The current knowledge of the physiological ecology of vascular epiphytes is reviewed here with an emphasis on the most recent literature. It is argued that by far the most relevant abiotic constraint for growth and vegetative function of vascular epiphytes is water shortage, while other factors such as nutrient availability or irradiation, are generally of inferior importance. However, it is shown that the present understanding of epiphyte biology is still highly biased, both taxonomically and ecologically, and it is concluded that any generalizations are still preliminary. Future studies should include a much wider range of taxa and growing sites within the canopy to reach a better understanding how abiotic factors are limiting epiphyte growth and survival which, in turn, should affect epiphyte community composition. Finally, a more integrative approach to epiphyte biology is encouraged: physiological investigations should be balanced by studies of other possible constraints, for example, substrate instability, dispersal limitation, competition or herbivory.
Human societies depend on an Earth System that operates within a constrained range of nutrient 68 availability, yet the recent trajectory of terrestrial nitrogen (N) availability is uncertain. 69 Examining patterns of foliar N concentrations ([N]) and isotope ratios (δ 15 N) from more than 42,000 samples acquired over years, here we show that foliar [N] declined by 8% and foliar δ 15 N declined by 0.8 -1.9 ‰. Examining patterns across different climate spaces, foliar δ 15 N declined across the entire range of MAT and MAP tested. These results suggest declines in N supply relative to plant demand at the global scale. In all, there are now multiple lines of evidence of declining N availability in many unfertilized terrestrial ecosystems, including declines in δ 15 N of tree rings and leaves from herbarium samples over the past 75-150 years. 76These patterns are consistent with the proposed consequences of elevated atmospheric CO 2 and longer growing seasons. These declines will limit future terrestrial C uptake and increase nutritional stress for herbivores. 235 much. Preventing these declines in N availability further emphasizes the need to reduce 236 anthropogenic CO 2 emissions.Data and code availability. The datasets generated during and/or analysed during the current study are available in the Dryad repository [link to be generated upon acceptance]. All code used for statistical analyses and figure generation are available on Dryad (XXX).
Vascular epiphytes were studied in forests at altitudes from 720 to 2370 m on the Atlantic slope of central Veracruz, Mexico. The biomass of all trees of each species > 10 cm diameter at breast height within plots between 625 and 1500 m 2 was estimated. The number of species per plot ranged between 22 and 53, and biomass between 9 and 249 g dry weight/m 2 . The highest values, both of species and biomass, were found at an intermediate altitude (1430 m). Habitat diversity may contribute to epiphyte diversity in humid forests, but the importance of this effect could not be distinguished from the influence of climate. A remarkably high number of bromeliads and orchids grew in relatively dry forests at low altitudes. In wet upper montane forests, bromeliads were replaced by ferns, while orchids were numerous at all sites, except for a pine forest. The number of epiphytic species and their biomass on a tree of a given site were closely related to tree size. According to Canonical Correspondence Analysis, the factor determining the composition of the epiphytic vegetation of a tree was altitude and to some extent tree size, whereas tree species had practically no influence. The only trees which had an evidently negative effect on epiphytes were pines, which were particularly hostile to orchids and to a lesser degree to ferns, and Bursera simaruba, which generally had few epiphytes due to its smooth and defoliating bark.
Resilient secondary tropical forests? Although deforestation is rampant across the tropics, forest has a strong capacity to regrow on abandoned lands. These “secondary” forests may increasingly play important roles in biodiversity conservation, climate change mitigation, and landscape restoration. Poorter et al . analyzed the patterns of recovery in forest attributes (related to soil, plant functioning, structure, and diversity) in 77 secondary forest sites in the Americas and West Africa. They found that different attributes recovered at different rates, with soil recovering in less than a decade and species diversity and biomass recovering in little more than a century. The authors discuss how these findings can be applied in efforts to promote forest restoration. —AMS
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