» Articles » PMID: 34928345

Distinguishing Carbon Gains from Photosynthesis and Heterotrophy in C3-hemiparasite-C3-host Pairs

Overview
Journal Ann Bot
Specialty Biology
Date 2021 Dec 20
PMID 34928345
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Background And Aims: Previous carbon stable isotope (13C) analyses have shown for very few C3-hemiparasites utilizing C4- or CAM-hosts the use of two carbon sources, autotrophy and heterotrophy. This 13C approach, however, failed for the frequently occurring C3-C3 parasite-host pairs. Thus, we used hydrogen stable isotope (2H) natural abundances as a substitute for 13C within a C3-Orobanchaceae sequence graded by haustoria complexity and C3-Santalaceae.

Methods: Parasitic plants and their real or potential host plants as references were collected in Central European lowland and alpine mountain meadows and forests. Parasitic plants included the xylem-feeding holoparasite Lathraea squamaria parasitizing on the same carbon nutrient source (xylem-transported organic carbon compounds) as potentially Pedicularis, Rhinanthus, Bartsia, Melampyrum and Euphrasia hemiparasites. Reference plants were used for an autotrophy-only isotope baseline. A multi-element stable isotope natural abundance approach was applied.

Key Results: Species-specific heterotrophic carbon gain ranging from 0 to 51 % was estimated by a 2H mixing-model. The sequence in heterotrophic carbon gain mostly met the morphological grading by haustoria complexity: Melampyrum- < Rhinanthus- < Pedicularis-type.

Conclusion: Due to higher transpiration and lower water-use efficiency, depletion in 13C, 18O and 2H compared to C3-host plants should be expected for tissues of C3-hemiparasites. However, 2H is counterbalanced by transpiration (2H-depletion) and heterotrophy (2H-enrichment). Progressive 2H-enrichment can be used as a proxy to evaluate carbon gains from hosts.

Citing Articles

Fire-modulated fluctuations in nutrient availability stimulate biome-scale floristic turnover in time, and elevated species richness, in low-nutrient fynbos heathland.

Verboom G, Slingsby J, Cramer M Ann Bot. 2023; 133(5-6):819-832.

PMID: 38150535 PMC: 11082518. DOI: 10.1093/aob/mcad199.


Water status and macronutrient concentrations, but not carbon status, of ssp. are determined by its hosts: a study across nine mistletoe-host pairs in central Switzerland.

Wang A, Bose A, Lehmann M, Rigling A, Gessler A, Yu L Front Plant Sci. 2023; 14:1142760.

PMID: 37223783 PMC: 10200922. DOI: 10.3389/fpls.2023.1142760.


Approaching a revolution in hemiparasitic plant biology? A commentary on 'Distinguishing carbon gains from photosynthesis and heterotrophy in C3-hemiparasite-C3-host-pairs'.

Tesitel J, Tesitelova T Ann Bot. 2022; 129(6):i-ii.

PMID: 35262668 PMC: 9113168. DOI: 10.1093/aob/mcac019.

References
1.
Tesitel J, Tesitelova T, Fisher J, Leps J, Cameron D . Integrating ecology and physiology of root-hemiparasitic interaction: interactive effects of abiotic resources shape the interplay between parasitism and autotrophy. New Phytol. 2014; 205(1):350-60. DOI: 10.1111/nph.13006. View

2.
Zimmer K, Hynson N, Gebauer G, Allen E, Allen M, Read D . Wide geographical and ecological distribution of nitrogen and carbon gains from fungi in pyroloids and monotropoids (Ericaceae) and in orchids. New Phytol. 2007; 175(1):166-175. DOI: 10.1111/j.1469-8137.2007.02065.x. View

3.
Yakir D, Deniro M . Oxygen and Hydrogen Isotope Fractionation during Cellulose Metabolism in Lemna gibba L. Plant Physiol. 1990; 93(1):325-32. PMC: 1062506. DOI: 10.1104/pp.93.1.325. View

4.
Ziegler H . [Not Available]. Ber Dtsch Bot Ges. 1968; 81:558-65. View

5.
Cernusak L, Pate J, Farquhar G . Oxygen and carbon isotope composition of parasitic plants and their hosts in southwestern Australia. Oecologia. 2004; 139(2):199-213. DOI: 10.1007/s00442-004-1506-6. View