[Taxacom] Dispersal clarifications

Robinwbruce at aol.com Robinwbruce at aol.com
Mon Jun 6 09:36:44 CDT 2011


Hi John,
 
My take on dispersal in current usage is range expansion with  the 
possibility of localized speciation as a further product.
 
My take of dispersal in Croizat's sense was of broad fronts/sheets of  
organisms expanding (or contracting) through time and space, and dependant on  
the relative degree of mobilism vs. immobilism and the morphogenetic 
potential  of the organisms, generating either deep or shallow differences of  form 
which could then be recognised, classified and systematised. Organisms  by 
their nature generate differences of form by various modes of  reproduction; 
time and space then canalise these differences into what  we recognise and 
develop as taxonomic patterns; all ranking is  derivative. The imperatives of 
such a system are temporal and  spatial coincidence, or at least proximity, 
and the generative nature  of organisms. Singular events, local effects and 
special ranks are  of little significance. Croizat's perspective was  
always Pan-biogeographical.
 
The current either/or form of vicariance/dispersal threatens to drain much  
meaning out of Croizat's efforts. Perhaps a more helpful and constructive  
outlook would be a bi-polar or multi-polar one, reflecting the global  
surface nature (assuming Tom Gold's ideas of deep organisms are just ideas)  of 
what we are trying to understand.   
 
Robin
 
 
 
 
     
 
 
In a message dated 6/4/2011 2:21:27 P.M. GMT Daylight Time,  
jgrehan at sciencebuff.org writes:

My take  on dispersal and biogeography is that biogeography is, in some 
ways, a test of  the assumptions about the role of means of dispersal (or the 
theorized ability  to translate an ability of individuals to move into a 
theory of how related  taxa come to occupy different sectors of the earth). 

In dispersalist  biogeography the ability to disperse seems to be often 
treated as an inherent  quality of an organism, so there are 'good' dispersers 
and 'bad' dispersers.  The bad ones explain why they are absent from 
particular sectors and visa  versa, and if a bad disperser does turn up then it 
obviously succeed by some  amazing or mysterious (and that word or similar has 
been used by  biogeographers), or a good disperser does not turn up then its 
just another  vagary of chance. 

Ecological work on the other hand seems to indicate  that dispensability is 
more an ecologically contingent quality, that one must  measure the 
ecological relationships between the organisms and the environment  to understand 
what dispersal is as a function of that relationship. Under one  set of 
ecological relationships the range of a species may be very stable, but  under 
another it may result in rapid and extensive changes in geographic  range. 
This must have occurred in many groups for there to be  trans-continental or 
global taxa. The correlation of such groups with Mesozoic  tectonics suggests 
that the ancestral range expansion did indeed occur in the  Mesozoic. So its 
not just a matter of whether or not to choose dispersal or  vicariance, but 
to have some way of estimating the spatial and temporal  context for their 
role in the origin of distribution in general.

The  case of Juan Fernandez having closer affinities on the other side of 
the  Pacific for some taxa is an example of where biogeography gives an 
insight  that is not possible simply from the assuming stratigraphic age and 
dispersal.  JF is not the only such example and even for the Galapagos there are 
 comparable patterns that hit the Galapagos, but not the American mainland. 
 

John Grehan



-----Original Message-----
From:  taxacom-bounces at mailman.nhm.ku.edu 
[mailto:taxacom-bounces at mailman.nhm.ku.edu]  On Behalf Of Jason Mate
Sent: Friday, June 03, 2011 6:22 PM
To:  Taxacom
Subject: Re: [Taxacom] Dispersal clarifications


Hi  Michael, my thoughts on your comments below:
MH:About the terms you  mention: 'dispersalist theory' and its advocates 
accept chance dispersal as a  mode of speciation. 
JFM:So is dispersal of a species from a mainland  source to an island 
acceptable dispersal?
MH:An organism 'disperses across  a barrier', often by mysterious means. 
For example, an organism that moves a  few centimeters in its lifetime is 
theorized to have jumped - just once - 10  000 km across the Pacific. Vicariance 
theory accepts that allopatric  speciation is caused by vicariance and that 
range expansion (physical  movement) only explains overlap.
JFM:Are all purported cases of dispersal  similarly extreme? Do you 
consider the dispersal of flying organisms equally  mysterious? Don´t you think 
that the probability of dispersal correlates with  the organisms ability to 
disperse?
MH:Chance: this term can be used in the  sense of sweeping something under 
the carpet - 'oh, event x must have just  been an accident'. Alternatively, 
you can go out and collect data and actually  work out the 'probabilities'. 
These are also referred to as 'chance' - as in  'the chance of event x 
happening', but 'chance' here is a completely different  concept. For example, a 
road accident may have happened on a corner where it  turns out, following a 
statistical analysis, 'accidents' regularly happen. It  wasn't simply an 
accident, there was a general, underlying explanation. This  change in 
approach was the psychological revolution of Fermat and Pascal that  gave birth to 
probability theory. 
JFM:This is a qualitative remark. A 1 in  a million event, although rare, 
although ´chance´, still has a probability,  and the sum of all the 
probabilities describes and event. Thus, although  accidents can cluster and these 
are what people may find interesting, a well  lit corner in a speed-controlled 
zone with good visibility can also have the  odd accident. The underlying 
cause of this accident may be something  completely random, with a low 
repeatability (maybe old drivers with  astigmatism at dusk fail to see 
pedestrians). But this isolated case is still  part of the totality of accidents for 
the area under study. So I´d say that  you are confusing probability with 
repeatability. By studying the biota of an  area you work out the frequency 
(probability) of each mechanism. Maybe  dispersal is not of interest to you 
since you are only interested in  vicariance, but to taxonomists or ecologists 
dispersal can be equally  interesting.
MH:Dispersal theory as seen in biogeography and systematics  journals deals 
with phylogeny and relies on 'chance' in the earlier sense. In  contrast, 
dispersal studies in ecological journals deal with observations (not  
inferences) of simple movement and are full of probability analyses - they use  
chance in the modern sense.
JFM:Chance in the earlier sense? You mean the  magical sense? Each throw of 
the dice is independent from the previous ones.  So even if I could work 
out the probability of dispersal under your system (I  can´t because your 
philosophical frame does not allow it) it would be based on  studying the origin 
of a certain number of clades and 

MH:'Ecological  dispersal' is just the simple movement of organisms 
observed every day. A weed  disperses into a garden, but it doesn't differentiate 
into a new taxon. An  organism can be where it is because it moved there or 
because it evolved  there.
JFM:The simple movement observed every day? So if you don´t observe  it 
every day it does not occur, i.e. migration? What about vagrant specimens?  
Dispersal is not an everyday, week or even year event. It is rare, precisely  
because it is a high failure, overwhelmingly lethal, no second prize  
strategy.
MH:Neatly allopatric (dovetailing) geographic structure repeated  in 
different groups can't be explained by (mere) 'chance'. It could be the  result of 
a general process such as vicariance.
JFM:You are the only one  here saying that vicariance is not an accepted 
mechanism that accounts for  organisms distributions. At the same time, you 
would expect that sources of  colonists would be limited to certain areas that 
have some sort of advantage  (i.e. currents, prevailing winds, shortest 
distance).
MH:Vicariance might  be falsified by finding that the distributions of taxa 
in a region don't share  similar phylogenetic/biogeographic breaks. But 
this could be due to original  allopatry followed by range expansion. Unlike 
the text-book examples which  everyone learns, most broad theories don't fall 
over instantaneously because  someone finds a single fact (see the detailed 
critiques of 'naive  falsificationism' by Lakatos, Feyerabend etc.). Usually 
there is a slow  accumulation of 'anomalous' data and eventually there is a 
broad shift of  opinion. If all the molecular phylogenies showed no 
geographic structure and  instead taxa tended to sort on colour or size or 
hairiness, rather than  locality, no-one would be looking at  vicariance and it 
would just fade  away. 
JFM:Once again, vicariance is an accepted mechanism.
MH:But the  clades nearly all show impressive allopatry - this is why so 
many authors  are  putting distribution maps of their clades in the graphical 
abstracts  at Mol. Phylogen. Evol. and lots of people are discussing 
vicariance. If you  Google scholar 'vicariance', here are the numbers of articles 
mentioning the  word for 5-year periods, starting with 1960-1965 when Croizat 
wrote his big  books on the topic: 27, 40, 66, 218, 770, 1040, 1380, 2280, 
4140, 6600  (2005-2010). 
JFM:So vicariance is the only mechanism allowable unless  everything there 
shows otherwise? Why would you assume that the entire biota  of an area got 
there by one mechanism only? What is the logical basis for  this?            
          
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