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Aretz et al_2011.pdf - ORBi - Université de Liège

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Kölner Forum Geol. P<strong>al</strong>äont., 19 (2011)<br />

M. ARETZ, S. DELCULÉE, J. DENAYER & E. POTY (Eds.)<br />

Abstracts, 11th Symposium on Fossil Cnidaria and Sponges, <strong>Liège</strong>, August 19-29, 2011<br />

_________________________________________________________________________________________________________<br />

P<strong>al</strong>aeodiversity and faun<strong>al</strong> dynamics of post-Frasnian Tabulates, Western<br />

P<strong>al</strong>aeot<strong>et</strong>hys<br />

Hans-Georg HERBIG, Elise NARDIN & Anke MÜLLER<br />

Universität zu Köln, Institut für Geologie und Miner<strong>al</strong>ogie, Zülpicher Straße 49a, D-50674 Köln;<br />

herbig.p<strong>al</strong>eont@uni-koeln.<strong>de</strong>; enardin@uni-koeln.<strong>de</strong>; ankeira@freen<strong>et</strong>.<strong>de</strong><br />

Introduction: Tabulate and rugose cor<strong>al</strong>s, and stromatoporids were the predominating framebuil<strong>de</strong>rs,<br />

bafflers and encrusters during the mid-P<strong>al</strong>aeozoic reef cycle. All were severely affected by the Frasnian-<br />

Famennian extinction event, but had a compl<strong>et</strong>ely different post-Frasnian history. P<strong>al</strong>aeozoic<br />

stromatoporids never recovered sufficiently and got extinct at the Devonian-Carboniferous boundary.<br />

Rugose cor<strong>al</strong>s radiated again during the latest Devonian (“Strunian”) and during the Mississippian. They<br />

flourished in carbonate platform s<strong>et</strong>tings and reinva<strong>de</strong>d the reef biotope, reaching <strong>al</strong>most their Devonian<br />

diversity (ARETZ 2010). Also tabulate cor<strong>al</strong>s recovered, but remained a mostly subordinate community<br />

element (SCRUTTON 1997).<br />

Problems and M<strong>et</strong>hods: Due to relative scarceness, missing biostratigraphic v<strong>al</strong>ue and difficult taxonomic<br />

treatment, post-Frasnian tabulates are not sufficiently studied in the western P<strong>al</strong>aeot<strong>et</strong>hys. We tried to<br />

ev<strong>al</strong>uate diversity and faun<strong>al</strong> dynamics at species level based on exhaustive bibliographic survey. Data<br />

were cross-checked and supplemented with those from the P<strong>al</strong>eobiology Database (http://paeodb.org), to<br />

reduce uncertainties due to unrevised faun<strong>al</strong> data. Fossil lists of that database were used, if entries are on<br />

species level and ranges confined at least to region<strong>al</strong> stages in <strong>de</strong>fined regions. Diversity was c<strong>al</strong>culated for<br />

western European region<strong>al</strong> stages in standardised regions, using the norm<strong>al</strong>ised diversity m<strong>et</strong>ric proposed<br />

by COOPER (2004). Defined standard regions are Ireland, northern England, southern England, Belgium,<br />

Rhenish Slate Mountains, Holy Cross Mountains, Silesia-Cracow Upland, Saxothuringia, Southern<br />

Portug<strong>al</strong>, Cat<strong>al</strong>onia, and the North African basins. P<strong>al</strong>aeogeographic relations were approached by cluster<br />

an<strong>al</strong>ysis based on the Dice similarity in<strong>de</strong>x using PAST software.<br />

P<strong>al</strong>aeodiversity and disparity: No tabulate cor<strong>al</strong>s are recor<strong>de</strong>d in the lower and middle Famennian of the<br />

western P<strong>al</strong>aeot<strong>et</strong>hys except for a faunula from the lower Famennian of Moravia (HLADIL 1987). Not a<br />

single “Strunian” or Carboniferous species is recor<strong>de</strong>d from pre-Famennian strata according to our<br />

knowledge. Thus, a compl<strong>et</strong>ely new faun<strong>al</strong> cycle started in the “Strunian”. It en<strong>de</strong>d in the Kasimovian,<br />

comprising <strong>al</strong>l tog<strong>et</strong>her about 75 species from 33 genera and 14 families.<br />

The diversity is relatively low in the “Strunian” but increases abruptly to reach an absolute maximum in<br />

the Molinacian. Then the diversity <strong>de</strong>cline from the Viséan to the Kasmovian is interrupted by an expressed<br />

Brigantian peak. The low “Strunian” -Hastarian diversity reflects the slow recovery after the Frasnian-<br />

Famennian extinction. Declining diversity during the Viséan is due to steadily increasing extinction and<br />

<strong>de</strong>creasing origination rate, a trend only reversed during the Brigantian. The Mississippian diversity curve<br />

for western European rugose cor<strong>al</strong>s (ARETZ 2010) is similar to that of tabulates. Both correlate well with<br />

Mississippian se<strong>al</strong>evel variations. The Molinacian maximum is probably related with the Avins event, a<br />

wi<strong>de</strong>ly recognized transgressive event, which introduced <strong>al</strong>so many rugose taxa. Of speci<strong>al</strong> interest is the<br />

Brigantian peak, which introduced some Asiatic taxa to Poland, Belgium, the B<strong>et</strong>ic Cordillera (own<br />

unpublished data) and Algeria (Multithecopora, Sinopora, Verolites). The quasi-extinction of tabulates at the<br />

end of the Viséan is related to the prograding Variscan orogeny, which caused emergence and wi<strong>de</strong>spread<br />

break-down of carbonate platforms. Moscovian and Kasimovian tabulates have been <strong>de</strong>scribed from<br />

Cantabria and the Carnic Alps, but un<strong>de</strong>scribed occurrences in the North African basins should increase<br />

Pennsylvanian diversity.<br />

Syringoporidae, Michelinidae and, to a lesser <strong>de</strong>gree, Favositidae are the most diverse and most<br />

abundantly occurring Carboniferous tabulate families in the western P<strong>al</strong>aeot<strong>et</strong>hys (Fig. 1A). The<br />

norm<strong>al</strong>ised diversity curves of the Syringoporidae and the Michelinidae par<strong>al</strong>lel the gener<strong>al</strong> trend of<br />

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