473 lines
26 KiB
Plaintext
473 lines
26 KiB
Plaintext
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Newsgroups: talk.origins
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From: bvickers@valentine.ics.uci.edu (Brett J. Vickers)
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Subject: Transitional Fossils FAQ (was Re: Duane T. Gish, Ph. D.)
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Message-ID: <2B645766.8197@ics.uci.edu>
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Organization: Univ. of Calif., Irvine, Info. & Computer Sci. Dept.
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Date: 25 Jan 93 21:11:02 GMT
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Lines: 475
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From Kathleen Hunt's excellent transitional fossil FAQ:
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===============================================================================
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Author: Kathleen Hunt (jespah@milton.u.washington.edu)
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Title: Transitional Fossils
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===============================================================================
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I've recently been re-reading Colbert's _Evolution of the Vertebrates_,
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and was reminded of the old "there aren't any transitional fossils"
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complaint that pops up on t.o. every now and then. That argument has long
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been obsolete and inaccurate, as a brief glance at the fossil record shows.
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I thought it might be of interest to have a list of some of the transitional
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vertebrate fossils known, so that future t.o.discussions of the fossil record
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can be somewhat more up-to-date and interesting (I can dream, can't I?).
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A couple people have asked me to post this as a f.a.q. file to t.o. So here
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goes. First, I'll present a *partial* list of known transitional fossils,
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compiled from Colbert's _Evolution of the Vertebrates_ (ref at end). Also
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at the end I have a short note about the significance of "transitional
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fossils".
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The fossils mentioned in this list are from species and/or genuses thought to
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represent transitions from one vertebrate group to another. This list is
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necessarily highly incomplete, because:
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a) I skipped entire sections of Colbert's text (rodents, bovids, dinosaurs,
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teleosts, and more).
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b) Colbert's text is *not* an encyclopedic list of all known fossils, but
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instead has detailed descriptions of *particular* fossils that Colbert
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thought were representative of that group at that time, or that were
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otherwise of special interest.
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c) Colbert's text is from 1980 and thus somewhat outdated. I've added in
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some recently discovered bird, whale, horse, and primate fossils. Please
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let me know of other recent discoveries.
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*******************************************************************
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[We start off with primitive jawless fish.]
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Transition from primitive jawless fish to sharks, skates, and rays:
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Cladoselachians (e.g., _Cladoselache_).
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Hybodonts (e.g. _Hybodus_)
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Heterodonts (e.g. _Heterodontus_)
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Hexanchids (e.g. _Chlamydoselache_)
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Transition from primitive bony fish to holostean fish:
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Palaeoniscoids (e.g. _Cheirolepis_); living chondrosteans such as
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_Polypterus_ and _Calamoichthys_, and also the living acipenseroid
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chondrosteans such as sturgeons and paddlefishes.
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Primitive holosteans such as _Semionotus_.
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Transition from holostean fish to advanced teleost fish:
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Leptolepidomorphs, esp. _Leptolepis_, an excellent holostean-teleost
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intermediate
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Elopomorphs, both fossil and living (tarpons, eels)
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Clupeomorphs (e.g. _Diplomystus_)
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Osteoglossomorphs (e.g. _Portheus_)
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Protacanthopterygians
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Transition from primitive bony fish to amphibians:
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Paleoniscoids again (e.g. _Cheirolepis_)
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_Osteolepis_ -- one of the earliest crossopterygian lobe-finned fishes,
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still sharing some characters with the lungfish (the other group of
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lobe-finned fish). Had paired fins with a leg-like arrangement of bones,
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and had an early-amphibian-like skull and teeth.
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_Eusthenopteron_ (and other rhipidistian crossopterygian fish) --
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intermediate between early crossopterygian fish and the earliest
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amphibians. Skull very amphibian-like. Strong amphibian-like backbone.
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Fins very like early amphibian feet.
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Icthyostegids (such as _Icthyostega_ and _Icthyostegopsis_) --
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Terrestrial amphibians with many of _Eusthenopteron_'s fish features
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(e.g., the fin rays of the tail were retained). Some debate about
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whether _Icthyostega_ should be considered a fish or an amphibian;
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it is an excellent transitional fossil.
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Labyrinthodonts (e.g., _Pholidogaster_, _Pteroplax_) -- still have some
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icthyostegid features, but have lost many of the fish features (e.g.,
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the fin rays are gone, vertebrae are stronger and interlocking, the
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nasal passage for air intake is well defined.)
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Transition from amphibians to reptiles:
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Seymouriamorph labyrinthodonts (e.g. _Seymouria_) -- classic labyrinthodont
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skull and teeth, with reptilian vertebrae, pelvis, humerus, and digits;
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amphibian ankle.
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Cotylosaurs (e.g. _Hylonomus_, _Limnoscelis_) -- slightly amphibian
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skull (e.g. with amphibian-type pineal opening), with rest of skeleton
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classically reptilian.
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The cotylosaurs gave rise to many reptile groups of tremendous variety. I
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won't go into the transitions from cotylosaurs to the advanced anapsid
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reptiles (turtles and possibly mesosaurs), to the euryapsid reptiles
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(icthyosaurs, plesiosaurs, and others), or to the lepidosaurs (eosuchians,
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lizards, snakes, and the tuatara), or to most of the dinosaurs, since I don't
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have infinite time. Instead I'll concentrate on the synapsid reptiles (which
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gave rise to mammals) and the archosaur reptiles (which gave rise to birds).
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Transition from reptiles to mammals:
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Pelycosaur synapsids -- classic reptilian skeleton, intermediate between
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the cotylosaurs (the earliest reptiles) and the therapsids (see next)
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Therapsids (e.g. _Dimetrodon_) -- the numerous therapsid
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fossils show gradual transitions from reptilian features to
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mammalian features. For example: the hard palate forms, the teeth
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differentiate, the occipital condyle on the base of the skull doubles,
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the ribs become restricted to the chest instead of extending down the
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whole body, the legs become "pulled in" instead of sprawled out, the ilium
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(major bone of the hip) expands forward.
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Cynodont theriodonts (e.g. _Cynognathus_) -- very mammal-like reptiles.
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Or is that reptile-like mammals? Highly differentiated teeth (a classic
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mammalian feature), with accessory cusps on cheek teeth; strongly
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differentiated vertebral column (with distinct types of vertebrae for
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the neck, chest, abdomen, pelvis, and tail -- very mammalian), mammalian
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scapula, mammalian limbs, mammalian digits (e.g. reduction of number of
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bones in the first digit). But, still has unmistakably *reptilian*
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jaw joint.
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Tritilodont theriodonts (e.g. _Tritylodon_, _Bienotherium_) -- skull
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even more mammalian (e.g. advanced zygomatic arches). Still has
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reptilian jaw joint.
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Ictidosaur theriodonts (e.g. _Diarthrognathus_) -- has all the mammalian
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features of the tritilodonts, and has a *double* jaw joint; both the
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reptilian jaw joint and the mammalian jaw joint were present, side-by-side,
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in _Diarthrognathus_'s skull. A really stunning transitional fossil.
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Morganucodonts (e.g. _Morganucodon_) -- early mammals. Double jaw joint,
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but now the mammalian joint is dominant (the reptilian joint bones are
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beginning to move inward; in modern mammals these are the bones of
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the middle ear).
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Eupantotheres (e.g. _Amphitherium_) -- these mammals begin to show the
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complex molar cusp patterns characteristic of modern marsupials and
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eutherians (placental mammals). Mammalian jaw joint.
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Proteutherians (e.g. _Zalambdalestes_) -- small, early insectivores with
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molars intermediate between eupantothere molars and modern eutherian
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molars.
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Those wondering how egg-laying reptiles could make the transition to
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placental mammals may wish to study the reproductive biology of the
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monotremes (egg-laying mammals) and the marsupials. The monotremes
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in particular could almost be considered "living transitional fossils".
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[see Peter Lamb's suggested marsupial references at end]
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Transition from reptiles to birds:
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_Lisboasaurus estesi_ and other "troodontid dinosaur-birds" -- a bird-like
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reptile with very bird-like teeth (that is, teeth very like those of
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early toothed birds [modern birds have no teeth]). May not have been
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a direct ancestor; may have been a "cousin" of the birds instead.
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_Protoavis_ -- this is a *highly controversial* fossil that may or may not be
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an extremely early bird. Not enough of the fossil was recovered to
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determine if it is definitely related to the birds, or not. I mention it
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in case people have heard about it recently.
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_Archeopteryx_ -- reptilian vertebrae, pelvis, tail, skull, teeth, digits,
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claws, sternum. Avian furcula (wishbone, for attachment of flight
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muscles), forelimbs, and lift-producing flight feathers. _Archeopteryx_
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could probably fly from tree to tree, but couldn't take off from
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the ground, since it lacked a keeled breastbone (for attachment of large
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flight muscles) and had a weak shoulder (relative to modern birds).
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"Chinese bird" [I don't know what name was given to this fossil] --
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A fossil dating from 10-15 million years after _Archeopteryx_.
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Bird-like claws on the toes, flight-specialized shoulders, fair-sized
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sternal keel (modern birds usually have large sternal keel); also
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has reptilian stomach ribs, reptilian unfused hand bones, & reptilian
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pelvis. This bird has a fused tail ("pygostyle"), but I don't know how
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long it was, or if it was all fused or just part of it was fused.
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"Las Hoyas bird" [I don't know what name was given to this fossil] --
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This fossil dates from 20-30 m.y. after _Archeopteryx_. It still
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has reptilian pelvis & legs, with bird-like shoulder. Tail is
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medium-length with a fused tip (_Archeopteryx_ had long, unfused tail;
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modern birds have short, fused tail). Fossil down feather was found with
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the Las Hoyas bird.
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Toothed Cretaceous birds, e.g. _Hesperornis_ and _Ichthyornis_. Skeleton
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further modified for flight (fusion of pelvis bones, fusion of hand
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bones, short & fused tail). Still had true socketed teeth, which are
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missing in modern birds.
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[note: a classic study of chicken embryos showed that chicken bills can
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be induced to develop teeth, indicating that chickens (and perhaps other
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modern birds) still retain the genes for making teeth.]
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Now, on to some of the classes of mammals.
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Transitional fossils from early eutherian mammals to primates:
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Early primates -- paromomyids, carpolestids, plesiadapids. Lemur-like
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clawed primates with generalized nails.
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_Notharctus_, an early Eocene lemur
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_Parapithecus_, a small Old World monkey (Oligocene)
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_Propliopithecus_, a small primate intermediate between _Parapithecus_
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and the more recent O.W. monkeys. Has several ape-like characters.
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_Aegyptopithecus_, an early ape.
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_Limnopithecus_, a later ape showing similarities to the modern gibbons.
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_Dryopithecus_, a later ape showing similarities to the non-gibbon apes.
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_Ramapithecus_, a dryopithecine-like ape showing similarities to the
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hominids but now thought to be an orang ancestor.
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_Australopithecus_ spp., early hominids. Bipedal.
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_Homo habilis_.
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_Homo erectus_. Numerous fossils across the Old World.
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_Homo sapiens sapiens_. This is us. (NB: "Cro-magnon man" belongs
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here too. Cro-magnons were a specific population of modern humans.)
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_Homo sapiens neanderthalensis_ (not on the direct line to _H. sapiens
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sapiens_, but worth mentioning).
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[I haven't described these fossils in detail because they're fairly well
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covered in any intro biology text, or in any of several good general-
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interest books on human evolution.]
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Transitional fossils from early eutherian mammals to rodents:
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Paramyids, e.g. _Paramys_ -- early "primitive" rodent
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_Paleocastor_ -- transitional from paramyids to beavers
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[yick. I was going to summarize rodent fossils but _Paramys_ and its
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friends gave rise to 5 enormous and very diverse groups of rodents, with
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about ten zillion fossils. Never mind.]
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Transitional fossils among the cetaceans (whales & dolphins):
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_Pakicetus_ -- the oldest fossil whale known. Only the skull was found.
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It is a distinct whale skull, but with nostrils in the position of a
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land animal (tip of snout). The ears were *partially* modified for
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hearing under water. This fossil was found in association with fossils
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of land mammals, suggesting this early whale *maybe* could walk on land.
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_Basilosaurus isis_ -- a recently discovered "legged" whale from the
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Eocene (after _Pakicetus_). Had hind feet with 3 toes and a tiny remnant
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of the 2nd toe (the big toe is totally missing). The legs were small and
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must have been useless for locomotion, but were specialized for swinging
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forward into a locked straddle position -- probably an aid to copulation
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for this long-bodied, serpentine whale.
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Archaeocetes (e.g. _Protocetus_, _Eocetus_) -- have lost hind legs entirely,
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but retain "primitive whale" skull and teeth, with forward nostrils.
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Squalodonts (e.g. _Prosqualodon_) -- whale-like skull with *dorsal*
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nostrils (blowhole), still with un-whale-like teeth.
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_Kentriodon_, an early toothed whale with whale-like teeth.
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_Mesocetus_, an early whalebone whale
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[note: very rarely a modern whale is found with tiny hind legs, showing
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that some whales still retain the genes for making hind legs.]
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Transitional fossils from early eutherian mammals to the carnivores:
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Miacids (e.g. _Viverravus_ and _Miacis_) -- small weasel-like animals
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with very carnivore-like teeth, esp. the carnassial teeth.
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Arctoids (e.g. _Cynodictis_, _Hesperocyon_) -- intermediate between
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miacids and dogs. Limbs have elongated, carnassials are more
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specialized, braincase is larger.
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_Cynodesmus_, _Tomarctus_ -- transitional fossils between arctoids
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and the modern dog genus _Canis_.
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_Hemicyon_, _Ursavus_ -- heavy doglike fossils between the arctoids
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and the bears.
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_Indarctos_ -- early bear. Carnassial teeth have no shearing action,
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molars are square, short tail, heavy limbs. Transitional to the
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modern genus _Ursus_.
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_Phlaocyon_ -- a climbing carnivore with non-shearing carnassials,
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transitional from the arctoids to the procyonids (raccoons et al.)
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Meanwhile back at the ranch,
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_Plesictis_, transitional between miacids (see above) and mustelids
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(weasels et al.)
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_Stenoplesictis_ and _Palaeoprionodon_, early civets related to the
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miacids (see above)
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_Tunguricits_, transitional between early civets and modern civets
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_Ictitherium_, transitional between early civets to hyenas
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_Proailurus_, transitional from early civets to early cats
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_Dinictis_, transitional from early cats to modern "feline" cats
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_Hoplophoneus_, transitional from early cats to "saber-tooth" cats
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Transitional fossils from early eutherians to hoofed animals:
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Arctocyonid condylarths -- insectivore-like small mammals with classic
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mammalian teeth and clawed feet.
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Mesonychid condylarths -- similar to the arctocyonids, but with blunt
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crushing-type cheek teeth, and flattened nails instead of claws.
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Late condylarths, e.g. _Phenocodus_ -- a fair-sized animal with
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hoofs on each toe (all toes were present), a continuous series of
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crushing-type cheek teeth with herbivore-type cusps, and no collarbone
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(like modern hoofed animals).
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Transitional fossils from early hoofed animals to perissodactyls:
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[Perissodactyls are animals with an *odd* number of toes; most of the
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weight is borne by the central 3rd toe. Horses, rhinos, tapirs.]
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_Tetraclaeonodon_ -- a Paleocene condylarth showing perissodactyl-like
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teeth
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_Hyracotherium_ -- the famous "dawn horse", an early perissodactyl, with
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more elongated digits and interlocking ankle bones, and slightly
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different tooth cusps, compared to to _Tetraclaeonodon_. A small, doggish
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animal with an arched back, short neck, and short snout; had 4 toes
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in front and 3 behind. Omnivore teeth.
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[The rest of horse evolution will be covered in an upcoming "horse
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fossils" post in a few weeks. To whet your appetite:]
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_Orohippus_ -- small, 4/3 toed, developing browser tooth crests
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_Epihippus_ -- small, 4/3 toed, good tooth crests, browser
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_Epihippus (Duchesnehippus)_ -- a subgenus with _Mesohippus_-like teeth
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_Mesohippus_ -- 3 toed on all feet, browser, slightly larger
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_Miohippus_ -- 3 toed browser, slightly larger [gave rise to lots of
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successful three-toed browsers]
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_Parahippus_ -- 3 toed browser/grazer, developing "spring foot"
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_'Parahippus' leonensis_ -- a _Merychippus_-like species of _Parahippus_
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_'Merychippus' gunteri_ -- a _Parahippus_-like species of _Merychippus_
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_'Merychippus' primus_ -- a more typical _Merychippus_, but still very
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like _Parahippus_.
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_Merychippus_ -- 3 toed grazer, spring-footed, size of small pony
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(gave rise to tons of successful three-toed grazers)
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_Merychippus (Protohippus)_ -- a subgenus of _Merychippus_ developing
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_Pliohippus_-like teeth.
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_Pliohippus_ & _Dinohippus_ -- *one*-toed grazers, spring-footed
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_Equus (Plesippus)_ -- like modern equines but teeth slightly simpler.
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_Equus (Hippotigris)_, the modern 1-toed spring-footed grazing zebras.
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_Equus (Equus)_, the modern 1-toed spring-footed grazing horses & donkeys.
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[note: very rarely a horse is born with small visible side toes, indicating
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that some horses retain the genes for side toes.]
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Meanwhile back at the ranch,
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Hyrachyids -- transitional from perissodactyl-like condylarths to tapirs
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Heptodonts, e.g. _Lophiodont_ -- a small horse-like tapir, transitional
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to modern tapirs
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_Protapirus_ -- a probable descendent of _Lophiodont_, much like modern
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tapirs but without the flexible snout.
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_Miotapirus_ -- an almost-modern tapir with a flexible snout, transitional
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between _Protapirus_ and the modern _Tapirus_.
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Meanwhile,
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Hyracodonts -- early "running rhinoceroses", transitional to modern rhinos
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_Caenopus_, a large, hornless, generalized rhino transitional between the
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hyracodonts and the various later groups of modern & extinct rhinos.
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Transitional fossils from early hoofed animals to some of the artiodactyls
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(cloven-hoofed animals):
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Dichobunoids, e.g. _Diacodexis_, transitional between condylarths
|
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|
and all the artiodactyls (cloven-hoofed animals). Very condylarth-like
|
||
|
but with a notably artiodactyl-like ankle.
|
||
|
_Propalaeochoerus_, an early pig, transitional between _Diacodexis_ and
|
||
|
modern pigs.
|
||
|
_Protylopus_, a small, short-necked, four-toed animal, transitional between
|
||
|
dichobunoids and early camels. From here the camel lineage goes through
|
||
|
_Protomeryx_, _Procamelus_, _Pleauchenia_, _Lama_ (which are still alive;
|
||
|
these are the llamas) and finally _Camelus_, the modern camels.
|
||
|
_Archeomeryx_, a rabbit-sized, four-toed animal, transitional between the
|
||
|
dichobunoids and the early deer. From here the deer lineage goes through
|
||
|
_Eumeryx_, _Paleomeryx_ and _Blastomeryx_, _Dicrocerus_ (with antlers) and
|
||
|
then a shmoo of successful groups that survive today as modern deer --
|
||
|
muntjacs, cervines, white-tail relatives, moose, reindeer, etc., etc.
|
||
|
_Palaeotragus_, transitional between early artiodactyls and the okapi &
|
||
|
giraffe. Actually the okapi hasn't changed much since _Palaeotragus_ and
|
||
|
is essentially a living Miocene giraffe. After _Palaeotragus_ came
|
||
|
_Giraffa_, with elongated legs & neck, and _Sivatherium_, large ox-like
|
||
|
giraffes that *almost* survived to the present.
|
||
|
|
||
|
*****************************************************************************
|
||
|
So, there's a *partial* list of transitional fossils.
|
||
|
|
||
|
This really only scratches the surface since I left out all groups that have
|
||
|
no surviving relatives, didn't discuss modern amphibians or reptiles, left
|
||
|
out most of the birds, ignored the diversity in modern fish, didn't discuss
|
||
|
the bovids or elephants or rodents or many other mammal groups....I hope this
|
||
|
gives a taste of the richness of the fossil record and the abundance of
|
||
|
transitional fossils between major vertebrate taxa.
|
||
|
|
||
|
By the way, notice that this list mostly includes transitional fossils that
|
||
|
happened to lead to modern, familiar animals. This may unintentionally give
|
||
|
the impression that fossil lineages proceed in a "straight line" from one
|
||
|
fossil to the next. That's not so; generally at any one time there are a
|
||
|
whole raft of successful species, only a few of which happened to leave
|
||
|
modern descendents. The horse family is a good example; _Merychippus_ gave
|
||
|
rise to something like 19 new three-toed grazing horse species, which
|
||
|
traveled all over the Old and New Worlds and were very successful at the
|
||
|
time. Only one of these lines happened to lead to _Equus_, though, so that's
|
||
|
the only line I talked about. Evolution is not a ladder, it's a branching
|
||
|
bush.
|
||
|
|
||
|
And now, for those of you who are still with me...
|
||
|
I have a few comments about "transitional fossils" in general. When _The
|
||
|
Origin Of Species_ was first published, the fossil record was poorly known.
|
||
|
At that time, the complaint about the lack of transitional fossils bridging
|
||
|
the major vertebrate taxa was perfectly reasonable. Opponents of Darwin's
|
||
|
theory of common descent (the theory that evolution has occurred; not to be
|
||
|
confused with the separate theory that evolution occurs specifically by
|
||
|
natural selection) were justifiably skeptical of such ideas as birds being
|
||
|
related to reptiles. The discovery of _Archeopteryx_ only two years after
|
||
|
the publication of _The Origin of Species_ was seen a stunning triumph for
|
||
|
Darwin's theory of common descent. _Archeopteryx_ has been called the single
|
||
|
most important natural history specimen ever found, "comparable to the
|
||
|
Rosetta Stone" (Alan Feduccia, in "The Age Of Birds"). O.C. Marsh's
|
||
|
groundbreaking study of the evolution of horses was another dramatic example
|
||
|
of transitional fossils, this time demonstrating a whole sequence of
|
||
|
transitions within a single family. Within a few decades after the _Origin_,
|
||
|
these and other fossils, along with many other sources of evidence (such as
|
||
|
developmental biology and biogeography) had convinced the majority of
|
||
|
educated people that evolution *had* occured, and that organisms *are*
|
||
|
related to each other by common descent. (Whether evolution occurs by
|
||
|
natural selection, rather than by some other mechanism, is *another question
|
||
|
entirely* and is the topic of current evolutionary research.)
|
||
|
|
||
|
Since then *many* more transitional fossils have been found. Typically, the
|
||
|
only people who still demand to see transitional fossils are creationists who
|
||
|
have been reading 100-year-old anti-evolution arguments, and who are either
|
||
|
unaware of the currently known fossil record or are unwilling to believe it
|
||
|
for some reason. When presented with a transitional fossil, such
|
||
|
creationists often then want to see the transitions between the transitions -
|
||
|
- or, as Pilbeam complained, "as soon as you find a missing link,
|
||
|
you've just created two more missing links". Alternatively,
|
||
|
creationists will often state that the two groups being bridged by the
|
||
|
transitional fossil are really the same "kind" (a term that has *no* meaning
|
||
|
in modern biology) and that therefore "real evolution" hasn't occurred. This
|
||
|
often leads to a weasely backtracking in which *no* transitional fossil,
|
||
|
however dramatic, no matter what disparate groups it connects, will ever be
|
||
|
accepted by a creationist. Biologists justifiably find this attitude
|
||
|
irritating, and any creationist taking this tack can expect to have testy
|
||
|
biologists demanding that he/she clearly define "kind" before the discussion
|
||
|
goes any further.
|
||
|
|
||
|
Creationists also sometimes say "All right, so you have a transitional fossil
|
||
|
from X to Y -- but you don't from Y to Z!" It is unreasonable to expect the
|
||
|
fossil record to be absolutely complete. It is highly unlikely for *any*
|
||
|
organism to get fossilized, and to demand a perfect sequence of fossils of
|
||
|
all species from all times and all locations, perfectly preserved in rocks
|
||
|
that are not plowed under or eroded away, and not taken by private collectors
|
||
|
and sold for thousands of dollars at some auction or used as a doorstop or a
|
||
|
paperweight, but instead are exposed just as one of the few working
|
||
|
paleontologists in the world happens to walk by -- well, we're lucky
|
||
|
that the known fossil record is as good as it is. Remember that even if only
|
||
|
*ONE* transitional fossil were known, it would be a tremendous support for
|
||
|
evolutionary theory. (Thus the tremendous impact of _Archeopteryx_ in 1861).
|
||
|
We now know of HUNDREDS of transitional fossils. It is logically absurd to
|
||
|
demand that a *particular* gap be filled, and if it can't be filled to then
|
||
|
say that evolution has been falsified -- meanwhile ignoring all the gaps that
|
||
|
*have* been filled.
|
||
|
|
||
|
I'll leave it at that. This has been a partial list of transitional fossils
|
||
|
among some of the major taxa of vertebrates. This list has been brought
|
||
|
to you by the numbers 1 and 7 and the letter E.
|
||
|
|
||
|
BIBLIOGRAPHY
|
||
|
"Chinese bird fossil: mix of old and new". 1990. Science News 138: 246-247
|
||
|
[this fossil was described at the 1990 annual meeting of the Society of
|
||
|
Vertebrate Paleontology, so there's probably a paper on it in the collected
|
||
|
meeting papers.]
|
||
|
|
||
|
Colbert, E. 1980. _Evolution of the Vertebrates_, 3rd ed. John Wiley &
|
||
|
Sons, New York.
|
||
|
|
||
|
Gould, S.J. 1983. _Hen's Teeth And Horse's Toes_. W.W. Norton, New York.
|
||
|
[The title essay discusses evidence that some species retain old genes
|
||
|
for traits that they no longer express -- teeth in chickens, side toes in
|
||
|
horses. ]
|
||
|
|
||
|
Feduccia, A. 1980. _The Age Of Birds_. Harvard University Press,
|
||
|
Cambridge, Mass.
|
||
|
|
||
|
Gingerich, P.D., Smith, B.H., Simons, E.L. 1990. Hind limb of Eocene
|
||
|
_Basilosaurus_: evidence of feet in whales. Science 249:154.
|
||
|
|
||
|
_The Lonely Bird_. 1991. Science News 140:104-105. [an article on the
|
||
|
controversy surrounding _Protoavis_. A monograph on _Protoavis_'s skull was
|
||
|
published in June 1991 in Phil. Trans. Royal Soc. London, if anyone cares;
|
||
|
this was the first publication on _Protoavis_, which was found years ago but
|
||
|
has been jealously guarded by its discoverer for some time.]
|
||
|
|
||
|
Milner, A.R., and S.E. Evans. 1991. The Upper Jurassic diapsid
|
||
|
_Lisboasaurus estesi_ -- a maniraptoran theropod. Paleontology 34:503-513.
|
||
|
[this is the bird-like archosaurian reptile]
|
||
|
|
||
|
Sanz, J.L., Bonaparte, J.F., and A. Lacassa. 1988. Unusual Early Cretaceous
|
||
|
birds from Spain. Nature 331:433-435. [This is about the Las Hoyas bird.
|
||
|
Also see Science News 133:102, "Bird fossil reveals history of flight", for
|
||
|
a brief synopsis.]
|
||
|
|
||
|
Horse references will be in horse post.
|
||
|
|
||
|
Marsupial references (suggested by Peter Lamb):
|
||
|
|
||
|
[1] Mervyn Griffiths, "The Platypus", Scientific American, May 1988 pp 60-67.
|
||
|
[2] Mervyn Griffiths, "The Biology of the Monotremes", Academic Press,
|
||
|
New York a.o., 1978
|
||
|
[3] Terence J.Dawson, "Monotremes and Marsupials: the other Mammals",
|
||
|
Arnold, London, 1983
|
||
|
|
||
|
--
|
||
|
Brett J. Vickers
|
||
|
bvickers@ics.uci.edu
|