Journal of Ecology

  0022-0477

  1365-2745

  Anh Quốc

Cơ quản chủ quản:  Wiley-Blackwell Publishing Ltd , WILEY

Lĩnh vực:
Plant ScienceEcologyEcology, Evolution, Behavior and Systematics

Các bài báo tiêu biểu

The world‐wide ‘fast–slow’ plant economics spectrum: a traits manifesto
Tập 102 Số 2 - Trang 275-301 - 2014
Peter B. Reich
Summary The leaf economics spectrum (LES) provides a useful framework for examining species strategies as shaped by their evolutionary history. However, that spectrum, as originally described, involved only two key resources (carbon and nutrients) and one of three economically important plant organs. Herein, I evaluate whether the economics spectrum idea can be broadly extended to water – the third key resource –stems, roots and entire plants and to individual, community and ecosystem scales. My overarching hypothesis is that strong selection along trait trade‐off axes, in tandem with biophysical constraints, results in convergence for any taxon on a uniformly fast, medium or slow strategy (i.e. rates of resource acquisition and processing) for all organs and all resources. Evidence for economic trait spectra exists for stems and roots as well as leaves, and for traits related to water as well as carbon and nutrients. These apply generally within and across scales (within and across communities, climate zones, biomes and lineages). There are linkages across organs and coupling among resources, resulting in an integrated whole‐plant economics spectrum. Species capable of moving water rapidly have low tissue density, short tissue life span and high rates of resource acquisition and flux at organ and individual scales. The reverse is true for species with the slow strategy. Different traits may be important in different conditions, but as being fast in one respect generally requires being fast in others, being fast or slow is a general feature of species. Economic traits influence performance and fitness consistent with trait‐based theory about underlying adaptive mechanisms. Traits help explain differences in growth and survival across resource gradients and thus help explain the distribution of species and the assembly of communities across light, water and nutrient gradients. Traits scale up – fast traits are associated with faster rates of ecosystem processes such as decomposition or primary productivity, and slow traits with slow process rates. Synthesis. Traits matter. A single ‘fast–slow’ plant economics spectrum that integrates across leaves, stems and roots is a key feature of the plant universe and helps to explain individual ecological strategies, community assembly processes and the functioning of ecosystems.
The Exchange of Dissolved Substances Between Mud and Water in Lakes
Tập 29 Số 2 - Trang 280 - 1941
C. H. Mortimer
The LEDA Traitbase: a database of life‐history traits of the Northwest European flora
Tập 96 Số 6 - Trang 1266-1274 - 2008
Michael Kleyer, R.M. Bekker, I.C. Knevel, J.P. Bakker, Ken Thompson, Michael Sonnenschein, Peter Poschlod, J.M. Van Groenendael, Leoš Klimeš, Jitka Klimešová, Stefan Klotz, Graciela M. Rusch, Martin Hermy, Dries Adriaens, Ger Boedeltje, Beatrijs Bossuyt, Andrea Dannemann, Patrick Endels, Lars Götzenberger, J. G. Hodgson, A. K. Jackel, Ingolf Kühn, D. Kunzmann, W.A. Ozinga, Christine Römermann, Michael Städler, Jürgen Schlegelmilch, H.J. Steendam, Oliver Tackenberg, Bodil Helene Wilmann, J. H. C. Cornelissen, Ove Eriksson, Éric Garnier, Begoña Peco
Some Ecological Consequences of a Computer Model of Forest Growth
Tập 60 Số 3 - Trang 849 - 1972
Daniel B. Botkin, J. F. Janak, James R. Wallis
Impact of invasive plants on the species richness, diversity and composition of invaded communities
Tập 97 Số 3 - Trang 393-403 - 2009
Martin Hejda, Petr Pyšek, Vojtĕch Jaros̆ı́k
Summary Much attention has been paid to negative effects of alien species on resident communities but studies that quantify community‐level effects of a number of invasive plants are scarce. We address this issue by assessing the impact of 13 species invasive in the Czech Republic on a wide range of plant communities. Vegetation in invaded and uninvaded plots with similar site conditions was sampled. All species of vascular plants were recorded, their covers were estimated and used as importance values for calculating the Shannon diversity index H′, evenness J and Sørensen index of similarity between invaded and uninvaded vegetation. With the exception of two invasive species, species richness, diversity and evenness were reduced in invaded plots. Species exhibiting the greatest impact reduced species numbers per plot and the total number of species recorded in the communities sampled by almost 90%. A strong reduction of species number at the plot scale resulted in a marked reduction in the total species number at the landscape scale, and in less similarity between invaded and uninvaded vegetation. The decrease in species richness in invaded compared to uninvaded plots is largely driven by the identity of the invading species, whereas the major determinants of the decrease in Shannon diversity and evenness are the cover and height of invading species, and differences between height and cover of invading and dominant native species, independent of species identity. Synthesis. Management decisions based on impact need to distinguish between invasive species, as their effects on diversity and composition of resident vegetation differ largely. Tall invading species capable of forming populations with the cover markedly greater than that of native dominant species exert the most severe effects on species diversity and evenness. Since a strong impact on the community scale is associated with reduction in species diversity at higher scales, invaders with a high impact represent a serious hazard to the landscape.
The Exchange of Dissolved Substances between Mud and Water in Lakes
Tập 30 Số 1 - Trang 147 - 1942
C. H. Mortimer
Identification of 100 fundamental ecological questions
Tập 101 Số 1 - Trang 58-67 - 2013
William J. Sutherland, Robert P. Freckleton, H. Charles J. Godfray, Steven R. Beissinger, Tim G. Benton, Duncan D. Cameron, Yohay Carmel, David A. Coomes, Tim Coulson, Mark Emmerson, Rosemary S. Hails, Graeme C. Hays, David J. Hodgson, Michael J. Hutchings, David Johnson, Julia P. G. Jones, Matt J. Keeling, Hanna Kokko, William E. Kunin, Xavier Lambin, Owen T. Lewis, Yadvinder Malhi, Nova Mieszkowska, E.J. Milner‐Gulland, Ken Norris, Albert B. Phillimore, Drew W. Purves, Jane M. Reid, Daniel C. Reuman, Ken Thompson, Justin M. J. Travis, Lindsay A. Turnbull, David A. Wardle, Thorsten Wiegand
Summary Fundamental ecological research is both intrinsically interesting and provides the basic knowledge required to answer applied questions of importance to the management of the natural world. The 100th anniversary of the British Ecological Society in 2013 is an opportune moment to reflect on the current status of ecology as a science and look forward to high‐light priorities for future work. To do this, we identified 100 important questions of fundamental importance in pure ecology. We elicited questions from ecologists working across a wide range of systems and disciplines. The 754 questions submitted (listed in the online appendix) from 388 participants were narrowed down to the final 100 through a process of discussion, rewording and repeated rounds of voting. This was done during a two‐day workshop and thereafter. The questions reflect many of the important current conceptual and technical pre‐occupations of ecology. For example, many questions concerned the dynamics of environmental change and complex ecosystem interactions, as well as the interaction between ecology and evolution. The questions reveal a dynamic science with novel subfields emerging. For example, a group of questions was dedicated to disease and micro‐organisms and another on human impacts and global change reflecting the emergence of new subdisciplines that would not have been foreseen a few decades ago. The list also contained a number of questions that have perplexed ecologists for decades and are still seen as crucial to answer, such as the link between population dynamics and life‐history evolution. Synthesis. These 100 questions identified reflect the state of ecology today. Using them as an agenda for further research would lead to a substantial enhancement in understanding of the discipline, with practical relevance for the conservation of biodiversity and ecosystem function.
Plant functional composition influences rates of soil carbon and nitrogen accumulation
Tập 96 Số 2 - Trang 314-322 - 2008
Dario Fornara, David Tilman
Summary The mechanisms controlling soil carbon (C) and nitrogen (N) accumulation are crucial for explaining why soils are major terrestrial C sinks. Such mechanisms have been mainly addressed by imposing short‐term, step‐changes in CO2, temperature and N fertilization rates on either monocultures or low‐diversity plant assemblages. No studies have addressed the long‐term effects of plant functional diversity (i.e. plant functional composition) on rates of soil C accumulation in N‐limited grasslands where fixation is the main source of N for plants. Here we measure net soil C and N accumulation to 1 m soil‐depth during a 12‐year‐long grassland biodiversity experiment established on agriculturally degraded soils at Cedar Creek, Minnesota, USA. We show that high‐diversity mixtures of perennial grassland plant species stored 500% and 600% more soil C and N than, on average, did monoculture plots of the same species. Moreover, the presence of C4 grasses and legumes increased soil C accumulation by 193% and 522%, respectively. Higher soil C and N accrual resulted both from increased C and N inputs via (i) higher root biomass, and (ii) from greater root biomass accumulation to 60 cm soil depth resulting from the presence of highly complementary functional groups (i.e. C4 grasses and legumes). Our results suggest that the joint presence of C4 grass and legume species is a key cause of greater soil C and N accumulation in both higher and lower diversity plant assemblages. This is because legumes have unique access to N, and C4 grasses take up and use N efficiently, increasing below‐ground biomass and thus soil C and N inputs. Synthesis. We demonstrate that plant functional complementarity is a key reason why higher plant diversity leads to greater soil C and N accumulation on agriculturally degraded soils. We suggest the combination of key C4 grass–legume species may greatly increase ecosystem services such as soil C accumulation and biomass (biofuel) production in both high‐ and low‐diversity N‐limited grassland systems.
Forest productivity increases with evenness, species richness and trait variation: a global meta‐analysis
Tập 100 Số 3 - Trang 742-749 - 2012
Yu Zhang, Han Y. H. Chen, Peter B. Reich
Summary1. Although there is ample support for positive species richness–productivity relationships in planted grassland experiments, a recent 48‐site study found no diversity–productivity relationship (DPR) in herbaceous communities. Thus, debate persists about diversity effects in natural versus planted systems. Additionally, current knowledge is weak regarding the influence of evenness on the DPRs, how DPRs are affected by the variation in life‐history traits among constituent species in polycultures and how DPRs differ among biomes. The impacts of these factors on DPRs in forest ecosystems are even more poorly understood.2. We performed a meta‐analysis of 54 studies to reconcile DPRs in forest ecosystems. We quantified the net diversity effect as log effect size [ln(ES)], the log ratio of the productivity in polycultures to the average of those in monocultures within the same type of mixture, site condition and stand age of each study. The first use of a boosted regression tree model in meta‐analysis, a useful method to partition the effects of multiple predictors rather than relying on vote‐counting of individual studies, unveiled the relative influences of individual predictors.3. Global average ln(ES) was 0.2128, indicating 23.7% higher productivity in polycultures than monocultures. The final model explained 21% of the variation in ln(ES). The predictors that substantially accounted for the explained variation included evenness (34%), heterogeneity of shade tolerance (29%), richness (13%) and stand age (15%). In contrast, heterogeneity of nitrogen fixation and growth habits, biome and stand origin (naturally established versus planted) contributed negligibly (each ≤ 4%). Log effect size strongly increased with evenness from 0.6 to 1 and with richness from 2 to 6. Furthermore, it was higher with heterogeneity of shade tolerance and generally increased with stand age.4.Synthesis.Our analysis is, to our knowledge, the first to demonstrate the critical role of species evenness, richness and the importance of contrasting traits in defining net diversity effects in forest polycultures. While testing the specific mechanisms is beyond the scope of our analysis, our results should motivate future studies to link richness, evenness, contrasting traits and life‐history stage to the mechanisms that are expected to produce positive net biodiversity effects such as niche differentiation, facilitation and reduced Janzen–Connell effects.
Land-Use History (1730-1990) and Vegetation Dynamics in Central New England, USA
Tập 80 Số 4 - Trang 753 - 1992
David R. Foster