Does the stability of phyla means phyla do not
evolve?
Summary of problems with claim:
Explore Evolution misunderstands the
definition of phyla.
Full discussion:
But stability also
characterizes the body designs of the organisms
representing the higher categories of life--the orders,
classes and phyla.(13)
Explore Evolution, p.
26
and in footnote #13 continues:
Technically, to say that
phyla remain stable is almost redundant. After all,
scientists define phyla by referring to an unchanging set
of anatomical characteristics. In another sense, however,
the stability of phyla is remarkable.
Think of the different phyla as though they were
arranged like bars on a bar chart. Each bar represents a
unique body plan. The farther apart two individual bars
are from one another, the more different the anatomical
characteristics are.
In nature, an animal body plan could theoretically fall
anywhere along this continuum, even in the gaps between
bars. Individual animals either falls [sic] within one of
the existing phyla, or in some instances new animals are
found that represent radically new body plans
altogether.Explore
Evolution, p. 26
This is problematic in many respects. By giving
this analogy to phyla arranged horizontally as bars in a
bar chart, and arguing that one can "fall within" these
bars, really misses the whole point of what phyla are.
Phyla are "body plans." They are the most
fundamental ways that bodies can be put together. Phyla
are based upon the internal, rather than external,
arrangement of organisms. Because of this, many
seemingly-similar animals (a number of phyla are "worms")
are grouped into separate phyla, while many
seemingly-different animals (jellies, anemones, corals
are all Phylum Cnidaria) are grouped together.
An analogy for phyla can be made for cars. Think
of all the different types of cars you see. They all have
four wheels, an engine, a windshield, and so on. But
beyond this, imagine that you were to classify cars into
different automobile phyla. You could make a phylum for
convertibles. Another for SUVs. Sedans get their own, as
do coupes. Are two-door sedans different enough from
four-door sedans that they deserve their own phylum?
These kinds of questions, when applied to animal bodies,
help scientists classify animals.
In recent years, advances in molecular biology
have shed even more light on phylogeny. DNA-DNA
hybridization, for example, takes single-strand DNA from
two different organisms and measures how well the single
strands bond together; the better the bonding, the more
closely the DNA pairs match. The advent of PCR
(polymerase chain reaction) allow DNA sequencing from
living and some extinct organisms. DNA sequencing
directly compares DNA at the base-pair level, yielding
even more information. Some proteins--for example,
cytochrome c--can be used as a "molecular clock" to judge
phylogenetic relationships.
Depending on the exact definition of phylum used,
the animal world can be divided into about 38 phyla.
These are
| #
| Phylum
| Features
| Example
|
|---|
| 1.
| Chordates
| spine or notochord
| fish, humans
|
| 2.
| Mollusca
| calcareous shell, muscular foot
| clams, octopi, nautiloids
|
| 3.
| Arthropods
| jointed, segmented exoskeleton
| crabs, spiders, insects
|
| 4.
| Echinoderms
| calcareous exoskeleton
| sea stars, sea urchins, sand dollars
|
| 5.
| Acanthocephala
| parasitic worm
| thorny-headed worm
|
| 6.
| Acoelomorpha
| no disgestive tract
| flatworms
|
| 7.
| Annelida
| complete digestive tract
| segmented worms
|
| 8.
| Brachiopoda
| similar to bivalves
| lamp shells
|
| 9.
| Chaetognatha
| long, streamlined body
| arrow worms
|
| 10.
| Cnidaria
| stinging cells (nematocysts)
| jellies, anemones, corals
|
| 11.
| Ctenophora
| no head, central nervous system
| comb jellies
|
| 12.
| Cycliophora
| lives in lobster mouths
| discovered 1995
|
| 13.
| Echuira
| unsegmented
| spoon worm
|
| 14.
| Entoprocta
| sessile
| goblet worm
|
| 15.
| Gastrotricha
| microscopic
| Meiofauna
|
| 16.
| Gnathostomulida
| hermaphroditic, 0.5-1.0 mm
| jaw worms
|
| 17.
| Hemichordata
| similar to worms
| acorn worms
|
| 18.
| Kinorhyncha
| <1 mm
| mud dragons
|
| 19.
| Loricifera
| sediment-dwelling, marine
| brush heads
|
| 20.
| Micrognathozoa
| <0.1mm, one of smallest animals known
| similar to Rotifera
|
| 21.
| Monoblastozoa
| "primitive" multicellular
|
|
| 22.
| Nematoda
| molting cuticle, 6 lips
| round worms
|
| 23.
| Nematophora
| parasites in arthopods
| horsehair worms
|
| 24.
| Nemertea
| unsegmented worms
| ribbon worms
|
| 25.
| Onycophora
| relatively large brain
| velvet worm
|
| 26.
| Orthonectida
| marine invertebrate parasite
|
|
| 27.
| Phoronida
| similar to worms
|
|
| 28.
| Placozoa
| pressure-filled body cavity
| tablet animal
|
| 29.
| Platyhgelminthes
| unsegmented worms
| flatworms
|
| 30.
| Porifera
| sessile suspension feeders
| sponges
|
| 31.
| Priapula
| marine worm
| "penis worm"
|
| 32.
| Rhombozoa
| cephalopod parasite
|
|
| 33.
| Rotifera
| microscopic
|
|
| 34.
| Siboglinidae
| no digestive system
| deep-sea vent worms, beard worms
|
| 35.
| Sipuncula
| mouth of tentacles
| peanut worms
|
| 36.
| Tardigrada
| four pairs clawed legs
| water bears, recently demonstrated to be able
to survive in the vacuum of space
|
| 37.
| Xenoturbellida
| no brain, no digestive tract
| similar to flatworm
|
These represent the full diversity of animal body
plans. But perhaps the most important thing about these
is that they are all found very early in the Cambrian
(542-488) fossil record (Gould, 2002, p. 1155). Only
Phylum Bryozoa developed after Cambrian times,
during the Ordovician (488-443 Ma).
Paleontologist Mike
Foote points out that, although we continue to find new
fossils, those we find belong to phyla and other major
groups that we already know about.Explore Evolution, p.
30
Trilobite: Elrathia (sp.) from the Burgess Shale. Photo by Steven Newton.
This statement implies that the fact that we only find
organisms that fit within our definitions of phyla is a
circular reasoning problem. This misunderstands the
fundamental tenet of common descent--that an animal has
to evolve from something rather than spontaneously
popping into existence.
According to Gould (1989), the fact that only 1
new phylum has originated since the Cambrian means that
animal diversity has actually decreased since
Cambrian times, since in early fauna such as the Burgess
Shale all of today's major phyla exist plus many other
phyla that are now extinct. There is considerable
disagreement over Gould's argument.
One implication of this is that the majority of
phyla came into being in a relatively short period of
time, the ten million years between 535-525 Ma, followed
by a dearth of new phyla. If a new body plan did not get
in at the very beginning, at the "ground floor," then
there would be little chance of its development at a
later time.
Molecular phylogeny suggest a rather different
story for the origin of the major phyla, in which:
1. echinoderms and chordates split ~ 670Ma (Ayala,
1998)
2. protosomes (arthopods, mollusks) and
deuterostomes (chordates, echinoderms)
split ~ 1.0-1.2 Ga (billion years ago) (Wray, 1996;
Bromham, 1998)
A problem with these estimates, based primarily on
protein-coding genes, is that rocks from the period of
1.2 Ga-0.67 Ga show little signs of active life at all.
Bioturbation, the mixing of sediment layers by burrowing
organisms, and trace fossils are not well expressed in
the fossil record until early Cambrian times.