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Effects of salinity and drought on physiology and chlorophyll fluorescence were used to evaluate stress in two coastal plants, Myrica cerifera (L.) and Phragmites australis (Cav.) Trin. ex Steud. Drought and salinity stress were induced and measurements of stomatal conductance, photosynthesis, xylem pressure potential (psi) and fluorescence were conducted following treatment. The onset of stress began at 2 g l(-1) for M. cerifera, and 5 g l(-1) for P. australis, as seen by significant decreases in physiological measurements. Despite the physiological effects of salinity, there was no significant difference in dark-adapted fluorescence (F(v)/F(m), where F(m) is the maximal fluorescence in dark-adapted leaves) for either species at any salinity level. Significant decreases in the light-adapted measurement Delta F/F'(m) (F'(m) is maximal fluorescence in light-adapted leaves) occurred at 10 g l(-1) in M. cerifera and P. australis, days before visible stress was evident. The quantum yield of xanthophyll-regulated thermal energy dissipation (Phi(NPQ), where NPQ is non-photochemical quenching of chlorophyll fluorescence) increased with decreasing Delta F/F'(m). Drought studies showed similar results, with significant decreases in physiological measurements occurring by day 2 in M. cerifera and day 4 in P. australis. Differences in Delta F/F'(m) were seen by day 5 for both species, whereas F(v)/F(m) showed no indication of stress, despite apparent visible signs. Xanthophyll-cycle-dependent energy dissipation may be the underlying mechanism in protecting photosystem II from excess energy in salinity- and drought-treated plants.

Photosynthesis, chlorophyll fluorescence, and hyperspectral reflectance were used to evaluate diurnal changes of Elaeagnus umbellata to quantify physiological responses of the invasive species during times of stress. Field measurements showed that E. umbellata is able to maintain higher levels of photosynthesis relative to nearby Quercus alba plants, with less water loss. Plants subjected to progressive drought were able to recover photosynthesis one day following re-watering. Laboratory and field measurements revealed decreasing DF/F 0 m values in response to drought stress, with little corresponding decrease in photochemical reflectance index values. This research supports the view that xanthophyll cycle dissipation is not the photoprotective mechanism at work for Elaeagnus species under water stress. Elaeagnus umbellata maintains photosynthetic carbon assimilation even under drought conditions, in part, due to chemical dissipation of excess light, and in part because of morphological features that limit excess radiation while maximizing photosynthetic carbon gain. These characteristics may contribute to the invasive success of E. umbellata.

Chlorophyll fluorescence and landscapelevel reflectance imagery were used to evaluate spatial variations in stress in Myrica cerifera and Iva frutescens during a severe drought and compared to an extremely wet year. Measurements of relative water content and the water band index (WBI 970 ) indicated that the water stress did not vary across the island. In contrast, there were significant differences in tissue chlorides across sites for both species. Using the physiological reflectance index (PRI), we were able to detect salinity stress across the landscape. For M. cerifera, PRI did not differ between wet and dry years, while for I. frutescens, there were differences in PRI during the 2 years, possibly related to flooding during the wet year. There was a positive relationship between PRI and DF=F 0 m for M. cerifera (r 2 = 0.79) and I. frutescens (r 2 = 0.72). The normalized difference vegetation index (NDVI), the chlorophyll index (CI), and WBI 970 were higher during the wet summer for M. cerifera, but varied little across the island. CI and WBI 970 were higher during 2004 for I. frutescens, while there were no differences in NDVI during the 2 years. PRI was not significantly related to NDVI, suggesting that the indices are spatially independent. These results suggest that PRI may be used for early identification of salt stress that may lead to changes in plant distributions at the landscape level, as a result of rising sea level. Comparsions between the two species indicate that variations in PRI and other indices may be species specific.

No abstract

Our study was aimed at understanding physiological responses to trinitrotoluene (TNT) soil contamination, and using optical methods to detect TNT-induced stress in a woody plant prior to visible changes. Myrica cerifera plants were potted in soil concentrations of TNT ranging from 30-500 mg kg −1 . Physiological measurements were significantly affected by TNT exposure at all treatment levels, and photosynthetic decline likely resulted from metabolic impairment rather than stomatal closure as the experiment progressed. Several reflectance indices were able to detect TNT-induced stress before any changes in chlorophyll concentrations occurred. The most sensitive index was the simple ratio R 761 /R 757 which is linked to fluorescence in-filling of the 0 2 atmospheric absorption. Changes at R 740 /R 850 and R 735 /R 850 may be attributed to both fluorescence and structural characteristics of leaf anatomy in the near infrared region. This could have been influenced by transformation and conjugation of TNT metabolites with other compounds. chlorophyll index (CHL) or in the water band index (WBI 970 ), which are indices typically associated with drought stress, and may provide a means of separating stress due to explosives. Further studies need to be conducted with a combination of stressors (TNT and natural) to determine if responses are in fact generalized or if any of these changes are separable from natural stress. AbbreviationsTNT Trinitrotoluene PPFD photosynthetic photon flux density g wv stomatal conductance A Net net photosynthetic rate F o minimal fluorescence in dark-adapted leaves F m maximal fluorescence in dark-adapted leaves F v /F m maximum quantum use efficiency of PSII in the dark-adapted state F′ o minimal fluorescence in light-adapted leaves F′ m maximal fluorescence in light-adapted leaves F s steady-state fluorescence ΔF/F′ m, fraction of absorbed photons that are used for photochemistry in a light-adapted leaf F′ v /F′ m effective quantum use efficiency of PSII in the light-adapted state PSII photosystem II WBI water band index Plant Soil (

No abstract

TNT is released into the soil from many different sources, especially from military and mining activities, including buried land mines. Vegetation may absorb explosive residuals, causing stress and by understanding how plants respond to energetic compounds, we may be able to develop non-invasive techniques to detect soil contamination. The objectives of our study were to examine the physiological response of plants grown in TNT contaminated soils and to use remote sensing methods to detect uptake in plant leaves and canopies in both laboratory and field studies. Differences in physiology and light-adapted fluorescence were apparent in laboratory plants grown in N enriched soils and when compared with plants grown in TNT contaminated soils. Several reflectance indices were able to detect TNT contamination prior to visible signs of stress, including the fluorescence-derived indices, R 740 /R 850 and R 735 /R 850 , which may be attributed to transformation and conjugation of TNT metabolites with other compounds. Field studies at the Duck, NC Field Research Facility revealed differences in physiological stress measures, and leaf and canopy reflectance when plants growing over suspected buried UXOs were compared with reference plants. Multiple reflectance indices indicated stress at the suspected contaminated sites, including R 740 /R 850 and R 735 /R 850 . Under natural conditions of constant leaching of TNT into the soil, TNT uptake would be continuous in plants, potentially creating a distinct signature from remotely sensed vegetation. We may be able to use remote sensing of plant canopies to detect TNT soil contamination prior to visible signs.