Multi-Stemmed Habit in Trees Contributes Climate Resilience in Tropical Dry Forest

Understanding how environmental adaptations mediate plant and ecosystem responses becomes increasingly important under accelerating global environmental change. Multi-stemmed trees, for example, differ in form and function from single-stemmed trees and may possess physiological advantages that allow for persistence during stressful climatic events such as extended drought. Following the worst drought in Hawaii in a century, we examined patterns of stem abundance and turnover in a Hawaiian lowland dry forest (LDF) and a montane wet forest (MWF) to investigate how multi-stemmed trees might influence site persistence, and how stem abundance and turnover relate to key functional traits. We found stem abundance and multi-stemmed trees to be an important component for climate resilience within the LDF. The LDF had higher relative abundance of multi-stemmed trees, stem abundance, and mean stem abundance compared to a reference MWF. Within the LDF, multi-stemmed trees had higher relative stem abundance (i.e., percent composition of stems to the total number of stems in the LDF) and higher estimated aboveground carbon than single-stemmed trees. Stem abundance varied among species and tree size classes. Stem turnover (i.e., change in stem abundance between five-year censuses) varied among species and tree size classes and species mean stem turnover was correlated with mean species stem abundance per tree. At the plot level, stem abundance per tree is also a predictor of survival, though mortality did not differ between multiple- and single-stemmed trees. Lastly, species with higher mean stem abundance per tree tended to have traits associated with a higher light-saturated photosynthetic rate, suggesting greater productivity in periods with higher water supply. Identifying the traits that allow species and forest communities to persist in dry environments or respond to disturbance is useful for forecasting ecological climate resilience or potential for restoration in tropical dry forests.

[1]  C. Giardina,et al.  Restoring Mexican Tropical Dry Forests: A National Review , 2022, Sustainability.

[2]  T. Ticktin,et al.  A Hawaiian Tropical Dry Forest Regenerates: Natural Regeneration of Endangered Species under Biocultural Restoration , 2022, Sustainability.

[3]  L. Sack,et al.  An extensive suite of functional traits distinguishes Hawaiian wet and dry forests and enables prediction of species vital rates , 2018, Functional Ecology.

[4]  J. Chave,et al.  biomass: an r package for estimating above‐ground biomass and its uncertainty in tropical forests , 2017 .

[5]  T. Giambelluca,et al.  Spatial trend analysis of Hawaiian rainfall from 1920 to 2012 , 2017 .

[6]  Annette M. Trierweiler,et al.  Will seasonally dry tropical forests be sensitive or resistant to future changes in rainfall regimes? , 2017 .

[7]  T. Bishop,et al.  Post-Fire Recovery of Eucalypt-Dominated Vegetation Communities in the Sydney Basin, Australia , 2016 .

[8]  Shixiao Yu,et al.  Tree aboveground carbon storage correlates with environmental gradients and functional diversity in a tropical forest , 2016, Scientific Reports.

[9]  T. Giambelluca,et al.  Comparison of geostatistical approaches to spatially interpolate month‐year rainfall for the Hawaiian Islands , 2016 .

[10]  Susana Paula,et al.  Towards understanding resprouting at the global scale. , 2016, The New phytologist.

[11]  R. Mendes R: The R Project for Statistical Computing , 2016 .

[12]  N. McDowell,et al.  Drought and resprouting plants. , 2015, The New phytologist.

[13]  I. Prentice,et al.  Improved simulation of fire–vegetation interactions in the Land surface Processes and eXchanges dynamic global vegetation model (LPX-Mv1) , 2014 .

[14]  Juli G Pausas,et al.  Evolutionary ecology of resprouting and seeding in fire-prone ecosystems. , 2014, The New phytologist.

[15]  B. Nelson,et al.  Improved allometric models to estimate the aboveground biomass of tropical trees , 2014, Global change biology.

[16]  R. Nilus,et al.  A trait-based trade-off between growth and mortality: evidence from 15 tropical tree species using size-specific relative growth rates , 2014, Ecology and evolution.

[17]  L. Sack,et al.  Forest Structure in Low-Diversity Tropical Forests: A Study of Hawaiian Wet and Dry Forests , 2014, PloS one.

[18]  Christophe Pélabon,et al.  Integrated phenotypes: understanding trait covariation in plants and animals , 2014, Philosophical Transactions of the Royal Society B: Biological Sciences.

[19]  T. Whitham,et al.  Climate relicts and their associated communities as natural ecology and evolution laboratories. , 2014, Trends in ecology & evolution.

[20]  J. Ahumada,et al.  Carbon storage in tropical forests correlates with taxonomic diversity and functional dominance on a global scale , 2014 .

[21]  J. Pausas,et al.  Physiological differences explain the co-existence of different regeneration strategies in Mediterranean ecosystems. , 2014, The New phytologist.

[22]  T. Sunderland,et al.  Tropical dry forests: The state of global knowledge and recommendations for future research , 2014 .

[23]  M. Adams,et al.  Stand water use status in relation to fire in a mixed species eucalypt forest , 2013 .

[24]  M. Lawes,et al.  Resprouting as a key functional trait: how buds, protection and resources drive persistence after fire. , 2013, The New phytologist.

[25]  R. Ostertag,et al.  Invasive feral pigs impact native tree ferns and woody seedlings in Hawaiian forest , 2013, Biological Invasions.

[26]  T. Gillespie,et al.  The rarest and least protected forests in biodiversity hotspots , 2012, Biodiversity and Conservation.

[27]  F. Ewers,et al.  Allocation tradeoffs among chaparral shrub seedlings with different life history types (Rhamnaceae). , 2012, American journal of botany.

[28]  W. Bond,et al.  Diverse functional responses to drought in a Mediterranean-type shrubland in South Africa. , 2012, The New phytologist.

[29]  R. Bradstock,et al.  Fire in Mediterranean Ecosystems: Ecology, Evolution and Management , 2011 .

[30]  Nathan J B Kraft,et al.  Functional traits and the growth-mortality trade-off in tropical trees. , 2010, Ecology.

[31]  N. Mouquet,et al.  Biodiversity and Climate Change: Integrating Evolutionary and Ecological Responses of Species and Communities , 2010 .

[32]  Robert D Holt,et al.  A framework for community interactions under climate change. , 2010, Trends in ecology & evolution.

[33]  R. Dirzo,et al.  Prevalence of Tree Regeneration by Sprouting and Seeding Along a Rainfall Gradient in Hawai'i , 2010 .

[34]  G. Asner,et al.  Convergent structural responses of tropical forests to diverse disturbance regimes. , 2009, Ecology letters.

[35]  A. Sparrow,et al.  Multi‐stemmed trees in montane rain forests: their frequency and demography in relation to elevation, soil nutrients and disturbance , 2009 .

[36]  Ian J. Fiske,et al.  Effects of Sample Size on Estimates of Population Growth Rates Calculated with Matrix Models , 2008, PloS one.

[37]  M. Lawes,et al.  Sprouting by remobilization of above-ground resources ensures persistence after disturbance of coastal dune forest trees , 2008 .

[38]  Responses of native and invasive plant species to selective logging in an Acacia koa-Metrosideros polymorpha forest in Hawai‘i , 2008 .

[39]  J. D. du Toit,et al.  Responses of woody saplings exposed to chronic mammalian herbivory in an African savanna , 2008 .

[40]  C. Pipper,et al.  [''R"--project for statistical computing]. , 2008, Ugeskrift for laeger.

[41]  S. Cordell,et al.  Functional diversity of carbon-gain, water-use, and leaf-allocation traits in trees of a threatened lowland dry forest in Hawaii. , 2007, American journal of botany.

[42]  S. Cordell,et al.  Effects of non-native grass invasion on aboveground carbon pools and tree population structure in a tropical dry forest of Hawaii , 2006 .

[43]  A. Scariot,et al.  Principles of Natural Regeneration of Tropical Dry Forests for Restoration , 2006 .

[44]  P. G. Murphy,et al.  The Influence of Hurricane Winds on Caribbean Dry Forest Structure and Nutrient Pools 1 , 2005 .

[45]  P. Clarke,et al.  Nutrient availability induces contrasting allocation and starch formation in resprouting and obligate seeding shrubs , 2005 .

[46]  F. Putz,et al.  Effect of disturbance intensity on regeneration mechanisms in a tropical dry forest , 2002 .

[47]  W. Bond,et al.  Ecology of sprouting in woody plants: the persistence niche. , 2001, Trends in ecology & evolution.

[48]  D. Mueller‐Dombois Rain forest establishment and succession in the Hawaiian Islands , 2000 .

[49]  Peter J. Bellingham,et al.  Resprouting as a life history strategy in woody plant communities , 2000 .

[50]  P. Vitousek,et al.  Microclimate Change and Effect on Fire Following Forest‐Grass Conversion in Seasonally Dry Tropical Woodland 1 , 1998 .

[51]  B. W. Wilgen,et al.  Fire and Plants , 1995, Population and Community Biology Series.

[52]  E. Wilson,et al.  Tropical Dry Forests The Most Endangered Major Tropical Ecosystem , 1988 .

[53]  P. G. Murphy,et al.  Ecology of Tropical Dry Forest , 1986 .

[54]  P. Reich,et al.  Water stress and tree phenology in a tropical dry forest in the lowlands of Costa Rica. , 1984 .