

Methods have recently become available for estimating the amount of leaf area at the surface of the Earth using satellite data. Also available are modeled estimates of what global leaf area patterns would look like should the vegetation be in equilibrium with current local climatic and soil conditions. The differences between the actual vegetation distribution and the potential vegetation distribution may reflect the impact of human activity on the Earth's surface. To examine model sensitivity to changes in leaf area index (LAI), global distributions of maximum LAI were used as surface boundary conditions in the National Center for Atmospheric Research community climate model (NCAR CCM2) coupled with the biosphere atmosphere transfer scheme (BATS). Results from 10‐year ensemble averages for the months of January and July indicate that the largest effects of the decreased LAI in the actual LAI simulation occur in the northern hemisphere winter at high latitudes despite the fact that direct LAI forcing is negligible in these regions at this time of year. This is possibly a result of LAI forcing in the tropics which has long‐ranging effects in the winter of both hemispheres. An assessment of the Asian monsoon region for the month of July shows decreased latent heat flux from the surface, increased surface temperature, and decreased precipitation with the actual LAI distribution. While the statistical significance of the results has not been unambiguously established in these simulations, we suspect that an effect on modeled general circulation dynamics has occurred due to changes of maximum LAI suggesting that further attention needs to be paid to the accurate designation of vegetation parameters. The incorporation of concomitant changes in albedo, vegetation fractional coverage, and roughness length is suggested for further research.

A global land primary productivity and phytogeography model

A global primary productivity and phytogeography model is described. The model represents the biochemical processes of photosynthesis and the dependence of gas exchange on stomatal conductance, which in turn depends on temperature and soil moisture. Canopy conductance controls soil water loss by evapotranspiration. The assignment of nitrogen uptake to leaf layers is proportional to irradiance, and respiration and maximum assimilation rates depend on nitrogen uptake and temperature. Total nitrogen uptake is derived from soil carbon and nitrogen and depends on temperature. The long‐term average annual carbon and hydrological budgets dictate canopy leaf area. Although observations constrain soil carbon and nitrogen, the distribution of vegetation types is not specified by an underlying map. Variables simulated by the model are compared to experimental results. These comparisons extend from biochemical processes to the whole canopy, and the comparisons are favorable for both current and elevated CO2atmospheres. The model is used to simulate the global distributions of leaf area index and annual net primary productivity. These distributions are sufficiently realistic to demonstrate that the model is useful for analyzing vegetation responses to global environmental change.

Canopy structure within a Quercus ilex forested watershed: variations due to location, phenological development, and water availability

Spatial and temporal changes in canopy structure were studied in 1988 and 1989 in a Mediterranean Quercus ilex forest in north-eastern Spain. Due to differences in precipitation patterns the 1989 growing season was drier than the 1988 growing season. Sampling was conducted in parallel at two sites which represent endpoints along a slope gradient within a watershed (ridge top at 975 m, and valley bottom at 700 m). At both sites, similar inter-annual changes in canopy structure were observed in response to differences in water availability. Samples harvested in the upper 50 cm of the canopy during 1989 exhibited a decrease in both average leaf size and the ratio of young to old leaf and stem biomass relative to samples obtained in 1988. At the whole canopy level, a decrease in leaf production efficiency and an increase in the stem to leaf biomass ratio was observed in 1989. Temporal changes in canopy leaf area index (LAI) were not statistically significant. Average LAI values of Q. ilex at the two sites were not significantly different despite differences in tree stature and density (4.6 m2 m−2 at the ridge top, and 5.3 m2 m−2 at the valley bottom). Vertical distribution of leaves and stems within the canopy was very similar at the two locations, with more than 60% of the total LAI in the uppermost metre of the canopy. The possible significance of such an LAI distribution on the canopy carbon budget is discussed.

Forest ecosystem processes at the watershed scale: sensitivity to remotely-sensed Leaf Area Index estimates

Abstract Recent research has shown that general trends in forest leaf area index along regional climatic gradients can be adequately characterized by using ratios of near-infrared and red reflectances. However it has proven difficult to represent properly the spatial distribution of Leaf Area Index (LAI) at sub-regional scales such as small catchments. The key problem at Thematic Mapper scale is the variation in canopy closure and understorey contribution, which dramatically influences near-infrared reflectance from conifer forests, [n this paper, a new spectral index is presented to estimate LAI of conifer forests using a combination of Red, NIR and mid-IR reflectances from the Landsat Thematic Mapper (TM). A simulation system (RHESSys) was used first, to generate potential vegetation patterns around a watershed in order to test them against remotely-sensed vegetation patterns, and secondly, to test the sensitivity of forest ecosystem processes to LAT estimated from combinations of the Thematic Mapper data The relation between Normalised Difference Vegetation Index (NDVI) and LAI is poorly defined at TM scale because of the outsized contribution of understorey vegetation and background materials to the NIR reflectance in open canopies. The mid-IR correction factor acting as a scalar for canopy closure scaled down the inflated NDVI in the open canopies, resulting in an improved relation between NDVI and LAT LAI, estimates from the MIR corrected NDVI better represented the vegetation patterns in Soup Creek watershed than those from uncorrected NDVI both in terms of magnitude and spatial patterns. Simulations using LAIs derived from corrected NDVI showed lower rates evapotranspiration and net photosynthesis. Differences in mean responses of evapotranspiration and photosynthesis were as large as 8cm and 2tonC ha-1 yr-1 respectively between simulation runs using LAIs from corrected and uncorrected NDVI.

Assessing seasonal leaf area dynamics and vertical leaf area distribution in eastern white pine (Pinus strobus L.) with a portable light meter.

We evaluated the ability of a portable light meter (Sunfleck Ceptometer, Decagon Devices, Pullman, WA, USA) to quantify seasonal photosynthetically active radiation (PAR, 400-700 nm) interception, projected stand leaf area index (LAI), and vertical LAI distribution in a 32-year-old eastern white pine (Pinus strobus L.) plantation. Canopy PAR transmittance measured with the ceptometer was converted to LAI with the Beer-Lambert Equation. The ceptometer was sensitive to changes in PAR transmittance resulting from foliage growth. Predicted stand LAI ranged from 3.5 in the dormant season to a maximum of 5.3 in late July. Predicted LAI values were within 9% of values determined from destructive sampling. Published canopy extinction coefficients (k) were inadequate for converting PAR transmittance data to stand LAI because a significant amount of PAR was intercepted by dead branches and stems below the forest canopy. Because of interception by dead branches and stems, we estimated k = 0.84, which is substantially higher than previously reported values. The ceptometer was also sensitive to seasonal changes in PAR transmittance within the canopy. However, in contrast to predictions based on the Beer-Lambert Law, the relationship between proportional PAR transmittance (Q(i)/Q(o)) and cumulative LAI within the canopy was linear. Thus, vertical LAI distribution was best estimated with a linear model, as opposed to the non-linear model assumed in the Beer-Lambert Equation. We hypothesize that the linear relationship was a result of a gap in the canopy which was not represented by the cumulative leaf area distribution estimation procedure.

Vertical distribution of leaf area in Larixoccidentalis: a comparison of two estimation methods

Total leaf-area index and the vertical distribution of leaf-area index were described for an unthinned stand (density 11 250 stems/ha) and a thinned stand (density 1660 stems/ha) of 30-year-old Larixoccidentalis Nutt. Two independent methods were used to estimate leaf-area index in each of the two stands. The first method is based on allometric relationships that are applied to stem measurements, and the second method is based on gap-fraction analysis of fisheye photographs. Leaf-area index estimates obtained by the two methods were not significantly different. The gap-fraction method provides a desirable alternative because much less fieldwork is required, however, use of this method is limited to canopies where the light-blocking elements are randomly displayed. Total leaf-area index values for the unthinned and thinned stands were 5.0 and 3.6, respectively. The vertical distribution of leaf-area index in the unthinned stand resembled a normal distribution. The vertical distribution of leaf-area index in the thinned stand would have resembled a normal distribution, except that thinning operations resulted in a truncated distribution of leaf-area index at the canopy base.

Estimating Oak Leaf Area Index and Gypsy Moth, Lymantria dispar (L.) (Lepidoptera: Lymantriidae), Defoliation Using Canopy Photographs

Oak leaf area index (LAI) was estimated using wide-angle photographs of the forest canopy taken from the ground at grid points throughout three sites on Cape Cod, Mass. Confidence intervals for these estimates and optimal sample sizes were calculated. Oak LAI estimates leveled off by early June when no defoliation was present. Within-plot two-dimensional spatial distribution of oak LAI was very similar to the spatial distribution of oak basal area. Consequently, there was a positive correlation between local oak leaf area and local basal area. Comparison of LAI estimates taken before and after gypsy moth, Lymantria dispar (L.), defoliation allowed the estimation of oak leaf area consumed. Leaf area loss was similar in areas of high and low host foliage densities. The correlation of leaf area lost with local density of early instars was greater than the correlation with the density of late instars.

Influence of krummholz mat microclimate on needle physiology and survival

Microclimate and photosynthesis of krummholz mat growth forms of Picea engelmanii (Parry) and Abies lasiocarpa [Hook.] Nutt. were investigated to determine structural features which may aid survival in alpine environments. The structure of krummholz mats was described in terms of the vertical distribution of leaf area index and leaf area density, which exceeded 50 m-1 (based on total leaf surface area) near the canopy surface and approached zero below 30 cm from the surface in both species. Photosynthetic photon flux density (PPFD, 0.4-0.7 μm wavelengths) and wind decreased by an average of 6 and 50-fold, respectively, between 1 m above and 10 cm below mat surfaces in both species. Needle temperatures on a P. engelmannii krummholz mat during July averaged about 2°C above air temperature during the day, with a maximum overtemperature of greater than 20°C above T air during one sunlit period. At night, needle temperatures averaged 3-4°C below T air.Net photosynthesis in year-old P. engelmannii shoots reached a maximum at 15-20°C during July and August. Surface shoots were light saturated at near 1200 μmoles m-2s-1 PPFD, and had higher photosynthetic rates than subsurface, predominantly shaded shoots above 800 μmoles m-2s-1. Shade shoots had higher photosynthetic rates when PPFD was below 600 μmoles m-2s-1, and at 250 μmoles m-2s-1 shade shoots maintained about 50% of the net photosynthetic rate of sun shoots at light saturation. Shade shoots appeared capable of benefitting photosynthetically from elevated temperatures within krummholz mats despite relatively low light levels. Especially rapid photosynthesis may occur when canopy needles are illuminated by sunflecks and needle temperatures rise by 10° C or more.Snow cover appears crucial for the survival of needles during winter. Snow accumulated within krummholz needle canopies before the sub-canopy zone of unfoliated branches became filled. The concentrated needle growth in the krummholz canopy captured snow in early autumn without support from ground-level snowpack. Early snow cover in both species prevented cuticle abrasion and resulted in high winter needle water contents and viabilities for subsurface compared to surface needles which became abraded, severely dehydrated, and had high mortality between December and February, especially on windward sides of shoots.Extremely high concentrations of needles within krummholz mat canopies created an aerodynamic structure which elevated needle temperatures to more optimal photosynthetic levels in summer and resulted in more efficient snow accumulation in winter. These factors appear crucial for winter needle survival. Thus, krummholz mats appear to be an important adaptation in growth form which provides survival benefits in both summer and winter.

Specific leaf area and leaf area index distribution in a young Douglas-fir plantation

The spatial distribution of specific leaf area and leaf area index of needles in different age classes has been investigated in a young and unthinned Douglas-fir (Pseudotsugamenziesii (Mirb.) Franco) plantation in Central Italy through the destructive analysis of 12 trees sampled in four diameter size classes. Specific leaf area decreased with leaf age and from crown base to apex. A clear interaction between the effects of age and position on specific leaf area was demonstrated. For the whole canopy the vertical distribution of leaf area was well fitted by a normal curve equation, which explained 97% of the variation. The midpoint of the leaf area distribution, estimated as a parameter of the normal curve, was found to be 1.2 m below the mean canopy depth. The standard deviation of leaf area with respect to height was 16.4%. The midpoint of leaf area distribution decreased as leaf age increased and increased as diameter size class increased. Strong and significant linear relationships were found between leaf biomass, leaf area, sapwood area, and diameter at breast height.

Light Distribution in Field Soybean Canopies1

AbstractA study was conducted to determine the pattern of light interception and distribution in a field soybean community. Light interception occurred primarily at the periphery of the canopy. When the open space between rows closed or when it was nearly closed, interception was primarily at the top of the canopy.The distribution of light through a soybean community could be approximated by an exponential distribution. The slope of the regression of the logarithm of percent light interception of leaf area index (LAI) above the point of light measurement was affected by the morphology of the community.From the distribution of percent light and cumulative LAI, an estimate of the “effective” LAI was determined. The large amount of self‐shading and predominant interception at the periphery of the canopy indicates that many lower leaves are not receiving adequate radiation. An increase in yield could possibly be achieved by selecting varieties whose natural inclination leads to deeper penetration of useful energy to a greater number of leaves.