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Filipendula ulmaria (Meadow Sweet)
The macrofossil evidence for Filipendula ulmaria is considerable, consisting of carpels that have lost their outer coat and have an asymmetric twisted form, crescentic in the side view and are quite recognisable when in this form and also when entire (Godwin 1975). They are also distinguishable from Filipendula vulgaris. The pollen grains of the two Filipendula species are not readily distinguishable and so fossil pollen records are not separated beyond the genus level. The recovery of Filipendula pollen in association with F. ulmaria macrofossils (Godwin 1975) encouraged the general attribution of fossil Filipendula grains to F. ulmaria, although some may well be F. vulgaris. Filipendula pollen has been recorded in all phases of all interglacials since the Cromerian (oxygen isotope stage 11) and in all sub-stages of the subsequent interglacials. Pollen records also occur from earlier interglacial contexts and from the early and late phases of glacial cold stages (Godwin 1975). Filipendula pollen is present in significant percentages in both the early and middle Devensian, but reaches high frequencies during the Devensian Late Glacial period and the transition to the Holocene. Although Filipendula is a high pollen producer, the evidence suggests that it was abundant during these periods, as it occurs in almost every site investigated and often in high percentages. Godwin (1975) notes that F. vulgaris is characteristic of present day cold steppe grassland and so the Devensian records may be referable to that species. The abundance of marshy habitats suitable for F. ulmaria in the Late Devensian, however, supports that as the species responsible for Late Glacial Filipendula abundance, especially as Filipendula ulmaria is today an important component of the kind of tall herb vegetation communities which were typical under Late Glacial environmental conditions. Great reductions in pollen frequencies for Filipendula during the cold and arid Late Devensian Stadial also suggest that F. ulmaria was the species involved. Filipendula ulmaria is also regarded as a thermophilous plant and was abundant in the early tall herb stage of transitional vegetation succession towards shrub and tree cover at the start of the Holocene. Such short-lived successional population expansion of thermophilous taxa on base-rich soils after climatic amelioration is typical of protocratic phase vegetation before tall shrub and tree expansion occurred (Birks 1986). The temporary high frequencies of Filipendula pollen will reflect the abundance of the plant around shallow lakes and marshes where it would be locally dominant in the earliest Holocene. Filipendula pollen is present throughout the rest of the Holocene in low frequencies and the species remained present in wetland communities as it does today. Higher pollen frequencies in the later Holocene are probably due to a spread of wetland habitats with climatic deterioration and are most apparent at sites in western parts of the British Isles (Godwin 1975). Clearance of woodland would have assisted that change and also increased the flowering and pollen transport of Filipendula. The pollen record indicates a probably continuous presence of Filipendula in the British Isles through several glacial/interglacial cycles (Godwin, 1975).

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