scholarly journals Intsia bijuga Is Moderately Tolerant of Flooding

HortScience ◽  
1996 ◽  
Vol 31 (4) ◽  
pp. 649c-649
Author(s):  
Thomas E. Marler ◽  
Louann C. Guzman

Growth and physiological responses of Intsia bijuga trees to flooding were determined in a series of five container experiments to assess the relative tolerance of this species to flooding. The first measurable response to flooding was reduced leaf gas exchange, which began within 5 to 6 days of the onset of flooding. Development of hypertrophied lenticels at the water line and paraheliotropic leaflet movement were evident by 17 days of flooding. Emergence of adventitious roots on the stem above the water line began after about 30 days of flooding. Leaflet abscission was greatly accelerated by flooding. After more than 3 months of flooding, regrowth of roots, stems, and leaves began within two weeks of draining the medium. The data and observations support a relative ranking of moderate flood tolerance for Intsia bijuga.

2010 ◽  
Vol 28 (3) ◽  
pp. 159-165
Author(s):  
Cliff G. Martin ◽  
Bruce Schaffer ◽  
Catharine Mannion

Abstract In south Florida nurseries, trees are often grown in marl soil, which is heavy, clay-like, calcareous soil that is slow to drain and prone to periodic flooding during the rainy season. Green buttonwood, mahogany, pond apple and Surinam cherry are grown in this soil. We tested effects of flooding on leaf gas exchange and growth of these four species to determine their flood tolerances in marl soil. Green buttonwood, mahogany, and Surinam cherry each had consistently lower leaf gas exchange and plant growth in flooded than in non-flooded marl soil, which suggests low tolerance to flooding. In contrast, flooding had little or no effect on leaf gas exchange and growth of pond apple, indicating that this species was tolerant of flooding in marl soil. Green buttonwood and pond apple had larger stem diameters and more hypertrophic stem lenticels when flooded than when not flooded. Flooded green buttonwood also developed adventitious roots. Pond apple appears to be a good choice for planting in low-lying areas in marl soil typical of outdoor nurseries in south Florida. In contrast, care should be taken to avoid planting green buttonwood, mahogany, and Surinam cherry in marl soil in flood-prone areas.


2021 ◽  
Author(s):  
Angelika Kübert ◽  
Kathrin Kühnhammer ◽  
Ines Bamberger ◽  
Erik Daber ◽  
Jason De Leeuw ◽  
...  

<p>Increasing drought in the tropics is a major threat to rainforests and can strongly harm plant communities. Understanding species-specific water use strategies to drought and the subsequent recovery is therefore important for estimating the risk to tropical rainforest ecosystems of drought. Conducting a large-scale long-term drought experiment in a model rainforest ecosystem (Biosphere 2 WALD project), we evaluated the role of plant physiological responses, above and below ground, in response to drought and subsequent recovery in five species (3 canopy species, 2 understory species). The model rainforest was exposed to a 9.5-week lasting drought. Severe drought was ended with a deep water pulse strongly enriched in <sup>2</sup>H, which allowed us to distinguish between deep and shallow rooting plants, and subsequent rain (natural abundance range of <sup>2</sup>H). We assessed plant physiological responses by leaf water potential, sap flow and high resolution monitoring of leaf gas exchange (concentrations and stable isotopes of H<sub>2</sub>O and CO<sub>2</sub>). Thereby, we could derive plant water uptake and leaf water use efficiency (WUE<sub>leaf</sub>) in high temporal resolution, revealing short-term and long-term responses of plant individuals to drought and rewetting. The observed water use strategies of species and plants differed widely. No uniform response in assimilation (A) and transpiration (T) to drought was found for species, resulting in decreasing, relatively constant, or increasing WUE<sub>leaf</sub> across plant individuals. While WUE<sub>leaf</sub> of some plant individuals strongly decreased due to a breakdown in A, others maintained relatively high T and A and thus constant WUE<sub>leaf, </sub>or increased WUE<sub>leaf</sub> by decreasing T while keeping A relatively high. We expect that the observed plant-specific responses in A, T and WUE<sub>leaf</sub> were strongly related to the plant individuals' access to soil water. We assume that plant individuals with constant WUE<sub>leaf</sub> could maintain their leaf gas exchange due to access to water of deeper soil layers, while plants with increasing/decreasing WUE<sub>leaf</sub> mainly depended on shallow soil water and only had limited or no access to deep soil water. We conclude that the observed physiological responses to drought were not only determined by species-specific water use strategies but also by the diverse strategies within species, mainly depending on the plant individuals' size and place of location. Our results highlight the plasticity of water use strategies beyond species-specific strategies and emphasize its importance for species’ survival in face of climate change and increasing drought.</p>


HortScience ◽  
1995 ◽  
Vol 30 (4) ◽  
pp. 780E-780
Author(s):  
Thomas E. Marler

A container study and a hydroponics study were conducted to determine gas-exchange and ion content of `Cariflora' papaya plants as influenced by a combination of salinity and flooding. Plants grown in nutrient solution were subjected to 1 or 8 dS·m–1 as salinity treatments and 6.54, 3.62, or 0.92 mg oxygen/liter as the flooding treatments. Plants in the container study were subjected to 0, 4, or 8 dS·m–1 as salinity treatments, and half of the plants in each salinity level were flooded. Leaf gas-exchange began to decline by day 1 in all plants receiving flooding, and was zero by day 5. In contrast, gas-exchange of plants experiencing salinity began a slow decline after 5 to 7 days. Stomatal conductance of salinized plants was 25% to 33% of the control plants in the container study after 39 days. No interaction occurred between flooding and salinity treatments since the stomatal response to flooding was so rapid across all levels of salinity. Roots and stems played a major role in storing Na+ and Cl– in salinized plants. For example, stems contained more than two times the dry weight concentration of both ions as did leaves. Older leaves accumulated more Na+ and Cl– than did younger leaves. Flooding decreased Na+ and Cl– accumulation in roots, stems, and leaves in all salinized plants.


HortScience ◽  
1996 ◽  
Vol 31 (4) ◽  
pp. 685e-685
Author(s):  
Thomas E. Marler ◽  
Yasmina Zozor

Whole plant growth, foliage mineral content, and leaf gas exchange were measured on Mammea americana seedlings exposed to salinity ranging from 0 to 8 dS·m–1 to determine relative tolerance of this species. In one study, growth measured as leaf area, trunk cross-sectional area, and total dry mass was reduced by 23 weeks of exposure to salinity. Growth of plants exposed to 8 dS·m–1 was ≈30% below that of control plants. Leaf gas exchange was reduced by salinity to a greater degree than the growth variables. Stomatal conductance of plants exposed to 8 dS·m–1 was ≈70% below that of control plants. Plants exposed to 8 dS·m–1 exhibited a seven-fold increase in leaf chloride and 13-fold increase in leaf sodium compared to the control plants. In a second study, 8 weeks of exposure to 8 dS·m–1 reduced net CO2 assimilation and apparent quantum yield to ≈50% of the values for the control plants. Dark respiration was not influenced by salinity. The results indicate that Mammea americana is moderately sensitive to salinity stress.


HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 540a-540
Author(s):  
K.J. Prevete ◽  
R.T. Fernandez

Three species of herbaceous perennials were tested on their ability to withstand and recover from drought stress periods of 2, 4, and 6 days. Eupatorium rugosum and Boltonia asteroides `Snowbank' were chosen because of their reported drought intolerance, while Rudbeckia triloba was chosen based on its reported drought tolerance. Drought stress began on 19 Sept. 1997. Plants were transplanted into the field the day following the end of each stress period. The effects of drought on transpiration rate, stomatal conductance, and net photosynthetic rate were measured during the stress and throughout recovery using an infrared gas analysis system. Leaf gas exchange measurements were taken through recovery until there were no differences between the stressed plants and the control plants. Transpiration, stomatal conductance, and photosynthesis of Rudbeckia and Boltonia were not affected until 4 days after the start of stress. Transpiration of Eupatorium decreased after 3 days of stress. After rewatering, leaf gas exchange of Boltonia and Rudbeckia returned to non-stressed levels quicker than Eupatorium. Growth measurements were taken every other day during stress, and then weekly following transplanting. Measurements were taken until a killing frost that occurred on 3 Nov. There were no differences in the growth between the stressed and non-stressed plants in any of the species. Plants will be monitored throughout the winter, spring, and summer to determine the effects of drought on overwintering capability and regrowth.


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