From owner-population-bio@net.bio.net Thu Apr 01 23:00:00 1993
Path: biosci!agate!usenet.ins.cwru.edu!magnus.acs.ohio-state.edu!zaphod.mps.ohio-state.edu!news.acns.nwu.edu!uicvm.uic.edu!yang.earlham.edu!jessec
From: jessec@yang.earlham.edu
Newsgroups: bionet.population-bio
Subject: Human population growth question
Message-ID: <1993Apr1.215017.22421@yang.earlham.edu>
Date: 2 Apr 93 02:50:17 GMT
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Hello--

   I'm a layperson with some exposure to the sciences.  In the human
population-biology section of my eco-bio class a while back, I recall
seeing at least one possible projection of future population growth that
had the world population peaking at some incredible level, dipping a bit,
then *levelling off* at some horrible number-- 12 billion, I think.  A
sort of plateau effect.
   What I can't remember is: who did this projection? When? And how many
population biologists think this is possible?
   If anyone can fill in the blanks, or wishes to comment on the general
reliability of such models, I'm all ears-- appreciative in advance--


   --Jesse.

"When I went to see *Blade Runner*, I panicked and fled from the theater."

   --William Gibson

From owner-population-bio@net.bio.net Fri Apr 02 23:00:00 1993
Path: biosci!uwm.edu!rpi!utcsri!newsflash.concordia.ca!mizar.cc.umanitoba.ca!etaylor
From: etaylor@ccu.umanitoba.ca (Euan R. Taylor)
Newsgroups: bionet.population-bio
Subject: Re: Teaching math to ecologists
Message-ID: <C4x5Mw.87I@ccu.umanitoba.ca>
Date: 3 Apr 93 17:52:08 GMT
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In <0096A482.45568440.19038@uamont.edu> zeide@UAMONT.EDU writes:

>In brief:

>     This review is the first step of a larger project, writing a
>text for undergraduate ecologists and foresters. We believe that
>ecologists, rather than mathematicians, are better equipped to
>convey the beauty and relevance of mathematics to our students.
>We hope that our text will be more inspiring than those written
>by professional mathematicians. Yet, it will not be just a
>cookbook spiced with ecological applications. Our approach to
>this project is outlined below. 

>    ------------------------------------------------------

>     We, ecologists, differ greatly in our attitude toward
>mathematics. (By mathematics I mean everything above high school
>arithmetic, algebra, and cookbooked defensive statistics.) Many
>ecologists hate all this differentiation and integration, maybe
>because they fail to understand it. For the same reason, others,
>like Darwin, hold math in awe. Some of us even dabble with
>differential equations, again usually without knowing much about
>what we are doing. 

>attempt to instill mathematical knowledge in students of biology
>and its applied branches such as forestry. This experiment has
>been conducted with an awful number of replications and variants
>in hundreds of institutions of higher education throughout the
>world. It makes sense to pause and look at the results of this
>experiment. No statistical analysis is required to see that math
>education of ecologists has been a failure.

>     This problem is not limited to the United States. I received
>all my degrees in Moscow, Russia, and can confirm that, although
>mathematical training there was more vigorous and extensive, it
>was also a complete waste. I retained nothing about calculus from
>college. If I know anything about it, it is because later on I
>learned calculus anew on my own. My interest was sparked by a
>very simple calculus text for votech schools which I happened
>across during a boring vacation. While reading and even enjoying
>this elementary book, I was amazed that I had forgotten even
>introductory concepts. The problem was not with my memory. More
>than just passive forgetting was involved. It was as if the brain
>actively, though subconsciously, had expunged all those dry
>abstract concepts as antithetical to our ecological vocation.

>     Yet, these concepts, after surmounting the barrier of
>initial rejection, appear as the most beautiful and relevant
>prerequisites of thinking in any science, ecology including.

>          Why have mathematicians failed to teach us?

>     There is a genuine lack of understanding between ecologists
>and mathematicians. It appears not only in teaching but in
>research as well. A biologist's way of thinking is different from
>that of a mathematician and, despite numerous attempts, examples
>of productive cooperation between biologists and mathematicians
>are as rare as the number of ecologists who mastered math as a
>university student. Those who create math and regard it as an end
>in itself are not necessarily the best at using it as a means to
>an end.

>     Analysis of this problem deserves a special inquiry, rather
>than offhand remarks, because it may help to find better ways of
>communication. Basically, there are two explanations. One is that
>in principle biology, unlike physics, cannot be explained in
>mathematical terms. These areas of knowledge belong to two
>inimical and mutually incomprehensible worlds. According to this
>explanation, when mathematicians venture to say something about
>biology, they are always wrong or, at best, irrelevant. Trofim
>Lysenko was the best known champion of this view in the fifties
>and Ernst Mayr is at present.

>     Mayr, an outstanding biologist who upon retirement turned to
>the history and philosophy of science, criticizes math in the
>course of his struggle with what he calls typological thinking.
>Instead, he advocates population thinking that "is a peculiarly
>biological concept, alien to the thinking of the physical
>scientist" (Mayr 1982, p. 487). Biology and historical sciences,
>he believes, deal with systems too complex to be expressed in
>mathematical formulas. Only misconceptions" can be produced as a
>result of "ill-advised application of mathematics" in biology.
>Equally expressive are comments like "It might be mentioned,
>incidentally, how misleading it is to refer to mathematics as the
>"queen of the sciences"." His thorough knowledge of the history
>of science allowed him to state that "even Kant, by 1790, had
>abandoned his subservience to mathematics. If the invalidity of
>the mathematical ideal of science had not been obvious before, it
>certainly became so with the publication of the Origin of
>Species" (Mayr 1982, p. 41). Besides these philosophical issues,
>Mayr demonstrated, using the argument between Darwin and Lord
>Kelvin, that biologists might be better at calculations than
>physicists.

>     Though less knowledgeable and articulate than Mayr, Lysenko
>was more effective: he simply prohibited all biologically-related
>math. Books on the subject were recalled from all libraries in
>the USSR and burned (not publicly). Teachers of this criminal
>discipline were exiled, fired, or, after proper public
>repentance, forgiven. It is curious that, despite great
>differences between the Harvard professor and Stalin's henchman,
>both used similar derisive terminology when referring to Mendel's
>typological theory of inheritance. Mayr calls it "bean-bag
>genetics", while Lysenko dubbed it "peas' laws."

>     An alternative explanation of our poor comprehension of math
>is less radical. It deals with the shortcomings of disciples
>rather than disciplines. These weaknesses are relative. They can
>be viewed as opposite sides of the assets of the respective
>disciplines. Ecologists have a better, though intuitive, grasp of
>complicated reality such as ecosystems. But their theories and
>explanations sometimes lack coherence and discipline. The strict
>rigor and precision, the hallmark of a mathematician, when
>applied to ecological problems, too often deteriorates into a
>concern about technicalities. These details appear irrelevant to
>an ecologist for whom math is not the end, but only a means.

>     We often casually say that sizes of plants or animals are
>normally distributed. This statement would not go unnoticed by a
>mathematician. "Do you really mean that some rabbits have a
>negative weight?" -  he or she would ask. A more serious
>predicament arises when we try to discuss our research. "Your
>problem is poorly defined" (or "ill-posed") is the most common
>response by a mathematician. As a rule, the cooperation stops
>here. In rare cases when it continues, a mathematician using
>impeccably correct methods will produce an outlandish answer,
>while an ecologist employing hopelessly faulty reasoning (and
>elusive intuition) will produce something more sensible.

>     The difference in the level of development of ecology and
>math does not foster understanding and cooperation. Ecosystems
>might be extremely complex and their explanation may require very
>sophisticated math, much of which is yet to be discovered.
>However, the present extent of our knowledge of ecological
>complexity is limited. From a mathematician's viewpoint, our
>greatest achievements so far have been the comprehension of
>exponentiation (as is the case with natural selection) and
>elementary combinatorics (Mendel's genetics). This disparity
>between developmental levels makes cooperation tenuous.  

>     Regardless of the reasons and explanations for this lack of
>mutual understanding, we must recognize that it does exist and
>that we should do something about it.

>                      What should we do?

>     If we have failed to learn from mathematicians, we should
>try something else: teach ourselves. Ecologically-inspired math
>is too important to be confined to esoteric graduate courses. It
>should be taught right at the beginning of our university
>education (and even prior) by mathematically-minded ecologists.
>Mathematicians will remain indispensable as consultants. They are
>at their best when they teach future mathematicians rather than
>biologists and engineers.

>     To start with, we need to write a good text for our
>undergraduates. Actually, many texts should be written in order
>to create the competitive environment needed to facilitate the
>evolution of our mathematical education. While there are decent
>books on mathematical ecology for graduate biology students,
>undergraduate texts are commonly written by mathematicians. Our
>text will be devoted to undergraduate ecological 
From owner-population-bio@net.bio.net Sat Apr 03 23:00:00 1993
Path: biosci!agate!ames!saimiri.primate.wisc.edu!usenet.coe.montana.edu!news.uoregon.edu!news.u.washington.edu!hardy.u.washington.edu!xia
From: xia@hardy.u.washington.edu (Xuhua Xia)
Newsgroups: bionet.population-bio
Subject: Questions on hatching of avian eggs.
Message-ID: <1pmvcoINNjd5@shelley.u.washington.edu>
Date: 4 Apr 93 15:38:00 GMT
References: <0096A482.45568440.19038@uamont.edu> <C4x5Mw.87I@ccu.umanitoba.ca>
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I should appreciate information on:

1) the relationship between egg size and hatching time (the period from
the date when the egg is laid to the date when it hatches, or the period
from the beginning of incubation to the date of hatching). I am not 
familiar with avian literature. A citation should be very helpful.

2) the cost of hatching after clutchmates.

Thanks in advance.

Xuhua

From owner-population-bio@net.bio.net Sun Apr 04 23:00:00 1993
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From: lhowes@kean.ucs.mun.ca
Newsgroups: bionet.population-bio
Subject: Re: Questions on hatching of avian eggs.
Message-ID: <1993Apr4.214908.1@kean.ucs.mun.ca>
Date: 5 Apr 93 01:19:08 GMT
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In article <1pmvcoINNjd5@shelley.u.washington.edu>, xia@hardy.u.washington.edu (Xuhua Xia) writes:
> I should appreciate information on:
> 
> 1) the relationship between egg size and hatching time (the period from
> the date when the egg is laid to the date when it hatches, or the period
> from the beginning of incubation to the date of hatching). I am not 
> familiar with avian literature. A citation should be very helpful.
> 
> 2) the cost of hatching after clutchmates.
> 
> Thanks in advance.
> 
> Xuhua
> 

I happen to be writing my thesis right now with some reference to that very
topic!  

Of course this depends on the species of bird that you are interested in. 
I happen to be working with Common and Arctic terns, and so can give you a
few refreences on these species. 

In general... Larger eggs in the clutch are the eggs that are laid first.  
They have the greatest chance at survival for several reasons, more of the 
females resourses, the first to hatch therefore getting a head start on 
sibs etc.... terns hatch in about 23 days or so.  First eggs often are not 
incubated as soon as they are laid.. clutches are completed before 
attentive incubation begins.  The cost of hatching after sibs is ofetn a 
matter of life and death in terns which often lay 3 eggs but are lucky to 
fledge 1 chick.  third chicks are smaller and do not recieve the continued
incubation that they need upon hatching since parents are off foraging.  
Also larger, older chicks out compete younger chicks for food.

Refs
Nisbet, I.C.T. 1978. Dependance of fledging success on egg-size, parental 
performance and egg comp....Ibis 120: 207-215.

Quinn, J.S. and R.D.Morris 1986. Intraclutch egg weight and chick
survival... Can. J. Zool. 64:2116-2122 

Bollinger, Bollinger and Malecki 1990. tests of three hyps of hatching 
asynchrony in the common tern the Auk 107: 696-706

Wiggins D.A. 1989 Consequences of varieation in brood size on the 
allocation of parental care... Can. J. zool. 67:2411-2413.

if you need more info than this feel free to contact me.

Les!

From owner-population-bio@net.bio.net Sun Apr 04 23:00:00 1993
Path: biosci!bcm!cs.utexas.edu!wupost!darwin.sura.net!newsserver.jvnc.net!yale.edu!news.yale.edu!YaleVM.YCC.Yale.Edu!NEIMANF
From: NEIMANF@YaleVM.YCC.Yale.Edu
Newsgroups: bionet.population-bio
Subject: Expected change under drift
Message-ID: <16BA6122C8.NEIMANF@YaleVM.YCC.Yale.Edu>
Date: 5 Apr 93 00:40:40 GMT
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Hi Folks,
 
Hope you all have the patience to point a tyro to a reference or two. I'd like
to hunt down a derivation of the amount of change (say, the squared euclidean
distance) to be expected between successive generations in a population
containing multiple (>2) alleles at a single locus, under equilibrium
conditions where drift and mutation balance each other out. The answer
is going to scale inversely with N(e), but I'd really like to see the maths by
which it is worked out.
 
Thanks very much for the help.
 
Fraser Neiman
Academic Computing User Services
Yale University

From owner-population-bio@net.bio.net Tue Apr 06 23:00:00 1993
Path: biosci!bcm!cs.utexas.edu!uunet!utcsri!newsflash.concordia.ca!mizar.cc.umanitoba.ca!etaylor
From: etaylor@ccu.umanitoba.ca (Euan R. Taylor)
Newsgroups: bionet.population-bio
Subject: Re: Questions on hatching of avian eggs.
Message-ID: <C54Kv1.BAD@ccu.umanitoba.ca>
Date: 7 Apr 93 18:04:12 GMT
References: <0096A482.45568440.19038@uamont.edu> <C4x5Mw.87I@ccu.umanitoba.ca> <1pmvcoINNjd5@shelley.u.washington.edu> <1993Apr4.214908.1@kean.ucs.mun.ca>
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In <1993Apr4.214908.1@kean.ucs.mun.ca> lhowes@kean.ucs.mun.ca writes:

>In article <1pmvcoINNjd5@shelley.u.washington.edu>, xia@hardy.u.washington.edu (Xuhua Xia) writes:
>> I should appreciate information on:
>> 
>> 1) the relationship between egg size and hatching time (the period from
>> the date when the egg is laid to the date when it hatches, or the period
>> from the beginning of incubation to the date of hatching). I am not 
>> familiar with avian literature. A citation should be very helpful.
>> 
>> 2) the cost of hatching after clutchmates.
>> 
>> Thanks in advance.
>> 
>> Xuhua
>> 

>I happen to be writing my thesis right now with some reference to that very
>topic!  

>Of course this depends on the species of bird that you are interested in. 
>I happen to be working with Common and Arctic terns, and so can give you a
>few refreences on these species. 

>In general... Larger eggs in the clutch are the eggs that are laid first.  
>They have the greatest chance at survival for several reasons, more of the 
>females resourses, the first to hatch therefore getting a head start on 
>sibs etc.... terns hatch in about 23 days or so.  First eggs often are not 
>incubated as soon as they are laid.. clutches are completed before 
>attentive incubation begins.  The cost of hatching after sibs is ofetn a 
>matter of life and death in terns which often lay 3 eggs but are lucky to 
>fledge 1 chick.  third chicks are smaller and do not recieve the continued
>incubation that they need upon hatching since parents are off foraging.  
>Also larger, older chicks out compete younger chicks for food.

I seem to rememmber form somewhere that in birds of prey where there are a
relatively small number of chicks and there is a heirarchy or competition
for parental feeding, the female although smaller than the male chicks
actually develops its motor skills much faster allowing it to compete
successfully for food.  Is that right, and if so is there a similar
situation outside of these types of species?

chers
euan
ps. I'm not an ornithologist, so sorry if this is a stupid question.

Usual disclaimers. These are my own opinions andprobably nobody else's.
etaylor@ccu.umanitoba.ca
"All great truths begin life as blasphemies"  George Bernard Shaw 



-- 
Usual disclaimers. These are my own opinions andprobably nobody else's.
etaylor@ccu.umanitoba.ca
"All great truths begin life as blasphemies"  George Bernard Shaw 

From owner-population-bio@net.bio.net Wed Apr 07 23:00:00 1993
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From: barkdoll@lepomis.psych.upenn.edu (Edwin Barkdoll)
Newsgroups: bionet.population-bio
Subject: Re: Questions on hatching of avian eggs.
Message-ID: <118899@netnews.upenn.edu>
Date: 8 Apr 93 02:38:42 GMT
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In article <C54Kv1.BAD@ccu.umanitoba.ca> etaylor@ccu.umanitoba.ca (Euan R. Taylor) writes:
>I seem to rememmber form somewhere that in birds of prey where there are a
>relatively small number of chicks and there is a heirarchy or competition
>for parental feeding, the female although smaller than the male chicks
>actually develops its motor skills much faster allowing it to compete
>successfully for food.  Is that right, and if so is there a similar
>situation outside of these types of species?

	Part of this seems to be backwards.  Female raptors tend to be
larger than the males, some dramatically larger.  Craighead and
Craighead (1956) _Hawks, Owls and Wildlife_ reported that the heavier
females could be detected by 5-6 days of age.

-- 
Edwin Barkdoll
barkdoll@lepomis.psych.upenn.edu
eb3@world.std.com

From owner-population-bio@net.bio.net Thu Apr 08 23:00:00 1993
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From: 891666t@dragon.acadiau.ca (Trish Turliuk)
Newsgroups: bionet.population-bio
Subject: FRACTAL DIMENSION ...anyone?
Message-ID: <1993Apr9.061032.4860@dragon.acadiau.ca>
Date: 9 Apr 93 06:10:32 GMT
Organization: Acadia University
Lines: 33

I'm a student of ecology and have recently become interested in fractal
geometry.  (I've done a *great* deal of reading in this past month)


I've decided to apply it in the field. 

The substrate is a mudflat in which many organisms inhabit. Organisms that
build their homes in the mud change it with their secretions and thereby
"strengthen" it. In the spring and summer, a marine invertebrate,
_Corophium volutator_ is extremely abundant.

My hypothesis is that there will be a different fractal dimension where
C.v are abundant than where they are not found.

My problem is in the logistics of the study. I assume that the d will lie
between 2 and 3 and I'm not sure exactly how to measure it. (I'm more
familiar with the 1-2 fractal measuring techniques)

Alternatively, I may focus my study on the changing distribution of the
C.v (their u-shaped tubes) over time. The literature suggests that the
distribution moves from being clumped, or patchy to uniformity at peak
densities. However, the method they use to reveal this is the
variance-to-mean ratio, which, to my understanding, would be an
inappropriate measure if dimension changes.

 Any advice would be greatly appreciated.


Trish Turliuk
trish.turliuk@acadiau.ca
Acadia University
Wolfville, Nova Scotia
Canada

From owner-population-bio@net.bio.net Thu Apr 08 23:00:00 1993
Path: biosci!bcm!cs.utexas.edu!wupost!uunet!pipex!uknet!uknet!daresbury!daresbury!news
From: Neve@ecol.ucl.ac.be (Gabriel NEVE)
Newsgroups: bionet.population-bio
Subject: Access to "Entomological Review"?
Message-ID: <1993Apr9.131238.8512@gserv1.dl.ac.uk>
Date: 9 Apr 93 13:58:02 GMT
Sender: GANEVE@be.ac.ucl.rice.Vm1
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Organization: Universite Catholique de Louvain
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Original-To: pop-bio@uk.ac.daresbury


Dear networkers,

Here is a request on the verge of our usual subject requests.
A Lithuanian colleague of mine is writing a paper using references to papers
originally published in Russian in
"Entomologicheskoye obozreniye", and he would like to join the
exact references to these papers in the English translation of this
journal, published in the USA under the name "Entomological Review".
Here are the seeked references. If any of you could find the exact references
(English titles and page numbers etc), I would be most grateful.
Unfortunately, Entomological Review is not available in any University
Library in Belgium...

1.Noreika, RV, Review of the Gracillariid moths  (Lepidoptera)
  of Turkmenia. Ent. Oboz. 1991, 70, (2), 429-443
2. Sruoga, VA, On the fauna of the Gramineal Elachistid moths (Lepidoptera,
   Elachistidae) of the USSR. Ent. Oboz., 191, 70 (2), 444-454
3. Puplesis RK, Arutyunova NV. Two new species of Nepticulid moths (
   Lepidoptera, Nepticulidae), mining apple-tree leaves, from Tajikistan.
   Ent. Oboz., 1991, 70 (3), 571-573
4. Noreika RV, Puplesis RK. Description of new species of moths of the
   family Gracillariidae (Lepidoptera) from Azerbaijan and Middle Asia
   and synonymization of Gracillaria impictipennella Grsm. Ent. Oboz.
   1992, 71 (2), 414-421
5. Sruoga VA, Puplesis RK. New species of Gramineal Elachistid moths (Lep.,
   Elachistidae) from Middle Asia and Kazakhstan. Ent. Oboz. 1992, 71 (2),
   428-441.

Thanks,
          Gabriel

"The death of the butterfly is the ine drawback to an entomological career"
                                               Margaret E. Fountaine (1892)
=======================================================================
Gabriel NEVE
Unite d'Ecologie et de Biogeographie     EMAIL: NEVE@ECOL.UCL.AC.BE
Universite catholique de Louvain            or  GANEVE@BUCLLN11.BITNET
Croix du Sud 5                           Fax  : +32/10/473490
B-1348 Louvain-la-Neuve                  Tel  : +32/10/473495
Belgium

From owner-population-bio@net.bio.net Fri Apr 09 23:00:00 1993
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From: NEIMANF@YaleVM.YCC.Yale.Edu
Newsgroups: bionet.population-bio
Subject: Re: FRACTAL DIMENSION ...anyone?
Message-ID: <16BAC5AEC.NEIMANF@YaleVM.YCC.Yale.Edu>
Date: 10 Apr 93 10:27:47 GMT
References: <1993Apr9.061032.4860@dragon.acadiau.ca>
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In article <1993Apr9.061032.4860@dragon.acadiau.ca>
891666t@dragon.acadiau.ca (Trish Turliuk) writes:
 
>
>I'm a student of ecology and have recently become interested in fractal
>geometry.  (I've done a *great* deal of reading in this past month)
>
>
>I've decided to apply it in the field.
>
>The substrate is a mudflat in which many organisms inhabit. Organisms that
>build their homes in the mud change it with their secretions and thereby
>"strengthen" it. In the spring and summer, a marine invertebrate,
>_Corophium volutator_ is extremely abundant.
>
>My hypothesis is that there will be a different fractal dimension where
>C.v are abundant than where they are not found.
>
>My problem is in the logistics of the study. I assume that the d will lie
>between 2 and 3 and I'm not sure exactly how to measure it. (I'm more
>familiar with the 1-2 fractal measuring techniques)
>
>
 
Hi,
 
This was an area I did work in a while back, but am no longer current.
So be warned!
 
One approach to this problem is to use the slope of the log-log
semivariogram (b) to estimate the fractal dimension (d):  d1(4-b)/2.
A classic article is Burrough 1983 (J. Soil Sci 34:577-597).
 
Another approach to the problem is described by Clark 1986 (Computers and
Geosciences 12:713-722).
 
I liked the semi-variogram approach because it is based on a
graphical display of autocorrelation structure, which is a helpful
exploratory tool.
 
Hope this helps a bit.
 
Best,  F.
 
-------------------------------------------------------------------------------
Fraser Neiman                          |
Academic Computing User Services       |  BITNET:   neimanf@yalevm
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From owner-population-bio@net.bio.net Wed Apr 14 23:00:00 1993
Path: biosci!daresbury!doc.ic.ac.uk!agate!spool.mu.edu!darwin.sura.net!news-feed-1.peachnet.edu!umn.edu!umeecs!zip!bagchi
From: bagchi@eecs.umich.edu (Ranjan Bagchi)
Newsgroups: bionet.population-bio,sci.fractals,sci.physics
Subject: Frequency Internment
Message-ID: <BAGCHI.93Apr14170432@quip.eecs.umich.edu>
Date: 14 Apr 93 22:04:32 GMT
Sender: news@zip.eecs.umich.edu (Mr. News)
Distribution: bionet
Organization: Recreational Creationists, Inc.
Lines: 19
Xref: biosci bionet.population-bio:417 sci.fractals:1450 sci.physics:13852


	Hi folks, 

	I'm working with a variant of the Gilpin attractor
(Lotka-Volterra eqns with logistic density dependence) where
I add in an extra oscillator.  I'm varying the properties of
the oscillator to investigate effect on the other equations.

	(Sorry, I'm being fairly imprecise.. I don't exactly
understand what I'm doing, but hopefully you get the idea.)

	Does anyone know of any references to this kind
of stuff?

	-rj

--
Ranjan Bagchi					       Ranjan.Bagchi@umich.edu
oo   oooo  o oo   ooo oo oo   oo       o o  oooo ooo o       o        oooooooo

From owner-population-bio@net.bio.net Wed Apr 14 23:00:00 1993
Path: biosci!daresbury!buzz.bmc.uu.se!corax.udac.uu.se!sunic!uunet!haven.umd.edu!darwin.sura.net!zaphod.mps.ohio-state.edu!moe.ksu.ksu.edu!ux1.cso.uiuc.edu!news.iastate.edu!iscsvax.uni.edu!yu0024
From: yu0024@iscsvax.uni.edu
Newsgroups: bionet.population-bio
Subject: I NEED HELP
Message-ID: <1993Apr14.234858.12383@iscsvax.uni.edu>
Date: 15 Apr 93 05:48:58 GMT
Organization: University of Northern Iowa
Lines: 53

I am sitting here for some hours try to start a paper, which is the requirment
for population ecology.   Without any ideal come to my mind, I think maybe it
is good ideal to post the requirment here, and hope you can disscuss your ideal
with me.

Here is the story

Disscuss one species, any species you chose, and then describe followings:

Evolution
Genetics
  Inbreeding
  Genetic disease
Physical Factors, how the species deal w/ the factors
  Temperature
  Moisture
  others (pH, atmosphere, soil, nutrition......
Habitat selection, whate and why
  Physical
  biological
Population Processes
  Birth rate
  Death Rate
  Immigration/emigration
  Total Growth rate
  Present Population size
  Cycles
Population Interactions
  Competition
  Predation
  Other (mutualism, commensalism, amensalism....
Conservation
  Habitate
  Corridors
  Transplants
  Harvest consideration
  Pest Control
Management Recommendation


For each topic, you may found tons of literature, the difficult is found all
the imformation for one species-----that's difficult

I guess Drosophila is the species to talk, since the research on this guy is
detailed.  But I am plant man, not familiar with it, the libary here is limited
So if you have any information, please e-mail me, and please tell me the
literature you cited if you do cited one.   If you think any other species is
more suitable, please let me know.

Any comments or suggestion will be greatly appreciated

Thanks advance
  

From owner-population-bio@net.bio.net Wed Apr 21 23:00:00 1993
Path: biosci!GENETICS.WASHINGTON.EDU!joe
From: joe@GENETICS.WASHINGTON.EDU (Joe Felsenstein)
Newsgroups: bionet.population-bio
Subject: SOME AVAILABLE PHYLOGENY PROGRAMS (LONG)
Message-ID: <9304222230.AA27807@evolution.genetics.washington.edu>
Date: 22 Apr 93 22:30:50 GMT
Sender: daemon@net.bio.net
Distribution: bionet
Lines: 356


                       SOME AVAILABLE PHYLOGENY PROGRAMS

     The following material (except item 0) is  from  the  PHYLIP  version  3.5
documentation.   I  post  it  because it may be a useful compilation.  Here are
some of the phylogeny packages that I know about.  Some of them  are  available
over  Internet  from  ftp  server  machines.  If you are on Internet you should
familiarize yourself with ftp and with them (see entries 6 and 7 below for more
information).
                               Table of Contents

      0. PHYLIP	             9. VOSTORG	             16. COMPROB
      1. PAUP	            10. MEGA	             17. MARKOV
      2. BIOSYS-1	    11. Evomony	             18. PHYSYS
      3. MacClade	    12. COMPONENT	     19. SINCAIDEN
      4. Hennig86	    13. Turbotree	     20. MUST
      5. ClaDOS	            14. Molevol   	     21. GDE
      6. TreeAlign	    15. CLINCH    	     22. TreeTool
      7. Clustal		

     0.  PHYLIP is a  free  package  of  programs  for  inferring  phylogenies,
including  programs  to  carry  out  parsimony, compatibility, distance matrix,
invariants ("evolutionary parsimony") and likelihood methods on  a  variety  of
different  kinds  of  data.   It is available in the recently-released versions
3.5c and 3.5p as C or Pascal source code and documentation, and in  four  forms
of  executables:  (i) for 386 and 486 systems under PCDOS, (ii) for 386 and 486
systems under Windows, (iii) for non-386 and non-486 PCDOS  systems,  and  (iv)
for  Macintosh  systems.   The  C  source code will also compile easily on most
workstations  and  mainframes  that  have  a  C  compiler.    PHYLIP  has  been
distributed  by  me  since  1980, with over 2000 registered installations.  New
features  include  programs  to  compute   protein   sequence   distances,   to
interactively  modify  a  phylogeny,  and  to compute likelihoods in coalescent
models from samples of genealogies.  Most programs in the C version  no  longer
have  arbitrary  limits  on the numbers of sites of or species.  Many other new
features have been  added  as  well,  such  as  new  models  for  variation  of
evolutionary rates among sites in the DNA likelihood programs.

     PHYLIP      is      available      by       anonymous       ftp       from
evolution.genetics.washington.edu   (IP   number   128.95.12.41)  in  directory
pub/phylip.  Users who cannot get it this way can also  send  enough  formatted
diskettes,  which  will be returned with the particular form of the package and
its documentation written on them.  Contact me (preferably by electronic  mail)
for details of the diskette distribution or further information about anonymous
ftp distribution.  The latest version of PHYLIP is  version  3.51  which  fixes
some bugs present in 3.5.

     1.  David Swofford of the Laboratory of  Molecular  Systematics,  National
Museum of Natural History, Smithsonian Instition, Washington, D.C.  has written
PAUP (Phylogenetic Analysis Using Parsimony).   It  can  be  ordered  from  the
Center  for  Biodiversity,  Illinois  Natural  History Survey, 607 East Peabody
Drive, Champaign, Illinois  61820, U.S.A.

     Since  December,  1985,  Swofford  has  been  distributing  a  precompiled
executable object-code versions of PAUP for the IBM PC and other MSDOS systems.
As of this writing (February, 1993) he has released version  3  (PAUP/Mac)  for
the  Macintosh,  and  later  hopes  to  release version 3 for PCDOS systems and
ultimately for mainframes.  The cost was $50, which will increase to $100 soon.
Orders  received  for  the  Mac  version  will  be filled but the final printed
documentation will arrive later, as it is not completed yet.

     PAUP 3.0 is probably the most sophisticated parsimony program.  It  allows
multistate  characters,  user-defined  weights on individual state transitions,
Wagner,  Camin-Sokal  and  Dollo  parsimony   methods,   bootstrap   confidence
intervals,  and  finding  all  most parsimonious trees by branch-and-bound.  It
also has provision for computing Lake's linear phylogenetic  invariants.   PAUP
is (a great) many times faster than the parsimony programs in PHYLIP.

     2. Swofford also distributes  an  older  package  of  programs,  BIOSYS-1,
including some phylogeny estimation programs, for use with gene frequency data,
with particular attention to distance methods.  BIOSYS-1 is distributed  on  an
IBM PC-formatted floppy disk.  Included are precompiled versions for the IBM PC
and source code for uploading to IBM, VAX/VMS, Unix, Prime and  CDC  mainframes
and  minicomputers.   The  price  is  $25.00,  from  the  same address as PAUP.
BIOSYS-2 is under development, but it is too early to anticipate  a  completion
date.

     3.  If you have a Macintosh computer and any  interest  in  discrete-state
parsimony  methods (including DNA and protein parsimony), you should definitely
get MacClade.  It was written by Wayne  Maddison  and  David  Maddison  of  the
University  of  Arizona.  All distribution is by Sinauer Associates, Sunderland
Massachusetts 01375, USA.  Their phone number is: (413) 665  3722,  FAX:  (413)
665  7292.   A  disk with program, help file, and example data files, plus book
(which has about 100 pages of intro to phylogenetic theory, and  250  pages  of
program  instructions),  is  $75  U.S. ($40 for the book alone).  Site licenses
also available.   An earlier and less capable  Version  2  (which  for  example
cannot  read  nucleic  acid  sequences  and  has  fewer  features  for discrete
characters) is also available by anonymous  ftp  from  the  EMBL,  Indiana  and
Houston  molecular  biology  software servers.  Their addresses are given below
under the descriptions of TreeAlign and ClustalV.  MacClade 2.1 will  be  found
among their Mac software, as a squeezed and then binhexed file.

     MacClade enables you to use the  mouse-window  interface  to  specify  and
rearrange  phylogenies by hand, and watch the number of character steps and the
distribution of states of a given character on the tree change as  you  do  so.
MacClade  is  positively addictive and will give you a much better feel for the
tree and your data.  It's the closest thing to a phylogeny video  game  that  I
have  seen.   It  has been influential in spurring the inclusion of interaction
and graphics into other phylogeny programs.   (I  have  tried  to  supply  this
functionality  in  PHYLIP  by  incorporating  the  programs  MOVE, DOLMOVE, and
DNAMOVE,  which  act  somewhat  like  MacClade).   MacClade  does  not  have  a
sophisticated  search algorithm to find best trees: it largely relies on you to
do  it  by  hand  (which  is  surprisingly  effective),  with  only   a   local
rearrangement algorithm available to improve on that tree.

     4.  J. S. Farris has produced Hennig86, a fast parsimony program including
branch-and-bound  search  for  most  parsimonious  trees  and  interactive tree
rearrangement.  Although complete benchmarks have not been published it is said
to  be faster than Swofford's PAUP; both are a great many times faster than the
parsimony programs in PHYLIP.  The program is distributed in executable  object
code  only  and  costs $50, plus $5 mailing costs ($10 outside of of the U.S.).
The user's name should be  stated,  as  copies  are  personalized  as  a  copy-
protection  measure.   It  is  distributed  by  Arnold  Kluge,  Amphibians  and
Reptiles, Museum of  Zoology,  University  of  Michigan,  Ann  Arbor,  Michigan
48109-1079,  U.S.A.  It runs on PC-compatible microcomputers with at least 512K
of RAM and needs no math coprocessor or graphics monitor.  It can handle up  to
180  taxa  and 999 characters.  An 80386 version, Hennig386, is currently being
tested but no release date has yet been announced.

     5. ClaDOS, an interactive program which allows rearrangement of trees  and
their  evaluation,  mapping of characters into them, and more, is available for
PCDOS systems from Kevin Nixon, L. H. Bailey Hortorium, Cornell University, 467
Mann  Library,  Ithaca, New York  14853.  I have been unable to get information
on its cost or method of distribution.

     6. Jotun Hein, (Institute of Genetics and Ecology, University  of  Aarhus,
8000  Aarhus  C, Denmark) has produced TreeAlign, a multiple sequence alignment
program that builds trees as it aligns DNA or protein  sequences.   It  uses  a
combination  of  distance  matrix and approximate parsimony methods.  TreeAlign
uses too much memory for it to run on PC's (DOS or Mac systems) but  is  really
designed  for  a workstation or mainframe.  It is available by anonymous ftp at
the Indiana, Houston, and EMBL molecular biology software  distribution  sites.
Their    network    addresses    are    respectively:      ftp.bio.indiana.edu,
ftp.bchs.uh.edu, and ftp.embl-heidelberg.de.  In the Indiana archive  one  must
enter  dir
From owner-population-bio@net.bio.net Thu Apr 22 23:00:00 1993
Path: biosci!bcm!cs.utexas.edu!swrinde!zaphod.mps.ohio-state.edu!howland.reston.ans.net!darwin.sura.net!welchgate.welch.jhu.edu!danj
From: danj@welchgate.welch.jhu.edu (Dan Jacobson)
Newsgroups: bionet.general,bionet.population-bio,bionet.molbio.gene-linkage
Subject: Bibliography of Theoretical Population Genetics by gopher
Message-ID: <1993Apr23.164056.2248@welchgate.welch.jhu.edu>
Date: 23 Apr 93 16:40:56 GMT
Organization: Johns Hopkins Univ. Welch Medical Library
Lines: 49
Xref: biosci bionet.general:4671 bionet.population-bio:420 bionet.molbio.gene-linkage:182



The Bibliography of Theoretical Population Genetics by Joseph Felsenstein
is now available by gopher.  Just point your gopher client at 
merlot.welch.jhu.edu and select the following:


 -->  12. Search Databases at Welchlab (Vectors, Promoters, NRL-3D, EST, OMI../

     -->  13. Search the Bibliography of Theoretical Population Genetics <?>

You may search this database using booleans (and, or, not), phrase
searches ("     ") and wildcards (*).
                                      
A typical entry s as follows:

----------

Franklin, I.  and M. W. Feldman
Two loci with two alleles: linkage equilibrium and linkage disequilibrium can 
be simultaneously stable
Theoretical Population Biology  12: 95-113  1977

----------


All contents of this bibliography (c) Copyright 1988 by 
Joseph Felsenstein.  This bibliography covers the years 1867-1981.

You can reach the author at the following addresses:

Electronic mail addresses:                     Joe Felsenstein
 Internet: joe@genetics.washington.edu         Department of Genetics SK-50
 Bitnet:  felsenst@uwavm                       University of Washington
phone: (206)-543-0150                          Seattle, WA  98195
fax:   (206)-543-0754


If you've never heard of gopher don't worry it's free and on the net,
just write me a note if you'd like information on how to get started.


Happy Searching,

Dan Jacobson

danj@welchgate.welch.jhu.edu

Johns Hopkins University

From owner-population-bio@net.bio.net Tue Apr 27 23:00:00 1993
Path: biosci!enterpoop.mit.edu!gatech!howland.reston.ans.net!zaphod.mps.ohio-state.edu!caen!kuhub.cc.ukans.edu!jimdb
From: jimdb@kuhub.cc.ukans.edu
Newsgroups: bionet.biology.tropical,bionet.population-bio,bionet.general,bionet.jobs,bionet.sci-resources,sci.bio,sci.environment,sci.research,talk.environment
Subject: Field Assistants Needed For Summer Pronghorn Antelope Study
Message-ID: <1993Apr28.000150.49566@kuhub.cc.ukans.edu>
Date: 28 Apr 93 06:01:50 GMT
Organization: University of Kansas Academic Computing Services
Lines: 33
Xref: biosci bionet.biology.tropical:202 bionet.population-bio:421 bionet.general:4711 bionet.jobs:1745 bionet.sci-resources:723 sci.bio:3085 sci.environment:5896 sci.research:735 talk.environment:3551

>>I am posting this for a friend, please reply to him directly<<
 
Field assistants are needed in the summer (June-August) and the 
fall (September-November) to help in a long-term study of the
behavior and ecology of pronghorn antelope in Colorado.  Any
students interested in behavior and evolution are welcome to apply. 
Primary duties include behavioral observations and videotaping of
focal bucks, and vegetational sampling of territories.  Basic
observational equipment (binoculars, spotting scope) and patience
are required.  Housing will be provided and additinal funds are
pending.  To apply, please send a letter describing your
qualifications and interests, and the names, addresses and phone
numbers of two references to one of the following addreses:
 
Before 15 May 1993:
Sherwick Min
Department of Systematics and Ecology
University of Kansas
Lawrence, KS   66045-2106
email:    MIN@UKANVM
 
After 15 May 1993:
P.O. Box 144
Kremmling, CO  80459
 
 
Thanks for your interest.

-- 
----------------------------------------------------------------------
Jim Danoff-Burg     (Snow Museum, Univ. of Kansas, Lawrence, KS 66045)
Bitnet: JIMDB@UKANVAX                Internet:jimdb@kuhub.cc.ukans.edu
"Myrmecophiles-R-Us"

From owner-population-bio@net.bio.net Thu Apr 29 23:00:00 1993
Path: biosci!daresbury!buzz.bmc.uu.se!corax.udac.uu.se!sunic!pipex!uknet!mcsun!Germany.EU.net!gmd.de!newsserver.jvnc.net!news.cac.psu.edu!howland.reston.ans.net!gatech!usenet.ufl.edu!gnv.ifas.ufl.edu!jma
From: jma@gnv.ifas.ufl.edu (JULIO M. ARIAS (813)956-1151 X 302)
Newsgroups: bionet.population-bio
Subject: Ecology and Environ. conf. -  Call for papers
Message-ID: <1993Apr29.155157.2374@gnv.ifas.ufl.edu>
Date: 29 Apr 93 20:51:57 GMT
Lines: 140

Sent to:
ECOLOG-L@UMDD
CONSLINK@SIVM
OTS-L@YALEVM
ECOSYS-L@DEARN
ENTOMOL@UGUELPH
biodiv-l@bdt.ftpt.br

	Dear netters:
		Please spread this out, apologies to those who sign in
more than one of this mailing lists.

Julio M. Arias
University of Florida
Department of Entomology

----------------------------

I have received a request from Costa Rica to publicize the enclosed call
for contributions, and I would be very grateful if you could help in this
regard.
 
With best regards,
 
Ignacio Trejos
Programming Research Group, Oxford University
 
---
INTERNATIONAL CONFERENCE ON ECOLOGY AND ENVIRONMENT
 
Drake Bay, PenInsula de Osa, Costa Rica
 
June  20-24th,  1994  (Indian Summer)
 
CALL FOR PAPERS
 
1.  La FundaciOn para la ProtecciOn del Bosque Primario
(FUNBOSPRI)  (Foundation for Primary Forest Protection)  Id.
3-006-115104-17 is calling for papers to specialists,
organizations and people interested in ecology and
environment and related fields.
 
The goal of the conference is to share experiences,  to get
perspectives and to discuss problems related with ecology
and environment and to join individuals and institutions
interested in this topic.   It is also to give the
opportunity to enjoy some of the most beautiful places of
our country and discuss about the ecological problems of the
area in order to propose a solution.   In this respect, I
would like to submit for your consideration, by the first
week of may, a list of problems we are facing and the
context in which they arose.   We hope  we will get a better
perspective to face our problems with your contributions.
 
2. Location of the conference.   For us it was difficult to
decide where this conference would take place.  The final
decision was "Peninsula de Osa".  This decision was
supported by arguments like this: Although there are cheaper
- and even more confortable- places in our country, it is
better to pay  a little extra cost and  give the opportunity
to enjoy  the natural riches of Peninsula de Osa, its
biological varieties - unique of the region-, and its
refreshing sights.
 
Peninsula de Osa is located 350 kms south of the
international airport.  It is one of the most beautiful
places of Costa Rica and one of the most appreciated regions
internationally. There are two ways of transportation: by
air and by  a combination of  land and river. We suggest  to
travel by land. The travel can be divided into two parts:
the first from San Jose to Sierpe and the other from
Sierpe to Drake Bay. The people who have visited this
region were stroken by these sights. This second part of the
travel is particularly exciting: navegating by Rio Sierpe
appreciating beautiful places, multicolor sand, clear water,
marshes at both sides of the river and other attractions.
This event will give you the opportunity of knowing these
places and seeing one of the locations that deserve
conservation and care.  The conference will take place
during five days.  Two trips are planned during the
conference: the first to Isla de CaNo, one of the most
exciting places, and the second to the Corcovado's National
Park, characterized by the primary forest and exotic
biological varieties.  The conference schedule is planned so
that it allows people to travel during the week.
 
3.  Main topics:
 
The main topics considered at the conference are the
following:
   Ecological Experiences
   Models for Development and Planning
   Pacific uses of Nuclear Energy and Environment
   Quality  Control and Environment
   Conservation and Management
   Community and Ecology
   Ecology and Education
   Native Cultures and Ecology
 
Related topics can be considered.
 
4. Deadlines:
 
Abstracts:  December 15th, 1993. Summaries no longer than 200
words.
Acceptance notification:   february 1994.
Papers:  April 15th,  1994
Conference's schedule availabe by:  early  May  1994.
 
5. Expenses:   $1,200.  Including  accomodations, meals, and
trips during the event; a copy of the proceedings and
transportation from the airport to peninsula and back.  If
you want to enjoy the beauties of the peninsula after or
before the event,  extra costs must be covered.    The
available kind of food  includes: 100 % natural vegetables
and fruits, meats and fish.   For washing,  cleaning  and
shower we use only biodegradable products.
 
6. Information:
 
We have pictures and more detailed information about the
region.  If you need any further information related with
the event or mailing documents, please write:
 
Celso Vargas
Departamento de ComputaciOn
ITCR, Aptdo 159, Cartago, Costa Rica
FAX (506) 51 53 48
email:  vargase@bitnet.ucrvm2 or vargase@earn.ucrvm2
or
Apartado 7137-1000 San JosE, Costa Rica.
 
JosE Castro
Apartado 7137-1000 San JosE, Costa Rica.
 
7. Executive committee
     Celso Vargas
     Elizabeth ArnAez
     JosE Antonio Vargas
     JosE Castro

