Abstract
Seasonal changes in the concentration of abscisic acid (ABA) in current-year needles of two different genotypes (AB-NSD-004 and AB-NSD-184) were monitored in branches collected from 20-year-old balsam fir (Abies balsamea L. (Mill.)) trees over a period of 11 months. A significant genotype × harvesting time interaction was observed for endogenous ABA levels and postharvest needle retention duration (NRD). A consistent pattern of seasonal variation in ABA concentration was observed in both genotypes, with the highest amount of ABA (7,887 ng g−1 DW) accumulating in April and May. The highest levels of ABA coincided with the lowest postharvest NRD regardless of genotype. Nevertheless, genotypes differed in their ABA concentrations. Branches of genotype AB-NSD-184 sampled during August exhibited 170 days of NRD whereas those collected in May and June registered the lowest NRD of around 40 days. There was a significant negative correlation (P < 0.05) between endogenous ABA concentrations and postharvest NRD in genotype AB-NSD-184. Also, an inverse relationship was observed between the average daily photoperiod and the postharvest NRD (R 2 = 0.35; P = 0.000) in the same genotype. Together with average daily temperature, the R 2 value for this correlation reached the highest (0.75; P ≤ 0.00). Genotypes differed in their physiological responses to environmental cues and thus differed in their postharvest qualities. Average daily photoperiod and maximum daily temperature are strongly linked to the postharvest NRD through modulating endogenous ABA concentration.
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Albers HH, Davis AK (1997) The wonderful world of Christmas trees. Mid-Prairie Books, Parkersburg
Alvim R, Hewett EW, Saunders PF (1976) Seasonal variation in the hormone content of willow: I. Changes in abscisic acid content and cytokinin activity in the xylem sap. Plant Physiol 57:474
Bauerle WL, Inman WW, Dudley JB (2006) Leaf abscisic acid accumulation in response to substrate water content: Linking leaf gas exchange regulation with leaf abscisic acid concentration. J Am Soc Hort Sci 131:295–301
Chen HH, Li PH, Brenner ML (1983) Involvement of abscisic acid in potato cold acclimation. Plant Physiol 71:362–365
Choat B, Pittermann J (2009) New insights into bordered pit structure and cavitation resistance in angiosperms and conifers. New Phytol 182:557–560
Christmann A, Havranek W, Wieser G (1999) Seasonal variation of abscisic acid in needles of Pinus cembra L. at the alpine timberline and possible relations to frost resistance and water status. Phyton (Horn) 39:23–30
CTCNS (2012) Christmas Tree Council of Nova Scotia. Available at www.ctcns.com (accessed 8 April 2013)
Dumbroff EB, Cohen DB, Webb DP (1979) Seasonal levels of abscisic acid in buds and stems of Acer saccharum. Physiol Plant 45:211–214
Environment Canada (2010) Climate Trends and Variations Bulletin—Autumn 2010. http://www.ec.gc.ca/adsc-cmda/default.asp?lang=en&n=A49944AE-1#a2. Accessed 20 Sept 2010
Greer DH, Robinson LA, Hall AJ, Klages K, Donnison H (2000) Frost hardening of Pinus radiata seedlings: effects of temperature on relative growth rate, carbon balance and carbohydrate concentration. Tree Physiol 20:107–114
Guy CL, Haskell D (1988) Detection of polypeptides associated with the cold acclimation process in spinach. Electrophoresis 9:787–796
Hinesley L, Snelling L (1997) Drying and rehydration of Atlantic white cedar, Arizona cypress, eastern white pine, Leyland cypress, and Virginia pine Christmas trees. Hort Sci 32:1252–1254
Jones GE, Cregg BM (2006) Screening exotic firs for the Midwestern United States: Interspecific variation in adaptive traits. Hort Sci 41:323–328
Kraus M, Ziegler H (1993) Quantitative analysis of abscisic acid in needles of Abies alba Mill. by electron capture gas chromatography. Trees Struct Funct 7:175–181
Kume S, Kobayashi F, Ishibashi M, Ohno R, Nakamura C, Takumi S (2005) Differential and coordinated expression of Cbf and Cor/Lea genes during long-term cold acclimation in two wheat cultivars showing distinct levels of freezing tolerance. Genes Genet Syst 80:185–197
Li CY, Puhakainen T, Welling A, Vihera-Aarnio A, Ernstsen A, Junttila O, Heino P, Pavla ET (2002) Cold acclimation in silver birch (Betula pendula). Development of freezing tolerance in different tissues and climatic ecotypes. Physiol Plant 116:478–488
MacDonald M, Lada R (2008) Cold acclimation can benefit only the clones with poor needle retention duration (NRD) in balsam fir. Hort Sci 43:1273
MacDonald M, Lada R, Martynenko AI, Dorais M, Pepin S, Desjardins Y (2010) Ethylene triggers needle abscission in root-detached balsam fir. Trees Struct Funct 24:879–886
Mitcham-Butler EJ, Hinesley L, Pharr D (1988) Effect of harvest date, storage temperature, and moisture status on postharvest needle retention of Fraser fir. J Environ Hort 6:1–4
Murphy EM, Ferrell WK (1982) Diurnal and seasonal changes in leaf conductance, xylem water potential, and abscisic acid of Douglas-fir [Pseudotsuga menziesii (Mirb.) Franco] in five habitat types. Forest Sci 28:627–638
Nielsen UB, Chastagner GA (2005) Genetic variation in postharvest needle retention among Nordmann fir families and grafted clones. Scand J Forest Res 20:304–312
Quarrie S, Whitford PN, Appleford NE, Wang TL, Cook SK, Henson IE, Loveys BR (1988) A monoclonal antibody to (S)-abscisic acid: its characterisation and use in a radioimmunoassay for measuring abscisic acid in crude extracts of cereal and lupin leaves. Planta 173:330–339
Rajasekaran LR, Blake TJ (1999) New plant growth regulators protect photosynthesis and enhance growth under drought of jack pine seedlings. J Plant Growth Regul 18:175–181
Reed BM (1993) Responses to ABA and cold acclimation are genotype dependent for cryopreserved blackberry and raspberry meristems. Cryobiology 30:179–184
Reich PB, Oleksyn J, Modrzynski J, Tjoelker MG (1996) Evidence that longer needle retention of spruce and pine populations at high elevations and high latitudes is largely a phenotypic response. Tree Physiol 16:643–647
Saxton AM (1988) A macro for converting mean separation output to letter groupings in Proc Mixed. In: Proceedings of the 23rd SAS users group international, pp 1243–1246
Schachtman D, Goodger J (2008) Chemical root to shoot signaling under drought. Trends Plant Sci 13:281–287
Thiagarajan A, Rajasekaran LR, Pepin S, Forney C, Desjardins Y, Dorais M (2012) Characterization of phytohormonal and postharvest senescence responses of balsam fir (Abies balsamea L. (Mill.)) to short-term low temperature exposure. Trees Struct Funct 26:1545–1553
Welling A, Moritz T, Palva ET, Junttila O (2002) Independent activation of cold acclimation by low temperature and short photoperiod in hybrid aspen. Plant Physiol 129:1633–1641
Zhang M, Yuan B, Leng P (2009) The role of ABA in triggering ethylene biosynthesis and ripening of tomato fruit. J Exp Bot 60:1579–1588
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Thiagarajan, A., Lada, R., Pepin, S. et al. Temperature and Photoperiod Influence Postharvest Needle Abscission of Selected Balsam Fir (Abies balsamea L. (Mill.)) Genotypes by Modulating ABA Levels. J Plant Growth Regul 32, 843–851 (2013). https://doi.org/10.1007/s00344-013-9349-1
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DOI: https://doi.org/10.1007/s00344-013-9349-1