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Review of the Cohesion Concept of Species

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Title: Review of the Cohesion Concept of Species


1
Review of the Cohesion Concept of Species
  • John Collier
  • University of KwaZulu-Natal
  • www.ukzn.ac.za/undphil/collier

2
Phylogenetic species
  • Phylogenetics The Theory and Practice of
    Phylogenetic Systematics, E.O. Wiley, 1981
  • Species determined by phylogeny. Historical
    individuals.
  • not phenotypic similarity
  • traits are signs of lineage
  • diagnostic traits determined by considerations of
    evolutionary history, derivation of traits,
    making some traits more reliable for diagnosis
    than others
  • evolutionary processes constrained by synchronic
    and diachronic constraints Wiley called
    horizontal and vertical cohesion
  • cohesion determines species identity

3
Information flow
  • Evolution as Entropy, Brooks and Wiley, 1986
  • Phylogeny as a process of information flow.
  • Historical constraints (vertical cohesion) and
    ecological constraints (horizontal cohesion) plus
    self organization within information flow govern
    speciation.
  • Cohesion determines species identity
  • Speciation is a disruption of species cohesion
  • Species cohesion determines species macrostates,
    with variation within species determining
    microstates
  • Entropy of species (as determined by
    informational macrostate/microstate relation) is
    typically not maximal
  • This allows self-organization and disruption of
    cohesion by self-organizing bifurcation.

4
Information Flow 2
  • Brooks and Wiley, 1986 (continued)
  • Focus of information is on genes (and chemical
    DNA), but this is not required, and some
    exceptions are noted.
  • Distinction between internal and external (within
    and without the flow of genetic information)
    noted. Sexual selection a case of an internal
    process, natural selection an external
    constraint. Developmental constraints are also
    assumed to be internal, though development is
    also treated as a case of information flow with
    vertical and horizontal constraints. External
    constraints (e.g., selection) said to be purely
    rate-determining
  • Restrictions on gene flow and equilibrium with
    constraints are assumed and treated statistically
    with the entropy concept.
  • Kinetics (both internal and external) largely
    ignored (mistakenly Harrison)

5
Cohesion concept of Species
  • The meaning of species and speciation, Templeton,
    1989
  • Explicit use of cohesion to define species
  • Fully gene centred species determined by gene
    flow (intrinsic cohesion mechanisms)
  • Process oriented, but no explicit distinction
    between vertical and horizontal cohesion.
  • No theoretical unification, just a collection of
    mechanisms (next slide) that confine and separate
    gene flow
  • Cohesion both separates species (isolation) and
    unifies species (facilitation of gene flow)
  • Speciation as disruption of cohesion

6
Cohesion concept of Species 2
  • Cohesion mechanisms (Templeton 1989)
  • Genetic exchangeability
  • 1. Promotion (facilitation)
  • 2. Isolation
  • Demographic exchangeability (constraints from
    selection and drift)
  • 1. Replaceability (genetic drift promotes
    genetic identity)
  • 2. Displaceability
  • i. Selective fixation
  • ii. Adaptive transitions (natural selection)
  • a. constraints on the origin of heritable
    variation
  • b. constraints on the fate of heritable
    variation
  • ecological, developmental, historical,
    population genetic (all extrinsic to
    genes, presumably)

7
Some remarks on the phylogenetic and cohesion
approaches
  • Wileys approach is more general because it does
    not specify heredity mechanisms
  • Templetons approach is more operational, but
    difficult to generalize
  • Brooks and Wiley regard sexual selection and
    developmental constraints as internal, whereas
    Templeton regards sexual selection as a form of
    natural selection (intrinsic to gene flow), but
    developmental constraints are extrinsic
  • The last is a significant difference following
    from Templetons focus on genes alone (and
    assuming implicitly that selection is on genes,
    thus intrinsic to gene flow), and Brooks and
    Wileys focus on information flow.

8
  • We need a general account of cohesion to give
    generality to accommodate non-genetic heredity
    and the formal parity of constraints with
    information and cohesion in order to evaluate the
    views and extend them.
  • This requires an analysis of the concept of
    cohesion.

9
The cohesion concept
  • First of all, cohesion is an identity concept, so
    we start there.
  • Identity, A B
  • Logical condition, same for all things
  • Equivalence relation symmetric, transitive,
    closed
  • A B implies that B has every property that A
    has, and vice versa
  • This tells us virtually nothing, since it is a
    purely logical relation, but it does put these
    logical constraints on any concept of autonomy.
    The next move is to look at what makes parts of
    something parts of that thing. This is provided
    by the unity relation.

10
Unity
  • Unity, U(A)
  • Unity is the relation among the parts of a thing
    A such that
  • If a and b are parts of A, then aUb, and bUa
    (symmetric)
  • If a and b are parts of A, then aUb and bUc
    implies aUb (transitive)
  • By a. and b., U is an equivalence relation
  • U(A) is the closure of U, given any initial part.
  • By a. to d., U(A) contains all and only the parts
    of A.
  • It is empirical question what satisfies U(A) for
    a given A. Typically the type of unity relation
    will depend on the sort of thing A is.

11
Cohesion, the dividing glue
  • Cohesion, C(A), dynamical unity
  • Cohesion is the unity relation for dynamical
    objects, such that
  • All parts aCb are dynamical
  • C is dynamical
  • Simple examples of cohesion
  • a quartz crystal
  • a gas in a box
  • Note that in each case the cohesion is not
    absolute it is a matter of degree.
  • We should expect difficult intermediate cases.
  • Cohesion can differ in strength in different
    dimensions (factors)

12
The Tautology Problem
  • Gold (2001)
  • Hey decries this popularly acclaimed definition.
    He unmasks it as a tautology framed in the
    ostensibly palpable, yet suffering a lack of
    utility. Hey urges us to substitute the word
    cohesion with any other word and suggests we
    will find equal meaning. (Ghiselin later made
    efforts to repair Templetons mis-construction by
    identifying a species as that which is by what it
    does, specifically defining species as the
    products of speciation.)

13
The tautology non-problem
  • The cohesion concept has alternatives that might
    be correct, e.g., phenetic concepts or essential
    properties concepts
  • The cohesion concept neither endorses or
    prohibits particular contributions to cohesion.
    This is an empirical matter.
  • This empirical matter is testable.

14
Phylogenetic species are cohesion species
  • Though tautology is a non-problem, if we assume a
    phylogenetic account of species as historical
    entities, it is necessary that cohesion is the
    determiner of species identity.
  • If we use the cohesion account of species, then
    the phylogenetic view of species follows
  • So the accounts are equivalent if not identical

15
Pluralism?
  • There are many contributors to cohesion, so we
    might take it that we need a pluralistic account
    of species to accommodate all of these.
  • This seems plausible given Templetons menu of
    cohesion factors.
  • On the Wiley account, however, various factors
    contribute to overall species cohesion, giving a
    net effect, as in forces in Newtonian mechanics.
  • We dont think that Newtonian systems are
    pluralistic, so by parity we should not consider
    species concepts to be pluralistic there are
    just different aspects of species identity

16
Pluralism? 2
  • However, if we have different loci of action then
    the argument is not so simple.
  • The genetic view of Templeton provides a single
    locus of action, arguably.
  • But if extra-genetic factors are in play, it is
    not obvious that there is a single locus of
    action.
  • I have not yet worked this out fully.
  • It would interesting if there are speciation
    events that do not involve genetic differences.

17
  • Thank you
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