Aretz et al_2011.pdf - ORBi - Université de Liège
Aretz et al_2011.pdf - ORBi - Université de Liège
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 />
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A comparison of Mississippian coloni<strong>al</strong> rugose cor<strong>al</strong>s from Western<br />
Europe and South China<br />
Edouard POTY 1 , Markus ARETZ 2 & XU Shaochun 3<br />
1 Service <strong>de</strong> P<strong>al</strong>éontologie anim<strong>al</strong>e <strong>et</strong> humaine, Département <strong>de</strong> Géologie, <strong>Université</strong> <strong>de</strong> <strong>Liège</strong>, Bat. B18,<br />
Allée du Six-Août, Sart Tilman, B-4000 <strong>Liège</strong>, Belgium; e.poty@ulg.ac.be<br />
2 <strong>Université</strong> <strong>de</strong> Touloluse (UPS), GET (OMP), 14, Avenue Edouard Belin, 31400 Toulouse, France;<br />
markus.ar<strong>et</strong>z@g<strong>et</strong>.obs-mip.fr<br />
3 Algoma University College, Ontario, Canada<br />
Sections in Hunan, Guanxhi and Guiyang were investigated or revised during the last years and their<br />
biostratigraphy (foraminifers and rugose cor<strong>al</strong>s) and sequence stratigraphy were precised (POTY <strong>et</strong> <strong>al</strong>. 2006;<br />
HANCE <strong>et</strong> <strong>al</strong>. in press). They provi<strong>de</strong> a composite section from the uppermost Famennian to the lowermost<br />
Serpukhovian which was correlated with Western Europe. The systematics and the stratigraphy of the<br />
South-Chinese coloni<strong>al</strong> rugose cor<strong>al</strong>s of this interv<strong>al</strong> were revised and <strong>al</strong>low to do comparisons with those<br />
present in Western Europe and to precise their relationships and their p<strong>al</strong>aeogeography.<br />
From the lower Tournaisian to the lowermost Namurian (Serpukhovian), 14 genera of coloni<strong>al</strong> rugose<br />
cor<strong>al</strong>s were recognized in Western Europe (WE) and 11 in South China (SC), that is a tot<strong>al</strong> of 17, 8 being<br />
common to both regions. But these latters have not the same stratigraphic distributions, none of them<br />
appearing at the same level in the two regions (Fig. 1).<br />
The ol<strong>de</strong>st Tournaisian coloni<strong>al</strong> rugose cor<strong>al</strong> is Parastelechophyllum which appeared only in China. It is<br />
closely related to Stelechophyllum (POTY & XU 1996) which is known in the North-American re<strong>al</strong>m and in<br />
Centr<strong>al</strong> Asia. Its stratigraphic distribution is limited to the Ur<strong>al</strong>inia tangpakouensis Cor<strong>al</strong> Zone (MFZ3).<br />
H<strong>et</strong>erostrotion and its closely related Soleno<strong>de</strong>ndron (POTY & XU 1997) are the ol<strong>de</strong>st European Tournaisian<br />
coloni<strong>al</strong> genera, the first being previously known in the Uppermost Famennian of Poland. Both appeared in<br />
the RC3α Cor<strong>al</strong> Subzone (base of MFZ5) in the lower part of the Ivorian (Upper Tournaisian). H<strong>et</strong>erostrotion<br />
is known only from one loc<strong>al</strong>ity in North France and limited to only one level, but the second extends up to<br />
the uppermost Viséan. Both can be consi<strong>de</strong>red as migrants from an outsi<strong>de</strong> area. In SC, Soleno<strong>de</strong>ndron was<br />
not recor<strong>de</strong>d, but H<strong>et</strong>erostrotion got into a little later than in WE (upper MFZ5). It became very common and<br />
exten<strong>de</strong>d up to the top of the Livian (Middle Viséan). It gave rise to a cerioid form (possibly corresponding<br />
to the not well <strong>de</strong>fined Lithostrotionella YABE & HAYASAKA 1915) at the base of the Keyserlingophyllum-<br />
Dorlodotia interv<strong>al</strong> Cor<strong>al</strong> Zone (base of MFZ7) and to Stylostrotion possibly in the upper part of the same<br />
Cor<strong>al</strong> Zone (base of MFZ10). That evolution can be consi<strong>de</strong>red as par<strong>al</strong>lel to the evolution of<br />
Lithostrotionids in WE and its surrounding regions. Dorlodotia is known from the RC4β1 Cor<strong>al</strong> Zone<br />
(MFZ7) in WE and from the base of the Dorlodotia Zone (MFZ11) in SC. It extends up to the top of the<br />
Moliniacian (RC5 – MFZ11 Zones) in WE, but up to the top of the Livian (top of MFZ12) in SC.<br />
Siphono<strong>de</strong>ndron introduced in WE from the base of the RC5 Zone (upper MFZ11) was common until the<br />
Namurian. It gave rise to Lithostrotion during the earliest Livian, and to Diphyphyllum, Nemistium and<br />
Orionastrea during the Warnantian. Siphono<strong>de</strong>ndron, Lithostrotion and Diphyphyllum got into China later,<br />
during the late Warnantian (MFZ15). Aulina is the only genus recor<strong>de</strong>d earlier in SC (late Warnantian,<br />
MFZ15) than in WE (Namurian, RC9-MFZ16).<br />
Therefore, most recor<strong>de</strong>d coloni<strong>al</strong> genera in SC are late migrants from outsi<strong>de</strong> regions, region<strong>al</strong><br />
radiation being traced only for h<strong>et</strong>erostrotionids. Note that some solitary genera known in WE got <strong>al</strong>so<br />
later into SC, for example Axophyllum and P<strong>al</strong>aeosmilia. Migrants got usu<strong>al</strong>ly earlier into WE, giving rise to<br />
lineages into the lithostrotionids, whereas originations can d<strong>et</strong>ermined for Lonsd<strong>al</strong>eia, P<strong>al</strong>astraea and<br />
possibly Corwenia.<br />
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