505I.506II.506III.508IV.512V.513VI.514515References515 Summary Fine roots acquire essential soil resources and mediate biogeochemical cycling in terrestrial ecosystems. Estimates of carbon and nutrient allocation to build and maintain these structures remain uncertain because of the challenges of consistently measuring and interpreting fine‐root systems. Traditionally, fine roots have been defined as all roots ≤ 2 mm in diameter, yet it is now recognized that this approach fails to capture the diversity of form and function observed among fine‐root orders. Here, we demonstrate how order‐based and functional classification frameworks improve our understanding of dynamic root processes in ecosystems dominated by perennial plants. In these frameworks, fine roots are either separated into individual root orders or functionally defined into a shorter‐lived absorptive pool and a longer‐lived transport fine‐root pool. Using these frameworks, we estimate that fine‐root production and turnover represent 22% of terrestrial net primary production globally – a c. 30% reduction from previous estimates assuming a single fine‐root pool. Future work developing tools to rapidly differentiate functional fine‐root classes, explicit incorporation of mycorrhizal fungi into fine‐root studies, and wider adoption of a two‐pool approach to model fine roots provide opportunities to better understand below‐ground processes in the terrestrial biosphere.

No abstract

Plant roots have greatly diversified in form and function since the emergence of the first land plants, but the global organization of functional traits in roots remains poorly understood. Here we analyse a global dataset of 10 functionally important root traits in metabolically active first-order roots, collected from 369 species distributed across the natural plant communities of 7 biomes. Our results identify a high degree of organization of root traits across species and biomes, and reveal a pattern that differs from expectations based on previous studies of leaf traits. Root diameter exerts the strongest influence on root trait variation across plant species, growth forms and biomes. Our analysis suggests that plants have evolved thinner roots since they first emerged in land ecosystems, which has enabled them to markedly improve their efficiency of soil exploration per unit of carbon invested and to reduce their dependence on symbiotic mycorrhizal fungi. We also found that diversity in root morphological traits is greatest in the tropics, where plant diversity is highest and many ancestral phylogenetic groups are preserved. Diversity in root morphology declines sharply across the sequence of tropical, temperate and desert biomes, presumably owing to changes in resource supply caused by seasonally inhospitable abiotic conditions. Our results suggest that root traits have evolved along a spectrum bounded by two contrasting strategies of root life: an ancestral 'conservative' strategy in which plants with thick roots depend on symbiosis with mycorrhizal fungi for soil resources and a more-derived 'opportunistic' strategy in which thin roots enable plants to more efficiently leverage photosynthetic carbon for soil exploration. These findings imply that innovations of belowground traits have had an important role in preparing plants to colonize new habitats, and in generating biodiversity within and across biomes.

Root turnover is important to the global carbon budget as well as to nutrient cycling in ecosystems and to the success of individual plants. Our ability to predict the effects of environmental change on root turnover is limited by the difficulty of measuring root dynamics, but emerging evidence suggests that roots, like leaves, possess suites of interrelated traits that are linked to their life span. In graminoids, high tissue density has been linked to increased root longevity. Other studies have found root longevity to be positively correlated with mycorrhizal colonization and negatively correlated with nitrogen concentration, root maintenance respiration and specific root length. Among fruit trees, apple roots (which are of relatively small diameter, low tissue density and have little lignification of the exodermis) have much shorter life spans than the roots of citrus, which have opposite traits. Likewise, within the branched network of the fine root system, the finest roots with no daughter roots tend to have higher N concentrations, faster maintenance respiration, higher specific root length and shorter life spans than secondary and tertiary roots that bear daughter roots. Mycorrhizal colonization can enhance root longevity by diverse mechanisms, including enhanced tolerance of drying soil and enhanced defence against root pathogens. Many variables involved in building roots might affect root longevity, including root diameter, tissue density, N concentration, mycorrhizal fungal colonization and accumulation of secondary phenolic compounds. These root traits are highly plastic and are strongly affected by resource supply (CO # , N, P and water). Therefore the response of root longevity to altered resource availability associated with climate change can be estimated by considering how changes in resource availability affect root construction and physiology. A cost-benefit approach to predicting root longevity assumes that a plant maintains a root only until the efficiency of resource acquisition is maximized. Using an efficiency model, we show that reduced tissue N concentration and reduced root maintenance respiration, both of which are predicted to result from elevated CO # , should lead to slightly longer root life spans. Complex interactions with soil biota and shifts in plant defences against root herbivory and parasitism, which are not included in the present efficiency model, might alter the effects of future climate change on root longevity in unpredicted ways.

Global data sets provide strong evidence of convergence for leaf structure with leaf longevity such that species having thick leaves, low specific leaf area, low mass-based nitrogen concentrations, and low photosynthetic rates typically exhibit long leaf life span. Leaf longevity and corresponding leaf structure have also been widely linked to plant potential growth rate, plant competition, and nutrient cycling. We hypothesized that selection forces leading to variation in leaf longevity and leaf structure have acted simultaneously and in similar directions on the longevity and structure of the finest root orders. Our four-year study investigated the links between root and leaf life span and root and leaf structure among 11 north-temperate tree species in a common garden in central Poland. Study species included the hardwoods Acer pseudoplatanus L., Acer platanoides L., Fagus sylvatica L., Quercus robur L., and Tilia cordata Mill.; and the conifers Abies alba Mill., Larix decidua Mill., Picea abies (L.) Karst., Pinus nigra Arnold, Pinus sylvestris L., and Pseudotsuga menziesii (Mirbel) Franco. Leaf life span, estimated by phenological observations and needle cohort measurements, ranged from 0.5 to 8 yr among species. Median fine-root life span, estimated using minirhizotron images of individual roots, ranged from 0.5 to 2.5 yr among species. Root life span was not correlated with leaf life span, but specific root length was significantly correlated with specific leaf area. Root nitrogen : carbon ratio was negatively correlated with root longevity, which corroborates previous research that has suggested a trade-off between organ life span and higher organ N concentrations. Specific traits such as thickened outer tangential walls of the exodermis were better predictors of long-lived roots than tissue density or specific root length, which have been correlated with life span in previous studies. Although theories linking organ structure and function suggest that similar root and leaf traits should be linked to life span and that root and leaf life span should be positively correlated, our results suggest that tissue structure and longevity aboveground (leaves) can contrast markedly with that belowground (roots).