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In vivo interspecific pollination success between Pinus radiata, P. maximinoi, P. oocarpa and P. tecunumanii

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Abstract

The objective of the study was to investigate in vivo interspecific pollination success between Pinus radiata, P. maximinoi, P. oocarpa and P. tecunumanii. Pinus radiata was control pollinated with pollen lots of P. maximinoi, P. oocarpa and P. tecunumanii in a P. radiata seed orchard at Karatara (Southern Cape, South Africa). Pollination success was determined by counting the number of visible ovules, pollen grains inside and outside P. radiata ovules, as well as pollen tubes visible inside P. radiata ovules. Conelets were harvested and studied at eight time intervals, including 24 h after pollination, and weekly for 7 weeks after pollination. Histology studies with a standard fixation-dehydration-embedding sequence and paraffin wax method were used to determine the number of visible pollen grains inside versus outside the ovules and number of pollen tubes. Results indicated that pollen grains did sift through the cone scales within 24 h after pollination. However, P. radiata differed significantly (time by type of cross interaction) from the other three hybrid combinations in terms of number of visible ovules, visible pollen grains inside and outside of the ovules as well as pollen tubes, confirming limited interspecific hybridisation success. Future studies need to determine the percentage of fertile ovules in cross combination as a tool in predicting pollination success.

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References

  • Bramlett DL (1981) Effectiveness of wind pollination in seed orchards. In: Franklin EC (eds) Pollen management handbook, USDA and Southern Forest Tree Improvement Committee, Agriculture Handbook nr. 587, Chapter 2

  • Bramlett DL, O’Gwynn CH (1981) Controlled pollination. In: Franklin ED (ed) Pollen management handbook. Agriculture Handbook Number 587, United States Department of Agriculture, Washington, pp 44–51

  • Brown S, Bridgewater F (1987) Observations on pollination in loblolly pine. Can J For Res 17:299–303

    Article  Google Scholar 

  • Cain S (1940) The identification of species in fossil pollen of Pinus by size-frequency determinations. Am J Bot 27:301–308

    Article  Google Scholar 

  • Caron G-E, Powell GR (1995) Pollen sizing in Jack pine (Pinus banksiana Lamb.) with a hemocytometer. Silvae Genetica 44:96–103

    Google Scholar 

  • Coetzee J (1982) Inleidende kursus in plantkundige mikrotegnieke [Introductory course in botanical microtechnics]. Stellenbosch University, Department of Botany, South Africa, p 80

  • Coura R, Prolla JC, Meurer L, Ashton-Prolla P (2005) An alternative protocol for DNA extraction from formalin fixed and paraffin wax embedded tissue. J Clin Pathol 58(8):894–895

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Critchfield WB (1975) Interspecific hybridisation in Pinus: a summary review. Symposium on interspecific and interprovenance hybridisation I forest trees. In: Fowler DP, Yeatman CY (ed) Proceedings 14th meeting, Canada tree improvement association part II. doi: https://www.treesearchfs.fed.us/pubs/32752

  • Dafni A, Pacini E, Nepi M (2005) Pollen and stigma biology. In: Dafni A, Kevan PG, Husband BC (eds) Practical pollination biology. Enviroquest Ltc., Cambridge, p 590

    Google Scholar 

  • Dungey HS, Carson MJ, Low CB, King NG (2003) Potential and niches for inter-specific hybrids with Pinus radiata in New Zealand. N Z J For Sci 33:295–318

    Google Scholar 

  • Dvorak WS (1985) One-year provenance/progeny results of Pinus tecunumanii from Guatemala established in Brazil and Colombia. Commonw For Rev 64:57–65

    Google Scholar 

  • Dvorak WS, Jordon AP, Hodge GP, Romero JL (2000) Assessing evolutionary relationships of pines in the Oocarpae and Australes subsections using RAPD markers. New For 20:163–192

    Article  Google Scholar 

  • Dvorak WS, Potter KM, Hipkins VD, Hodge GR (2009) Genetic diversity and gene exchange in Pinus oocarpa, a Mesoamerican pine with resistance to the pitch canker fungus (Fusarium circinatum). Int J Plant Sci 170:609–626

    Article  Google Scholar 

  • Ellstrand NC (2014) Is gene flow the most important evolutionary force in plants? Am J Bot 101:737–753

    Article  PubMed  Google Scholar 

  • Feder N, O’Brien TP (1968) Plant microtechnique: some principles and new methods. Am J Bot 55(1):123–142

    Article  Google Scholar 

  • Fernando DD (2014) The pine reproductive process in temperate and tropical regions. New For 45(3):333–352

    Article  Google Scholar 

  • Fernando DD, Long SM, Sniezko RA (2005) Sexual reproduction and crossing barriers in white pines: the case between Pinus lambertiana (sugar pine) and P. monticola (western white pine). Tree Genet Genomes 1:143–150

    Article  Google Scholar 

  • Funda T, Liewlaksaneeyanawin C, El-Kassaby YA (2014) Determination of paternal and maternal parentage in lodgepole pine seed: full versus partial pedigree reconstruction. Can J For Res 44(9):1122–1127

    Article  Google Scholar 

  • Greenwood MS (1980) Reproductive development in loblolly pine: I. The early development of male and female strobili in relation to the long shoot growth behavior. Am J Bot 67:1414–1422

    Article  Google Scholar 

  • Greenwood MS (1986) Gene exchange in loblolly pine: the relation between pollination mechanisms, female receptivity and pollen viability. Am J Bot 73:1433–1451

    Article  Google Scholar 

  • Griffin AR, Lindgren D (1985) Effect of inbreeding on production of filled seed in Pinus radiata—experimental results and a model of gene action. Theor Appl Genet 71:334–343

    Article  CAS  PubMed  Google Scholar 

  • Hagman M (1975) Incompatibility in forest trees. Proc R Soc Lond B 188:313–326

    Article  Google Scholar 

  • Hall JP, Brown IR (1977) Embryo development and yield of seed in Larix. Silvae Genetica 26:77–84

    Google Scholar 

  • Ham H, Botha A-M, Kanzler A, du Toit B (2017a) Pinus radiata interspecific hybridisation: environmental conditions inside pine pollination bags as a potential hybridisation barrier. Submitted to Annales of Forest Research, April 20th

  • Ham H, Botha A-M, Kanzler A, du Toit B (2017b) Pinus radiata hybridisation: pollen tube elongation and pollen grain size as possible reproductive barriers. Accepted but subjected to final corrections by iForest, April 30th

  • Ham H, du Plessis A, le Roux SG (2017c) Micro computer tomography (microCT) as a tool in Pinus tree breeding: case study. N Z J For Sci 47(1):2–8

    Article  Google Scholar 

  • Harushima Y, Nakagahra M, Yano M, Sasaki T, Kurata N (2001) A genome-wide survey of reproductive barriers in an interspecific hybrid. Genetics 159:883–892

    CAS  PubMed  PubMed Central  Google Scholar 

  • Huyn SK (1976) Interspecific hybridization in pines with the special reference to Pinus rigida x taeda. Silvae Genetica 25:188–191

    Google Scholar 

  • Johnsson H (1976) Contributions to the genetics of empty grains in the seed of pine (Pinus sylbestris). Silvae Genetica 25:10–15

    Google Scholar 

  • Konar R, Oberoi Y (1969) Recent work on reproductive structures of living conifers and taxads—a review. Bot Rev 35:89–116

    Article  Google Scholar 

  • Kormanik PP (1974) Conelet abortion in pines. In: Kraus J (ed) Seed yield from southern pine seed orchards. Georgia Forest Research Council, Macon, pp 42–48

    Google Scholar 

  • Lanner RM (1966) Needed: a new approach to the study of pollen dispersion. Silvae Genetica 15:50–52

    Google Scholar 

  • Lill BS (1976) Ovule and seed development in P. radiata D. Don: post meiotic development, fertilisation and embryogeny. Can J Bot 54:2141–2154

    Article  Google Scholar 

  • Lindgren D (1975) The relationship between self-fertilization, empty seeds and seeds originating from selfing as a consequence of polyembryology. Studia Forestalia Suecica 126

  • Little TM, Hills FJ (1978) Statistical methods in agricultural experimentation. University of California, Davis

    Google Scholar 

  • Major JE, Mosseler A, Johnsen KH, Rajora OP, Barsi DC, Kim K-H, Park J-M, Campbell M (2005) Reproductive barriers and hybridity in two spruces, Picea rubens and Picea mariana, sympatric in eastern North America. Can J Bot 83:163–175

    Article  Google Scholar 

  • Mathews S, Kramer EM (2012) The evolution of reproductive structures in seed plants: an r-examination based on insights from developmental genetics. New Phytol 194:910–923

    Article  CAS  PubMed  Google Scholar 

  • McWilliam JR (1958) The role of the micropyle in the pollination of Pinus. Bot Gaz 2:109–117

    Article  Google Scholar 

  • McWilliam JR (1959) Interspecific incompatibility in Pinus. Am J Bot 46:425–433

    Article  Google Scholar 

  • Mert C, Soylu A (2006) Flower and stamen structures of male-fertile and male-sterile chestnut (Castanea sativa Mill.) cultivars. J Am Soc Hortic Sci 131:752–759

    Article  Google Scholar 

  • Moody WR, Jett JB (1990) Effects of pollen viability and vigor on seed production of loblolly pine. South J Appl For 14:33–38

    Article  Google Scholar 

  • Moran GF, Griffin AR (1985) Non-random contribution of pollen in polycrosses of Pinus radiata D. Don. Silvae Genetica 34:117–121

    Google Scholar 

  • Moran GF, Bell JC, Matheson AC (1980) The genetic structure and levels of inbreeding in a Pinus radiata D. Don seed orchard. Silvae Genetica 29:190–193

    Google Scholar 

  • Nel A, van Staden J (2003) Micro-fibre pollination bags and high viability Pinus patula pollen enhance cone survival and seed set during controlled pollination. S Afr J Bot 69:469–475

    Article  Google Scholar 

  • Nel A, van Staden J (2005) Pollen morphological features of temperature on pollen germination of various Pinus species. S Afr J Bot 71:88–94

    Article  Google Scholar 

  • O’Leary S, von Aderkas P (2006) Post pollination drop production in hybrid larch is not related to the diurnal pattern of xylem water potential. Trends Ecol Evol 20:61–66

    Google Scholar 

  • Ott RL, Longnecker M (2001) An introduction to statistical methods and data analysis, 5th edn. Duxbury Press, Belmont, p 1273

    Google Scholar 

  • Owens JN, Bruns D (2000) Western white pine (Pinus monticola Dougl.) reproduction: I. Gametophyte development. Sex Plant Reprod 13:61–74

    Article  Google Scholar 

  • Owens JN, Fernando DD (2007) Pollination and seed production in western white pine. Can J For Res 37:260–275

    Article  Google Scholar 

  • Owens JN, Simpson SJ, Molder M (1981) Sexual reproduction of Pinus contorta. I. Pollen development, the pollination mechanism, and early ovule development. Can J Bot 59:1828–1843

    Article  Google Scholar 

  • Owens JN, Bennett J, L’Hirondelle S (2005) Pollination and cone morphology affect cone and seed production in lodgepole pine seed orchards. Can J For Res 35:383–400

    Article  Google Scholar 

  • Plomoin C, Chagné D, Pot D, Kumar S, Wilcox PL, Burdon RD, Prat D, Peterson DG, Paiva J, Chaumeil P, Vendramin GG, Sebastiani F, Nelson CD, Echt CS, Savolainen O, Kubisiak TL, Cervera MT, de Marìa N, Islam-Faridi MN (2007) Pines. In: Kole C (ed) Genome mapping and molecular breeding in plants, forest trees, vol 7. Springer, Berlin, p 220

    Google Scholar 

  • Santos-del-Blanco L, Climent J (2014) Costs of female reproduction in a conifer tree: a whole-tree level assessment. J Ecol 102(5):1310–1317

    Article  Google Scholar 

  • Sarvas R (1962) Investigations on the flowering and seed crop of Pinus sylvestris. Commun Inst Fenn 53:1–198

    Google Scholar 

  • Sass EJ (1958) Botanical microtechnique. Iowa State University Press, Iowa Ames, p 228

    Google Scholar 

  • Schwendemann AB, Wang G, Mertz ML, McWilliams RT, Thatcher SL, Osborn JM (2007) Aerodynamics of saccate pollen and its implications for wind pollination. Am J Bot 94:1371–1381

    Article  PubMed  Google Scholar 

  • Shapiro SS, Wilk MB (1965) An analysis of variance test for normality (complete samples). Biometrika 52:591–611

    Article  Google Scholar 

  • Slee MU, Abbott DC (1990) Pollination investigations for production of the hybrid between slash and Caribbean Pines. South Afr For J 152:7–16

    Google Scholar 

  • Solga MJ, Harmon JP, Ganguli AC (2014) Timing is everything: an overview of phenological changes to plants and their pollinators. Nat Areas J 34:227–234

    Article  Google Scholar 

  • Stephenson AG (1981) Flower and fruit abortion: proximate causes and ultimate functions. Ann Rev Ecol Syst 12:253–279

    Article  Google Scholar 

  • Sweet GB (1977) Pollination in Pinus radiata. N Z J For Sci 7(1):21–34

    Google Scholar 

  • Sweet GB, Thulin IJ (1969) The abortion of conelets in Pinus radiata. N Z J For 14:59–67

    Google Scholar 

  • Tjoel DM (1983) AGS (Alcian Green Safranin)—a simple differential staining of plant material for the light microscope. In: Royal Microscopical Society (ed) Proceedings—royal microscopical society, vol 18, pp 149–151

  • Tomlinson P (1994) Functional morphology of saccate pollen in conifers with special reference to the Podocarpaceae. Int J Plant Sci 155:699–715

    Article  Google Scholar 

  • Tomlinson P, Braggins J, Rattenbury J (1997) Contrasted pollen capture mechanisms in Phyllocladaceae and certain Podocarpaceae (Coniferales). Am J Bot 84:214–223

    Article  CAS  PubMed  Google Scholar 

  • Trigiano RN, Gray DJ (2011) Plant tissue culture, development, and biotechnology. CRC Press, Boca Raton, p 608

    Google Scholar 

  • Varis S, Santanen A, Pakkanen A, Pulkkinen P (2008) The importance of being the first pollen in the strobili of Scots pine. Can J For Res 38:2976–2980

    Article  Google Scholar 

  • Williams CG (2009) Conifer reproductive biology. Springer, Berlin, p 172

    Book  Google Scholar 

  • Winsor L (1994) Tissue processing. Laboratory histopathology. Churchill Livingstone, New York. Available online: https://www.researchgate.net/file.PostFileLoader.html?id=5536a4d8d767a649648b4575&assetKey=AS%3A273761889128455%401442281329466. Assessed 20 Nov

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Acknowledgements

We would also like to thank the MTO Forestry research team for technical support, Mardé Booysen for assistance with the statistical analyses, and Bill Dvorak for guidance during project initiation.

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Correspondence to Hannél Ham.

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Project funding: This work was financially supported by the grants from the National Research Foundation (TP 1207 122 754), Department of Agriculture, Forestry and Fisheries, Mountain to Ocean, and Camcore.

The online version is available at http://www.springerlink.com

Corresponding editor: Yu Lei.

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Ham, H., Botha, AM., Kanzler, A. et al. In vivo interspecific pollination success between Pinus radiata, P. maximinoi, P. oocarpa and P. tecunumanii. J. For. Res. 30, 817–826 (2019). https://doi.org/10.1007/s11676-018-0653-2

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