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Evaluating different soil and plant hydraulic constraints on tree function using a model and sap flow data from ponderosa pine
Relationships between tree size and physiological processes such as transpiration may have important implications for plant and ecosystem function, but as yet are poorly understood. We used a process‐based model of the soil–plant–atmosphere continuum to investigate patterns of whole‐tree sap flow in...
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Published in: | Plant, cell and environment cell and environment, 2001-07, Vol.24 (7), p.679-690 |
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description | Relationships between tree size and physiological processes such as transpiration may have important implications for plant and ecosystem function, but as yet are poorly understood. We used a process‐based model of the soil–plant–atmosphere continuum to investigate patterns of whole‐tree sap flow in ponderosa pine trees of different size and age (36 m and ∼250 years versus 13 m and 10–50 years) over a developing summer drought. We examined three different hypothetical controls on hydraulic resistance, and found that size‐related differences in sap flow could be best explained by absolute differences in plant resistance related to path length (hypothesis 1) rather than through different dynamic relationships between plant resistance and leaf water potential (hypothesis 2), or alterations in rates of cumulative inducement and repair of cavitation (hypothesis 3). Reductions in sap flow over time could be best explained by rising soil–root resistance (hypothesis 1), rather than by a combination of rising plant and soil–root resistance (hypothesis 2), or by rising plant resistance alone (hypothesis 3). Comparing hourly predictions with observed sap flow, we found that a direct relationship between plant resistance and leaf water potential (hypothesis 2) led to unrealistic bimodal patterns of sap flow within a day. Explaining seasonal reduction in sap flow purely through rising plant resistance (hypothesis 3) was effective but failed to explain the observed decline in pre‐dawn leaf water potential for small trees. Thus, hypothesis 1 was best corroborated. A sensitivity analysis revealed a significant difference in the response to drought‐relieving rains; precipitation induced a strong recovery in sap flow in the hypothetical case of limiting soil–root resistance (hypothesis 1), and an insignificant response in the case of limiting plant resistance (hypothesis 3). Longer term monitoring and manipulation experiments are thus likely to resolve the uncertainties in hydraulic constraints on plant function. |
doi_str_mv | 10.1046/j.1365-3040.2001.00715.x |
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J. ; Ryan, M. G.</creator><creatorcontrib>Williams, M. ; Bond, B. J. ; Ryan, M. G.</creatorcontrib><description>Relationships between tree size and physiological processes such as transpiration may have important implications for plant and ecosystem function, but as yet are poorly understood. We used a process‐based model of the soil–plant–atmosphere continuum to investigate patterns of whole‐tree sap flow in ponderosa pine trees of different size and age (36 m and ∼250 years versus 13 m and 10–50 years) over a developing summer drought. We examined three different hypothetical controls on hydraulic resistance, and found that size‐related differences in sap flow could be best explained by absolute differences in plant resistance related to path length (hypothesis 1) rather than through different dynamic relationships between plant resistance and leaf water potential (hypothesis 2), or alterations in rates of cumulative inducement and repair of cavitation (hypothesis 3). Reductions in sap flow over time could be best explained by rising soil–root resistance (hypothesis 1), rather than by a combination of rising plant and soil–root resistance (hypothesis 2), or by rising plant resistance alone (hypothesis 3). Comparing hourly predictions with observed sap flow, we found that a direct relationship between plant resistance and leaf water potential (hypothesis 2) led to unrealistic bimodal patterns of sap flow within a day. Explaining seasonal reduction in sap flow purely through rising plant resistance (hypothesis 3) was effective but failed to explain the observed decline in pre‐dawn leaf water potential for small trees. Thus, hypothesis 1 was best corroborated. A sensitivity analysis revealed a significant difference in the response to drought‐relieving rains; precipitation induced a strong recovery in sap flow in the hypothetical case of limiting soil–root resistance (hypothesis 1), and an insignificant response in the case of limiting plant resistance (hypothesis 3). Longer term monitoring and manipulation experiments are thus likely to resolve the uncertainties in hydraulic constraints on plant function.</description><identifier>ISSN: 0140-7791</identifier><identifier>EISSN: 1365-3040</identifier><identifier>DOI: 10.1046/j.1365-3040.2001.00715.x</identifier><identifier>CODEN: PLCEDV</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science, Ltd</publisher><subject>Agronomy. Soil science and plant productions ; Animal and plant ecology ; Animal, plant and microbial ecology ; Autoecology ; Biological and medical sciences ; Economic plant physiology ; Fundamental and applied biological sciences. 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G.</creatorcontrib><title>Evaluating different soil and plant hydraulic constraints on tree function using a model and sap flow data from ponderosa pine</title><title>Plant, cell and environment</title><description>Relationships between tree size and physiological processes such as transpiration may have important implications for plant and ecosystem function, but as yet are poorly understood. We used a process‐based model of the soil–plant–atmosphere continuum to investigate patterns of whole‐tree sap flow in ponderosa pine trees of different size and age (36 m and ∼250 years versus 13 m and 10–50 years) over a developing summer drought. We examined three different hypothetical controls on hydraulic resistance, and found that size‐related differences in sap flow could be best explained by absolute differences in plant resistance related to path length (hypothesis 1) rather than through different dynamic relationships between plant resistance and leaf water potential (hypothesis 2), or alterations in rates of cumulative inducement and repair of cavitation (hypothesis 3). Reductions in sap flow over time could be best explained by rising soil–root resistance (hypothesis 1), rather than by a combination of rising plant and soil–root resistance (hypothesis 2), or by rising plant resistance alone (hypothesis 3). Comparing hourly predictions with observed sap flow, we found that a direct relationship between plant resistance and leaf water potential (hypothesis 2) led to unrealistic bimodal patterns of sap flow within a day. Explaining seasonal reduction in sap flow purely through rising plant resistance (hypothesis 3) was effective but failed to explain the observed decline in pre‐dawn leaf water potential for small trees. Thus, hypothesis 1 was best corroborated. A sensitivity analysis revealed a significant difference in the response to drought‐relieving rains; precipitation induced a strong recovery in sap flow in the hypothetical case of limiting soil–root resistance (hypothesis 1), and an insignificant response in the case of limiting plant resistance (hypothesis 3). Longer term monitoring and manipulation experiments are thus likely to resolve the uncertainties in hydraulic constraints on plant function.</description><subject>Agronomy. Soil science and plant productions</subject><subject>Animal and plant ecology</subject><subject>Animal, plant and microbial ecology</subject><subject>Autoecology</subject><subject>Biological and medical sciences</subject><subject>Economic plant physiology</subject><subject>Fundamental and applied biological sciences. 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Soil science and plant productions</topic><topic>Animal and plant ecology</topic><topic>Animal, plant and microbial ecology</topic><topic>Autoecology</topic><topic>Biological and medical sciences</topic><topic>Economic plant physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Plants and fungi</topic><topic>Water relations, transpiration, stomata</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Williams, M.</creatorcontrib><creatorcontrib>Bond, B. J.</creatorcontrib><creatorcontrib>Ryan, M. G.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><jtitle>Plant, cell and environment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Williams, M.</au><au>Bond, B. J.</au><au>Ryan, M. G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluating different soil and plant hydraulic constraints on tree function using a model and sap flow data from ponderosa pine</atitle><jtitle>Plant, cell and environment</jtitle><date>2001-07</date><risdate>2001</risdate><volume>24</volume><issue>7</issue><spage>679</spage><epage>690</epage><pages>679-690</pages><issn>0140-7791</issn><eissn>1365-3040</eissn><coden>PLCEDV</coden><abstract>Relationships between tree size and physiological processes such as transpiration may have important implications for plant and ecosystem function, but as yet are poorly understood. We used a process‐based model of the soil–plant–atmosphere continuum to investigate patterns of whole‐tree sap flow in ponderosa pine trees of different size and age (36 m and ∼250 years versus 13 m and 10–50 years) over a developing summer drought. We examined three different hypothetical controls on hydraulic resistance, and found that size‐related differences in sap flow could be best explained by absolute differences in plant resistance related to path length (hypothesis 1) rather than through different dynamic relationships between plant resistance and leaf water potential (hypothesis 2), or alterations in rates of cumulative inducement and repair of cavitation (hypothesis 3). Reductions in sap flow over time could be best explained by rising soil–root resistance (hypothesis 1), rather than by a combination of rising plant and soil–root resistance (hypothesis 2), or by rising plant resistance alone (hypothesis 3). Comparing hourly predictions with observed sap flow, we found that a direct relationship between plant resistance and leaf water potential (hypothesis 2) led to unrealistic bimodal patterns of sap flow within a day. Explaining seasonal reduction in sap flow purely through rising plant resistance (hypothesis 3) was effective but failed to explain the observed decline in pre‐dawn leaf water potential for small trees. Thus, hypothesis 1 was best corroborated. A sensitivity analysis revealed a significant difference in the response to drought‐relieving rains; precipitation induced a strong recovery in sap flow in the hypothetical case of limiting soil–root resistance (hypothesis 1), and an insignificant response in the case of limiting plant resistance (hypothesis 3). Longer term monitoring and manipulation experiments are thus likely to resolve the uncertainties in hydraulic constraints on plant function.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science, Ltd</pub><doi>10.1046/j.1365-3040.2001.00715.x</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Agronomy. Soil science and plant productions Animal and plant ecology Animal, plant and microbial ecology Autoecology Biological and medical sciences Economic plant physiology Fundamental and applied biological sciences. Psychology Plants and fungi Water relations, transpiration, stomata |
title | Evaluating different soil and plant hydraulic constraints on tree function using a model and sap flow data from ponderosa pine |
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