Summary
The distributions of Primula vulgaris, P. elatior and P. veris in the British Isles are partly dependent on differences in waterlogging and drought tolerance. Comparison of biomass production and root length on soils with different water tables ranked the species in order of increasing waterlogging-tolerance: P. veris < P. vulgaris < P. elatior. P. veris and P. vulgaris were most sensitive to waterlogging during the first three months of growth. Waterloggingtolerance in P. elatior was associated with the ability to maintain an oxygen flux from the roots in anoxic media, which was not present in the other species. Solution culture experiments indicated that poor growth of P. vulgaris on saturated soils was a consequence of anoxia but gave no explanation for the waterlogging-intolerance of P. veris.
Maximum photosynthetic rate recovered rapidly in P. vulgaris and P. veris following drought. In P. elatior, however, recovery was slower and associated with the production of new leaf area. Older, wilted leaves senesced rapidly and reduced the overall photosynthetic performance of the plant. Comparison of cumulative water loss on a leaf area basis against the proportion of maximum photosynthetic rate prior to soil drought, ranked the species in order of increasing drought tolerance; P. veris>vulgaris>elatior.
The habitats of P. vulgaris and P. elatior are recognisably distinct where the species occur together as a consequence of differences in their drought and waterloggingtolerances. Amongst other factors, the more developed drought tolerance of P. veris enables it to exploit drier, more open, situations.
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References
Abeywickrama BA (1949) Ph D dissertation, University of Cambridge. A study of the field layer vegetation of two Cambridgeshire woodlands
Adamson RS (1910) Note on the relationships of P. elatior and P. vulgaris to soil conditions. Trans Bot Soc Edinb 24:84–86
Armstrong W (1967a) The use of polarography in the assay of oxygen diffusing from roots in anaerobic media. Physiologia Plant 20:540–553
Armstrong W (1967b) The oxidising activitiy of roots in waterlogged soils. Physiologia Plant 20:920–926
Armstrong W, Boatman DJ (1967) Some field observations relating the growth of bog plants to conditions of soil aeration. J Ecol 55:101–110
Armstrong W, Wright EJ (1975) A polarographic assembly for multiple sampling of soil oxygen flux in the field. J appl Ecol 13:849–856
Bartlett RJ (1961) Iron oxidation proximate to plant roots. Soil Sci 92:372–379
Boggie R (1972) Effect of water table height on root development of Pinus contorta on deep peat in Scotland. Oikos 23:304–312
Bradfield EG, Gultridge CG (1979) the dependance of calcium transport and leaf tipburn in strawberry on relative humidity and nutrient solution concentration. Ann Bot 43:363–372
Bunce JA, Chabot BF, Miller LN (1979) Role of annual leaf carbon balance in the distribution of plant species along an elevational gradient. Bot Gaz 140:288–294
Cannon WA (1940) Oxygen relations in Hydrophytes. Science, NY 91:43–44
Christy RM (1884) On the species of the genus Primula in Essex; with observations on their variation and distribution, and their relative numbers and fertility in nature of the two forms of flower. Trans Essex Field Club 3:148–211
Forster E (1844) Note on Primula elatior. Phytologist 1:974–975
Gaastra P (1959) Photosynthesis of crop plants as influenced by light, CO2, temperature and stomatal diffusive resistance. Meded Langhoogesch Wageningen 59:1–68
Gilbert EG (1903) The oxlip, cowslip and primrose. J Bot (Lond) 41:280–282
Good RD (1944) On the distribution of primrose in a southern county. Naturalist (Hull) p 41–46
Harper JL, Sagar GR (1953) Some aspects of the ecology of buttercups in permanent grassland. Proc Br Weed Control Conf 1:256–265
Healy MT, Armstrong W (1972) The effectiveness of internal oxygen transport in a mesophyte (Pisum sativum L). Planta 103:302–309
Hegi G (1924) Illustrierte Flora von Mittel-Europa 5(3) Carl Hanser, München
Keith-Lucas M (1968) PhD dissertation, University of Cambridge. Shade tolerance in Primula
Ludlow MM, Ng TT, Ford CW (1980) Recovery after water stress of leaf gas exchange in Panicum maximum var trichoglume. Aust J Pl Phys 7:299–313
Martin MH (1968) Conditions affecting the distribution of Mercurialis perennis in certain Cambridgeshire woodlands. J Ecol 56:777–793
Malloch AJC (1971) Vegetation of the maritime cliff tops of the Lazard and Lands End Peninsulas, West Cornwall. New Phytol 70:115–1197
Packham JR, Willis AJ (1977) The effects of shading on Oxalis acetosella. J Ecol 65:619–643
Poszwinska J (1965) Introgression between Primula elatior and P. officinalis. Acta Soc Bot Polon 34:45–71
Rackham O (1980) Ancient woodlands: its history vegetation and uses in England. Edward Arnold, London
Valentine DH (1948) Studies in British Primulas. II Ecology and taxonomy of primrose and cowslip. New Phytiol 47:111–130
Valentine DH (1966) The experimental taxonomy of some Primula species. Trans Bot Soc Edinb 40:169–180
Weirsum LK (1960) Some experiences in soil aerobic measurements and relationsships to depth of rooting. Neth J Agric Sci 8:245–252
Whale DM (1982a) Ph D dissertation, University of Oxford. A physiological study of habitat preference in Primula species
Whale DM (1982b) Measurement of O2 flux in two woodland soils. Soil and Plant 68:353–359
Whale DM (1983) Laboratory and field studies of seasonal changes in gas exchange characteristics of Primula species. Oecologia (Berlin) (In press)
Woodell SRJ (1969) Natural hybridization in Britain between the primrose and the oxlip. Watsonia 7:115–127
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Whale, D.M. The response of Primula species to soil waterlogging and soil drought. Oecologia 58, 272–277 (1983). https://doi.org/10.1007/BF00399231
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DOI: https://doi.org/10.1007/BF00399231