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And Now Begins Our Tour of The Kingdoms.
We've already met the THREE DOMAINS
Domain Bacteria - the "true bacteria"
Domain Archaea - the archaebacteria
Domain Eukarya - the eukaryotes
The evolutionary relationships have been determined via comparison of DNA,
mRNA and rRNA sequences.
Signature sequences (base sequences at specific locations
along the rRNA) are comparable and relatively taxon specific,
yielding powerful evidence for recency of common descent of Archaea
(specifically, the thermophiles) and Eukarya.
We've already seen that prokaryotes display a wide array of metabolic
pathways, with a variety of elements/compounds used as oxidizing
agents and terminal electron acceptors.
In EUKARYOTES, only one of two pathways is seen:
- aerobic metabolism (oxygen as terminal electron acceptor)
- fermentation
This suggests that prokaryotes may have evolved several times,
whereas eukaryotes are more likely to share a common ancestor.
There are two models for eukaryotic origin:
- THE AUTOGENOUS MODEL
Eukaryotes arose when the outer membranes of ancestral
prokaryotes underwent extensive inpocketing and
pinching off to form complex internal network of membranes.
- Evidence: some extant species of cyanobacteria (e.g., Gloeocapsa)
have complex internal membrane systems and resemble simple chloroplasts.
- THE ENDOSYMBIONT MODEL
Proposed by Lynn Margulis (University of Massachusetts), this model holds that small,
energy-transducing prokaryotes
took up residence (either by being ingested as prey, or as internal
symbionts) inside larger prokaryotes, where they survived just fine.
Eventually, host and symbiont became inextricably linked
in a symbiotic relationship.
- Evidence:
- such symbioses exist today (e.g. Chaos, which resembles a very
large amoeba, but has symbiotic, energy-transducing bacteria instead of
mitochondria)
- there are extant species of cyanobacteria and heterotrophic bacteria
that strongly resemble chloroplasts and mitochondria, respectively.
- the enzymes embedded in mitochondrial and chloroplast internal
membrantes are more similar to those of
prokaryotes than they are to other enzymes found in eukaryotes
- ribosome enzymes in the mitochondria and chloroplasts
are more like those of prokaryotes than those of eukaryotes
- mitochondria and chloroplasts have their own genome,
separate from and largely independent of the nuclear genome.
- mtDNA and cpDNA are circular, and though there may be multiple
copies, all are genetically identical within a given cell (hence, these
organelles are--like bacteria--essentially haploid
- mtDNA and cpDNA circular chromosomes have no associated histones or RNA
- cytochromes and other transport proteins used in mitochondria and
chloroplasts are made in situ, without cooperation from nuclear
genome enzyme products.
- mitochondria and chloroplasts reproduce via binary fission very
similar to that seen in prokaryotes.
- nucleus, mitochondria and chloroplasts all have a double membrane
system
Here's an overview of the two models:
Until fairly recently, the "protists" were all included in a single form taxon,
Kingdom Protista.
Now that more sophisticated methods for determining similarities and
differences among cells are in use (DNA, RNA analysis; cell
ultrastructural analysis, etc.), the polyphyly of that "Kingdom" is
painfully obvious.

The Earliest Eukaryotes were Protists
The oldest known eukaryote fossils (2.1 billion years old, found in
pre-Cambrian fossil beds in Michigan) are called "acritarchs"
acrit = "confused"
(Gr)
arch = "beginning"
(Gr.)
What do "protists" have in common?
Other than their unicellularity, few characters link them as a large
group. Rather, they are now being divided into the candidate kingdoms we
see above.
Protists may be
- unicellular
- colonial
- colonial with a division of labor among cells
- planktonic (free-floating in a marine or freshwater water column)
- terrestrial
- photoautotrophic
- chemoheterotrophic, including
- predatory
- parasitic
- commensal
- mutualistic
- detritivorous (feeding on dead, organic matter and turning it into
smaller organic molecules, but NOT decomposing it)
Let's have a look at some of the protists we know today, and the most
educated suspicions about their evolutionary relationships. For a really
excellent overview of current protist biology and systematics, visit this
comprehensive site U.C.
Berkeley. (Go, Bears.)
CANDIDATE KINGDOM ARCHAEZOA
This may be a polyphyletic garbage can akin to the old "Kingdom Protista,"
as it contains a variety of protists whose evolutionary affinities are not
clear. A broad, non-committal overview of the most primitive protists can be seen HERE.
A parasitic species Giardia lamblia serves as a good example of the
primitive characters shown by many of the organisms in this assemblage.
- it is flagellated (though flagellum has typical eukaryote morphology: two
central microtubules surrounded by nine paired microtubules)
- pathogenic (transmitted via contact with infected
water; causes severe diarrhea and intestinal cramps in a variety of
mammals and birds). If you're interested in learning more about
giardiasis, and in seeing pictures of this evolutionary wonder, click
HERE.
- lacks mitochondria or any type of plastids
- has a very simple cytoskeleton
- contains two haploid nuclei
- Is Giardia's anatomy a holdover of its ancestor's autogeny? Or
perhaps endosymbiosis? Or maybe both?
Did the diplomonads branch off the evolutionary tree before mitochondrial
incorporation and before karyogamy of an ancestral eukaryote? (Remember:
prokaryotes are essentially haploid). No one knows.
CANDIDATE KINGDOM EUGLENOZOA
This includes
-
euglenoids
- kinetoplastids (such as
Trypanosoma
spp., the
causative
agents of such deadly diseases as Chaga's Disease, leishmaniasis and Sleeping Sickness.)
Both euglenoids and kinetoplastids were once lumped in the Phylum
Mastigophora ("flagellates"), which no longer exists. The flagellum is
apparently a very primitive eukaryotic structure, and gives little
information useful for classifying anything with a flagellum into a less
inclusive taxon.
CANDIDATE KINGDOM ALVEOLATA
These are linked by the presence of alveoli under the plasma membrane,
which is highly complex in function and anatomy.
Includes the
CANDIDATE KINGDOM STRAMENOPILA - a.k.a. the "Chromista"
Includes the
The diversity of their names reflects that biosystematists once thought
these organisms belonged to taxa as diverse and different as "algae"
(whatever that means) and fungi.
CANDIDATE KINGDOM RHODOPHYTA - The Red Algae
The "Red
Algae" were once linked to cyanobacteria because of similarity
in their photosynthetic pigments (phycocyanins and phycoerythrins).
Whether these pigments are analogous (homoplasies) or homologous is not
yet known for certain.
CHLOROPHYTA: PLANTS OR THEIR OWN KINGDOM?
The Chlorophyta undoubtedly share a most recent common ancestor with
plants, because of the following synapomorphies unique to plants and green
algae, but absent in other taxa.
Remember that the above characters are synapomorphies with respect to
the taxa which branched off earlier on the phylogenetic tree.
These same characters are
considered to be symplesiomorphies with respect to the green algae
and plants considered as a group.
These characters are thus not informative in determining further
clades within the green algae and plants.
SYNAPOMORPHIES of plants relative to their green algae
relatives set them apart from green algae. These include:
CHLOROPHYTA has many members which exhibit
a progression of complexity (e.g., the volvocine line of evolution).
This should NOT be taken to represent a progression towards Kingdom
Plantae. It merely shows that many algae are genetically predisposed
to have a division of labor among their cells. This predisposition also
may have been
present in the ancestral plant.
We'll return to this later, when we study Kingdom Plantae.