Can sugar maple establish into the boreal forest? Insights from seedlings under various canopies in southern Quebec

Understanding tree recruitment dynamics in various growth environments is essential for a better assessment of tree species’ adaptive capacity to climate change. We investigated the microsite factors influencing survival, growth, and foliar nutrition of natural and planted sugar maple seedlings (Acer saccharum) along a gradient of tree species that reflect the change in composition from temperate hardwoods to boreal forests of eastern Canada. We specifically tested whether the increasing abundance of conifers in the forest and its modifications on soil properties negatively affects foliar nutrition of natural seedlings as well as the survival and growth of seedlings planted directly in the natural soil and in pots filled with enriched soil. Results of natural seedlings indicate that under conifer-dominated stands, lower soil pH, accelerated dissolution of some minerals, lower temperature and moisture, and higher levels of phenolic compounds have created microsites that are less suitable for sugar maple foliar nutrition and regeneration. These conditions were omnipresent under hemlock. The growth of seedlings planted in the natural soil was negatively impacted by the overall low soil quality under all forest types (as compared to seedlings planted in pots with enriched soil). However, survival and growth of the seedlings were not negatively affected by conifers, regardless of planting type, likely because of stored nutrients from the nursery. Also, lower survival was found under maple–birch stands for seedlings planted both in the natural soil and in pots with enriched soil due to higher shading. This study has identified key microsite factors created by specific conifers that may impede or benefit the potential of sugar maple to maintain its current range or expand its range northward under climate change.

[1]  C. Messier,et al.  Conifer Presence May Negatively Affect Sugar Maple’s Ability to Migrate into the Boreal Forest Through Reduced Foliar Nutritional Status , 2017, Ecosystems.

[2]  C. Messier,et al.  Contrasting Nutritional Acclimation of Sugar Maple (Acer saccharum Marsh.) and Red Maple (Acer rubrum L.) to Increasing Conifers and Soil Acidity as Demonstrated by Foliar Nutrient Balances , 2016, Front. Ecol. Evol..

[3]  N. Thiffault,et al.  Phosphate-solubilizing bacteria isolated from ectomycorrhizal mycelium of Picea glauca are highly efficient at fluorapatite weathering , 2016 .

[4]  R. Long,et al.  Ecological benefits and risks arising from liming sugar maple dominated forests in northeastern North America , 2015 .

[5]  M. Vellend,et al.  Non-climatic constraints on upper elevational plant range expansion under climate change , 2014, Proceedings of the Royal Society B: Biological Sciences.

[6]  P. Reich,et al.  First‐year seedlings and climate change: species‐specific responses of 15 North American tree species , 2014 .

[7]  J. Battles,et al.  Determinants of survival over 7 years for a natural cohort of sugar maple seedlings in a northern hardwood forest , 2014 .

[8]  James S. Clark,et al.  Competition‐interaction landscapes for the joint response of forests to climate change , 2014, Global change biology.

[9]  I. Dickie,et al.  Ecological significance of mineral weathering in ectomycorrhizal and arbuscular mycorrhizal ecosystems from a field-based comparison , 2014 .

[10]  Y. Bergeron,et al.  Geographical variation in reproductive capacity of sugar maple (Acer saccharum Marshall) northern peripheral populations , 2014 .

[11]  Christian Messier,et al.  Root production of hybrid poplars and nitrogen mineralization improve following mounding of boreal Podzols , 2013 .

[12]  J. Puértolas,et al.  Nutrient loading of forest tree seedlings to promote stress resistance and field performance: a Mediterranean perspective , 2013, New Forests.

[13]  E. Thiffault,et al.  Influence of afforestation on soil: The case of mineral weathering , 2013 .

[14]  J. HilleRisLambers,et al.  Climate isn't everything: competitive interactions and variation by life stage will also affect range shifts in a warming world. , 2013, American journal of botany.

[15]  F. Courchesne,et al.  Constraining soil mineral weathering 87Sr/86Sr for calcium apportionment studies of a deciduous forest growing on soils developed from granitoid igneous rocks , 2012 .

[16]  B. Wemple,et al.  Forest influences on snow accumulation and snowmelt at the Hubbard Brook Experimental Forest, New Hampshire, USA , 2012 .

[17]  B. Velde,et al.  Weathering of biotite in the presence of arbuscular mycorrhizae in selected agricultural crops , 2012 .

[18]  D. Beerling,et al.  Evolution of trees and mycorrhizal fungi intensifies silicate mineral weathering , 2012, Biology Letters.

[19]  James S. Clark,et al.  Failure to migrate: lack of tree range expansion in response to climate change , 2012 .

[20]  R. Farrell,et al.  Intercropping Caragana arborescens with Salix miyabeana to Satisfy Nitrogen Demand and Maximize Growth , 2012, BioEnergy Research.

[21]  R. Ohlemüller,et al.  Rapid Range Shifts of Species Associated with High Levels of Climate Warming , 2011, Science.

[22]  J. Kattge,et al.  Improving assessment and modelling of climate change impacts on global terrestrial biodiversity. , 2011, Trends in ecology & evolution.

[23]  P. Balandier,et al.  Influence of several tree traits on rainfall partitioning in temperate and boreal forests: a review , 2009, Annals of Forest Science.

[24]  Ülo Niinemets,et al.  Responses of forest trees to single and multiple environmental stresses from seedlings to mature plants: Past stress history, stress interactions, tolerance and acclimation , 2010 .

[25]  Y. Bergeron,et al.  Response of northeastern North American forests to climate change: Will soil conditions constrain tree species migration? , 2010 .

[26]  C. Holmden,et al.  Influence of landscape on the apportionment of Ca nutrition in a Boreal Shield forest of Saskatchewan (Canada) using 87Sr/86Sr as a tracer. , 2010 .

[27]  C. Field,et al.  The velocity of climate change , 2009, Nature.

[28]  R. Ouimet,et al.  Present-day expansion of American beech in northeastern hardwood forests: does soil base status matter? , 2009 .

[29]  R. Hallett,et al.  Sugar maple growth in relation to nutrition and stress in the northeastern United States. , 2009, Ecological applications : a publication of the Ecological Society of America.

[30]  K. Gaston Geographic range limits: achieving synthesis , 2009, Proceedings of the Royal Society B: Biological Sciences.

[31]  G. Tutz,et al.  An introduction to recursive partitioning: rationale, application, and characteristics of classification and regression trees, bagging, and random forests. , 2009, Psychological methods.

[32]  T. Hothorn,et al.  Simultaneous Inference in General Parametric Models , 2008, Biometrical journal. Biometrische Zeitschrift.

[33]  C. Rosenzweig,et al.  Attributing physical and biological impacts to anthropogenic climate change , 2008, Nature.

[34]  S. S. Clair,et al.  Key interactions between nutrient limitation and climatic factors in temperate forests: a synthesis of the sugar maple literature , 2008 .

[35]  S. Hamburg,et al.  A sequential extraction to determine the distribution of apatite in granitoid soil mineral pools with application to weathering at the Hubbard Brook Experimental Forest, NH, USA , 2007 .

[36]  D. Houle,et al.  Foliar and wood chemistry of sugar maple along a gradient of soil acidity and stand health , 2007, Plant and Soil.

[37]  P. Legendre,et al.  packfor: Forward Selection with permutation (Canoco p.46), version 0.0-8 , 2007 .

[38]  P. Legendre,et al.  Variation partitioning of species data matrices: estimation and comparison of fractions. , 2006, Ecology.

[39]  R. Ouimet,et al.  Ten-year effect of dolomitic lime on the nutrition, crown vigor, and growth of sugar maple , 2006 .

[40]  A. Richardson,et al.  Response of sugar maple to calcium addition to northern hardwood forest. , 2006, Ecology.

[41]  P. Arp,et al.  Determination and Mapping Critical Loads of Acidity and Exceedances for Upland Forest Soils in Eastern Canada , 2006 .

[42]  Paul G. Schaberg,et al.  Associations of calcium and aluminum with the growth and health of sugar maple trees in Vermont , 2006 .

[43]  U. Blum,et al.  Allelopathy: A soil system perspective , 2006 .

[44]  Thomas Drouet,et al.  Strontium isotope composition as a tracer of calcium sources in two forest ecosystems in Belgium , 2005 .

[45]  C. Wirth Fire regime and treediversity in boreal forests: implications for the carbon cycle , 2005 .

[46]  R. B. Jackson,et al.  THE UPLIFT OF SOIL NUTRIENTS BY PLANTS: BIOGEOCHEMICAL CONSEQUENCES ACROSS SCALES , 2004 .

[47]  T. Kuyper,et al.  The role of fungi in weathering , 2004 .

[48]  Mark W. Schwartz,et al.  How fast and far might tree species migrate in the eastern United States due to climate change , 2004 .

[49]  K. Greer,et al.  The effect of interspecific competition on conifer seedling growth and nitrogen availability measured using ion-exchange membranes , 2004 .

[50]  D. Paré,et al.  Is the use of trees with superior growth a threat to soil nutrient availability? A case study with Norway spruce , 2004 .

[51]  S. Hamburg,et al.  Phytotoxicity of American beech leaf leachate to sugar maple seedlings in a greenhouse experiment , 2003 .

[52]  G. Yohe,et al.  A globally coherent fingerprint of climate change impacts across natural systems , 2003, Nature.

[53]  M. Nilsson,et al.  Nitrogen mineralization and phenol accumulation along a fire chronosequence in northern Sweden , 2002, Oecologia.

[54]  Daniel Houle,et al.  Basal area growth of sugar maple in relation to acid deposition, stand health, and soil nutrients. , 2002, Journal of environmental quality.

[55]  G. Likens,et al.  Mycorrhizal weathering of apatite as an important calcium source in base-poor forest ecosystems , 2002, Nature.

[56]  G. Likens,et al.  Tree seedling growth and mortality responses to manipulations of calcium and aluminum in a northern hardwood forest , 2002 .

[57]  F. Dijkstra,et al.  Tree Species Effects on Calcium Cycling: The Role of Calcium Uptake in Deep Soils , 2002, Ecosystems.

[58]  J. Fyles,et al.  Rates of litter decomposition over 6 years in Canadian forests: influence of litter quality and climate , 2002 .

[59]  Nicolas Bélanger,et al.  Simulation of soil chemistry and nutrient availability in a forested ecosystem of southern Quebec - I. Reconstruction of the time-series files of nutrient cycling using the MAKEDEP model , 2002, Environ. Model. Softw..

[60]  E. Vaganov,et al.  Effects of Fire and Climate on Successions and Structural Changes in The Siberian Boreal Forest , 2001 .

[61]  R. Clárk,et al.  Mineral acquisition by arbuscular mycorrhizal plants , 2000 .

[62]  L. Augusto,et al.  Impact of forest tree species on feldspar weathering rates , 2000 .

[63]  P. Vitousek,et al.  The role of polyphenols in terrestrial ecosystem nutrient cycling. , 2000, Trends in ecology & evolution.

[64]  M. Olsson,et al.  Mycorrhizal weathering: A true case of mineral plant nutrition? , 2000 .

[65]  I. Yevdokimov,et al.  In Situ extraction of rhizosphere organic compounds from contrasting plant communities , 2000 .

[66]  J. Fyles,et al.  Litter decomposition rates in Canadian forests , 1999 .

[67]  Christian P. Giardina,et al.  Why do Tree Species Affect Soils? The Warp and Woof of Tree-soil Interactions , 1998 .

[68]  Charles D. Canham,et al.  CANOPY TREE–SOIL INTERACTIONS WITHIN TEMPERATE FORESTS: SPECIES EFFECTS ON pH AND CATIONS , 1998 .

[69]  Charles T. Driscoll,et al.  Factors regulating throughfall flux in a New Hampshire forested landscape , 1996 .

[70]  O. Chadwick,et al.  Base cation biogeochemistry and weathering under oak and pine: a controlled long-term experiment , 1996 .

[71]  Randy A. Dahlgren,et al.  Polyphenol control of nitrogen release from pine litter , 1995, Nature.

[72]  B. Côté,et al.  Application of leaf, soil, and tree ring chemistry to determine the nutritional status of sugar maple on sites of different levels of decline , 1995 .

[73]  P. Stenberg,et al.  Performance of the LAI-2000 plant canopy analyzer in estimating leaf area index of some Scots pine stands. , 1994, Tree physiology.

[74]  Benoît Côté,et al.  Effects of base cation fertilization on soil and foliage nutrient concentrations, and litter-fall and throughfall nutrient fluxes in a sugar maple forest , 1994 .

[75]  Lee E. Frelich,et al.  Patch Formation and Maintenance in an Old‐Growth Hemlock‐Hardwood Forest , 1993 .

[76]  H. Graham Stabilization of the Prussian blue color in the determination of polyphenols , 1992 .

[77]  J. Wilson,et al.  Positive-feedback Switches in Plant Communities , 1992 .

[78]  R. Doig U-Pb Zircon Dates of Morin Anorthosite Suite Rocks, Grenville Province, Quebec , 1991, The Journal of Geology.

[79]  T. Kavanagh,et al.  Influence of stand age and spatial location on throughfall chemistry beneath black spruce , 1990 .

[80]  F. I. Woodward,et al.  Stomatal numbers are sensitive to increases in CO2 from pre-industrial levels , 1987, Nature.

[81]  J. Hett A Dynamic Analysis of Age in Sugar Maple Seedlings , 1971 .