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

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<strong>the</strong> <strong>Middle</strong> <strong>Miocene</strong> and caused signifi cant<br />

extension <strong>of</strong> <strong>deposit</strong>s in fl uvial, lacustrine and<br />

swampy environments in <strong>the</strong> Polish Lowland<br />

area. Humid and warm-temperate climate close<br />

to subtropical one in <strong>Middle</strong> <strong>Miocene</strong> favoured<br />

<strong>the</strong> peat-producing vegetation, forming <strong>the</strong> 2 nd<br />

Lusatian group <strong>of</strong> seams (<strong>the</strong> Lusatian <strong>lignite</strong><br />

seam in <strong>the</strong> studied area). Origin <strong>of</strong> this seam<br />

is connected with extensive swamps occurring<br />

on coastal plains surrounded a bay <strong>of</strong> <strong>the</strong><br />

<strong>the</strong>n North Sea, extended far to <strong>the</strong> East. In<br />

western and partially central Poland, where<br />

this group <strong>of</strong> seams has a continuous range,<br />

<strong>the</strong> brown coal is <strong>of</strong> paralic origin, whereas<br />

in isolated basins in south-western, central<br />

and eastern Poland it is <strong>of</strong> limnic or limn<strong>of</strong>l<br />

uvial origin. The Lusatian group <strong>of</strong> seams is<br />

a marker <strong>of</strong> <strong>the</strong> great lithostratigraphical correlative<br />

importance, composed <strong>of</strong> 1–4 horizons<br />

usually making toge<strong>the</strong>r more than 3 m thick<br />

seam (Piwocki 1992, 1998).<br />

Presence <strong>of</strong> this seam in <strong>the</strong> <strong>Legnica</strong> <strong>deposit</strong><br />

<strong>complex</strong> has been confi rmed in boreholes from<br />

<strong>the</strong> west fi eld – <strong>Legnica</strong> 5/53, 7/49, 7/58, and<br />

8/59 (Sadowska et al. 1976), as well as <strong>the</strong><br />

east fi eld – <strong>Legnica</strong> 33/56, 41/52, 41/56, 41/64,<br />

47/55, 47/62, 47/68, and 53/56 (Sadowska et al.<br />

1981, Nowak 1998, Wacnik & Worobiec 2001).<br />

Two <strong>of</strong> <strong>the</strong>se cores (33/56 and 41/52) were<br />

subjects <strong>of</strong> current study. In all pr<strong>of</strong>i les from<br />

<strong>the</strong> <strong>Legnica</strong> <strong>deposit</strong> results <strong>of</strong> pollen analysis<br />

were similar. Pollen grains <strong>of</strong> conifers were<br />

numerous (mainly Taxodiaceae/Cupressaceae<br />

– up to 50%, with a signifi cant contribution<br />

<strong>of</strong> Sequoia, as well Pinus – up to 50%, with<br />

domination <strong>of</strong> Pinus sylvestris type). Among<br />

<strong>the</strong> angiosperms, pollen grains <strong>of</strong> Tricolporopollenites<br />

pseudocingulum (in previous studies<br />

misidentifi ed as Rhus), Quercoidites henrici<br />

(up to 15–25%), Araliaceoipollenites edmundi<br />

(=Tricolporopollenites edmundi), and o<strong>the</strong>r<br />

Araliaceae (up to 8–10%), as well as Myrica,<br />

Ilex, Alnus, Liquidambar, Nyssa, Quercus,<br />

Engelhardia, Ericaceae, and palms (usually<br />

less than 10%) prevailed. There were also found<br />

Abies, Sciadopitys, Betula, Fagus, Castanea,<br />

Ulmus, Carya, Rosaceae, Fabaceae (=Leguminosae),<br />

Symplocos, Celtis, and single pollen<br />

grains <strong>of</strong> o<strong>the</strong>r plants. Tricolporopollenites<br />

liblarensis (+ T. fallax) and T. cingulum were<br />

present in all pr<strong>of</strong>i les (Sadowska et al. 1976,<br />

1981, Nowak 1998, Wacnik & Worobiec 2001).<br />

In <strong>the</strong> <strong>Legnica</strong> <strong>deposit</strong> (for example in <strong>Legnica</strong><br />

47/68 pr<strong>of</strong>i le) <strong>the</strong> Lusatian seam is divided into<br />

73<br />

two horizons, what was caused by <strong>the</strong> situation<br />

<strong>of</strong> <strong>the</strong> <strong>deposit</strong> in <strong>the</strong> marginal zone <strong>of</strong> <strong>the</strong><br />

basin and strong lability <strong>of</strong> this zone during<br />

<strong>the</strong> sedimentation time (Sadowska et al. 1981).<br />

At Ruja it has a form <strong>of</strong> one compact seam in<br />

central part, and 2–3 (or more) horizons at <strong>the</strong><br />

western and nor<strong>the</strong>rn margins (Dyląg 1995).<br />

Plant communities, both <strong>the</strong> swamps and<br />

<strong>the</strong> mesophilous forests growing outside <strong>the</strong><br />

swampy basins, were fl oristically rich and had<br />

a relatively signifi cant contribution <strong>of</strong> plants<br />

<strong>of</strong> <strong>the</strong> palaeotropical ge<strong>of</strong>l ora, which contained<br />

<strong>the</strong> tropical (P1) and subtropical (P2) elements<br />

<strong>of</strong> large taxonomic differentiation (Tab. 1), with<br />

a considerable role <strong>of</strong> warm-temperate plants<br />

(A1). Picture <strong>of</strong> vegetation shown by <strong>the</strong> pollen<br />

diagrams (Figs 3–5) implies a warm and humid<br />

climate, favourable for abundant peat-producing<br />

vegetation. This was <strong>the</strong> warmest phase <strong>of</strong><br />

<strong>the</strong> <strong>Legnica</strong> pr<strong>of</strong>i les, when swamp and peat-bog<br />

vegetation dominated. Large areas were constantly<br />

covered by shallow water or marshes.<br />

Only on elevations <strong>the</strong>re existed patches <strong>of</strong><br />

riparian and mesophilous vegetation. Swamp<br />

forests were luxuriant and dominated by Taxodium,<br />

Glyptostrobus, Nyssa, and Alnus. In <strong>the</strong><br />

upper part <strong>of</strong> <strong>the</strong> bottom section <strong>of</strong> <strong>Legnica</strong><br />

33/56 pr<strong>of</strong>i le <strong>the</strong> contribution <strong>of</strong> bush swamp<br />

elements: Cyrillaceae, Clethraceae, Ericaceae,<br />

Ilex, and Myrica, as well as Sequoia increases,<br />

what indicates more mesophilous conditions<br />

during <strong>the</strong> sedimentation.<br />

Results <strong>of</strong> palynological investigations <strong>of</strong><br />

<strong>the</strong> <strong>Legnica</strong> pr<strong>of</strong>i les are similar to spectra<br />

from <strong>the</strong> 2 nd group <strong>of</strong> seams correlated with<br />

<strong>the</strong> V spore-pollen zone – Quercoidites henrici<br />

phase, distinguished by several authors<br />

(Ziembińska-Tworzydło & Ważyńska 1981,<br />

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

Ziembińska-Tworzydło 1998, Słodkowska<br />

1998). Deposits <strong>of</strong> this phase occur on large<br />

areas <strong>of</strong> <strong>the</strong> Polish Lowland, mainly in western,<br />

south-western (Nowe Czaple, Zielona Góra<br />

– Sadowska 1977), north-western and central<br />

(Wyrzysk region – Kohlman-Adamska 1993,<br />

Bełchatów B seam – Stuchlik et al. 1990, Lubstów<br />

near Konin – Ciuk & Grabowska 1991),<br />

as well as nor<strong>the</strong>rn parts (Grabowska 1987,<br />

Grabowska & Ważyńska 1997).<br />

Upper part <strong>of</strong> <strong>the</strong> bottom section <strong>of</strong> <strong>the</strong> <strong>Legnica</strong><br />

33/56 pr<strong>of</strong>i le refers to <strong>the</strong> VI spore-pollen<br />

zone – Tricolporopollenites megaexactus<br />

phase, previously distinguished as <strong>the</strong> Cyrillaceae<br />

phase by Raniecka-Bobrowska (1970)

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