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Terrestrial Palaeoecology and Global Change

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Chapter 3. <strong>Palaeoecology</strong><br />

69<br />

etum, a pioneer stream-side growths fringing distributary channels, represented by allochthonous<br />

material alone, replaced toward the delta interior by (5) Elatididetum expansae,<br />

a back-marsh bog forest, of the widest facies range, merging on (6) Elatidi-<br />

Pityophylletum, a coniferous peat-bog assemblage, <strong>and</strong> (6) Elatidi-Nilssoniopteridetum,<br />

a bennettitalean peat-bog shrubl<strong>and</strong>. The allochthonous Phoenicopsis <strong>and</strong> Ginkgoites<br />

represent dryl<strong>and</strong> vegetation.<br />

Of special interest is the succession of osmundaceous ferns: Cladophlebis kamenkensis<br />

– C. denticulata – Todites (Cladophlebis) williamsonii – Todites (Cladophlebis)<br />

haiburnensis, perhaps reflecting a zonation of the fern-marh community partly<br />

extending over the horsetail mire <strong>and</strong> ascending as understorey to the Elatidion.<br />

Many uncertainties remained that could only be resolved by comparison with analogous<br />

successions in other sedimentary basins.<br />

Umalta. In the mid-Jurassic (Callovian) regressive sequence of Umalta, Bureya Basin,<br />

Russian Far East, Dicksonia (Coniopteris) burejensis <strong>and</strong> Osmunda diamensis are<br />

dominant in the basal deltaic facies that rest conformably on shallow marine s<strong>and</strong>stones<br />

with ammonite shells <strong>and</strong> still contain marine phytoplankton, as well as occasional limulid<br />

remains. The catenic position of the fern assemblage might have been as at Kamenka<br />

(above). Horsetails, much smaller than at Kamenka, patchily occur as an edaphic variant<br />

of the coastal marshl<strong>and</strong>. Bulk maceration of a fern bed soil brought fossil mites,<br />

diverse bryophytes of the ground cover (Krassilov, 1973c), fern sporangia, as well as<br />

scattered scale-leaves <strong>and</strong> shoot fragments of Elatides ovalis, the latter dominant in the<br />

next catenic assemblage upsection, the back-marsh Elatidion.<br />

This, however, is less prominent than at Kamenka. Conversely, Czekanowskia (with<br />

Leptostrobus-type cupules) is more abundant in the flood-plain deposits. Leaf-mats grading<br />

on leaf-coals consist of Czekanowskia accompanied, or locally replaced, by a needleleaved<br />

conifer Pityophyllum or a narrow-leaved ginkgophyte Pseudotorellia. Their<br />

frequent associates are Osmunda diamensis <strong>and</strong> Sphenobaiera, a ginkgophyte with<br />

deeply dissected leaves. Nilssonia, Podozamites <strong>and</strong> their reproductive remains cooccur<br />

with Czekanowskia in the coarser levee facies.<br />

The peatl<strong>and</strong> vegetation is thereby reconstructed as a Pityo-Pseudotorellietum (Sphenobaieretum)<br />

mosaic marginally admixed with a riparian Czekanowskietum <strong>and</strong> with a<br />

fern growth as understorey or over the gaps. All plant assemblages of this stage contain<br />

allochthonous remains of Phoenicopsis, which comes to dominance over a sequence of<br />

the fluvial s<strong>and</strong>stone/siltstone cyclothems above.<br />

Seral links between Czekanowskia, a pioneer form of the delta-plain to flood-plain<br />

alluvium, <strong>and</strong> Phoenicopsis, a lowl<strong>and</strong> climax dominant, are confirmed by repeated<br />

observations of their stratigraphic successions <strong>and</strong> concurrent facies changes in a large<br />

number of Siberian localities (II.7.1). Over the Umalta Section, their succession is catenic,<br />

as well as seral.<br />

The regressive sequence is overlain by a series of coal-bearing cyclothems, in<br />

which an avulsion autocyclicity is periodically truncated by a thick lamellate s<strong>and</strong>-

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