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Growth of Eucalyptus pellita in mixed species and monoculture plantations (2007)
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@MISC{Bristow07growthof,
author = {Mila Bristow},
title = {Growth of Eucalyptus pellita in mixed species and monoculture plantations},
year = {2007}
}
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Abstract
Eucalyptus pellita is a commercially important plantation hardwood species for the humid tropics of north Queensland. This species is favoured by both small-scale growers for use in mixed species woodlots targeting low-volume high-value sawn timber, and also by industrial forest companies growing monocultures for integrated pulp – sawn timber regimes. This study investigated whether mixed-species designs can increase the growth of this tropical eucalypt when compared to monocultures. A replacement series experiment with monocultures of Eucalyptus pellita (E) and Acacia peregrina (A) and mixtures in various proportions (75E:25A, 50E:50A, 25E:75A) was used to examine questions about growth and productivity. The trial was located on the Atherton Tablelands of north Queensland, Australia. High mortality in the establishment phase due to repeated damage by tropical cyclones altered the trial design. Effects of experimental designs on tree growth were estimated using a linear mixed effects model with restricted maximum likelihood analysis (REML). Volume growth of individual eucalypt trees were positively affected by the presence of acacia trees at age five years and this effect generally increased with time up to age 10 years. However, the stand volume and basal area increased with increasing proportions of E. pellita, due to its larger individual tree size. Conventional analysis did not offer convincing support for mixed-species designs. Preliminary individual-based modelling using a modified Hegyi competition index offered a solution and an equation that indicates acacias have positive ecological interactions (facilitation or competitive reduction), and definitely do not cause competition like E. pellita. These results suggest that significantly increased growth rates could be achieved with mixed-species designs over E. pellita monocultures. This statistical methodology could enable a better understanding of species interactions in similarly altered experiments, or undesigned mixed-species plantations. The effects of trees on soils are highly variable and highly site and species specific. That trees can change soil chemistry over time is well established. The soil chemical properties under the eucalypt: acacia experiment were compared to several potential baseline data sources: the reference description of this soil type; those measured at 7 months after planting; and with those of soils under two adjacent vegetation types (forest and pasture) when the experiment was aged 9 years. At 9 years after planting soil total nitrogen increased with increasing proportion of acacias in the treatment. The mean total N under the acacia monoculture was significantly higher (P = 0.041) than that of either the eucalypt monoculture, or the surrounding pasture. The proportion of acacia in the treatment was positively linearly correlated with soil total N (r2 = 0.46; P = 0.018). Soils under the eucalypt monocultures were more similar to those under pasture for a range of soil chemical properties, compared with soils under treatments containing acacias. Results from this site show that the two species alter the soil chemistry in different ways. It is possible that the increased total N under the acacias could be facilitating the growth of the E. pellita, however without n-fixation analysis or tissue sampling it is not possible to confirm that the eucalypt is using the N. Similar cause and effect (or ‘supply and use’) questions also remain for soil pH and available phosphorus changes with increasing acacia in treatment. This study also demonstrates the difficulty in monitoring changes in soil properties over long cycles of forest plantations. The photosynthetic response to light was assessed in the stratified canopy of the mixed species field trial of the eucalypt: acacia experiment, and among commonly planted taxa of E. pellita in glasshouse pot trials. In the field trial photosynthetic capacity of fully expanded sun and shade leaves of both species was measured. E. pellita has a wide natural distribution with considerable variation in morphology and growth within the species, with several provenances commonly planted in north Queensland. Photosynthetic capacity and leaf nutrient content of three of these taxa (two from northern occurrences and one from southern occurrences of E. pellita) were measured on two occasions in glasshouse pot trials. A non rectangular hyperbolic function was used to describe the light response curves, and analysis of variance was used to determine differences in the biologically relevant curve parameters between treatments. In the field trial sun and shade leaves of E. pellita produced similar light saturated photosynthetic rates, and experienced little competition for light from the acacia crowns. In contrast there was significant variation in the photosynthetic response between acacia sun and shade leaves. In the glasshouse trials, differences in leaf and petiole morphology were observed, which were coupled with differences in leaf nutrient content and highly significant variation in light saturated photosynthetic rate between the three taxa. This study characterised the light response of E. pellita and suggests that differences in physiological responses to resource availability should be expected among taxa within this species, which may be important for forest productivity models which endeavour to predict tree growth and resource use. An empirical model of growth of E. pellita from a designed monocultures vs. mixed species experiment has been used to explore system behaviour rather than predict production of this species from specific forests. This approach has allowed examination of the effect of plantation design on competition, soil nutrient pool change with time and physiological responses to light; leading to a greater understanding of why mixtures can lead to greater productivity than monocultures.
Keyphrases
eucalyptus pellita mixed specie monoculture plantation mixed-species design north queensland shade leaf photosynthetic response leaf nutrient content soil chemistry glasshouse pot trial eucalypt monoculture acacia experiment soil chemical property physiological response tree growth significant variation photosynthetic rate field trial sun relevant curve parameter humid tropic establishment phase individual tree size site show light response hegyi competition index acacia tree long cycle surrounding pasture industrial forest company statistical methodology similar light soil property several provenance soil nutrient pool change growth rate resource use non rectangular hyperbolic function altered experiment restricted maximum likelihood analysis soil total nitrogen soil type mixed specie experiment productivity model mixed specie field trial light response curve tropical eucalypt integrated pulp sawn timber regime stratified canopy replacement series experiment southern occurrence available phosphorus change atherton tableland wide natural distribution reference description linear mixed effect positive ecological interaction pellita monoculture experimental design adjacent vegetation type undesigned mixed-species plantation trial design tropical cyclone important plantation hardwood specie photosynthetic capacity small-scale grower soil total conventional analysis different way northern occurrence n-fixation analysis petiole morphology acacia peregrina acacia sun empirical model plantation design stand volume similar cause basal area individual eucalypt tree various proportion preliminary individual-based modelling several potential baseline data source predict production soil ph little competition acacia monoculture acacia crown specific forest specie interaction high mortality monitoring change field trial photosynthetic capacity low-volume high-value sawn timber considerable variation volume growth competitive reduction glasshouse trial mean total
