Biomass equations are a helpful tool to estimate the tree and stand biomass production and standing stock. Such estimations are of great interest for science but also of great importance for global reports on the carbon cycle and the global climate system. Even though there are various collections and generic meta-analyses available with biomass equations for mature trees, reports on biomass equations for juvenile trees (seedlings and saplings) are mainly missing. Against the background of an increasing amount of reforestation and afforestation projects and forests in young successional stages, such equations are required. In this study we have collected data from various studies on the aboveground woody biomass of 19 common tree species growing in Europe. The aim of this paper was to calculate species-specific biomass equations for the aboveground woody biomass of single trees in dependence of root-collar-diameter (RCD), height (H) and the combination of the two (RCD2 H). Next to calculating species-specific biomass equations for the species available in the dataset, we also calculated generic biomass equations for all broadleaved species and all conifer species. The biomass equations should be a contribution to the pool of published biomass equations, whereas the novelty is here that the equations were exclusively derived for young trees

A method for computing leaf area of isolated trees from perspective photographs was developed. The method is based on gap fraction inversion. Photographs are discretized into picture zones where gap fraction is computed from image processing. Canopy volume and leaf area density associated with each picture zone are computed from geometrical considerations and inversion of gap fraction equations. Total leaf area and the vertical profile of leaf area are computed from the product of associated volume and its density. The method has been implemented in software called Tree Analyser, written in C++. The method has been tested by comparison with direct estimation of leaf area of three-dimensional (3D) digitized trees of walnut, peach, mango, olive and rubber. Estimated leaf area was sensitive to picture discretization, individual leaf size and leaf inclination distribution. Optimal size of picture discretization was 17 times projected leaf size. Total leaf area was estimated by using a set of eight photographs taken around the tree in the main horizontal directions: deviation ranged from -11% in peach tree to +5% in rubber tree. The method allows fast and nondestructive monitoring of leaf area of individual tree canopies. The next version of the method will include the estimation of 3D leaf area distribution within the canopy.

No abstract

Rubber plantations have rapidly replaced natural forests (NFs) in Mainland Southeast Asia, yet the relevant impacts on the terrestrial carbon cycle remain uncertain especially with an increase in drought frequency. Our study compared eddy‐covariance measurements of carbon and water fluxes from two rubber monoculture plantations (at a northern marginal site and a southern traditional plantation site) with a second‐growth NF between 2015 and 2018, and their responses to a prolonged drought during 2015/2016. The NF had higher light use efficiency, water use efficiency and gross primary productivity (GPP, 2.94 ± 0.41 kg C m−2 yr−1) than the northern rubber (NR) monoculture (2.45 ± 0.17 kg C m−2 yr−1), while lower ecosystem carbon use efficiency (eCUE) caused a lower net ecosystem productivity (NEP, 0.75 ± 0.25 kg C m−2 yr−1) compared to the plantation (1.19 ± 0.22 kg C m−2 yr−1). Drought decreased the NF eCUE by 23% with significant carbon uptake restrictions across multiple seasons, while the rubber GPP reduction was only substantial in the warm‐dry season with an overall 17% decline in eCUE. The NR site's GPP was mainly controlled by soil water content throughout the year. Higher light availability offset the negative effect of drier conditions on the rubber GPP, resulting in larger carbon uptake compared to the southern plantation (GPP, 2.12 ± 0.12 kg C m−2 yr−1; NEP, 1.07 ± 0.14 kg C m−2 yr−1). In contrast, the NF GPP was mainly restricted by vapor pressure deficit, especially during the drought.

Rubber trees (Hevea brasiliensis) are the main source of natural rubber, extracted from latex, which exudes from the trunk after tapping. Tapped trees require large amounts of carbon (C) to regenerate the latex after its collection. Knowing the contribution of C sources involved in latex biosynthesis will help in understanding how rubber trees face this additional C demand. Whole crown 13CO2 pulse labelling was performed on 4-year-old rubber trees in June, when latex production was low, and in October, when it was high. 13C content was quantified in the foliage, phloem sap, wood, and latex. In both labelling periods, 13C was recovered in latex just after labelling, indicating that part of the carbohydrate was directly allocated to latex. However, significant amounts of 13C were still recovered in latex after 100 d and the peak was reached significantly later than in phloem sap, demonstrating the contribution of a reserve pool as a source of latex C. The contribution of new photosynthates to latex regeneration was faster and higher when latex metabolism was well established, in October, than in June. An improved understanding of C dynamics and the source–sink relationship in rubber tree is crucial to adapt tapping system practices and ensure sustainable latex production.