Investigating old‐growth ponderosa pine physiology using tree‐rings, δ13C, δ18O, and a process‐based model

dc.contributor.authorUlrich, Danielle E. M.
dc.contributor.authorStill, Christopher
dc.contributor.authorBrooks, J. Renée
dc.contributor.authorKim, Youngil
dc.contributor.authorMeinzer, Frederick C.
dc.date.accessioned2023-09-27T21:04:05Z
dc.date.available2023-09-27T21:04:05Z
dc.date.issued2019-06
dc.description.abstractIn dealing with predicted changes in environmental conditions outside those experienced today, forest managers and researchers rely on process‐based models to inform physiological processes and predict future forest growth responses. The carbon and oxygen isotope ratios of tree‐ring cellulose (δ13Ccell, δ18Ocell) reveal long‐term, integrated physiological responses to environmental conditions. We incorporated a submodel of δ18Ocell into the widely used Physiological Principles in Predicting Growth (3‐PG) model for the first time, to complement a recently added δ13Ccell submodel. We parameterized the model using previously reported stand characteristics and long‐term trajectories of tree‐ring growth, δ13Ccell, and δ18Ocell collected from the Metolius AmeriFlux site in central Oregon (upland trees). We then applied the parameterized model to a nearby set of riparian trees to investigate the physiological drivers of differences in observed basal area increment (BAI) and δ13Ccell trajectories between upland and riparian trees. The model showed that greater available soil water and maximum canopy conductance likely explain the greater observed BAI and lower δ13Ccell of riparian trees. Unexpectedly, both observed and simulated δ18Ocell trajectories did not differ between the upland and riparian trees, likely due to similar δ18O of source water isotope composition. The δ18Ocell submodel with a Peclet effect improved model estimates of δ18Ocell because its calculation utilizes 3‐PG growth and allocation processes. Because simulated stand‐level transpiration (E) is used in the δ18O submodel, aspects of leaf‐level anatomy such as the effective path length for transport of water from the xylem to the sites of evaporation could be estimated.en_US
dc.identifier.citationUlrich, D. E., Still, C., Brooks, J. R., Kim, Y., & Meinzer, F. C. (2019). Investigating old‐growth ponderosa pine physiology using tree‐rings, δ13C, δ18O, and a process‐based model. Ecology, 100(6), e02656.en_US
dc.identifier.issn0012-9658
dc.identifier.urihttps://scholarworks.montana.edu/handle/1/18120
dc.language.isoen_USen_US
dc.publisherWileyen_US
dc.rightscc-byen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.subjectcarbon isotope ratiosen_US
dc.subjecteffective path lengthen_US
dc.subjectoxygen isotope ratiosen_US
dc.subjectphysiological Principlesin Predicting Growthen_US
dc.subjectprocess-based modelingen_US
dc.subjecttree ringsen_US
dc.titleInvestigating old‐growth ponderosa pine physiology using tree‐rings, δ13C, δ18O, and a process‐based modelen_US
dc.typeArticleen_US
mus.citation.extentfirstpage1en_US
mus.citation.extentlastpage18en_US
mus.citation.issue6en_US
mus.citation.journaltitleEcologyen_US
mus.citation.volume100en_US
mus.data.thumbpage13en_US
mus.identifier.doi10.1002/ecy.2656en_US
mus.relation.collegeCollege of Letters & Scienceen_US
mus.relation.departmentEcology.en_US
mus.relation.universityMontana State University - Bozemanen_US

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