Wetland forests, known as coal forests, extended over large areas of the palaeotropics during the Late Carboniferous and the Permian Periods. They were initiated during the Serpukhovian Age as a response to lowering sea levels having exposed large areas of continental shelf. They expanded dramatically during the late Bashkirian Age, but then contracted by over one‐half during the Kasimovian Age. The estimated loss of carbon sink probably resulted in an annual increase in atmospheric CO2 of about 2–5 ppm, and coincided with clear evidence of global warming in both the northern and southern high latitudes. A return to cooler conditions in very Early Permian times coincided with an expansion of the palaeotropical coal forests in the Far East, but this was short‐lived and most of the rest of the Permian was a time of global warming. The Palaeozoic evidence clearly confirms that there is a correlation between levels of atmospheric CO2 and global climates. However, care must be taken in extrapolating this evidence to the present‐day tropical forests, which do not act as a comparable unsaturated carbon sink.

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IMPF: 00.66A synthesis of the upper Moscovian sedimentotogical and palaeontological record of terrestrial habitats across the Variscan foreland and adjacent intramontane basins (an area which is referred to here as Variscan Euramerica) suggests a contraction and progressive westward shift of the coal swamps. These changes can be correlated with pulses of tectonic activity (tectonic phases) resulting from the northwards migration of the Variscan Front. This tectonic activity caused disruption to the landscapes and drainage patterns where the coat swamps were growing, which became less suitable to growth of the dominant plants of the swamps, the arborescent lycopsids. They were progressively replaced by vegetation dominated by marattialean ferns, which through a combination of slower growth and larger canopies resulted in less evapo-transpiration. This in turn caused localised reductions in rainfall, which further affected the ability of the lycopsids to dominate the swamp vegetation. These changes were initially localised and where the coat swamps were able to survive the lycopsids and pteridosperms show little change in either species diversity or biogeography, indicating that at this time there was minimal regional-scale climate change taking place. By Asturian times, however, the process had accelerated and the swamps in Variscan Euramerica became progressively replaced by predominantly conifer and cordaite vegetation that favoured much drier substrates. Except in localised pockets in intramontane basins of the Variscan Mountains, the last development of coat swamps in Variscan Euramerica was of early Cantabrian age. Further west, lycopsid-dominated coal swamps persisted for a little longer. The last remnants of the lycopsid-dominated coal swamps in the Illinois Basin disappeared probably by middle-late Cantabrian times, as the cycle of contracting wetlands and regional reductions in rainfall generated its own momentum, and no longer needed the impetus of tectonic instability. This tectonically-driven decline in the Euramerican coal swamps was probably responsible for an annual increase in atmospheric CO2 of c. 0.37 ppm, and may have been implicated in the marked increase in global temperatures near the Moscovian - Kasimovian boundary, and the onset of the Late Pennsylvanian interglacial.Peer reviewe

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The South Wales Coalfield has the most complete Westphalian macrofloral record anywhere on the Variscan Foreland or adjacent basins, with 135 biodiversity-meaningful morphospecies having been recognized. All of the standard macrofloral biozones of the Westphalian Stage have been recognized, although a detailed comparison with the Central Pennines Coalfields has indicated some discrepancies in the relative positions of the biozonal boundaries. Total Species Richness progressively increases through the Langsettian Substage, and then remains relatively stable through most of the Duckmantian and Bolsovian substages. There is a distinct reduction in Total Species Richness towards the top of the Bolsovian Substage, but this partially recovers in the middle Asturian Substage with the appearance of a range of marattialean ferns, and medullosalean and callistophytaleans pteridosperms. There is no evidence of any significant drop in Total Species Richness towards the top of the succession, indicating that conditions at this time were relatively stable. The change from coastal floodplain to alluvial braidplain conditions in middle Bolsovian times correlates with a marked increase in the proportion of medullosalean remains being preserved in the adpression record, reflecting an expansion of the clastic-substrate habitats.

Cactus ackermannii LindleyLindley (1830) did not mention any preserved specimen, but he utilized a description by Haworth (1829), which was based on a living specimen, "examined ... at Mr. Tate's choice nursery". Lindley's

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