A standardized protocol for the determination of specific leaf area and leaf dry matter content

Summary 1 The impact of sample preparation, rehydration procedure and time of collection on the determination of specific leaf area (SLA, the ratio of leaf area to leaf dry mass) and leaf dry matter content (LDMC, the ratio of leaf dry mass to fresh mass) of mature leaves was studied in three wild species growing in the field, chosen for their contrasting SLA and LDMC. 2 Complete rehydration was achieved 6 h after samples were placed into water, but neither of the procedures tested – preparation of samples before rehydration or temperature applied during rehydration – had a significant effect on the final values of SLA or LDMC. 3 As expected, water-saturated leaves had a lower LDMC than non-rehydrated leaves; more surprisingly, their SLA was also higher. The impact of rehydration on SLA was especially important when the SLA of the species was high. 4 There was no significant effect of time of sampling on either trait in any species over the time period covered (09·00–16·30 h). 5 These results suggest that SLA and LDMC obtained on water-saturated leaves (SLASAT and LDMCSAT) can be used for species comparisons. We propose a standardized protocol for the measurement of these traits. This would allow for better consistency in data collection, a prerequisite for the constitution of large databases of functional traits.

[1]  Eric Garnier,et al.  Consistency of species ranking based on functional leaf traits. , 2001, The New phytologist.

[2]  B. Shipley Plasticity in relative growth rate and its components following a change in irradiance , 2000 .

[3]  Mark Westoby,et al.  EVOLUTIONARY DIVERGENCES IN LEAF STRUCTURE AND CHEMISTRY, COMPARING RAINFALL AND SOIL NUTRIENT GRADIENTS , 1999 .

[4]  M. Roderick,et al.  Challenging Theophrastus: A common core list of plant traits for functional ecology , 1999 .

[5]  Ülo Niinemets,et al.  Research review. Components of leaf dry mass per area – thickness and density – alter leaf photosynthetic capacity in reverse directions in woody plants , 1999 .

[6]  P. Reich,et al.  Generality of leaf trait relationships: a test across six biomes: Ecology , 1999 .

[7]  K. Thompson,et al.  Specific leaf area and leaf dry matter content as alternative predictors of plant strategies , 1999 .

[8]  N. Bertin,et al.  Contribution of carbohydrate pools to the variations in leaf mass per area within a tomato plant , 1999 .

[9]  I. Noble,et al.  The relationship between leaf composition and morphology at elevated CO2 concentrations , 1999 .

[10]  François Tardieu,et al.  Modelling leaf expansion in a fluctuating environment: are changes in specific leaf area a consequence of changes in expansion rate? , 1999 .

[11]  Hendrik Poorter,et al.  A comparison of specific leaf area, chemical composition and leaf construction costs of field plants from 15 habitats differing in productivity , 1999 .

[12]  Bill Shipley,et al.  Interacting determinants of specific leaf area in 22 herbaceous species: effects of irradiance and nutrient availability , 1999 .

[13]  N. Bertin,et al.  Short and Long Term Fluctuations of the Leaf Mass Per Area of Tomato Plants—Implications for Growth Models , 1998 .

[14]  S. Lavorel,et al.  Plant functional classifications: from general groups to specific groups based on response to disturbance. , 1997, Trends in ecology & evolution.

[15]  J. Guehl,et al.  Concentration and σ13C of leaf carbohydrates in relation to gas exchange in Quercus robur under elevated CO2 and drought , 1997 .

[16]  Ü. Niinemets Role of foliar nitrogen in light harvesting and shade tolerance of four temperate deciduous woody species , 1997 .

[17]  E. Garnier,et al.  Specific leaf area and leaf nitrogen concentration in annual and perennial grass species growing in Mediterranean old-fields , 1997, Oecologia.

[18]  Bill Shipley,et al.  Structured interspecific determinants of specific leaf area in 34 species of herbaceous angiosperms , 1995 .

[19]  H. Medrano,et al.  Effect of Water Stress on Photosynthesis, Leaf Characteristics and Productivity of Field-Grown Nicotiana tabacum L. Genotypes Selected for Survival at Low CO2 , 1992 .

[20]  D. Krieg,et al.  Osmotic Adjustment in Sorghum: II. Relationship to Gas Exchange Rates. , 1992, Plant physiology.

[21]  D. Krieg,et al.  Osmotic adjustment in sorghum: I. Mechanisms of diurnal osmotic potential changes. , 1992, Plant physiology.

[22]  P. Reich,et al.  Leaf Life‐Span in Relation to Leaf, Plant, and Stand Characteristics among Diverse Ecosystems , 1992 .

[23]  P. Keddy A pragmatic approach to functional ecology , 1992 .

[24]  S. O. Link,et al.  Rehydration‐induced changes in pressure‐volume relationships of Artemisia tridentata Nutt. ssp. tridentata , 1990 .

[25]  M. Abrams,et al.  Leaf structural characteristics of 31 hardwood and conifer tree species in central Wisconsin: influence of light regime and shade-tolerance rank. , 1990 .

[26]  A. Tyree,et al.  Vulnerability of Xylem to Cavitation and Embolism , 1989 .

[27]  T. W. Jurik,et al.  Temporal and spatial patterns of specific leaf weight in successional northern hardwood tree species , 1986 .

[28]  J. M. Cutler,et al.  The Importance of Cell Size in the Water Relations of Plants , 1977 .

[29]  Diurnal Change in Specific Leaf Weight of Medicago sativa L. and Zea mays L. 1 , 1972 .

[30]  J. Ritchie,et al.  Influence of soil water stress on evaporation, root absorption, and internal water status of cotton. , 1971, Plant physiology.

[31]  C. Stewart,et al.  Effect of Wilting on Carbohydrates during Incubation of Excised Bean Leaves in the Dark. , 1971, Plant physiology.

[32]  T. T. Kozlowski,et al.  Determination of water deficits in plant tissues. , 1968 .

[33]  B. D. Millar Relative Turgidity of Leaves: Temperature Effects in Measurement , 1966, Science.

[34]  H. Barrs,et al.  A Re-Examination of the Relative Turgidity Technique for Estimating Water Deficits in Leaves , 1962 .