Abstract
Even though drought impacts on tree physiology have been identified, whether drought affects leaf litter chemistry that, in turn, influences litter decay rates is still poorly understood. We compared litter quality and decomposition for two cohorts of leaves from five co-occurring seasonally deciduous tree species: Acer saccharum, Tilia americana, Quercus rubra, Quercus alba, and Ostrya virginiana. One cohort experienced a growing-season drought, and the other cohort came from the same trees in the ensuing, post-drought growing season. Leaf litter production was greater for drought litter than post-drought litter for all five species. Specific leaf area and nitrogen concentrations were 20% greater for the drought cohort than the post-drought cohort. Concentrations of non-structural carbohydrates were about 14% greater for the drought cohort, except for greater values for post-drought A. saccharum litter. Pectin in the middle lamella of leaf litter was 31% lower for the drought cohort compared to post-drought cohort. We found few differences in litter decay rates between drought and post-drought cohorts, although Q. rubra litter had more decomposition for the post-drought cohort than the drought cohort, whereas A. saccharum litter had more decomposition for the drought cohort than the post-drought cohort. Leaf litter decay rates for the drought cohort were related to litter nitrogen and lignin concentrations, whereas decay rates for the post-drought cohort were related to litter carbohydrate concentrations. Our findings suggest that the role of drought events on seasonally deciduous forest ecosystems must recognize species-specific, idiosyncratic responses in leaf litter quality and decomposition.
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References
Abrams MD, Kubiske ME (1990) Leaf structural characteristics of 31 hardwood and conifer tree species in central Wisconsin: influence of light regime and shade-tolerance rank. Forest Ecol Manag 31:245–253
Abrams MD, Nowacki GJ (2016) An interdisciplinary approach to better assess global change impacts and drought vulnerability on forest dynamics. Tree Physiol 36:421–427
Azuma W, Nakashima S, Yamakita E, Ishii HR, Kuroda K (2017) Water retained in tall Cryptomeria japonica leaves as studied by infrared micro-spectroscopy. Tree Physiol 37:1367–1378
Bates D, Mächler M, Bolker B, Walker S (2014) Fitting linear mixed-effects models using lme4. J Stat Softw 67:1–48
Berg B, McClaugherty C (2020) Plant litter, 4th edn. Springer, Switzerland
Carpita NC (1984) Fractionation of hemicelluloses from maize cell walls with increasing concentrations of alkali. Phytochemistry 23:1089–1093
Cassab GI (1998) Plant cell wall proteins. Ann Rev Plant Biol 49:281–309
Chapman HD, Morris VJ, Selvendran RR, O’Neill MA (1987) Static and dynamic light-scattering studies of pectic polysaccharides from the middle lamellae and primary cell walls of cider apples. Carbohyd Res 165:53–68
Cosgrove DJ (2015) Plant expansins: diversity and interactions with plant cell walls. Curr Opin Plant Biol 25:162–172
de Dios VR, Gessler A (2021) Sink and source co-limitation in the response of stored non-structural carbohydrates to an intense but short drought. Trees 35:1751–1754
Dempsey MA, Fisk MC, Yavitt JB, Fahey TJ, Balser TC (2013) Exotic earthworms alter soil microbial community composition and function. Soil Biol Biochem 67:263–270
Dietze MC, Sala A, Carbone MS, Czimczik CI, Mantooth JA, Richardson AD, Vargas R (2014) Nonstructural carbon in woody plants. Ann Rev Plant Biol 65:667–687
Dixon RA, Paiva NL (1995) Stress-induced phenylpropanoid metabolism. Plant Cell 7:1085–1097
Dyer JM (2006) Revisiting the deciduous forests of eastern North America. Bioscience 56:341–352
Esquerré-Tugayé MT, Boudart G, Dumas B (2000) Cell wall degrading enzymes, inhibitory proteins, and oligosaccharides participate in the molecular dialogue between plants and pathogens. Plant Physiol Biochem 38:157–163
Evans GC (1972) The quantitative analysis of plant growth. Blackwell, Oxford
Gawkowska D, Cybulska J, Zdunek A (2018) Structure-related gelling of pectins and linking with other natural compounds: a review. Polymers 10:762
Hendrix DL (1993) Rapid extraction and analysis of nonstructural carbohydrates in plant tissues. Crop Sci 33:1306–1311
Horowitz ME, Fahey TJ, Yavitt JB, Feldpausch TR, Sherman RE (2009) Patterns of late-season photosynthate movement in sugar maple saplings. Can J Forest Res 39:2294–2298
Houben K, Jolie RP, Fraeye I, Van Loey AM, Hendrickx ME (2011) Comparative study of the cell wall composition of broccoli, carrot, and tomato: structural characterization of the extractable pectins and hemicelluloses. Carbohyd Res 346:1105–1111
Jamet E, Canut H, Boudart G, Pont-Lezica RF (2006) Cell wall proteins: a new insight through proteomics. Trends Plant Sci 11:33–39
Jarvis MC (1982) The proportion of calcium-bound pectin in plant cell walls. Planta 154:344–346
Jiao T, Williams CA, De Kauwe MG, Schwalm CR, Medlyn BE (2021) Patterns of post-drought recovery are strongly influenced by drought duration, frequency, post-drought wetness, and bioclimatic setting. Glob Change Biol 27:4630–4643
Karberg NJ, Scott NA, Giardina CP (2008) Methods for estimating litter decomposition. In: Hoover CM (ed) Field measurements for forest carbon monitoring. Springer, Dordrecht, pp 103–111
Kettler TA, Doran JW, Gilbert TL (2001) Simplified method for soil particle-size determination to accompany soil-quality analyses. Soil Sci Soc Am J 65:849–852
Klotzbücher T, Kaiser K, Guggenberger G, Gatzek C, Kalbitz K (2011) A new conceptual model for the fate of lignin in decomposing plant litter. Ecology 92:1052–1062
Knight CA, Ackerly DD (2003) Evolution and plasticity of photosynthetic thermal tolerance, specific leaf area and leaf size: congeneric species from desert and coastal environments. New Phytol 160:337–347
Knutson RM (1997) An 18-year study of litterfall and litter decomposition in a northeast Iowa deciduous forest. Am Midl Nat 138:77–83
Kozlowski TT (1992) Carbohydrate sources and sinks in woody plants. Bot Rev 58:107–222
Lechowicz MJ (1984) Why do temperate deciduous trees leaf out at different times? Adaptation and ecology of forest communities. Am Nat 124:821–842
Lisboa MS, Schneider RL, Sullivan PJ, Walter MT (2020) Drought and post-drought rain effect on stream phosphorus and other nutrient losses in the Northeastern USA. J Hydrol Reg Stud 28:100672
Loomis WD, Battaile J (1966) Plant phenolic compounds and the isolation of plant enzymes. Phytochemistry 5:423–438
Maher JM, Markey JC, Ebert-May D (2013) The other half of the story: effect size analysis in quantitative research. CBE Life Sci Educ 12:345–351
McDowell NG (2011) Mechanisms linking drought, hydraulics, carbon metabolism, and vegetation mortality. Plant Physiol 155:1051–1059
McKown AD, Guy RD, Azam MS, Drewes EC, Quamme LK (2013) Seasonality and phenology alter functional leaf traits. Oecologia 172:653–665
McLeod AR, Newsham KK, Fry SC (2007) Elevated UV-B radiation modifies the extractability of carbohydrates from leaf litter of Quercus robur. Soil Biol Biochem 39:116–126
Medrano H, Escalona JM, Bota J, Gulías J, Flexas J (2002) Regulation of photosynthesis of C3 plants in response to progressive drought: stomatal conductance as a reference parameter. Ann Bot 89:895–905
Meentemeyer V (1978) Macroclimate and lignin control of litter decomposition rates. Ecology 59:465–472
Melillo JM, Aber JD, Muratore JF (1982) Nitrogen and lignin control of hardwood leaf litter decomposition dynamics. Ecology 63:621–626
Moller IE, Henrik H, Harholt J, Willats WG, Boomsma JJ (2011) The dynamics of plant cell-wall polysaccharide decomposition in leaf-cutting ant fungus gardens. PLoS ONE 6(3):e17506
Murdoch L, Corbel JC, Reis D, Bertheau Y, Vian B (1999) Differential cell wall degradation by Erwinia chrysanthemi in petiole of Saintpaulia ionantha. Protoplasma 210:59–74
Nakagawa S, Cuthill IC (2007) Effect size, confidence interval and statistical significance: a practical guide for biologists. Biol Rev 82:591–605
Newman GS, Arthur MA, Muller RN (2006) Above-and belowground net primary production in a temperate mixed deciduous forest. Ecosystems 9:317–329
Niinemets Ü, Valladares F (2006) Tolerance to shade, drought, and waterlogging of temperate northern hemisphere trees and shrubs. Ecol Monogr 76:521–547
Parsons JW, Tinsley J (1960) Extraction of soil organic matter with anhydrous formic acid. Soil Sci Soc Am J 24:198–201
Peaucelle A, Braybrook SA, Höfte H (2012) Cell wall mechanics and growth control in plants: the role of pectins revisited. Front Plant Sci 3:121
Popkin G (2019) How much can forests fight climate change? Nature 565:280–283
Prado FE, González JA, Boero C, Sampietro AR (1998) A simple and sensitive method for determining reducing sugars in plant tissues. Application to quantify the sugar content in quinoa (Chenopodium quinoa Willd.) seedlings. Phytochem Anal 9:58–62
Saleska SR, Didan K, Huete AR, Da Rocha HR (2007) Amazon forests green-up during 2005 drought. Science 318:612
Sariyildiz T, Anderson JM, Kucuk M (2005) Effects of tree species and topography on soil chemistry, litter quality, and decomposition in Northeast Turkey. Soil Biol Biochem 37:1695–1706
Scalbert A (1992) Quantitative methods for the estimation of tannins in plant tissues. In: Hemingway RW, Laks PE (eds) Plant polyphenols. Springer, Boston, pp 259–280
Schlesinger WH, Dietze MC, Jackson RB, Phillips RP, Rhoades CC, Rustad LE, Vose JM (2016) Forest biogeochemistry in response to drought. Glob Change Biol 22:2318–2328
Selvendran RR, O’Neill MA (1987) Isolation and analysis of cell walls from plant material. Method Biochem Anal 32:25–153
Suárez ER, Fahey TJ, Yavitt JB, Groffman PM, Bohlen PJ (2006) Patterns of litter disappearance in a northern hardwood forest invaded by exotic earthworms. Ecol Applic 16:154–165
Suseela V, Tharayil N, Xing B, Dukes JS (2013) Labile compounds in plant litter reduce the sensitivity of decomposition to warming and altered precipitation. New Phytol 200:122–133
Suseela V, Tharayil N, Xing B, Dukes JS (2015) Warming and drought differentially influence the production and resorption of elemental and metabolic nitrogen pools in Quercus rubra. Glob Change Biol 21:4177–4195
Sweet SK, Wolfe DW, DeGaetano A, Benner R (2017) Anatomy of the 2016 drought in the Northeastern United States: implications for agriculture and water resources in humid climates. Agric Forest Meteorol 247:571–581
Van Soest PJ (1994) Nutritional ecology of the ruminant. Cornell University Press, Ithaca
Wright IJ, Reich PB, Cornelissen JH, Falster DS, Groom PK, Hikosaka K, Lee W, Lusk CH, Niinemets Ü, Oleksyn J, Osada N (2005) Modulation of leaf economic traits and trait relationships by climate. Glob Ecol Biogeogr 14:411–421
Yavitt JB, Williams CJ (2015a) Conifer litter identity regulates anaerobic microbial activity in wetland soils via variation in leaf litter chemical composition. Geoderma 243:141–148
Yavitt JB, Williams CJ (2015b) Linking tree species identity to anaerobic microbial activity in a forested wetland soil via leaf litter decomposition and leaf carbon fractions. Plant Soil 390:293–305
Yavitt JB, Fahey TJ, Sherman RE, Groffman PM (2015) Lumbricid earthworm effects on incorporation of root and leaf litter into aggregates in a forest soil, New York State. Biogeochemistry 125:261–273
Zukswert JM, Prescott CE (2017) Relationships among leaf functional traits, litter traits, and mass loss during early phases of leaf litter decomposition in 12 woody plant species. Oecologia 185:305–316
Acknowledgements
We thank Molly E Huber, Gwendolyn T Pipes, and Emily C Olmos for laboratory assistance. We thank ad hoc reviewers and editors for comments and suggestions that greatly improved the clarity of the presentation.
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AM Wilson was supported by a Rawlings Cornell Presidential Research Scholarship for undergraduate student research.
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All authors conceived and designed the study and participated in the fieldwork. AMW and JBY analyzed litter and soil samples. JCB and AMW analyzed the data. AMW initiated paper writing and all authors provided editorial advice.
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Wilson, A.M., Burtis, J.C., Goebel, M. et al. Litter quality and decomposition responses to drought in a northeastern US deciduous forest. Oecologia 200, 247–257 (2022). https://doi.org/10.1007/s00442-022-05263-z
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DOI: https://doi.org/10.1007/s00442-022-05263-z