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1.
利用桂东南桉树(Eucalyptus spp.)主产区5个不同林龄(1a、2a、3a、5a和8a)15个样点45个样地调查数据,分析桂东南尾巨桉(Eucalyptus urophylla×E.grandis)人工林的碳格局及其动态变化特征。结果表明:(1)尾巨桉人工林生态系统总碳储量表现为3a林龄(195.25t·hm-2)5a林龄(169.57t·hm-2)8a林龄(166.70t·hm-2)2a林龄(165.00t·hm-2)1a林龄(111.84t·hm-2);不同林龄碳储量分布格局均为土壤层植被层凋落物层,地下部分地上部分;其中植被层为4.87~80.54t·hm-2,占总碳储量的4.36%~48.31%,随林龄的增加而增加;凋落物层为0.92~3.25t·hm-2,占0.82%~1.91%,随林龄增加呈递减趋势;土壤层为3a林龄(162.53t·hm-2,83.24%)2a林龄(141.55t·hm-2,85.79%)5a林龄(112.26t·hm-2,60.22%)1a林龄(106.05t·hm-2,94.82%)8a林龄(84.50t·hm-2,50.69%)。(2)植被层碳储量以乔木层最大(3.10~78.97t·hm-2),占63.64%~99.25%,其中乔木层各器官碳储量以树干最大(1.58~68.84t·hm-2),占乔木层碳储量的50.90%~87.18%,随林龄的增加而增加,枝、叶、根分别占4.97%~12.17%、1.97%~22.36%和5.87%~14.57%,均随林龄而下降。(3)桂东南尾巨桉人工林生态系统年净固碳量平均为11.73t·hm-2·a-1,2a林龄(16.03t·hm-2·a-1)最大,3a林龄的固碳能力也很高,8a林龄年净固碳量与5a林龄持平,高达11.96t·hm-2·a-1,是较好的碳汇林业树种。提高桉树林的生态服务功能、降低其负面效应将有利于桉树人工林生产的发展。  相似文献   

2.
米老排人工林碳素积累特征及其分配格局   总被引:1,自引:0,他引:1  
在生物量调查的基础上,对桂西南地区28年生米老排人工林生态系统的碳素积累特征及分配格局进行了研究.结果表明:米老排各器官碳含量在522.8~560.2 g·kg-1,大小排序为:树叶(560.2 g·kg-1)>树干(542.8 g·kg-1)>树根(530.9 g·kg-1)>树皮(530.8 g·kg-1)>树枝(522.8 g·kg-1);土壤碳含量以表土层最高,且随土层深度的增加而降低;米老排人工林乔木层碳贮量为147.90 t·hm-2,其中,树干占乔木层碳贮量的63.72%;米老排人工林生态系统碳贮量为285.36 t·hm-2,各组分的分配顺序为乔木层>土壤层>凋落物层>灌木层>草本层;植被层碳贮量为土壤层(0~100 cm)的1.1倍.  相似文献   

3.
连栽桉树人工林生产力和植物多样性及其相关性分析   总被引:3,自引:0,他引:3  
对不同连栽代次的尾巨桉人工林进行长期定位观测,研究林分各组成部分生物量及林下植物多样性的变化,并采用趋势面分析方法分析生物量与植物多样性之间的关系.结果表明:(1)第1、2、3代7年生尾巨桉人工林的群落生物量基本相同,分别为102.22、105.11、102.66 t/hm2,其中乔木层林分生物量随着连栽代次呈增加趋势,第1代到第3代林分分别为81.48、88.36、92.28 t/hm2,平均净生产力分别为11.64、12.62、13.18 t/hm2·a,林分各器官生物量分配无明显差异,但在各生长年份,随着代数增加也呈增加趋势.(2)尾巨桉林下植物及枯落物生物量明显下降,第1、2、3代灌木层生物量分别为8.47、6.89、3.09 t/hm2,草木层生物量分别为1.93、1.21、0.35 t/hm2,枯落层生物量分别为10.34、8.64、6.94 t/hm2.(3)连栽尾巨桉人工林植物多样性指数、均匀度指数、丰富度指数随着连栽代次的增加而明显下降,即林下植物多样性随连栽代次的增加而减少,物种生态优势度增加.(4)采用趋势面分析方法结果表明,不同连栽代次尾巨桉林地植物多样性增加则林地根系生物量和林下植物生物量显著增加,而对林分总生物量及其它器官生物量影响不大.  相似文献   

4.
南亚热带不同林龄红锥人工林碳贮量与碳固定特征   总被引:6,自引:0,他引:6  
采用乡土珍贵阔叶树种改造大面积针叶人工纯林已经成为我国亚热带地区人工林近自然化经营的有效模式.采用样地调查与生物量实测方法,研究了我国南亚热带广西3个不同林龄红锥人工林(10、20和27年生)的不同器官、凋落物层和土壤层的碳含量,以及不同林龄红锥人工林的乔木层、凋落物层和土壤层碳贮量及其分配特征.结果表明:红锥不同器官碳含量为49.7%~57.9%;凋落物层碳含量为40.8% ~ 50.5%,而且未分解层>半分解层;土壤层(0~60 cm)碳含量随林龄增加而增大,随土层深度的增加而下降.10、20和27年生红锥人工林碳贮量分别为182.42、234.75和269.75 t·hm-2,其中,乔木层分别占19.8%、32.0%和32.8%,凋落物层分别占1.5%、1.6%和1.3%,土壤层分别占78.7%、66.4%和65.9%.3个红锥人工林的年净固碳量分别为4.70、5.64和5.18 t· hm-2.红锥具有较高的固碳能力,是发展多目标森林经营模式的理想树种.  相似文献   

5.
量化橡胶树和桉树人工林碳储量,为评价海南地区碳汇功能和可持续管理功能提供重要依据。在海南省儋州市选择不同林龄的橡胶树和桉树人工林,设置样地测算乔木层、林下植被和枯落物的生物量,土壤分层采集0—100cm土样,依据相对方程,计算橡胶树和桉树人工林生态系统的碳含量和碳储量。结果表明:不同林龄橡胶树和桉树人工林林下植被碳含量变化幅度为38.09%—45.31%,枯落物碳含量为38.50%—47.52%之间。0—100 cm土层碳含量变化幅度为0.31%—1.62%,各林分土壤含碳率均随土层深度增加而减少,除底层(50—100cm)土壤外,其它层次不同林分土壤有机碳的含量均表现为橡胶林桉树林。橡胶树、桉树人工林生态系统总碳储量分别为160.01和86.33 t C·hm~(-2),桉树人工林生态系统碳储量均表现为随林龄的增加而增加,橡胶树各林龄碳储量均高于桉树。橡胶树、桉树人工林乔木碳储量分别占其总碳储量的36.87%和23.92%。橡胶树和桉树人工林下植被碳储量表现为橡胶树(0.78 t C·hm~(-2))桉树(0.49 t C·hm~(-2)),枯落物碳储量分别占其总碳储量的1.00%和1.56%。橡胶树、桉树人工林土壤碳储量分别为96.22和63.88 t C·hm~(-2),橡胶树人工林土壤碳储量高于桉树,0—50 cm土层碳储量成为土壤的主体,橡胶树0—50 cm土层碳储量占其土壤总碳储量的64.39%,桉树为54.35%。乔木层和土壤层碳储量是整个森林生态系统碳贮量的主要部分。橡胶人工林生态系统的固碳速率和固碳潜力分别为4.20 t C·hm~(-2)·a~(-1)和64.78 t C·hm~(-2),桉树人工林生态系统的固碳速率和固碳潜力分别为11.06 t C·hm~(-2)·a~(-1)和23.98 t C·hm~(-2)。两个树种均具有较高的固碳能力,是海南营造高效固碳人工林的理想树种。  相似文献   

6.
鼎湖山马尾松林生态系统碳素分配和贮量的研究   总被引:36,自引:1,他引:35  
方运霆  莫江明 《广西植物》2002,22(4):305-310
鼎湖山马尾松林中 ,马尾松各器官碳含量平均为 5 4.46%,灌木层植物 48.1 0 %,草本层植物40 .2 1 %,地表现存凋落物层 5 4.40 %,以上各组分总平均为 49.2 9%。土壤碳密度为 7.3 7kg· m- 2 (深 1 0 0cm)。生态系统各组分碳贮量分别为 :乔木层 68.876t·hm- 2 ,林下植物层 6.0 3 0 t· hm- 2 ,凋落物层 5 .892 t·hm- 2 ,土壤层 73 .70 5 t· hm- 2。根据研究结果 ,还对广东省马尾松林的现有碳贮量和碳吸存潜力进行了估算和讨论。  相似文献   

7.
广西主要人工林凋落物分解过程及其对淋溶水质的影响   总被引:3,自引:0,他引:3  
为探讨不同人工林各组分凋落物分解过程特征及其释放物质对淋溶水质的影响,恒温(28℃)培养条件下,在室内人工定期淋水模拟自然环境中凋落物的淋溶过程,对1年生和4年生尾巨桉、7年生杂交相思、13年生马尾松以及软阔林5种人工林的凋落叶、凋落枝、凋落皮进行255 d的模拟淋溶.结果表明:1年生和4年生尾巨桉各组分凋落物分解0~105 d的淋溶液色度和化学需氧量(COD)、总N和总P含量显著高于杂交相思、马尾松、软阔林,淋溶液pH值显著低于其他3种林分人工林;至255 d,1年生和4年生尾巨桉凋落叶淋溶液的COD累积量(193.9和212.8 g·kg-1)分别是杂交相思、马尾松、软阔林的4.2、4.0、4.3倍和5.3、4.4、4.7倍;1年生尾巨桉凋落叶质量损失率、N和P淋失率显著大于杂交相思、马尾松和软阔林,凋落皮显著大于马尾松,而凋落枝与后三者基本相当.1年生尾巨桉凋落叶和凋落皮比4年生尾巨桉更易被分解淋溶,但凋落枝差异不显著.5种林分凋落物不同组分间,凋落叶最易被分解淋溶,凋落枝难于被分解淋溶.尾巨桉凋落物淋溶液pH值与色度、COD含量呈显著负相关,COD与色度、总N和总P呈显著正相关.  相似文献   

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以不炼山+人工穴垦、不炼山+机械带垦和炼山+机械全垦3种不同整地组合下的2.5年生尾巨桉人工林为对象,对其碳储量及其分配格局进行研究。结果表明:(1)3种整地组合下尾巨桉各器官碳含量平均值为44.37%~57.42%,大小顺序为叶>干>枝>根>皮,带垦最大(51.21%),炼山全垦最小(49.95%);不同整地组合尾巨桉人工林林下地被物层的碳含量均无显著差异(P>0.05);土壤层(0~100 cm)碳含量均随土层深度的增大而减小,各层土壤平均碳含量总体趋势表现为带垦>炼山全垦>穴垦。(2)穴垦、带垦、炼山全垦措施下乔木层总碳储量依次为18.01、30.49和23.56 t.hm-2,各器官碳储量大小顺序为干>根>叶>枝>皮;除皮外,其余器官碳储量排序均为带垦>炼山全垦>穴垦。(3)尾巨桉人工林生态系统的总碳储量表现为带垦(197.03 t.hm-2)>炼山全垦(161.16t.hm-2)>穴垦(144.77 t.hm-2);不同整地措施碳储量分配格局均为土壤层>植被层>枯落物层。土壤层和乔木层碳储量均是带垦最大,在整个生态系统碳储量中处于主导地位,占整个系统碳储量在93%以上;不同整地组合措施对枯落物层的碳储量无显著影响。因此,从提高尾巨桉林分系统碳储量方面考虑,在雷州半岛及相似立地条件地区进行尾巨桉人工林造林时宜采取不炼山+机械带垦的整地组合方式。  相似文献   

9.
不同林龄尾巨桉人工林的生物量及其分配特征   总被引:2,自引:0,他引:2  
根据1,2,3,5,8a共5个不同年龄的15块1000 m2尾巨桉样地(3次重复)调查资料,利用18株不同年龄和径阶的样木数据,建立以胸径(D)为单变量的生物量回归方程。采用样木回归分析法(乔木层)和样方收获法(灌木层、草本层、地上凋落物)获取不同林龄尾巨桉人工林的生物量,分析了其组成、分配及不同林龄生物量的变化趋势。结果表明:林分总生物量随林龄而增加,1,2,3,5年生和8年生尾巨桉人工林生物量分别为12.49,47.75,64.51,105.77和137.51 t/hm2,其中活体植物占85.60%—97.61%,地上凋落物占2.39%—14.40%;层次分配方面乔木层占绝对优势,占54.80%—91.56%,且随林龄的增加而增大,其次为凋落物,灌木层和草本层生物量较小,分别占1.02%—6.47%和0.28%—24.33%,均随林龄的增加呈递减趋势;乔木层以干所占比例最高,占51.07%—98.48%,且随林龄而增加,枝、叶、根分别占5.76%—11.80%,2.17%—21.01%和6.72%—14.87%,均随林龄而下降;灌木层以枝所占比例最高,为37.89%—56.79%,叶和根分别占16.35%—34.24%和19.52%—39.52%,随林龄的变化均不大;草本层分配1—5年生以地上所占比例较大,8年生地下所占比例高达63.87%;尾巨桉人工林乔木层各器官、地上凋落物及总生物量具有良好的优化增长模型,其总生物量的增长模型为Y=-1.693×104+3.337×104X-1.761X2;8年生尾巨桉人工林总生物量与30年生的木莲人工林持平,低于热带雨林,但其年均净生产量高达17.19 t/hm2,是一个光合效率高、固碳潜力大的速生丰产优良造林树种。  相似文献   

10.
以福建长乐滨海沙地上3种人工林(尾巨桉、纹荚相思、木麻黄)土壤为研究对象,设置去除凋落物、去除根系和对照3种处理,观测1年后分析改变地上、地下有机质输入对沙地土壤碳氮储量、可溶性有机碳(DOC)氮(DON)和微生物量碳(MBC)氮(MBN)的影响。结果表明:不同树种人工林间土壤碳氮储量无显著差异;不同树种人工林间土壤活性碳氮组分差异显著,木麻黄土壤DOC含量显著高于纹荚相思,纹荚相思土壤DON显著高于木麻黄和尾巨桉,尾巨桉土壤MBN显著高于木麻黄和纹荚相思。改变地上地下有机质输入对滨海沙地土壤碳氮库有显著影响且这种影响随树种而异。去除凋落物后纹荚相思、木麻黄土壤碳储量分别下降38.0%、25.1%,氮储量分别下降12.9%、12.5%;去除凋落物后尾巨桉、纹荚相思、木麻黄土壤DOC分别下降37.5%、30.6%、52.9%,MBC分别下降31.0%、56.9%、29.7%,MBN分别下降50.7%、34.9%、42.2%;去除根系后尾巨桉、纹荚相思土壤MBC分别下降57.7%、15.4%。回归分析显示,滨海沙地土壤DOC、MBC与土壤碳储量呈显著正相关,土壤DOC和MBC分别能够解释土壤碳储量变化的47.7%和57.7%。研究表明:树种通过调控地上、地下输入影响可溶性有机碳氮和微生物量碳氮,进而影响土壤碳氮库。  相似文献   

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In experiments on Black Sea skates (Raja clavata), the potential of the receptor epithelium of the ampullae of Lorenzini and spike activity of single nerve fibers connected to them were investigated during electrical and temperature stimulation. Usually the potential within the canal was between 0 and –2 mV, and the input resistance of the ampulla 250–400 k. Heating of the region of the receptor epithelium was accompanied by a negative wave of potential, an increase in input resistance, and inhibition of spike activity. With worsening of the animal's condition the transepithelial potential became positive (up to +10 mV) but the input resistance of the ampulla during stimulation with a positive current was nonlinear in some cases: a regenerative spike of positive polarity appeared in the channel. During heating, the spike response was sometimes reversed in sign. It is suggested that fluctuations of the transepithelial potential and spike responses to temperature stimulation reflect changes in the potential difference on the basal membrane of the receptor cells, which is described by a relationship of the Nernst's or Goldman's equation type.I. P. Pavlov Institute of Physiology, Academy of Sciences of the USSR, Leningrad. I. M. Sechenov, Institute of Evolutionary Physiology and Biochemistry, Academy of Sciences of the USSR, Leningrad. Pacific Institute of Oceanology, Far Eastern Scientific Center, Academy of Sciences of the USSR, Vladivostok. Translated from Neirofiziologiya, Vol. 12, No. 1, pp. 67–74, January–February, 1980.  相似文献   

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Shapes of curves of pH-dependence of reactions   总被引:14,自引:14,他引:0  
A simple case is considered in which the rate of a two-step reaction depends on pH because the intermediate formed in the first step has to gain (or lose) a proton before it can react in the second step, and in which the rate-determining step therefore changes with pH. The curves of reaction rate against pH are shown to be symmetrical, and the sharpest peak possible has a width at half its height of 1.53pH units, i.e. of 2log(3+2 radical2). Any particular curve for this situation proves to be identical with a curve that could be generated for the pH-dependence of a single-step reaction in which the rate is proportional to the concentration of a particular ionic form of a reactant. Curves for the latter situation, however, can have forms impossible for the former case in which the rate-determining step changes, but only if the protonations that activate and deactivate the reactant are co-operative. The peak can then become even sharper, and its width at half its height can fall to 1.14pH units, i.e. to 2log(2+ radical3).  相似文献   

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Dietary intakes of tomatoes and tomato products containing lycopene have been shown to be associated with decreased risk of chronic diseases such as cancer and cardiovascular diseases in numerous studies. Serum and tissue lycopene levels have also been inversely related to the risk of lung and prostate cancers. Lycopene functions as a very potent antioxidant, and this is clearly a major important mechanism of lycopene action. In this regard, lycopene can trap singlet oxygen and reduce mutagenesis in the Ames test. However, evidence is accumulating for other mechanisms as well. Lycopene at physiological concentrations can inhibit human cancer cell growth by interfering with growth factor receptor signaling and cell cycle progression specifically in prostate cancer cells without evidence of toxic effects or apoptosis of cells. Studies using human and animal cells have identified a gene, connexin 43, whose expression is upregulated by lycopene and which allows direct intercellular gap junctional communication (GJC). GJC is deficient in many human tumors and its restoration or upregulation is associated with decreased proliferation. The combination of low concentrations of lycopene with 1,25-dihydroxyvitamin D3 exhibits a synergistic effect on cell proliferation and differentiation and an additive effect on cell cycle progression in the HL-60 promyelocytic leukemia cell line, suggesting some interaction at a nuclear or subcellular level. The combination of lycopene and lutein synergistically interact as antioxidants, and this may relate to specific positioning of different carotenoids in membranes. This review will focus on the growing body of evidence that carotenoids have unexpected biologic effects in experimental systems, some of which may contribute to their cancer preventive properties in models of carcinogenesis. Consideration of solubility in vitro, comparison with doses achieved in humans by dietary means, interactions with other phytochemicals, and other potential mechanisms such as stimulation of xenobiotic metabolism, inhibition of cholesterogenesis, modulation of cyclooxygenase pathways, and inhibition of inflammation will be considered. This review will point out areas for future research where more evidence is needed on the effects of lycopene on the etiology of chronic disease.  相似文献   

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