Biomass accumulation in rapidly growing loblolly pine and sweetgum |
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| Affiliation: | 1. DCC – Universidade Federal de Minas Gerais, Belo Horizonte 31270-010, Brazil;2. CCET – Unimontes, Montes Claros, Brazil;3. Microsoft Research, Redmond, USA;1. Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen, Fujian 361005, China;2. Fujian Key Laboratory of Advanced Materials, Xiamen University, Xiamen, Fujian 361005, China;1. Federal University of Rio Grande do Sul, School of Physical Education, 750 Felizardo Street, Porto Alegre City, Rio Grande do Sul State, Brazil;2. Hospital de Clínicas de Porto Alegre, 2350 Ramiro Barcelos Street, Porto Alegre City, Rio Grande do Sul State, Brazil;1. NANO-SciTech Centre, Institute of Science, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia;2. Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia;3. NANO-ElecTronic Centre, Faculty of Electrical Engineering, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia;4. Centre of Excellent in Nanotechnology and Department of Chemistry, King Fahd University of Petroleum and Minerals, Dhahran 31261, Saudi Arabia;1. Department of Mathematics, National Technical University of Athens, Zografou Campus, 15780 Athens, Greece;2. Mathematics Department, Washington State University, Pullman, WA 99164-3113, USA |
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| Abstract: | Loblolly pine (Pinus taeda) and sweetgum (Liquidambar styraciflua) trees, growing in International Paper Company's study of intensive management on marginal agricultural land near Bainbridge GA, were destructively sampled at the end of the sixth growing season. All trees were single family blocks of genetically superior trees planted 2.5 m apart on sub-soiled rows 3.6 m apart and grown with complete competition control. Management treatments were: control, irrigation, irrigation plus fertilization, and irrigation plus fertilization plus pest control. Tree measures were basal diameter, DBH, height of live crown, diameter at base of live crown, and total height. Twenty trees of each species were destructively sampled. Stems were sectioned at 1 m intervals, stem diameter determined at each end and sections were weighed green. Branches were removed and height, basal diameter, and length were measured on each branch. Branches were separated into foliated and unfoliated segments and weighed green. A stem disk and branch from each meter were returned to the lab to determine dry weight: green weight ratio. Foliated limb: foliage ratios were also determined from sub-sampled branches. Intensive culture resulted in larger growth differences for sweetgum (most intensive treatment 9.5 m tall, 13.1 cm DBH; control trees 5.0 m tall, 6.3 cm DBH) than in pine (most intensive treatment 10.3 m tall, 17.7 cm DBH; control, 7.6 m tall, 13.4 cm DBH). The pipe model of tree development explained dimensions of the upper 5 m of crown with leaf biomass highly correlated to branch basal area (r2 from 0.697 to 0.947). There was a constant ratio of leaf biomass to branch basal area (50 gm/cm2 for pine, 30 gm/cm2 for sweetgum). We also found a constant ratio of bole basal area to cumulative branch basal area throughout the crowns. Rapidly growing pines produced about 49 Mg ha?1 of stem biomass, 11 Mg ha?1 of dead branch biomass, and 17 Mg ha?1 of unfoliated branch biomass at the end of six years. |
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