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Transcript
The Evolution of the Caribbean Seaway: Jurassic to Present
Manuel A. Iturralde-Vinent
Museo Nacional de Historia Natural
Obispo No. 61, Plaza de Armas
La Habana Vieja 10100, Cuba
www.medioambiente.cu/museo
Abstract
This paper presents a summary of the history of the Caribbean Seaway, from its
Lower to Middle Jurassic Pangaean epicontinental sea precursor (rift valleys), its debut as an
oceanic seaway in the Oxfordian, and its subsequent evolution until the Present. Since
Oxfordian, marine connectivity between the Tethys/Atlantic and the Pacific oceans along the
Caribbean Seaway have been shaped by the occurrence of different topographic barriers,
sometimes as isolated islands and submarine highs, sometimes as continuous land barriers.
This scenario can be used to evaluate possible biotic interchange, either by land between the
American continents or by water between the Pacific and Tethys/Atlantic oceans. It is
demonstrated that during the Eocene-Oligocene transition (35-33 Ma) there was a land
barrier in the Caribbean (Gaarlandia), that precluded free ocean water circulation between
the Pacific and the Atlantic/Caribbean, probably contributing to the climatic change that took
place at this time interval. This barrier was progresively drowned during the Oligocene,
restoring the Circumtropical current that warmed up temperature within the Caribbean Sea
and the Tropical Pacific.
1
Introduction
It is well known that, due to changing Earth paleogeography, global ocean water
circulation has changed, controlled by the configuration of the continents, islands, oceans,
seas and shallow submarine areas, as well as atmospheric and water composition and
dynamic factors (Barrow and Peterson, 1989). As a consequence, present-day patterns of
marine circulation cannot be extrapolated to evaluate paleobiogeographic scenarios
(Berggren and Hollister, 1974; Frakes et al., 1992; Parrish, 1992). For these reasons, in
this paper I briefly explore the origin and evolution of the Caribbean area, using the
database compiled by Iturralde-Vinent and MacPhee (1999), as well as the paleogeographic
reconstructions published recently (Iturralde-Vinent and MacPhee, 1999; Kerr et al., 1999;
Iturralde-Vinent, 1998, Lawver et al., 1999). This is a necessary step toward the
understanding of the history of marine biotic exchange between the Pacific and
Tethyan/Atlantic oceans.
In order to summarize the evolution of the Caribbean Seaway, figure 1 is presented
to illustrate the history of topographic barriers between North and South America, and their
bearing on the history of marine flow across the area. This history can be subdivided into
the following major steps: 1. The Western Pangaean epicontinental seaway, 2. The early
opening of the Caribbean Seaway, 3. The Mesozoic evolution of the Caribbean Seaway, 4.
The early Cenozoic evolution, and 5. The latest Eocene to Recent evolution of the Seaway.
Acknowledgement. This is a contribution to UNESCO/IUGS IGCP Project 433 Caribbean Plate
Tectonics. The author wish to thanks his colleague Ross MacPhee (American Museum of
Natural History), and an anonymous reviewer, for important suggestions to the original
typescript and drawings. Attending the GSA Penrose Conference on The Marine EoceneOligocene Transition (Seattle, 1999) was possible thanks to a grant from the Cuba Group of
SSRC. Field work in the Greater Antilles for this paper was partially supported by a NGS
Grant to the author. Laboratory work at the Institute for Geophysics of the University of
Texas at Austin (UTIG) was possible thanks to grants from the Institute for Latin American
Studies (UTEXAS) and UTIG.
The Western Pangaean epicontinental Seaway
Similarities among several groups of marine animals (pelecipods, ammonites, marine
reptiles) that occur both in the western Tethys and the East Pacific suggest that since the
2
Pliensbachian-Hettangian (nearly 190±5 m.y. ago) an aquatic connection existed between
these regions (Smith, 1983; Damborenea and Maceñido, 1979; Ricardii, 1991; Gasparini,
1992, 1996). Although the connection, theoretically, may have taken place eastward across
the eastern Tethys into the Pacific Ocean, similarities between the western Tethyan and the
East Pacific taxa suggest that the connection passed trough the central part of the Pangaean
supercontinent (Gasparini, 1978; Smith, 1983; Riccardi, 1991; Gasparini, 1978, 1992,
1996; Gasparini and Fernández 1996; Damborenea, 2000, Aberham, 2001).
This
connection first yielded a limited exchange of shallow marine taxa (Smith, 1983;
Damborenea, 2000, Aberham, 2001), but with time the waterway widened (Pindell, 1994;
Lawver et al., 1999) allowing an increasing exchange of marine animals, including both open
and shallow marine taxa, limited during the Bathonian-Oxfordian, and extensive since the
Oxfordian (Westermann, 1981; Westermann, 1992; Hilldebrandt, 1981; Hilldebrandt et al.,
1992: Imlay, 1984; Sandoval and Westermann, 1986; Bartok et al., 1985; Riccardi, 1991;
Gasparini, 1978, 1992, 1996; Gasparini and Fernández, 1996; Iturralde-Vinent and Norell,
1996; Damborenea, 2000). According to recent paleogeographic reconstructions, this
passway was established before the break-up of Pangaea, probably across a dominantly
shallow siliciclastic interior sea located within western Pangaea (Fig. 1; Salvador, 1987;
Pindell, 1994; Pindell and Tabbutt, 1995).
The fact that large ocean dwelling saurians are recorded from the Middle Jurassic of the
southeastern Pacific (Gasparini, 1992; Gasparini and Fernández, 1996) suggest that the
western Pangaean epicontinental seaway may have been transected by some deep water
channels, probably along grabens and semigrabens produced by crustal extension (rift
valleys). This hypothesis is supported by the existence of "continental margin and marine
facies" in the preOxfordian probably Bathonian-Bajocian siliciclastic rocks of western Cuba
(San Cayetano Formation), with sedimentary features suggesting the occurrence of
paleoslopes from fluvio-marine facies into marine environments (Haczewski, 1976;
Pszczolkowski, 1978); and by the occurrence of Jurassic rift grabens and semigrabens in the
eastern and southern continental margin of North America (Salvador, 1987; Pindell, 1994;
Marton and Buffler, 1994, Bullard et al., 1965; Klitgord et al., 1988; Gradstein et al., 1990;
Jones et al., 1995, Pindell and Talbut, 1995; Milani and Tomas Filho, 2000).
The Pangaean Epicontinental Sea should not be thought of as the ProtoCaribbean basin
itself, but as a precursor situated within western Pangaea (Iturralde-Vinent and MacPhee,
1999). For this reason, I propose to avoid the confusing terms "Hispanic Corridor" or
"Caribbean Corridor" to designate this seaway and refer to it instead by a more descriptive
term, the Western Pangaean Epicontinental Seaway and rift valley system (Fig. 1).
3
The early opening of the Caribbean Seaway
As the break-up of Western Pangaea completely separates Laurasia and Gondwana, a
new paleogeographic feature formed: the Caribbean Seaway. This Seaway is here
understood as a truly oceanic basin located between the North and South American
continental landmasses. This seaway represents a linkage between the Pacific and the
Atlantic/Tethyan Oceans. In order to explore the origin of this basin, two sources of
information are needed: Earliest Mesozoic occurrence of ocean crustal indicators and the
first occurrence of true marine environments.
The earliest occurrence of Mesozoic oceanic crustal indicators within the Mesoamerican
realm comprise the pillow basalts and associated marine sediments reported from the
Andean terranes of northern South America (Bajocian/Bathonian Siquisique basalts: Bartok
et al. 1985) and from the Guaniguanico terrane of western Cuba (Oxfordian El Sábalo
basalts: Pszczolkowski, 1994; Kerr et al., 1999). The original position of the Siquisique
basalts is not yet well understood, but probably they belong to the Pacific margin of
Pangaea, as do the Andean terranes (Pindell, 1994; Pindell and Tabbutt, 1995, Aleman, A.
and V.A. Ramos, 2000). If this is true, they predate the formation of the early Caribbean
oceanic crust (Iturralde-Vinent, 1998). This is not the case for the El Sábalo basalts, which
probably formed on the Mayan (Yucatan) block margin facing the Caribbean (IturraldeVinent, 1994; Hutson et al., 1999), so they can be thought of as representing a magmatic
event related to the initiation of ocean spreading within the Caribbean (Iturralde-Vinent,
1998; Iturralde-Vinent and MacPhee, 1999; Kerr et al., 1999). This inference is corroborated
by the occurrence of an important assemblage of Oxfordian marine animals (pelecipods,
ammonites, ganoid fish and marine reptiles) in the Guaniguanico terrane of western Cuba
(Iturralde-Vinent and Norell, 1996) that are clearly related to both the western Tethys and
the eastern Pacific faunas (Ricardii, 1991; Gasparini, 1992; Gasparini and Fernández, 1996;
Fernández and Iturralde-Vinent, 2000).
The opening of the Caribbean Seaway represents an important paleoceanographic golden
spike, --the initiation of Mesozoic deep circumequatorial ocean water circulation that linked
the Tethys, the Central Atlantic and the Pacific oceans.
The Mesozoic evolution of the Caribbean Seaway
4
It is generally understood that active seafloor spreading between North and South
America lasted from Late Jurassic through late Albian, widening the gap between the
continents (Pindell, 1994). Subsidence of the crust produced abyssal water depth sections
within the area, as early as the Tithonian (Pszczolkowski, 1978; 1982; Iturralde-Vinent,
1998; Iturralde-Vinent and MacPhee, 1999). These processes generally improved the
chances for inter-oceanic marine communication across the Caribbean Seaway. This
paleoceanographic scenario allowed extensive biotic exchange between the Tethys, the
Caribbean and the Pacific, as recorded by the distribution of several mollusks taxa (Shol and
Kollmann, 1985; Ricardii, 1991; Rojas et al., 1996; Boitrón-Sánchez and López-Tinajero,
1996).
Some numerical models of Cretaceous ocean circulation across the Tethys suggest
that the main circulation was directed eastward (Barron and Peterson, 1989). This
hypothesis is contradicted by the pattern of ammonite (cephalopod), acteonelid (gastropod)
and rudist (pelecipod) dispersion from east to west (Shol and Kollmann, 1985; Ricardii,
1991; Rojas et al., 1996; Boitrón-Sánchez and López-Tinajero, 1996).
Marine connectivity along the Caribbean Seaway was eventually moderated by local
and regional uplift within the Caribbean (Fig. 1). Iturralde-Vinent and MacPhee (1999) have
compiled abundant information concerning the occurrence of locals and regional
unconformities and hiatuses, as well as the presence of shallow-water banks, indicating both
subaereal exposure and/or submarine topographic highs during the time interval under
consideration. These positive topographies must have ultimately interrupted deep ocean
circulation, and forced circulation along deep trenches and channels. However, the present
state of our knowledge precludes accurate reconstruction of the specific paleoceanographic
scenarios.
An important permanent barrier that occurs within the Caribbean Seaway is the
Bahamas. By Late Jurassic-Early Cretaceous, this shallow water structure included presentday Florida and Bahamas, but since Aptian this megaplatform has been subdivided into
smaller platforms separated by a network of abyssal channels (Buffler and Hurts, 1985;
Iturralde-Vinent, 1994; 1998). This general barrier allowed restricted deep marine
circulation through the channels, but had the special effect of concentrating the main
circulation across the Strait of Florida and the Central Atlantic Ocean. Some other barriers
probably occurred as islands chains (erosional surfaces and hiatuses within the volcanic
sections) and shallows (interbedded shallow marine limestones) along the active volcanic
arcs of the Caribbean realm (Iturralde-Vinent and MacPhee, 1999), but these topographic
features, during the Cretaceous, were mostly located on the western periphery of the
5
Caribbean (Pindell, 1994; Iturralde-Vinent, 1998). Within these volcanic terranes major
uplift events are recorded during the Neocomian, Aptian-Albian, and Coniancian-Santonian;
but these barriers were surely non-permanent, because subsidence and deposition of marine
rocks are also recorded in them after each uplift (Iturralde-Vinent and MacPhee, 1999).
The documented interchange of large terrestrial tetrapods between North and South
America, late in the Cretaceous, strongly suggests that there was a landbridge between
these continents (Gingerich, 1985; Gayet et al., 1992). Iturralde-Vinent and MacPhee
(1999) suggested that this landbridge probably coincided in time with the regional uplift that
took place by late Campanian-early Maastrichtian along the Antillean Cretaceous volcanic arc
(Fig. 1). This event would have closed the Caribbean Seaway for a period of 1-3 Ma.,
producing a major change in ocean water circulation and global climate, as the one recorded
after the formation of the Panamanian bridge in the Pliocene. The pre late Campanian
topographic barriers within the Cretaceous volcanic arcs where ephemeral and probably not
continuous landmasses and shallows separated by local deep-water channels (IturraldeVinent and MacPhee, 1999), so their effect on the marine flow across the Caribbean Seaway
was not so drastic (Fig. 1).
The early Cenozoic evolution of the Caribbean Seaway
The end of the Cretaceous in the Caribbean realm was accompanied by strong
modifications in the tectonic regime of the area. Rock deformation and collisional tectonics
associated with important vertical movements played an outstanding role since latest
Campanian and the formation and destruction of topographic barriers was a common
phenomenon during the Cenozoic (Khudoley and Meyerhoff, 1971; Pszczolkowski and Flores,
1986; Droxler, et al., 1998; Iturralde-Vinent and MacPhee, 1999). This dynamic of the
crustal movements within the Caribbean also produced a more complicated landscape, as
several volcanic chains and ridges were present, with a clear tendency toward the reduction
of the size of the marine basins (Iturralde-Vinent and MacPhee, 1999: Figs. 6-8).
Nevertheless, those barriers did not prevent marine currents from flowing across the
Caribbean Seaway (Fig. 1), as Paleogene and Neogene biotas from the Pacific and
Atlantic/Tethys intermingled in the Caribbean and/or migrated between these oceans
(Papers in this volume; Duque Caro, 1990; Collins, 1996; Iturralde-Vinent, et al., 1997).
This biotic interchange was particularly marked during the periods of high stand, recorded
by the frequent occurrence of deep water environments within Caribbean early Cenozoic
stratigraphic sections (Iturralde-Vinent and MacPhee, 1999).
6
Consequently, during the Paleocene and Eocene, the so-called Circumglobal
equatorial current (Droxler, et al., 1998) flowed between the Tethys/Atlantic and the
Caribbean/Pacific across the Caribbean Seaway. Figure 2 (60-35 Ma) illustrates, in a very
general manner, the Caribbean paleogeography during this time interval.
The latest Eocene to Recent evolution of the Caribbean Seaway
The transition between the end of the Eocene and the beginning of the Oligocene
(zones P16 to P18 of Berggren et al., 1995) coincides with the Pyrenean phase of
tectogenesis (Leonov and Khain, 1987), the effects of which are well represented in the
Caribbean Region (MacPhee and Iturralde-Vinent, 1995; Iturralde-Vinent and MacPhee,
1999). During this phase, regional tectonic uplift coincided with a major eustatic sea level
drop at ca. 35 Ma (Miller et al., 1996). As a result, subaerial exposure within the Caribbean
Region was probably more extensive then than at any other time in the Cenozoic, including
the late Quaternary. The map (Fig. 2: 35-33 Ma) reflects this fact. However, it is important
to compare this map with other “Oligocene” reconstructions which represent this period as
one of overall minimum land exposure (e.g., González de Juana et al., 1980; Galloway et
al., 1995; Macellari, 1995). The explanation for the difference in treatment lies in the fact
that most Oligocene reconstructions depict the paleogeography of the mid- to later
Oligocene, by which time the Pyrenean orogenic phase had terminated (Iturralde-Vinent and
MacPhee, 1999).
Evidence for Pyrenean uplift can be seen in stratigraphic sections as well as
submarine dredge samples, drill cores, and seismic lines recovered from many parts of the
Caribbean and surrounding continental borderlands (Table1). Many stratigraphic sections
consistently lack marine sediments of latest Eocene-Early Oligocene age, presenting instead
hiatuses, red beds, and other kinds of terrestrial deposits (Iturralde-Vinent and MacPhee,
1999). In many sedimentary basins located near former topographic highs, latest EoceneEarly Oligocene sediments carry abundant land-derived debris, chiefly very coarse
conglomerates (matrix or clast-supported) and sandstones. This type of sedimentary unit is
so common in the Caribbean realm that Iturralde-Vinent and MacPhee (1999) dubbed it the
"Eocene-Oligocene transition conglomerate event". In places far removed from terrestrial
sediment sources, such as the Colombian, Venezuelan and Yucatan basins, deep-marine
deposition was condensed (Edgar et al., 1973; Sigurdsson et al., 1997).
The Aves Ridge is considered to have constituted the southeastern continuation of
the Greater Antilles ridge in latest Eocene-Early Oligocene time. Iturralde-Vinent and
7
MacPhee (1999) argue that exposure of the ridgecrest created, for a short time ca. 33-35
Ma, a series of large, closely-spaced islands or possibly a continuous peninsula (as part of
Gaarlandia) stretching from northern South America to the Puerto Rico-Virgin Islands to
Central Cuba. Noteworthy, during the Eocene-Oligocene transition is the fact that western
Cuba was uplifted, but separated by the Havana-Matanzas deep-water channel from central
Cuba (actually from Garrlandia), and by the Strait of Yucatan from the Yucatan Peninsula
(Fig. 2; Iturralde-Vinent et al., 1996). Some positive topographic features characteristic of
the present Caribbean sea floor did not exist in Eocene-Oligocene times (and are therefore
not depicted in Fig. 2). These are the Cayman Trench, Mona Channel, Anegada Trough, etc.
(see discussion by MacPhee and Iturralde-Vinent, 1994, 1995).
About Latest Eocene, after the colision of the Antillean arc with the Bahamas, general
uplift started all along the axis of the present day Greater Antilles, about 37 Ma ago
(Iturralde-Vinent and MacPhee, 1999). Short after, during the Eocene-Oligocene transition
(c.a. 35-33 Ma) a pronounced topographic barrier (Gaarlandia) reduced to a minimum water
exchange between the Atlantic and the Caribbean/Pacific, and a special pattern of ocean
water circulation similar to present day was established for a short time (Fig. 2), probably
contributing to the climatic change recorded at the Eocene-Oligocene transition (Prothero,
1994).
Since the Lower Oligocene, Gaarlandia progressively drowned. Inundation of
terrestrial environments began as early as zone P19 (Berggren et al., 1995) and continued
into zone P22, as it is indicated by the widespread occurrence of transgresive Oligocene
marine sediments in the Caribbean Region (Iturralde-Vinent and MacPhee, 1999, its table 3
and appendix 1). Marine communication between the Atlantic and Pacific reestablished, and
the Circumtropical current warmed up the water temperature within the Caribbean Seaway
and the equatorial Pacific (Droxler, et al., 1998). This scenario lasted until the Middle
Miocene (Fig. 2: 33-9 Ma), and by Late Miocene water circulation across the Caribbean
Seaway was restricted again by regional uplift during the Late Miocene (Fig. 2: 9-7 Ma;
Coates and Obando, 1996; Iturralde-Vinent and MacPhee, 1999), as is suggested by a
foraminiferal faunal turnover in the Panamanian area, by the abundance of high latitude
Californian elements in the Panamanian fauna, and the occurrence of South American land
mammals in the Late Miocene-Pliocene of North America (Gingerich, 1985; Duque-Caro,
1990; Collins, 1996). The Panamanian barrier was drowned at the end of the Miocene (Fig.
2: 7-3.7 Ma), and soon erected again, first as a shallow submarine ridge, later as a
landbridge between North and South American continents (Fig. 2 3.7-0 Ma; Duque-Caro,
1990; Collins, 1996; Coates and Obando, 1996).
8
Conclusions
The history of the Caribbean Seaway is very complicated, but can be generally
explored with the available data. Figure 1 is a summary of the history of marine
connections and topographic barriers within the Caribbean area. This scenario can be used
to evaluate possible biotic interchange, either by land between the American continents or
by water between the Pacific and Tehys/Atlantic oceans. Figure 2 illustrates the Paleocene to
Recent evolution of the seaway, which is the main interest of the present volume. In
general, the evolution of the Caribbean Seaway must have had a strong bearing on the
global patterns of ocean circulation and climate change in the past, but this is an issue that
remains to be studied in more details.
References
Aberhan, M., 2001, Bivalve paleogeography and the Hispanic corridor: time of opening and
effectiveness of a proto-Atlantic seaway, Paleogeography, Paleoclimatology and
Paleoecology, v. 165 p. 375-394.
Aleman, A. and V.A. Ramos, 2000, Northern Andes, In U.C. Cordani, E.J. Milani, A. Thomaz
Filho and D.A. Campos eds., Tectonic evolution of South America, 31st International
Geological Congress, p. 453-480.
Barron, E.J. and Peterson, W.H., 1989. Model simulation of the Cretaceous Ocean
circulation. Science 244(may):684-686.
Bartok, P.E., O. Renz and G.E.G. Westermann, 1985. The Siquisique ophiolites, Northern
Lara State, Venezuela: A discussion on their Middle Jurassic ammonites and tectonic
implications. GSA Bull. 96:1050-1055.
Berggren, W.A. and C.D. Hollister, 1974, Paleogeography, paleobiogeography and the
history of circulation in the Atlantic Ocean, In W.W. Hay ed., Studies in paleooceanography, Society of Economic Paleontologists and Mineralogists, Special Publ.,
v. 20 p. 126-186.
Berggren, W. A., D. V. Kent, C. C. Swisher, and M.-P. Aubry, 1995.A revised Cenozoic
geochronology and chronostratigraphy. Spec. Publ. Soc. Econ. Paleontol. Mineral. 54:
129-212.
9
Boitrón-Sánchez, B. and López-Tinajero, Y., 1996. Mollusk gastropods in a Lower Cretaceous
rudist-bearing formation of Jalisco, west central Mexico. Rev. Mexicana de Ciencias
Geológicas, 12(2):157-168.
Buffler, R.T. and J.M. Hurst, 1995, Disintegration of the Jurassic-Lower Cretaceous
Megabank, Cuba-Florida-Bahamas (abs): First SEPM Congress on Sedimentary
Geology, Congress Program and Abstracts, p. 35. St. Pete Beach, Florida
Coates, A. G. and Obando, J. A., 1996. The geologic evolution of the Central American
isthmus. In J.B.C. Jackson, A.F. Budd and A.G. Coates (Eds.) Evolution and
environment in Tropical America, 21-56, The Univ. of Chicago Press, Chicago and
London.
Collins, L. S., 1996. Environmental changes in the Caribbean shallow waters relative to
closing tropical American Seaway. In J.B.C. Jackson, A.F. Budd and A.G. Coates (Eds.)
Evolution and environment in Tropical America, 130-167, The Univ. of Chicago Press,
Chicago and London
Damborenea, S.E., 2000, Hispanic corridor: Its evolution and the biogeography of bivalve
molluscs, In R.L. Hall and P.L. Smith eds., Advances in Jurassic Research 2000,
Transtech Publications, Switzerland, GeoResearch Forum v. 6 p. 369-380,
Damborenea, S. E., and Maceñido, M. O., 1979. On the paleogeographical distribution of
pectinid genus Weyla (Bivalvia, Lower Jurassic). Palaeogeography, Palaeoclimatology,
Palaeoecology, 27:85-102.
Droxler, A. W., K. Burke, A. D. Cunningham, A. C. Hine, E. Rosencrantz, D. S. Duncan, P.
Hallock, E. Robinson, 1998, Caribbean constraints on circulation between Atlantic and
Pacific oceands over the past 40 million years in T. Crowley and K. Burke (Ed) Tectonic
Boundary Conditions for Climate Reconstruction, Oxford Monograph on Geology and
Geophysics. 160-191.
Duque Caro, H., 1990. Major neogene events in Panamanian South America. in R. Tsuchi
(ed.) Pacific Neogene events, their timing, nature and interrelationships. 101-114,
Tokyo.
Fernández, M. and M. Iturralde-Vinent, 2000. An Oxfordian ichthyosauria (Reptilia) from
Viñales, western Cuba: Paleobiogeographic significance. J. Vertebrate Paleontology
20(1):191-193.
10
Frakes, L.A., J, E, Francis and J.I. Syktus, 1992, Climate modes of the Phanerozoic, The
history of Earth’s climate over the past 600 million years, Cambridge University
Press, 274 p,
Galloway, W. E., D. G. Bebout, W. L. Fisher, J. B. Dunlap, Jr., R. Cabrera-Castro, J. E. Lugo
Rivera, and T. M. Scott, 1991.Cenozoic, In Salvador, A. (ed.), The Geology of North
America, vol. J, The Gulf of Mexico basin, pp. 245-324. Boulder, CO: Geological
Society of America.
González de Juana, C., J. M. Iturralde de Arozena, X. Picard Cadillat, 1980. Geología de
Venezuela y de sus cuencas petrolíferas, 2 vol. Caracas: Ediciones Foninves, 1031 p.
Gasparini, Z., 1978, Consideraciones sobre los Metrorhynchidae (Crocodylia, Mesosuchia):
su origen, taxonomía y distribución geográfica, Obra del Centenario del Museo de La
Plata, 5, Paleontología, p. 1-9, La Plata.
Gasparini, Z., 1992. Marine reptiles of the circum Pacific region. In G.E.G. Westermann
(Ed.), The Jurassic of the Circum Paciific, World and regional Geology 3:361-364,
Cambridge Univ. Press, London.
Gasparini, Z., 1996. Biogeographic evolution of the South American crocodilians. in G.
Arratia (ed.) Contributions of South America to Vertebrate paleontology. Münchner
Geowiss. Abh.A(30):159-184.
Gasparini, Z. and M. Fernández, 1996, Biogeographic affinities of the Jurassic marine reptile
fauna of South America, In A.C. Riccardi ed., Advances in Jurassic Research, Transtec
Publications, Switzerland, GeoResearch Forum, v. 1-2 p. 443-449.
Gayet, M., J. C. Rage, T. Sampere, P. Y. Gagnier, 1992. Modalité des exchanges de
vertebrés continentaux entre l'Amerique du Nord et l'Amerique du Sud au Cretacé
superior et au Paleocene. Bull. Soc. Geol. France 163: 781-791.
Gingerich, P. D., 1985. South American mammals in the Paleocene of North America. In F.
G. Stehli and S. D. Webb (eds.), The Great American Biotic Interchange, pp. 123-137.
New York: Plenum Press.
González de Juana, C., J. M. Iturralde de Arozena, X. Picard Cadillat, 1980.Geología de
Venezuela y de sus cuencas petrolíferas, 2 vol. Caracas: Ediciones
Gradstein, F.M., L.F. Jansa, S.P. Srivastava, M.A. Williamson, G. Bonham Carter and B.
Stam, 1990, Aspects of North Atlantic paleo-oceanography, In M.J. Keen and G.L.
Williams eds., Geology of the continental margin of Canada, Geological Survey of
Canada, Geology of Canada, v. 2 p. 351-389.
11
Haczewski, G., 1976. Sedimentological reconnaissance of the San Cayetano Formation. An
accumulative continental margin in the Jurassic. Acta Geologica Polonica 26(2):331-353
Hutson, F., P. Mann, P. Renne, 1999. 40Ar / 39Ar dating of single muscovite grains in
Jurassic siliciclastic rocks (San Cayetano Formation): Constraints on the paleoposition
oif western Cuba. Geology 26(1):83-86.
Iturralde-Vinent, M., 1994. Cuban Geology: A new plate tectonic synthesis: Journal of
Petroleum Geology, 17:39-70.
Iturralde-Vinent, M., 1998. Sinopsis de la constitución geológica de Cuba, In: J.C. Melgarejo
and J.A. Proenza (eds.). Geología y Metalogénia de Cuba: una introducción. Acta
Geológica Hispánica 33(1-4):9-56.
Iturralde-Vinent, M. and M. Norell, 1996. Synoptic catalog of Late Jurassic marine reptiles
from Cuba. Am. Mus. Novitates 3164:1-17.
Iturralde-Vinent, M., G. Hubbell, and R. Rojas, 1996. Catalog of Cuban fossil Elasmobranchii
(Paleocene-Pliocene) and paleogeographic implications of their Lower to Middle Miocene
occurrence. Journ. Geol. Soc. Jamaica, XXXI:7-22.
Iturralde-Vinent, M.A., R.D.E. MacPhee, 1999. Paleogeography of the Caribbean region:
implications for the Cenozoic biogeography. Bull. American Museum of Natural History,
238:1-95.
Jones, E.J.W., S.C. Cande and F. Spathopoulos, 1995, Evolution of a major oceanographic
pathway: the equatorial Atlantic, In R.A. Scrutton, M.S. Stoker, G.B. Shimmield and
A.W. Tudhope eds., The tectonics, sedimentation and paleooceanography of the North
Atlantic region, London Geological Society Special Publication, v. 9 p. 199-213.
Khudoley, K. y A. Meyerhoff, 1971. Paleogeography and geological history of Greater
Antilles. GSA Mem. 129:1-199
Klitgord, K.D., D. R. Hutchinson and H. Schouten, 1988, U.S. Atlantic continental margin;
structural and tectonic framework, In R.E Sheridan and J.A. Grow eds., The Geology of
North America, v. 1-2, The Atlantic continental margin, Geological Society of America, p.
19-55.Kerr, A. C., M. Iturralde-Vinent, A. D. Saunders, T. L. Babbs, J. Tarney 1999. A
geochemical reconnaissance of Cuban Cretaceous volcanic rocks: Implications for plate
tectonic models of the Caribbean. GSA Bull. 111(11):1581-1599.
Lawver, L.A., M.F. Coffin, I.W.D. Dalziel, L.M. Gahagan and R.M. Schmitz, 1999, Plates
1999, Atlas of Paleogeographic reconstructions, PLATES Progress Report No. 350799, University of Texas Institute for Geophysics, 84 p.
12
Leonov, Yu. G., and V.E. Khain, 1987. Problems of a systematic approach to the study and
correlation of tectonic phases. In Yu. G. Leonov, and V.E. Khain (eds.), Global
correlation of tectonic movements, pp. 1.12. New York: Wiley
Macellari, C. E., 1995.Cenozoic sedimentation and tectonics of the southwestern Caribbean
pull-apart basin, Venezuela and Colombia. In A. J. R. Tankard, R. Suarez Soruco, and
H.J. Welsink (eds.), Petroleum basins of South America, Mem. Amer. Assoc. Petrol.
Geol. 62: 757-780.
MacPhee, R. D. E., and M. A. Iturralde-Vinent, 1994.First Tertiary land mammal from
Greater Antilles: An Early Miocene sloth (Xenarthra, Megalonychidae) from Cuba.
Amer. Mus. Novitates 3094: 1-13.
MacPhee, R. D. E., and M. A. Iturralde-Vinent, 1995.Origin of the Greater Antillean land
mammal fauna, 1: New Tertiary fossils from Cuba and Puerto Rico. Amer. Mus.
Novitates, 3141: 1-31.
Marton, G., Buffler, R. T., 1994. Jurassic reconstruction of the Gulf of Mexico basin.
International Geology Review, 36, 545-586.
Miller, K. G., G. S. Mountain, Leg 150 Shipboard Party, and members of New Jersey Coastal
Plain Drilling Project. 1996.Drilling and dating New Jersey Oligocene-Miocene
sequences: ice volume, global sea level, Exxon record: Science 271: 1092-1095.
Parrish, J.T., 1992, Climatology and oceanology, In G.E.G. Westermann ed., The Jurassic of
the circum-Pacific, Cambridge University Press, p. 365-379.
Pindell, J. 1994. Evolution of the Gulf of Mexico and the Caribbean, in S.K. Donovan and T.A.
Jackson (Eds.) Caribbean Geology, an introduction. The University of West Indians
Publishers. Ass., 13-40, Jamaica.
Prothero, D.R., 1994. The Eocene-Oligocene transition. In D.J. Bottjer and R.K. Bambach
(Ed.) Critical moments in the paleobiology and Earth History Series, 281 pp., Columbia
Univ. Press, New York.
Pszczolkowski, A. 1978. Geosynclinal sequences of the Cordillera de Guaniguanico in western
Cuba; their lithostratigraphy, facies development and paleogeography: Acta Geol.
Polonica 28 (1): 1-96.
Pszczolkowski, A. 1982. Cretaceous sediments and paleogeography in the western part of
the Cuban miogeosyncline: Acta Geol. Polonica 32 (1-2): 135-161.
13
Pszczolkowski, A., 1994. Lithostratigraphy of Mesozoic and Paleogene rocks of Sierra del
Rosario, western Cuba. Studia Geologica Polonica, 105:39-66.
Pszczolkowski, A. and Flores, R., 1986. Fases tectónicas del Cretácico y del Paleógeno en
Cuba occidental y central. Bull. Polish Acad. Sci., Earth Sci., 34(1):95-111.
Ricardii, A.C., 1991. Jurassic and Cretaceous marine connections between the southeast
Pacific and Tethys. Palaeogeography, Palaeoclimatology, Palaeoecology, 87:155-189.
Rojas, R., M. Iturralde-Vinent and P. Skelton 1995. Stratigraphy, composition and age of
Cuban rudist-bearing deposits. Revista Mexicana de Ciencias Geológicas, 12 (2) 272-291
Salvador, A., 1987. Late Triassic-Jurassic paleogeography and origin of the Gulf of Mexico
basin: AAPG Bull. 71(4):419-451.
Shol, N.F. and Kollmann, H.A., 1985. Cretaceous actaeonellid gastropods from the western
hemisphere. U. S. Geological Survey, Prof. Pap. 1304:1-104.
Smith, P.L., 1983. The Pliensbachian ammonite Dayiceras dayiceroides and Early Jurassic
paleogeography. Can. J. Earth Sci., (20):86-91.
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FIGURES
Figure 1. Major events in the evolution of the Caribbean Seaway from Jurassic to Recent. Data from
Iturralde and MacPhee (1999:Fig. 12 and tables 1 - 4). On the left part of the graphic, the dotted
vertical strips are the permanent continental masses of North and South America (NA and SA),
the central patternless zone represent the Caribbean marine area, and the bubble rows indicate
topographic barriers within the Caribbean. The right part of the graphic bring information about
the topographic barriers and the marine seaway. The thin vertical strip within the textual area is
intended to show in black major shutdowns of the flow along the Caribbean Seaway, and with
15
horizontal pattern the time lapses when water exchange was possible between the Pacific and
Atlantic/Tethyan oceans. Chronology not to scale.
Figure 2. Main scenarios of Late Eocene to Recent marine surface circulation across the
Caribbean Seaway. After data from Prothero (1994), Coates and Obando (1996), Droxell
et al. (1998), Iturralde-Vinent and MacPhee (1999: Fig. 10). Since the Late Eocene the
course of westward-flowing currents in the mid-Atlantic/Tethys across the Caribbean
Seaway has been greatly affected by the appearence and disappearence of various
topographic barriers. Thus, the Circumtropical current, which originally passed into the
western Pacific (Late Eocene) was temporarily disrupted during the Eocene-Oligocene
transition by the emergence of Gaarlandia, during the Late Miocene by the partial
emergence of Central America, and was permanently disrupted by the uplift of Central
America in the Late Pliocene.
16
Table 1. Stratigraphic indicators for land, shallow marine, and deep marine environments
during the latest Eocene-early Oligocene (35-33 Ma, Zones P16-18) interval within the
Caribbean realm and its surroundings. Some present-day geographic areas are not listed
because they do not existed at this time interval (Cayman Trench, Windward Passage, Mona
Passage, Anegada Trough, etc.). Compiled from Iturralde-Vinent and MacPhee, 1999, table 2
and appendix 1.
Location
Land indicators
Shallow marine and
Deep marine
(hiatuses, red beds,
costal indicators
indicators
alluvia, paleosls,
(lagoonal sediments,
(Globigerine ooze,
terrestrial plant and
carbonate shelf, etc.)
etc.)
animal fossils,
nearshore
conglomerates)
Florida Peninsula
X
X
-
Bahamas Platform
X
X
X
Southern Mexico
X
X
X
Yucatan Peninsula
X
X
X
Northern Central
X
-
-
-
X
X
X
X
X
X
X
-
Nicaragua Rise
X
X
-
Cayman Ridge
X
X
-
Beata Ridge
-
X
-
Aves Ridge
X
X
-
Cuba
X
X
X
Jamaica
X
X
X
Hipaniola
X
X
X
Puerto Rico-Virgin
X
X
-
Lesser Antilles
X
X
?
Yucatan Basin and
-
?
X
America
Southern Central
America
Northeastern South
America
Northeastern South
America shelf and
islands
Islands
17
Cayman Rise
Colombia and
-
-
X
-
X
X
Venezuela Basins
Grenada Basin
18