Anne Raymond

CARBONIFEROUS PALEOGEOGRAPHIC, PHYTOGEOGRAPHIC, AND PALEOCLIMATIC RECONSTRUCTIONS

Abstract Two revised paleogeographic reconstructions of the Visean and Westphalian C-D stages are presented based on recent paleomagnetic, phytogeographic, stratigraphic, and tectonic data. These data change the positions of some continental blocks, and allow the definition of several new ones. The most important modifications that have been incorporated in these reconstructions are: (1) a proposed isthmus linking North America and Siberia across the Bering Strait; and (2) the separation of China and Southeast Asia in six major blocks, including South China, North China, Shan Thai-Malaya, Indochina, Qangtang, and Tarim blocks. Evidence is presented that suggests that at least the South China, Shan Thai-Malaya, and Qangtang blocks were derived from the northern margin of Gondwana. Multivariate statistical analysis of phytogeographic data from the middle and late Paleozoic allow definition of a number of different phytogeographic units for four time intervals: (1) the Early Devonian, (2) Tournaisian—early Visean, (3) Visean, and (4) late Visean—early Namurian A. Pre-late Visean—early Namurian A floral assemblages from South China show affinities with northern Gondwana floras suggesting a southerly position and provides additional support for our reconstruction of South China against the northern margin of Gondwana. There is a marked decrease in the diversity of phytogeographic units in the Namurian and younger Carboniferous. This correlates closely with the time of assembly of most of Pangaea. The general pattern of Carboniferous phytogeographic units corresponds well with global distribution of continents shown on our paleogeographic reconstructions. In addition, we have constructed paleoclimatic maps for the two Carboniferous time intervals. These maps stress the distribution of rainfall, as this should be strongly correlated with the floras. There is marked change in the rainfall patterns between the Visean and Westphalian C-D. This change corresponds with the closing of the Appalachian-Ouachita ocean between Laurussia and Gondwana, and reflects the removal of a low-latitude moisture source that probably gave rise to monsoonal conditions along the northern margin of Gondwana in the Visean and earlier times. As well, the presence of a substantial heat source at high elevation in the Late Carboniferous significantly influenced the distribution of climatic belts.

Coal, climate and terrestrial productivity: the present and early Cretaceous compared

Abstract At the present time, rainfall sufficient and consistent enough for swamp formation and peat preservation occurs in the equatorial and temperate belts. Evaporite deposits and aeolian sandstones occur in the consistently dry areas, while the intermediate areas of seasonal rainfall tend not to have any of these climatically significant sediments. In the Cretaceous, the temperate belts are well represented by coals as today, but the tropical belt is not, and the same can be said of other Mesozoic and early Cenozoic periods. Instead, the tropics are represented by low diversity floras and sediments, like the Nubian Sandstone, which can be interpreted as representative of climates in which precipitation was markedly seasonal. The inference is that the Intertropical Convergence Zone was less latitudinally confined during the warmer ‘greenhouse’ periods, and that this might have been due to weaker polar fronts.

Rates of burial and disturbance of experimentally-deployed molluscs; implications for preservation potential

Rates of burial and transport of molluscan remains are essentially unknown for deeper continental shelf and slope environments, especially over periods of years. An understanding of the rates of taphonomic loss are critical to paleoecological analyses and to paleoenvironmental studies in general. The post-depositional history of organic remains is highly dependent on the length of time the material remains at or near the sediment/water interface. In order to measure these rates, 100 gastropod and bivalve shells were scattered over a marked area of sea bottom at 21 sites in seven environments of deposition (EOD9s) in the Gulf of Mexico and at five EOD9s on the Bahamas platform edge. A total of over 2600 shells were deployed. Each site was thoroughly documented with video photography. After one year in the Bahamas and after two years in both the Gulf of Mexico and Bahamas, these sites were re-photographed and video-taped to measure rates of burial and movement of shells. Shell condition (e.g., articulation, encrustation, and color loss) for those shells that remained exposed was also determined. Shells deployed in Gulf of Mexico petroleum seep sites, on the open continental shelf, and on the continental slope experienced high rates of burial (0.5-3.0 cm) within two years. Shells at these sites generally were not transported or disturbed, and disarticulation rates were low. In the Bahamas, shells on the platform shelf were completely buried within one year. On the steep platform edge from 70 to 300 m, shells on hardground ledges remained exposed, whereas shells in carbonate sands were buried by up to 3.5 cm of sediment. Transport was more common on the steep slopes of the platform edge. Net sedimentation rates for the outer continental shelf and slope of 0.01-0.06 cm yr-1 are well below our observed burial rates of 31 cm yr (super -1) . Thus, burial rate may be somewhat independent of sedimentation rate due to local reworking of sediments by storms at shallower depths and mechanisms such as deep bottom currents or bioturbation at deeper sites. Therefore, the potential for fossil preservation in offshore areas with low sedimentation rates may be much greater than previously assumed.

Laurussian land-plant diversity during the Silurian and Devonian: mass extinction, sampling bias, or both?

In phytogeographic data sets, the number of assemblages or floras from each interval may provide a test of the influence of sampling intensity on land-plant diversity. Using a data set of Silurian and Devonian compression-impression plant genera from Laurussia and the Acadian terrain, regression of five measures of land-plant diversity (total diversity, mean genus richness of floras, median assemblage diversity, most diverse assemblage, and standing diversity at interval boundaries) against the number assemblages or floras from thirteen intervals suggests that sampling bias influences all of the diversity measures to some extent, including within-habitat measures. The standing diversity of land plants at interval boundaries, the measure least influenced by sampling ( r = 0.65, p = 0.05), increased steadily from the Middle Silurian to the late Givetian/early–middle Frasnian boundary, fell sharply in the early–middle Frasnian and remained low throughout the late Frasnian–middle Famennian. Standing diversity rose dramatically in the late Famennian and Strunian (latest Devonian): the Frasnian–Famennian extinction event may have affected land plants. The standing diversity of Silurian and Devonian microspore genera at interval boundaries mirrors that of compression-impression genera: neither record supports a land-plant diversity equilibrium during the Devonian.

Taphonomy on the continental shelf and slope: two-year trends ^ Gulf of Mexico and Bahamas

Abstract The Shelf and Slope Experimental Taphonomy Initiative was established to measure taphonomic rates in a range of continental shelf and slope environments of deposition (EODs) over a multiyear period. We deployed experiments on the forereef slope off Lee Stocking Island, Bahamas, and on the continental shelf and slope of the Gulf of Mexico for 2 yr in 18 distinctive EODs at depths from 15 to 530 m. Overall, most shells deployed at most sites had relatively minor changes in shell condition. Most EODs generated relatively similar taphonomic signatures. A few sites did produce taphonomic signatures clearly distinguishable from the central group and these sites were characterized by one or more of the following: high rates of oxidation of reduced compounds, presence in the photic zone, and significant burial and exhumation events. Thus, unique taphonomic signatures are created by unique combinations of environmental conditions that include variables associated with regional gradients, such as depth and light, and variables associated with edaphic processes, such as the seepage of brine or petroleum or the resuspension and redeposition of sediment. Most sites, however, showed similar taphonomic signatures, despite the variety of EOD characteristics present, suggesting that insufficient time had elapsed over 2 yr to generate a more diverse array of taphonomic signatures. Discoloration and dissolution were by far the dominant processes over the 2-yr deployment period. Periostracum breakdown, loss of shell weight, and chipping and breakage was less noticeable. EODs were chosen based on the expectation that the process of burial and the influence of depth and sediment type should play the greatest roles in determining between-EOD differences in taphonomic signature. EOD-specific edaphic factors often overrode the influence of geographic-scale environmental gradients. Taphonomic alteration was greater on hardgrounds and in brine-exposed sites than on terrigenous muds. Dissolution was less effective at sites where burial was greatest. Discoloration occurred most rapidly at shallower sites and on hardgrounds. Water depth was less influential in determining taphonomic signature than burial state or sediment type. The limited influence of water depth is likely due to the presence of shallow sites that, for one reason or another, were protected from certain taphonomic processes and deeper sites that were characterized by unusually strong taphonomic signals.

Taphonomic Trends Along a Forereef Slope: Lee Stocking Island, Bahamas. I. Location and Water Depth

Abstract The Shelf and Slope Experimental Taphonomy Initiative (SSETI) Program was established to measure taphonomic rates in a range of continental shelf and slope environments. Experiments were deployed on the forereef slope off Lee Stocking Island, Bahamas, for one and two years along two transects (AA and BA) in seven distinctive environments of deposition (EODs) along each transect: in sand channels on the platform top (15 m) and the platform edge (30 m), on ledges down the wall (70–88 m), on the upper (183 m—transect BA only) and lower (210–226 m) talus slope below the wall, and on the crest (256–264 m) and in the trough (259–267 m) of large sand dunes. Discoloration was by far the dominant taphonomic process over the two-year deployment period, with dissolution or maceration of shell carbonate a close second. Periostracum breakdown was not significant, nor was loss of shell weight. Chipped edges and breakage (assayed by the edge alteration variable) were much less common, but were important in some species. The degrees of edge alteration and dissolution were correlated with discoloration more frequently than expected by chance, emphasizing that the process of discoloration progressed in a coordinated fashion with the other two over time. The degree of burial or the interaction between degree of burial and water depth explained most of the trends observed in discoloration. The deep water sites, below the photic zone, including the talus slope and dune EODs, had very similar taphonomic signatures. Shells were characterized by a low degree of discoloration, little edge alteration, and varying degrees of dissolution. Photic zone sites, including the platform top and wall locations, followed the opposite trends, with the shallowest site, on the platform top, typically attaining the most extreme degree of alteration. The wall location was most similar to the platform top despite the greater depth and less rigorous physical and sedimentological regime. The platform edge occupied an intermediate position, likely due to the greater degree of burial that resulted in shells at this site being at least as frequently under aphotic conditions as under photic conditions. The data indicate that similar taphonomic signatures can be attained in distinctly different ways over a two-year exposure period, complicating the interpretation of taphofacies and the taphonomic process.

Ice and Its Consequences: Glaciation in the Late Ordovician, Late Devonian, Pennsylvanian‐Permian, and Cenozoic Compared

Comparison of the duration, onset conditions, and biotic response to the four Phanerozoic glaciations suggests that there are two Phanerozoic glacial modes. Late Ordovician glaciation typifies short‐duration, high atmospheric CO2 events, characterized by cosmopolitan faunal distributions and two episodes of catastrophic extinction. Pennsylvanian‐Permian and Cenozoic glaciation typify long‐duration, low atmospheric CO2 events, characterized by abundant biogeographic differentiation and stable or rising biotic diversity. Late Devonian glaciation appears most similar to Late Ordovician glaciation: it had a short duration; Late Devonian biotas were cosmopolitan; and Late Devonian glaciation was associated with increased extinction at the Devonian‐Carboniferous boundary. On the basis of biotic response, we would predict high atmospheric CO2 levels at the time of Devonian glaciation. However, the Berner GeoCarb curve suggests relatively low atmospheric CO2 levels in the Late Devonian.

Taphonomic Trends Along a Forereef Slope: Lee Stocking Island, Bahamas. II. Time

Abstract The Shelf and Slope Experimental Taphonomy Initiative (SSETI) Program was established to measure taphonomic rates in a range of continental shelf and slope environments over a long period of time. For this report, mollusk shells were deployed for one and two years at seven different environments of deposition (EODs) along two onshore-offshore transects off Lee Stocking Island in the Bahamas. The experimental sites were located: in sand channels on the platform top (15 m) and the platform edge (33 m); on ledges down the wall (70–88 m); on the upper (183 m) and lower (210–226 m) talus slope below the wall; and on the crest (256–264 m) and in the trough (259–267 m) of large sand dunes. Shell condition was assessed using a range of taphonomic attributes including dissolution, abrasion, edge alteration, discoloration, and changes in shell weight. After two years, taphonomic alteration was not particularly intense in any EOD. No species was particularly susceptible or resistant to taphonomic alteration. Taphonomic processes were unexpectedly complex. Effects of location, transect, water depth, and degree of exposure all had significant effects. On average, shells deployed in shallow sites were altered significantly from the controls more frequently than shells deployed at deeper sites. However, the number of significant interaction terms between time and the other main effects indicates a complex interaction between taphonomic processes and the local environment that, over the short term, defies any attempt at delineating taphofacies over a broader spatial area than a single deployment site. Some locations attained the same taphonomic signature in different ways making discrimination of taphonomic rules difficult. For example, deeper-water sites and shallow sites where burial rates were high yielded similar taphonomic signatures because shells were in the aphotic zone in both cases, and this limited the rate and range of taphonomic interactions. Taphonomic processes were strongly nonlinear in time for all taphonomic attributes in all species and all EODs. Nonlinear taphonomic rates hinder the interpretation of single-point-in-time studies in understanding the taphonomic process and buttress a commitment to long-term experiments.

Floral diversity, phytogeography, and climatic amelioration during the Early Carboniferous (Dinantian)

Phytogeographic analysis of three Early Carboniferous intervals (Tournaisian–early Visean, Visean, and late Visean–early Namurian A) indicates a high level of phytogeographic differentiation in the beginning of the Early Carboniferous that decreases toward the end of this period. Climatic amelioration (warmer or wetter conditions) in the north middle and high latitudes, caused by the collision of Laurussia and Gondwana at the end of the Early Carboniferous, may be responsible for this decrease in phytogeographic provinciality. Toward the end of the Early Carboniferous, a large number of equatorial genera expand their ranges northward, and the average generic diversity of assemblages in the north high latitudes (Siberia) also rises. Both support the hypothesis of climatic amelioration. Northward migration of equatorial forms and the appearance of new genera endemic to Siberia both contributed to the rise in Siberian diversity. Although this trend is not statistically significant, additional evidence of diversity increase in northern high latitudes tied to climatic amelioration comes from the northernmost limit of diverse (≥ 10 genera) assemblages, which rises from 20°N at the beginning to 55°N at the end of the Early Carboniferous. Global plant diversity assessed at the generic level remained constant during the Early Carboniferous. The increase in Siberian diversity was offset by a decrease in equatorial diversity, perhaps due to the loss of pronounced latitudinal climatic gradients between north-middle and equatorial latitudes.

Evidence for an Upper Carboniferous mangrove community

The morphological and paleogeographic evidence suggesting that cordaitean-dominated swamps from the early Westphalian D (= 295 m.y.b.p.) of Iowa grew in salt water swamps is reviewed. Cordaitean trees, Psaronius tree ferns, and Medullosa seed ferns contributed 95% of the peat in coal-ball samples taken from three Iowa mines. Ordination analysis shows that associations dominated by Psaronius and Medullosa succeeded an association dominated by cordaitean trees at each site. Based on comparisons with Upper Carboniferous compression flora deposits, Psaronius and Medullosa seem to have grown in freshwater or only slightly brackish water habitats. The root morphology of cordaitean trees from Iowa and the paleogeographic position of these swamps suggest that cordaitean trees which produced Nucellangium glabrum and Cardiocarpus spinatus seeds grew in salt water. Results of the ordination analysis suggest that cordaitean trees which produced Mitrospermum seeds grew in freshwater or only slightly brackish habitats. The methods used to assess these deposits as mangrove peats can be applied to any structurally preserved peat. Most other putative mangrove communities in the fossil record have been described from compression-flora deposits. The non-morphological criteria for assessing these floras as mangrove swamp deposits are reviewed.