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Middle Miocene palynoflora of the Legnica lignite deposit complex ...

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78<br />

and Osmunda are numerous (Sadowska et al.<br />

1976, 1981).<br />

The plant communities, both swamp and<br />

mesophilous forests outside <strong>the</strong> marsh basins,<br />

became once more fl oristically rich, and dominated<br />

by plants <strong>of</strong> relatively high climatic<br />

requirements, representing warm-temperate<br />

element, whereas palaeotropical element was<br />

distinctly poorer and with smaller taxonomic<br />

differentiation (Tab. 1). In comparison with<br />

<strong>the</strong> Lusatian seam <strong>the</strong> proportion <strong>of</strong> Tricolporopollenites<br />

pseudocingulum, Engelhardia,<br />

Quercoidites henrici, Araliaceae (excluding<br />

<strong>Legnica</strong> 7/58 pr<strong>of</strong>i le), and Ilex pollen is low.<br />

In addition, here <strong>the</strong>re are more pollen grains<br />

<strong>of</strong> Nyssa, Alnus, Quercus, and Fagus. Pollen<br />

grains <strong>of</strong> Tricolporopollenites liblarensis<br />

(+ T. fallax) occur sporadically (Sadowska et al.<br />

1976, 1981). The climate was warm-temperate<br />

and humid. There was again <strong>the</strong> time <strong>of</strong> slowly<br />

fl owing waters and large-area marshes with<br />

low peat-bogs on <strong>the</strong> accumulation terraces<br />

(Piwocki & Ziembińska-Tworzydło 1995, 1997).<br />

In <strong>the</strong> <strong>Legnica</strong> region swamp forests and bush<br />

swamps grew. In drier terrains <strong>the</strong>re existed<br />

favourable conditions for mixed mesophitic<br />

forests with <strong>the</strong> domination <strong>of</strong> warm-temperate<br />

taxa, and with an admixture <strong>of</strong> evergreen<br />

plants, mainly forming <strong>the</strong> undergrowth. In<br />

samples from <strong>the</strong> grey clays arctotertiary taxa<br />

prevail, but relatively high diversity <strong>of</strong> palaeotropical<br />

element (Tab. 1) points out a still<br />

warm, mild and humid climate, favourable for<br />

swamp and riparian plant communities.<br />

In pollen diagrams <strong>of</strong> <strong>the</strong>se sediments from<br />

various regions <strong>of</strong> Poland (both distant and<br />

near ones, even in <strong>the</strong> same locality), we can<br />

observe differences in contributions <strong>of</strong> pollen<br />

grains <strong>of</strong> individual taxa (genera and families),<br />

which refl ect changes <strong>of</strong> plant communities.<br />

These differences agree with <strong>the</strong> kind <strong>of</strong> sediment<br />

and are connected with changes <strong>of</strong> edafi c<br />

conditions. This problem has been studied by<br />

Dyjor and Sadowska (1977). On <strong>the</strong> basis <strong>of</strong><br />

pr<strong>of</strong>i les <strong>of</strong> <strong>the</strong> Henryk seam from many localities<br />

(Nowe Czaple, Tuplice, Staszów, Mirostowice,<br />

Gozdnica, Ruszów, Milików, Wołów,<br />

Łojowice, Jaworzyna, Żarów, Rusko, Jerzmanowa,<br />

Tarpno, Chróścina, and Wielowieś)<br />

<strong>the</strong> main features differing this seam from<br />

o<strong>the</strong>r ones have been given (Dyjor & Sadowska<br />

op. cit.). In addition, pr<strong>of</strong>i les from <strong>the</strong> Zielona<br />

Góra region (Sadowska et al. 1973, 1974), Żary<br />

and Mirosławice (=Mirostowice; Doktorowicz-<br />

Hrebnicka 1954, 1956b), Rogóźno <strong>deposit</strong> (Doktorowicz-Hrebnicka<br />

1961, Mam czar 1961),<br />

Konin region (Kremp 1949, Mamczar 1960),<br />

margin <strong>of</strong> <strong>the</strong> Bełchatów graben (Sadowska<br />

1974), upper coal series from Bełchatów<br />

(Kościelniak & Wanat 1974), and Ustronie<br />

(Ziembińska & Niklewski 1966, Ziembińska-<br />

Tworzydło 1974) were recognized as analogical<br />

ones. The main stratigraphic criterion was<br />

a variable percentage <strong>of</strong> pollen grains <strong>of</strong> <strong>the</strong>rmophilous<br />

families and genera (Quercoidites<br />

henrici, Myrica, Tricolporopollenites pseudocingulum,<br />

Engelhardia, Symplocos, Araliaceae,<br />

Araliaceae/Cornaceae, Araliaceoipollenites<br />

edmundi (=Tricolporopollenites edmundi),<br />

Itea, Arceuthobium, Meliaceae, Solanaceae,<br />

palms, and Tricolpopollenites liblarensis) in<br />

individual stages <strong>of</strong> <strong>the</strong> <strong>Miocene</strong>. In samples<br />

from <strong>the</strong> Henryk seam <strong>the</strong>y make up on <strong>the</strong><br />

average 5.8% (in comparison in <strong>the</strong> 2 nd Lusatian<br />

seam 14.9%, in <strong>the</strong> Kędzierzyn seam 2.5%).<br />

In comparisons <strong>of</strong> <strong>the</strong>se pr<strong>of</strong>i les <strong>the</strong> attention<br />

was also paid to percentage contribution <strong>of</strong> pollen<br />

grains <strong>of</strong> temperate and warm-temperate<br />

plants, including Abies, Picea, Tsuga, Sciadopitys,<br />

Betula, Carpinus, Corylus, Ostrya, Quercus,<br />

Fagus, Castanea, Ulmus, Celtis, Parrotia,<br />

and Acer. In samples from <strong>the</strong> Henryk seam<br />

<strong>the</strong>y make up an average <strong>of</strong> 25.4% (in <strong>the</strong> 2 nd<br />

Lusatian seam 17.5%, in <strong>the</strong> Kędzierzyn seam<br />

39.2%). Sporomorphs <strong>of</strong> <strong>the</strong> facial element<br />

have <strong>the</strong> highest frequency (60–80%) in all<br />

<strong>the</strong>se pr<strong>of</strong>i les. Their differentiation in individual<br />

pr<strong>of</strong>i les is a result <strong>of</strong> various ecological and<br />

regional conditions (Dyjor & Sadowska 1977).<br />

In many palynological pr<strong>of</strong>i les from <strong>the</strong><br />

Polish Lowland (for example from <strong>the</strong> Wyrzysk<br />

region – Kohlman-Adamska 1993) towards <strong>the</strong><br />

top <strong>of</strong> cores an increase <strong>of</strong> <strong>the</strong> contribution <strong>of</strong><br />

Alnus pollen grains can be observed, what is<br />

interpreted as a result <strong>of</strong> changes in taxonomical<br />

composition <strong>of</strong> <strong>the</strong> swamp forest. During <strong>the</strong><br />

sedimentation <strong>of</strong> <strong>the</strong> 2 nd Lusatian seam <strong>the</strong>re<br />

probably were forests with <strong>the</strong> domination <strong>of</strong><br />

Taxodium, Nyssa and Glyptostrobus, while<br />

during <strong>the</strong> sedimentation <strong>of</strong> <strong>the</strong> 1 st seam <strong>the</strong>re<br />

were forests with a considerable role <strong>of</strong> Alnus.<br />

In <strong>the</strong> <strong>Legnica</strong> pr<strong>of</strong>i les pollen grains <strong>of</strong> Alnus<br />

reach a few per cent in <strong>the</strong> Lusatian seam, in<br />

<strong>the</strong> Mużaków series – up to 70%, in <strong>the</strong> Henryk<br />

seam – up to 16%, and in <strong>the</strong> grey clay<br />

horizon – up to 50%. So, we can assume that<br />

during accumulation time <strong>of</strong> <strong>the</strong> Mid-Polish<br />

group <strong>of</strong> seams (Henryk seam) and grey clays

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