The Carbon Isotope Composition of Epiphytes Depends Not Only on Their Layers, Life Forms, and Taxonomical Groups but Also on the Carbon and Nitrogen Indicators of Host Trees.

The carbon isotopic composition of plant tissues is a diagnostic feature of a number of physiological and ecological processes. The most important of which is the type of photosynthesis. In epiphytes, two peaks of δ13C values are known to correspond to C3 and CAM photosynthesis and some variants of transitional forms between them. But the diagnosis of δ13C may not be limited to the type of photosynthesis. This makes it necessary to study trends in the distribution of δ13C in a broader ecological context. In this study, we present trends in the distribution of δ13C epiphytes and other structurally dependent plants and their relationship with other isotopic and elemental parameters (δ15N, C%, N%, and C/N) and with life forms of epiphytes, taxonomic or vertical groups in crowns (synusia), and the parameters of the trees themselves. In all communities except for the moss forest, δ13C in epiphyte leaves was significantly higher (less negative) than in phorophyte leaves. In general, δ13C in epiphytes in mountain communities (pine forest and moss forest) was more negative than in other communities due to the absence of succulents with CAM. δ13C in the leaves of all epiphytes was negatively related to the percentage of carbon and δ15N in the leaves of the phorophyte. When considering the Gaussian distributions of δ13C with the method of modeling mixtures, we observe the unimodal, bimodal, and trimodal nature of the distribution.

Orchid epiphytes do not receive organic substances from living trees through fungi.

Numerous studies of terrestrial orchids have demonstrated widespread partial mycoheterotrophy, particularly the possibility of obtaining organic matter from surrounding trees through a common fungal network. Fungi are also widespread in epiphytic orchid roots, but there have been no attempts to determine if epiphytes accept organic matter from the living stems of their phorophytes. We hypothesise that such transfer does not exist because epiphytes and phorophytes harbour different fungal communities. To test this hypothesis, we tagged three short Randia sp. trees with 13C-enriched CO2 and examined 13C transfer from the phorophyte into the epiphytic orchids Grosourdya appendiculata, Dendrobium oligophyllum and Gastrochilus sp. in Cat Tien National Park, (South Vietnam, Cat Tien National Park, plot size approx. 1 ha). The coincidence of fungal sequences in the orchid roots and in the branches on which they grew was also examined. We did not detect 13C label moving from phorophytes to epiphytes. Using Illumina sequencing, 162 fungal operational taxonomic units (OTUs) were detected. The fungal communities were significantly different between the roots of epiphytes and branches of phorophytes, although no strict fungal specificity at the species level was found in either epiphytes or phorophytes.