s 22 s
The Ocean Hoppers
Geographical
Limitations of Species
Throughout
the millions of years complex life has been on this planet, species have
usually been geographically limited by the oceans. For example, if a certain creature lives in
Europe, it will not be able to cross the Atlantic and go to the Americas, nor
will it be found in Australia, but it might cross Arabia into Africa, or Russia
into Asia. Consequently, we might find
related species in Europe and Africa and Asia; however, we should not expect to
see related species in both Europe and America, or Europe and Australia, unless
introduced by humans.
Indeed,
this rule holds true in most cases, as the fossil record attests. Isolated landmasses like Australia and
Madagascar sport unique animals like kangaroos and mongooses, because they have
been evolutionarily isolated for a long time.
Madagascar lost contact with Africa around 130 million years ago. Australia's most recent connections have been
with Antarctica, a continent rather devoid of life anyway. South America also used to be home to many
unique animals, before the isthmus of Panama came into existence about 4
million years ago. South American
fossils from before 4 million years ago typically represent evolutionary
lineages that are unknown to the rest of the world.
This
phenomenon is to be expected under normal evolutionary conditions. Natural selection will yield different
results on different continents. The
terrestrial life forms that evolve on unconnected continents will remain
different from each other, as long as vast oceans restrict them from invading
each other's geographic range. For the
most part, the fossil record establishes that this is indeed the case.
However,
exceptions do exist. The geographic
restriction of terrestrial life forms is occasionally violated by anomalies in
the fossil record. Certain families and
genera show up in parts of the world where they should not be. They appear on two or more continents that
were separated by broad oceans, often with no likely explanation for how they
got there. Examining these anomalies is
the subject of this chapter.
Noah's Ark of Marsupials
Toward
the end of the dinosaurs' long reign, there lived a marsupial whose name was Glasbius. 20 specimens have been found among the
Lancian rocks of North America,[1]
dating to the range of 67-65 million years ago.
Glasbius disappeared from
North America 65 million years ago, along with the dinosaurs.
However,
immediately after the extinction, some close relatives of Glasbius appeared in South America.
These relatives were so similar to Glasbius
that they are classified together in the same family – that is
Caroloameghiniidae, or super-family Caroloameghinioidea.[2] [3] [4] Glasbius
may be a close cousin of its South American relatives.[5] Glasbius
and the South American Carolameghiniidae are similar enough that an
evolutionary relationship would normally be presumed.
Yet
nothing like Glasbius or the
Caroloameghiniidae existed in South America before the dinosaurs went extinct. Their debut in South America occurs in the
Tiupampa fossil beds of Bolivia.[6] The Tiupampa is the early Paleocene,
immediately after the dinosaurs, and immediately after Glasbius went extinct from North America. A couple of other close kin of Glasbius are also known from the
Paleocene of South America.[7] Hence, before the dinosaurs went extinct, the
Caroloameghiniidae are known only from North America; yet after the dinosaurs
went extinct, they are known only from South America.
It's
as if the whole lineage migrated from North America to South America. The problem is, Central America had not yet
formed at that time. A wide ocean
separated North America from South America.
There was no Panama land bridge between the two as there is today. Thus, it is difficult to explain why or how
these animals relocated from North America to South America. Particularly, why would such a relocation
just happen to coincide with the extinction of the dinosaurs?
One
explanation could be that extraterrestrial and/or supernatural intervention
saved the Caroloameghiniidae. Perhaps
the gods saw fit to save this creature from the cataclysm that killed the
dinosaurs, and so they protected a few of them and transplanted them to South
America. Much like Noah saving a few
animals before the Flood, it appears that some benevolent god loaded these
creatures onto some kind of boat or craft and saved them from destruction.
But
why would the gods rescue the Caroloameghiniidae and not rescue other
species? One plausible answer might be
that the gods saw evolutionary potential in the Caroloameghiniidae, because
they were somewhat like primates.[8] As such, they had the potential to evolve
along the same lines as apes and eventually humans. As it turned out, the true primates beat them
to the punch, and so the rescue mission was an exercise in futility. None the less, it was a reasonable gamble for
the gods to take given the evolutionary odds of developing an intelligent
creature.
Another
genus within the family is Chulpasia, which
is similar to Thylacotinga from
Australia.[9] If all these belong to the same lineage, as
their similarity suggests, it would mean, perhaps, that the Caroloameghiniidae
were also airlifted to the distant continent of Australia; however, it is
currently believed that such migrations to Australia occurred over a land
bridge via Antarctica, as Antarctica was warmer then.
The
Pediomyidae were another family of marsupial mammals, which seem to have disappeared
from North America along with the dinosaurs, but then inexplicably reappeared
in South America immediately after the dinosaurs became extinct. The Pediomyidae were found in South America
in the Laguna Umayo Formation,[10]
which was at first thought to be Cretaceous in age, but was later demonstrated
to be early Paleocene.[11] One can clearly see that the Pediomyidae
suffered complete extinction from North America at the same time the dinosaurs
suffered extinction, for nearly 100 fossilized specimens have been found in
North America from the time immediately before the end of the dinosaurs, but
none have been found after the end of the dinosaurs.[12] Only in South America did they reappear. Nor is this because more advanced animals
replaced these marsupials, for the early Paleocene fauna of North America
consists largely of primitive marsupials and multituberculates, which were
common on both sides of the extinction event – not being replaced by advanced
mammals until the Eocene.
The
mainstream explanation is as follows:
These marsupials evolved first on North America, then migrated to South
America over an elusive land bridge,[13]
which allegedly rose and fell multiple times.[14] Then, some of them moved from South America
to Antarctica over another elusive land bridge, where they thrived because the
earth was warmer back then. Finally,
they arrived in Australia, because Australia at that time was still connected
to Antarctica. That's the naturalistic
explanation for how marsupials got to South America and Australia. But why did these migrations just happen to
coincide with the extinctions of the same lineages from North America? Moreover, if there was a landbridge, then why
didn't more species cross it? For the
most part, North American and South American fauna were different –
Caroloameghiniidae and Pediomyidae are the exception, not the rule.
Monkeys
Ever
since monkeys first emerged in the Oligocene, they appear to have lived on both
sides of the Atlantic Ocean. The
Atlantic Ocean is nearly 1,800 miles from the western-most coasts of Africa to
the eastern-most coasts of South America.
In the early Oligocene, the distance was perhaps 1,000 miles – still a
formidable obstacle for any land animal to cross. Moreover, the impossibility of a land bridge
or series of islands that could facilitate migrations is confirmed by the fact
that this region of the South Atlantic is consistently deep and devoid of
underwater mountain building. No Bering
Strait here.
The
Old World monkeys and the New World monkeys are so similar that convergent
evolution may be ruled out. Science
believes that the monkeys migrated from Africa to South America about 37
million years ago. Furthermore, this
remarkable journey across the Atlantic only happened once. According to Wicander and Monroe,
No evidence exists of any
prosimian or other primitive primates in Central or South America nor of any
contact with Old World monkeys after the initial immigration from Africa.[15]
That a migration happened might
be remotely plausible, given the possibility that the monkeys rafted across the
Atlantic on dead trees; but if it happened once, we should expect it to happen
again and again. Yet such is not the case. There is but one single lineage of New World
monkeys, which demands that there was at most just one single migration
event. Moreover, this migration event
just happened to occur at the very same time the monkeys first evolved. Is this coincidence or something more?
Perhaps
the gods were having more than a barrel of fun with the monkeys, so they
transported some monkeys to South America to enlarge their habitat and
population. Or, perhaps they considered
it advantageous to have the ancestors of potentially intelligent life forms
evolving on two different continents, to enhance the potential of positive
evolutionary advancements within the primate group.
A
similar situation exists with the carnivores of Madagascar, for molecular DNA
evidence demonstrates that they are all one single lineage. This fact indicates that there was one and
only one migration of carnivores from Africa to Madagascar.[16] Again, the same question should be asked – if
animals can cross the ocean once, why didn't they do so again and again? Why was there only one migrational event of
carnivores across the ocean from Africa to Madagascar?
Large Animals Crossing the Ocean
It
would be quite amazing to see a marsupial or a monkey gripping a log and
crossing the ocean on it, but it would be utterly unthinkable to see an
elephant or a giant ground sloth doing the same thing.
In
the mid-Cenozoic, Africa and Arabia were moving north together, slowly closing
the ancient Tethys Sea. Eventually, this
northward drift caused Africa and Arabia to join with Asia. The fusion of these continents split the
Tethys Sea into the current day Mediterranean Sea and Persian Gulf. The time of this event was at first thought
to have been 17.5 million years ago.
Before then, Africa and Arabia were supposedly isolated from
Eurasia. However, this has subsequently
been called into question on account of African elephants appearing in Asia
during the late Oligocene, which is at least 7 million years beforehand. This leaves open the question of how the elephants
got across the Tethys Sea, and has spawned a theory that temporary land bridges
emerged before the collision.[17] Alternatively, it could mean the elephants
were transported.
Concerning the large-bodied terrestrial
South American mammals known as xenarthtra, which includes anteaters,
armadillos, and giant ground sloths, Pujos et al reported:
The presence of xenarthra in other
continents remains ambiguous. Purported
xenarthrans have been reported from the Eocene of Europe (the
"anteateroid" Eurotamandua from Messel, Germany; Storch, 1981)
and Asia (the "pseudo-xenarthrans," Ernanodon and Asiabradypus
from the late Paleocene of China; Ding, 1979; Radinsky and Ding, 1984;
Nessov, 1987 and Chungchienia from the Middle Eocene of China; Chow,
1963; Chow et al., 1996; Rose et al.,
2005).[18]
Hunter and Janis also noted the
anomalous presence of xenarthrans in Europe and Asia, such as Palaeanodonta, Ernandon, and Eurotamandua.[19] Given that xenarthra originated in South
America and are common only to that continent, and given that South America was
isolated from the rest of the world during the entire time of xenarthran
existence, up to 4 million years ago when Panama rose from the sea; it is
strange to find xenarthrans on other continents prior to 4 million years
ago. Could it be that something, or
someone, transported them there?
George Gaylord Simpson's Sweepstakes
George
Gaylord Simpson, one of the most widely respected paleontologists of all time,
mentioned a few bio-geographical oddities himself. Among them was the horse Anchitherium, which existed in both Spain and North America, and
the elephantine Mastodon, which
originated in Africa but somehow got to North America. Simpson proposed that such distributions of
animals across continents was best attributed to plate tectonics – that is,
continents moving around and crashing into one another, thus allowing animals
to migrate from one continent to another across dry land.[20] Today, plate tectonics are relatively well
understood, and we can date the approximate times that certain continents were
connected by land bridges, and when they were not. The ability to date the locations of the continents
imposes some limitations to Simpson's theory, because not all strange
distributions of animals across continents can be explained when certain
constraints in deep time place vast oceans in the way of immigrations that we
know must have happened. But Simpson
also had a second theory on migration which addresses this problem.
Simpson
proposed that some animals get "sweepstakes tickets" across large
bodies of water. According to the
theory, a pregnant animal hops on a log or sturdy mat of vegetation that floats
out to sea, and somehow the animal stays afloat and hydrated until it reaches a
foreign continent. The new continent is
then populated by means of incest among the children of the immigrant. However unlikely such a journey may be, it
stands to reason, so they say, that it happens once every billionth blue
moon. In such a fashion, it is believed,
monkeys and marsupials crossed over to South America, and a multitude of other
lucky land mammals traversed the waters between Eurasia and the islands of
proto-Spain and proto-India, and others from Asia to the East Indies.
Rodents – A Challenge to Simpson's Sweepstakes
A
problem with the theory concerns the lack of rodents who made these alleged
epic journeys on the high seas. If
monkeys and marsupials can hop on logs and cross an ocean, then certainly
squirrels and rats should be capable of doing so also. There are several factors which make rodents
prime characters for testing the sweepstakes theory. First, rodents are small enough to float on a
log without weighing it down. Second,
they have claws which can cling to a log tossed about by waves. Third, rodents have an excellent fossil
record. Their fossils can be found in
abundant numbers, much more so than the majority of other terrestrial
vertebrates. If they made it to a certain
continent, we should expect to find fossil evidence for their arrival.
However,
such is not the case. Of the 151 genera
of mice and rats listed in McKenna and Bell, not a single genus appears
indigenously on both sides of a large ocean when there is no plausible
terrestrial connection – not a single one.
Granted, they got to Australia, but this only happened at a very late
date, and only because of the low sea levels caused by the ice ages. For the vast majority of the time mice and
rats have been on this planet, the bulk of which was before the ice ages, they
were absent from Australia. Mice and
rats never did make it to the Americas – not by natural means.[21] It took Christopher Columbus to bring them to
the New World. If there were ever an animal
that was small enough, agile enough, with claws clingy enough, and with enough
of a limit to its fresh water requirements due to its small size, to climb
aboard a tree branch and float across the turbulent high seas, shouldn't we
expect a mouse to do it?
Concerning
the broader category of rodents as a whole, of the 246 families, subfamilies,
tribes, and subtribes listed in McKenna and Bell, three clear examples exist
where the same group appears on both sides of a wide ocean without a plausible
landbridge.[22]
Porcupines
are the biggest of the three mysteries.
Of all the rodents that might grip a log and hold on for a thousand
miles of mighty waves, porcupines are one of the least likely candidates. They are large and unstable compared to
squirrels, mice, and a host of other rodents, both extant and extinct. Porcupines first appear in the Oligocene of
South America. Rodents as a whole had
originated in Asia – the farthest place on Earth from South America. So how did porcupine ancestors get from Asia
to South America? One thing is
certain: they could not have come via
North America. Although Beringia
(Alaska-Siberia) was functioning as a landbridge for much of the Cenozoic, the
Panamanian landbridge did not exist until just 4 million years ago. Moreover, there are no fossil porcupine
species in North America until after the Panamanian landbridge was established
– meaning that North American porcupines came from South America, not
vice-versa. Could they have come from
Africa? The problem here is also
two-fold; first, because Africa was already separated from South America long
before rodents even existed, and second, because porcupine relatives in Africa
do not appear until the Miocene, which is after they first appeared in South
America. It is possible that porcupines
were in Europe during the Oligocene,[23]
in which case we are left with the unlikely proposition that the porcupines
pulled a Christopher Columbus across the widest part of the Atlantic.
The
other two inexplicable rodent distributions are the case of the African rodent
family Zegdoumyidae, and the genus Protophiomys.[24] These appear in the African Eocene long
before Africa was attached to Asia via the Suez. The Afro-Arabian continental plate separated
from Eurasia while the age of the dinosaurs was still young, and it did not
rejoin Eurasia until the time of human-like apes. The Eocene is after the former but before the
latter. Thus, Africa was an island continent
when these lineages of rodents somehow immigrated to it.
The
history of rodents is well known from the fossil record. They originated in Asia during the Paleocene,
from whence they quickly migrated to Europe and onward to North America across
the Greenland-Norway landbridge. After
Greenland and Norway were permanently separated by ocean about 40 million years
ago, Beringia still provided for North America and Eurasia to continue sharing
their mutual rodent infestations. In the
Miocene, temporal landbridges or closely spaced islands allowed rodents to
cross into Africa in large numbers. But
from Africa, they could not cross over to Madagascar until the ice ages lowered
the sea level. Therefore, Madagascar was
free of rodents even while Africa swarmed with rodents for over 10 million
years! The same is true for New Guinea
and Australia, which were entirely free of rodents until the ice ages lowered
sea levels, thus creating opportunities for the rodents of Asia to island hop
their way to the land down under.[25]
Hence,
there is considerable evidence that rodents are in fact constrained by large
oceans, and do not cross them much easier than any other type of terrestrial
animal. If they cannot cross oceans,
even with their small and agile frame, and clinging claws, then how is it that
larger animals crossed the oceans?
For
these reasons, it is at least plausible to suppose that paranormal or
extraterrestrial entities have transported creatures across continents. Indeed, it may be the only likely
explanation.
Alien Abduction
What happened in Enoch’s time, when angels came down from
heaven and began to procreate with animals and humans, is also happening today,
only today it is no longer attributed to angels, but is recognized as alien
abduction. Alien abduction of both
animals and humans is a longstanding phenomenon known to those who study
UFOs. Sometimes, when the aliens are
finished probing, terrifying, defiling, and otherwise abusing their abductees,
they unceremoniously dump them in whatever random location is convenient. In this manner, we might explain the occasional
fossil which shows up on a continent it does not belong.
The agenda of the extraterrestrials is to use human sexual
mechanisms to create one or more new species.
At the moment, they don't want to conquer us as Hollywood pictures in
the movies, nor do they want to help us as the New Agers hope. Instead, UFO researchers report a scenario
much more akin to the situation in Enoch’s time – that is, heavenly entities
secretly coexist with us for the purpose of genetic engineering.
One of the most widely respected UFO
researchers is Dr. David Jacobs, who has effectively reduced UFO abduction
research into a science that can be studied using large sets of quantifiable
data. According to Jacobs,
The
evidence suggests that all the alien procedures serve a reproductive
agenda. And at the heart of the
reproductive agenda is the Breeding Program, in which the aliens collect human
sperm and eggs, incubate fetuses in human hosts, to produce alien-human
hybrids, and cause humans to mentally and physically interact with these
hybrids for the purposes of their development…[26] The production of a hybrid species appears to
be the means to the aliens’ goal. So
far, researchers have been unable to uncover any other purpose for the UFO and
abduction phenomena, and the Breeding Program.[27]
Leading
UFO researcher Budd Hopkins adds confirmation.
About his first alien abduction case in 1983 he writes that it was,
The first
of hundreds of similar cases I subsequently investigated in which women
reported being abducted and apparently artificially inseminated, after which
they found themselves pregnant. Then
equally mysteriously, about the end of the first trimester, but often weeks or
months later, the pregnancies disappeared, with no trace of fetal tissue.[28]
Jacobs
adds,
On many
occasions, abductees have reported scheduling an abortion only to find an empty
uterus during the actual procedure.[29]
For
the skeptics, Jacobs lays down several reasons for why alien abductions are
real:
Abductees
are physically missing during the event.
The abductee is not where he is supposed to be; people who search for
him cannot find him. The abductee is
usually aware that there is a gap of two or three hours that neither he nor
anyone else can account for… Approximately 20 percent of abductions include two
or more people who see each other during the abduction event.[30]
These
factors make it improbable, even impossible, that the abduction phenomena are
only psychological delusions.
Hopkins and Jacobs claim that female
abductees typically develop health problems associated with their reproductive
organs, even to the point where hysterectomies are common. During hysterectomy operations, doctors
sometimes notice scar tissue has developed on the ovaries or the fallopian
tubes, indicating that something or someone penetrated the abductees’ stomachs
to retrieve or impregnate eggs.[31] [32]
This aspect of the alien abduction
phenomena is consistent with the fact that female abductees typically report
the aliens inserting a long needle into their stomach. This procedure is a constant component of the
abduction experience, going back to the very first time a woman was allegedly
abducted by aliens. In 1961, Barney and
Betty Hill made history by becoming the first victims of alien abduction to have
their experience widely published. The
couple reported that the aliens ran a long needle into Betty’s stomach, telling
her it was a pregnancy test. Such a
procedure was entirely unknown in 1961, but is commonly done today for the
purpose of removing eggs for in-vitro fertilization. After the abduction experience, Barney
contracted genital warts, possibly from the aliens.[33] Jacobs attests that of 700 abduction cases he
has studied, almost 150 of them contain abductee testimony that eggs were taken
during the abduction.[34]
Another very early UFO abduction incident,
which allegedly took place in 1957, concerned a Brazilian farmer named Villas
Boas who was ostensibly forced to engage in sexual intercourse with a naked
female human-like alien. After the
sexual encounter, the alien pointed to her stomach and then pointed upward to
the sky, suggesting that she would become pregnant with his child, and that it
would be born in the sky with her. The
pattern of alien-human sexual activity for the purposes of reproducing a hybrid
species has been a consistent component of the alien abduction phenomena ever
since it began in the 1950's, and ever since it first began in the time of
Enoch.
Concerning bestiality, cattle mutilations
also play a likely role in the reproductive goals of the aliens. In typical cattle mutilations, animals such
as cows, sheep, goats, or horses are slaughtered, but without any trace of
blood. Internal organs are removed, and
UFO sightings often accompany the event.
UFO writer and Ugaritic scholar Heiser notes that a bovine uterus is
very similar to a human uterus. The
aliens are apparently killing cows to take their uteruses. Then they incubate hybrid human-alien fetuses
inside of the bovine uteruses.[35] This explains why the cattle mutilations are
occurring.
A Condylarth Who Crossed Two Oceans
The
condylarths were an ancient group of mammals that lived soon after the
dinosaurs became extinct. From 65 to 40
million years ago, they roamed across the northern supercontinent of Eurasia-North
America, which was at first connected via Greenland and later by Beringia. The earth was much warmer then, and the
continents farther south, so many species easily traversed Greenland and
Alaska.
There
were also condylarths in Africa and in South America. However, the species on those two southern
continents were different from those in the north. While the ancestors of deer, horses, and pigs
roamed the northern continents, a weird camel-like creature called litopterna
roamed South America, and the hyracoids roamed Africa. This was because the condylarths were
separated by vast oceans, which kept them from intermingling. Africa was separated from Europe by the Tethys
Sea – a large and turbulent ocean that had existed deep into the age of the
dinosaurs. Spain was far distant, and a
good deal of the Middle East had not even risen from the ocean yet. Africa was an island continent. So too was South America.
Yet
despite this, a certain lineage of condylarths was able to cross the ocean –
not just once, but twice. This was a
rare feat seeing that few other condylarths accomplished even one oceanic
crossing. This lineage, variously called
the Mioclaenidae or the Kollpaniinae, was previously known from North America,
South America, and Europe.[36] Recently, it was discovered in Africa
also. Although the African condylarth Abdounodus displays a fair degree of
difference from its cousins on other continents, it is referred to the same
family Mioclaenidae. Gheerbrant et al
mention the possibility of convergent evolution, yet prefer to view the African
specimen as a descendent of condylarths from the northern continents, and
suggest the condylarths found a way across the Tethys Sea.[37]
The
possibility of a viable land bridge or series of closely spaced islands
connecting Europe with Africa is a convenient assumption, but rests on shaky
evidence. If such a land bridge truly
existed, then we should see a mass migration of many species between Africa and
Europe. In other landbridge events, the
fossil record clearly proves that there was a massive exchange of species
between North and South America when the isthmus of Panama arose 4 million
years ago, and also proves a massive exchange occurred between Siberia and
Alaska when Beringia was dry-shod. Yet
the supposed trans-Tethyan link, if it existed, certainly did not allow large
numbers of European species to migrate into Africa, nor vice-versa. Hence, the existence of such a land bridge is
not well supported. If one species can
cross a landbridge, others can too. But
in this case, only the condylarth crossed.
Hence,
if the supposed land bridges never existed, then this would mean that the
Mioclaenidae crossed two oceans. They
crossed the ocean dividing South America from North America, and they also
crossed the Tethys Sea which divided Africa from Europe. If they crossed by swimming, then this was
quite an accomplishment for a condylarth, since condylarths possess long narrow
limbs made for running, not swimming.
Likewise, it is hard to see how they rafted on driftwood, since their
lanky legs are ill-suited for gripping driftwood, and because ocean currents
would have been mainly contrary to the directions they traveled. Thus, the possibility of supernatural or
extraterrestrial transport provides a plausible solution for an otherwise
inexplicable problem.
India
and the Rest of Gondwana
In the Jurassic, the
Indian subcontinent was part of a large supercontinent called Gondwana,
comprised of Africa, Antarctica, South America, Madagascar, Australia, and
India. India broke away from this
massive continent early in the Cretaceous about 140 or 130 million years
ago. It began a long voyage northward,
through the Indian Ocean, finally colliding with Asia in the late Paleocene
and/or early Eocene. The collision
probably began about 55 million years ago and culminated just under 50 million
years ago.[38] Hence, India was an island continent for the
great majority of the Cretaceous period and on into the Paleocene.
However, a variety of
mammals from the Cretaceous have been found on India which should not be there
if India were isolated by ocean. During
the Cretaceous, there was a definite distinction between the typical mammals of
the southern continents of Gondwana on one hand, and the mammals of the northern
continents on the other hand. Since
India was part of Gondwana, we should generally not expect to find
northern-type mammals on it before its collision with Asia 55 million years
ago. Nevertheless, several fossils of
northern-type Cretaceous mammals on southern continents have been found,
despite a lack of geological evidence for terrestrial connections between the
continents. Wilson et al called such
north-south migrations "infrequent dispersal events," and posed the
question, "What biogeographic filters allowed their dispersal but
prevented the dispersal of other taxa?[39]
The implication is
that something other than a land bridge was responsible for the transportation
of northern animals to southern continents, for when a landbridge is crossable,
a large and diverse assemblage of species migrates across it, yet in the
Cretaceous of Gondwana, such a large scale interchange is not readily
apparent. Even though terrestrial
connections with other continents have not been ruled out,[40]
terrestrial connections themselves cannot account for the migrations, because
if they did, then there should have been a wholesale interchange of species
across continents. As it was, only a few
species crossed over to other continents.
Arctostylopids
In
1915, a certain group of North American mammals called arctostylopids were
identified as relatives of the notoungulates.[41] The problem is, the notoungulates are only
found on South America. Years later,
when this was realized, the similarities between the arctostylopids and the
notoungulates were deemed due to convergent evolution, and the arctostylopids
were reassigned to their own order.[42] [43] This is only one example of how cladists tend
to raise new taxa when geographical considerations prohibit identification with
existing taxa. This tendency is rooted
in the assumption that the dispersal of animals is limited by geography – an
assumption which, although it is well substantiated in the fossil record most
of the time, does not always hold true, as we have seen. This tendency to raise new taxa in light of
biogeographical considerations results in the danger that extraterrestrial
transportation events may fail to be recognized as such, and thus evidence for
divine and/or alien involvement in earth history may be inadvertently masked by
the biogeographical assumptions of cladistics.
The Case of the Kidnapped Opossum
A
genus of possum-like creatures called Peradectes
lived in North America in the Paleocene and Eocene periods, after the dinosaurs
went extinct.[44] Some apparently migrated to Europe over the
Greenland-Norway land bridge about 50 million years ago, for they are found in
the Messel Pits of Germany. At that
time, the expanding Atlantic Ocean had not yet completely separated Greenland
from Europe.
What
is more difficult to explain is how this ancient possum got to South
America. It is known that at least one
of these possums existed in South America about 63-65 million years ago, for a
specimen was found in the Tiupampan strata of Peru.[45] But there was no land bridge to South America
at that time, so there was really no way this possum could have migrated to
South America via dry land. Lofgren et
al suggested that the fossil record indicates two migrations from North America
to South America during the Paleocene, the first one in the late Puercan or
early Torrejonian (63 million years ago), and another in the late Tiffanian (57
million years ago).[46]
It
cannot be explained by convergent evolution on both continents, as the mammals
of South America immediately preceding them in the late Cretaceous were of an
entirely different structure.[47] As in Europe, the mammals of South America
suffered mass annihilation in the dinosaur extinction – to a greater degree
than did the mammals of North America and Asia.
After the extinction, new mammal populations were imported into Europe
and South America from North America, and to a lesser extent from Asia.[48] There is really no chance this same type of
possum could have evolved by coincidence in two separate places. This is because duplicate evolutionary events
generally do not happen in the fossil record at the level of genus and family.
There
is some question whether the Peruvian specimen should be assigned to the genus Alphadon, which is a close relative of Peradectes. Alphadon
existed in North America during the Campanian and Maastrichtian times of the
late Cretaceous, over the period of 84-65 million years ago. Not that it matters, since there was no more
a land bridge to South America for Alphadon
than there was for Peradectes.
Puzzling Snake Distributions
In
another example, snake fossils recovered from the Cerro Azul Formation of
Argentina confirm that viperid snakes were present in South America from the
late Miocene forward. The timing of the
viperids' first appearance in South America occurs after they first emerged on
other continents during the early Miocene.
Hence, it is agreed that the viperid snakes must have migrated to South
America from another continent. The
problem is, how did they get there?
There is no proof for the existence of a terrestrial connection between
North and South America during the Miocene,[49]
and Africa had separated from South America long before the Miocene.
Could
snakes have found a way across the ocean?
One may note that snakes inhabit Australia. However, many islands such as Iceland, New
Zealand, and even Ireland are devoid of indigenous snakes. If it were so easy for snakes to cross an
ocean, why did they not cross the narrow channels of the British Isles?
Tetrapods
The
earliest legged vertebrates are called tetrapods. They arose first on Old Red Sandstone, where
they were geographically confined for a short while.[50] Old Red Sandstone was comprised of eastern
North America, Greenland, and transalpine Europe, which were at that time
joined as a single, tropical continent.
But tetrapod fossils soon appeared in other widely diverse
locations. The first tetrapods in China
appear at 355 million years ago.[51] China was at that time a series of large
islands on the other side of the world, and was separated by a vast ocean. The tetrapods also spread to Australia about
the same time, as known from the discovery of Metaxygnathus.[52] By
333 million years ago, tetrapods in Australia were diverse, advanced, and they
represented those known elsewhere in the world.[53] Interestingly, the tetrapods in Australia
looked a lot like those in North America, implying that some kind of migration
occurred.
The
wide distribution of terrestrial and fresh water tetrapods raises interesting
questions on how migrations happened.
Ahlberg et al, who described the Australian specimen, suggest that the
conventional wisdom concerning the position of the continents is just plain
wrong, and that Australia was further north and nearly adjacent to Greenland.[54] Daeschler pointed to the fact that early
tetrapods existed on North America, Europe, Eurasia, and Australia; and
therefore surmised that tetrapod migrations to such diverse locales must be
explained either in terms of the tetrapods' abilities to navigate salt water
oceans or by continental connections.[55] Carroll submitted that they at least
inhabited the coastal waters, pointing to the marine affinities of Tulerpeton.[56]
As
a case in point, the proto-tetrapod-like lungfish Soederberghia has been found in southeastern Australia, which is on
the other side of the world from Greenland, where it was first found. Southeastern Australia was at that time
located very close to the South Pole.
Greenland, in contrast, was smack dab on the equator, and halfway around
the globe. It is strange to find the
same genus occupying such diverse ecosystems.
Moreover, this fish was confined to fresh water and estuaries. We know because it is only found in fossil
beds where marine invertebrates are lacking.
In the Devonian, there was a very large ocean separating Greenland on
one hand from Australia on the other – the former being part of Old Red
Sandstone and the latter being part of Gondwana. How did this non-marine fish get across that
ocean?
Thulborn
et al described North America, which was connected to Greenland, as being
"virtually at the opposite pole of the Early Carboniferous globe"
from Australia. To overcome this, they
asserted that Gondwana had already collided with North America, thus linking
Old Red Sandstone to Gondwana, and that Australia was in a tropical location –
somehow being positioned northeastward from its presumed near Antarctic
position.[57]
Yet,
if Australia was tropical, then Antarctica was temperate, since it was
connected to Australia's southern edge at the time; and if Antarctica was
temperate, then why don't we find tetrapods on Antarctica at that time? Tetrapods took a lot longer to get to
Antarctica, where they first appeared in the earliest Triassic, over 100
million years since they first appeared on Old Red Sandstone, China, and
Australia.[58] Moreover, the Carboniferous ice age scarred
Antarctica with glaciers – hardly the mark of a temperate climate. To surmount the Carboniferous ice age
problem, it must be supposed that Australia-Antarctica sped southward from the
tropics to the South Pole in about 20 or 25 million years – a speed much
greater than that which hurled India into Tibet thus forming the
Himalayas. In terms of climate and the
Antarctic fossil record, it is perhaps better to stick with the original map
drawn by plate tectonics, which shows Antarctica near the South Pole, and hence
Gondwana still a good ways south of Old Red Sandstone, not in collision with
it. This is more consistent with what we
know of the Carboniferous era than supposing Australia was tropical. If this more conventional map is accepted,
then the tetrapods must have traversed cold ocean water to the other side of
the world in Australia.
Or,
if cold ocean water be thought too harsh for them, they were airlifted by
extraterrestrials.
If
we assume that continental connections between Gondwana and Old Red Sandstone
were already happening in the late Devonian, then why don't we find any early
tetrapods in Africa? The point of
contact between the two super-continents happened along the Morocco-Appalachian
mountain ranges, at a time when they were positioned in the tropics. The tetrapod-rich fossil beds that are found
in Pennsylvania and eastern Canada are lacking in northwestern Africa. Where are the tetrapods of Morocco?
This
problem can be submitted as evidence for a supernatural or extraterrestrial
presence in distant antiquity, which transported living creatures to places
they could not otherwise have traveled.
Freshwater Fish Across Continents
For
freshwater fish, obstacles such as mountains, deserts, and climate can slow the
spread of their range, but do not prohibit their geographic expansion
indefinitely. According to Darlington,
"The only barriers that are fully effective against freshwater fishes seem
to be those of salt water."[59] Perhaps the best example of this is the
Australian continent and its subsidiaries, New Guinea and New Zealand. Although these locations do contain
aboriginal freshwater fishes, they are generally of a type not found
elsewhere. One exception occurs in the
genus Scleropages, which is found in
both Australia and on the Asian mainland.
Darlington writes,
Whether Scleropages reached Australia through river systems, over ancient
land connection, or partly through the sea I shall not try to say.[60]
River systems or land connection
is very improbable, since if such a situation existed, more than just one genus
would have crossed from Asia into Australia – because massive migrations of
many species occur when land bridges are formed.
There
is also a British fish in Africa. The
freshwater fish Clupisudis is known
from the Eocene of Britain, but is found also in Africa.[61] The fact that the Straits of Gibraltar, which
separate Europe from Africa, were at one time a wide ocean in the
not-so-distant past complicates any supposed terrestrial connection, and may
indicate some paranormal or extraterrestrial source of transportation was involved.
Catfish
Catfish
first emerged in the Campanian of South America. In less than 18 million years, these mostly
freshwater fish had become established all over the world. Catfish fossils are found in North America,
Spain, Africa, and in India before the extinction of the dinosaurs. What's remarkable is that all these
continents were isolated from each other by large oceans during this time. A few catfish are tolerable to brackish or
marine waters. It is possible that they
traversed the oceans to all continents.
If true, they quickly adapted to freshwater, for the Mesozoic catfish of
India appear to have been freshwater fish.
India was in the middle of the ocean at this time, halfway between Asia
and Madagascar, hence entirely isolated from non-native freshwater fish
migrations.[62]
The
probability that catfish ventured outside the lakes and rivers of South
America, into the ocean, even beyond the continental shelves into the deep
ocean, and subsequently adapted again to freshwater on all continents, finally
loosing their saltwater tolerance on nearly a worldwide basis, and
accomplishing all this in just the last two phases of the Cretaceous, while
other fresh water fish have not been able to do the same – the odds of this
happening are not too far from the odds a skeptic would give extraterrestrial
transport. It is easy to see why
sexually perverted space aliens might have been attracted to catfish. They have so much in common – both are slimy,
gray, mean, and ugly.
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[2] Marshall, L G; de Muizon, C. The Dawn of the Age of Mammals in South America. 1988, National Geographic Research 4, p 23-55
[3] Jehle, Martin. Paleocene Mammals of the World, www.paleocene-mammals.de/pal1.htm, data were downloaded Dec 2007; Ameghino 1901
[4] Marshall, L G; de Muizon, C. The Dawn of the Age of Mammals in South America. 1988, National Geographic Research 4, p 23-55
[5] Goin, Francisco; Candela, Adriana M; de Muizon, Christian. The Affinities of Roberthoffstetteria Nationalgeographica (Marsupilia) and the Origin of the Polydolopine Molar Pattern. 2003, Journal of Vertebrate Paleontology 23(4), p 869-876
[6] De Muizon, Christian; Cifelli, Richard L. A New Basal "Didelphoid" (Marsupialia, Mammalia) from the Early Paleocene of Tiupampa (Bolivia). 2001, Journal of Vertebrate Paleontology 21(1), p 87-97
[7] Jehle, Martin. Paleocene Mammals of the World, www.paleocene-mammals.de/pal1.htm, data were downloaded Dec 2007
[8] Goin, F J. A Review of the Caroloameghiniidae, Paleogene South American "Primate-Like" Marsupials (?Didelphimorphia, Peradectoidea). 2006, E Schweizerbart'sche Verlagsbuchhandlung, Palaeontographica Abteilung A 278(1), p 57-67
[9] Sige, B; Archer, M; Godthelp, H; Hand, S; Crochet, J Y. Peruvian-Australian Paleogene Mammal Connection. 1995, Fifth Conference on Australian Vertebrate Evolution, Palaeontology and Systematics 1:2
[10] Sige, B. La Faunule des Mammiferes du Cretace Superieur de Laguna Umayo (Andes Peruviennes). 1972, Bulletin du Museum National d'Histoire Naturelle, 3e ser, Sciences de la Terre 99, p 375-405
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[13] Simpson, G G. Early Mammals in South America: Fact, Controversy, and Mystery. 1978, Proceedings of the American Philosophical Society 122, p 318-328
[14] De Muizon, Christian; Cifelli, Richard L. A New Basal "Didelphoid" (Marsupialia, Mammalia) from the Early Paleocene of Tiupampa (Bolivia). 2001, Journal of Vertebrate Paleontology 21(1), p 87-97
[15] Wicander, Reed; Monroe, James S. Historical Geology: Evolution of Earth and Life Through Time, 4th Ed. 2004, Brooks/Cole – Thomson Learning, Belmont, CA p 374-375, 335
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[17] Antoine, Pierre-Olivier; Welcomme, Jean-Loup; Marivaux, Laurent; Baloch, Ibrahim; Benammi, Mouloud; Tassy, Pascal. First Record of Paleogene Elephantoidea (Mammalia, Proboscidea) from the Bugti Hills of Pakistan. 2003, Journal of Vertebrate Paleontology 23(4), p 977-980
[18] Pujos, Francois; de Iuliis, Gerardo. Late Oligocene Megatherioidea Fauna (Mammalia: Xenarthra) from Salla-Luribay (Bolivia): New Data on Basal Sloth Radiation and Cingulata-Tardigrada Split. 2007, Journal of Vertebrate Paleontology 27(1), p 132-144
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[22] McKenna, Malcolm C; Bell, Susan K. ibid, p 114-210
[23] McKenna, Malcolm C; Bell, Susan K. ibid, p 191-193
[24] McKenna, Malcolm C; Bell, Susan K. ibid, p 185, 187
[25] McKenna, Malcolm C; Bell, Susan K. ibid, p 114, 140, 157, 161
[26] Jacobs, David M. The Threat: Revealing the Secret Alien Agenda. 1998, Simon & Schuster, New York, NY, p 61
[27] Jacobs, David M. ibid, p 128
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[30] Jacobs, David M. The Threat: Revealing the Secret Alien Agenda. 1998, Simon & Schuster, New York, NY, p 38-39
[31] Hopkins, Budd; Rainey, Carol. Sight Unseen: Science, UFO Invisibility, and Transgenic Beings. 2003, Pocket Books, Simon & Schuster, New York, NY, p 398
[32] Jacobs, David M. The Threat: Revealing the Secret Alien Agenda. 1998, Simon & Schuster, New York, NY, p 64
[33] Marrs, Jim. Alien Agenda: Investigating the Extraterrestrial Presence Among Us. 1997, HarperCollins Publishers, New York, NY, p 296-298
[34] Jacobs, David M. The Threat: Revealing the Secret Alien Agenda. 1998, Simon & Schuster, New York, NY, p 22-23
[35] Heiser, Michael S. The Facade. 2001, SuperiorBooks.com, p 163
[36] McKenna, Malcolm C; Bell, Susan K. Classification of Mammals Above the Species Level. 1997, Columbia University Press, New York, NY, p 362-363
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[38] Rose, K D; Smith, T; Rana, R S; Sahni, A; Singh, H; Missiaen, P; Folie, A. Early Eocene (Ypresian) Continental Vertebrate Assemblage from India, with Description of a New Anthracobunid (Mammalia, Tethytheria). 2006, Journal of Vertebrate Paleontology 26(1), p 219-225
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[43] Zack, Shawn P. An Early Eocene Arctostylopid (Mammalia: Arctostylopida) from the Green River Basin, Wyoming. 2004, Journal of Paleontology 24(2), p 498-501
[44] The Paleobiology Database, www.paleodb.org. Search Parameter: Taxon "Peradectes," data were downloaded Oct 6, 2008
[45] Marshall, L G; de Muizon, C. The Dawn of the Age of Mammals in South America. 1988, National Geographic Research 4, p 23-55; see also Jehle, Martin. Paleocene Mammals of the World, www.paleocene-mammals.de/
[46] Lofgren, Donald L; Lillegraven, Jason A; Clemens, William A; Gingerich, Philip D; Williamson, Thomas E. Paleocene Biochronology: The Puercan Through Clarkforkian Land Mammal Ages. Compiled and edited in Woodburne, Michael O. Late Cretaceous and Cenozoic Mammals of North America: Biostratigraphy and Geochronology. 2004, Columbia University Press, New York, NY, p 95
[47] Lofgren, Donald L; et al. ibid, p 92
[48] Lofgren, Donald L; et al. ibid, p 88, 90, 92
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[50] Clack, Jennifer A. Gaining Ground: The Origin and Evolution of Tetrapods. 2002, Indiana University Press, Bloomington, IN, p 97
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[52] Campbell, K S W; Bell, M W. A Primitive Amphibian from the Late Devonian of New South Wales. 1977, Alcheringa 1, p 369-381
[53] Thulborn, Tony; Warren, Anne; Turner, Susan; Hamley, Tim. Early Carboniferous Tetrapods in Australia. 1996, Nature 381, p 777-779
[54] Ahlberg, Per E; Johanson, Zerina; Daeschler, Edward B. The Late Devonian Lungfish Soederberghia (Sarcopterygii, Dipnoi) From Australia and North America and Its Biogeographical Implications. 2001, Journal of Vertebrate Paleontology 21(1), p 1-12
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[57] Thulborn, Tony; Warren, Anne; Turner, Susan; Hamley, Tim. Early Carboniferous Tetrapods in Australia. 1996, Nature 381, p 777-779
[58] Collinson, J W; Hammer, W R. Migration of Triassic Tetrapods to Antarctica: A Keystone in a Changing World. 2007, Online Proceedings of the 10th ISAES X; edited by Cooper, A K; Raymond, C R, et al. US Geological Survey Open File Report 2007-1047, extended abstract 047
[59] Darlington, Philip J Jr. Zoogeography: The Geographical Distribution of Animals. 1957, John Wiley & Sons, New York, NY, p 79
[60] Darlington, Philip J Jr. ibid, p 52
[61] Darlington, Philip J Jr. ibid, p 52
[62] Cione, Alberto L; Prasad, G V R. The Oldest Known Catfish (Teleostei:Siluriformes) from Asia (India, Late Cretaceous). 2002, Journal of Paleontology 76(1), p 190-193