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Data include sample replication (N) and flood-ring frequencies (F1, F2) derived from black ash (Fraxinus nigra Marsh.) trees growing in the floodplain of the Driftwood River in northwestern Ontario reported in "Flood ring production modulated by river regulation in eastern boreal Canada" published in "Frontiers in Plant Science - Quantitative Wood Anatomy to Explore Tree Responses to Global Change" by Nolin et al. in 2021c. DriftwoodFR.csv, as in Fig. 4, F1 and F2 flood-rings chronologies per sites and distance class with sample replication (N) to reproduce the flood-ring frequencies. Harricana River F1 and F2 flood ring chronologies from Nolin et al., 2021b are also provided. DriftwoodRW.csv, as in Fig. 5, the mean site chronologies of total ring width with sample replication (N). LAT_LON_Driftwood.kml, the coordinate data for each F. nigra stand sampled on the Driftwood River, including Monteith dam location, in Google Earth format (.kml) meatadatas.txt, a set of self-explanatory instructions and descriptions for data files. All other data are available upon request to the corresponding author at alexandreflorent.nolin@uqat.ca (institutional email), alexandreflorent.nolin@gmail.com (permanent email).
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In recent years, the utility of earlywood vessels anatomical characteristics in identifying and reconstructing hydrological conditions has been fully recognized. In riparian ring-porous species, flood rings have been used to identify discrete flood events, and chronologies developed from cross-sectional lumen areas of earlywood vessels have been used to successfully reconstruct seasonal discharge. In contrast, the utility of the earlywood vessel chronologies in non-riparian habitats has been less compelling. No studies have contrasted within species their earlywood vessel anatomical characteristics, specifically from trees that are inversely exposed to flooding. In this study, earlywood vessel and ring-width chronologies were compared between flooded and non-flooded control Fraxinus nigra trees. The association between chronologies and hydroclimate variables was also assessed. Fraxinus nigra trees from both settings shared similar mean tree-ring width but floodplain trees did produce, on average, thicker earlywood. Vessel chronologies from the floodplain trees generally recorded higher mean sensitivity (standard deviation) and lower autocorrelation than corresponding control chronologies indicating higher year-to-year variations. Principal components analysis (PCA) revealed that control and floodplain chronologies shared little variance indicating habitat-specific signals. At the habitat level, the PCA indicated that vessel characteristics were strongly associated with tree-ring width descriptors in control trees whereas, in floodplain trees, they were decoupled from the width. The most striking difference found between flood exposures related to the chronologies' associations with hydroclimatic variables. Floodplain vessel chronologies were strongly associated with climate variables modulating spring-flood conditions as well as with spring discharge whereas control ones showed weaker and few consistent correlations. Our results illustrated how spring flood conditions modulate earlywood vessel plasticity. In floodplain F. nigra trees, the use of earlywood vessel characteristics could potentially be extended to assess and/or mitigate anthropogenic modifications of hydrological regimes. In absence of major recurring environmental stressors like spring flooding, our results support the idea that the production of continuous earlywood vessel chronologies may be of limited utility in dendroclimatology.
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Data include tree-ring widths and wood anatomical chronologies of Pinus banksiana and Fraxinus nigra trees growing in eastern boreal Canada, as well as the reconstructed spring mean temperature, reported in "A 247-years tree-ring reconstruction of spring temperature and relation to spring flooding in eastern boreal Canada" published in "International journal of Climatology" by Nolin et al., 2021. PIBA_FRNI_Chronos.csv, the tree-ring widths and wood anatomical chronologies (1706-2017) used in this study (species and sites are coded as in Table 1); PIBA_FRNI_SampDepth.csv, the annual replication of samples used to produce each chronologies (1706-2017); PIBA_FRNI_RecSpringTemp.csv, the reconstructed mean spring temperature (1770 to 2016) LAT_LON_SpringTemp.kml, the coordinate data for each sampling site: metadatas.txt, a set of self-explanatory instructions and descriptions for data files. All other data are available upon request to the corresponding author at alexandreflorent.nolin@uqat.ca (institutional email), alexandreflorent.nolin@gmail.com (permanent email).