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Wednesday 24 August 2016

Canopy foliation and area as predictors of mortality risk from episodic drought for individual trees of Ashe juniper

Published Date
Volume 217, Issue 9, pp 1105–1114

Title 
Canopy foliation and area as predictors of mortality risk from episodic drought for individual trees of Ashe juniper

  • Daniel M. Johnson
  • Robert B. Jackson

  • Abstract

    Drought is killing an increasing number of trees globally, yet mortality risk remains difficult to predict at fine spatial scales. We sought to identify metrics of living individuals that could be used to estimate mortality risk of Ashe juniper (Juniperus ashei) trees and eventually to estimate the fraction of juniper populations at risk from drought. Ashe juniper is a keystone species in the Edwards Plateau region in central Texas, USA. We analyzed tree rings from both living and dead trees to determine growth rate prior to an historic drought in 2011 and measured morphological, physiological, and stand-level variables hypothesized to link growth rate and mortality risk. Slowly growing trees were disproportionately vulnerable to mortality. Fractional mortality of sampled trees was correlated to the difference between the mean predrought basal area increment (BAI) per tree and the predrought BAI of minimally stressed trees growing on deep soil (=BAI90 − BAI). Slowly growing trees had sparsely foliated canopies. BAI90 − BAI was positively correlated to the difference between: (1) leaf area per unit of projected canopy area per tree (LA) and the LA of minimally stressed trees and (2) projected canopy area (CA) and the CA of comparably sized trees. By contrast, there was no correlation between growth of living trees and light interception by neighboring trees, soil depth, or two functional metrics, the stem–leaf Ψ gradient and leaf light use efficiency. Mortality risk in Ashe juniper populations can be estimated from nondestructive measurements of leaf and canopy area of individual trees using relationships among risk, growth, and leaf and canopy area.

    References

    1. Adams HD, Luce CH, Breshears DD, Allen CD, Weiler M, Hale VC, Smith AMS, Huxman TE (2012) Ecohydrological consequences of drought- and infestation-triggered tree die-off: insights and hypotheses. Ecohydrology 5:145–159CrossRef
    2. Allen CD, Breshears DD (1998) Drought-induced shift of a forest-woodland ecotone: rapid landscape response to climate variation. Proc Natl Acad Sci USA 95:14839–14842CrossRefPubMedPubMedCentral
    3. Begg JE, Turner NC (1970) Water potential gradients in field tobacco. Plant Physiol 46:343–346CrossRefPubMedPubMedCentral
    4. Bennett AC, McDowell NG, Allen CD, Anderson-Teixeira KJ (2015) Larger trees suffer most during drought in forests worldwide. Nat Plants. doi:10.1038/nplants.2015.139
    5. Bowker MA, Muñoz A, Martinez T, Lau KM (2012) Rare drought-induced mortality of juniper is enhanced by edaphic stressors and influenced by stand density. J Arid Environ 76:9–16CrossRef
    6. Breshears DD, Myers OB, Meyer CW, Barnes FJ, Zou CB, Allen CD, McDowell NG, Pockman WT (2009) Tree die-off in response to global change type drought: mortality insights from a decade of plant water potential measurements. Front Ecol Environ 7:185–189CrossRef
    7. Cade BS, Noon BR (2003) A gentle introduction to quantile regression for ecologists. Front Ecol Environ 1:412–420CrossRef
    8. Camarero JJ, Gazol A, Sangüesa-Barreda G, Oliva J, Vicente-Serrano SM (2015) To die or not to die: early warnings of tree dieback in response to severe drought. J Ecol 103:44–57CrossRef
    9. Carnicer J, Coll M, Ninyerola M, Pons X, Sánchez G, Peñuelas J (2011) Widespread crown condition decline, food web disruption, and amplified tree mortality with increased climate change-type drought. Proc Natl Acad Sci USA 108:1474–1478CrossRefPubMedPubMedCentral
    10. Deines JM, Hellmann JJ, Curran TJ (2011) Traits associated with drought survival in three Australian tropical rainforest seedlings. Aust J Bot 59:620–628CrossRef
    11. Gamon JA, Serrano L, Surfus JS (1997) The photochemical reflectance index: an optical indicator of photosynthetic radiation use efficiency across species, functional types, and nutrient levels. Oecologia 112:492–501CrossRef
    12. Greenwood DL, Weisberg PJ (2008) Density-dependent tree mortality in pinyon-juniper woodlands. For Ecol Manag 255:2120–2137CrossRef
    13. Gu L, Pallardy SG, Hosman KP, Sun Y (2015) Drought-influenced mortality of tree species with different predawn leaf water dynamics in a decade-long study of a central US forest. Biogeosciences 12:2831–2845CrossRef
    14. Heres AM, Camarero JJ, López BC, Martínez-Vilalta J (2014) Declining hydraulic performances and low carbon investments in tree rings predate Scots pine drought-induced mortality. Trees 28:1737–1750CrossRef
    15. Huang C, Asner GP, Barger NN, Neff JC, Floyd ML (2010) Regional aboveground live carbon losses due to drought-induced tree dieback in piñon-juniper ecosystems. Remote Sens Environ 114:1471–1479CrossRef
    16. Intergovernmental Panel on Climate Change (2013) The physical science basis: contribution of Working Group I. Cambridge University Press, Cambridge
    17. Jiang X, Rauscher SA, Ringler TD, Lawrence DM, Williams AP, Allen CD, Stiner AL, Cai DM, McDowell NG (2013) Projected future changes in vegetation in western North America in the twenty-first century. J Clim 26:3671–3687CrossRef
    18. Kukowski KR, Schwinning S, Schwartz BF (2013) Hydraulic responses to extreme drought conditions in three co-dominant tree species in shallow soil over bedrock. Oecologia 171:819–830CrossRefPubMed
    19. Littell RS, Stroup WW, Freund RJ (2002) SAS for linear models, 4th edn. SAS Institute Inc, Cary
    20. Manion PD (1981) Tree disease concepts. Prentice Hall, Upper Saddle River
    21. Ogle K, Whitham TG, Cobb HS (2000) Tree-ring variation in pinyon predicts likelihood of death following severe drought. Ecology 81:3237–3243CrossRef
    22. Pangle RE, Limousin J-M, Plaut JA, Yepez EA, Hudson PJ, Boutz AL, Gehres N, Pockman WT, McDowell NG (2015) Prolonged experimental drought reduces plant hydraulic conductance and transpiration and increases mortality in a piñon-juniper woodland. Ecol Evol 5:1618–1638CrossRefPubMedPubMedCentral
    23. Pedersen BS (1998) The role of stress in the mortality of midwestern oaks as indicated by growth prior to death. Ecology 79:79–93CrossRef
    24. Peng CH, Ma ZH, Lei XD, Zhu QA, Chen H, Wang WF, Liu SR, Li WZ, Fang XQ, Zhou XL (2011) A drought induced pervasive increase in tree mortality across Canada’s boreal forests. Nat Clim Change 1:467–471CrossRef
    25. Reidy JL, Thompson FR III, Schwope C, Rowin S, Mueller JM (2016) Effects of prescribed fire on fuels, vegetation, and Golden-cheeked warbler (Setophaga chrysoparia) demographics in Texas juniper-oak woodlands. For Ecol Manag 376:96–106CrossRef
    26. Riskind DH, Diamond DD (1988) An introduction to environments and vegetation. In: Amos BB, Gehlbach FR (eds) Edwards Plateau vegetation: plant ecological studies in central Texas. Baylor Univ Press, Waco, pp 1–15
    27. Schwantes AM, Swenson JJ, Jackson RB (2016) Quantifying drought-induced tree mortality in the open canopy woods of central Texas. Remote Sens Environ 181:54–64CrossRef
    28. Schwinning S (2008) The water relations of two evergreen tree species in a karst savanna. Oecologia 158:373–383CrossRefPubMed
    29. Smeins FE, Merrill LB (1988) Long-term change in a semi-arid grassland. In: Amos BB, Gehlbach FR (eds) Edwards Plateau vegetation: plant ecological studies in central Texas. Baylor University Press, Waco, pp 101–114
    30. Suarez ML, Ghermandi L, Kitzberger T (2005) Factors predisposing episodic drought-induced tree mortality in Nothofagus: site, climatic sensitivity, and growth trends. J Ecol 92:954–966CrossRef
    31. Swaty RL, Deckert RJ, Whitham TG, Gehring CA (2004) Ectomycorrhizal abundance and community composition shifts with drought: predictions from tree rings. Ecology 85:1072–1084CrossRef
    32. Taucer PI, Munster CL, Wilcox BP, Owens MK, Mohanty BP (2008) Large-scale rainfall simulation experiments on juniper rangelands. Trans ASABE 51:1951–1961CrossRef
    33. Twidwell D, Wonkka CL, Taylor CA Jr, Zou CB, Twidwell JJ, Rogers WE (2014) Drought-induced woody plant mortality in an encroached semi-arid savanna depends on topoedaphic factors and land management. Appl Veg Sci 17:42–52CrossRef
    34. US Global Change Research Program (2009) Global climate change impacts in the United States. Karl TR, Melillo JM, Peterson TC (eds). Cambridge University Press, Cambridge. http://www.globalchange.gov/usimpacts. Accessed 10 Feb 2016
    35. van Mantgem PJ, Stephenson NL, Byrne JC, Daniels LD, Franklin JF, Fule PZ, Harmon ME, Larson AJ, Smith JM, Taylor AH, Veblen TT (2009) Widespread increase of tree mortality rates in the western United States. Science 323:521–524CrossRefPubMed
    36. Weiner J, Thomas SC (2001) The nature of tree growth and the “age-related decline in forest productivity”. Oikos 94:374–376CrossRef
    37. Williams AP, Allen CD, Macalady AK, Griffin D, Woodhouse CA, Meko DM, Swetnam TW, Rauscher SA, Seager R, Grissino-Mayer HD, Dean JS, Cook ER, Gangodagamage C, Cai M, McDowell NG (2013) Temperature as a potent driver of regional forest drought stress and tree mortality. Nat Clim Change 3:292–297CrossRef
    38. Wold S, Ruhe A, Wold H, Dunn WJ III (1984) The collinearity problem in linear regression. The partial least squares (PLS) approach to generalized inverses. SIAM J Sci Stat Comput 5:735–743CrossRef
    39. Zou CB, Turton DJ, Will RE, Engle DM, Fuhlendorf SD (2014) Alteration of hydrological processes and streamflow with juniper (Juniperus virginiana) encroachment in a mesic grassland catchment. Hydrol Process 28:6173–6182CrossRef

    For further details log on website :
    http://link.springer.com/article/10.1007%2Fs11258-016-0636-3

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