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Root Function (root + function)
Selected AbstractsBiological and environmental factors controlling root dynamics and function: effects of root ageing and soil moistureAUSTRALIAN JOURNAL OF GRAPE AND WINE RESEARCH, Issue 2010L.H. COMAS Abstract Understanding factors controlling root dynamics and functioning can lead to more efficient and profitable vineyard management. However, our current understanding of root dynamics and their regulation by plant and environmental factors is limited, particularly under field conditions. This paper presents current understanding of grape root dynamics, highlighting studies using minirhizotron cameras, which directly assess root dynamics, and experiments on roots of known age, which link root phenology and function. Data summarised here show timing of grape root production varies widely among different regions, as well as among rootstocks and canopy management systems in the same region. Timing of production can be responsive to differences in soil moisture. Lifespan of grape roots, however, appears less affected by soil moisture because of nocturnal hydraulic redistribution. Root function, such as capacity for P and N uptake, declines rapidly with root age. Differences in timing and spatial distribution of root production can effect above-ground growth and vineyard water-use efficiency. Improving our understanding of when roots grow and are functionally active in agricultural systems can lead to improved water and fertiliser applications, and more precise vineyard management. Because both environmental and biological factors affect root dynamics, simple predictions of timing of root production or standing populations with shoot development are unlikely to be achieved. However, with multi-year data on root dynamics, and environmental and biological factors, regionally specific models of root populations and their functioning may be possible to develop. [source] A multi-trait test of the leaf-height-seed plant strategy scheme with 133 species from a pine forest floraFUNCTIONAL ECOLOGY, Issue 3 2010Daniel C. Laughlin Summary 1.,Westoby's [Plant and Soil (1998), 199, 213] Leaf-Height-Seed (LHS) plant strategy scheme quantifies the strategy of a plant based on its location in a three-dimensional space defined by three functional traits: specific leaf area (SLA), height, and seed mass. This scheme is based on aboveground traits and may neglect strategies of belowground resource capture if root functioning is not mirrored in any of the axes. How then do fine roots fit into the LHS scheme? 2.,We measured 10 functional traits on 133 plant species in a ponderosa pine forest in northern Arizona, USA. This data set was used to evaluate how well the LHS scheme accounts for the variation in above and belowground traits. 3.,The three most important plant strategies were composed of multiple correlated traits, but SLA, seed mass, and height loaded on separate principle components. The first axis reflected the widely observed ,leaf economics spectrum'. Species at the high end of this spectrum had high SLA, high leaf and fine root nitrogen (N) concentration, and low leaf dry matter content. The second axis reflected variation in seed mass and fine root morphology. Plants at the positive end of this spectrum were plants with large seeds and low specific root length (SRL). The third axis reflected variation in height and phenology. Plants at the positive end of this spectrum were tall species that flower late in the growing season. 4.,Leaf N concentration was positively correlated with fine root N concentration. SRL was weakly positively correlated with SLA. SRL was not correlated with fine root N concentration. Leaf litter decomposition rate was positively correlated with the leaf economics spectrum and was negatively correlated with the height and phenology spectrum. 5.,Leaf traits, seed mass, and height appear to be integrating properties of species that reflect much of the variation in plant function, including root function. Fine root N concentration was positively mirrored by the leaf economics spectrum, and SRL was inversely mirrored by seed mass. The leaf and height axes play a role in controlling leaf litter decomposability, indicating that these strategy axes have important consequences for ecosystem functioning. [source] Commentary: Mining for nutrients , regulatory aspects of cluster root function and developmentNEW PHYTOLOGIST, Issue 4 2010Günter Neumann First page of article [source] Evolution of epiphytes in Davalliaceae and related fernsBOTANICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 4 2006CHIE TSUTSUMI The evolution of epiphytes in Davalliaceae was investigated by field observations and molecular phylogenetic analyses. Field studies revealed that in Davalliaceae and related ferns, epiphytes in a broad sense are classified into climber, secondary hemi-epiphyte, and obligate epiphyte, based on combinations of the places (ground vs. tree) of inferred spore germination and sporophyte growth. Some species of Davalliaceae have multiple life forms, i.e. secondary hemi-epiphyte and obligate epiphyte, whereas others are obligate epiphytes. Phylogenetic trees obtained from rbcL and accD gene sequences supported that secondary hemi-epiphytic Oleandra is sister to the epiphytic Davalliaceae and polygrammoid ferns. Analyses of life form evolution based on the phylogenetic relationships suggested that obligate epiphytes of the Davalliaceae and polygrammoid ferns evolved from secondary hemi-epiphytes, or less likely from climbers. We hypothesized a scenario for the evolution of life forms in Davalliaceae and related groups that involves successive changes in rhizome habit, root function, and germination place. Rhizome dorsiventrality and scale morphology, shared by climbers, secondary hemi-epiphytes, and obligate epiphytes examined, may be other innovations for the ferns to have evolved into epiphytes. © 2006 The Linnean Society of London, Botanical Journal of the Linnean Society, 2006, 151, 495,510. [source] Dynamics of heterorhizic root systems: protoxylem groups within the fine-root system of Chamaecyparis obtusaNEW PHYTOLOGIST, Issue 2 2005Takuo Hishi Summary ,,To understand the physiology of fine-root functions in relation to soil organic sources, the heterogeneity of individual root functions within a fine-root system requires investigation. Here the heterogeneous dynamics within fine-root systems are reported. ,,The fine roots of Chamaecyparis obtusa were sampled using a sequential ingrowth core method over 2 yr. After color categorization, roots were classified into protoxylem groups from anatomical observations. ,,The root lengths with diarch and triarch groups fluctuated seasonally, whereas the tetrarch root length increased. The percentage of secondary root mortality to total mortality increased with increasing amounts of protoxylem. The carbon : nitrogen ratio indicated that the decomposability of primary roots might be greater than that of secondary roots. The position of diarch roots was mostly apical, whereas tetrarch roots tended to be distributed in basal positions within the root architecture. ,,We demonstrate the heterogeneous dynamics within a fine-root system of C. obtusa. Fine-root heterogeneity should affect soil C dynamics. This heterogeneity is determined by the branching position within the root architecture. [source] | ||||||||||