Geography Reference
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terns may need to be treated within a multiple time plane approach (Rosen
and Smith 1988) or time slicing (Upchurch et al. 2002). The latter term cor-
respondstothe analysisofbiotic distributional data accordingtoasequence
of individual stratigraphic intervals (time slices).
Let us consider an example. Originally (time t 0 ), we have a biotic com-
ponent A. Then a vicariance event at time t 1 produces two biotic compon-
ents endemic to areasB andC. At time t 2 these biotic components converge
in a single biotic component in area D because of geographic coalescence,
but a trace of the previous endemism may be still recognizable. Finally, at
time t 3 two new endemic biotic components occur in areas E and F after
another vicariance event that subdivided the former component inhabiting
area D. How does one recognize the vicariance event at t 1 if the effects
of biogeographic convergence that formed the biotic component of area D
overwhelmed the biotic fingerprint on the two original biotic components B
and C? How does one recognize what happened at times t 1 and t 2 if one
studies only the latest time plane (t 3 ) and the lineages occurring in areas E
and F?
Events of biogeographic convergence such as those described for
Mesozoic ammonites (Cecca 2002) or for plant and animal taxa from the
Mexican Transition Zone (Halffter 1987) produce a sort of overprinting of
past biogeographic histories by more recent patterns (e.g., reticulated area
histories). This overprinting lowers the chances of establishing area relation-
ships through congruence, which is the final goal of cladistic biogeography.
The solution to problems posed by instances of biogeographic convergence
is time slicing (Grande 1985; Upchurch and Hunn 2002). Although assess-
ments of faunal similarity usually are undertaken with faunas of successive
geological ages, traditional cladistic biogeography has used data on organ-
ism relationships and spatial distributions only on a single time plane (usu-
ally the present). Time slicing may reconcile the use of time and a synchron-
icapproach.Ideally,paleobiogeographersshouldbeabletouseasynchron-
ic approach for each time slice they identify. This is difficult because of the
limits imposed by geological constraints (e.g., insufficient precision or resol-
ution of chronological correlations, incompleteness of the fossil record).
Methods: Temporally Partitioned Component Analysis
In order to apply time slicing, three methods are available. Two of them,
parsimony analysis of endemicity and area cladistics, have been already
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