@flmnh.ufl - sgp.org.pe · heydt & dijkstra 2006 5000 2500 nof and van gorder 2003 2500....
TRANSCRIPT
Orange=warm shallow waters
Blue=cold deep waters
Thermohaline Circulation
Broecker et al 1987; Lozier 2010
BIRTH OF CARIBBEAN SEA
Caribbean
non-seasonal
nutrient-poor
high-carbonates (corals)
Pacific
Seasonality
rich in nutrients
low carbonates (few corals)
Classic “Panamanian Isthmus Rise” Literature
(more than 1800 citations over past 30 years)
Title Author/Publication Date
Total citations (Web of Knowledge)
Total citations (Google Scholar)
The geology of the Darien, Panama, and the late Miocene-Pliocene collision of the Panama Arc with northwestern South
America Coates et al., 2004 84 100
Early Neogene history of the Central American arc from Bocas del Toro, western Panama Coates et al., 2003 43 41
Effect of the formation of the Isthmus of Panama on Atlantic Ocean thermohaline circulation Haugh, 1998 356 408
The geologic evolution of the Central American isthmus Coates & Obando, 1996 - 460
Closure of the Isthmus of Panamá: The near-shore marine record of Costa Rica and western Panama Coates et al., 1992 - 306
The Choco Block in the Northwestern corner of South America: structural, tectonostratigraphic and paleogeographic implications Duque, 1990 - 78
Neogene stratigraphy, paleoceanography and paleobiogeography in northwest South America and evolution of
the Pama Seaway Duque, 1990 181 217
The great American biotic interchange Stehli & Webb, 1985 - 258
Splendid Isolation: The Curious History of South American Mammals Simpson, 1983 - 366
Pliocene closing of the Isthmus of Panama, based on biostratigraphic evidence from nearby Pacific Ocean and
Caribbean Sea cores Lloyd, 1978 - 222
“no vicariant date [3.5 Ma] is better dated than the Isthmus (Lessios et al 2008)”
Thermochronology
Farris et al 2011 Montes et al 2012
42-46 23-25
10-12 Panama block initial collision
with South America, initial uplift eastern Andes northern
South America
Farris, et al in review
The very shallow crystallization depth of Late basalt indicates no exhumation since the Miocene, or at the very least burial=exhumation
.
~16 Ma CANAL BASIN
(central Panama)
Lowland pollen flora
Cucaracha & Culebra Fm
Early Miocene (~18 Ma)
Panama Canal
Lowland flora
Barro Colorado Island 50ha plot
Extant
Panama Canal
Jaramillo et al 2014
Az
Az
BCI
Miocene
A 20 million year old rainforests based on permineralized
fruits and seeds from the Cucaracha Formation
Lauraceae Juglandaceae Parinari
Sacoglottis Spondias Vitaceae Annonaceae
Herrera et al, in press
FRESH-WATER TURTLES, EARLY MIOCENE, CUCARACHA/CULEBRA
TESTUDINES
CRYPTODIRA
Geoemydidae
Rhinoclemmys panamaensis new speies
Early-middle Miocene
Cucaracha Formation, Panama
Estimated carapace length: 41 cm.
Cadena et. al. 2012
TESTUDINES
CRYPTODIRA
Kinosternidae
Staurotypus moschus new species
Early-middle Miocene
Cucaracha Formation
Estimated carapace length: 27cm
TESTUDINES
CRYPTODIRA
Trionychidae Incertae sedis
Early-middle Miocene
Cucaracha Formation
Cadena et. al. 2012
NA->CA
NA->CA
NA->CA
TESTUDINES
PLEURODIRA
Podocnemididae Incertae sedis
Early Miocene
Culebra Formation, Panama
Estimated large size of the shell:
100 cm.
SA->CA
Culebrasuchus mesoamericanus
cf. Purussaurus sp
SA->CA
Sister taxa to all Caimaninae
SA->CA
Hasting et. al. 2012
Crocodiles
EARLY MIOCENE
The colonization of Central America by South American
Pristimantis involved at least 11 independent events.
At least 8 of these invasions into CA
took place prior to 4 Ma, mainly in the Miocene (6-14Ma)
Pinto et al, 2012
rain frogs, largely restricted to moist, forested habitats
part of of SA clade Terrarana
Coates et al 2004
Montes et al 2012
Very similar models
but our model 1)quantify
the width of seaway (~200km)
and 2)terrestrial fossils indicate
a continuous land connection
of canal basin with NA
CAS
~21 Ma
Coates et al 2004
Montes et al 2012 ~10 Ma
Both models show a collision
of SA & Panama microplate
by 10 Ma CAS
connection is closed
No
CAS
No
CAS
Vargas and
Mann 2013
The collision
of Panama
Indenter produces
a tear across the
Andes, The Caldas
Tear, that starts
~10 Ma
*After McDougall’s (1996) taxonomical identification
-1.0 -0.5 0.0 0.5 1.0
-1.0
-0.5
0.0
0.5
1.0
ord$points[,1]
ord
$poin
ts[,
2]
Dimension 1
Dim
en
sio
n 2
Pleistocene
Pliocene
MessinianSite 503 (Pacific)
Site 502 (Caribbean)
Site 503
Site 502
Deep benthic foraminifera
Data after McDougall (1996)
MDS
By late Miocene, already separated
CAS paleoceanographic models
author CAS depth (m) CAS width (Km)
Mikolajewicz and Browley 1997 2100 90
Steph et al 2006 800 200
Scheider and Schmittner 2006 130;700;2000 450
Murdock et al 1997 3600 700
Nisancioglu et al 2003 1000;2700 840
Butzin et al 2011 250;500;1000;3000 900
Prange and Schulz, 2004 700 1000
Klocker et al 2005 700 1000
Steph et al 2010 700 1000
Lunt et al 2008 370 1400
Maier-Reimer et al 1990 2711 1700
Mikolajewicz et al 1993 2711 1700
Heydt & Dijkstra 2005 5000 2500
Heydt & Dijkstra 2006 5000 2500
Nof and van Gorder 2003 2500
Surface waters
A->P
Intermediate waters
P->A
Deep waters
P->A
-Net Flow P->A
-reduces salinity of A
-slows down
AMOC (Atlantic
Meridional Overturning
Circulation)
CAS
-400km wide
-Along a
parallel
Sepulchre et al 2014
NET FLOW P->A
7.8Sv ---------- Sill 1500m deep
5.4Sv----------- Sill 500m
0.4Sv----------- Sill 200m
-3.8Sv---------- Sill 50M
Major drop in P-A flow exchange once
a 200m deep CAS is reached
AMOC
NO
AMOC
Northern hemisphere glaciation (NHG)
CAS closure, End of permanent El Nino, CO2
threshold, cooling of Antarctica, unknown mechanism