[Taxacom] Biogeography of Australasia

Michael Heads m.j.heads at gmail.com
Tue Mar 25 02:59:07 CDT 2014


Surprisingly, even species with long-lived, planktonic larval stages also
show very high levels of geographic structuring.

Michael


On Tue, Mar 25, 2014 at 7:26 PM, Stephen Thorpe
<stephen_thorpe at yahoo.co.nz>wrote:

> Yes, marine species with direct development (no larval stage) can show
> local endemism (the sea to them is like the air to us!)
>
> Stephen
>
> --------------------------------------------
> On Tue, 25/3/14, Michael Heads <m.j.heads at gmail.com> wrote:
>
>  Subject: Re: [Taxacom] Biogeography of Australasia
>  To: "Stephen Thorpe" <stephen_thorpe at yahoo.co.nz>
>  Cc: "JF Mate" <aphodiinaemate at gmail.com>, "Taxacom" <
> taxacom at mailman.nhm.ku.edu>
>  Received: Tuesday, 25 March, 2014, 6:14 AM
>
>  A lot of reef
>  organisms show very high levels of genetic/geographic
>  structure (allopatry). This discovery has caused a paradigm
>  shift in marine biology, and the recognition of local
>  endemics. In much the same way, the high levels of
>  geographic structure even in microrganisms have caused a
>  revolution and the rejection of the old idea that
>  'everything is everywhere and the environment
>  selects'.
>   Michael
>
>  On Tue, Mar 25, 2014
>  at 5:11 PM, Stephen Thorpe <stephen_thorpe at yahoo.co.nz>
>  wrote:
>
>
>  Shallow water species would need to lack actively
>  swimming or planktonic or phoretic larvae ...
>
>
>
>
>
>
>  From: Michael Heads
>  <m.j.heads at gmail.com>
>
>  To: Stephen
>  Thorpe <stephen_thorpe at yahoo.co.nz>
>
>  Cc: JF Mate
>  <aphodiinaemate at gmail.com>;
>  Taxacom <taxacom at mailman.nhm.ku.edu>
>
>
>  Sent: Tuesday,
>  25 March 2014 5:07 PM
>  Subject: Re:
>  [Taxacom] Biogeography of Australasia
>
>
>
>
>
>
>
>  Many cases of vicariance in island groups are most
>  easily explained if the organisms regularly move between
>  nearby islands, as a metapopulation on individually
>  ephemeral islands. If the island group is rifted apart, the
>  metapopulation may be divided by vicariance into two, as
>  between Vanuatu and Fiji for example. This process can
>  operate on terrestrial biota, but also reef groups that
>  require shallow water.
>
>
>  Michael
>
>
>
>
>  On Tue, Mar 25, 2014 at 4:50 PM, Stephen Thorpe <
> stephen_thorpe at yahoo.co.nz>
>  wrote:
>
>
>
>
>
>  The distinction between vicariance vs.
>  dispersal scenarios really only makes sense for terrestrial
>  allopatric species separated on oceanic islands. Then we can
>  ask if one of the species is derived from ancestors which
>  did not need to swim or fly from another island. This would
>  be vicariance. Amphibians are good examples, as they
>  can't fly (actively or passively) and they can't
>  tolerate seawater.
>
>
>  Stephen
>
>
>
>
>  From: Michael Heads
>  <m.j.heads at gmail.com>
>
>  To: JF Mate
>  <aphodiinaemate at gmail.com>
>  Cc: Taxacom <taxacom at mailman.nhm.ku.edu>
>
>  Sent: Tuesday,
>  25 March 2014 4:27 PM
>  Subject: Re: [Taxacom]
>  Biogeography of Australasia
>
>
>
>
>
>  Hi Jason,
>
>  You said:
>
>  'This is a play on words. There is no
>  valid/clear-cut distinction
>  between
>  "chance dispersal", "range extension" or
>  your "dispersal" vs
>
>  the meaning of the word as used by most biologists. I
>  understand that
>  panbiogeography requires
>  this (non-existant) difference to distinguish
>  itself, but in the end you only need a few
>  observed cases of organisms
>
>  crossing barriers to show that, given the right conditions,
>  dispersal
>  is a valid mechanism.'
>
>  The difference between normal,
>  observed dispersal discussed by ecologists
>
>  (e.g. weeds dispersing into a garden), and chance,
>  'jump' or 'long
>  distance'
>  dispersal as invoked by evolutionists, is that the former
>  does
>  not involve differentiation, whereas
>   the latter is proposed as a mode of
>  speciation.
>
>  Dispersal theory explains range overlap by
>  dispersal, but also explains
>  allopatry by
>  dispersal. Vicariance theory explains range overlap by
>
>  dispersal, but explains allopatry by vicariance. Note that
>  the dispersal
>  invoked in vicariance theory
>  is caused by geological change, whereas
>  dispersal as invoked by dispersal theory to
>  explain allopatry, is caused by
>
>  chance.
>
>  Michael
>
>
>  On Sun, Mar
>  23, 2014 at 8:03 AM, JF Mate <aphodiinaemate at gmail.com> wrote:
>
>
>  > Mostly a reply to John but a
>  sprinkling to Michael as well
>  >
>  > The use of quotes
>   such as "It was Darwin who invoked the concept of
>  > miracles for anyone denouncing his theory
>  of centers of origin and
>  > dispersal.
>  You are welcome to believe in extraordinary events
>  ..."
>
>  > suggests that, either by accident or design, you (John)
>  are implying
>  > dispersal is a mechanism
>  akin to religion. That and the daily readings
>  > suggest baiting.
>  >
>
>  > As to why congruence of phylogeny and known geological
>  events is
>  > important (your words):
>  "...sequence of geological events may
>  > indicate that the phylogeny predates the
>  geology, is related to a
>
>  > different geology, or that the geological
>  reconstruction is wrong."
>  > John,
>  this makes Panbiogeography unfalsifiable. Your fallback line
>  is
>  > "geology/genes/phylogeny"
>  could be wrong if they don“t
>   match a purely
>  > vicariant model. Yes, I
>  am sure that as more evidence acumulates the
>  > biogeographical scenarios of certain
>  groups will have to change. But
>  > where
>  panbiogeography fails is in the closed, one size-fits-all
>
>  > mechanism department. Science is never "the last
>  word" but the best
>  > fit to facts.
>  By using this to shield Panbiogeography you are
>  > purposefully using scientific uncertainty
>  to protect your ideas.
>
>  >
>  > As to "The significance of
>  observed cases of dispersal of highly
>  >
>  vagile species as evidence of chance dispersal being a
>  significant
>  > force in biogeography is
>  questionable and does not predict the
>
>  > tectonic correlations between good and poor dispersers
>  (in the sense
>  > of means of
>  dispersal)." There are plenty of examples of
>   species
>  > (mostly good flyers) which
>  have crossed significant barriers (even
>  >
>  oceans) and colonized new areas in recent history. How are
>  these
>  > examples not appropriate to the
>  discussion? As for successful
>
>  > colonization, just look at gardeners in Europe or NA.
>  Thousands of
>  > introduced, carefully
>  nurtured plants, often cultured for generations
>  > and only a small fraction ever becomes
>  naturalized. I acknowledge the
>
>  > fact that successful dispersal over significant
>  barriers (sea, major
>  > ranges) can be an
>  unlikely event on a daily event but over millions of
>  > years a small probability can really make
>  a impact. The mechanism is
>
>  > certainly common enough to suggest it does not require
>  divine
>  > intervention to happen.
>  >
>  > "Similarly,
>   repopulation does not substanciate chance dispersal as a
>  > significant force in the sense of chance
>  dispersal being a major
>  > mechanism in
>  biogeography." and Michael "No-one is arguing
>  that
>
>  > dispersal is a significant force. All organisms have
>  dispersed to
>  > their current locations.
>  Dispersal can be observed every day.
>  >
>  Vicariance biogeography has never denied dispersal - you
>  can't just
>
>  > have vicariance otherwise there would only be a single
>  taxon in any
>  > area."
>  >
>  > This is a play on
>  words. There is no valid/clear-cut distinction
>
>  > between "chance dispersal", "range
>  extension" or your "dispersal" vs
>  > the meaning of the word as used by most
>  biologists. I understand that
>  >
>  panbiogeography requires this (non-existant) difference to
>  distinguish
>
>  > itself, but in the end you only need a few observed
>  cases of organisms
>  > crossing barriers to
>  show that, given the right conditions, dispersal
>  > is a valid mechanism. Maybe not 99% of the
>  time, but chance plays a
>
>  > bigger part in evolution than 0, and that is what
>  matters.
>  >
>  > Best
>  >
>  > Jason
>  >
>  >
>  _______________________________________________
>
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>  > Taxacom at mailman.nhm.ku.edu
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>
>  > The Taxacom Archive back to 1992 may be
>   searched at:
>  > http://taxacom.markmail.org/
>
>  >
>  > Celebrating
>  27 years of Taxacom in 2014.
>  >
>
>
>
>  --
>  Dunedin, New Zealand.
>
>
>  My recent books:
>
>  *Molecular panbiogeography of the
>  tropics.* 2012. University of California
>  Press, Berkeley. www.ucpress.edu/book.php?isbn=9780520271968
>
>
>  *Biogeography of Australasia:  A molecular
>  analysis*. 2014. Cambridge
>  University Press,
>  Cambridge. www.cambridge.org/9781107041028
>
>
>  _______________________________________________
>  Taxacom Mailing List
>  Taxacom at mailman.nhm.ku.edu
>
>  http://mailman.nhm.ku.edu/mailman/listinfo/taxacom
>  The Taxacom Archive back to 1992 may be
>  searched at: http://taxacom.markmail.org/
>
>
>  Celebrating 27 years
>  of Taxacom in 2014.
>
>
>
>
>
>  --
>
>
>  Dunedin, New Zealand.
>
>
>  My recent books:
>
>  Molecular panbiogeography of the tropics.
>  2012.University of California Press, Berkeley.
> www.ucpress.edu/book.php?isbn=9780520271968
>
>
>  Biogeography of Australasia:  A molecular
>  analysis. 2014. Cambridge University Press, Cambridge.
>  www.cambridge.org/9781107041028
>
>
>
>
>
>  --
>  Dunedin, New Zealand.
>   My recent
>  books:
>  Molecular panbiogeography of the tropics.
>  2012. University of California Press, Berkeley.
> www.ucpress.edu/book.php?isbn=9780520271968
>   Biogeography of Australasia:  A
>  molecular analysis. 2014. Cambridge University Press,
>  Cambridge. www.cambridge.org/9781107041028
>
>
>
>


-- 
Dunedin, New Zealand.

My recent books:

*Molecular panbiogeography of the tropics.* 2012. University of California
Press, Berkeley. www.ucpress.edu/book.php?isbn=9780520271968

*Biogeography of Australasia:  A molecular analysis*. 2014. Cambridge
University Press, Cambridge. www.cambridge.org/9781107041028



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