Cretaceous Ammonite Distributions and the Opening of the South Atlantic

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Cretaceous Ammonite Distributions and the Opening of the South Atlantic Cretaceous ammonite distributions and the opening of the South Atlantic WILLIAM JAMES KENNEDY & MICHAEL COOPER SUMMARY Analysis of distribution patterns of middle to absence of early Turonian marine deposits in late Cretaceous ammonites along the line of Southern Africa), but such evidence as is the opening S. Atlantic suggest that open available also suggests continued connection. marine connections, if not actual rifting, Palaeobiogeographic evidence is thus corn- developed during early upper Albian times, patible with sea floor spreading and palaeo- and extended continuously to the close of the magnetic data, rather than in conflict, as Cenomanian. Evidence of early Turonian previouslysuggested. distributions is equivocal (due largely to an PALAEOMAONETIC and sea floor spreading data (Creer et al. I965; Amaral et al. I966; McDougaU & Ruegg I966; Saito et al. x966; Siedner & Miller x968; Maxwell et al. I97o; Valencio & Vilas I97o ) have suggested to recent authors that initial rifling between Africa and S. America began in early or mid- Cretaceous times, while the recovery of chalks and nannofossil oozes of Albian to Cenomanian date from the Walvis Ridge (Pastouret & Goslin I974) confirms this view. In contrast, studies of distribution patterns of Cretaceous marine invertebrates, notably ammonites, from coastal basins flanking the south Atlantic (Beurlen I96I , Reyment i969-72 , Reyment & Tait I972, Cooper x972-I974) are held to indicate that a continuous marine connection between N. and S. Atlantic areas was not established until the close of the early Turonian. We would suggest on the basis of recent work on mid to late Cretaceous faunas from Angola (Cooper I972-I974) , Zululand and Natal (South Africa) (Kennedy & Klinger I97I , in press) that faunal distributions rather confirm a far earlier open marine N.-S. connection, although this may have been no more than flooding of a downwarped area of continental crust rather than an actual oceanic rift. The S. African and Angolan ammonite faunas (Fig. i) discussed here may have reached these areas either via the shelf seas flanking the western Indian Ocean, via the line of the Atlantic, or via a so-called trans-Saharan seaway (Reyment & Tait I972 ). Reyment & Tait (i972) concluded that Africa and South America remained connected during early middle Albian times, on the basis of the geographic restriction of the oxytropiceratid subgenus Venezoliceras. We can confirm this view on the basis of rich Oxytropidoceras faunas of early middle Albian date from Dombe Grande, south of Benguella (Angola), which show little resemblance to the equally rich contemporaneous Oxytropidoceras faunas from Texas (Young x966 ). In contrast, the associated douvilliceratids D. mammillatum (Schlotheim) and D. orbigni Hyatt are forms well known from S. Africa and Madagascar Jl geol. 8oc. Lond. vol. x3x, x975, PP. 283-288, x fig. Printed in Northern Ireland. Downloaded from http://pubs.geoscienceworld.org/jgs/article-pdf/131/3/283/4884980/gsjgs.131.3.0283.pdf by guest on 30 September 2021 284 W. J. Kennedy & M. Cooper (Collignon I963) , appearing to be migrants to Angola via the Cape Seaway (Dingle & Klinger i97i , Jones I972, Dingle x972). Evidence of a continued barrier between northern and southern proto Atlantic (latter term used in the sense of the opening Mesozoic ocean, rather than the Palaeozoic seaway of Tuzo Wilson et al.) areas during early upper Albian times may also be indicated by the distribution of the essentially endemic south Atlantic genera Elobiceras, Neokentroceras and Angolaites, well known from Angola, Brazil and Nigeria (Reyrnent & Tait I972; Howarth I965; Spath I922; Haas z942), with records from Madagascar (Collingnon I963) again suggesting an open Cape Seaway. These taxa occur, however, in upper Albian faunas (approximately H. varicosum subzone) from Lobito and Hanha, Angola (Cooper x973; Haas I942) which have long been considered to have close affinities with those of N. Africa, Europe and S. Africa. We would add that a whole series of mortoniceratids are also known to be common to areas of trans-Pecos Texas, Chihuahua, northern Coahuila (Mexico) and Angola at this time, e.g. Mortoniceras (Boeseites) roemeri (Haas), M. (B.) perarmata Haas, M. (B.) proteus (Haas), M. (B.) el. howelli (Haas), M. (B.) of. barbouri (Haas) and Prohysteroceras cf. hanhaense Haas (Young i968 ). Equally strong evidence of an open southern proto Atlantic seaway at a slightly j olorado,~,~l A ~'~Texas / Venezuela Postulat~ Angola Barrier' FIG. I. Location of principal Cretaceous faunas discussed in text, and possible migration routes of South i:iiii Atlantic faunas. A: proto-Atlantic, B: trans-Saharan, C C: Cape. Downloaded from http://pubs.geoscienceworld.org/jgs/article-pdf/131/3/283/4884980/gsjgs.131.3.0283.pdf by guest on 30 September 2021 Cretaceous ammonite distributions and the opening of the South Atlantic 285 later date (approximately C. auritus subzone) is given by the strong similarities between faunas from the La Puya Member of the Penas Altas Formation in the Venezuelan Andes and contemporary deposits in West and South Africa and Madagascar (Renz 1968). The following species are common to Venezuela and E. Africa (Zululand, Mozambique, and Madagascar)" Mortoniceras (Mortoniceras) pricei (Spath), M. (M.) pricei var. intermedium Spath, M. (M.) africanum (Spath), M. (M.) arietiforme andranofotsyense (Collignon), M. (M.) cf. recticostatum (Spath), M. (Deiradoceras) prerostratum (Spath), M. (D.) devonense Spath, M. (D.) mokara- haense (Collignon), M. (D.) cf. exile (Van Hoepen), M. (Rusoceras) nothum (Van Hoepen), Hysteroceras carinatum Spath, H. orbignyi (Spath), Puzosia (Anapuzosia) saintoursi Collignon, Bhimaites aontzyensis Collignon, B. stoliczkai (Kossmat) and Oxytropidoceras (Venezoliceras) madagascariense Collignon. Species common to Vene- zuela and Angola include Hysteroceras orbignyi (Spath), H. orbignyi evolutum Haas, H. carinatum Spath, H. carinatum aft. robusteocostatum Haas, H. choffati Spath and Mortoniceras (Mortoniceras) arietiforme arietiforme (Spath). This leaves little doubt that there was free faunal migration between the E. coast of Africa and Venezuela during the low upper Albian. Uppermost Albian (dispar Zone) faunas are rather poorly known from Brazil and Nigeria (Reyment & Tait 1972, Reyment 1955) but we now have extensive faunas of this date from Egito in Angola and from Zululand. Occurrence ofhetero- morph species such as Anisoceras perarmatum Pictet & Campiche, A. arrogans (Giebel) (=A. campichei Spath) and A. jacobi Breistroffer (=A. picteti Spath) together with Mortoniceras (Durnovarites) from Texas, N. Mexico and Africa down to Angola and to Zululand confirm a continued seaway. Particularly convincing is the distribution of Stoliczkaia of the africana (Pervinqui6re) group, known from England, Texas, Switzerland, N. Africa (Algeria and Tunisia), Nigeria, Brazil (although said to be of Cenomanian age) (Reyment & Tait i972), Angola and Zululand. Absence of records of this species group from the Middle East, Mada- gascar and S. India strongly suggests migration along a southern proto Atlantic seaway. Cenomanian faunas recently recorded from Angola (Cooper 1972) again support an open connection" forms such as Stomoham#es aft. simplex (d'Orbigny), Anisoceras plicatile (J. Sowerby), Turrilites costatus Lamarck, T. acutus Passy, Forbesiceras obtectum (Sharpe), Calycoceras coleroonense percostata Collignon, C. annulatum Collignon, Euomphaloceras cunningtoni meridionale (Stoliczka) and Acan- thoceras cf. tunetana Pervinqui6re (Cooper x972) showing strong links with NW. European and N. African faunas in many respects, but also include Malagasy and Zululand species. Latest Cenomanian faunas from Angola, correlative with the N. American Sciponoceras gracile Zone and the European Metoicoceras gourdoni-geslinianum Zones, again support continued connection and free interchange with Europe and N. America. Ammonites from Salinas, Angola (Cooper 1972) including Metoico- ceras whitei Hyatt, Sciponocerasgracile (Shumard), Kanabiceras septemseriatum (Cragin) Calycoceras naviculare (Mantell) and Pseudocalycoceras of the angolaense (Spath)- dentonense (Moreman) group from an assemblage identical with that known in Texas (Moreman 1927, 1942) and the U.S. Western Interior (Cobban & Scott Downloaded from http://pubs.geoscienceworld.org/jgs/article-pdf/131/3/283/4884980/gsjgs.131.3.0283.pdf by guest on 30 September 2021 286 W. J. Kennedy & M. Cooper I972 ) and Europe (Kennedy i97i , Juignet et al. I973) , and also repre- sented by sparse assemblages from Nigeria (Reyment x955) and Morocco (Collignon x966 ) (Metoicocerus ornatum Moreman of these authors is a synonym of M. whitei). The species Austiniceras dibleyi Spath is in fact only known from S. England and Angola (Kennedy x97 I). Considerable weight has been placed upon early Turonian distributions, with a suggestion of a northern Selwynoceras association typifying northern S. America, Mexico, Texas and parts of W. Europe and with the area of the southern proto Atlantic typified by a vascoceratid association with links across the Sahara to the Middle East. The Angolan Turonian is poorly understood, although one of us (Cooper I972 ) has described a condensed Turonian to Coniacian sequence yielding the ammonite genera Mammites, Proplacenticeras, Subprionocyclus, Baculites, Mesopuzosia, Hauericeras, Puebloites, Gaudryceras, Anagaudryceras, Damesites, Kossmati- ceras, Subtissotia ? and Hypophylloceras. It is arguable that absence of such
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