Kansas City, Mo. (March 6, 2006) - Jacqueline Kim Dale, Ph.D.,
formerly a Senior Research Associate at the Stowers Institute for
Medical Research, and Olivier Pourquie, Ph.D., Stowers Institute
Investigator and an investigator with the Howard Hughes Medical
Institute, have demonstrated that the long-studied family of
transcription factors called Snail is expressed in a cyclic fashion
during the formation of the vertebral precursors in the mouse and chick
embryo.
The findings, which were published in the March 7 issue of
Developmental Cell, indicate that the genes governing many cellular
properties are downstream of the segmentation clock, the mechanism that
controls the formation of the vertebral column.
Gabora,
L. & Aerts, D. (2005). Evolution as context-driven actualization of
potential: Toward an interdisciplinary theory of change of state. Interdisciplinary
Science Reviews, 30(1), 69-88.
Abstract:
It is increasingly evident that there is more to biological evolution
than natural selection; moreover, the concept of evolution is not
limited to biology. We propose an integrative framework for
characterizing how entities evolve, in which evolution is viewed as a
process of context-driven actualization of potential (CAP). Processes
of change differ according to the degree of nondeterminism, and the
degree to which they are sensitive to, internalize, and depend upon a
particular context. The approach enables us to embed phenomena across
disciplines into a broad conceptual framework. We give examples of
insights into physics, biology, culture and cognition that derive from
this unifying framework.
Mammals
of the Mesozoic era (248 to 65 million years ago) generally are
considered to be primitive, shrew-like creatures living in the shadow
of the dinosaurs (1). Only after the extinction of the dinosaurs at the
end of the Cretaceous era (144 to 65 million years ago) did they have a
chance to explore a greater variety of ecological niches. During the
adaptive radiation that began about 65 million years ago, mammals were
able to invade all kinds of terrestrial environments, even the aquatic
and aerial realms. Pushing back the mammalian conquest of the waters by
more than 100 million years, Ji et al. (2) report on page 1123 of this
issue a Middle Jurassic, 164-million-year-old skeleton with a
beaverlike tail and seal-like teeth perfectly adapted for an aquatic
lifestyle.
A
docodontan mammaliaform from the Middle Jurassic of China possesses
swimming and burrowing skeletal adaptations and some dental features
for aquatic feeding. It is the most primitive taxon in the mammalian
lineage known to have fur and has a broad, flattened, partly scaly tail
analogous to that of modern beavers. We infer that docodontans were
semiaquatic, convergent to the modern platypus and many Cenozoic
placentals. This fossil demonstrates that some mammaliaforms, or
proximal relatives to modern mammals, developed diverse locomotory and
feeding adaptations and were ecomorphologically different from the
majority of generalized small terrestrial Mesozoic mammalian
insectivores.
The links work OK but email
me if you have any problems (I made a typo on the research
article url and got "We've redesigned
our Web site, and some Carnegie Museum of Natural History pages have
gone the way of the dinosaurs."!)
From symmetry to asymmetry: Phylogenetic patterns of asymmetry
variation in animals and their evolutionary significance
Abstract:
Phylogenetic analyses of asymmetry variation offer a powerful tool for
exploring the interplay between ontogeny and evolution because (i)
conspicuous asymmetries exist in many higher metazoans with widely
varying modes of development, (ii) patterns of bilateral variation
within species may identify genetically and environmentally triggered
asymmetries, and (iii) asymmetries arising at different times during
development may be more sensitive to internal cytoplasmic
inhomogeneities compared to external environmental stimuli. Using four
broadly comparable asymmetry states (symmetry, antisymmetry, dextral,
and sinistral), and two stages at which asymmetry appears
developmentally (larval and postlarval), I evaluated relations between
ontogenetic and phylogenetic patterns of asymmetry variation. Among 140
inferred phylogenetic transitions between asymmetry states, recorded
from 11 classes in five phyla, directional asymmetry (dextral or
sinistral) evolved directly from symmetrical ancestors proportionally
more frequently among larval asymmetries. In contrast, antisymmetry,
either as an end state or as a transitional stage preceding directional
asymmetry, was confined primarily to postlarval asymmetries. The
ontogenetic origin of asymmetry thus significantly influences its
subsequent evolution. Furthermore, because antisymmetry typically
signals an environmentally triggered asymmetry, the phylogenetic
transition from antisymmetry to directional asymmetry suggests that
many cases of laterally fixed asymmetries evolved via genetic
assimilation.
--- In evomech@yahoogroups.com, "John Latter" <jorolat@...> wrote: > > [A. Richard Palmer. "Antisymmetry." In Variation, Editors B Hallgrimmson and BK Hall. Elsevier (2005): 359-397] > > Introduction: > > The notion of antisymmetry likely strikes most people as bizarre. How can any > variation exist that is "anti-" something else? To dismiss antisymmetry as mere > intellectual catnip of academic snoots would seem easy. To dismiss it too hastily > would be a big mistake. > > Antisymmetry is a peculiar kind of variation whose evolutionary significance is > surprisingly unappreciated, no doubt in part because the term seems odd and foreboding. However, the phenomenon, with its particularly apt moniker, is actually > widespread and offers the promise of valuable insights into a century-old debate > about the interplay between development and evolution.
From: "John Latter" <jorolat@...>
> Subject: [evomech] Limbs in whales and limblessness in other
> vertebrates: mechanisms of evolutionary and developmental
> transformation and loss. [Bejder & Hall, Evolution &
> Development, '02]
> text; http://whitelab.biology.dal.ca/lb/Bejder%20and%20Hall.pdf
> We address the developmental and evolutionary mechanisms
> underlying fore- and hindlimb development and progressive
> hindlimb reduction and skeletal loss...
There's nothing in the article about the evolutionary origin of
limbs.
That little point is glossed over in this discussion of
development
and of the evolutionary reduction of limbs.
> Limblessness in most snakes is also associated with adoption
>of a new (burrowing) lifestyle...
Were early snakes tunnelers? Or does this new burowing include
merely burrowing through surface debis? Just wondering.
> An evolutionary change in Hox gene expression--as occurs
> in snakes--or in Hox gene regulation--as occurs in some limbless
> mutants--is unlikely to have initiated loss of the hindlimbs in
> cetaceans. Selective pressures acting on a wide range of
> developmental processes and adult traits other than the
> limbs are likely to have driven the loss of hindlimbs in whales.
Are they suggesting that a change occurring via Hox genes or
their regulation can occur more quickly? Selective pressure may
drive the loss of a feature, but how do we know whether or not
Hox genes are involved?
Cliff
We address the developmental and evolutionary mechanisms underlying
fore- and hindlimb development and progressive hindlimb reduction and
skeletal loss in whales and evaluate whether the genetic,
developmental, and evolutionary mechanisms thought to be responsible
for limb loss in snakes "explain" loss of the hindlimbs in whales. Limb
loss and concurrent morphological and physiological changes associated
with the transition from land to water are discussed within the context
of the current whale phylogeny. Emphasis is placed on fore- and
hindlimb development, how the forelimbs transformed into flippers, and
how the hindlimbs regressed, leaving either no elements or vestigial
skeletal elements. Hindlimbs likely began to regress only after the
ancestors of whales entered the aquatic environment: Hindlimb function
was co-opted by the undulatory vertical axial locomotion made possible
by the newly evolved caudal flukes. Loss of the hindlimbs was
associated with elongation of the body during the transition from land
to water. Limblessness in most snakes is also associated with adoption
of a new (burrowing) lifestyle and was driven by developmental changes
associated with elongation of the body. Parallels between adaptation to
burrowing or to the aquatic environment reflect structural and
functional changes associated with the switch to axial locomotion.
Because they are more fully studied and to determine whether hindlimb
loss in lineages that are not closely related could result from similar
genetically controlled developmental pathways, we discuss developmental
(cellular and genetic) processes that may have driven limb loss in
snakes and leg-less lizards and compare these processes to the loss of
hindlimbs in whales. In neither group does ontogenetic or phylogenetic
limb reduction result from failure to initiate limb development. In
both groups limb loss results from arrested development at the limb bud
stage, as a result of inability to maintain necessary inductive tissue
interactions and enhanced cell death over that seen in limbed
tetrapods. An evolutionary change in Hox gene expression--as occurs in
snakes--or in Hox gene regulation--as occurs in some limbless
mutants--is unlikely to have initiated loss of the hindlimbs in
cetaceans. Selective pressures acting on a wide range of developmental
processes and adult traits other than the limbs are likely to have
driven the loss of hindlimbs in whales.
Conrad Hal Waddington was a leading embryologist and geneticist from
the 1930s to the 1950s. He is remembered mainly for his concepts of the
'epigenetic landscape' and 'genetic assimilation'. This article reviews
his life and work, and enquires to what extent his ideas are relevant
tools for understanding the biological problems of today.
The early studies of evolutionary developmental biology (Evo-Devo) come
from several sources. Tributaries flowing into Evo-Devo came from such
disciplines as embryology, developmental genetics, evolutionary
biology, ecology, paleontology, systematics, medical embryology and
mathematical modeling. This essay will trace one of the major pathways,
that from evolutionary embryology to Evo-Devo and it will show the
interactions of this pathway with two other sources of Evo-Devo:
ecological developmental biology and medical developmental biology.
Together, these three fields are forming a more inclusive evolutionary
developmental biology that is revitalizing and providing answers to old
and important questions involving the formation of biodiversity on
Earth. The phenotype of Evo-Devo is limited by internal constraints on
what could be known given the methods and equipment of the time and it
has been framed by external factors that include both academic and
global politics. [Evolution]
--- In evomech@yahoogroups.com, "John Latter" <jorolat@...> wrote: > > [Palmer, Science, Oct '04] > > Abstract: > > " Because of its simplicity, the binary-switch nature of left-right asymmetry permits meaningful comparisons among many different organisms. Phylogenetic analyses of asymmetry variation, inheritance, and molecular mechanisms reveal unexpected insights into how development evolves. First, directional asymmetry, an evolutionary novelty, arose from nonheritable origins almost as often as from mutations, implying that genetic assimilation ("phenotype precedes genotype") is a common mode of evolution. Second, the molecular pathway directing hearts leftward—the nodal cascade—varies considerably among vertebrates (homology of form does not require homology of development) and was possibly co-opted from a preexisting asymmetrical chordate organ system. Finally, declining frequencies of spontaneous asymmetry reversal throughout vertebrate evolution suggest that heart development has become more canalized." > > Copies of the full article can be obtained either by emailing Rich direct or from myself here >
[Pfennig, American Scientist Book Review, Jan '04]
Developmental Plasticity and Evolution. Mary Jane
West-Eberhard.
An unfortunate outgrowth of the modern revolution in genetics is the
widespread belief that the genes of an individual organism determine
its appearance, physiology and behavior. The genome does not, of
course, completely determine how an organism is constructed: The
environment is an essential partner. Nowhere is this point more clearly
illustrated than by the principle of developmental plasticity—the
tendency for genetically identical organisms to differ in response to
various environmental stimuli, or for individuals to vary over time as
the result of changing conditions in their surroundings...
... In Developmental Plasticity and Evolution, Mary Jane
West-Eberhard, an evolutionary biologist at the Smithsonian Tropical
Research Institute and a member of the National Academy of Sciences,
undertakes to explain how developmental plasticity fits within a
genetic theory of evolution. She believes (with considerable
justification) that evolutionary and developmental biologists have
failed to incorporate developmental plasticity into their framework for
understanding the living world.
Under the influence of natural selection development tends to become
canalized so that more or less normal organs and tissues are produced
even in the face of slight abnormalities of the genotype or of the
external environment (Waddington, 1940).
It has been suggested that if an animal is subjected to unusual
circumstances to which it can react in an adaptive manner, the
development of the adaptive character might itself become so far
canalised that it continued to appear even when the conditions returned
to the previous norm (Waddington, 1942). This mechanism would provide a
means by which an "acquired character" in the conventional sense could
be "assimilated" by the genotype, and eventually appear comparitively
independent of any specific environmental influence.
Schmalhausen (1947) has independently suggested a very similar process,
which he has discussed at some length under the name "stabilising
selection"; a phrase which, however, he uses in a number of different
senses, as Simpson (1947) has pointed out.
[Collin & Cipriani, Proceedings of the Royal Society of London B , Dec '03]
Abstract:
Gastropods have lost the quintessential snail feature, the coiledshell, numerous times in evolution. In many cases these animals havedeveloped a limpet morphology with a cap-shaped shell and a large foot.Limpets thrive in marginal habitats such as hydrothermal vents, thehigh-energy rocky intertidal areas and fresh water, but they areconsidered to be evolutionary dead-ends, unable to re-evolve a coiledshell and therefore unable to give rise to the diversity seen amongcoiled snails. The re-evolution of a coiled shell, or any complexcharacter, is considered unlikely or impossible (Dollo's law) becausethe loss of the character is followed by the loss of the geneticarchitecture and developmental mechanisms that underlie that character.Here, we quantify the level of coiling in calyptraeids, a family ofmostly uncoiled limpets, and show that coiled shells have re-evolved atleast once within this family. These results are the firstdemonstration, to our knowledge, of the re-evolution of coiling in agastropod, and show that the developmental features underlying coilinghave not been lost during 20-100 Myr of uncoiled evolutionary history.This is the first example of the re-evolution of a complex charactervia a change in developmental timing (heterochrony) rather than achange in location of gene expression (heterotopy).
Gone does not necessarily mean forgotten, especially in biology. A
recent finding by researchers at the University of Wisconsin, Madison,
and colleagues from the University of Manchester have found new
evidence that the ability to form previously lost organs--in this case,
teeth--can be maintained millions of years after the last known
ancestor possessed them.
Birds do not have teeth. However, their ancestors did--about 70 - 80
million years ago. The evolutionary loss of teeth corresponded to the
formation of the beak that is present in all living birds. Nonetheless,
it has been known that if mouse tooth-forming tissue is in contact with
bird jaw tissue, the bird tissue is able to follow the instructions
given by the mouse tissue and participate in making teeth, and that
these teeth look very much like those of mammals. However, Drs. Matthew
Harris and John F. Fallon and colleagues have found that modern birds
retain the ability to make teeth even without instruction from their
tooth-bearing cousins.
2) The Development of Archosaurian First-Generation Teeth in a
Chicken Mutant
[Harris et al., Current Biology, Feb '06]
Summary:
Modern
birds do not have teeth. Rather, they develop a specialized keratinized
structure, called the rhamphotheca, that covers the mandible, maxillae,
and premaxillae. Although recombination studies have shown that the
avian epidermis can respond to tooth-inductive cues from mouse or
lizard oral mesenchyme and participate in tooth formation 1; 2,
attempts to initiate tooth development de novo in birds have failed.
Here, we describe the formation of teeth in the talpid2 chicken mutant,
including the developmental processes and early molecular changes
associated with the formation of teeth. Additionally, we show
recapitulation of the early events seen in talpid2 after in vivo
activation of β-catenin in wild-type embryos. We compare the formation
of teeth in the talpid2 mutant with that in the alligator and show the
formation of decidedly archosaurian (crocodilian) first-generation
teeth in an avian embryo. The formation of teeth in the mutant is
coupled with alterations in the specification of the oral/aboral
boundary of the jaw. We propose an epigenetic model of the
developmental modification of dentition in avian evolution; in this
model, changes in the relative position of a lateral signaling center
over competent odontogenic mesenchyme led to loss of teeth in avians
while maintaining tooth developmental potential.
The genetic basis of vertebrate morphological evolution has
traditionally been very difficult to examine in naturally occurring
populations. Here we describe the generation of a genome-wide linkage
map to allow quantitative trait analysis of evolutionarily derived
morphologies in the Mexican cave tetra, a species that has, in a series
of independent caves, repeatedly evolved specialized characteristics
adapted to a unique and well-studied ecological environment. We focused
on the trait of albinism and discovered that it is linked to Oca2, a
known pigmentation gene, in two cave populations. We found different
deletions in Oca2 in each population and, using a cell-based assay,
showed that both cause loss of function of the corresponding protein,
OCA2. Thus, the two cave populations evolved albinism independently,
through similar mutational events.
1) Research points to new theory driving evolutionary changes (Press Release)
DALLAS - Dec. 13, 2004 - Researchers at UT Southwestern Medical Center at Dallas have used canine DNA to identify a genetic mutation mechanism they believe is responsible for rapid evolutionary changes in the physical appearance of many species.
The findings, based on data gathered from hundreds of museum specimens of dogs and from blood samples of volunteered live dogs, offer a new explanation for the sudden, rapid rise of new speciesfound in the fossil record. They also help explain the variability inappearance among individual members of a species, such as the length of the nose in different breeds of domestic dogs.
"We're offering an explanation for a lot of differentcomponents of evolution, one that goes against the central dogma thatcurrently explains how certain aspects of evolution take place," said Dr. Harold "Skip" Garner.
2) Molecular origins of rapid and continuous morphological evolution
[Garner & Fondon, PNAS, Dec '04]
Abstract:
Mutations in cis-regulatory sequences have been implicated asbeing the predominant source of variation in morphologicalevolution.We offer a hypothesis that gene-associatedtandem repeat expansionsand contractions are a majorsource of phenotypic variationin evolution. Here, wedescribe a comparative genomic studyof repetitiveelements in developmental genes of 92 breeds ofdogs. Wefind evidence for selection for divergence at codingrepeatloci in the form of both elevated purity and extensivelengthpolymorphism among different breeds. Variations in thenumberof repeats in the coding regions of the Alx-4 (aristaless-like4) and Runx-2 (runt-related transcription factor 2)genes werequantitatively associated with significantdifferences in limband skull morphology. We identifiedsimilar repeat length variationin the coding repeats ofRunx-2, Twist, and Dlx-2 in severalotherspecies. The high frequency and incremental effects ofrepeatlength mutations provide molecular explanations for swift,yettopologically conservative morphological evolution.
A monstrous discovery suggests that viruses, long regarded as lowly
evolutionary latecomers, may have been the precursors of all life on
Earth
Extracts:
Few things on Earth are spookier than viruses. The very name virus,
from the Latin word for "poisonous slime," speaks to our lowly regard
for them...
...Now, with the recent discovery of a truly monstrous virus,
scientists are again casting about for how best to characterize these
spectral life-forms. The new virus, officially known as Mimivirus
(because it mimics a bacterium), is a creature "so bizarre," as The
London Telegraph described it, "and unlike anything else seen by
scientists . . . that . . . it could qualify for a new domain in the
tree of life." Indeed, Mimivirus is so much more genetically complex
than all previously known viruses, not to mention a number of bacteria,
that it seems to call for a dramatic redrawing of the tree of life...
...Viruses, long thought to be biology's hitchhikers, turn out to have
been biology's formative force. This is striking news,
especially at a moment when the basic facts of origins and evolution
seem to have fallen under a shroud. In the discussions of intelligent
design, one hears a yearning for an old-fashioned creation story, in
which some singular, inchoate entity stepped in to give rise to complex
life-forms—humans in particular. Now the viruses appear to present a
creation story of their own: a stirring, topsy-turvy, and decidedly
unintelligent design wherein life arose more by reckless accident than
original intent...
...The discovery of Mimivirus lends weight to one of the more
compelling theories discussed at Les Treilles. Back when the three
domains of life were emerging, a large DNA virus very much like Mimi
may have made its way inside a bacterium or an archaean and, rather
than killing it, harmlessly persisted there. The eukaryotic cell
nucleus and large, complex DNA viruses like Mimi share a compelling
number of biological traits. They both replicate in the cell cytoplasm,
and on doing so, each uses the same machinery within the cytoplasm to
form a new membrane around itself. They both have certain enzymes for
capping messenger RNA, and they both have linear chromosomes rather
than the circular ones typically found in a bacterium. "If this is
true," Forterre has said of the viral-nucleus hypothesis, "then we are
all basically descended from viruses."...
...We have been looking for our designer in all the wrong places. It
seems we owe our existence to viruses, the least of semiliving forms,
and about the only thing they have in common with any sort of
theological prime mover is their omnipresence and invisibility. Once
again, viruses have altered the way that we view them and, by
extension, ourselves. As it turns out, they are not the little
breakaway shards of our biology - we are, of theirs.
[Lenski & Sniegowski, Annual Review of Systematics, Nov '95]
Abstract:
A central tenet of evolutionary theory is that mutation is random with
respect to its adaptive consequences for individual organisms; that is,
the production of variation precedes and does not cause adaptation.
Several recent experimental reports have challenged this tenet by
suggesting that bacteria (and yeast) ''may have mechanisms for choosing
which mutations will occur'' (6, p. 142). The phenomenon of nonrandom
mutation claimed in these experiments was initially called ''directed
mutation'' but has undergone several name changes during its brief and
controversial history. The directed mutation hypothesis has not fared
well; many examples of apparently directed mutation have been rejected
in favor of more conventional explanations, and several reviews
questioning the validity of directed mutation have appeared (53, 54,
59-61, 79, 80). Nonetheless, directed mutation has recently been
reincarnated under the confusing label ''adaptive mutation'' (5, 23, 24,
27, 35, 74). Here we discuss the many experimental and conceptual
problems with directed/adaptive mutation, and we argue that the most
plausible molecular models proposed to explain ''adaptive mutation'' are
entirely consistent with the modern Darwinian concept of adaptation by
natural selection on randomly occurring variation. In the concluding
section of the paper, we discuss the importance of an informed
evolutionary approach in the study of the potential adaptive
significance of mutational phenomena. Knowledge of the molecular bases
of mutation is increasing rapidly, but rigorous evolutionary
understanding lags behind. We note that ascribing adaptive significance
to mutational phenomena (for example, ''adaptive mutation'') is beset
with some of the same difficulties as ascribing adaptive significance to
features of whole organisms (29). We consider some examples of
mutational phenomena along with possible adaptive and nonadaptive
explanations.
Full text at:
https://vnet.uh.edu/vrecord_data/vclass/resource/sniegowski_9211.pdfhttp://myxo.css.msu.edu/lenski/pdf/1995,%20ARES,%20Sniegowski%20&%20Lenski.pdf
John Latter
--
*Model of an Internal Evolutionary Mechanism*:
http://members.aol.com/jorolat/index.html
technorati tags: central+tenet
<http://www.technorati.com/tags/central+tenet>, evolutionary+theory
<http://www.technorati.com/tags/evolutionary+theory>, evolution
<http://www.technorati.com/tags/evolution>, variation
<http://www.technorati.com/tags/variation>, adaptation
<http://www.technorati.com/tags/adaptation>, mechanism
<http://www.technorati.com/tags/mechanism>, nonrandom
<http://www.technorati.com/tags/nonrandom>, phenomena
<http://www.technorati.com/tags/phenomena>, controversy
<http://www.technorati.com/tags/controversy>, directed+mutation
<http://www.technorati.com/tags/directed+mutation>, adaptive+mutation
<http://www.technorati.com/tags/adaptive+mutation>, darwinian
<http://www.technorati.com/tags/darwinian>, natural+selection
<http://www.technorati.com/tags/natural+selection>
On pages 48 and 49 of "The Great Evolution Mystery" (Secker
& Warburg version - page numbers may be different in Abacus or
MacDonald editions) Gordon Rattray Taylor wrote:
"Fifty years ago, for instance, one Harry Schroeder conducted an
intriguing experiment with the willow-moth caterpillar. This
caterpillar places itself on a leaf and rolls the leaf around itself
before pupating, fastening it down with a web.
Normally, it starts by drawing the tip of the leaf over itself, but
Schroeder, with fiendish cunning, systematically cut off the tips of
all the leaves on which caterpillars had taken up position. Sensibly
enough, they responded by drawing the side of the leaf over instead.
When these caterpillars had produced another generation, Schroeder
found that, of nineteen offspring, four drew the side of the leaf over,
not the tip, when their time to pupate came around.
It may be said that this was inheritance of an acquired behavior, not a
structure, but there may not be much difference from a genetic point of
view, as we shall see.
Perhaps the same might be said of an unique series of experiments by
Frederick Griffiths, who placed rats on slowly revolving turntables for
periods of up to one and a half years. When the wretched animals were
freed their heads constantly flicked in the direction in which they had
been rotated, and their eyes flicked also. This flicking automatism
reappeared in their progeny."
Both of the above experiments exhibit characteristics consistent with
the proposed homeostatic internal evolutionary mechanism I am currently
researching. Unfortunately, however, Taylor gives no citations and
there are no further references to Schroeder and Griffiths in either
the Bibliography or the Sources.
Should anyone comes across any information regarding these experiments
- or others of a similar nature - I would be very grateful if you could
let me know: jorolat@...
"The Great Evolution Mystery" is no longer in print although
used copies are still listed at:
"If you read much popular science,
you’d be forgiven for thinking that biology has become something of a
banana republic. A seemingly endless series of books and newspaper
articles reports that biology is being roiled by any number of
revolutions. Take your pick: genomics, proteomics, medical genetics,
and, now, something called evo devo. Some of the revolutionary rhetoric
is surely hype, but these are, undeniably, exciting times in biology.
Entire genomes are being decoded at an astounding rate (nearly three
hundred species have been done, and more than seven hundred others are
in the works), and new high-tech approaches to old problems seem to
appear by the week. The result of all this has been some genuinely
surprising scientific findings. And some of the biggest have come from
the new science of evo devo."
On 15/02/2006 johnhewitt22 wrote: > Dear John Latter and other regular
contributors to this group,
>
> I have been a member of the group for just a couple of weeks now
and I
> have looked at the web site from which it draws inspiration. > I understand that what is being
advanced is the idea of some kind of
> internal mechanism for evolution but I am not too clear about how
this
> translates into a general programme or what exact mechanism is
being
> advanced. > Could I ask that a simple, slimmed
down version of the group's basic
> ideas and objectives be given? Something so bare as to be suitable
for
> a bear with very little brain.
>
> Sincerely
>
> John Hewitt
> http://www.sexandphilosophy.co.uk
John,
The group homepage contains a description of the group's
'aims/interests' at:
And Warren has posted his views on a number of occasions - these can be
found using the search facility on the group homepage.
Currently I'm engaged in researching material for a rewrite of a
proposed testable homeostatic internal mechanism - I'm pretty
sure group members are busy in other areas!
Dear John Latter and other regular contributors to this group,
I have been a member of the group for just a couple of weeks now and I
have looked at the web site from which it draws inspiration.
I understand that what is being advanced is the idea of some kind of
internal mechanism for evolution but I am not too clear about how this
translates into a general programme or what exact mechanism is being
advanced.
Could I ask that a simple, slimmed down version of the group's basic
ideas and objectives be given? Something so bare as to be suitable for
a bear with very little brain.
Sincerely
John Hewitt
http://www.sexandphilosophy.co.uk
[Editor’s
note: This essay will be published in the Spring 2006 issue of VQR in a
special portfolio on Darwin, evolution, and intelligent design. The
portfolio will also feature essays by Michael Ruse, Thomas Eisner, and
Robert M. Sapolsky, and an excerpt from David Quammen’s forthcoming
book The Reluctant Mr. Darwin: An Intimate Portrait of Charles Darwin
and the Making of His Theory of Evolution. To pre-order the Spring
issue, click here.]
"I came to evolution in a roundabout
way. Sure, as a kid I had seen the dinosaurs at the American Museum of
Natural History—and had heard a bit about evolution in high school. But
I was intent on studying Latin and maybe going to law school.
Development of the animal body plan is controlled by large gene
regulatory networks (GRNs), and
hence evolution of body plans must depend upon change in the
architecture of developmental
GRNs. However, these networks are composed of diverse components that
evolve at different rates
and in different ways. Because of the hierarchical organization of
developmental GRNs, some kinds
of change affect terminal properties of the body plan such as occur in
speciation, whereas others
affect major aspects of body plan morphology. A notable feature of the
paleontological record
of animal evolution is the establishment by the Early Cambrian of
virtually all phylum-level body
plans. We identify a class of GRN component, the 'kernels' of the
network, which, because of
their developmental role and their particular internal structure, are
most impervious to change.
Conservation of phyletic body plans may have been due to the retention
since pre-Cambrian
time of GRN kernels, which underlie development of major body parts.
Reprints available from Eric Davidson at the email address on the
following link or contact jorolat@... :
A leading evolutionist recently observed that the great questions in
evolutionary theory
remain much the same today as they were in Darwin’s time. Certainly
this observation
applies to the debate over the inheritance of acquired characters,
commonly known as
Lamarckism, after Jean Lamarck, author of the first systematic theory
of evolution. The
debate over the reality of Lamarckian ideas has raged for the better
part of a century and
a half and shows no signs of abating. Indeed, as I write, the
controversy has been
rekindled over the announcement of new experiments allegedly supporting
the possibility
of inheritance of acquired characters.
In an attempt to understand the historical background and theoretical
significance of this
controversy we will offer here a brief outline of the history of the
inheritance of acquired
characters. This outline will include a summary of Lamarck’s theory of
evolution; an
assessment of the validity of its rejection by Weismann and
Neo-Darwinism; and a
discussion of recent developments including the modern revival of the
inheritance of
acquired characters by Steele and Gorczynski.
[Puglicci, Trends in Ecology and Evolution, Sept '05]
Abstract:
The study of phenotypic plasticity has progressed significantly over
the past few decades. We have moved from variation for plasticity being
considered as a nuisance in evolutionary studies to it being the
primary target of investigations that use an array of methods,
including quantitative and molecular genetics, as well as of several
approaches that model the evolution of plastic responses. Here, I
consider some of the major aspects of research on phenotypic
plasticity, assessing where progress has been made and where additional
effort is required. I suggest that some areas of research, such the
study of the quantitative genetic underpinning of plasticity, have been
either settled in broad outline or superseded by new approaches and
questions. Other issues, such as the costs of plasticity are currently
at the forefront of research in this field, and are likely to be areas
of major future development.