Structure and Function of High Altitude Forests of Central Himalaya II. Nutrient Dynamics

This paper deals with nutrient dynamics in horse chestnut, silverfir and kharsu oak forests in a high altitude region of CentralHimalaya. In general, the nutrient concentrations in differentlife forms were of the order: herb > seedling > shrub> sapling > tree, whereas the standing state of nutrientswere of the order: tree > herb > shrub > sapling >seedling. Of the total nutrients in the system, soil litterand vegetation, respectively accounted 66·5, 0·6and 32·9% in horse chestnut, 61·4, 0·8and 37·8% in silver fir, 58·1, 0·8 and41·1% in kharsu oak forests. Considerable reductionsin concentrations of nutrients in leaves occurred during senescence.Annual transfer of litter (above-ground+below-ground) to thesoil by vegetation of all forests ranged from 68-163 for N,4-7 for P, 26-48 for K, 62-150 for Ca and 2-4 kg ha^-1 year^-1for Na. Turnover time for different nutrients ranged between1·41 and 1·75 years for horse chestnut, 1·33and 2·13 years for silver fir, and 1·32 and 1·75years for kharsu oak forests. The distribution of nutrient contentsand net annual fluxes within the system have been developedto represent nutrient dynamics in compartment models.Copyright1995, 1999 Academic Press Standing state, turnover, retranslocation, nutrient concentration, internal cycling, uptake     

Structure and Function of Oak Forests in Central Himalaya. I. Dry Matter Dynamics

The present study deals with structure and functioning of threeareas of Himalayan oak forest. Low- and mid-altitude oaks, namelyQuercus leucotrichophora, and Quercus floribunda, form predominantevergreen forests in Central and Western Himalaya. The totaltree basal cover ranged between 33·89 m² ha^–1 (Q.floribunda site) to 36·83 m² ha^–1 (Q. leucotrichophorasite). The density ranged between 570 and 760 individuals ha^–1.Allometric equations relating biomass of different tree componentsto GBH (girth at breast height) were significant with the exceptionof leaf biomass in Q. leucotrichophora and Rhododendron arboreum.Total vegetation biomass (29·40–467·0 tha^–1) was distributed as 377·1 t ha^–1 intrees, 5·40 t ha^–1 in shrubs and 1·23 tha^–1 in herbs. Total forest floor biomass ranged between4·6 and 6·2 t ha^–1. Of the total annuallitter fall (4·7–4·8 t ha^–1), 77·5% was contributed by leaf litter, 17·8 % by wood litterand 4·7 % by miscellaneous litter. Turnover rate of treelitter varied from 0·66 to 0·70. Net primary productionof total vegetation ranged between 15·9 and 20·6t ha^–1 yr^–1, of which the contribution of trees,shrubs and herbs was 81·2 %, 8·6 % and 10·2%, respectively. A compartment model of dry matter on the basisof mean data across sites was developed to show dry matter storageand flow of dry matter within the system. Quercus leucotrichophora forest, Q. floribunda forest, Q. lanuginosa forest, biomass, litter fall, net primary production, compartmental transfer     

Structure and Function of an Age Series of Poplar Plantations in Central Himalaya: I Dry Matter Dynamics

The biomass and net primary productivity (NPP) of 5- to 8-year-oldpoplar (Populus deltoides Marsh, Clone D₁₂₁) plantations growingin the Tarai belt (low-lying plains with high water table adjacentto foothills of central Himalaya) were estimated. Allometricequations for all the above-ground and below-ground componentsof trees and shrubs were developed for each stand. Understorey,forest floor biomass, and litter fall were also estimated fromstands. The biomass of plantation, forest floor litter mass,tree litter fall and net primary productivity (NPP) of treesand shrubs increased with increase in plantation age, whereasherb biomass and NPP significantly (P < 0·01) decreasedwith increasing plantation age. The total plantation biomassincreased from 84·0 in the 5-year-old to 170·0t ha^-1 in the 8-year-old plantation and NPP from 16·8t ha^-1 year^-1 in the 5- and 6-year-old to 21·8 t ha^-1year^-1 in the 8-year-old plantation. The biomass accumulationratio (biomass: net production, BAR) for different tree componentsincreased with the age of plantation increase. The BAR ratioranged from 4·9 in the 5-year-old to 7·7 in the8-year-old plantation.Copyright 1995, 1999 Academic Press Populus deltoides plantations (Clone D₁₂₁), biomass, dry matter turnover, net primary productivity, Tarai belt of Central Himalaya     

Structure and Function of an Age Series of Eucalypt Plantations in Central Himalaya. I. Dry Matter Dynamics

The biomass and net primary productivity (NPP) of 2- to 8-year-oldplantations of Eucalyptus tereticornis Sm. (= E. hybrid) growingin the tarai (a level area of superabundant water) region ofCentral Himalaya were estimated. Allometric equations for allthe above-ground and below-ground components of trees and shrubswere developed for each stand. Understorey, forest floor biomassand litter fall were also estimated from stands. Shrubs appearedfirst at 5-year-old plantation. The biomass of vegetation, forestfloor littermass, tree litter fall and net primary productivity(NPP) of trees and shrubs increased with the increase in plantationage, whereas herb biomass and NPP significantly (P < 0·01)decreased with the increase in plantation age. The total plantationbiomass increased from 7·7 t ha^–1 in the 2-year-oldto 126·7 t ha^–1 in the 8-year-old plantation andNPP from 8·6 t ha^–1 year^–1 in the 2-year-oldto 23·4 t ha^–1 year^–1 in the 8-year-old plantation.The biomass accumulation ratio ranged from 0·81 to 5·93. Eucalyptus tereticornis Sm, plantation, biomass, forest floor, litter fall, net primary productivity, biomass accumulation ratio     

The Structure and Function of Pine Forest in Central Himalaya. I. Dry Matter Dynamics

The present study deals with structure and function of fourareas of Himalayan chir pine forest. Tree layer was monospecificon all sites with varied density and basal cover in the rangeof 540–1630 individuals per ha and 25·0–47·2m²ha^–1, respectively. Shrubs having low density were sparselydistributed. All allometric equations relating to biomass ofdifferent components, to circumference at breast height (cbh)were significant, with the exception of that for cone biomass.Total vegetation biomass (115–236 t ha^–1) was distributedas 113–283 t ha^–1 in trees. 0·56–0·82t ha^–1 in shrubs and 1·63–2·57 t ha^–1in herbs. Total forest floor biomass including herbaceous litterranged between 9·6 and 13·6 t ha^–1. Of thetotal annual litter fall (4·26–7·38 t ha^–1),60·3–75·1 per cent was distributed in leaflitter and 24·9–39·7 per cent in wood litter.Turnover rate of tree litter varied from 0·45 to 0·53,whereas rates for shrubs and herbs were assumed to 1. Net primaryproduction of total vegetation ranged between 9·91 and21·2 t ha^–1 year^–1, of which the contributionof trees, shrubs and herbs was 76·5– 88·1per cent 0·6–1·8 per cent and 11·3–21·5per cent, respectively. A compartment model of dry matter onthe basis of mean data across sites was developed to show drymatter storage and flow of dry matter within the ecosystem. Pinus roxburghii forest, biomass, litter fall, net primary production, compartmental transfer     

Structure and Function of Oak Forests in Central Himalaya. II. Nutrient Dynamics

This paper elucidates nutrient dynamics in oak forests previouslyinvestigated for dry matter dynamics. The nutrient concentrationsin different life forms were of the order: herb > shrub >tree, whereas the standing state of nutrients were of the order:tree > shrub > herb. Soil, litter and vegetation, respectively,accounted for 32·4–98·0 %; 0·3–3·5%, and 10·2–66·6 % of the total nutrientsin the system. Considerable reductions (8·5–41·7%)in concentrations of nutrients in leaves occurred during senescence.The uptake of nutrients by vegetation, and also by differentcomponents with and without adjustment for internal recycling,has been calculated separately. Annual transfer of litter (above+ below ground) to the soil by vegetation was 115·9–187N, 7·5–15·6 P, 122·7–195·1Ca, 36·1–48·8 K and 2·88–5·16Na kg ha^–1 yr^–1. Turnover rate and turnover timefor different nutrients ranged between 0·66–0·84yr^–1 and 1·19–1·56 yr^–1, respectively.Compartment models for nutrient dynamics have been developedto represent the distribution of nutrient contents and net annualfluxes within the system. Quercus leucotrichophora forest, Q.floribunda forest, Q. lanuginosa forest, Nutrient concentration, standing state, uptake, internal cycling, turnover     

Fine Root Productivity and Turnover in Two Evergreen Central Himalayan Forests

Fine root production and mortality in central Himalayan evergreenforests consisting of Quercus leucotrichophora (banj oak) andPinus roxburghii (chir pine) were measured. Fine root productionand mortality decreased with increasing soil depth. Annual fineroot production was higher in the broadleafed forest than inthe coniferous forest, across months and seasons (1.3 and 1.5-timesmore living and dead root biomass, respectively in banj oakthan in chir pine). Live fine root production was 2508 kg ha^-1year^-1inchir pine forest and 3631 kg ha^-1year^-1in banj oak forest. Deadfine roots accumulated at a rate of 1197 and 1525 kg ha^-1year^-1inchir pine and in banj oak forest, respectively. In both forests,the greatest fine root production was recorded in the rainyseason followed by summer and winter seasons. Both soil androot nitrogen concentration decreased with increasing soil depth.Nitrogen uptake was higher in banj oak forest (12.1 kg ha^-1year^-1)than chir pine forest (7.2 kg ha^-1year^-1).Copyright 1999 Annalsof Botany Company Fine root production, fine roots, necromass, banj oak, chir pine, Quercus leucotrichophora , Pinus roxburghii .     

Structure and Function of an Age Series of Poplar Plantations in Central Himalaya. II Nutrient Dynamics

This paper elucidates nutrient dynamics in 5- to 8-year-oldpoplar (Populus deltoides) clone D₁₂₁ plantations previouslyinvestigated for dry matter dynamics. The nutrient concentrationin different layers of the vegetation were in the order: tree> shrub > herb, whereas the standing state of nutrientswere in the order: tree > herb > shrub. Soil, litter andvegetation, respectively, accounted for 80-89, 2-3 and 9-16%of the total nutrients in the system. Considerable reductions(trees 42-54, shrubs 31-37 and herbs 15-23%) in concentrationof nutrients in leaves occurred during senescence. The uptakeof nutrients by the vegetation and also by the different components,with and without adjustment for internal recycling, has beencalculated separately. Annual transfer of litter nutrient tothe soil by vegetation was 113·7-137·6 N, 11·6-14·6P and 80·1-83·2 K kg ha^-1 year^-1. Turnover rateand time for different nutrients ranged between 0·72-0·89year^-1 and 1·12-1·39 years, respectively. Thehigh turnover rate of litter on the forest floor indicates thegreater productivity of the stands, which was due to the higherdry matter dynamics and nutrient release for the growing vegetation.The nutrient use efficiency in poplar plantations ranged from159-175 for N, 1405-1569 for P and 295-332 for K. Compared withEucalyptus, there was a higher proportion of nutrient retranslocationin poplars largely because of higher tissue nutrient concentrations;this indicates lower nutrient use efficiency as compared tothe eucalypt plantation. Compartment models for nutrient dynamicshave been developed to represent the distribution of nutrientpools and net annual fluxes within the system.Copyright 1995,1999 Academic Press Populus deltoides plantations (Clone D₁₂₁), nutrient retranslocation, net nutrient uptake, nutrient use efficiency, nutrient cycling, nutrient pool, nutrient fluxes     

Nutrient Movement in Litter Fall and Precipitation Components for Central Himalayan Forests

The annual total litter fall in six Central Himalayan forestsranged from 2.1 to 3.8 t C ha^–1, of which 54 to 82 percent was leaf litter, 9–20 per cent wood litter and 6–14per cent other litter. In all forests the order of relativeabundance of nutrients (kg ha^-1 year^-1) in litter fall was Ca(50.8–91.6) > N (47.7–72.2) > K (22.8–37.1)> P (4.1–6.4). Leaf litter accounted for 63–95per cent of the total nutrients returned through litter fall. In these forests throughfall ranged from 71.3 to 81.4 per cent,stemflow from 0.50 to 2.16 per cent and canopy interceptionfrom 17.7 to 28.2 per cent of the gross rainfall. In the incidentrainfall the concentration and annual input of Ca was the greatestand of P the least. Canopy precipitation was richer in all nutrientscompared to incident rainfall. Net gain of nutrients from thecanopy ranged from 0.16 kg ha^-1 year^-1, for P, to 17.77 kg ha^-1year^-1 for K. Leaching was greatest for K and least for N. Ofthe total quantity of nutrients returned to the soil, 11 to46 per cent was accounted for by precipitation components. Thusprecipitation inputs play a significant role in nutrient cyclingof these forests. Himalaya, forest, litter fall, precipitation components, nutrients     

Nutrient Dynamics in Himalayan Alder Plantations

Dynamics of four macro-nutrients were studied in an age series(7, 17, 30, 46 and 56 years) of Himalayan alder (Alnus nepalensisD. Don) plantations in the Kalimpong forest division of theeastern Himalayas. Concentrations of nutrients were in the orderN > K > Ca > P in most of the tree components and inunderstorey vegetation. There was an inverse relationship betweennutrient concentrations of perennial parts and diameter at breastheight. The relative contributions of standing state of nutrientsin different tree components of mature plantations were in theorder; bole > branch > below-ground part > twig andleaf > catkin. Sequential arrangement of nutrient storagein tree components was: N > K > Ca > P. Soil totalN and available P increased with plantation age. Annual inputsof nutrients (kg ha^-1) to the forest-floor via litterfall were:183-235 N, 4·9-7·0 P, 33·5-39·5K, and 9·2-10·8 Ca. Total annual accretion ofN through biological fixation ranged from 29 to 117 kg ha^-1in different plantations. Turnover rate and turnover time fordifferent nutrients in the age series of plantations fluctuatedbetween 0·10-0·55 year^-1 and 1·8-9·3years, respectively. Nutrient use efficiencies decreased withplantation age for all nutrients except for calcium. Uptakeof nutrients is a more energy consuming process than release.Copyright1993, 1999 Academic Press Alnus nepalensis D. Don, plantation age, nitrogen accretion, nutrient concentration, standing state, uptake, turnover     

Biomass, Productivity and Energetics in Himalayan Alder Plantations

Biomass, net primary production and energy fixation in an agesequence of Himalayan alder (Alnus nepalensis D. Don) plantationswere estimated in the Kalimpong forest division of the easternHimalayas. Biomass in the plantations ranged from 106 t ha^–1(7-year stand) to 606 t ha^–1 (56-year stand) demonstratingthe potential of the alder for accumulating large biomass. Netprimary production and net energy fixation rates of the plantationswere reduced by nearly half in the 7-year stand (25 t ha^–1year^–1; 421 x 10⁶ kJ ha^–1 year^–1) comparedwith the 56-year stand (13 t ha^–1 year^–1; 215 x10⁶ kJ ha^–1 year^–1). Compartmental models of energystorage and flow rates were developed for the 7-year and 56-yearstands. The production efficiency, energy conversion efficiencyand energy efficiency in N₂ fixation have inverse relationshipswith plantation age. These efficiencies, when treated with eachother, showed significant exponential functions. Alnus nepalensis D. Don, Himalayan alder, plantation age, biomass, net primary production, energy flow, efficiencies     

Dynamics of Nutrient Translocation in Stemwood across an Age Series of a Eucalyptus Hybrid

Despite the continuous nature of growth of eucalyptus hybridsin Congo, taper functions fitted to stem profiles of one clonethroughout stand development, combined with annual tree measurements,made it possible to locate accurately the position of annualrings in stems. Annual rings were identified on discs of woodsampled every 4 m in four trees cut from 1-, 2-, 3-, 4-, 5-,6- and 7-year-old stands. Chemical analysis, performed individuallyfor each ring per level and per tree sampled, made it possibleto quantify the changes in nutrient content of the rings duringstand development. Nutrient translocation in stemwood was thuscalculated in a stepwise manner between trees of two successiveages. The cumulated nutrient translocations in stemwood fromthe 1-year-old stage to the 6-year-old stage amounted to 18·5kg ha^-1N, 4·2 kg ha^-1P, 38·8 kg ha^-1K, 1·5kg ha^-1Ca and 3·2 kg ha^-1Mg. They represented 11, 18,121, 6, and 15% of the amounts of N, P, K, Ca and Mg accumulatedin stemwood, respectively, at the 7-year-old stage (loggingage). Negative translocations of N, P, Ca and Mg in stemwoodbetween 6 and 7 years might indicate an improvement in the nutritivestatus of the stand at the end of the rotation. Much translocationof K in stemwood suggests that this process might be involvedin the high use efficiency of this element. Copyright 2001 Annalsof Botany Company Translocation, stemwood, ring, nutrient, Eucalyptus, age series     

Species Structure, Dry Matter Dynamics and Carbon Flux of a Dry Tropical Forest in India

Species composition, plant biomass and net primary productivitywere studied on three sites of a dry tropical forest The forestwas characterized by small structure with 38–10.4 m2 ha^–1tree and 3 1–7 8 m² ha^–1 shrub basal cover Speciesdiversity was highest for the mid-slope site while the concentrationof dominance was greatest for the hill-top stand The beta diversitywas 3 1 Total standing crop of vegetation averaged 66 98 t ha^–1with 46 70 t ha^–1 in the tree layer, 13.97 t ha^–1in the shrub layer, 0.35 t ha^–1 in the herb layer, 2 83t ha^–1 in the litter layer and 3 13 t ha^–1 in fineroots Of the total annual litterfall (4 88–6.71 t ha^–1),69% was accounted for by leaves and 31% by non-leaf matter Netprimary production (NPP) ranged between 11 3 and 19 2 t ha^–1year^–1, to which the contributions of trees, shrubs andherbs averaged 72, 22 and 6%, respectively Contribution of rootsto NPP was substantial and ranged from 2 9 to 5 3 t ha^–1year^–1 A total of 83% of vegetation carbon was storedin the above-ground plant parts while the above-ground NPP wasresponsible for 72% of the total carbon input into the systemThe contribution of foliage, herbaceous vegetation and fineroots to carbon turnover was disproportionately larger comparedto their share in the total standing crop Carbon budgeting indicatedthat the forest was an accumulating system, over at least theshort term Dry tropical forest, biomass, litterfall, net primary production, carbon budget, carbon flux     

Above- and belowground organic matter storage and production in a tropical pine plantation and a paired broadleaf secondary forest

The distribution of tree biomass and the allocation of organic matter production were measured in an 11-yr-old Pinus caribaea plantation and a paired broadleaf secondary forest growing under the same climatic conditions. The pine plantation had significantly more mass aboveground than the secondary forest (94.9 vs 35.6 t ha^-1 for biomass and 10.5 vs 5.0 t ha^{-1 for litter}), whereas the secondary forest had significantly more fine roots (⩽2 mm diameter) than the pine plantation (10.5 and 1.0 t ha^-1, respectively). Standing stock of dead fine roots was higher than aboveground litter in the secondary forest. In contrast, aboveground litter in pine was more than ten times higher than the dead root fraction. Both pine and secondary forests had similar total organic matter productions (19.2 and 19.4 t ha^-1 yr^-1, respectively) but structural allocation of that production was significantly different between the two forests; 44% of total production was allocated belowground in the secondary forest, whereas 94% was allocated aboveground in pine. The growth strategies represented by fast growth and large structural allocation aboveground, as for pine, and almost half the production allocated belowground, as for the secondary forest, illustrate equally successful, but contrasting growth strategies under the same climate, regardless of soil characteristics. The patterns of accumulation of organic matter in the soil profile indicated contrasting nutrient immobilization and mineralization sites and sources for soil organic matter formation.     

Internal Nutrient Translocation in Chestnut Tree Stemwood: III. Dynamics Across an Age Series of Castanea sativa (Miller)

Nutrient translocation in chestnut tree stemwood was calculatedfrom the distribution of nutrient content throughout the tissuelife-span. The dynamics of internal translocation were followedduring the crop rotation by means of an age series of five coppicedstands (2–19 years). N, P, K, Ca and Mg contents in treerings were estimated from the concentrations along a verticaland radial gradient and from the ring volume obtained usingstem ring analysis.Real nutrient translocation was calculatedstepwise between successive stages in the age series;apparenttranslocation was computed on a complete tree rotation by comparingthe initial content just after the ring was formed with themineral content in the oldest stand. There was a marked translocationof N, P, K and Ca when the rings were physiologically-activetissues. Real translocation of N, P and K (but not Ca) increasedwith stand age, obviously in parallel with the enlarged stemwoodbiomass reaching 23.2 and 20.6 kg ha^-1for K and N in the lastyears of rotation, nearly 5 kg ha^-1for Mg and about 3 kg ha^-1forCa and P. Potassium was the most mobile element since translocationreached 60% of the total amount immobilized in the stemwoodat the end of the rotation, whereas values for N, P and Mg wereapproximately 25% and 10% for calcium. Total apparent translocationreached respectively 39.2 and 32.4 kg ha^-1for K, N, approximately12 and 7 kg ha^-1for Mg and Ca and only 4.4 kg ha^-1for P. Totalapparent translocation as a percentage of total wood immobilizationwas 114% for K, 83% for Mg, 63% for P, but only 39% for N and24% for calcium. Translocation; nutrient content; stemwood; tree ring; coppice; age series; dynamics; chestnut tree; Castanea sativa Miller     

Determination of a Critical Nitrogen Dilution Curve for Winter Wheat Crops

A set of N-fertilization field experiments was used to determinethe 'critical nitrogen concentration', i.e, the minimal concentrationof total N in shoots that produced the maximum aerial dry matter,at a given time and field situation. A unique 'critical nitrogendilution curve' was obtained by plotting these concentrationsN_ct (% DM) vs. accumulated shoot biomass DM (t ha^-1). It couldbe described by the equation: N_ct = 5·35DM^-0·442 when shoot biomass was between 1·55 and 12 t ha^-1. Anexcellent fit was obtained between model and data (r² = 0·98,15 d.f.). A very close relationship was found using reducedN instead of total N, because the nitrate concentrations inshoots corresponding to critical points were small. The criticalcurve was rather close to those reported by Greenwood et al.(1990) for C₃ plants. However, this equation did not apply whenshoot biomass was less than 1·55 t ha^-1. In this case,the critical N concentration was independent of shoot biomass:the constant critical value N_ct = 4·4% is suggested forreduced-N. The model was validated in all the experimental situations,in spite of large differences in growth rate, cultivar, soiland climatic conditions; shoot biomass varying from 0·2to 14 t ha^-1. Plant N concentration was found to vary by a factor of fourat a given shoot biomass level. In the heavily fertilized treatments,shoot N concentration could be 60% higher than the criticalconcentration. Most (on average 80%) of the extra N accumulatedwas in the form of reduced N. The proportion of nitrate to totalN in shoot mainly depended on the crop stage of development.It was independent of the nitrogen nutrition level.Copyright1994, 1999 Academic Press Winter wheat, Triticum aestivum, arable crops, plant N concentration, aerial biomass, critical nitrogen, dilution curve, fertilization, reduced N, nitrate     

Mass loss and nitrogen dynamics in decomposing acid forest litter in the Netherlands at increased nitrogen deposition

Litterbag experiments were carried out in five forest ecosystems in the Netherlands to study weight loss and nitrogen dynamics during the first two years of decomposition of leaf and needle litter. All forests were characterized by a relatively high atmospheric nitrogen input by throughfall, ranging from 22–55 kg N ha^–1 yr^–1.Correlation analysis of all seven leaf and needle litters revealed no significant relation between the measured litter quality indices (nitrogen and lignin concentration, lignin-to-nitrogen ratio) and the decomposition rate. A significant linear relation was found between initial lignin-to-nitrogen ratio and critical nitrogen concentration, suggesting an effect of litter quality on nitrogen dynamics.Comparison of the decomposition of oak leaves in a nitrogen-limited and a nitrogen-saturated forest suggested an increased nitrogen availability. The differences in capacities to retain atmospheric nitrogen inputs between these two sites could be explained by differences in net nitrogen immobilization in first year decomposing oak leaves: in the nitrogen-limited oak forest a major part (55%) of the nitrogen input by throughfall was immobilized in the first year oak leaf litter.The three coniferous forests consisted of two monocultures of Douglas fir and a mixed stand of Douglas fir and Scots pine. Despite comparable litter quality in the Douglas fir needles in all sites, completely different nitrogen dynamics were found.     

Microbial Community Structure and Density Under Different Tree Species in an Acid Forest Soil (Morvan, France)

Overexploitation of forests to increase wood production has led to the replacement of native forest by large areas of monospecific tree plantations. In the present study, the effects of different monospecific tree cover plantations on density and composition of the indigenous soil microbial community are described. The experimental site of “Breuil-Chenue” in the Morvan (France) was the site of a comparison of a similar mineral soil under Norway spruce (Picea abies), Douglas fir (Pseudotuga menziesii), oak (Quercus sessiflora), and native forest [mixed stand dominated by oak and beech (Fagus sylvatica)]. Sampling was performed during winter (February) at three depths (0–5, 5–10, and 10–15 cm). Abundance of microorganisms was estimated via microbial biomass measurements, using the fumigation–extraction method. The genetic structure of microbial communities was investigated using the bacterial- and fungal-automated ribosomal intergenic spacer analysis (B-ARISA and F-ARISA, respectively) DNA fingerprint. Only small differences in microbial biomass were observed between tree species, the highest values being recorded under oak forest and the lowest under Douglas fir. B- and F-ARISA community profiles of the different tree covers clustered separately, but noticeable similarities were observed for soils under Douglas fir and oak. A significant stratification was revealed under each tree species by a decrease in microbial biomass with increasing depths and by distinct microbial communities for each soil layer. Differences in density and community composition according to tree species and depth were related to soil physicochemical characteristics and organic matter composition.     

Plant Biomass,Nutrient Concentration and Nutrient Storage in a Tropical Dry Forest in the South–west of Madagascar

Plant biomass, mineral composition and the amounts of nutrients in the different fractions of the vegetation were determined for a dense dry deciduous forest growing on light red sands in south-western Madagascar. Complete harvesting and soil coring were used to determine the above- and below-ground biomass respectively. The above-ground biomass, weighing 118 t ha⁻¹ (dry matter), was mostly (96%) made up of phanerophytes (woody trees and shrubs >25 cm tall). Dead material (litter and dead wood on the soil surface) represented 13.8 t ha⁻¹. These results fit well into the range of values reported for other tropical ecosystems. The below-ground biomass was 17.8 t ha⁻¹ giving a root/shoot ratio of 0.15. Rooting is superficial. The nutrient concentration in this dry forest on light reddish-brown sands is, as in other dry forests, considerably higher than that usually found for humid forests. Calcium is the most abundant element. The plant biomass Ca/K ratio is much higher than that of humid tropical forests. In spite of its high originality, this Madagascan dry forest has the same behaviour as other dry forests of the world.     

Estimates of biomass and primary productivity in a high-altitude maple forest of the west central Himalayas

The paper describes the biomass and productivity of maple (Acer cappadocicum) forest occurring at an altitude of 2,750 m in the west central Himalayas. Total vegetation biomass was 308.3 t ha⁻¹, of which the tree layer contributed the most, followed by herbs and shrubs. The seasonal forest-floor litter mass varied between 5.4 t ha⁻¹ (in rainy season) and 6.6 t ha⁻¹ (in winter season). The annual litter fall was 6.2 t ha⁻¹, of which leaf litter contributed the largest part (59% of the total litter fall). Net primary productivity of total vegetation was 19.5 t ha⁻¹ year⁻¹. The production efficiency of leaves (net primary productivity/leaf mass) was markedly higher (2.9 g g⁻¹ foliage mass year⁻¹) than those of the low-altitude forests of the region.