Hydraulic and photosynthetic co‐ordination in seasonally dry tropical forest trees

By Tim J. Brodribb, N. Michele Holbrook, M. Gutiérrez. 2002

286 citations recorded by the source corpus.

Subfields: Atmospheric Science, Global and Planetary Change, Nature and Landscape Conservation

View Paper: https://www.semanticscholar.org/paper/c45e0713c87d0d8c3f9540441c8ce14247f23d08

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Citations in the corpus

Evidence for Adaptation to Fire Regimes in the Tropical Savannas of the Brazilian Cerrado (2012, background): “For example, Brodribb et al. (2002) showed that Curatella americana, a dominant species in the Cerrado, was able to maintain stem-specific conductivity at a basically constant level through dry and wet seasons in the Santa Rosa National Park, Costa Rica.”
Leaf hydraulics. (2006, background): “For 34 species of a range of life forms, the leaf, including petiole, contributed on average ≈30% of Rplant (Rplant = 1/Kplant) (99).”
Relations between stomatal closure, leaf turgor and xylem vulnerability in eight tropical dry forest trees (2003, background): “This is especially so when considered in the light of variation in hydraulic strategies that are known to exist even amongst co-occurring species (Kolb & Davis 1994; Jarbeau, Ewers & Davis 1995; Nardini, Lo Gullo & Salleo 1999; Brodribb et al. 2002).”
Hydraulic properties and photosynthetic rates in co-occurring lianas and trees in a seasonal tropical rainforest in southwestern China (2009, background): “Since water supply influences leaf water potential and stomatal conductance, hydraulic conductance is strongly correlated with photosynthetic capacity of plants (Brodribb and Feild 2000; Brodribb et al. 2002).”
Dark and disturbed: a new image of early angiosperm ecology (2004, background): “…(maximum photosynthetic electron transport rate and light-saturation point) was typical of shade-adapted tropical understory plants (Table 1, Appendix 3) (Bilger et al. 1995; Chazdon et al. 1996; Brodribb and Hill 1997; Brodribb and Feild 2000; Brodribb et al. 2002; Franco and Lüttge 2002).”
Leaf phenology is associated with soil water availability and xylem traits in a tropical dry forest (2012, background): “In other dry tropical forests (such as Santa Rosa, Costa Rica, which has a relatively high annual rainfall of 1,500 mm per year), evergreens include species with high-density wood, low hydraulic conductivity and high resistance to embolism and are found on the driest parts of the landscape (Brodribb”
Stomatal Closure during Leaf Dehydration, Correlation with Other Leaf Physiological Traits1 (2003, background): “…www.plantphysiol.org © 2003 American Society of Plant Biologists the leaf, given that leaf minor veins appear more prone to cavitation than stems (Nardini et al., 2001), and that leaves represent a large proportion of the whole plant hydraulic resistance (Nardini, 2001; Brodribb et al., 2002).”
The Ancestral Ecology of Angiosperms: Emerging Perspectives from Extant Basal Lineages (2003, background): “…properties (maximum photosynthetic electron transport rate and light saturation point) most similar to those of shade-adapted tropical understory angiosperms and conifers (table 2; Chazdon et al. 1996; Brodribb and Hill 1997; Brodribb and Feild 2000; Brodribb et al. 2002; Franco and Lüttge 2002).”
The importance of wood traits and hydraulic conductance for the performance and life history strategies of 42 rainforest tree species. (2010, background): “It has been frequently demonstrated that hydraulics affect photosynthetic carbon gain (Brodribb & Field, 2000; Brodribb et al., 2002; Santiago et al., 2004).”
Changes in leaf hydraulic conductance during leaf shedding in seasonally dry tropical forest (2003, background): “While leaf shedding in some seasonally dry forest species is associated with xylem cavitation, in others stem conductivity remains high during leaf shedding (Brodribb et al., 2002a).”
Time-dependent effects of climate and drought on tree growth in a Neotropical dry forest: Short-term tolerance vs. long-term sensitivity (2014, background): “…and Zeyheria, species 325 showing the highest growth sensitivity to precipitation, can exhibit hydraulic patterns similar to 326 those reported by Brodribb et al. (2002) for the first deciduous tree species, whereas the least 327 sensitive species (Caesalpinia) could behave similarly to the…”
Hydraulic architecture of deciduous and evergreen dry rainforest tree species from north-eastern Australia (2005, background): “Borchert 1994a, b; Brodribb et al. 2002, 2003 ), and the situation is likely to be similar in Australian forests.”