Dynamics of nonstructural carbohydrates and biomass yield in a fodder legume tree at different harvest intensities

Tropical tree fodder is harvested by frequent prunings, and resprouting depends on nonstructural carbohydrate reserves in the remaining tree parts. We studied the effects of three pruning intensities (removal of all leaves and branches leaving 1 m of stem once a year (T-12), or every 6 months (T-6), and about 50% pruning every 2 months (P-2)) on regrowth and the dynamics of soluble sugars and starch in the legume tree Gliricidia sepium (Jacq.) Walp. growing under humid tropical conditions in Guadeloupe, Lesser Antilles. Carbohydrates were sampled in roots, stems and branches. Among pruned trees, trees in the T-6 harvest regime had the highest leaf fodder yield (0.73 kg tree(-1) year(-1)). High litter loss reduced leaf yield of T-12 trees, but compared with the other treatments, T-12 trees produced the most branch biomass (3.43 kg tree(-1)). Among treatments, P-2 trees had an intermediate leaf fodder yield and the lowest branch production. Sucrose, glucose and fructose were the most common sugars in all biomass compartments. Mannose, pinitol and an unidentified cyclitol were relatively abundant in branches. Root sugar and starch concentrations were unaffected by harvest regime. There was a significant interactive effect of harvest intensity and regrowth time on stem sugar concentration. Stem starch concentration was highest in T-12 trees. After a year of fodder harvesting, whole-tree reserves of nonstructural carbohydrates were highest in T-12 trees; however, a larger proportion of reserves were located in roots and stems of T-6 and P-2 trees. These reserves, which were not lost in pruning and contributed to regrowth of G. sepium after pruning, may explain the relatively small effects of harvesting regime on soluble sugar and starch concentrations.     

Dynamics of non-structural carbohydrate reserves in pruned <Emphasis Type="Italic">Erythrina poeppigiana</Emphasis> and <Emphasis Type="Italic">Gliricidia sepium</Emphasis> trees

In alley cropping systems, fast growing leguminous trees are pruned to reduce competition with crops for light and to provide organic inputs for crop nutrition. Tree regrowth depends on non-structural carbohydrate reserves in the remaining tree parts. In this study, the dynamics of starch and soluble carbohydrates in roots and stems of completely pruned (all shoots removed), partially pruned (one branch retained on the pruned stump) and unpruned Erythrina poeppigiana (Walp.) O.F. Cook and Gliricidia sepium (Jacq.) Kunth ex Walp. trees were studied under humid tropical conditions in Turrialba, Costa Rica. Measurements on starch and soluble carbohydrates in roots and stems were made at 0, 2, 6 and 12 weeks after pruning during both a “rainy” and a “dry” season. In general, the dynamics of non-structural carbohydrates in roots and stems of pruned E. poeppigiana and G. sepium trees were similar. Starch concentration was highest in unpruned trees and higher in roots than in stems of pruned trees. The effect of pruning intensity was first observed in stems, and starch reserves were more depleted in stems than in roots, an effect more evident during the “dry” season. The critical tree regrowth stage for starch mobilisation was that of vigorous sprout development at six or four weeks after pruning particularly in completely pruned trees. At this time, fine root biomass and length and nodule biomass in pruned trees decreased. Survival of fine roots and nodules was greater in partially pruned than in completely pruned trees. Starch accumulation in roots recommenced at 12 weeks after pruning in G. sepium, and later than 12 weeks after pruning in E. poeppigiana roots. This study showed that E. poeppigiana responded better to pruning regimes than G. sepium. Recovery of trees after pruning is better when trees are partially pruned than when completely pruned.     

Biomass allocation and nodulation of Gliricidia sepium under two cut-and-carry forage production regimes

The effects of two pruning regimes on the above-ground biomass allocation and nodulation of Gliricidia sepium (Jacq.) Walp. (Leguminosae: Robinieae) were studied in a cut-and-carry forage production system under humid tropical conditions in Guadeloupe, French Antilles. The grass layer composed of a mixture dominated by Paspalum notatum Flügge (80%) and Digitaria decumbens Stent. The pruning regimes were partial pruning (ca. 50%) every two months and complete pruning every six months. The complete pruning caused an almost complete turnover of N2 fixing nodules. The nodule biomass decreased after the partial pruning, but the turnover was not complete. The nodule to foliage biomass ratio followed the same pattern under both treatments, and the values of the ratio converged towards the end of the experimental period. The maxima of standing nodule biomass were 7.2 and 13.0 kg ha−1 in the partially and completely pruned trees, respectively. The cumulative leaf fodder harvest was higher under partial pruning management, due to smaller litter loss. The branch biomass production was higher under complete pruning management. Grass production was not affected by the pruning pattern of G. sepium. It was concluded that the partial pruning management produces more fodder in the studied association, and the nodulation probably adjusts to the canopy N requirements. The potential N release to soil in the turnover of nodules of G. sepium (max. 0.82 kg ha−1) is negligible compared to the N export in tree and grass fodder harvest, 190 and 215 kg ha−1 in partially and completely pruned plots, respectively. This revised version was published online in June 2006 with corrections to the Cover Date.     

Effect of pruning on branch production and water relations in widely spaced ponderosa pines

This study dealt with the effects of pruning on branch and leaf area (F _a) production of ponderosa pines growing in silvopastoral systems in Patagonia. We hypothesized that pruning positively influences the number of branches per whorl and their basal area growth rate, changing F _a production. In addition, we studied some water relations in order to explain potential differences in branch growth rates between treatments. Two mathematical models were developed to estimate branch and total F _a. The averaged diameter at the third year of pruning was, for high-pruned trees 3.1 and 3.6 cm at the bottom and middle of the crown, against 4 and 4.4 cm for low-pruned trees. Pruning did not produce changes in the number of branches per whorl (approximately 7.6 branches per whorl). Water stress may be responsible of this lower branch growth in pruned trees. Water potential, stomatal conductance and transpiration were lower in high- than in low-pruned trees.     

Effect of pruning on nitrogen dynamics within crowns of Pinus radiata

Stem injection of (15)N-labeled ammonium sulfate was used to determine effects of pruning on canopy nitrogen dynamics in open-grown Pinus radiata D. Don in New Zealand. Trees were planted in July 1990 and the isotope introduced in December 1994. Tree crowns were divided into three zones: base section, from which branches of pruned trees were removed; mid section, between the pruned zone and the height of the trees at the start of the year in which they were pruned; and top section, which grew predominantly after the isotope was applied. Pruning removed 32% of the green crown length, representing 75% of foliage biomass. Needles were sampled from each region of the crown until July 1996. Branch growth was used to predict foliage biomass for each sampling occasion. Approximately 45% of the applied isotope was recovered from needles sampled in December 1994 (1 week after application and immediately before pruning), two-thirds of which occurred in needles in the base section. Thereafter, changes in isotope content of needles in the base section of unpruned trees largely reflected foliage biomass fluctuations and dilution of the isotope by continued uptake from the unlabeled soil nitrogen pool. Recovery of isotope in needles from the mid-crown section increased by 58 and 86% from December 1994 to July 1995 in control and pruned trees, respectively. Within this crown section, there was evidence of isotope translocation from old to new needles, with both isotope dilution and efflux observed in the needle cohorts that had been present at the time the isotope was applied. Therefore, isotope dynamics did not reflect the dynamics of the total nitrogen pool in the mid-crown section. By July 1996, a small proportion of the applied isotope was recovered from the new foliage formed in the top section of the crown. Within the top section, isotope dynamics closely matched total nitrogen fluxes. Pruning the lower crown did not affect nitrogen dynamics elsewhere in the crown for the following 18 months.     

Root growth and carbohydrate responses in bearing citrus trees following partial canopy removal

In August, eight 4-m tall citrus trees were pruned by removing the top third of their canopy. Eight unpruned trees served as controls. Root growth, which was examined nondestructively with minirhizotrons over a four-month period, tended to be less in the pruned than unpruned trees seven days after pruning and this difference was significant (P < 0.05) from 14 to 49 days after pruning. Total reducing and ketone sugars (includes free fructose, sucrose and fructans) in the fine roots were less in pruned than unpruned trees 20 days after pruning, but not thereafter. By 30 days after pruning, at least 20% of the roots of the pruned trees at a soil depth of 9 to 35 cm apparently died. By 63 days after pruning, root length density had recovered to that of the unpruned trees, although starch reserves were 18% less in the fine roots of pruned than unpruned trees at this time. Nine to eleven months after pruning (May to July), total biomass of leaves and fine roots to a depth of 1 m were similar in pruned and unpruned trees. However, fruit biomass harvested in April from pruned trees was only 24% of that in the unpruned trees. In May, nonstructural carbohydrates in the fine and coarse roots of pruned trees were generally greater than in unpruned trees, possibly reflecting previous differences in fruit production.     

Effects of pruning on radial growth and biomass increment of trees growing in homegardens of Kerala, India

To evaluate the effects of pruning on stem radial growth increment and leaf and twig biomass production, an experiment with four pruning intensities (0, 50, 75 and 90%) on ten locally important tree species (Ailanthus triphysa, Albizia odoratissima, Artocarpus hirsutus, Bombax malabarica, Bridelia crenulata, Erythrina indica, Grewia tiliifolia, Macaranga peltata, Terminalia paniculata and Xylia xylocarpa ), was carried out. The results did not support the contention that a certain level of pruning promotes stem growth in trees. Instead, all species have a level of pruning that reduces annual increment in stem diameter. In Ailanthus triphysa and Artocarpus hirsutus trees subjected to different pruning intensities showed a decline in the annual increment in stem diameter while in other species diameter increment reduced when the pruning intensity was 75% and 90%. Response to pruning in terms of biomass production also varied from species to species. In Erythrina indica, Macaranga peltata and Terminalia paniculata annual foliage and branch production in pruned trees was significantly more than that of the un-pruned trees. However, in Ailanthus triphysa, Albizia odoratissima, Artocarpus hirsutus, Bridelia crenulata, Grewia tiliifolia and Xylia xylocarpa pruned trees produced comparatively more amount of foliage and branches produced annually than that by the un-pruned trees when the pruning was carried out once in 2 years. Based on these observations it is recommended that trees of Erythrina indica, Macaranga peltata and Terminalia paniculata may be pruned at 50% level annually while the trees of Ailanthus triphysa, Albizia odoratissima, Artocarpus hirsutus, Bridelia crenulata, Grewia tiliifolia and Xylia xylocarpa may be pruned at the same pruning intensity once in 2 years.     

Tree/crop complementarity in an arid zone runoff agroforestry system in northern Kenya

We tested the hypothesis that shallow-rooted crops and deep-rooted trees will share the available water in a complementary manner, when grown together, in a field trail in the Turkana district of northern Kenya during 1994 to 1996. Such studies have been few in dryland agroforestry. The effects of two different Acacia saligna (Labill.) H. Wendl. tree planting densities (2500 and 833 trees per ha), tree pruning (no pruning vs. pruning) and annual intercrops (no intercrop vs. intercrop) on total biomass production and their interactions were tested. In 1996 Sorghum bicolor (L.) Moench was used during the first vegetation period and Vigna unguiculata (L.) Walp. during the second. We used naturally generated runoff water for irrigation to supplement low rainfall amounts typical for the area. High biomass production (> 13 t ha^–1 over a two year period) was observed irrespective of intercropping of pruned trees or sole tree stands. Although the pruning treatment reduced total tree biomass yields by a quarter, the introduction of annual intercrops after the pruning of trees outweighed this loss. The yields of the intercrops in the pruned tree treatments were similar to their yields when grown as monocrops. The calculation of land equivalent ratios showed overyielding for intercropped, pruned systems. The high values for LER (1.36 at low and 1.47 at high density of trees) indicate that there is complementarity in resource use between the different species.This revised version was published online in November 2005 with corrections to the Cover Date.     

Nitrogen and fine root length dynamics in a tropical agroforestry system with periodically pruned Erythrina poeppigiana

The effect of pruning all branches (complete pruning) or retaining one branch (partial pruning) on the dynamics of nitrogen cycling in aboveground biomass, nitrogen supplying power of an amended Eutric Cambisol, and fine root length, was studied in an Erythrina poeppigiana (Walp.) O.F. Cook—tomato (Lycopersicon esculentum Mill.) alley cropping practice in Turrialba, Costa Rica during 1999–2000. Over the 1 year pruning cycle, in which trees were completely or partially pruned four times, respective aboveground biomass production was 4.4 Mg or 7 Mg ha⁻¹ (2-year-old trees) and 5.5 Mg or 9 Mg ha⁻¹ (8-year-old trees); N cycled in aboveground biomass was 123 kg or 187 kg ha⁻¹ (2-year-old trees) and 160 kg or 256 kg N ha⁻¹ (8-year-old trees); mean fine root length was 489 or 821 m (2-year-old-trees), 184 or 364 m per tree (8-year-old-trees). Pruning intensity did not significantly affect net N mineralisation and net nitrification rates during the tomato-cropping season. For the tomato crop, pre-plant mean net N mineralisation rate of 2.5 mg N kg⁻¹ soil day⁻¹ was significantly lower than 16.7 or 11.6 mg N kg⁻¹ soil day⁻¹ at the end of vegetative development and flowering, respectively. Mean net nitrification rates of 3.5, and 4.3 mg N kg⁻¹ soil day⁻¹, at pre-plant and end of vegetative development, respectively, were significantly higher than 0.3 mg N kg⁻¹ soil day⁻¹ at end of flowering. In humid tropical low-input agroforestry practices that depend on organic inputs from trees for crop nutrition, retention of a branch on the pruned tree stump appears to be a good alternative to removal of all branches for reducing N losses through higher N cycling in aboveground biomass, and for conserving fine root length for higher N uptake, although it might enhance competition for associated crops.     

Fine root and nodule dynamics of Erythrina poeppigiana in an alley cropping system in Costa Rica

Fine root and nodule production and turnover in pruned 2- and 8-yr-old Erythrina poeppigiana (Walp.) O.F. Cook trees were estimated under humid tropical conditions by applying the compartment flow model (CFM) to fine root and nodule biomass and necromass measured in sequentially taken core samples. Shoot pruning intensities compared were complete pruning (i.e., complete removal of shoots) and partial pruning (i.e., retention of one branch on the pruned stump). The CFM provided reasonable estimates of nodule dynamics but did not apply to fine root data. Over a five-month observation period, nodule production in completely and partially pruned 2-yr-old trees was 58.2 and 115 g tree^–1, respectively, and the corresponding values in 8-yr-old trees were 26.8 and 26.4 g tree^–1. Senescent nodules and fine roots pass to soil organic matter via decomposition. Partially and completely pruned 2-yr-old trees added 95.4 and 50.4 g tree^–1 decomposed nodules to soil, respectively. The respective value for 8-yr-old trees were 26.7 and 36.5g tree^–1. Nodule and fine root turnover was compensated for by new production at 10–14 weeks after pruning. The retention of a branch on the pruned E. poeppigiana tree stump allows better fine root and nodule survival, and enhances tree biomass production.This revised version was published online in November 2005 with corrections to the Cover Date.     

The influence of severe shoot pruning on growth,carbon and nitrogen status in young peach trees (Prunus persica)

One-year-old peach trees (Prunus persica (L.) Batsch) were severely pruned in July by removing 60% of the shoots. Tree responses were analyzed in terms of architecture and nutritional status. Tree growth was recorded from July to September by nondestructive (leaf production, thickening and branching of the remaining secondary axes) and destructive measurements (biomass partitioning and concentrations of total nitrogen (N) and nonstructural carbohydrates (NC) in specific tissues). The dry weights of pruned trees were lower than those of control trees at the end of the growing season (i.e., 2.5 months after pruning), whereas shoot:root ratios were restored to the initial values. Tree response occurred in two stages. During the first 24 days following pruning, the growth components of the remaining secondary axes were similar to the control, and new secondary axes were produced. During the next 17 days, increases in both diameter and branching of secondary axes contributed to the maintenance of pruned tree growth rate (similar to that of control trees) and restoration of initial shoot:root ratios. No significant effect of pruning was observed on NC concentrations, whereas N concentrations increased in several organs of the pruned trees during the first growth period. The transient increase in internal N availability contributed to the initiation of new axes and the restoration of a more functional biomass partitioning between shoots and roots.     

The effects of early and intense pruning on light penetration,tree growth,and epicormic shoot dynamics in a young hybrid larch stand

We examined the effect of early and intense pruning on light intensity under the canopy, individual growth, diameter–height relationships, and epicormic shoot dynamics in young hybrid larch (Larix gmelinii var. japonica × L. kaempferi) to establish a new effective management method for hybrid larch plantations. The objective is to produce high-quality wood while reducing silviculture costs using a combination of low-density planting and early and intense pruning. In a young hybrid larch plantation, we pruned branches to two different heights (2 and 4 m above ground level) using a no-pruning treatment as a control. Although the growth rates were lower in the heavy pruning treatment (4 m above the ground level) than in other treatments in the year following pruning, when measured 4 years later, growth did not differ between treatments. The number of epicormic shoots increased in the year following pruning, as did the relative photosynthetic photon flux density (rPPFD). The number of epicormic shoots was also dependent on the size of individual trees. However, survival of epicormic shoots was not sufficiently high to be problematic for high-quality timber production. If branches are pruned carefully such that the rPPFD does not rise above 20%, the emergence of epicormic shoots can also be controlled. Our results indicate that early and intense pruning is an effective component of a new management system for hybrid larch plantations.     

To prune or not to prune Faidherbia albida: competing needs for water,wheat and tree products in semi-arid Ethiopia

Faidherbia albida is one of the scattered trees commonly intercropped with most cereals in Ethiopia due to its positive impacts. The tree is pruned for various purposes including for fencing and fuelwood. In this study, the impact of pruning on water relations of F. albida and on understorey wheat productivity was investigated. The on-farm study was conducted in Ejerssa Joro, semi-arid Ethiopia. Six mature trees were selected; three were fully pruned and three were left unpruned. Sap flow and leaf water potential were measured on these trees. Crop gas exchange, aboveground biomass and grain yield were measured under and outside tree canopies. The highest and the lowest sap volumes, recorded from unpruned F. albida, during the dry period, were 153 L day^?1 and 20 L day^?1, respectively. The highest and the lowest sap volumes were 13.4 L day^?1 and 0.04 L day^?1 recorded during the wet period. Wheat CO₂ assimilation was highest (7.8 µmolm^?2 s^?1) at 1 m distance and declined away from the tree trunk under unpruned trees. Aboveground biomass and grain yield under unpruned treatments were significantly (P?<?0.05) higher than outside of canopy of same tree and outside canopies of pruned trees. Pruning reduced aboveground biomass and grain yield by 30% and 27%, respectively; despite the higher water uptake by unpruned trees. We recommend that intensive pruning of F. albida be discouraged and propose further studies on optimal pruning for increased food production and provision of tree products to meet farmers’ needs.

     

Impact of artificial pruning on growth and secondary shoot development of wild cherry (Prunus avium L.)

Producing high value veneer wood requires that the tree bole be branch-free. This can be accomplished by natural or artificial pruning. Since wild cherry does not self prune well, pruning artificially is the only practical option. The study analysed the effect of conventional whorl-wise pruning and selective pruning, on height growth, diameter growth and secondary shoot development of wild cherry. Four pruning treatments were applied on cherry trees in summer 2007, one group of cherries was left unpruned to serve as a control: treatment C1 (upper 5 whorls left), C2 (upper 3 whorls left), S1 (removal of branches larger than 3 cm or with an angle to the stem < 40°), S2 (removal of branches larger than 2 cm or with an angle to the stem < 40°), N (unpruned). Data showed that height growth was not affected by pruning. In contrast, diameter growth at breast height of the C2 pruned cherry was reduced by approximately 5% (SE = 2.7%) in the year of pruning (trees were pruned in July). This pruning treatment produced significant (p = 0.028) nine percent less diameter growth than the control in the second year following pruning. The diameter increment of the C1 pruned trees with five whorls left after pruning and the selective pruned cherries were only about 4% (SE = 4.0%) smaller than the control after two years. This loss was statistically not significant. Analyses showed that on selective pruned trees the survival rate of secondary shoots was significantly reduced compared to those on whorl-wise pruned trees. Significant differences in the size of the secondary shoots were only found between the C1 and S1 (p < 0.05) pruned trees. We did not find differences in the total number of secondary shoots per tree among pruning treatments. Solely from a tree growth perspective, the moderate whorl-wise pruning treatment C1 and the selective prunings were equally effective in minimizing the reduction of diameter growth and are recommended in practice. However it was found that the survival of secondary shoots was reduced on selective pruned trees although the amount of pruning work needed in selective pruning was slightly greater than conventional moderate pruning.     

Effects of pruning on the concentration of secondary metabolites in Colophospermum mopane leaves

Colophospermum mopane, commonly known as mopane, produces secondary metabolites during the growing season. However, there is still insufficient knowledge on the quantity of secondary metabolites and the effect of browsers on the concentration of secondary metabolites. A pruning experiment was conducted in the Musina Nature Reserve, Limpopo province, South Africa, to simulate the effect of browsers on the concentration of secondary metabolites in mopane leaves. The twigs from 40 selected experimental mopane trees were pruned back 50 mm from their tips using a hand shear. The total amount of leaf and shoot biomass removed from branches of selected experimental trees was less than 10%. Three independent samples composed of seven mopane leaves per 40 mopane trees were randomly collected from the canopies of experimental and control trees per sampling event. The dried leaves from each three independent samples were then mixed separately and a pooled sample of 10 g per treatment per sample cycle (55 d) was used for determination of total phenols (TP), condensed tannins (CT) and protein-precipitating tannins (PPT). Results showed that <10% pruning does not have an effect on the amount of secondary metabolites in the mopane leaves. The concentration of TP, CT and PPT increased during leaf flush in October and then declined as the leaves matured and aged. It is concluded that the amount of secondary metabolites in mopane leaves is not dependent on <10% pruning, but appeared to be associated with leaf growth stages. The ability of mopane to produce secondary metabolites has implications on the seasonal diet composition and distribution of browsers in mopane woodland.     

Effects of oak root pruning in forest nurseries on potential pathogen infections

Despite the general practice of root pruning, little is known about the potential impact of reducing shoot/root systems of oak seedlings in this way on their future susceptibility to pathogens, for example Cylindrocarpon spp., Fusarium spp., Ilyonectria spp., Pythium spp. Phytophthora spp. or Rhizoctonia spp. In this study, root‐pruned and non‐pruned seedlings of Quercus robur grown under controlled conditions were inoculated with aggressive and less‐aggressive pathogens. Results indicated, in contrast to our initial assumption, that pathogens significantly reduced lateral root biomass more in non‐pruned seedlings, the extent of the response depending on the pathogens species. In response to pathogen pressure, pruned seedlings tended to attain a higher dry stem mass fraction, but lower dry leaf mass fraction. Pathogens also suppressed leaf mass in total root dry mass fraction (dry leaf mass/total root dry mass ratio, in g × g^?1) more in pruned than in non‐pruned seedlings. These results suggest differences in growth between non‐pruned and pruned seedlings in response to pathogen stress. In nurseries, root pruning of oak trees may enhance the reduction in leaf mass in lateral roots mass fraction resulting from pathogen infections, which may decrease seedling quality. It is therefore important to ensure a low level of inoculum of soil‐borne pathogens to minimize the risk of seedling infection.     

Effects of curtain-like pruning on distribution and seasonal patterns of carbohydrate reserves in plane (Platanus acerifolia Wild) trees

The maintenance of plane trees (Platanus acerfolia Wild) by regular curtain-like pruning during the vegetative period induced modifications in the distribution and seasonal patterns of carbohydrate reserves in the perennial parts. The unpruned trees were characterized by high and fairly constant concentrations of starch in roots > 5 cm in diameter and a decreasing gradient of starch from the base to the top of the trunk. Starch also accumulated at the trunk-branch junction and at the base of large branches. Curtain-like pruning caused the starch gradient in the trunk to disappear and induced well marked seasonal variations in the starch concentration of roots > 5 cm in diameter. Pruning also eliminated the accumulation of starch at the trunk-branch junction during summer, but it had no effect on the accumulation of starch at the base of large branches. Concentrations and seasonal fluctuations of carbohydrates in roots < 0.5 cm in diameter were similar in both pruned and unpruned trees. Repeated cuts or "short head pruning" induced the formation of excrescences at the tips of branches that accumulated starch.     

Rejuvenating indigenous trees in agroforestry parkland systems for better fruit production using crown pruning

The effects of crown pruning of mature indigenous fruit trees of Vitellaria paradoxa C. F Gaertn (commonly known as karité) and Parkia biglobosa (Jacq.) R. Br. ex G. Don (commonly known as néré) on recovery of crown size and fruit yield were assessed during 6 years in an agroforestry parkland system in Burkina Faso. Three treatments of crown pruning (total-pruning, half-pruning and a control of no-pruning) were applied to karité and néré. Each treatment comprised ten individuals of each species or a total of 60 trees of both species. Six years after pruning, higher recovery (81%) of crown diameter was achieved in total-pruned trees of néré as opposed to karité which recovered by only 73%. On the contrary, fruit production in total-pruned trees of karité recovered by 83% 5 years after pruning and fully (100%) 6 years after pruning as opposed to néré which recovered by only 57% 5 years after pruning but declined to 16% on the sixth year probably due to interannual variability. Fruit yields did not differ significantly between unpruned and half-pruned trees of both species throughout the experiment period. Total pruning may, therefore, be recommended to farmers to rejuvenate old trees of karité in parklands on the basis of fast recovery of fruit and slow recovery of crown in the species. Slow recovery of crown in pruned trees is the most desirable characteristic in parklands in order to avoid the negative effect of tree shade on adjacent crop.     

Effects of <Emphasis Type="Italic">Inga densiflora</Emphasis> on the microclimate of coffee (<Emphasis Type="Italic">Coffea arabica</Emphasis> L.) and overall biomass under optimal growing conditions in Costa Rica

The advantages of associating shade trees in coffee agroforestry systems (AFS) are generally thought to be restricted mostly to poor soil and sub-optimal ecological conditions for coffee cultivation whereas their role in optimal conditions remains controversial. Thus, the objective of this study was to investigate, under the optimal coffee cultivation conditions of the Central Valley of Costa Rica, the impact of Inga densiflora, a very common shade tree in Central America, on the microclimate, yield and vegetative development of shaded coffee in comparison to coffee monoculture (MC). Maximum temperature of shaded coffee leaves was reduced by up to 5°C relative to coffee leaf temperature in MC. The minimum air temperature at night was 0.5°C higher in AFS than air temperature in MC demonstrating the buffering effects of shade trees. As judged by the lower relative extractable water (REW) in the deep soil layers during the dry season, water use in AFS was higher than in MC. Nevertheless, competition for water between coffee and associated trees was assumed to be limited as REW in the 0–150 cm soil layer was always higher than 0.3 in shaded coffee compared to 0.4 in monoculture. Coffee production was quite similar in both systems during the establishment of shade trees, however a yield decrease of 30% was observed in AFS compared to MC with a decrease in radiation transmittance to less than 40% during the latter years in the absence of an adequate shade tree pruning. As a result of the high contribution (60%) of shade trees to overall biomass, permanent aerial biomass accumulation in AFS amounted to two times the biomass accumulated in MC after 7 years. Thus provided an adequate pruning, Inga-shaded plantations appeared more advantageous than MC in optimal conditions, especially considering the fact that coffee AFS provides high quality coffee, farmers’ revenue diversification and environmental benefits.     

Modeling the effect of physiological responses to green pruning on net biomass production of Eucalyptus nitens

Green pruning of Eucalyptus nitens (Deane and Maiden) Maiden increases instantaneous rates of light-saturated CO(2) assimilation (A), and changes patterns of total leaf area and foliage distribution. We investigated the importance of such changes on the rate of recovery of growth following pruning. A simple process-based model was developed to estimate daily net biomass production (G(d)) of three-year-old plantation-grown trees over a 20-month period. The trees had been pruned by removal of 0, 50 or 70% of the length of green crown, equivalent to removal of 0, 55 or 88% of leaf area, respectively, when the plantation verged on canopy closure. Total G(d) was reduced by only 20% immediately following the 50%-pruning treatment, as a result of both the high leaf dark respiration and low A in the portion of the crown removed compared to the top of the crown. Pruning at the time of canopy closure preempted a natural and rapid decline in G(d) of the lower crown. Although leaf area index (L) was approximately 6.0 at the time of pruning, high light interception (95%) occurred with an L of 4.0. The 50%-pruning treatment reduced L to 3.5, but the physiological responses to pruning were sufficient to compensate fully for the reduction in intercepted radiation within 110 days of pruning. The 70%-pruning treatment reduced L to 1.9, and reduced G(d) by 77%, reflecting the removal of branches with high A in the mid and upper crown. Physiological responses to the 70%-pruning treatment were insufficient to increase G(d) to the value of unpruned trees during the study. Model sensitivity analysis showed that increases in A following pruning increased G(d) by 20 and 25% in the 50- and 70%-pruned trees, respectively, 20 months after pruning. Changes in leaf area/foliage distribution had a greater effect on G(d) of 50%-pruned trees (47% increase) than did changes in A. However, the reduction in photosynthetic potential associated with the 70%-pruning treatment resulted in only small changes in leaf area/foliage distribution, which consequently had little effect on G(d). The effects of physiological processes occurring within the crown and in response to green pruning on G(d) are discussed with respect to pruning of plantations.