Agroforestry in the arid zones of India

The arid regions of India cover over 300,000 km² and are spread over six States, mostly in the northwestern parts of the country. In spite of the hostile environmental conditions, several indigenous agroforestry practices are being practised in this region. The Central Arid Zone Research Institute (CAZRI) has made considerable progress in improving these indigenous practices and also developing new land use technologies some of which involve agroforestry approaches. Notable among these include sand-dune stabilization, shelterbelt plantations, tree planting techniques in difficult land forms, silvopastoral and agrisilvicultural systems, introduction and improvement of fruit trees and other indigenous trees, etc. Some of these technologies are adopted on a large scale by farmers in the arid zone of India, and have attracted international attention in other arid parts of the world. This paper is a summary of the results of these agroforestry initiatives of CAZRI.     

Hill agroforestry systems in south Sikkim,India

In the Mamlay watershed of south Sikkim, India, about 80% of the population depend on land for their livelihood. The agricultural land-use activity includes agroforestry, horticulture and animal husbandry besides growing crops in irrigated or unirrigated fields. Trees are maintained in the farms mainly for fodder and rarely for fuel purposes. Cropping system is characterised by cultivation of cereals and cash crops to ensure supply of food grains and returns for daily needs. This paper presents data on crop production and farm management aspects including the linkages among tree-crop-animal components of a hill agriculture system. Crop diversity is high and crop combinations are fixed and well tested. Unpalatable grasses are used for composting by mixing with cow dung to meet high demand for manure and thus exhibit efficient recycling of plant material. The system is at low input level, and is therefore adopted by even the poorest section of society. Limited infrastructure facilities, sloping terrain, inaccessibility to most agricultural zone, depletion of natural resources from forests, water scarcity during lean period and heavy rainfall during monsoon, and erosion are, the main constraints which need to be improved through research using scientific means.     

5α-Reductase inhibitory component from leaves ofArtocarpus altilis

The inhibitory effects of 17 samples prepared from Thailand plants on 5-reductase activity were examined. The acetone extract of leaves ofArtocarpus altilis showed potent 5-reductase inhibitory activity. Fractionation guided by 5-reductase inhibition led to the isolation of 2-geranyl-2,3,4,4-tetrahydroxydihydrochalcone from the acetone extract of leaves ofA. altilis. This compound showed more potent inhibitory effect (IC₅₀=38M) than-linolenic acid known as a naturally occurring potent inhibitor.     

Specific degradation ofβ-aryl ether linkage in synthetic lignin (dehydrogenative polymerizate) by bacterial enzymes ofSphingomonas paucimobilis SYK-6 produced in recombinantEscherichia coli

Sphingomonas paucimobilis SYK-6 produces unique and specific enzymes, such as-etherases,O-demethylases, and ring fission dioxygenases, for lignin degradation. Cleavage of arylglycerol--aryl ether linkage is the most important process in the lignin metabolic pathway ofS. paucimobilis SYK-6. We reported the genes (ligD, ligE, ligF) for enzymes that cleaved-aryl ether linkage of dimeric compounds in previous studies. In this study we synthesized the fluorescent high-molecular-weight lignin (UBE-DHP) by dehydrogenative polymerization. We investigated the-aryl ether cleavage ability of these enzymes produced in recombinantEscherichia coli. When UBE-DHP was incubated with LigF, 4-methylumbeliferone was released as a result of-aryl ether cleavage of O-methylumbelliferyl--hydroxypropiovanillone (compound III) incorporated in UBE-DHP. Here, we report that-etherase ofS. paucimobilis SYK-6 can be expressed inE. coli and is able to cleave the-aryl ether linkage in synthetic high-molecular-weight lignin.     

Five years of Paulownia field trials in North Carolina

Performance of Paulownia elongata, Paulownia fortunei, and Paulownia×Henan 1 was monitored at three sites in North Carolina between 1996 and 2000, and P. elongata clones were tested at an additional two sites. The primary objective was to define the potential for growing Paulownia in the state. Species and clones within species differed in survival and height and diameter growth whenever genotype was included as a treatment. P. elongata was superior at two and P. fortunei was superior at one of the three sites that included P. elongata, P. fortunei, and P.×Henan 1. Trees produced through vegetative means were more likely to survive and were taller and of greater DBH than seed produced trees. Mortality in trees produced from seed was greater for P. fortunei and P. ×Henan 1 than for P. elongata. Application of animal waste or different rates of nitrogen as inorganic fertilizer did not have a pronounced effect on tree survival and growth.     

Length of cuttings in juvenile development of a hybrid poplar clone

The influence of length of cuttings on establishment of a short rotation plantation was investigated over a period of two years using direct field planting of unrooted Populus Rasumowskiana cuttings. The longer the cuttings, the higher were the survival and dry mass production. Survival at the end of the second growing season varied from 75% to 97%. In two years, the two longest cutting lengths (40 cm and 50 cm) produced about 100 g dry mass per living cutting; but owing to the higher survival rate of the longest cuttings, there was a difference per area unit: 360 g/m² for 40 cm and 400 g/m² for 50 cm-long cuttings. The shortest (10 cm) cuttings produced only 115 g/m².     

Synthesis of dihydroxyphenacyl glycosides for biological and medicinal study: β-oxoacteoside from Paulownia tomentosa

The protected structure of -oxoacteoside (tomentoside A), 2-oxo-2-(3,4-dihydroxyphenyl)ethyl 3-O-(2,3,4-tri-O-acetyl--l-rhamnopyranosyl)-4-O-caffeoyl--d-glucopyranoside 14 was synthesized in 14% overall yield in 11 steps, starting from d-glucose for biological and medicinal studies of phenylpropanoid glycosides. The first step was the preparation of a 3-O-rhamnopyranosyl disaccharide sugar core 2 from a suitably protected rhamnosyl trichloroacetimidate 10 and glucose derivative (diacetone-d-glucose 1) in 71% yield. To the glucose moiety of this sugar core, several protection/deprotection procedures were performed sequentially to obtain a fully acetylated sugar core 7 with a 4-OH group on the glucose moiety, in 57% yield in five steps. Thereafter, to the 4-OH group of the glucose moiety, selective 4-O-caffeoylation was achieved by proton-transfer esterification with 3,4-di-O-allylcaffeic acid 16 to give the caffeoyl disaccharide 11 in 97% yield. Then, it was converted to trichloroacetimidate 13 for a glycosylation donor in 90% in two steps. Finally, anomeric glycosylation was conducted with 2-oxo-2-(3,4-di-allyloxyphenyl)ethyl alcohol 19 with catalytic amounts of BF₃·Et₂O to give 2-oxo-2-(3,4-di-allyloxyphenyl)ethyl 2,6-di-O-acetyl-3-O-(2,3,4-tri-O-acetyl--l-rhamnopyranosyl)-4-O-(3,4-di-allyloxycaffeoyl)--d-glucopyranoside 14 in 60% yield. Deprotected intermediates of compounds 2, 11, 14, and 19 which were obtained in high yield would be useful for biological and medicinal studies of phenylpropanoid glycosides.Part of this study was presented at the 52nd Annual Meeting of the Japan Wood Research Society, Gifu, April, 2002     

Studies on the synthesis and properties of terpene-phenol-aldehyde resin with a high softening point

Synthesis conditions of terpene-phenol-aldehyde resin with a high softening point were studied based on the reactions among-pinene, phenol, and formaldehyde. A suitable catalyst system and the best processing conditions were obtained by laboratory experiments. The influence of the raw materials ratios, reaction temperature, reaction time, and catalyst dose on the softening point, yield, and color of the synthesized resin was examined. The physical and chemical characteristics of the resin were determined: softening point 140°C (ball and ring method); color value 7 (Gardner); acid value (KOH mg/g) <1; bromine value (Br₂ mg/100g) <64; saponification value (KOH mg/g) <1; average molecular weight 830. The yield of resin was more than 85% (based on the total raw material).     

Factors influencing the variability of Mg, Ca and K in waters of a mangrove creek in Bragança, North Brazil

Sodium, potassium, magnesium, calcium and physicochemical parameters were monitored for one year in a mangrove tidal creek near Bragança, North Brazil, to determine their tidally induced and seasonal variations and the main parameters controlling the concentration of these cations. On a daily basis, cation concentrations showed a strong tidal rhythm due to the mixing of estuarine and mangrove waters. Mean concentrations were highest at the end of the dry season (December 1996) and lowest (April 1997) towards the end of the rainy season. Average values over one year were: Na+ = 329± 118mM, K+ = 6.9±2.5mM, Mg++=37 ±14 mM and Ca++= 6.9±2.4mM. Dissolved oxygen concentration was higher during the dry season due to enhanced aquatic primary production, with a maximum daily average value of 8.5mg/L in July 1996, and a minimum value of 4mg/L in June 1997. Cation concentrations were transformed relating them to the respective average values in standard seawater at salinity 35. Although cation concentrations and salinity tightly correlated, this standardization showed that the concentrations of K+, Ca++ and Mg++ did not depend solely on salinity and reflected the seasonal variation in aquatic primary production. It also allowed the discrimination of their sources (marine, riverine and groundwater). Thermodynamic equilibrium calculations indicate that phytoplankton may be regulating the concentration of these cations in the water column indirectly by inducing precipitation through pH increase and directly through metabolic uptake.     

5<Emphasis Type="Italic">Α</Emphasis>-Reductase inhibitory tannin-related compounds isolated from <Emphasis Type="Italic">Shorea laeviforia</Emphasis>

Five tannin-related compounds – gallic acid, flavogallonic acid dilactone, valoneic acid dilactone, gallagyldilactone, ellagic acid – were isolated from the heartwood of Shorea laeviforia, and the inhibitory activity of each against rat liver 5-reductase was evaluated. Valoneic acid dilactone and gallagyldilactone exhibited positive inhibitory activity, but gallic acid and ellagic acid did not. Flavogallonic acid dilactone stimulated 5-reductase activity, even though this compound is structurally similar to valoneic acid dilactone. The kinetic study of valoneic acid dilactone and gallagyldilactone indicated that the inhibitory behavior of 5-reductase were not competitive against the substrate (testosterone) and were partially competitive against the cofactor (NADPH). Additionally, double inhibition analysis of valoneic acid dilactone and NADP⁺ showed synergetic inhibition. These results suggested that neither valoneic acid dilactone nor gallagyldilactone can affect the binding of testosterone but that either compound could interact with an enzyme–NADP⁺ complex to inhibit 5-reductase.     

The effects of sulfometuron on the root growth of loblolly pine

The effect of sulfometuron (Oust) on the root growth of loblolly pine (Pinus taeda L.) seedlings was studied in the field and in two soil types in the greenhouse. In the greenhouse study sulfometuron was applied to the foliage only, the soil only, and to both foliage and soil at the rates of 0.10, 0.21, and 0.42 kg ai/ha. Twenty-eight days after application root growth significantly decreased for all methods of application and with increasing rates e.g., 0.10, 0.21, and 0.42 kg ai/ha sulfometuron reduced new root length by 42%, 53%, and 64%, respectively. Application in the field at the rate of 0.30 kg ai/ha resulted in a 68% reduction in root growth. However, by the end of the growing season treated seedling root and shoot biomass were 115% and 64% greater, respectively. To ensure earlier season survival the rate of sulfometuron applied should be kept at a minimum level that will allow both weed control and adequate root growth. Low rates would be particularly important during a dry planting season.     

Lignans ofLinum flavum var.compactum

A new dibenzylbutyrolactone lignan 7.6-dihydroxybursehernin, together with six known lignans (pinoresinol, lariciresinol, secoisolariciresinol,-peltatin,-peltatin, 5-methoxypodophyllotoxin) were isolated from the methanol extracts ofLinum flavum var.compactum. The enantiomeric analysis of pinoresinol and lariciresinol isolated from the species, which are upstream lignans in the lignan biosynthetic pathway, indicated that they are not optically pure, which is in accordance with our recent findings on lignans occurring in other plant species.Parts of this report were presented at the 42nd Lignin Symposium, Sapporo, October 1997; and the 43rd Lignin Symposium, Fuchu, October 1998     

Validation of a small-area method for estimating the spatial distribution of the degree of tree damage

This article presents a validation of a method, proposed in Podlaski (2003), for estimating the degree of tree damage. This method belongs to a group of small-area methods. To estimate the degree of tree damage in individual P₃ sub-blocks of the SINUS system of information on the natural environment, a classification based on the degree of defoliation was used. Spatial distribution of the degree of tree damage was estimated through unrestricted simple random sampling. The maximum total estimation error for proportions of fir and beech with a damage degree of zero, and also with second and third degrees jointly, reached a maximum of 35.6% for fir, and 33.8% for beech. P₃ sub-blocks characterised by the highest proportion of the healthiest trees (at least 15% being undamaged trees) occurred in patches in the case of fir, and in larger, compact areas in the case of beech. Because spatial diversification in the health of fir, and to a smaller degree in the case of beech, occurs at small scales, small-area methods for estimating tree condition are necessary. An analogous scheme, combining small-area with large-area methods (utilising sub-blocks of the network of large-area systems in a small-area inventory, and establishing a common database), could be used on a wider scale; for example, by supplementing the program of estimating tree health carried out by the United Nations Economic Commission for Europe (Lorenz et al. 2002) with local inventories.     

Antioxidative activity of tree phenolic constituents 1: Radical-capturing reaction of flavon-3-ols with radical initiator

The present work was undertaken from the standpoint of radical-capturing ability with regard to the antioxidative ability of flavonoids, especially flavonols distributed widely in woody plants. In regard to the flavonols, six methyl derivatives were initially prepared from quercetin and its litinoside. Their radical-capturing constants were determined strictly by the stopped-flow spectroscopic method. It was proved that the radical-capturing ability of quercetin mainly involves the vicinal C₃. and C₄, hydroxyl groups and the C₃ hydroxyl group. To clarify the reaction mechanism begun at the C₃ hydroxyl group of quercetin, 5,7,3,4-tetramethylquercetin (TMQ), flavon-3-ol (F30) and so on were treated with 2,2-azo-bis-(2,4-dimethylvaleronitrile) (AMVN). Six products (1–6) containing one depside and its two hydrolytic products, two valeronitrile adducts, and others were isolated from the reaction mixture of TMQ and their structures determined by instrumental analyses. Similarly, F30 gave four products, 7–10, which corresponded to the above products 1–3 and 5 (one depside, its two hydrolytic products, and one adduct), respectively. 3,5,7,3,4-Pentamethylquercetin (PMQ) and flavon-3-O-methylate (F3M) gave no products. The quantitative change of the products with reaction time was determined spectroscopically. An initial reaction pathway for the radical-capturing reaction of flavon-3-ols with AMVN was proposed based on the products and their amounts. The main route — formation of depside and its hydrolytic products via ketohydroperoxide (3) or ketohydroperoxy radical (4) - was similar to that of the oxidation reaction of quercetin with quercetinase and light.Part of this paper was presented at the 46th and 47th annual meetings of the Japan Wood Research Society, Kumamoto and Kouchi, April 1996 and 1997     

Dynamic properties of three types of wood-based composites

This study used a vibration test method to show that grain angles of face veneer have substantial effects on sound velocities and dynamic Youngs moduli of three types of wood-based composites. The sound velocity at 0° grain angle of face veneer was the highest, and it decreased with increasing grain angle in the range of 0° to 90°. This tendency was similar to that for dynamic Youngs modulus. The relationship between the grain angle of face veneer and the sound velocity of three types of wood-based composites can be expressed in the form of Hankinsons equation or a second-order parabolic equation. This study also showed that the application of orthotropic elasticity theory was valid for the three types of wood-based composites. The relationship between the grain angle of the face veneer and the Youngs modulus of three types of wood-based composites can be expressed in the form of the Jenkin equation, Hankinsons equation, or a second-order parabolic equation. Rule of mixture can also be used to predict the Youngs modulus of wood-based composite from the Youngs moduli of the two elements.Part of this study was presented at the 53rd Annual Meeting of the Japan Wood Research Society, Fukuoka, Japan, March 2003 and the 15th Annual Meeting of Chugoku Shikoku Branch of the Japan Wood Research Society, Higashi-Hiroshima, Japan, September 2003     

Preparation of polyols from methyl-α-d-glucoside and cyclic esters for design and fabrication of biodegradable polyurethane foams

A ring-opening polymerization of cyclic esters -caprolactone (CL) and/or l-lactide (LACD) was carried out in the presence of methyl--d-glucoside (m-Glc) as an activated substrate and tin(II) 2-ethylhexanoate (SnEht₂) as a catalyst. This led to successful synthesis of an armed polyester polyol with m-Glc as the core. These polyols were characterized through gel permeation chromatography, hydroxyl value assessment, differential scanning calorimetry, and viscosity measurements. It was clarified that the thermal properties and tractability of the synthesized polyols are closely related to the structural characteristics of the side chain polyesters, such as their length and chemical composition. Polyurethane foams were also prepared by mixing an appropriate amount of the polyols with diphenyl methane diisocyanate, a foaming agent (water), and other additives, and their mechanical properties were examined. Two polyurethane foams manufactured from polycaprolactone-polyols that were synthesized at a CL/m-Glc ratio of 2 or 5, were used in a biodegradation test in a closed system of activated sludge suspension. Evidence of their biodegradation is presented based on data showing oxygen consumption by the pulverized samples.     

Characterization of the lignin-derived products from wood as treated in supercritical water

Sugi (Cryptomeria japonica D. Don) and buna (Fugus crenata Blume) woods were treated with supercritical water (>374°C, >22.1 MPa) and fractionated into a water-soluble portion and a water-insoluble residue. The latter was washed with methanol to be fractionated further into a methanol-soluble portion and a methanol-insoluble residue. Whereas the carbohydrate-derived products were in the water-soluble portion, most of the lignin-derived products were found in the methanol-soluble portion and methanol-insoluble residue. The lignin-derived products in the methanol-soluble portion were shown to have more phenolic hydroxyl groups than lignin in original wood. The alkaline nitrobenzene oxidation analyses, however, exhibited much less oxidation product in the methanol-soluble portion and methanol-insoluble residue. These lines of evidence suggest that the ether linkages of lignin are preferentially cleaved during supercritical water treatment. To simulate the reaction of lignin, a study with lignin model compounds was performed;-O-4-type lignin model compounds were found to be cleaved, whereas biphenyl-type compounds were highly stable during supercritical water treatment. These results clearly indicated that the lignin-derived products, mainly consisting of condensed-type linkages of lignin due to the preferential degradation of the ether linkages of lignin, occurred during supercritical water treatment.This study was presented in part at the 45th lignin symposium, Ehime, Japan, October, 2000; and the 49th Annual Meeting of the Japan Wood Research Society, Tokyo, April 1988     

Erythro/threo ratio ofβ-O-4 structures as an important structural characteristic of lignin. I: Improvement of ozonation method for the quantitative analysis of lignin side-chain structure

Ozonation as a quantitative tool to analyze the stereo structures of arylglycerol--aryl ether linkages was examined using wood meal, milled wood lignin, and a lignin model compound, 1-(3,4-dimethoxyphenyl)-2-(2-methoxyphenoxy)-1,3-propanediol (veratrylglycerol--guaiacyl ether, VG). The procedure was improved. When mild postreduction was conducted for ozonation products, the total yield of erythronic and threonic acids from this model compound was 74%, which is 15% higher than the yield without postreduction. A decrease in the recovery of these two acids under prolonged ozonation treatment was successfully suppressed by postreduction. Theerythro/threo ratio of VG determined by the ozonation method with postreduction is in good agreement with the ratio determined by¹H-nuclear magnetic resonance. Excellent reproducibility of the yield was obtained by adopting a procedure that included trimethylsilylation of ammonium salts of ozonation products using a dimethylsulfoxide-hexamethyldisilazane-trimethylchlorosilane mixture and subjecting it to gas chromatography analysis. It was concluded that arylglycerol--aryl ether structures comprise at least 35% of the C₃-C₆ structure in birch wood meal, with anerythro/threo ratio of 2.8.This paper was presented at the 43rd Lignin Symposium, Fuchu, Japan, October 1998; and at the 10th ISWPC, Yokohama, Japan, June 1999