吉林省蛟河市针阔混交林林层结构与地形的关系

探讨不同林层群落结构动态及其与地形因子之间的关系,为群落结构优化和可持续经营管理提供理论支持。基于吉林蛟河30 hm²针阔混交林固定监测样地的野外调查数据,以2010和2015年胸径（DBH）≥1 cm的木本植物为研究对象,分析了不同林层物种组成、林分密度、群落结构多样性差异及其5年间的动态变化,利用偏相关分析研究了不同林层群落结构特征和地形因子的关系。结果表明：（1）林下层物种丰富度略高于林冠层,林冠层蓄积生产力是整个森林群落蓄积生产力的主要贡献者,林下层的物种多样性和林分结构多样性变化较林冠层明显;（2）林冠层优势树种的重要值在群落演替过程中逐渐扩大,整个样地林冠层树木个体数量减少了175株,林下层树木个体增加了3503株;（3）地形因子中海拔是影响群落结构动态最主要的因子,通过影响土壤和光照等条件从而影响群落结构变化。该林分处于相对稳定状态,不同林层群落结构特征差异显著,正确把握地形因子与不同林层群落结构动态变化的关系对森林的可持续经营具有重要意义。     

天目山常绿落叶阔叶林群落垂直结构与群落整体物种多样性的关系

以浙江省天目山1 hm²常绿落叶阔叶混交林样地调查数据为基础,运用K-means聚类方法将DBH≥1 cm的个体根据树高划分为不同林层,研究比较了各个林层的物种多样性特点;利用通径分析方法和决策系数定量计算各个林层物种多样性对群落整体物种多样性的直接作用和间接作用,天目山常绿落叶阔叶林垂直结构对群落物种多样性构成的影响。结果表明：（1）天目山常绿落叶阔叶林群落层次结构丰富,树高由1.4-36.5 m依次可分为灌木层、亚冠层、林冠下层、林冠中层和林冠上层。（2）天目山常绿落叶阔叶林群落从灌木层依次往向上,物种丰富度、多度、特有种数量、Shannon-Weiner指数和Simpson指数均呈下降趋势。（3）灌木层对群落物种多样性的贡献最大且远高于其他四个林层,其中灌木层对群落整体物种多样性Shannon-Wiener指数、Pielou指数以及Simpson指数的决策系数分别为0.850、0.651、0.755。（4）林冠下层、林冠中层和林冠上层密度的大小对灌木层的物种数目有明显的影响,林冠层密度越大,灌木层群落的物种数目越少,复杂程度越低;偶见种和稀有种对群落物种多样性的维持具有特殊作用。综上,研究认为森林群落的垂直结构在维持森林群落整体物种多样性中具有关键作用,而灌木层在群落整体物种多样性构成中具有决定作用,森林群落中稀有种、偶见种多少在群落物种多样性构成中具有特殊作用。     

鼎湖山南亚热带常绿阔叶林群落垂直结构及其物种多样性特征

群落结构在森林生态系统中具有重要作用, 其构建机制一直是森林生态学的研究核心。群落结构不仅包括水平方向上的物种分布格局, 还包括垂直方向上的物种分层结构。本文基于鼎湖山南亚热带常绿阔叶林塔吊样地, 利用林冠塔吊和测高杆精准测量样地内每个个体(胸径大于1 cm)的树高, 并划分群落的垂直层次, 研究了每层的群落多样性特征(α多样性)和林层间的群落多样性变化特征(β多样性)。结果表明: (1)样地群落垂直层次由下至上分为5层: 灌木层、亚冠层、林冠下层、林冠中层和林冠上层。(2)随林层向上, 物种丰富度、多度和Shannon-Wiener指数均下降, Pielou均匀度指数在林冠下层最大。(3)利用POD法计算并分解β多样性, 发现随林层向上, β多样性在灌木层与其他各层间呈递增趋势, 在相邻林层间呈单峰型, 不同林层间的物种组成差异主要由丰富度差异造成。 但在林冠下层与林冠中层间丰富度差异较小, 物种替换组分增大, 可能与林冠下层所处特殊位置有关。(4)各林层内微环境从灌木层向上, 趋于高温、强光照和低空气相对湿度, 但林冠下层平均日光强最低。综上, 鼎湖山南亚热带常绿阔叶林林冠下层可能存在强烈的环境筛选作用, 且光照可能是影响群落垂直结构形成的限制因子。     

林分因子对神木垒不同森林群落林下植物多样性的影响

为探究神木垒不同森林群落林下植物多样性的差异，本研究采用典型样地法，以夹金山神木垒的5种主要森林群落：云杉林、丽江云杉林、红杉林、针阔混交林、阔叶林为研究对象，对不同森林群落林下植物物种组成和物种多样性进行比较，并对林分因子和林下植物多样性进行冗余分析，确定影响林下植物多样性的主要林分因子，为当地森林经营管理提供理论依据。结果表明：（1）在研究区内共记录林下植物147种，隶属于61科，108属；云杉林群落林下植物的科属种组成最丰富。（2）各类型群落的H值、H"值、D值、JSW值均为：草本层＞灌木层；灌木层多样性最高的群落为云杉林群落，草本层多样性最高的群落为丽江云杉林群落，针阔混交林群落、阔叶林群落林下植物多样性较差。（3）平均枝下高与林分密度是影响灌木层物种多样性的主要林分因子（P<0.01），平均枝下高与灌木层的D值、H值、H"值呈负相关关系，林分密度与灌木层4个多样性指数均呈正相关关系；平均枝下高是影响草本层物种多样性的主要林分因子（P<0.01），平均枝下高与草本层H值、H"值、JSW值呈正相关关系。本研究认为，云杉林群落与丽江云杉林群落的林下植物多样性水平较高，平均枝下高与林分密度是影响神木垒不同森林群落林下植物多样性的主要林分因子。     

大明山常绿阔叶林冠层垂直结构与林下植物更新

2009—2011年,在广西大明山常绿阔叶林一个典型坡面的上坡、中坡和下坡分别建立24个20 m×20 m的固定样地,测定不同林冠层次(上层、中层和下层冠高分别为:>8、4～8和0～4 m)的覆盖度并监测林下植物的更新,研究林冠垂直结构的动态变化及其对林下植物更新的影响.结果表明: 随着2008年特大冰冻灾害后森林的恢复,林冠总覆盖度显著增加,从2009年的54.0%提高到2011年的67.4%,不同冠层覆盖度和恢复增长存在显著差异,上层林冠覆盖度显著高于中、下层,而中、下层林冠的恢复增长显著优于上层林冠.林下更新的木本植物共55种,优势科和优势种与现有群落的基本一致.同一年份不同坡位林下更新植物的物种多样性指数差异不显著,但同一坡位不同年份间存在显著差异.不同冠层的覆盖度与更新植物的物种丰富度和多度相关性不显著;中层、下层和林冠总覆盖度与林下更新植物的Shannon指数、Simpson指数和Pielou均匀度指数呈显著负相关,表明冠层覆盖度显著影响着林下更新,中、下层林冠对林下更新植物多样性的作用更明显.     

吉林蛟河针阔混交林生物量时间稳定性驱动机制

生态系统稳定性是森林群落结构和功能的综合特征。通过长期大样地的监测数据,探究森林生态系统稳定性机制。本研究以吉林蛟河21.12 hm²天然针阔混交林固定样地中连续10年的野外调查数据(即2009年、2014年和2019年3次复测)为基础,分析了物种异步性、物种多样性、结构多样性、林分密度和海拔与生物量时间稳定性的直接和间接关系,探究并确定了生物量时间稳定性各驱动因素的相对重要性。结果显示,生物量时间稳定性与物种异步性、林分密度和海拔呈极显著正相关(P<0.001),路径系数分别为0.546、0.249和0.151。生物量时间稳定性与物种丰富度呈显著正相关(P<0.05),路径系数为0.086,而与林分结构的关系不显著(P>0.05),路径系数为0.021。海拔与林分密度呈显著正相关(P<0.001),路径系数为0.443,对生物量时间稳定性有极显著的间接作用。相较于其他林分因子,物种异步性是温带森林生物量时间稳定性的关键驱动因素,生物多样性通过物种异步效应提高生物量时间稳定性。基于结构方程模型的结果,分析生物与非生物因素对天然针阔混交林生物...     

青海大通典型林分冠层结构与林下植被物种多样性关系研究

为探究青海高寒山区典型林分冠层结构与林内光环境中维持林下植被物种多样性稳定的关键因素,该研究以青海大通县青海云杉林(Ⅰ)、青杨林(Ⅱ)、华北落叶松-青海云杉混交林(Ⅲ)、青杨-白桦混交林(Ⅳ)和白桦-青海云杉混交林(Ⅴ)5种典型人工林分为研究对象,运用冠层分析仪采集数据,并结合实地调查,研究冠层结构与林内光环境特征及其对林下植被的影响。结果表明:(1)林分Ⅰ、Ⅲ的林冠开度显著低于林分Ⅱ、Ⅳ、Ⅴ(P0.05),各林分叶面积指数大小顺序为ⅢⅠⅡⅤⅣ,总体表现为阔叶林的林冠开度大于针叶林,但其叶面积指数小于针叶林;林分Ⅱ、Ⅳ的直射辐射、散射辐射及总辐射均显著高于林分Ⅰ、Ⅲ、Ⅴ(P0.05),其中林下总辐射与散射辐射表现为ⅡⅣⅤⅠⅢ,直射辐射为ⅡⅣⅠⅢⅤ;林分Ⅱ、Ⅳ、Ⅴ的消光系数均显著高于Ⅰ、Ⅲ,总体上均表现为阔叶林针叶林。(2)相关分析结果表明,林冠开度与林下光照指标呈极显著正相关关系(P0.01),叶面积指数与林下光照指标呈极显著负相关关系(P0.01),且其对林下散射辐射的控制能力最强;典型相关分析表明,纯林的林冠开度对冠层结构的贡献和解释能力较叶面积指数和平均叶倾角大,混交林的叶面积指数对林下光照的影响大于纯林。(3)混交林的林下物种多样性指数(H)及丰富度指数(P)均高于纯林;林下草本层物种多样性指数(H)及丰富度指数(P)与林冠开度及林下光辐射呈显著正相关关系,与叶面积指数呈显著负相关关系(P0.05);物种均匀度(J_(sw))与平均叶倾角呈极显著负相关关系(P0.01),与林下散射辐射呈显著正相关关系(P0.05)。研究认为,在人工纯林改造和结构调整中,对乔木层适当补植伴生树种,并逐步调整为多树种混交林,增加冠层结构和林下光照异质性,将更有利于林下植被物种多样性的维持。     

树冠结构对典型阔叶红松林生产力的影响

阔叶红松(Pinus koraiensis)林是东北东部山区的地带性森林植被, 阐明其生产力的影响因素, 对于理解温带森林生产力维持机制具有重要意义。该研究依托小兴安岭典型阔叶红松林9 hm²动态监测样地, 基于2005和2015年的30 m × 30 m样方内所有胸径>6.5 cm的木本植物的调查数据, 计算各样方的树冠结构复杂性、物种多样性和林分胸高断面积, 结合各样方的地形和土壤理化性质数据, 拟合结构方程模型, 定量分析影响典型阔叶红松林生产力的直接和间接因素。研究结果显示: 树冠结构复杂性和物种多样性与生产力显著正相关, 且树冠结构复杂性对生产力的影响显著高于物种多样性; 树冠结构复杂性对生产力的作用分为树冠垂直分层和树冠可塑性, 其中树冠垂直分层是树冠结构复杂性影响阔叶红松林生产力的主要因素, 而树冠可塑性无显著影响; 林分胸高断面积与生产力显著正相关, 其解释权重仅次于树冠结构复杂性, 树冠结构复杂性与物种多样性均通过影响林分胸高断面积对阔叶红松林生产力产生间接影响; 考虑不同树冠结构复杂性时, 坡度和土壤全磷含量代表的环境因素在调节生产力上发挥的作用存在差异, 移除树冠垂直分层的作用后两者与生产力呈显著的负相关关系。综上可知, 在典型阔叶红松林中, 树冠结构复杂性比物种多样性更有效地解释了生产力的变化, 同时不可忽视其他生物和非生物因素对生产力的作用。     

环境因子对山西太岳山典型森林类型物种多样性及其功能多样性的影响

该研究采用典型样地法,调查群落内物种分布并测量植物功能性状(叶面积和植株高度),对山西太岳山不同坡位华北落叶松-白桦混交林以及辽东栎次生林物种多样性及其功能多样性进行比较分析,探究环境因子对不同群落层次(乔木、灌木、草本)物种多样性及其功能多样性的影响机制,以及环境因子与群落构建之间的联系,为森林生态系统多样性研究以及经营管理提供理论依据。结果显示:(1)华北落叶松-白桦混交林的物种分布更加均匀,物种多样性和功能多样性(乔木层)均显著高于辽东栎次生林。(2)华北落叶松-白桦混交林乔木层功能均匀度与功能分散指数显著高于辽东栎次生林,但灌木草本层低于辽东栎次生林。(3)不同群落层次的物种多样性与功能多样性均呈正相关关系,影响物种分布和性状分布的环境因子存在差异,物种多样性受多种环境因子的综合影响,而单个环境因子对功能多样性影响较大,环境解释力与林分类型和群落层次相关。(4)乔木层物种多样性主要受土壤pH、冠层结构(MLA、林分开度)以及光照影响,灌木层物种多样性与土壤pH和MLA密切相关,林下总辐射、土壤养分(SOC、STN)、土壤相对含水率是影响草本层物种分布的主要环境因子;冠层结构(MLA、林分开度)是影响乔木层功能多样性最主要的环境因子,土壤pH和坡位分别是华北落叶松-白桦混交林和辽东栎次生林灌木层功能多样性的主要影响因子,影响草本层功能多样性的主要环境因子是土壤相对含水率与LAI。研究表明,在垂直分层的森林生态系统中,不同群落层次竞争的主要环境资源存在差异,乔木层通过改变冠层结构和林内环境限制林下物种分布和性状分布。     

宁南山区华北落叶松林下草本层群落特征及其影响因素

林下草本植物是森林生态系统的基本组成要素,对森林的更新、生态系统结构、功能的维持和提升具有重要作用,理解林下草本层群落特征及其影响因素,有助于构建理想的林-草结合模式。本研究以宁南山区泾源县无人为干扰的华北落叶松林人工林、间伐处理的华北落叶松林人工林和华北落叶松与白桦自然混交林为研究对象,探究林下草本层群落特征(物种多样性和地上生物量)及其与土壤理化特性(土壤容重、含水量、全碳含量、全氮含量及全磷含量)和林分结构(密度和郁闭度)的关系。结果表明：(1)与人工林相比,自然混交林林下草本植物组成最丰富(34种),且物种多样性和地上生物量也最高;(2)自然混交林林下土壤特性均优于人工林,但间伐处理的人工林林下土壤特性较无人为干扰的人工林土壤特性有显著提高;(3)冗余分析表明,林下草本层物种多样性主要与土壤含水量、土壤全碳、全氮和全磷含量呈正相关,与土壤容重、林分密度和郁闭度呈负相关,且林分密度、0～20 cm土层含水量对林下草本物种多样性有显著影响(P<0.05);(4)回归分析结果表明,0～20 cm土层的土壤特性、物种丰富度和优势度、林分密度及郁闭度显著影响林下草本地上生物量的积累...     

Functional identity of overstorey tree height and understorey conservative traits drive aboveground biomass in a subtropical forest

The niche complementarity hypothesis has received empirical support but species differ in functional strategies for their contribution to ecosystem function, as predicted by the mass ratio hypothesis. Our understanding of how functional identity of conservative and acquisitive strategies of trees predicts aboveground biomass across forest strata (i.e. overstorey and understorey) remains unclear. Aboveground biomass, community-weighted mean (CWM − functional identity) of trait values (6 leaf and 2 stem traits), and soil physicochemical properties were estimated for 125 plots in a 5-ha subtropical forest in Eastern China. We used multiple linear regressions models to relate aboveground biomass to CWM indices at overstorey and understorey strata separately, and whole-community level. We finally employed the structural equation model to test for the effects of overstorey on understorey strata, in addition to the effects of soil physicochemical properties. Forest strata optimal models showed that overstorey strata had high aboveground biomass when they are dominated by functional identity of tree height, whereas high aboveground biomass in understorey strata was driven by functional identity of dense-wooded conservative strategy. Whole-community optimal model showed that communities dominated by functional identity of leaf dry matter content and mean leaf area had high aboveground biomass. Aboveground biomass was negatively related to soil nutrients across forest strata and whole-community level. The structural equation model showed that CWM of overstorey tree height did not affect understorey functional identity and aboveground biomass, when soil physicochemical properties were accounted. Soil nutrients had positive effect on functional identity of overstorey tree height whereas negative effect on functional identity of understorey dense-wooded strategy. This study highlights the fundamental roles of forest strata where overstorey and understorey strata contribute to their corresponding aboveground biomass with contrasting functional strategies across a range of soil nutrients. High aboveground biomass was potentially driven by functional identity of tree height through making use of plentiful soil nutrients at overstorey strata, whereas by conservative strategy at understorey strata through enduring nutrient-poor soils. To better understand the roles of functional identity of conservative and acquisitive strategies in driving ecosystem functions, it is worth to analyse forest strata separately.     

Testing indicators of sustainable forest management on understorey composition and diversity in southern Italy through variation partitioning

Tree species composition and stand structural complexity are valuable indicators of sustainable forest management. This article aims to investigate the relative influence of forest overstorey composition and structural attributes on understorey composition and diversity, taking into account also site characteristics and broad-scale environmental variables. We sampled vascular plant species composition and forest structure in 132 plots in the Cilento and Vallo di Diano National Park (southern Italy). Spearman’s non-parametric correlation coefficients were calculated between overstorey and understorey diversity indices, beech percentage, and altitude and environmental indices. A complete partitioning of the variation in understorey composition was then performed through canonical correspondence analysis considering four sets of variables: (1) overstorey composition, (2) structural attributes, (3) topography, and (4) landscape abiotic variables. Finally, we constructed a regression tree analysis of understorey species richness using the same explanatory variables. Understorey diversity indices were positively correlated with overstorey diversity indices and with environmental indices (i.e., light and soil heterogeneity). Overstorey and understorey diversity indices were negatively correlated with both altitude and the dominance of beech in the overstorey. Compositional variation was due primarily to overstorey composition and secondarily to structural attributes. Regression tree analysis revealed that altitude, overstorey species richness, and structural attributes play an important role in determining understorey species richness. According to our results, understorey composition and diversity are strongly related to overstorey composition and structural attributes. Indeed, the latter proved to be effective indicators of understorey characteristics in the study area.     

Drivers of understorey biomass: tree species identity is more important than richness in a young forest

林下生物量影响因素：幼龄林树种特性比丰富度更重要 生物多样性与生态系统功能的正相关关系已被广泛报道,其主要来源于对草原生态系统的研究。然而,该结论并不一定适用于更复杂的环境,例如具有不同垂直层次的森林。举例而言,已有研究表明上层乔木树种丰富度与林下生产力降低有关。树种丰富度是否会通过增加(由于生境异质性)或降低(通过增强竞争)资源的可利用性进而影响林下生产力,以及林下生产力是否受树种特性的影响更大,这些影响机制都可能会随着时间的推移而改变。此外,研究还表明,丰富度-生产力关系随着环境背景的变化而改变。本研究利用可以操控树种丰富度的实验林场研究了这些不同垂直层位里的时间和环境动态。在中国亚热带森林生物多样性与生态系统功能(BEF-China)研究计划的框架下,我们在3年时间里沿树种丰富度梯度反复采集林下生物量样本,研究了不同环境处理中树种丰富度、树种特性和时间对林下生物量的影响。尽管我们发现乔木层特性对林下生物量有显著和一致的影响,但是树种丰富度对后者却不具有这种影响。另外,在森林结构层之间,可能并不存在单一的、具有普遍性的上层乔木树种丰富度与林下生产力的相关关系,并且与上层乔木相关的环境因素(如透光率)对林下生产力的贡献程度会随着时间而变化。总体而言,我们的结果表明,在研究森林结构层之间的关系时应将时间动态变化考虑在内。     

南亚热带常绿阔叶林树木多样性与生物量和生产力的关联及其影响因素

生物多样性和生态系统功能的关系直接或间接地影响着生产力, 是生态学研究的关键问题。本研究旨在定量探讨亚热带自然林演替后期森林生态系统树木多样性与生物量或生产力的关系。本研究基于中国南亚热带长期永久性样地的群落调查数据以及地形和土壤养分数据, 分析了南亚热带常绿阔叶林树木多样性与生物量和生产力的关联及其影响因素。相关性分析结果表明, 物种多样性与生物量呈显著负相关, 与生产力呈显著正相关; 结构多样性与生物量呈显著正相关, 与生产力呈显著负相关。此外, 不同环境因子对多样性、生物量和生产力的影响具有显著差异, 其中土壤含水量对生产力有显著影响, 物种多样性指标与部分地形和土壤因子均有相关性, 而群落结构多样性指标与土壤因子的相关性更强。方差分解结果表明, 结构多样性对生物量和生产力的单独效应的解释率最大, 分别为35.39%和5.21%; 其次是结构多样性和物种多样性的共同效应, 对生物量和生产力的解释率分别为13.66%和3.53%; 地形和土壤因子的解释率较小。同时, 结构方程结果也表明, 结构多样性对生物量有较强的直接正影响; 生物量对生产力有强烈的直接负影响, 结构多样性通过增加生物量明显地减少了生产力; 土壤和地形因子主要是通过物种和结构多样性间接影响生物量和生产力。综上, 本研究认为在南亚热带森林演替顶极群落中, 群落结构复杂性和物种多样性的提高对促进群落生产力和生物量具有重要作用。     

Relationships between species diversity or community structure and productivity of woody-plants in a broad-leaved Korean pine forest in Jiaohe,Jilin, China

Aims Based on the dataset of a broad-leaved Korean pine forest in Jiaohe, Jilin Province, this research compared the influences of species diversity and community structure on productivity. We aim to explain the relationship between diversity and productivity for better forest management. Methods We used the data of 10 973 woody-plants in a 11.76 hm² large sample plot and analyzed the correlations between 7 different indices of species diversity or community structure and productivity. Structural equation model was used to compare the effects of species diversity and community structure on productivity. Important findings The results showed that: (1) Both species diversity and community structure had significant effects on productivity when they were considered separately in linear regression analysis, i.e. species evenness was negatively correlated with productivity, the Shannon index of community structure was positively correlated with productivity and the Gini index was negatively correlated with productivity. (2) In the structural equation model, when simultaneously considered, community structure had stronger influence on productivity than species diversity. Our research suggests that, the effects of community structure on productivity are greater than species diversity and it is important to increase community structure complexity to improve forest productivity during forest management.     

基于结构方程模型分析林分空间结构对草本物种多样性的影响

林分空间结构的改变直接影响林下草本物种的多样性。以针叶纯林、针阔混交林和常绿阔叶林为研究对象,采用结构方程模型研究了林分空间结构对林下草本物种多样性的影响,并探讨了林分水平空间结构,垂直空间结构以及林木竞争态势对林下草本物种多样性的影响的相对重要性。结果表明,林分水平空间结构对林下草本的物种多样性指数和物种均匀性指数均存在极显著的影响（P < 0.001）,影响系数高达0.96和0.89,对林下草本物种丰富度存在显著影响（P < 0.01）,影响系数为0.22;林分垂直空间结对林下草本丰富度和物种均匀性指数均存在极显著的影响（P < 0.001）,影响系数分别为0.86和0.43,对林下草本物种多样性指数存在显著影响（P < 0.01）,影响系数为0.16;林木竞争指数与林下草本丰富度和物种多样性指数也均存在极显著的影响（P < 0.001）,但影响系数较小,分别为-0.47和-0.30,而对林下草本物种均匀性指数未达到显著影响作用（P > 0.05）,影响系数仅为-0.04。整体上看,林分水平空间结构、垂直空间结构和林木竞争态势均对林下草本物种多样性有较强的影响作用,但从影响系数看,林分水平空间结构的影响作用最大,垂直空间结构次之,林木竞争态势的影响作用最小。因此,欲维持或改善林下草本物种多样性,应采取调整林分水平空间结构为主,垂直空间结构调整为辅,并适当降低林木竞争程度的综合经营措施。     

Vertical distribution of fruit‐feeding butterflies with evidence of sex‐specific differences in a Tanzanian forest

Tropical forests accommodate rich species diversity, particularly among insects. Habitat heterogeneity along the vertical gradient extending from the forest understorey to the tree canopy influences diversity. The vertical distribution of forest insects is poorly understood across Africa, most especially eastern Africa. Food‐baited traps were used to study the vertical stratification of adult fruit‐feeding nymphalid butterflies in Mtai Forest Reserve, north‐eastern Tanzania. Traps were located in the forest canopy and understorey. A total of 277 individuals of 24 species were captured. Species composition differed by trap locations: 33% of the species captured were found in both the canopy and understorey strata; however, significantly more species were captured in the understorey (54%) than canopy (13%). Males were significantly more abundant than females and captured in both strata. A greater proportion of females were captured in the understorey than the canopy. The time of day affected capture rates, with more individuals caught in the afternoon; however, there was no association between the time period and the sex of individuals captured in canopy versus understorey locations. Understanding how the sexes of butterflies vary in understorey versus canopy offers new biological insights into the vertical stratification of insects.     

Effect of forest canopy composition on soil nutrients and dynamics of the understorey: mixed canopies serve neither vascular nor bryophyte strata

Question: The effect of overstorey composition on above‐ground dynamics of understorey vegetation is poorly understood. This study examines the understorey biomass, production and turnover rates of vascular and non‐vascular plants along a conifer–broadleaf gradient of resource availability and heterogeneity. Location: Canadian boreal forests of northwest Quebec and Ontario. Methods: We sampled mature stands containing various proportions of black spruce (Picea mariana (Mill.) BSP), trembling aspen (Populus tremuloides Michx.) and jack pine (Pinus banksiana Lamb.). Above‐ground biomass of the understorey vegetation was assessed through harvesting; annual growth rates were calculated as the differences between biomass in 2007 and 2008, as estimated by allometric relationships, and turnover rates were estimated as net primary production divided by the biomass in 2007. Results: Higher aspen presence, linked to greater nutrient availability in the forest floor, was generally associated with higher vascular biomass and production in the understorey. This effect was less pronounced in sites of high intrinsic fertility. In contrast, bryophyte biomass was positively associated with conifer abundance, particularly in wet sites of the Quebec study area. Non‐linear responses resulted in total understorey biomass being lower under mixed canopies than under pure aspen or pure conifer canopies. Turnover rates did not differ with overstorey composition. Conclusions: While resource availability is a main driver of understorey productivity, resources as drivers appear to differ with differences in understorey strata components, i.e. vascular versus non‐vascular plants. Resource heterogeneity induced by a mixed canopy had overall negative effects on understorey above‐ground productivity, as this productivity seemed to rely on species adapted to the specific conditions induced by a pure canopy.     

The balance between the foliage projective covers of overstorey and understorey strata in Australian vegetation

Foliage Projective Cover of the overstorey (canopy) of a‘climax’community appears to reach an equilibrium value determined largely by the prevailing climate. Overstorey FPC decreases in‘climax’communities in a graded series from humid to arid regions. Understorey cover (of all strata below the canopy) in‘climax’communities attains a balance with overstorey FPC. Disturbance (gaps, microhabitats, fire, overgrazing, invasion of woody weeds, etc.) may reduce the overstorey cover which will be compensated by an increase in understorey cover. Secondary succession back to the‘climax’structure will follow a path maintaining an inverse linear relationship between understorey cover and overstorey cover. At the same time, species diversity appears to decrease as overstorey cover increases.