Three most promising protection methods of pine pulp wood stacks against the attacks of Tomicus piniperda L. were compared. The methods were the covering of stacks by fibreglass-strengthened paper or twofold achrylene netting, removing the upper parts of stacks, and enhanced planning of the placement of the timber store using ARC/INFO GIS-software. T. piniperda was observed to strongly prefer the upper parts of the stacks: 90 % of the beetles occurred within 0.5 meters of the top of the stacks. Covering of the stacks decreased the attack density of T. piniperda, and the protection effect of covering was 80 %. Due to long transport distances and fragmentation of forest landscape the relocation of timber store was found to be an unsuitable method in the practical level. Also, taking into account the costs of the method, removing of the upper parts of stacks was considered to be the optimal solution.
Drying of pulpwood bolts of Scots pine (Pinus sylvestris L.), birch (Betula spp.) and Norway spruce (Picea abies (L.) H. Karst.) was studied by measuring the drying of sample bolts placed in experimental piles. The results revealed that the main factors affecting timber drying are debarked surface area, moisture content at the time of felling and the size of the bolt. Furthermore, pine and spruce bolts located in the upper part of the pile dry better than bolts near the ground.
The investigation of green weight changes of whole piles of pine and birch was based on data collected in 1987–91. The green weight of piles was dependent mainly on storage time and on region; effect of weather variables could not be distinguished. Specific calibrating coefficients for motor-manual and mechanical cutting were included in the green weight equations.
Comparison between green weight equations and detected weight losses of sample piles indicates that fitted models seem to produce at least approximate results for the green weights, the said results thus lending themselves to be utilized as part of a transportation cost model.
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Shoot losses due to maturation feeding by pine shoot beetles (Tomicus piniperda (L.) and T. minor (Hart.), Col., Scolytidae) and subsequent growth losses were studied in Scots pine (Pinus sylvestris L.) stands growing at different distances from a timber yard, where pine timber was stored during the years 1982–84. In autumn 1985, pine trees were felled at 20, 40, 80, 500 and 1,500 m distance from the timber yard, five trees in each distance class. Trees were analysed for beetle attack, needle biomass and growth. In autumn 1988, increment cores were taken from 20 trees in each distance class.
In 1985, different damage estimates showed that beetle damage was more than 10-fold in the crowns of pine trees growing close to the timber yard as compared to less damaged trees in greater distance. Crude needle biomass estimates indicated that the trees attacked most had lost more than half of the total foliage. Following three years of attack, basal area growth decreased for 2–3 years and recovered during the subsequent 3 years, the total period of loss thus being 5–6 years. The loss in volume growth during 1983–85 was ca. 70, 40, 20 and 10% at 20, 40, 80 and 500 m distance from the beetle source, respectively, compared to the stand at 1,500. Growth losses did not occur until the number of beetle-attacks, ”pegs”, exceeded ca. 200 per tree. The highest observed growth losses occurred in trees with more than 1,000 pegs per tree.
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Six seed collections were made in September–December 1984 in a natural Scots pine (Pinus sylvestris L.) stand in Southern Finland. The seeds were germinated immediately after the cone collection and three photoperiods (0.8 and 24 hours) were used in germination tests.
The seeds collected in September and October possessed relative dormancy, i.e. they did not germinate in darkness and at 10°C. Later in November and December the seeds were capable to germinate in darkness and at low temperature also. The gradual change in germination capacity is attributed to chilling temperatures in natural environments or in cone storage.
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On the basis of a limited material, the drying of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) timber at room temperature decreased the thickness of the bark proportionally to the decrease in the moisture content. The decrease was the greatest in the middle portion of the trunk. In the spruce material, the decrease in bark thickness was exceeded by the shrinkage of the wood. During soaking, the bark thickness of both tree species decreased, too, contrary to the presupposed hypothesis. In both cases, the shrinkage was the greatest in the middle portion of the trunk. In the spruce material, the decrease in bark thickness was exceeded by the shrinkage of the wood. Possible explanation for the phenomenon is discussed.
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Soft X-ray radiation (Grenz rays) has been used in the X-ray radiography of seeds. It is based on the principle that the different parts of the seed absorb X-rays to a slightly varying extent. Empty seeds and empty regions in the seeds appears as dark areas on the film. X-ray radiography without staining and X-ray contrast radiography were compared to study the stored seeds of Scots pine (Pinus sylvestris L.). The results were compared with the results of germination in a Jacobsen germinator according to ISTA norms.
Normal X-ray radiography gave too good estimates of germinative capacity of the seeds, and was shown to suit only when it is used to study fully ripe seeds which have recently been collected in an undamaged condition. The results of X-ray contrast radiography when barium chloride was used as the stain, however, followed closely the germination results.
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Seedlings of three different Scots pine (Pinus sylvestris L.) nursery stock, 1+0 ,1+1, and 2+0, were kept over the winter, after they had been packed in polythene bags, in three different ways: 1) In a refrigerated storage room, 2) in a wooden crate in the ground, 3) submerged in a lake. The seedling to which they were to be compared with were left over the winter in a nursery bed. The 1,800 seedlings were planted out in the spring 1966 in 15 random blocks. Their development was scrutinized during the three subsequent falls.
The seedlings which had been stored in the lake all died. The seedlings which had been stored along the 1st and 2nd method, managed almost as well as the ones which had been kept over the winter in the nursery bed, except for those of 1+0 stock.
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Scots pine (Pinus sylvestris L.) seedlings were stored for five days in an ordinary wood shed. One half of the seedlings were planted out directly, and another half after soaking the roots of the seedlings for 3–6 hours in water to compensate the possible water deficit developed. According to the results of the experiment, the effect of watering was extremely small. The difference observed, which was in favour of the trees that had been watered during storage, was discernible only in the needle length and in the number of lateral buds; in mortality or in the growth of the seedlings no difference could be observed.
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The aim of this study was to investigate how the weight loss and water content of cold stored plants depend on the storage conditions, and if there is a clear connection between these factors and the field survival of the planting stock. The experiments were carried out in a climate chamber at about +2°C and at three moisture levels (about 70, 85, and 95%) from November 1968 to May 1969. Three-year-old seedlings of Scots pine (Pinus sylvestris L.) average length 127 mm, diameter 3.5 mm and the top/root-ratio of fresh weight 1.93, were stored in open and sealed plastic bags. In addition, a transpiration retardant (Silvaplast) was used. The plastic bags (10 plants each) were weighted every 4. week. The remaining 270 seedlings were planted out and inspected after one growing season.
Although the experiment was made in a small scale, the results showed clearly that plant mortality, varying between 3 and 97%, was due to the storage conditions. The weight loss ranged between 2 and 50%, and the correlation between the weight loss and the mortality in the field was high. The water content of the seedlings was about 61%. The correlation between water content and survival was very high. Thus, the determination of weight loss or water content could be a useful method in observing the changes of water balance of the seedling stock during winter-storage. Further investigations are needed to show the tolerable rate of drying out for different sorts of plants. The Silvaplast-treatment had no visible effect either on the drying out or on the field survival.
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The aim of the study was to investigate the effect of four packing methods on the field survival and growth of seedlings and transplants of Scots pine (Pinus sylvestris L.) stored over the winter in a cold-storage cellar. The following sorts of plants were used: one-year-old seedlings (1+0) grown in a plastic greenhouse, two-year-old (2+0) open grown seedlings and three-year-old open grown transplants. These plants were stored in open wooden boxes, in sealed plastic bags, in boxes with wet peat on the bottom and in plastic-laminated paper bags.
The control plants were of the same types and were kept in a nursery over the winter. The storage was carried out in a mantle-chilled cold-storage from October 1966 to May 1967. The temperature in the cold-storage was kept around -2 °C and the relative humidity of the air over 90%. The water content of a randomly selected sample plants showed no increase in water deficit after the storing. Part of the seedlings were transplanted in the nursery and the rest were planted in a clear-cut area. A number of the latter plants were treated with an insecticide (1% Intaktol, which contains DDT, Lindane and dieldrin) before planting. All the experiments were examined after one growing season and the planting experiments the next fall.
The transplants (2+1) in the nursery, and in the forest had survived and grown better than the seedlings. In the nursery the 1+0 seedlings survived and grew better than the 2+0 seedlings. There was no difference in mortality between the seedlings. After the first growing season occasional significant differences between the packing methods were observed, but they disappeared during the second growing season. Thus, all packing methods proved to be as successful as the control method without winter storage.
Transplants were more often attacked by the large pine weevil (Hylobius abietis L.) than the smaller seedlings. The damage, however, was considerably greater on the seedlings because of their lower resistance. No significant differences in the Hylobius-attack between the packing methods could be observed. The Intaktol-treated plants were as often attacked as the untreated ones, but the damage was slighter on the treated ones.
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The aim of the present study was to establish, by means of planting experiments, the influence of different packing, heeling-in and watering as well as the length of the storage period on the development of Scots pine (Pinus sylvestris L.) seedlings, in all 2,090 seedlings, that had been lifted from the nursery bed in spring. The plants were packed in bundles and into plastic sacks in 1965 (6 storage methods) and in 1966 (3 storage methods). Control seedlings were planted without storing at the time when storage of the test material begun. The plantations were followed 3–4 years.
Storage for two weeks in the different ways and planting without storage gave similar results when seedling survival was compared. Storage in plastic sack proved to be as good as storage in bundles in a cellar, and healing-in in moist soil or in a drain were both usable methods. Watering the seedlings did not improve the results, which indicates that the storage caused no serious lack of water.
After four growing seasons an average of 19,6% of the seedlings of the 1965 experiment died, the bulk of them by the end of the first growing season. Despite control treatment, Hylobious abietis caused serious damages. In the plantations of the year 1966 mortality of the seedlings was under 5% by the end of third growing season. During the first two growing seasons after planting differences in growth of the seedlings stored in different ways could be observed in the plantations of the year 1965, but the differences levelled out later. In the plantations established in 1966 no differences in growth occurred.
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The aim of the study was to establish how the cold storage of cones of Norway spruce (Picea abies (L.) H. Karst.) affects the viability of the seeds and the percentage ratio in 7 days. A parallel study was made of the longevity of seed in barn-stored cones subject to weather fluctuations and the longevity of seed extracted immediately and stored in the conventional way in an air-tight container. The cones were collected near Kuopio in Central Finland and near Tampere.
The viability and germination rate of the control sample was constant throughout the storage period. This storage method proved the best. The viability of seeds kept in cones declined in cold storage after 3 ½ months. The cones collected in Tampere were damaged by Laspeyresia strobilella, which affected the viability of the seeds.
The viability of seeds stored in cones in a barn had not weakened by the end of May, however, they deteriorated during the summer, as did the seeds stored in cones in the cold storage. Viability of the seeds was still 94% in October. The germination rate was constant in each lot up to the end of May, after which it decreased to 81.7–86.1% in October.
The results show that healthy spruce cones can be stored in paper sacks in a single layer in cold storage and in an ordinary barn for several months without it affecting the viability of the seeds.
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Seed storing experiments with cones of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) H. Karst.) were conducted in Oitti seed extracting plant in Southern Finland from February to December 1955. The pine cones were stores for 267 and the spruce coned for 304 days. In four of the storage methods the cones were packed in sacks and another four in wooden boxes. Sample of cones were taken once a month, seeds were extracted and the germinative capacity was tested. The remaining extracted seeds were placed in storage, and in January 1956 moved to cold seed cellar until 1962, when the viability of the seeds was tested.
According to the results, cleaned pine cones can be stores for at least nine months using almost all methods of storage which are commonly used at our seed traction plants, without hazarding the usability of the seeds. The seeds in spruce cones, however, seemed to be more sensitive to conditions during the storage. The germinative capacity of the spruce seeds began to decrease after the beginning of May. Later the seeds were infected with mould, which increased towards the end of the experiment.
Thus, preservation of the germinative capacity of the seeds of pine and spruce requires storage in different conditions. The results suggest that extraction of spruce seeds should be finished during the cold winter months. It seems that seed in the cones of pine and spruce endure storage in piles of paper or cloth sacks at least as well as in wooden boxes. Occasional warming of the storage, snow and foreign material among the cones and an over meter thick cone layer decreased the germinative capacity of spruce seeds during spring and summer. Spruce seeds that had been extracted immediately after collecting of the cones preserved their germinative capacity well during an eight years storage period.
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This study was carried out in 1966 in the nursery at Hyytiälä, Korkeakoski Forest District, in Southern Finland. The influence of lifting date (two liftings), way of packing (two methods) and length of storage (one, three and six weeks) on the development of Scots pine (Pinus sylvestris L.), 2 + 1, during the four years following planting was assessed. On the seedlings stored for six weeks, the influence of compensating for the water deficit was also studied.
According to the results, the lifting carried out later, i.e. when the seedlings had already started growth, gave slightly better results than when seedlings were lifted earlier. No difference could be observed for seedlings stored for one week, but for the seedlings stored for three or six weeks, mortality in the lot lifted earlier was 6- to 7-fold that of the seedlings lifted later. The main reason for this was probably that the seedlings of the earlier lifting suffered from lack of water at the time of lifting.
The growth of the seedlings lifted earlier and stored for three weeks showed a decrease compared to those lifted later. For the seedlings stored for six weeks, on the other hand, faster growth was recorded for both the seedlings of the earlier and the later lifting in comparison with those stored for shorter times. Watering increased to some extent the growth of the seedlings stored for six weeks.
During the normal, one- and three-week storing periods, seedlings were well preserved when packed both in bundles and in polythene sacks. Three years after the planting the average mortality was about 10%. Effect of watering was large for those seedlings that had been longer in the storage.
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The aim of this study was to find out the planting vigour of Scots pine (Pinus sylvestris L.) stored over the winter either in winter storage mainly in the temperature of 4 – -6 °C or in nursery beds. The experimental planting included about 4,500 of 2+1 transplants in Northern Finland. In spring 1965 the control plants were lifted in the spring before budbreak and stored in closed bags in a cold store, in the following year the control plants were lifted in June when the growth had started.
Winter storage of pine transplants in a cold store, tightly closed into bags for the major period, did not, according to the results, increase plant mortality as compared to lifting in the spring. Soaking the stored-plant roots did not affect plant mortality. Mortality was rather small in all treated lots and probably more dependent on planting site and other local factors.
No consistent difference on the leader growth, needle length, bud number and plant grade was found between the plants stored over winter and those lifted in the spring. Sealing the plants into tight bags for winter proved to be suitable method, efficiently preventing water shortage in the plants. No moulds or fungal diseases were found in the plants. In the exceptionally cold 1965–1966 winter, temperature in the cold store sank to -15 °C, but in spite of the temperatures below the recommended storing temperature, the plants survived well. The reason was that the plants froze slowly in the fall and thawed out slowly in the spring.
The value of vigour grade in predicting plant-characteristic development proved to be good, and predicted plant development also in the following year fairly well.
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We used forest ecosystem model simulations to study how forest conservation and management intensity affected timber yield, ecosystem carbon stocks, amount of dead wood, and habitat suitability area in a middle boreal forest region of Finland under changing climate over a 90-year simulation period. We used the following forest conservation and management scenarios: baseline forest management (BM), BM with 10 or 20% increase of conservation area with or without intensified forest management (i.e. improved forest regeneration material and forest fertilization). The simulations were done under current climate (reference period of 1981–2010), and Representative Concentration Pathway (RCP) climate change projections under the RCP2.6 and RCP4.5 forcing scenarios. Overall, increasing the forest conservation area decreased timber yield and increased the ecosystem carbon stock, the amount of dead wood and consequently the area of suitable habitat for saproxylic species. The use of intensified forest management reduced the loss of timber yield, increased ecosystem carbon stock, the amount of dead wood and area of suitable habitat for saproxylic species. At the end of simulation period, the use of intensified forest management even overcompensated (4–6% higher) the timber loss from 10% increase of conservation area. Under changing climate, timber yield, the amount of dead wood and the area of suitable habitats for saproxylic species increased. To conclude, with intensified forest management it is possible, in the short term, to decrease the loss of timber yield through increased forest conservation area and in the long term maintain or even increase it compared to baseline forest management.
The situation on the log yard changes seasonally and also over the years. The quantities of assortments to be stored, their number and also the type of wood can change. To respond to this, we have developed a dynamic log yard planning model for assigning roundwood to specific ejection boxes and storage areas in order to minimise the overall transport distances of the loaded transportation vehicles on the log yard, including any possible re-allocation of assortments. The study centres on the log yard of a medium-sized hardwood sawmill in Europe, with actual cutting data from a six-month period. We are comparing a multi-period binary integer program with a model that operates on a period per period basis and a solution approach that splits the problem into two subproblems and solves them sequentially. The models undergo testing with decreasing space capacities at the storage boxes on the log yard and are compared. If capacity is continuously decreasing from 100% to 80%, then period per period planning is on average 13% worse than multi-period planning. We also investigate how the solutions change when twice as many or half as many assortments are stored at the log yard. In addition, we study how much the solutions improve when logs can be removed from the storage boxes to clear them and release them for other material in the following period.
Bark beetles are amongst the most aggressive pest agents of coniferous forests. Due to this, many boreal countries have designated laws aiming to lower the risk of bark beetle epidemics. Finland’s forest legislation has pre-emptive measures targeted against bark beetles, and for Scots pine (Pinus sylvestris L.), the law concerns pine shoot beetles (Tomicus spp.). This study used data collected around 25 piles of Scots pine roundwood that were harvested in the winter but left in the forest until the following November. Thus, the pine shoot beetles were able to use the piles for breeding. We assessed the number of emerged insects from the piles and the cascading damage they caused in the surrounding forests. All roundwood piles, regardless of their volume, were used by the beetles for breeding. Highest densities of beetle exit holes were found from the parts of the log with thick and intact bark. If the bark of the log was damaged by the harvester head, the number of beetles decreased significantly. Depending on the volume of the roundwood pile, the cascading damage (fallen shoots) was noticeable up to ca. 40–60 m from the roundwood pile. Storing of piles smaller than 50 m3 did not cause excess damage. The number of fallen shoots per tree was generally below the known thresholds for when growth losses can occur. However, the study was conducted in mature forests, and it can be assumed that the recorded damage levels would severely affect the growth of young pines, raising the question of where to store the roundwood. As with other bark beetles, the role of Tomicus beetles as damage agents may change in the future, but based on this as well as past studies, the species can be viewed as a notable damage agents only around long-term wood storage sites in the current northern conditions.
Accurate estimates of aboveground biomass (AGB) strongly depend on the suitability and precision of allometric models. Diospyros mespiliformis Hochst. ex A. DC. is a key component of most sub-Sahara agroforestry systems and, one of the most economically important trees in Africa. Despite its importance, very few scientific information exists regarding its biomass and carbon storage potential. In this study direct method was used to develop site-specific biomass models for D. mespiliformis tree components in Burkina Faso. Allometric models were developed for stem, branch and leaf biomass using data from 39 tree harvested in Sudanian savannas of Burkina Faso. Diameter at breast height (DBH), tree height, crown diameter (CD) and basal diameter (D20) were regressed on biomass component using non-linear models with DBH alone, and DBH in combination with height and/or CD as predictor variables. Carbon content was estimated for each tree component using the ash method. Allometric models differed between the experimental sites, except for branch biomass models. Site-specific models developed in this study exhibited good model fit and performance, with explained variance of 81–98%. Using models developed from other areas would have underestimated or overestimated biomass by between –72% and +98%. Carbon content in aboveground components of D. mespiliformis in Tiogo, Boulon and Tapoa-Boopo was 55.40% ± 1.50, 55.52% ± 1.06 and 55.63% ± 1.00, respectively, and did not vary significantly (P-value = 0.909). Site-specific models developed in this study are useful tool for estimating carbon stocks and can be used to accurately estimate tree components biomass in vegetation growing under similar conditions.
Stored nutrient reserves are closely correlated with survival and growth of transplanted seedlings. Previous studies have proven that combining pre-hardening fertilization (PF) with fall fertilization (FF) built seedling nutrient reserves more effectively; however, their effect on transplanting performance is poorly documented. We investigated the independent and interacting effects of 2 levels of PF and 4 levels of FF on seedling growth, nutrient acquisition and accumulation during different growth phases 1 year after transplanting of Quercus variabilis Blume in a nursery. High PF benefited nutrient reserves and subsequent transplanted seedling growth and tissue nutrient storage at the end of the rapid growth and hardening phases. Fall fertilization with 36 mg N increased stem dry mass and tissue nutrient content at the end of the hardening phase. At the conclusion of establishment, PF and FF showed a significant interaction for N and K uptake from soil. At the end of the rapid growth and hardening phases, high PF consistently increased nutrient uptake. Enhanced N and K uptake occurred following application of 36 mg N of FF at the end of the hardening phase. Distinct roles for PF and FF on 3 phases of transplanted seedlings demonstrated the necessity to evaluate fertilization in terms of nutrient reserves and subsequent transplanting performance in consecutive phases. Combining 100 mg N seedling–1 during pre-hardening with 36 mg N seedling–1 during fall yielded ideal transplanting performance for Quercus variabilis seedlings.
The primary aim of this study was to clarify the chipping productivity and fuel consumption of tractor-powered and truck-mounted drum chippers when chipping pine pulpwood at a terminal. The secondary aim was to evaluate the impact of wood storage time on the chemical and physical technical specifications of wood chips by chipping pulpwood from eight different storage time groups, using Scots pine (Pinus sylvestris) pulpwood stems logged between 2 and 21 months previously at the terminal with the above-mentioned chippers. Thirdly, the impact of sieve mesh size on the particle size distribution of wood chips from different age groups was compared by using an 80 mm × 80 mm sieve for a tractor-powered chipper and a 100 mm × 100 mm sieve for a truck-mounted chipper. With both chippers, the chipping productivity grew as a function of grapple load weight. The average chipping productivity of the tractor-powered chipper unit was 19 508 kg (dry mass) per effective hour (E0h), and for the truck-mounted chipper the average productivity was 31 184 kg E0h–1. The tractor-powered drum chipper’s fuel consumption was 3.1 litres and for the truck-mounted chipper 3.3 litres per chipped 1000 kg (dry mass). The amount of extractives or volatiles did not demonstrate any statistically significant differences between storage time groups. The particle size distributions with both chippers were quite uniform, and the storage time of pulpwood did not have a significant effect on the particle size distribution in any chip size classes. One reason for this might be that the basic density of chipped wood was homogenous and there was no statistical difference between different storage times. The use of new sharp knives is likely to have affected chip quality, as witnessed by the absence of oversized particles and the moderate presence of fines. The use of narrower 80 mm × 80 mm sieves on Scots pine material does not seem to offer any benefit compared to 100 mm × 100 mm from the chip quality point of view.
For sawmills, paper mills, particleboard, oriented strand board (OSB), fiberboard and other wood production factories, the log yard is the first step, where raw materials are sorted and stored before production begins. Due to the size of these production sites great potential exists for the optimisation of internal logistics. In this paper the different planning problems of the log yard are introduced and existing literature examined. Beginning with the tactical problems of structure, such as assessing material flow, planning facility layout and assigning storage areas, it continues with operational problems such as vehicle movement planning within the log yard, empty trip minimisation and the seasonality of raw material availability. Data derived from this study reveals a variety of possible solution methods, the applicability of which depends on the precise nature of the log yard operations. Additionally, several real life examples are provided which illustrate the potential for operational improvement.
Species-specific allometric equations for shrubs and small trees are relatively scarce, thus limiting the precise quantification of aboveground biomass (AGB) in both shrubby vegetation and forests. Fourteen shrub and small tree species in Eastern China were selected to develop species-specific and multispecies allometric biomass equations. Biometric variables, including the diameter of the longest stem (D), height (H), wet basic density (BD), and crown area and shape were measured for each individual plant. We measured the AGB through a non-destructive method, and validated these measurements using the dry mass of the sampled plant components. The AGB was related to biometric variables using regression analysis. The species-specific allometric models, with D and H as predictors (D-H models) accounted for 70% to 99% of the variation in the AGB of shrubs and small trees. A multispecies allometric D-H model accounted for 71% of the variation in the AGB. Although BD, as an additional predictor, improved the fit of most models, the D-H models were adequate for predicting the AGB for shrubs and small trees in subtropical China without BD data.