Relationships of culm surface area to other culm dimensions for bamboo, Phyllostachys pubescens

We determine the relationships of culm surface area to other culm dimensions for one of the largest bamboo species, Phyllostachys pubescens Mazel ex Houzeau de Lehaie. A total number of 150 sample culms were collected from a stand of P. pubescens in Mt. Toshima, Kumamoto Prefecture, western Japan. The culm surface area for each sample was calculated, and then the relationships of the culm surface area to basal area and product of diameter at breast height (dbh) and culm height were analyzed. The relationship between culm surface area and basal area could be described successfully by the power equation, whereas there was a linear relationship of culm surface area to product of dbh and height. Although the regression equations determined here would be useful in estimating culm surface area of P. pubescens, it is necessary to select an appropriate equation depending on the purpose and available time and labor.     

Tree size dependence of litter production, and above-ground net production in a young Hinoki (Chamaecyparis obtusa) stand

The study was carried out in a 9-year-old hinoki cypress (Chamaecyparis obtusa (Sieb. et Zucc.) Endl.), stand over a span of three years from July 1992 to June 1995, primarily to predict litter production from exteral tree dimensions by combining open-top clothtrap and clipping methods. Litter production was virtually concentrated in October and November. Stem cross-sectional area at the crown base was proved to be the reliable predictor of litter production, and that single regression model was evolved irrespective of year. The regression model had proportional constants of 2.696 × 10⁻² and 3.540 × 10⁻² kg cm⁻² year⁻¹ for leaf litter and total litter production, respectively. Utilizing the model, leaf litter production of the stand was assessed to be 5.04, 5.12, and 4.99, and total litter production to be 6.48, 6.58, and 6.40 Mg ha⁻¹ year⁻¹ for the first, second and third year, respectively. Biomass increment was 6.67, 7.80, and 7.70, tree mortality was 0.15, 0.13, and 0.41, and insect grazing was 0.09, 0.05, and 0.002 Mg ha⁻¹ year⁻¹ for the first, second and third year, respectively. Above-groud net production was therefore 13.39, 14.55, and 14.51, Mg ha⁻¹ year⁻¹, and biomass accumulation ratio (biomass/net production) was 1.86, 2.21, and 2.76 year for the first, second and third year, respectively. Considering data from earlier studies and the results of this study, biomass accumulation ratio,BAR (year), of hinoki stands was best related to above-ground biomass,y (Mg ha⁻¹), using the power function:BAR=0.112y ^0.936. Excluding seedling stands, leaf efficiency (above-ground net production per unit leaf mass) of hinoki stands was 0.91±0.02 (SE) Mg Mg⁻¹ year⁻¹, irrespective of stand biomass or age.     

Evaluation of drag coefficients of poplar-tree crowns by a field test method

To estimate the wind force that causes windthrow damage to a tree, the drag coefficients of actual-sized trees were evaluated by a field test method. In this method, wind velocity and stem deflection were monitored simultaneously. The wind force acting on a tree crown was calculated from stem deflection; stem stiffness was evaluated by conducting tree-bending tests. The results of tests conducted on three poplar trees showed that drag coefficient decreased with an increase in wind velocity. Although the variation in the drag coefficient was large at low wind velocity because of the vibrating behavior of the stem subjected to variable wind force, the variation at wind velocities above 10 m/s was small. The average drag coefficient at a wind velocity of 30 m/s was estimated by the curve-fitting of a power function to the wind velocity-drag coefficient relationship to be 0.102, which was smaller than that of actual-sized conifers studied in previous wind tunnel experiments. The drag coefficients of these crown areas in the defoliation season were smaller than those measured in the leafy season.     

Genetic mapping of AFLP markers in Japanese bunching onion (<Emphasis Type="Italic">Allium fistulosum</Emphasis>)

Summary The first genetic linkage map of Japanese bunching onion (Allium fistulosum) based primarily on AFLP markers was constructed using reciprocally backcrossed progenies. They were 120 plants each of (P₁)BC₁ and (P₂)BC₁ populations derived from a cross between single plants of two inbred lines: D1s-15s-22 (P₁) and J1s-14s-20 (P₂). Based on the (P₂)BC₁ population, a linkage map of P₁ was constructed. It comprises 164 markers – 149 amplified fragment length polymorphisms (AFLPs), 2 cleaved amplified polymorphic sequences (CAPSs), and 12 simple sequence repeats (SSRs) from Japanese bunching onion, and 1 SSR from bulb onion (A. cepa) – on 15 linkage groups covering 947 centiMorgans (cM). The linkage map of P₂ was constructed with the (P₁)BC₁ population and composed of 120 loci – 105 AFLPs, 1 CAPS, and 13 SSRs developed from Japanese bunching onion and 1 SSR from bulb onion – on 14 linkage groups covering 775 cM. Both maps were not saturated but were considered to cover the majority of the genome. Nine linkage groups in P₂ map were connected with their counterparts in P₁ map using co-dominant anchor markers, 13 SSRs and 1 CAPS.     

Development of a new high-throughput and small-size method for measuring sediment oxygen demand in lakes

Journal of Soils and Sediments - Sediment oxygen demand (SOD) measurement currently requires a long preparation time and bulky experimental equipment, which represent major obstacles to conducting...     

Both stem and crown mass affect tree resistance to uprooting

To examine the hypothesis that both stem and crown mass affect the resistance of a tree to uprooting and that tree resistance increases with increasing crown mass, we conducted tree-pulling experiments on three Picea glehnii plantations (stands A, B, and C: 27–32 years old) that differed in tree density and slenderness ratio. Allometries between crown and stem masses and between the critical uprooting moment and stem mass differed significantly among the three stands, with the crown mass and critical moment significantly larger in stand C than in stands A or B, despite the same stem mass. These results quantitatively verified our hypothesis. Allometries between crown and stem masses and between critical uprooting moment and stem mass were highly significant in each stand but were stand specific. Therefore, these allometries can be used to estimate tree resistance to uprooting in a given stand but not for data compiled from stands of various conditions and tree shapes. The allometry between critical moment and aboveground mass did not differ among the three Picea stands; thus, it is not stand specific and is generally appropriate to use for estimating tree resistance. To increase tree resistance to uprooting, we recommend light management for Picea glehnii plantations and probably other coniferous plantations as well.     

A model of seasonal foliage dynamics of the subtropical mangrove species Rhizophora stylosa Griff.growing at the northern limit of its distribution

Background： Progress of forest production in response to the environment requires a quantitative understanding of leaf area development. Therefore, it is necessary to investigate the dynamics of seasonal crown foliage in order to understand the productivity of mangroves, which play an important role in the subtropical and tropical coastlines of the world. Method： Crown foliage dynamics of the mangrove Rhizophora styloso were studies to reveal patterns of leaf recruitment, survival and seasonal leaf area growth. Results： Flushing of leaves occurred throughout the year, but both flushing and leaf area growth pattern of leaves varied with season. Maximum flushing occurred in summer, but leaf areas did not differ significantly with season. The half-expansion period is longer, and the intrinsic rate of increase was lower in winter. Summer flushed leaves grew faster at their initial stage and reached their maximum area over a shorter period of time. The difference in temperature and air vapor pressure deficit （VPD） between summer and winter contributed to the present dynamics of foliage patterns. The mean leaf longevity was estimated to be 13.1 month. The crown foliage area was almost stable throughout the year. Conclusions： Homeostatic control of the crown foliage area may be accompanied by the existence of ecophysiological mechanisms in R. stylosa. Integrating crown foliage dynamics into forest models represents an important step towards incorporating physiological mechanisms into the models for predicting growth responses to environmental changes and for understanding the complex responses of tree growth and litter production.     

Nondestructive measurement of cross-sectional shape of a tree trunk

To evaluate windthrow resistance with respect to stem breakage, a nondestructive method for determining the shape of trunk cross sections was developed. In this method, the coordinates of multiple gauge points set on the perimeter of a trunk are calculated by measuring the distances between them. The shape between the gauge points is generated with the use of a profile gauge placed between them. Measurement tests were conducted using profile gauges with lengths of 300 and 900 mm on model specimens with four shape patterns and four different diameters. The accuracy of the estimation was verified by comparing the section modulus calculated for the generated image and for the photograph. The average ratio of section modulus (generated/photo) for all specimens was 0.994, which indicates that the proposed method is highly accurate. The section moduli of hollow trunks can be evaluated using the profile method together with the drill resistance technique on the condition that 26% of the trunk diameter could be drilled without skew.