Variation in leaf life—span has long been considered of ecological significance.Despite this, quantitative evaluation of the relationships between leaf life—span and other plant and ecosystem characteristics has been rare. In this paper we ask whether leaf life—span is related to other leaf, plant, and stand traits of species from diverse ecosystems and biomes. We also examine the interaction between leaf, plant, and stand traits and their relation to productivity and ecological patterns. Among all species, both mass— (Amass) and area—based (Aarea) maximum net photosynthesis decreased with increasing leaf life—span, but the relationship was stronger on a mass (P .25, r2 = 0.01). Specific leaf area (SLA, leaf area/leaf dry mass) and leaf diffusive conductance also decreased with increasing leaf life—span. Decreasing Amass with increasing leaf life—span results from the impact of decreasing Nmass and SLA on Amass. Variation in leaf traits as a function of leaf life—span was similar for broad—leaved and needle—leaved subsets of the data. These leaf—scale data from several biomes were compared to a data set from a single biome, Amazonia. For several leaf traits (e.g., SLA, Nmass, and Amass) the quantitative relationship with leaf life—span was similar in the two independent data sets, suggesting that these are fundamental relations applicable to all species. Amass was a linear function of Nmass (P .001, r2 = 0.74) with a regression similar to previous analyses, while Aarea was not significantly related to Narea. These results suggest that the photosynthesis—leaf N relationship among species should be considered universal when expressed on a mass, but not on a leaf area, basis. Relative growth rates (RGR) and leaf area ratio (LAR, the whole—plant ratio of leaf area to total dry mass) of seedlings decreased with increasing leaf life—span (P < .001, r2 = 0.61 and 0.89, respectively). LAR was positively related to both RGR and Amass (r2 = 0.68 and 0.84, respectively), and Amass and RGR were also positively related (r2 = 0.55). Absolute height growth rates of young trees decreased with increasing leaf life—span (P < .001, r2 = 0.72) and increased with Amass (P < .001, r2 = 0.78). It appears that a suite of traits including short leaf life—span and high leaf Nmass, SLA, LAR, and Amass interactively contribute to high growth rates in open—grown individuals. These traits interact similarly at the stand level, but stands differ from individuals in one key trait. In closed—canopy forests, species with longer lived foliage (and low LAR as seedlings) have greater foliage mass per unit ground area (P < .001, r2 = 0.74) and a greater proportion of total mass in foliage. The aboveground production efficiency (ANPP/foliar biomass) of forest stands decreased markedly with increasing leaf life—span or total foliage mass (P < .001, r2 = 0.78 and 0.72, respectively), probably as a result of decreasing Amass, Nmass, and SLA, all of which were positively related with production efficiency and negatively related to total foliage mass. However, high foliage mass of species with extended leaf life—spans appears to compensate for low production per unit foliage, since aboveground net primary production (ANPP, in megagrams per hectare per year) of forest stands was not related to leaf life—span. Extended leaf life—span also appears to compensate for lower potential production per unit leaf N per unit time, with the result that stand—level N use efficiency is weakly positively related to leaf life—span. We hypothesize that co—variation among species in leaf life—span, SLA, leaf Nmass, Amass, and growth rate reflects a set of mutually supporting traits that interact to determine plant behavior and production, and provide a useful conceptual link between processes at short—term leaf scales and longer term whole plant and stand—level scales. Although this paper has focused on leaf life—span, this trait is so closely interrelated with several others that this cohort of leaf traits should be viewed as casually interrelated. Generality in the relationships between leaf life—span and other plant traits across diverse communities and ecosystems suggests that they are universal in nature and thus can provide a quantitative link and/or common currency for ecological comparisons among diverse systems.

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Leaf Life-Span in Relation to Leaf, Plant, and Stand Characteristics among Diverse Ecosystems

What determines the number and size of the seeds produced by a plant? How often should it reproduce them? How often should a plant produce them? Why and how are seeds dispersed, and what are the implications for the diversity and composition of vegetation? These are just some of the questions tackled in this wide-ranging review of the role of seeds in the ecology of plants. The authors bring together information on the ecological aspects of seed biology, starting with a consideration of reproductive strategies in seed plants and progressing through the life cycle, covering seed maturation, dispersal, storage in the soil, dormancy, germination, seedling establishment, and regeneration in the field. The text encompasses a wide range of concepts of general relevance to plant ecology, reflecting the central role that the study of seed ecology has played in elucidating many fundamental aspects of plant community function.

The ecology of seeds

Immunosuppressive tumor microenvironments can restrain antitumor immunity, particularly in pancreatic ductal adenocarcinoma (PDA). Because CD40 activation can reverse immune suppression and drive antitumor T cell responses, we tested the combination of an agonist CD40 antibody with gemcitabine chemotherapy in a small cohort of patients with surgically incurable PDA and observed tumor regressions in some patients. We reproduced this treatment effect in a genetically engineered mouse model of PDA and found unexpectedly that tumor regression required macrophages but not T cells or gemcitabine. CD40-activated macrophages rapidly infiltrated tumors, became tumoricidal, and facilitated the depletion of tumor stroma. Thus, cancer immune surveillance does not necessarily depend on therapy-induced T cells; rather, our findings demonstrate a CD40-dependent mechanism for targeting tumor stroma in the treatment of cancer.

https://science.sciencemag.org/content/sci/331/6024/1612.full.pdf

CD40 Agonists Alter Tumor Stroma and Show Efficacy Against Pancreatic Carcinoma in Mice and Humans

Despite a growing awareness that the herbaceous layer serves a special role in maintaining the structure and function of forests, this stratum remains an underappreciated aspect of forest ecosystems. In this article I review and synthesize information concerning the herb layer's structure, composition, and dynamics to emphasize its role as an integral component of forest ecosystems. Because species diversity is highest in the herb layer among all forest strata, forest biodiversity is largely a function of the herb-layer community. Competitive interactions within the herb layer can determine the initial success of plants occupying higher strata, including the regeneration of dominant overstory tree species. Furthermore, the herb layer and the overstory can become linked through parallel responses to similar environmental gradients. These relationships between strata vary both spatially and temporally. Because the herb layer responds sensitively to disturbance across broad spatial and temporal scal...

/pdf/the-ecological-significance-of-the-herbaceous-layer-in-2ejcg4fqii.pdf

The Ecological Significance of the Herbaceous Layer in Temperate Forest Ecosystems

The biodiversity-productivity relationship (BPR) is foundational to our understanding of the global extinction crisis and its impacts on ecosystem functioning. Understanding BPR is critical for the accurate valuation and effective conservation of biodiversity. Using ground-sourced data from 777,126 permanent plots, spanning 44 countries and most terrestrial biomes, we reveal a globally consistent positive concave-down BPR, showing that continued biodiversity loss would result in an accelerating decline in forest productivity worldwide. The value of biodiversity in maintaining commercial forest productivity alone-US$166 billion to 490 billion per year according to our estimation-is more than twice what it would cost to implement effective global conservation. This highlights the need for a worldwide reassessment of biodiversity values, forest management strategies, and conservation priorities.

/pdf/positive-biodiversity-productivity-relationship-predominant-1sw0qb4uti.pdf

Positive biodiversity-productivity relationship predominant in global forests

Biogeoclimatic ecosystem classification in British Columbia

Towards a Taxonomic Classification of Humus Forms

Indicator Plants of Coastal British Columbia

We studied growth, crown architecture, and specific leaf area acclimation of a shade-intolerant species, Pinuscontorta Dougl. ex Loud. var. latifolia Engelm., and a moderately shade-tolerant specie...

Effects of light on growth, crown architecture, and specific leaf area for naturally established Pinuscontorta var. latifolia and Pseudotsugamenziesii var. glauca saplings

Karel Klinka

Papers

Biogeoclimatic ecosystem classification in British Columbia

Towards a Taxonomic Classification of Humus Forms

Indicator Plants of Coastal British Columbia

Effects of light on growth, crown architecture, and specific leaf area for naturally established Pinuscontorta var. latifolia and Pseudotsugamenziesii var. glauca saplings

Variation in shade tolerance of Douglas fir, western hemlock, and western red cedar in coastal British Columbia