秦岭南坡油松-锐齿槲栎混交林群落不同层次多样性特征及环境解释

在秦岭山脉南坡陕西省境内设置11个样地进行实地调查,从植物物种组成、多样性指数差异以及多样性指数沿环境梯度排序等方面对该区域油松-锐齿槲栎天然混交林的群落总体以及乔木层、灌木层、草本层的各自4个α多样性指数（Patrick丰富度指数、Simpson优势度指数、Shannon-Wiener多样性指数、Pielou均匀度指数）特征进行分析,以揭示该群落多样性特征及其与环境因素的关系。结果显示：（1）11个样地共记录维管束植物112种,隶属于45科77属,分布较广的物种有蔷薇科、菊科、百合科、松科、禾本科和忍冬科。（2）研究区群落中建群种锐齿槲栎和油松的优势地位突出,乔木层伴生种稀少,平均仅为4.8种,多样性水平较低;灌木层物种组成丰富,平均11.4种;草本层次之,平均9种。（3）单因素方差分析表明,该群落不同层次的多样性指数之间均存在极显著差异（P<0.01）;LSD多重比较及多样性指数变化趋势分析表明,群落多样性水平表现为总体>灌木层>草本层>乔木层。（4）CCA法将群落不同层次多样性指数沿地形因子和土壤养分等12项环境指标梯度的分布划分为界线明显的3个区域,即Ⅰ区（中等浓度土壤磷素和有机质制约区）、Ⅱ区（非环境因子制约区）和Ⅲ区（高浓度土壤磷素制约区）;群落总体多样性主要受灌木层影响,同时也受乔木层均匀度影响,但环境因子对乔木层多样性基本无限制性作用。（5）土壤速效磷、全磷和有机质是造成研究区群落不同层次多样性差异的主要因素,海拔、坡向等地形因子对群落多样性影响不大,可能是由于土壤养分的直接影响削弱了地形因子的间接性生态作用。研究表明：保持中等水平的土壤速效磷（3.775±1.529 mg·kg^-1）和有机质含量［（4.079±1.001）%］,并通过合理补植松栎幼树和伐除枯死木等抚育手段提高乔木层均匀度是维持秦岭南坡油松-锐齿槲栎混交林群落生物多样性的有效措施。     

灵空山油松种群年龄结构与动态分析

对山西灵空山自然保护区的油松（Pinus tabulaeformis）种群进行了调查,利用生存分析理论及谱分析理论,分析了油松种群径级结构和静态生命表,绘制了存活曲线,同时分析了种群数量的周期性。主要结果如下：（1）油松种群幼苗幼树个体数较多,中径级的个体数较稳定,而高径级由于种间竞争及环境因子的影响,个体数明显下降。（2）油松种群的存活曲线呈现Deevey-Ⅱ型。动态表现为前期增长,中期稳定,后期衰退。（3）油松种群波动存在小周期,但变化不大,说明油松种群发展较为稳定。     

酸雨背景下缙云山典型林分凋落物量和营养元素含量及其释放特征

选取缙云山针阔混交林、常绿阔叶林、楠竹林和灌木林作为研究对象,对4种林分的凋落物储量和营养元素释放量等进行观测,并应用室内模拟酸雨实验对4种林分凋落物进行淋溶模拟。结果表明:缙云山各林分现存凋落物厚度为1.4～4.5 cm,具有明显的分层结构;林分未分解U层、半分解S层和分解D层现存凋落物量分别为1.97～8.59、2.84～10.18和3.58～17.43 t·hm-2,林分年凋落物量为2.17～9.86 t·hm-2·a-1,凋落物总储量为14.21～32.42 t·hm-2,凋落物分解常数为0.15～0.31,林下凋落物分解95%时所需时间针阔混交林和楠竹林均在10年以上,凋落物分解速率比较缓慢;林下凋落物层营养元素含量以Ca、N为主,Fe、K、Mg次之;凋落物总的营养元素释放率表现为常绿阔叶林(0.80)>灌木林(0.72)>针阔混交林(0.50)>楠竹林(-0.17);与叶片相比,凋落物中N、K、Mn 3种营养元素含量明显降低;为探明酸雨影响营养元素循环的作用机理,对模拟酸雨的离子含量与凋落物淋滤液盐基离子含量进行了分析,其相关性大小表现为楠竹林(相关系数0.895)>针阔混交林(0.826)>灌木(0.700)>常绿阔叶林(0.699),楠竹林凋落物营养元素的淋滤受酸雨影响最大,常绿阔叶林受其影响最弱;推测在这一过程中以凋落物的吸附作用为主。     

西藏高原云南松生物量模型及碳储量

云南松林是西藏高原亮针叶林生态系统的重要组成部分,准确估算其生态系统碳储量不但有助于弄清西藏森林生态系统固碳现状,而且可为准确估算青藏高原乃至全国森林生态系统的固碳潜力和固碳速率提供基础数据.本研究以云南松为研究对象,采用实地调查与建模相结合的方法,建立了各器官(叶、枝、干、根)与株高、胸径的生物量回归方程,并以此为基础计算了云南松幼龄林、中龄林、近熟林和成熟林生态系统的生物量和碳储量.结果表明:(1)用胸径和树高估测单株林木器官生物量的较优模型为指数模型,所建立的生物量回归方程相关性较好(R2＞0.90),估计精度较高.(2)在云南松幼龄林、中龄林、近熟林和成熟林生态系统中植被总生物量分别为(63.80±9.21)、(134.76+12.69)、(142.91±13.02)、(316.72+42.57)t·hm-2,其中乔木层生物量分别为(49.48±10.32)、(120.57±9.37)、(124.70±12.92)、(304.76±32.47)t·hm-2,灌草层生物量为(13.09±3.02)、(12.81±2.54)、(11.88±3.12)、(3.47±0.98)t·hm-2,凋落物生物量为(1.23±0.24)、(1.38±0.31)、(0.72±0.11)、(1.13±0.39)t·hm-2.(3)各龄级云南松林生态系统植被碳储量分别为(30.67±7.13)、(67.63±19.06)、(71.00±4.15)、(159.32±39.95)t·hm-2,碳储量随林龄增加的变化规律明显,碳汇潜力巨大.     

马尾松松针挥发油提取工艺研究

本文研究水蒸气蒸馏法提取马尾松松针挥发油的工艺。通过单因素试验考察液固比、提取时间、松针长度、浸泡时间4个因素对马尾松松针挥发油得率的影响,运用L9(34)正交试验探索最佳工艺条件。结果表明,浸泡时间对挥发油提取有显著影响(P=0.045),最佳时间为7 h;液固比、提取时间、松针长度无显著影响(P>0.05)。最佳工艺条件为液固比9∶1、提取时间3 h、松针长度5 mm、浸泡时间7 h,通过验证实验验证此工艺稳定可行。     

马尾松和苦槠林根际土壤矿化和根系分解CO2释放的温度敏感性

以中亚热带马尾松林和苦槠林为对象,原位收集根际和非根际土壤、树木不同生态功能的根系,开展15℃、25℃、35℃和45℃恒温培养模拟试验,采用密闭气室碱液吸收法测定53 d内CO2释放的动态变化.结果表明:两种森林类型不同温度下土壤矿化CO2释放速率的根际效应介于1.12 ～3.09,且培养前期高于培养后期;15℃下马尾松林和苦槠林差异不显著,25℃和35℃下前者低于后者,45℃下则相反.不同培养温度下两树种吸收根分解的CO2释放速率均高于过渡根和贮存根,且马尾松均低于苦槠.两种森林类型CO2释放的Q10值均为土壤(1.21 ～1.83)显著高于根系(0.96 ～1.36).两种森林类型土壤矿化CO2释放的Q10值差异不显著,而马尾松根系分解CO2释放的Q10值高于苦槠.推断全球变暖导致的土壤矿化CO2释放的增量将远远高于根系分解,且马尾松林高于苦槠林;地带性顶极群落应对气候变化的抵抗力强于先锋树种群落.     

Variation in biomass and carbon storage by stand age in pine (Pinus tabulaeformis) planted ecosystem in Mt. Taiyue,Shanxi, China

Forest ecosystems play dominant roles in global carbon budget because of the large quantities stored in live biomass, detritus, and soil organic matter. Researchers in various countries have investigated regional and continental scale patterns of carbon (C) stocks in forest ecosystems; however, the relationship between stand age in different components (vegetation, forest floor detritus, and mineral soil) and C storage and sequestration remains poorly understood. In this paper, we assessed an age sequence of 18-, 20-, 25-, 38-, and 42-year-old Pinus tabulaeformis planted by analyzing the vertical distribution of different components biomass with similar site conditions on Mt. Taiyue, Shanxi, China. The results showed that biomass of P. tabulaeformis planted stands was ranged from 88.59 Mg ha^?1 for the 25-year-old stand to 231.05 Mg ha^?1 for the 42-year-old stand and the major biomass was in the stems. Biomass of the ground vegetation varied from 0.51 to 1.35 Mg C ha^?1 between the five stands. The forest floor biomass increased with increasing stand age. The mean C concentration of total tree was 49.94%, which was higher than C concentrations of ground vegetation and forest floor. Different organs of trees C concentration were between 54.14% and 47.74%. C concentrations stored in the mineral soil for each stand experienced decline with increasing soil depth, but were age-independent. Total C storage of five planted forests ranged from 122.15 to 229.85 Mg C ha^?1, of which 51.44–68.38% of C storage was in the soil and 28.46–45.21% in vegetation. The study provided not only with an estimation biomass of P. tabulaeformis planted forest in Mt. Taiyue, Shanxi, China, but also with accurately estimating forest C storage at ecosystem scale.     

Scots pine growing on forested mires in Abernethy Forest,Strathspey, Scotland

Summary

A substantial proportion of the Abernethy Forest Reserve has Scots pine (Pinus sylvestris) growing on the surfaces of a variety of mires. The hydrology of the mires has been affected by drainage and peat cutting but this area is unusual in having had a long period of protection from grazing by domestic stock. There are three main types of pine populations found on these mires. Woodland bog comprises predominantly bog vegetation with abundant pine seedlings due to the heavy seed rain from the surrounding woodland. Only a few very small trees survive, which are stunted, heavily diseased and have very low seed production. Wooded bog also comprises predominately bog vegetation but there are scattered mature trees of a moderate height with an open canopy. The trees are fertile and can form uneven aged stands with regeneration. Bog woodland is a predominantly woodland vegetation with tall, dense tree cover on deep peat. The trees are well grown with a dense canopy. A few remnants of bog vegetation remain in the ground flora although most have been replaced by woodland bryophytes and shrubs. Each of these three types is described and their development is discussed.     

Composition and Chemical Variability of the Needle Oil from Pinus halepensis growing in Corsica

The composition of oil samples isolated from needles of Pinus halepensis growing in three locations in Corsica (Saleccia, Capo di Feno, and Tre Padule) has been investigated by combination of chromatographic (GC with retention indices) and spectroscopic (MS and ¹³C‐NMR) techniques. In total, 35 compounds that accounted for 77 – 100% of the whole composition have been identified. α‐Pinene, myrcene, and (E)‐β‐caryophyllene were the major component followed by α‐humulene and 2‐phenylethyl isovalerate. Various diterpenes have been identified as minor components. 47 Oil samples isolated from pine needles have been analyzed and were differentiated in two groups. Oil samples of the first group (15 samples) contained myrcene (M = 28.1 g/100 g; SD = 10.6) and (E)‐β‐caryophyllene (M = 19.0 g/100 g; SD = 2.2) as major components and diterpenes were absent. All these oil samples were isolated from pine needles harvested in Saleccia. Oil samples of the second group (32 samples) contained mostly (E)‐β‐caryophyllene (M = 28.7 g/100 g; SD = 7.9), α‐pinene (M = 12.3 g/100 g; SD = 3.6), and myrcene (M = 11.7 g/100 g; SD = 7.3). All these oil samples were isolated from pine needles harvested in Capo di Feno and Tre Padule.     

Morphological and niche divergence of pinyon pines

The environmental variables that define a species ecological niche should be associated with the evolutionary patterns present in the adaptations that resulted from living in these conditions. Thus, when comparing across species, we can expect to find an association between phylogenetically independent phenotypic characters and ecological niche evolution. Few studies have evaluated how organismal phenotypes might mirror patterns of niche evolution if these phenotypes reflect adaptations. Doing so could contribute on the understanding of the origin and maintenance of phenotypic diversity observed in nature. Here, we show the pattern of niche evolution of the pinyon pine lineage (Pinus subsection Cembroides); then, we suggest morphological adaptations possibly related to niche divergence, and finally, we test for correlation between ecological niche and morphology. We demonstrate that niche divergence is the general pattern within the clade and that it is positively correlated with adaptation.