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Intransitive competition is often projected to be a widespread mechanism of species coexistence in ecological communities. However, it is unknown how much of the coexistence we observe in nature results from this mechanism when species interactions are also stabilized by pairwise niche differences. We combined field-parameterized models of competition among 18 annual plant species with tools from network theory to quantify the prevalence of intransitive competitive relationships. We then analyzed the predicted outcome of competitive interactions with and without pairwise niche differences. Intransitive competition was found for just 15–19% of the 816 possible triplets, and this mechanism was never sufficient to stabilize the coexistence of the triplet when the pair-wise niche differences between competitors were removed. Of the transitive and intransitive triplets, only four were predicted to coexist and these were more similar in multidimensional trait space defined by 11 functional traits than non-coexisting triplets. Our results argue that intransitive competition may be less frequent than recently posed, and that even when it does operate, pairwise niche differences may be key to possible coexistence.

Coevolution can promote long-term coexistence of two competing species if selection acts to reduce the fitness inequality between competitors and/or strengthen negative frequency dependence within each population. However, clear coevolution between plant competitors has been rarely documented. Plant invasions offer opportunities to capture the process of coevolution. Here we investigated how the developing relationship between an invasive forb, Alliaria petiolata, and a native competitor, Pilea pumila, may affect their long-term coexistence, by testing the competitive effects of populations of varying lengths of co-occurrence on each other across a chronosequence of invasion history. Alliaria petiolata and P. pumila tended to develop greater tolerance to competition over invasion history. Their coexistence was promoted more by increases in stabilizing relative to equalizing processes. These changes likely stem in part from reductions in allelopathic traits in the invader and evolution of tolerance in the native. These results suggested that some native species can evolve tolerance against the competitive effects of strong invaders, which likely promoted their persistence in invaded communities. However, the potential for coevolutionary rescue of competing populations is likely to vary across native species, and evolutionary processes should not be expected to compensate for the ecological consequences of exotic invasions.

Poly(vinyl chloride) (PVC) is widely used in various fields and requires the use of thermal stabilizers to enhance its thermal stability during processing because of its poor thermal stability. Layered double hydroxides (LDHs) are widely considered to be one kind of highly efficient and environmentally friendly PVC thermal stabilizer. To investigate the thermal stabilizing process of layered double hydroxides (LDHs) in PVC resin, PVC and MgAl-LDHs powders with different interlayer anions (CO32−, Cl−, and NO3−) were physically mixed and aged at 180 °C. The structure of LDHs at different aging times was studied using XRD, SEM, and FT-IR. The results show that the thermal stabilizing process of LDHs on PVC mainly has three stages. In the first stage, the layers of LDHs undergo a reaction with HCl, which is released during the thermal decomposition of PVC. Subsequently, the ion exchange process occurs between Cl− and interlayer CO32−, resulting in the formation of MgAl-Cl-LDHs. Finally, the layers of MgAl-Cl-LDHs react with HCl slowly. During the thermal stabilizing process of MgAl-Cl-LDHs, the peak intensity of XRD reduces slightly, and no new XRD peak emerges. It indicates that only the first step happens for MgAl-Cl-LDHs. The TG-DTA analysis of LDHs indicates that the interaction of LDHs with different interlayer anions has the following order: NO3− < CO32− < Cl−, according to the early coloring in the thermal aging test of PVC composites. The results of the thermal aging tests suggest that LDHs with a weak interaction between interlayer anions and layers can enhance the early stability of PVC significantly. Furthermore, the thermal aging test demonstrates that LDHs with high HCl absorption capacities exhibit superior long-term stabilizing effects on PVC resin. This finding provides a valuable hint for designing an LDHs/PVC resin with a novel structure and excellent thermal stability.

1. Increased species diversity promotes ecosystem function; however, the dynamics of multi-species grassland systems over time and their role in sustaining higher yields generated by increased diversity are still poorly understood. We investigated the development of species' relative abundances in grassland mixtures over 3 years to identify drivers of diversity change and their links to yield diversity effects. 2. A continental-scale field experiment was conducted at 31 sites using 11 different four-species mixtures each sown at two seed abundances. The four species consisted of two grasses and two legumes, of which one was fast establishing and the other temporally persistent. We modelled the dynamics of the four-species mixtures, and tested associations with diversity effects on yield. 3. We found that species' dynamics were primarily driven by differences in the relative growth rates (RGRs) of competing species, and secondarily by density dependence and climate. The temporally persistent grass species typically had the highest RGRs and hence became dominant over time. Density dependence sometimes induced stabilising processes on the dominant species and inhibited shifts to monoculture. Legumes persisted at most sites at low or medium abundances and persistence was improved at sites with higher annual minimum temperature. 4. Significant diversity effects were present at the majority of sites in all years and the strength of diversity effects was improved with higher legume abundance in the previous year. Observed diversity effects, when legumes had declined, may be due to (i) important effects of legumes even at low abundance, (ii) interaction between the two grass species or (iii) a store of N because of previous presence of legumes. 5. Synthesis. Alongside major compositional changes driven by RGR differences, diversity effects were observed at most sites, albeit at reduced strength as legumes declined. This evidence strongly supports the sowing of multi-species mixtures that include legumes over the long-standing practice of sowing grass monocultures. Careful and strategic selection of the identity of the species used in mixtures is suggested to facilitate the maintenance of species diversity and especially persistence of legumes over time, and to preserve the strength of yield increases associated with diversity.

Interspecific competition in natural plant communities is highly dependent on nutrient availability. At high levels of nutrient availability, competition is mainly for light. As light is a unidirectional resource, high-nutrient habitats are dominated by fast-growing perennials with a tall stature and a rather uniform vertical distribution of leaf area. Moreover, these species have high turnover rates of leaves and roots and a high morphological plasticity during the differentiation of leaves. There is less consensus, however, about the importance and intensity of interspecific competition in nutrient-poor environments. It is argued that selection in nutrient-poor habitats is not necessarily on a high competitive ability for nutrients and a high growth rate, but rather on traits which reduce nutrient losses (low tissue nutrient concentrations, slow tissue turnover rates, high nutrient resorption efficiency). Due to evolutionary trade-offs plants can not maximize both growth rate and nutrient retention. Thus, the low growth rate of species from nutrient-poor habitats should be considered as the consequence of nutrient retention rather than as a feature on which direct selection takes place. The contrasting traits of species from nutrient-poor and nutrient-rich habitats mutually exclude them from each others' habitats. Moreover, these traits have severe consequences for litter decomposability and thereby also for nutrient cycling. This leads both in nutrient-poor and nutrient-rich habitats to a positive feedback between plant species dominance and nutrient availability, thereby promoting ecosystem stability.

Various claims have been made about the ecological significance of plant-to-plant carbon movement through common mycorrhizal networks (CMNs). Most suggest that resource competition among interconnected plants should be less important than previously thought. If true, that would profoundly alter our perception of how plants interact among themselves and with their environment. However, there are difficulties in quantifying the amounts of resource transferred via CMNs, ensuring that transfer is genuinely through hyphae, not soil, and understanding its control. Carbon movement has not been quantified in many of the published studies. Where it has, its likely functional role has not been clarified. Some recent, well-publicized research suggests that carbon transferred to trees via an ectomycorrhizal (EcM) network may be physiologically and ecologically important. Our view, however, is that the evidence for this remains equivocal. Appropriate controls for the possibility of carbon transfer via soil were not used under field conditions. In laboratory experiments, controls failed to clarify the role of EcM links in carbon transfer. To resolve some areas of uncertainty, abundances of 13C have been measured to estimate carbon transfers via an arbuscular mycorrhizal (AM) network connecting grasses and forbs of the same or different species. Permeable barriers to roots and hyphae allowed any direct carbon transfer via soil to be detected. Large amounts of carbon (typically 10% of that in roots) were transferred between linked plants via the CMN. Transferred carbon was never transported into shoots of ‘receiver’ plants. It remained in roots, probably inside fungal structures and, therefore, unavailable to the plants into which it was apparently transferred. Carbon transfer via an AM network does not allow ‘resource sharing’ among linked plants. It is probably irrelevant to the botanical components of a community, but it may be fundamental for fungal members. The ‘mycocentric’ view is that fungal structures within roots are parts of extended mycelia through which fungi move carbon according to their own carbon demands, not those of their autotrophic hosts.

Plants generate and perceive informational signals. An interaction (between plants) is considered to be informational when it involves the exchange of an insignificant amount of matter or energy, in quantitative terms, but in spite of this has a profound effect on plants by modulating their developmental programme. This article discusses how plants 'use' light signals to detect neighbouring plants and outlines the implications of shade-avoidance responses for the development of size and fitness hierarchies in canopies. The role of shade avoidance as a stabilizing force in monospecific canopies is noted.

A conceptual model of resource acquisition and allocation within a generalized, individual plant growing vegetatively in competition with others is presented. The model considers C and N acquisition, synthesis of assimilates and their transport and partitioning, growth of new tissues, reserve formation and recycling, and losses due to root exudation and respiration. These processes are regulated by the relative size of the C and N substrate pools in shoot and roots, in relation to meristematic sink strength. Translocation and allocation patterns are represented according to the Minchin phloem transport model. The current model is used to consider the impact of competition on resource acquisition and allocation, first by considering a plant growing in isolation and its response to manipulation of light, CO2 and N supplies. Secondly, competitive plants are introduced and the direct effects on plant responses in terms of resource depletion are considered separately from indirect effects such as potential changes in the quality of resources available (e.g. light quality or soil N sources). In the past, many studies of plant competition have not established the importance of these indirect effects because they have not established all the processes involved in competition. This model can be used to interpret responses of whole plants to their neighbours in terms of the relative importance of both the direct and indirect effects of competition.

A model for mimicking land plant evolution is here expanded and re-evaluated. The model consists of (1) a morphospace containing on the order of 10(9) phenotypic variants, (2) 15 different fitness landscapes, each defined on the basis of performing one or more of four tasks (i.e. maximizing light interception, mechanical stability and reproduction, and minimizing total surface area), and (3) an algorithm driving a search through fitness landscapes for more fit variants. The model is used to predict the effects of the number of simultaneously performed tasks ('complexity'), abrupt changes in environmental conditions (mimicked by random replacement of one fitness landscape with another), and developmental barriers (mimicked by barring searches from entering specific subdomains in the morphospace) on number and accessibility of variants occupying fitness maxima. The model predicts that (1) the number and accessibility of fitness peaks will increase (while the difference between the relative fitness of peaks and valleys will decrease) in proportion to functional complexity, (2) abrupt shifts in landscapes will increase rather than decrease phenotypic diversity, and (3) obstructed searches have an equal or higher probability of reaching fitness peaks than unfettered searches. These results follow axiomatically from the way hypothetical variants are spatially ordered in the morphospace, the manner in which relative fitness is defined, and the protocol used to locate fitness peaks. A critique of the model's predictions and desiderata for future research are provided.

Despite extensive research for several decades, there remains a lack of understanding of the processes that determine the dynamics of natural plant communities. In this paper some current concepts in vegetation dynamics are reviewed and an attempt is made to provide a perspective of the way in which data for molecular diversity might be used to help in developing an understanding of population processes. It is proposed that data from assessments of general population diversity, and specific ecophysiological traits can be used to assess the potential for individual species to compete and substitute for each other in a community.