From daemon  Mon Feb  2 12:28:03 1998
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To: annelida@net.bio.net
From: "Peter Olive" <p.j.w.olive@ncl.ac.uk>
Reply-To: annelida@net.bio.net
Date:          Mon, 2 Feb 1998 14:13:33 +0000
Subject:       Re: Nereis - nomenclature

Erik  Kristensen

writes to Annelida about the use of subgenus names for Nereids.

I look forward to seeing the reply from those expert in such matters. I
have (for fear of doing the wrong thing) been writing about Nereis
(Neanthes) virens and Nereis (Hediste) diversicolor  and Nereis (Nereis)
pelagica - but I would much rather stick to Nereis.  The literature from
the New world seems to favour the use of Neanthes. 

I shall be glad to know what is considered the correct form of address for
these worms.

Peter Olive
<p.j.w.olive@ncl.ac.uk>

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From daemon  Tue Feb  3 07:19:15 1998
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To: annelida@net.bio.net
Date:          Tue, 03 Feb 1998 09:49:26 +0000
Reply-To: annelida@net.bio.net
From: "Dr M.G. Bentley" <mgb@st-and.ac.uk>
Subject:       Nereis nomenclature

I too should be glad for some guidance on the current accepted (correct)
usage of Nereis (Neanthes) virens and Nereis (Hediste) diversicolor. I
notice that much of the Environment Agency, SEPA, JNCC, SNH, literature
here in Britain use Hediste diversicolor routinely.

Any help would be most welcome.

Matt Bentley

******************************************************************
Dr M.G. Bentley
Marine Invertebrate Reproduction Group
Gatty Marine Laboratory
School of Environmental and Evolutionary Biology
University of St Andrews
St Andrews KY16 8LB
Scotland UK
 
Tel: +44 1334 463444
Fax: +44 1334 463443
e-mail: mgb@st-andrews.ac.uk
********************************************************************

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From daemon  Tue Feb  3 17:54:42 1998
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To: annelida@net.bio.net
Date:          Tue, 3 Feb 1998 20:19:41 -0500
Reply-To: annelida@net.bio.net
From: judy A Fournier <110275.1004@compuserve.com>
Subject:       Euphrosinidae - Feeding Guild?

Dear Annelidans,

Could someone tell me what feeding guild the Euphrosinidae should be
referred to?  I am posting this on behalf of a colleague who suspects
"subsurface deposit feeder" would be close.  I tend to agree about
"deposit feeder" but do not know if they are surface or subsurface.  We
are looking mainly at arctic species.

        Any help would be greatly appreciated.

        Judy Fournier
<110275.1004@compuserve.com>

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From daemon  Tue Feb  3 18:33:31 1998
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To: annelida@net.bio.net
Date:          Tue, 3 Feb 1998 12:18:12 -0500 (EST)
Reply-To: annelida@net.bio.net
From: Aaron Bartholomew <bart@vims.edu>
Subject:       Re: Nereis nomenclature

Ditto on the nomenclature issue, I'm not sure whether to use Neanthes or
Nereis for species I identify either. -Thanks

On Tue, 3 Feb 1998, Dr M.G. Bentley wrote:

> I too should be glad for some guidance on the current accepted (correct)
> usage of Nereis (Neanthes) virens and Nereis (Hediste) diversicolor. I
> notice that much of the Environment Agency, SEPA, JNCC, SNH, literature
> here in Britain use Hediste diversicolor routinely.

Aaron Bartholomew <bart@vims.edu>
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From daemon  Tue Feb  3 23:38:34 1998
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To: annelida@net.bio.net
From: "Helmut Zibrowius" <hzibrowi@com.univ-mrs.fr>
Reply-To: annelida@net.bio.net
Date:          Wed, 4 Feb 98 07:33:36 MST
Subject:       Re: Euphrosinidae - Feeding Guild?

On Tue, 3 Feb 1998 20:19:41 -0500, judy A Fournier wrote:

>Could someone tell me what feeding guild the Euphrosinidae should be
>referred to? I am posting this on behalf of a colleague who suspects
>"subsurface deposit feeder" would be close. I tend to agree about
>"deposit feeder" but do not know if they are surface or subsurface. We
>are looking mainly at arctic species.

   Considering their tentacle crown and easily observable behaviour, there
may be little doubt on the general way Serpulids feed (the only family I
am somewhat familiar with). In other cases I often wonder if it is
reasonable that whole families are appointed members of that or that
feeding guild. For example because mouthparts of just one species had
been considered good for predating, or because some ancient author had
thought they could do this or that. Surely, it is very convenient to rely
to once for ever decided rigid categories ....

   Could someone tell me what feeding guild the Darwin Finches should be
referred to?

  ----------------------------------- 
  Helmut ZIBROWIUS
  (Centre d'Oceanologie de Marseille)
  Station Marine d'Endoume
  Rue Batterie des Lions
  13007 Marseille / France
  E-MAIL:  hzibrowi@com.univ-mrs.fr
  TEL: within France  0491041624  from abroad +33 491041624
  FAX: within France  0491041635  from abroad +33 491041635  
  ---------------------------------------------------------


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From daemon  Wed Feb  4 01:25:36 1998
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To: annelida@net.bio.net
Date:          Wed, 4 Feb 1998 00:39:01 -0800
Reply-To: annelida@net.bio.net
From: "Derek C. Moore" <mooredc@marlab.ac.uk>
Subject:       Nereis, Neanthes, Hediste

In reply to Matt Bentley's comment on the EA, SEPA, JNCC and SNH in the
UK using Hediste diversicolor routinely, this is because UK benthic
ecologists have agreed (in general) to employ the nomenclature contained
in the so-called MCS Species Directory, which has recently emerged as a
second edition.

In this new edition the annelid section, admirably compiled by Andy
Mackie, gives full genus status to Hediste and Neanthes but clearly states
the synonomy with Nereis recognised by Chambers and Garwood (1992).

Regards

Derek C Moore

--------------------------------------------------------------------------   
Derek C Moore, Senior Scientific Officer       LAB TEL (44)(0)1224 876544    
Environmental Protection Section (EPS)         DIR TEL (44)(0)1224 295441*   
Fisheries Research Services                    LAB FAX (44)(0)1224 295511    
Marine Laboratory, Aberdeen                    EPS FAX (44)(0)1224 295524*   
PO Box 101, Victoria Rd                        EMAIL MOOREDC@MARLAB.AC.UK    
Aberdeen AB11 9DB, UK                            http://www.marlab.ac.uk  
--------------------------------------------------------------------------   

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From daemon  Wed Feb  4 07:30:30 1998
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To: annelida@net.bio.net
Date:          Wed, 4 Feb 1998 05:44:50 -0800
Reply-To: annelida@net.bio.net
From: "Derek C. Moore" <mooredc@marlab.ac.uk>
Subject:       Apologies to Christer Erseus!

Dear All,

I should have made clear that Prof. Christer Erseus co-authored the
chapter on Annelids with Andy Mackie ...  my apologies for this omission,


Regards

Derek C Moore

--------------------------------------------------------------------------   
Derek C Moore, Senior Scientific Officer       LAB TEL (44)(0)1224 876544    
Environmental Protection Section (EPS)         DIR TEL (44)(0)1224 295441*   
Fisheries Research Services                    LAB FAX (44)(0)1224 295511    
Marine Laboratory, Aberdeen                    EPS FAX (44)(0)1224 295524*   
PO Box 101, Victoria Rd                        EMAIL MOOREDC@MARLAB.AC.UK    
Aberdeen AB11 9DB, UK                            http://www.marlab.ac.uk  
--------------------------------------------------------------------------   

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From daemon  Wed Feb  4 14:12:50 1998
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To: annelida@net.bio.net
Date:          Wed, 4 Feb 1998 10:13:21 -0800 (PST)
Reply-To: annelida@net.bio.net
From: Marine Biology Laboratory <mblcsdla@netcom.com>
Subject:       Re: Nereis, Neanthes, Hediste


I have just seen the posting by Derek Moore on the Neanthes name issue and
wonder if the MCS Species Directory he referred to is available for
distribution?  Is it available electronically?  How could I get the
directory?

Thanks for any assistance

bye for now

Thomas Parker
mblcsdla@netcom.com

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From daemon  Wed Feb  4 14:18:50 1998
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To: annelida@net.bio.net
From: "Geoff Read" <g.read@niwa.cri.nz>
Reply-To: annelida@net.bio.net
Organization:  NIWA (Nat. Inst. Water & Atmos. Research)
Date:          Thu, 5 Feb 1998 11:08:53 +1100
Subject:       Re: Nereis, Neanthes, Hediste

> I have just seen the posting by Derek Moore on the Neanthes name issue
> and wonder if the MCS Species Directory he referred to is available for
> distribution?  Is it available electronically?  

At a guess no. The Mackie/Erseus annelid list WAS available electronically
but withdrawn. A link to this page has been on Annelida resources for a
long time (hoping it would come back). It would be nice if it could be made
available somehow as the whole book is rather expensive.

>How could I get the directory?

A bit of ferreting around Bernard Picton's pages revealed:

http://www2.tcd.ie/People/Bernard.Picton/species/index.html

"The Species Directory of the marine fauna and flora of the British Isles
and surrounding seas." Howson, C.M. & Picton, B. E. (Eds.) 508 pages Ulster
Museum and Marine Conservation Society, Belfast and Ross-on-Wye. ISBN 0
94815006 8

Available from: 
The Marine Conservation Society, 9 Gloucester Road, Ross-on-Wye,
Herefordshire, HR9 5BU, England, UK Telephone: Int + 44 1989 566017 or UK:
01989 566017 Price 53 pounds sterling plus post and packing. 

--
  Geoff Read <g.read@niwa.cri.nz>

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From daemon  Wed Feb  4 21:33:52 1998
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To: annelida@net.bio.net
From: "Geoff Read" <g.read@niwa.cri.nz>
Reply-To: annelida@net.bio.net
Organization:  NIWA (Nat. Inst. Water & Atmos. Research)
Date:          Thu, 5 Feb 1998 18:16:58 +1100
Subject:       Libbie Hyman

Hi folks,

A snippet of info:

By chance today I came across a web'ised (not elegant  but no matter) short
autobiography  of Libbie Hyman of fame through "The invertebrates"
multi-volume treatise. I recommend it to you all as a worthwhile read when
you have a free moment to look. It is rather a surprise, and sad that her
personal life was so difficult.

Also surprising to me is  that her doctoral thesis was "An Analysis of the
Process of Regeneration in Certain Microdrilous Oligochaetes".  I knew she
had done a handful of  papers impinging on annelids.

http://www.ul.cs.cmu.edu/books/biographical_memoirs/bio108.htm

Deceased 1969. Now which of you own up to meeting her?   :-)

Geoff
--
  Geoff Read <g.read@niwa.cri.nz>


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From daemon  Thu Feb  5 12:56:57 1998
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To: annelida@net.bio.net
From: DanauSakai@aol.com
Reply-To: annelida@net.bio.net
Date:          Thu, 5 Feb 1998 12:42:39 EST
Subject:       Re: Libbie Hyman

Thanks for the website.  You mentioned her difficult personal life.  To flip
the coin, what is amazing is that those of us (myself included) with an easy
personal life have accomplished so little by comparison.

You failed to mention the author, G. Evelyn Hutchinson, considered the
grandfather of ecology in the U.S.  Many (most?) ecologists in major
universities of the U.S. can trace their lineage back to Hutchinson.

Last, as a graduate student in the early 70's visiting Friday Harbor Labs
of the University of Washington, the staff pointed out an old abandoned
building outside of the town of Friday Harbor hanging over the waters. 
They told us that this was Libbie Hyman's lab and how she would simply
drop a bucket over the edge into the waters to get samples to look at
specimens for her treatises.  I wonder if it still there?

Walt

Walter H. Sakai                              "MIGRATE WITH THE MONARCHS"
Professor of Biology         
Santa Monica College                   Research Associate, Entomology Section
1900 Pico Blvd                             Los Angeles Co. Museum of Natural
History
Santa Monica, CA 90405-1268
Tele:  (310)450-5150 X9702           FAX: (310)581-8624     
Emails:  sakai_walter@smc.edu; DanauSakai@aol.com
Master Bird Banding Permit No. 22030

"The best way to learn something is to teach it."

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From daemon  Thu Feb  5 13:07:02 1998
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To: annelida@net.bio.net
Date:          Thu, 05 Feb 1998 20:22:46 +0000
Reply-To: annelida@net.bio.net
From: Pei_Yuan Qian <boqianpy@usthk.ust.hk>
Subject:       Professor Wu Baoling


Dear Friends and fellow polychaete scientists,

Grievously inform you that Prof. Wu Baoling passed away at 2:45 this
morning (Feb 5,1998).   I will fly back to Qingdao to attend his funeral
and to be with his family.   Professor Wu has been the best polychaete
scientist in China and contributed a great deal to the marine science
research in this region.  He has also promoted international exchange
programs between China and the rest of the world.  It is too sad and too
difficult for me to express my deep sorrow at this moment.   I think that
many friends may share the same feeling as I do.    

The obituary and member of his funeral office has been formed. His
funeral will be held at 10:00 of Jan 9, 1998 at Qingdao Funeral Parlor. 
For those of you who want to pay your sympathy to his family, please send
your message through fax at 86-532-2867468.

Pei-Yuan Qian
Associate Professor in Biology
Hong Kong University of Science and Technology
Clear Water Bay, Hong Kong
Tel: 0852-2358-7331/7336/7337
Fax: 0852-2358-1559
<boqianpy@usthk.ust.hk>


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From daemon  Thu Feb  5 14:18:28 1998
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To: annelida@net.bio.net
Date:          Thu, 05 Feb 1998 13:25:37 -0800
Reply-To: annelida@net.bio.net
From: Kirk Fitzhugh <fitzhugh@almaak.usc.edu>
Subject:       Thailand contact


Dear Annelidans:

Does any one know a person to contact in Thailand working on freshwater
invertebrates, especially snails? Greg Rouse and I are trying to obtain
travel funds to collect the sabellid _Caobangia_ from northern Thailand.
It would be appropriate to work in collaboration with specialists in that
country.

Any suggestions would be greatly appreciated.

Thanks much,

Kirk Fitzhugh
<fitzhugh@almaak.usc.edu>


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From daemon  Sun Feb  8 13:56:01 1998
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To: annelida@net.bio.net
From: Jacques.Grall@univ-brest.fr
Reply-To: annelida@net.bio.net
Date:          Fri, 6 Feb 1998 12:16:35 +0100 (MET)
Subject:     Chemo-autotrophy

Message from Pr M. GLEMAREC

Dear Annelidans, 

I am wondering if any capitellid species is able to perform
Chemo-autotrophy when living inside anoxic sediments ? Does anyone of you
have any references on that subject? Thanks in advance. M. GLEMAREC

Please reply to Jacques.Grall@univ-brest.fr
---------------------------------------------------
Jacques GRALL
UMR CNRS 6539- Ecologie Benthique-
Institut Universitaire Europeen de la Mer
Place Copernic 29280 PLOUZANE  France
Tel : 33 (0)2 98 49 86 77
Fax : 33 (0)2 98 49 86 45

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From daemon  Sun Feb  8 21:03:13 1998
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To: annelida@net.bio.net
From: "Geoff Read" <g.read@niwa.cri.nz>
Reply-To: annelida@net.bio.net
Organization:  NIWA (Nat. Inst. Water & Atmos. Research)
Date:          Mon, 9 Feb 1998 17:48:44 +1100
Subject:       Re: Nereis - nomenclature

Erik Kristensen wrote:

> ... However, I am a
> little frustrated about the increasing number of papers using new genus
> names for nereids, e.g. Hediste diversicolor instead of Nereis
> diversicolor and Neanthes virens instead of Nereis virens.

Hardly new - Hediste is 1867, Neanthes is 1866.  They are ancient and
venerable, if rather flimsily defined. Neanthes has probably been in
continuous use since, and Hediste has undergone a revival over some years
now.   Biologists can use them  at the level they wish without fear of
censure either way. It's not important.

But please, when you really want to say "We prefer Hediste here, others may
call it Nereis diversicolor," DO NOT  make Nereis apparently a subgenus of
Hediste as in the bizarre formation 'Hediste (Nereis) diversicolor'
(examplars: the 4th Conference vol. abstracts p.623,  p631, p638).

--
  Geoff Read <g.read@niwa.cri.nz>


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From daemon  Mon Feb  9 13:00:25 1998
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To: annelida@net.bio.net
Date:          Mon, 09 Feb 1998 19:09:18 +0100
Reply-To: annelida@net.bio.net
From: "Helmut Goerke" <hgoerke@awi-bremerhaven.de>
Organization:  AWI
Subject:       Re: Nereis - nomenclature

In my view, Hediste, Neanthes and Nereis are subgenera of the genus Nereis
LINNE, 1758. The common characteristics outweigh the small differences in
the arrangement of setae by far. 
Subgenus Nereis has homogomph spinigers and homogomph falcigers in the
middle and posterior notopods. 
Subgenus Neanthes has only homogomph spinigers in the notopods.
Subgenus Hediste also has only homogomph spinigers in the notopods and one
homogomph falciger above the acicula in the middle and posterior neuropods
additionally. Shaft and apical element of this seta can be more or less
fused. 
In my opinion Eunereis also belongs as subgenus to Nereis. Eunereis has
also homogomph falcigers in middle and posterior notopods as the subgenus
Nereis has. Subgenus Eunereis differs from the other subgenera by the weak
development of the paragnaths (they are very small and less numerous) in
the maxillar ring of the proboscis; occasionally they are even absent
there.

All these differences are distinct, but they are small in comparison with
the many common Nereis characteristics. This is why the nomenclature
exemplified by Nereis (Hediste) diversicolor, Nereis (Neanthes) virens and
Nereis (Nereis) pelagica should be retained.

Gesa Hartmann-Schroeder

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

Since Dr. Gesa Hartmann-Schroeder has no access to "Annelida", I am
communicating her response to Erik Kristensen's inquiry. I shall send any
further notes on this topic by surface mail to her. 

The 2nd. revised edition of Annelida, Borstenwuermer, Polychaeta by Gesa
Hartmann-Schroeder, Part 58 of Die Tierwelt Deutschlands und der
angrenzenden Meeresteile nach ihren Merkmalen und nach ihrer Lebensweise,
Gustav Fischer Verlag, Jena, appeared in 1996. ISBN 3-437-35038-2.

Helmut Goerke
Alfred-Wegener-Institut fuer Polar- und Meeresforschung
D-27515 Bremerhaven, Germany
hgoerke@awi-bremerhaven.de

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From daemon  Mon Feb  9 14:03:04 1998
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To: annelida@net.bio.net
Date:          Mon, 09 Feb 1998 13:36:08 -0800
Reply-To: annelida@net.bio.net
From: Kirk Fitzhugh <fitzhugh@almaak.usc.edu>
Subject:       Re: Nereis - nomenclature

We seem to be missing the mark in these discussions on Hediste, Neanthes, &
Nereis. If we are to assume that our use of names is to reflect the reality
that surrounds us then we must provide reasons that substantiate our
interpretations of reality. The only way to settle the matter of which
genera to use is to present data showing each to be monophyletic, unless
one wishes to claim monophyly an unnecessary consideration. Taking the
latter position would be unfortunate since reality is no longer a concern -
which takes the process outside the realm of science. Once one recognizes
which nereidid genera are not monophyletic, there is a fairly clear sense
of the revisionary work needed. I havn't seen even this first step taken
yet.

Kirk Fitzhugh

------------------------------------------  
Kirk Fitzhugh, Ph.D.
Associate Curator of Polychaetes
Research & Collections Branch
Los Angeles County Museum of Natural History
900 Exposition Blvd
Los Angeles CA 90007
Phone:   213-763-3233
FAX:     213-746-2999
e-mail:  fitzhugh@bcf.usc.edu
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From daemon  Mon Feb  9 16:55:17 1998
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To: annelida@net.bio.net
From: "Wilson, Robin" <RWILSON@mov.vic.gov.au>
Reply-To: annelida@net.bio.net
Subject:       Re: Nereis - nomenclature
Date:          Tue, 10 Feb 1998 11:21:13 +1000


> We seem to be missing the mark in these discussions on Hediste,
> Neanthes, & Nereis. ...
> Once one recognizes which nereidid genera are not monophyletic, there
> is a fairly clear sense of the revisionary work needed. I havn't seen
> even this first step taken yet.
> 
> Kirk Fitzhugh

Kirk is right, the issue is monophyly of these generic combinations.
But I am embarassed to have to admit (after remaining silent on this
subject for a week!)  that the first step HAS been taken, but only as an
unpublished part of my PhD thesis.  I have held back from publication
because my cladistic analysis gave weak support for several of these genera
and strongly indicated that some, like Neanthes s.s., are paraphyletic, or
maybe even polyphyletic.  I have been unwilling to propose new generic
definitions until I had independent supporting data. But not many authors
are so reticent with their taxonomies, and many have pushed me to get this
out so that at least there is something more concrete to argue about, so I
will have to get busy ...

In the meantime, for practical purposes, it is more or less as Gesa
Hartmann-Schroder (and Fauchald 1977!) said: Hediste are those taxa with
paragnaths on oral and maxillary rings and fused neuropodial falcigers
posteriorly; Nereis are those with notopodial homogomph falcigers; and
"Neanthes" are the rest (!).  But I must disagree with Gesa's comment on
common characteristics.  Similarities (character states) shared by these 3
taxa are also shared by several other nereidid genera,  and it seems to me
that these 3 are no more closely related than they are to several other
valid genera.  It is unimportant and arbitrary whether one refers to these
combinations as genera or subgenera, but from my comments you will guess
that I strongly favour elevating all subgenera to genus status.

I am sorry I can not direct interested persons to a paper (yet).

bye

Robin

 Robin Wilson			
 Museum of Victoria
 71 Victoria Crescent
 Abbotsford  3067
 Australia  
 telephone (61) 3 9284 0216; fax (61) 3 9416 0475 
 rwilson@mov.vic.gov.au
 Polychaetes of Australia URL http://www.mov.vic.gov.au/poly

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From daemon  Mon Feb  9 17:53:18 1998
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To: annelida@net.bio.net
Date:          Mon, 9 Feb 1998 20:06:57 -0500
Reply-To: annelida@net.bio.net
From: judy A Fournier <110275.1004@compuserve.com>
Subject:       Re: Nereis - nomenclature

Dr. Hartmann-Schroeder's response is typical of the opinion of those who
look at the keys and the literature but misses the point.  A careful
examination of the type specimens of these three genera will show that
they differ significantly in the structure of the parapodia, particularly
the presence and form of the pre-, post, and acicular lamellae found in
Neanthes.  These differences far outweigh the differences in setae and
paragnaths.

I agree with with Kirk that substantial revision of the Nereididae is
overdue.  We must take a long, careful look at these worms to determine
their true relationships.  Based on the structure of parapodial lamellae,
Neanthes is quite removed from Nereis.

Judith A. Fournier
<110275.1004@compuserve.com>

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From daemon  Tue Feb 10 12:40:59 1998
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To: annelida@net.bio.net
Date:          Tue, 10 Feb 1998 11:15:28 -0800
Reply-To: annelida@net.bio.net
From: Kirk Fitzhugh <fitzhugh@almaak.usc.edu>
Subject:       Re: Nereis - nomenclature

I'm thrilled to hear that Robin Wilson has a cladistic analysis just
waiting to be published. Robin, don't hold off on this. The whole point of
publishing such an analysis is to get people thinking and talking about
these issues. It should come as little surprise to many that Neanthes
could be paraphyletic. Keep in mind as well that cladistic analyses don't
carry with them the requirement that taxonomic revisions be performed.
The analysis provides illumination for us all as to what problem areas
need to be addressed regardless of whether one revises a group or not. For
example, I have two papers coming out this year on cladistic
relationships among fabriciin sabellid genera. Among the thousands of
trees I looked at, there are many topologies with some major genera as
para- or polyphyletic. I'm certainly not going to sink a whole bunch of
genera right now from these analyses because I suspect much of the problem
is the rapid increase in species discovered and the small number of
characters I have. What I think is more important at this time is to make
accessible the data that are available. 

Good luck Robin.

Kirk Fitzhugh

------------------------------------------  
Kirk Fitzhugh, Ph.D.
Associate Curator of Polychaetes
Research & Collections Branch
Los Angeles County Museum of Natural History
900 Exposition Blvd
Los Angeles CA 90007
Phone:   213-763-3233
FAX:     213-746-2999
e-mail:  fitzhugh@bcf.usc.edu
------------------------------------------

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From daemon  Tue Feb 10 12:41:00 1998
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To: annelida@net.bio.net
Reply-To: annelida@net.bio.net
From: Torleif Holthe <vmzothol@vm.ntnu.no>
Subject:       Accents in "JELDES & LEFEVERE"
Date:          Tue, 10 Feb 1998 14:06:04 +0100

The paper by Jeldes & Lefevere (1959) with i.a. the description of
Amphicteis pennata has been a tricky one to quote correctly. I've got a
copy of the original paper where the authors' names are printed in
capitals. Olga Hartman (appendix to the catalogue) used plain lower case,
but I do wonder: should there be any accents in those names? 

Torleif Holthe
Museum of Natural History and Archaeology
NTNU
Trondheim, Norway
<vmzothol@vm.ntnu.no>


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From daemon  Tue Feb 10 13:48:08 1998
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To: annelida@net.bio.net
Date:          Tue, 10 Feb 1998 16:17:36 -0500
Reply-To: annelida@net.bio.net
From: Kristian Fauchald <FAUCHALD.KRISTIAN@nmnh.si.edu>
Subject:       Re: Nereis - nomenclature -Reply

I had not really planned to get involved in this debate:  To a certain
extent I made my opinion rather clear already in 1977 in the Key. 
However, I believe there are some important points that must be considered
here.

There are two distinct problems; one is strictly taxonomic and has to do
with the names only; the other has to do with biology and the information
content in the use of a given name.  

The Code lumps the "sub" categories with their respective main category:
subspecies with species, subgenera with genera and subfamilies with
families.  It talks about them as species-level, generic-level and
family-level taxa.  The rules for each is then specified. Thus for
taxonomic purposes it is simpler to avoid the use of the sub-categories
and very little is gained by using them in a taxonomic sense, except
making the names longer and more likely to be mis-spelled or mis-used.  As
pointed out by Geoff Read, the formulation Hediste (Nereis) is just awful
and completely incorrect.  It is not a new problem.  I believe I have seen
both in Blainville's and Grube's publication from early-mid last century.

In an informative sense, we name monophyletic taxa; the use of a
particular name, such as "Hediste" instead of "Neanthes" implies a
hypothesis of monophyly (except of course in cases where a specific
analysis has been done and monophyly demonstrated).   In keys and
overviews, we tend to use the simplest possible characters to use in
identifications.  Quite often simple presence/absence characters are to be
preferred in a key, to a shape designation, since the latter frequently
does not translate well into other languages etc.  (I can vividly remember
trying figure out what the shapes of the phyllodocid dorsal cirri was
supposed to look like as a young student in Norway).  However, as pointed
out by Judy Fournier, there is a lot more to the differences of shapes than
those used in keys; the parapodial structures are really very different and
can be well characterized and may well turn out to be the kinds of
apomorphies we end up using for demonstrating the monophyly of these
clades.    The process of demonstrating monophyly, once done, may make it
possible for us to feel certain that the simple characters we have been
using have validity (or not, depending on the analysis of course).  

The nereidids are biologically often very similar as pointed out by Dr.
Goerke, who knows more about these worms than anybody else I know about.
However, such generalizations may or may not be supported by an analysis
of relationships.  I hope that this will turn out to be the case, because
at that time, the more inclusive clades than the species may turn out to
be supported not only by morphological characteristics but also by
characterizable biological/ecological characteristics, surely as
inheritable as the morphological ones.

I hope somebody will do the analysis we need, and we need it badly,
since the nereidids are such favorite subjects for experiments and so
forth.   

Kristian Fauchald
<FAUCHALD.KRISTIAN@NMNH.SI.EDU>

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From daemon  Tue Feb 10 16:59:17 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id QAA29554
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To: annelida@net.bio.net
From: "Chris Glasby" <c.glasby@niwa.cri.nz>
Reply-To: annelida@net.bio.net
Organization:  NIWA
Date:          Wed, 11 Feb 1998 13:36:24 +12
Subject:       Re: Nereis - nomenclature

I was a bit slow off the mark this morning, and Kristian put it 
better than I could have any way! .....

.... I agree with all of the recent contributions to this thread, but there
appears to be a wider issue here that has been missed (except by 
Kristian).

Robin Wilson says

> Similarities (character states) shared by these 3 taxa are also
> shared by several other nereidid genera,  and it seems to me that
> these 3 are no more closely related than they are to several other
> valid genera. 

OK so it looks as though Nereis s.s., Neanthes s.s. and Hediste may
not be each others closest relatives, and therefore that the placement of
all three as subgenera under Nereis may not reflect reality (to borrow
Kirk's term). Not to mention that Neanthes s.s. is probably not
monophyletic.

I suspect that this scenario may be true of many 
polychaete subgenera and of relationships between subgenera 
under their parent genus. So why do we continue to recognise (and use) the
subgeneric category if their monophyly and relationships to one another
have not been substantiated by a cladistic analysis?

Robin goes on to say...

> It is unimportant and arbitrary whether one refers to these
> combinations as genera or subgenera ....

and Geoff ... 

> Biologists can use them [generic and subgeneric names]  at the level
> they wish without fear of censure either way. It's not important.

But, as is evident in the early messages in this thread, the fact that
there is this choice appears to be causing confusion out there among
biologists, conservation managers etc. The differences between say, Nereis
diversicolor, Nereis (Hediste) diversicolor and the incorrectly formed,
Hediste (Nereis) diversicolor, appear to be too subtle for the
non-taxonomist, and causing problems.

So shouldn't we just dump the subgeneric rank altogether? The pink
book pretty much took this approach I believe, and hopefully the
revised version in the pipeline will too. One less Linnean category is not
going to make a big difference. Sure there will be some species-rich genera
as a result (eg. Nereis), but in these days of computers (and not having to
rely so much on memory), it makes little difference!

Chris
Dr Chris Glasby
National Institute for Water & Atmospheric Research
PO Box 14-901, Kilbirnie
Wellington, New Zealand
email: c.glasby@niwa.cri.nz
phone: 64-4-386 0352; fax: 64-4-386 2153

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From daemon  Tue Feb 10 18:24:00 1998
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To: annelida@net.bio.net
Date:          Tue, 10 Feb 1998 18:01:00 -0800
Reply-To: annelida@net.bio.net
From: Kirk Fitzhugh <fitzhugh@almaak.usc.edu>
Subject:       Re: Nereis - nomenclature

I agree with Kristian's and Chris' opinions on subgenera. My personal
take on the more traditional use of subgenera stems from the desire to
reflect grade groups, ancestor-descendant relationships, levels of
divergence, etc., back when these were (and unfortunately still are)
fashionable. The problem has been compounded by the notion that some
characters deserve greater recognition than others. As we're seeing,
unless we're very clear about our intentions, both nomenclaturally and
systematically, there's the chance to introduce more confusion for many,
as noted by Chris. There may be times that subgenera are needed, but this
can only be determined when the cladograms are available or monophyly is
known. If formal classifications are intended to reflect what we observe,
then taxonomic ranks serve to denote monophyletic groups, not vice versa.
I have no problem with the use of subgenus - but polychaete systematists
must make clear their intent to use such a rank with monophyly in mind.

Kirk
------------------------------------------  
Kirk Fitzhugh, Ph.D.
Associate Curator of Polychaetes
Research & Collections Branch
Los Angeles County Museum of Natural History
900 Exposition Blvd
Los Angeles CA 90007
Phone:   213-763-3233
FAX:     213-746-2999
e-mail:  fitzhugh@bcf.usc.edu
------------------------------------------

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From daemon  Wed Feb 11 02:24:58 1998
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To: annelida@net.bio.net
From: "Helmut Zibrowius" <hzibrowi@com.univ-mrs.fr>
Reply-To: annelida@net.bio.net
Date:          Wed, 11 Feb 98 08:57:37 MST
Subject:       Polychaeta in a coral paper


Cairns S.D., Zibrowius H., 1997. Cnidaria Anthozoa: azooxanthellate
Scleractinia from the Philippine and Indonesian regions. In: Crosnier A.,
Bouchet P. (ed.), Resultats des campagnes MUSORSTOM, volume 16. Memoires
du Museum national d'histoire naturelle, 172: 27-243.

This contains a chapter mentioning polychaetes in symbiosis with corals.
Here the text of this chapter (p. 58-59):
------------

Commensal relationships

   Several types of specialized coral symbionts (other than simple 
epibionts) have been found associated with various members of the species-
rich fauna of the Philippines and Indonesia studied here. 

Lumbrinerid polychaete eroding the coral skeleton.
   This association has been described in detail by ZIBROWIUS et al. (1975) 
on the basis of material from the northeastern Atlantic and the 
southwestern Indian Ocean (South Africa), with additional records from 
Madagascar, the China Sea and Japan. The coral skeleton eroding polychaete 
Lumbrineris flabelliocola (Fage, 1936) inhabits a soft tube exteriorly 
attached to the host and causes a superficial to deep erosion of the coral 
skeleton. The worm itself is easily lost by the mechanical constraints of 
dredging and the subsequent manipulations, but frequently empty tube 
fragments remain attached to the coral, or a corrosion trace can be 
detected on the coral even after the worm and and the tube have 
disappeared. This association occurs in the Philippines and in Indonesia. 
Worms obtained during cruise MUSORSTOM 2 in the Philippines have been 
compared by T. MIURA with Lumbrineis flabellicola from the NE Atlantic and 
Japan and have been found to be the same species (L. flabellicola) in these 
widely distant areas (T. MIURA, in litt., 1989).   The following species 
have been found to be the coral partner of this association, specimens 
still bearing the worm (WO), or still having empty tubes fragments attached 
(ET), or showing only a characteristic erosion trace left over (TR):

- Caryophyllia (C.) transversalis: DEKI stn 32 (WO).

- Caryophyllia (C.) grayi: MUSORSTOM-2 stn 29 (ET); MUSORSTOM-3 stn 131 
(ET, TR).

- Caryophyllia (A.) spinigera: MUSORSTOM-2 stn 63 (WO).

- Caryophyllia (A.) spinicarens: "Albatross" stn 5256 (ET), stn 5418 (TR),
stn 5535 (ET), stn 5536 (TR), stn 5538 (TR); MUSORSTOM-1 stn 20 (TR?); 
MUSORSTOM-2 stn 63 (ET).

- Conotrochus brunneus: MUSORSTOM-3 stn 92 (ET, TR).

- Flabellum (F.) patens: KARUBAR stn 31 (TR).

- Flabellum (F.) lamellulosum: MUSORSTOM 1 stn 27 (TR?), stn 31 (TR);
MUSORSTOM-2 stn 63 (ET); MUSORSTOM-3 stn 86 (WO), stn 92 (WO, TR).

- Flabellum (F.) sp.: MUSORSTOM 3 stn. 133 (ET).

- Rhizotrochus typus: MUSORSTOM-3 stn 131 (ET).

- Balanophyllia sp.: MUSORSTOM-2 stn 33 (WO).

- Dendrophylliidae, colonial: MUSORSTOM 2 stn 33 (WO).


Eunicid polychaete causing deformation of the coral colony.
   Some colonies of Madrepora oculata from Indonesia ("Albatross" stn 5645;
KARUBAR stn 56) show deformations similar to those found in colonies of 
Madrepora oculata, Lophelia pertusa, and Solenosmilia variabilis from the 
northeastern Atlantic, in which the parchment-like tube of Eunice norvegica 
(Linnaeus, 1767) is overgrown by the coral coenosteum and incorporated into 
thecolony (Zibrowius, 1980). We have no information whether the 
deformations of Indonesian M. oculata is caused by the same Eunice species. 
Similar deformations characterize all colonies of Madrepora arbuscula and 
of Madrepora minutiseptum studied here. Even though no overgrown soft tube 
has been formally identified in this material and no worm been extracted, 
it is presumed that the causing organism is an eunicid polychaete. 
Overgrown parchment-like Eunice tubes have also been found in some colonies 
of Neohelia cf. porcellana.


Acrothoracic cirriped crustacean boring the coral skeleton.
   Acrothoracic cirripeds may bore the skeleton of live corals and when 
penetrating through the wall cause the polyp to deposit additional wall 
material that is intended to seal off the borer. The orifice of the burrow 
may migrate upward along the growing coral (GRYGIER & NEWMAN, 1985). 
Orifice motility is particularly marked in a specimen of Javania 
lamprotichum (MUSORSTOM-2 stn 53) bored by 4 large acrothoracids. Other 
species bored alive are Tethocyathus virgatus (MUSORSTOM-3 stn 108), 
Balanophyllia crassiseptum (KARUBAR stn 50) and Balanophyllia sp. 
(MUSORSTOM-1 stn. 61; MUSORSTOM-2 stn 32; MUSORSTOM-3 stn 131).


Ascothoracid crustacean inducing a skeleton gall.
   The most common aspect of this association has been described in detail 
by ZIBROWIUS & GRYGIER (1985) who already reported some examples the 
Philippines and Indonesia: "internal galls" are recognizable as a spongy 
proliferation of the columella that covers the underlying cavity occupied 
by the parasite. The list from the Philippines and Indonesia now includes 
Deltocyathoides orientalis ("Albatross" stn 5178, 5313, 5314, 5315, 5317, 
5403, 5569); Flabellum (F.) lamellulosum (MUSORSTOM-2 stn 83); 
Balanophyllia carinata (Siboga stn 240), Balanophyllia sp. (MUSORSTOM-2 stn 
34); Balanophyllia sp. (MUSORSTOM-3 stn 131); Dendrophyllia sp. cf. D. 
ijimai(MUSORSTOM-2 stn 33). A newly recognized expression (GRYGIER & 
CAIRNS, 1996) of ascothoracidan gall induction are abnormal hypertrophied 
corallites in Madrepora oculata ("Albatross" stn 5529; DEKI stn 50; "Hakuho 
Maru" stn KH-73-2-44-2; KARUBAR stn. 9, 13, 19, 77). 	


Cryptochirid crab inhabiting a crypt in the coral skeleton.    
   Cryptochirid (formerly hapalocarcinid) crabs are obligate symbionts of 
scleractinians. The crypts (or in some cases cage-like galls) they inhabit 
are due to dissolution of the coral skeleton and to induced modified coral 
growth (ZIBROWIUS, 1982; ZIBROWIUS & GILI, 1990). Previous to these authors 
cryptochirids had always been considered as typical of the reef fauna, but 
new deep-water species continue to be discovered. Zibrovia galea Kropp & 
Manning, 1995, has thus been found on Phyllangia papuensis from the 
Philippines (MUSORSTOM-2 stn 47) and from Madagascar.

---------------------------------------------------- 
  Helmut ZIBROWIUS
  (Centre d'Oceanologie de Marseille)
  Station Marine d'Endoume
  Rue Batterie des Lions
  13007 Marseille / France
  E-MAIL:  hzibrowi@com.univ-mrs.fr
  TEL: within France  0491041624  from abroad +33 491041624
  FAX: within France  0491041635  from abroad +33 491041635  
  ---------------------------------------------------------

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From: BIOSCI Administrator <biohelp@net.bio.net>
Subject:       BIOSCI/bionet miniFAQ & Fundraiser

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accessible on the World Wide Web at URL http://www.bio.net/.

If you can not find an answer to your question in this or other
documentation, the BIOSCI technical support staff answers e-mail
queries sent to

         biosci-help@net.bio.net

We can only answer questions about the use of the newsgroups and
mailing lists.  We unfortunately do not have the staff to do Internet
information searches or answer scientific questions.  Please post
those to the appropriate BIOSCI/bionet newsgroups.


 Contents:
 --------
 0) BIOSCI NEEDS YOUR SUPPORT!!

 1) Using the WWW to access the BIOSCI/bionet newsgroups.

 2) What to do about "spams," i.e., junk mail, ads, etc.

 3) Examples of subscribing and unsubscribing to the mailing lists.

 4) The BIOSCI user address and research interest directory.


0) BIOSCI NEEDS YOUR SUPPORT!!
------------------------------
BIOSCI's government funding has been expended, and we are now
operating solely from advertising revenue that we have raised from our Web
site at http://www.bio.net/.  We need just a few minutes of your time to
help us serve you.

You can do two important things which will take very little time for
you individually and will immensely help us continue to help you.

First, please use our WWW system at http://www.bio.net/ to access the
archives.  You can post or reply to messages via your Web browser as
described in item #1 below.  Your usage helps attract sponsors. If you
contact any of our sponsors, please be sure to thank them for supporting
BIOSCI. It is critical for them to get this feedback if they are to
continue their sponsorship for the long term.

Second, if you work for a company or organization that provides
products or services of interest to the biology community, please pass this
message on to your marketing or marketing communications department or
other appropriate group.  Please ask them to help support BIOSCI by
sponsoring our Web site and explain the uses and benefits of the system to
the biology community. If they are interested, they can then contact us for
further information at our tech support address, biosci-help@net.bio.net.


1) Using the WWW to access the BIOSCI/bionet newsgroups.
--------------------------------------------------------
As of 10 December 1995, all BIOSCI/bionet full newsgroups are
accessible through the World Wide Web (WWW) at URL http://www.bio.net. One
can read and reply publicly or privately to both recent postings and
archived messages through one's Web browser if it is configured properly to
send e-mail.  Each newsgroup is equipped with its own WAIS index.  The main
BIOSCI home page also has access to the BIO-JOURNALS Table of Contents
database WAIS index and the BIOSCI user address database described in
another item further below.


2) What to do about "spams," i.e., junk mail, ads, etc.
-------------------------------------------------------
BIOSCI is a set of parallel USENET newsgroups (the "bionet" groups),
mailing lists, and a hypermail archive at URL http://www.bio.net/.
The same postings are distributed on all media (except for a small
number of mailing-list-only groups at net.bio.net).  Unfortunately it
is becoming a despicable practice on the Internet (by a few people out to
make a fast buck) to do automated mass postings to thousands of newsgroups
and mailing lists.  These attempts to grab free advertising are refered to
as "spams" in the usual, somewhat boneheaded, net terminology.  USENET is
more susceptible to this practice, and many spams originate on the USENET
groups and then are passed on to the mailing lists.  However, spammers also
get lists of mailing addresses and hit these too, so neither medium is
immune.

What should you do personally if you get junk mail?
---------------------------------------------------
Just delete it and move on without reading it further.  Filing a
protest is becoming increasingly useless because spammers are often
disguising the addresses where the messages are sent from.  Unless you
really understand Internet mail systems, your attempt at protest by sending
replies to the message will often end up being sent to the address of an
innocent person that the spammer is victimizing.

What can BIOSCI/bionet do to protect its newsgroups?
----------------------------------------------------
The only solution currently available is to moderate the newsgroup.
If this newsgroup is already moderated, then you are in good shape.
Moderation protects the USENET distribution from about 95% of the
spams that are being sent to date and protects the mailing lists
completely.  Moderation means, however, that someone has to take the
time to review each message before it goes out.  We have set up
software here that simply allows the moderator to forward to an
address at net.bio.net messages that (s)he wishes to have distributed. This
takes no more time than that needed to read the message and pass it on, say
about 1 min. per message.

Most newsgroups currently have a discussion leader who is responsible
for their newsgroup.  The discussions leaders and their e-mail
addresses are listed in the BIOSCI Information Sheet which is
available on the Web at http://www.bio.net/.  If a newsgroup is being
hit with too many junk postings, please contact the discussion leader
for that group and see if there is interest in moderating the group.
Please do not assume that by simply posting a complaint to the
newsgroup itself, anyone on the BIOSCI staff will act on your
complaint.  With close to 100 newsgroups to run, the BIOSCI staff has
to rely on the discussion leaders of each newsgroup to report problems
directly to us at biosci-help@net.bio.net.

We will moderate any of our newsgroups if the discussion leader tells
us that the readership of the group wishes to do so and if a moderator is
willing to do the work.  For most BIOSCI/bionet groups, this entails only a
few minutes of work each day.

Moderating a newsgroup will resolve probably 95% of the junk postings
on the USENET distribution.  Unfortunately there are easy ways for
determined spammers to override the moderation mechanism on USENET,
but we can protect our e-mail subscribers from unwanted postings if
the newsgroup is moderated.  You can also access our newsgroups over
the WWW at URL http://www.bio.net.  While this Web interface will not
stop spammers from trying to post to the groups, this will give you
yet another way, besides using USENET news, to keep the junk out of
your personal mail files.  For those of you with local USENET news
systems, the Web interface will also give you faster access to new
newsgroups and recent postings.


3) Examples of subscribing and unsubscribing to the mailing lists.
------------------------------------------------------------------
PLEASE NOTE: The BIOSCI management does NOT act on
subscription/unsubscription requests that are posted improperly to the
newsgroups and mailing lists.  People who do this only bother everyone on
the lists to no avail.  Please be sure to follow the proper procedures
below.

Gory details are in the BIOSCI Information sheets on the Web at
http://www.bio.net.  Below we give an example utilizing the
METHODS-AND-REAGENTS list at both of our two BIOSCI sites:

Users in the Americas and Pacific Rim countries who use the BIOSCI
------------------------------------------------------------------
node at computer net.bio.net:
----------------------------

A) Determine the "listname" which is the <=8 character mail address
                                         ^^^^^^^^^^^^^
   for the group.  These can be found in the BIOSCI Info. Sheet.  For
   the METHODS-AND-REAGENTS group the mailing address is
   methods@net.bio.net.  The listname is the portion of the address to the
   left of the @ sign, i.e., "methods".  The listname is used with the
   "subscribe" and "unsubscribe" commands illustrated below.

B) Mail all commands in the body of a mail message addressed to
   biosci-server@net.bio.net.  Do NOT send commands to the newsgroup
   posting addresses!  Leave the Subject: line blank, any text on it
   will be ignored.

C) In the body of your message put one or more of the following
   commands with an "end" command on the last line, e.g.,

   subscribe methods
   unsubscribe methods
   end

   Do NOT put your e-mail address or other text on these lines.  The
   server only allows you to cancel your subscription if the address
   on your mail header matches the address on our mailing list.
   Please ask for help at biosci-help@net.bio.net if your address has
   changed, e.g., if you know you are on the list but the server tells you
   that you are not a member.


Users in Europe, Africa, and Central Asia who use the BIOSCI node at
--------------------------------------------------------------------
computer daresbury.ac.uk (also known as dl.ac.uk):
-------------------------------------------------

To subscribe and unsubscribe to/from the BIOSCI lists, you need to
specify the full USENET newsgroup name with "bionet-news." prepended.
The USENET newsgroup names are listed in the BIOSCI Information sheet
on the Web at http://www.bio.net/.  For the METHODS-AND-REAGENTS list
the USENET newsgroup name is bionet.molbio.methds-reagnts, thus the
appropriate commands are

    sub bionet-news.bionet.molbio.methds-reagnts

    unsub bionet-news.bionet.molbio.methds-reagnts

These commands are included in a message addressed to mxt@dl.ac.uk,
NOT to the newsgroup mailing addresses.  As usual, include the text in the
body of the message as text on the Subject: line is ignored.

To unsubscribe from all the lists at the UK node, use

    unsub bionet-news

Please note that if the address in the list is different than the one
in your mail message header, you will not be able to unsubscribe by
this method. If you have problems, please mail biosci@daresbury.ac.uk.


4) The BIOSCI user address and research interest directory.
-----------------------------------------------------------
Please take this opportunity to add your name, address, and research
interest information to the BIOSCI User Address Database if you have
not already done so.

You can fill out the address form directly through our Web page at URL
http://www.bio.net/adrform.html.

The address database is reindexed nightly for WWW access (the URL is
http://www.bio.net/).  If you are not directly on the Internet but can
reach it by e-mail, please use our waismail server to access the user
directory.  waismail use is described above.  You can also request a user
address form by e-mail from biosci-help@net.bio.net.

Please check your database entry from time-to-time to see if your
address information is still up-to-date.  Because of our limited
personnel resources, we ask that you resubmit a *complete* form to
revise your entry; we only replace complete entries and do not have
resources to edit old forms.

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From daemon  Fri Feb 13 10:08:38 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id KAA15587
Message-Id: <199802131808.KAA15587@net.bio.net>
To: annelida@net.bio.net
From: Salma Hassen Shalla <S.H.Shalla@liverpool.ac.uk>
Reply-To: annelida@net.bio.net
Subject:       Serpula vermicularis
Date:          Fri, 13 Feb 1998 10:41:00 +0000 (GMT)

I have been researching the ecology of reefs formed by the serpulid
Serpula vermicularis in the British Isles.  I have found some good
surveys, descriptions and ecological information on the reefs themselves,
but surprisingly little on very basic questions such as:

How long do individual worms live, what is their growth 
rate, how long do reefs take to build up etc.  

Also are there records of extensive reefs formed by this species
elsewhere? It has been suggested they may occur in the Mediterranean but
I can find nothing definitive on this. 

Any help would be very much appreciated.

Salma Shalla

----------------------
mb0s4005@liverpool.ac.uk


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From daemon  Fri Feb 13 10:08:36 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id KAA15578
Message-Id: <199802131808.KAA15578@net.bio.net>
To: annelida@net.bio.net
Date:          Fri, 13 Feb 1998 10:53:21 +0100
Reply-To: annelida@net.bio.net
From: "Harry A. ten Hove" <hove@bio.uva.nl>
Subject:       Re: Ficopomatus biology & ecology


>I am looking for any references (Biology and ecological preferences) on
>the Serpulidae polychaete : Ficopomatus enigmaticus (Fauvel 1923) (syn.
>Mercierella enigmaticus)
>
>Could somebody help me on that species?

>Jacques GRALL

I pasted below my letter:    

To: MCCANN@SERC.SI.EDU
From: hove@bio.uva.nl (Harry A. ten Hove)
Subject: RE: Fico.enigmaticus

Dear Linda,

>So Ficopomatus is found in salinities ranging from brackish to 55 '%'?
>That's quite a broad salinity tolerance!

Yes indeed.

>Jim Carlton and I are interested in writing a paper synthesizing all of
>the work on the genus. We are particularily interested in the zoogeography
>of the Ficopmatus enigmaticus, and in tracking down it's actual area of
>origin. Would this overlap with what you are doing too much? Any thoughts,
>papers we might look at? We are quite taken with this worm.

If people are enthusiastic about a subject, one should stimulate them
rather than discourage. Nevertheless, I have to utter a word of caution.
About 20 years ago a student of mine tried to synthesize the then known
papers on Ficopomatus (at that time still Mercierella), but gave up after
about 2 months, although I had almost all papers at hand (it thus was not
the practical problem of obtaining articles from relatively unknown
Russian or Spanish journals). Since that time the problem has simplified
to a certain degree, ten Hove & Weerdenburg at least sorted out the
taxonomic mess and made clear that F.enigmaticus is not likely to occur in
tropical waters. Nevertheless, (few) new papers have appeared reporting
F.enigmaticus from these unlikely habitats, so there still is some
confusion to be sorted out when compiling data. All together my files now
contain 350 papers mentioning F.enigmaticus (the previous estimate of 250
was a typing error discovered thanks to the fact that you were asking
questions).

The last distributional map of Ficopomatus to my knowledge is: Hove, H.A.
Ten, 1979a.- Tube worm. Yearb.Sci.Techn., McGraw-Hill, 1979: 400-402, 3
figs.

A thesis you should try to obtain if pushing on with Ficopomatus is David
Dixon's thesis, partly published in his two later papers: Dixon, D.R.,
1977.- The energetics of Mercierella enigmatica Fauvel. Thesis, Univ.of
London, 494 pp., 89 figs., 41 tabs. [mimeogr.] Dixon, D.R., 1980.- The
energetics of tube production by Mercierella enigmatica (Polychaeta:
Serpulidae). J.mar.biol.Ass.UK 60: 655-659, 2 figs. Dixon, D.R., 1981.-
Reproductive biology of the serpulid Ficopomatus (Mercierella) enigmatica
in the Thames estuary, S.E.England. J.mar.biol.Ass.UK 61: 805-815, 6
figs.

A must too is:
Vuillemin, S., 1965.- Contribution a l'etude ecologique du lac de Tunis.
Biologie de Mercierella enigmatica Fauvel. Thesis, Paris, A 4622 (5469),
554 pp., illustrated.

The last known hypothesis on the origin of enigmaticus is: Zibrowius, H.,
1992.- Ongoing modification of the Mediterranean marine fauna and flora
by the establishment of exotic species. Mesogee 51: 83-107. Interestingly,
and probably correctly he reaches exactly the opposite conclusion as
vented by: Williams, R.J., & E.J. van der Wal & J. Story, 1986.- Draft
inventory of introduced marine organisms. Austr.Mar.Sci.Bull.61: 12

If, after reading the above papers, you still want to go ahead, I might
send you a copy of my handwritten systemcards, mentioning author and year
only. I do not have the time to copy all 350 full references,
unfortunately these are only partially on disc yet.

Wormly, Harry



Harry A. ten Hove
Institute for Systematics and Population Biology
Zoological Museum, University of Amsterdam
POB 94766, 1090 GT AMSTERDAM

TEL. 3120 5256906
FAX. 3120 5255402
<hove@bio.uva.nl>



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From daemon  Fri Feb 13 10:08:35 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id KAA15572
Message-Id: <199802131808.KAA15572@net.bio.net>
To: annelida@net.bio.net
Date:          Fri, 13 Feb 1998 08:55:23 -0800 (PST)
Reply-To: annelida@net.bio.net
From: Debi Ingrao <debi@marinelab.sarasota.fl.us>
Subject:       Americonuphis


Where can I find I find taxonomic (and or any info ) on Americonuphis
magna?

Debra Ingrao
Mote Marine Laboratory		Phone: (941) 388-4441 EXT. 436
Benthic Ecology Program		Fax: (941) 388-4312
1600 Thompson Parkway			
Sarasota, Fl  34236		e-mail: debi@marinelab.sarasota.fl.us


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From daemon  Sun Feb 15 13:04:43 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id NAA03352
Message-Id: <199802152104.NAA03352@net.bio.net>
To: annelida@net.bio.net
Date:          Sun, 15 Feb 1998 11:25:44 -0800 (PST)
Reply-To: annelida@net.bio.net
From: Rolf Bissell Parker  <parkerr@ea.oac.uci.edu>
Subject:       Sorensen's Buffer recipe


 Hello Anneliders,

I can find many articles that refer to Sorensen's Buffer, but not any
current references that actually give the original source reference. 

What I actually need is a recipe for this buffer. Does anyone have this? 

Thanks,

  Rolf Parker
  ECO EVO DEPT
  UCAL IRVINE
  714 824 5324

  parkerr@uci.edu


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From daemon  Sun Feb 15 17:17:36 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id RAA28555
Message-Id: <199802160117.RAA28555@net.bio.net>
To: annelida@net.bio.net
From: "Geoff Read" <g.read@niwa.cri.nz>
Reply-To: annelida@net.bio.net
Organization:  NIWA (Nat. Inst. Water & Atmos. Research)
Date:          Mon, 16 Feb 1998 14:09:33 +1100
Subject:       Re: Ficopomatus biology & ecology


> The last known hypothesis on the origin of enigmaticus is: Zibrowius, H.,
> 1992.- Ongoing modification of the Mediterranean marine fauna and flora
> by the establishment of exotic species. Mesogee 51: 83-107.

Might we be told more? Not a widely available journal unfortunately.

--
  Geoff Read <g.read@niwa.cri.nz>

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From daemon  Mon Feb 16 02:19:44 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id CAA23306
Message-Id: <199802161019.CAA23306@net.bio.net>
To: annelida@net.bio.net
From: "Helmut Zibrowius" <hzibrowi@com.univ-mrs.fr>
Reply-To: annelida@net.bio.net
Date:          Mon, 16 Feb 98 10:45:26 MST
Subject:       speculations on F. enigmaticus origin


>The last known hypothesis on the origin of enigmaticus is: Zibrowius, H.,
>1992.- Ongoing modification of the Mediterranean marine fauna and flora
>by the establishment of exotic species. Mesogee 51: 83-107.

Referring to H.A. ten Hove's above message Geoff Read
(Mon, 16 Feb 1998 14:09:33 +1100) asked:
>Might we be told more? Not a widely available journal unfortunately.

Here the extract concerning polychaetes in that alien species compilation:

---------------------------------------
       Polychaeta (general information)

          Based on literature that unfortunately comprised some
       particularly unreliable older publications, Por (1978) listed 9
       species of polychaetes (including one species of Serpulidae) as
       high-probability, and 14 species (including one species of
       Serpulidae) as low-probability lessepsian migrants, and 20 species
       (including two species of Serpulidae) as antilessepsian migrants.
       A partial correction and updating was provided by Zibrowius
       (1983b); in particular, it was stated that considerably more
       serpulid species of Indo-Pacific origin had settled on the
       Levantine coasts. Por (1989, 1990) was able to refer to new data
       obtained by Ben-Eliahu (1989, 1991b) on Nereidae (6 species) and
       Serpulidae (see below), whereas data for other polychaete families
       remain problematical.

       Polychaeta Serpulidae and Spirorbidae

          The serpulids of Red Sea/Indo-Pacific origin presently known
       from the coasts of Israel and Lebanon are: Hydroides cf.
       brachyacantha Rioja, 1941; H. novaepommeraniae Augener, 1925 [= H.
       grubei Pillai, 1965]; H. heterocera (Grube, 1868); H. homocera
       Pixell, 1913; H. minax (Grube, 1878); H. operculata (Treadwell,
       1929); Pomatoleios kraussii (Baird, 1865); Spirobranchus
       tetraceros (Schmarda, 1861) (see Laubier, 1966; Zibrowius and
       Bitar, 1981; Ben-Eliahu, 1988, 1989, 1991a; Ben-Eliahu and Hove,
       1990, 1992). In addition to active dispersal by planktonic larvae,
       passive dispersal as ship fouling may have contributed to their
       present range. In fact, most of these species, together with
       Hydroides albiceps (Grube, 1870), and H. steinitzi Ben-Eliahu,
       1972 (both of Red Sea/Indo-Pacific origin), have also been found
       among the fouling sampled at Toulon harbour from a ship arriving
       from the Indian Ocean via the Suez canal (Zibrowius, 1979). As for
       Pomatoleios kraussii, it is wide-spread in the Indo-Pacific (from
       Japan to South Africa) and also occurs in the Gulf of Guinea. This
       disjunct distribution may well be due to early dispersal by
       navigation (Zibrowius, 1983b).

          Comprising world-wide > 80 species and particularly specious in
       tropical seas, the genus Hydroides is predominant not only among
       lessepsian migrants, but also includes the three earliest alien
       serpulids in the Mediterranean (Zibrowius, 1971, 1973, 1978,
       1983b; Zibrowius and Thorp, 1990). Hydroides dianthus (Verrill,
       1873), H. dirampha Moerch, 1863, and H. elegans Haswell, 1883, have
       been collected together at Naples from harbour fouling as early as
       1888, H. elegans being quantitatively dominant (an association
       currently observed in present harbour fouling throughout the
       Mediterranean). But two species can be traced back to an even
       earlier date: H. dianthus at Izmir (year of publication 1865) and
       at Trieste (year of collecting 1874); H. dirampha at Naples (year
       of publication 1870). All three species are now widely distributed
       in the Mediterranean in harbours and coastal lagoons. The
       distribution is disjunct, leaving out "natural" habitats of full
       marine salinity, except in areas immediately adjacent to harbours.
       Within this pattern, H. dirampha appears to be absent from the
       northernmost parts of the Mediterranean and to be more frequent in
       the south; its origin could be the tropical American Atlantic. H.
       elegans (frequently confused with the autochthonous northeastern
       Atlantic and Mediterranean H. norvegica Gunnerus, 1768) also
       appears to be of tropical/subtropical origin, but its native area
       is even less evident; being first described from Australia does
       not prove an Australian origin. H. dianthus appears native of the
       Atlantic coast of North America where it occurs in a variety of
       "natural" habitats. Possibly the arrival with ship fouling of the
       three Hydroides species in the Mediterranean considerably
       antedates their first records. Considerable fouling nuisances by
       H. elegans have been described by Parenzan (1965) and Paoletti and
       Sebastio (1973).

          Ficopomatus enigmaticus (Fauvel, 1923) probably was brought to
       Europe with ship fouling during the first world war. Dense
       brackish water populations were first noticed at London harbour
       and in a canal of northern France (Zibrowius and Thorp, 1990). A
       few years after its description F. enigmaticus invaded suitable
       biota in the Mediterranean where it is now wide-spread in coastal
       lagoons and estuaries. Its apparition in San Francisco Bay at the
       close of the first world war, as evidenced by local newspaper
       accounts (Carlton, 1975), was about contemporary with its
       apparition in Europe. Fauvel's hypothesis of an Indian/Indonesian
       origin, can be ruled out: other species of Ficopomatus, but not F.
       enigmaticus, exist in that area (Hove and Weerdenburg, 1978). The
       origin from a subtropical to temperate area, eventually southern
       Australia, appears more likely (Zibrowius, 1978, 1983b).

         The Spirorbidae Spirorbis marioni Caullery and Mesnil, 1897, and
       Pileolaria berkeleyana (Rioja, 1942) have originally been
       described from the eastern Pacific (Panama and Mexico). In 1979
       both species were discovered on stones in a harbour at Marseille
       where they did not exist some years before. Investigations of
       harbours and adjacent areas motivated by this discovery and
       conducted for several years showed that the two alien species
       were differently distributed in the Mediterranean (Zibrowius and
       Bianchi, 1981; Zibrowius, 1983a, 1983b). P. berkeleyana was found
       limited to harbours in the Marseille area sensu lato (from the
       Gulf of Fos in the west to Les Lecques in the east) whereas S.
       marioni was already wide-spread, from Morocco through Spain and
       France to Italy (southern limit of explorations at Monte
       Argentario promontory), including Elba, Corsica and Sardinia. Both
       species frequently occur in dense populations. It was also found
       that S. marioni and P. berkeleyana had been present in the
       Marseille area, and S. marioni at Genova, as early as 1977. Both
       spirorbids are able to spread from harbour to harbour by ship
       navigation since many of the investigated harbours shelter mainly
       small sailing and motor boats that do not travel far. S. marioni
       appears to have better spreading abilities, but the previously
       studied coasts should be checked again in order to see whether P.
       berkeleyana has extended its area.

          In 1987 S. marioni has also been found in Izmir Bay and
       elsewhere on the Turkish coast of the Aegean Sea, always in
       harbour areas (Knight-Jones et al., 1991). It would be of interest
       to extend these investigations in view of alien spirorbids to
       other parts of the Mediterranean.


  ----------------------------------- 
  Helmut ZIBROWIUS
  (Centre d'Oceanologie de Marseille)
  Station Marine d'Endoume
  Rue Batterie des Lions
  13007 Marseille / France
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  FAX: within France  0491041635  from abroad +33 491041635  
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From daemon  Tue Feb 17 02:37:27 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id CAA16966
Message-Id: <199802171037.CAA16966@net.bio.net>
To: annelida@net.bio.net
Date:          Tue, 17 Feb 1998 10:27:01 +0100
Reply-To: annelida@net.bio.net
From: "Harry A. ten Hove" <hove@bio.uva.nl>
Subject:       Serpulid reefs, Filograna & S.vermicularis

>Annelidians,
>
>I need information on reefbuilding Serpulidae, especially about Filograna
>implexa and the fauna within the coloni.

>How long do individual worms live, what is their growth
>rate, how long do reefs take to build up etc.


You might find some references in the following papers of which I
unfortunately do not have reprints left.

HOVE, H.A. TEN, 1979a.- Tube worm. Yearb. Sci. Techn., McGraw-Hill, 1979 :
400-402, 3 figs.

HOVE, H.A. TEN, 1979b.- Different causes of mass occurrence in serpulids.
p.282-298 in: G. LARWOOD & B.R. ROSEN (eds), 1979.- Biology and systematics
of colonial organisms. Syst. Ass. Spec. Vol.11, xxxv + 589 pp., illustr.

HOVE, H.A. TEN, & P. VAN DEN HURK, 1993.- A review of Recent and fossil
serpulid "reefs"; actuopaleontology and the 'Upper Malm' serpulid
limestones in NW Germany. Geol. Mijnbouw, 72: 23-67, 12 figs., 5 tabs.

wormly

Harry A. ten Hove
Institute for Systematics and Population Biology
Zoological Museum, University of Amsterdam
POB 94766, 1090 GT AMSTERDAM

TEL. 3120 5256906
FAX. 3120 5255402


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From daemon  Wed Feb 18 21:19:29 1998
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To: annelida@net.bio.net
Date:          Wed, 18 Feb 1998 18:14:03 -0500
Reply-To: annelida@net.bio.net
From: "Dr. Andrew G. McArthur" <mcarthur@onyx.si.edu>
Subject:       Invertebrate Molecular Systematics

RESEARCHER IN INVERTEBRATE MOLECULAR SYSTEMATICS
SEEKING POSTDOCTORAL RESEARCH POSITION

EDUCATION:
PhD 1996, University of Victoria, Canada
Postdoctoral Fellowship 1997, Laboratory of Molecular Systematics, National
Museum of Natural History, Smithsonian Institution

SKILLS:
Invertebrate Zoology, Molecular Systematics, Use of Formalin Preserved
Museum Specimens, Maximum Likelihood Approaches, Systematics of the
Gastropoda, Deep-Sea Biogeography

CURRICULUM VITAE AND OTHER INFORMATION:
http://www.geocities.com/CapeCanaveral/8431/Vitae.html

CANADA OR THE UNITED STATES ONLY

CONTACT: Dr. Andrew G. McArthur (mcarthur@onyx.si.edu)

Effective February-March, 1998:
------------------------------------------------------------
Dr. Andrew G. McArthur, Guest Investigator, Biology Department, Woods Hole
Oceanographic Institution, U.S.A., Ph. (301) 238-3444 Ext. 112, Fax (508)
457-2134, Email: mcarthur@onyx.si.edu,
http://www.geocities.com/CapeCanaveral/8431/

** Do not send unsolicted mail - please request current mailing address.


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From daemon  Thu Feb 19 13:19:29 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id NAA08010
Message-Id: <199802192119.NAA08010@net.bio.net>
To: annelida@net.bio.net
Date:          Thu, 19 Feb 1998 07:45:49 -0800 (PST)
Reply-To: annelida@net.bio.net
From: Marine Biology Laboratory <mblcsdla@netcom.com>
Subject:       Re: Sorensen's Buffer recipe


Greetings:

A recipe for the phosphate buffer is in Humanson's, "Animal Tissue
Techniques" Fourth edition, page 556.

Bye for now,

Tom Parker
mblcsdla@netcom.com

On Sun, 15 Feb 1998, Rolf Bissell Parker wrote:

> I can find many articles that refer to Sorensen's Buffer, but not any
> current references that actually give the original source reference. 

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From daemon  Thu Feb 19 18:52:06 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id SAA20238
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To: annelida@net.bio.net
From: "Geoff Read" <g.read@niwa.cri.nz>
Reply-To: annelida@net.bio.net
Organization:  NIWA (Nat. Inst. Water & Atmos. Research)
Date:          Fri, 20 Feb 1998 15:39:26 +1100
Subject:       With similar rami

Annelidans,

I am looking at the characters in Rouse and Fauchald (1997) "Cladistics &
polychaetes," one of two important papers that Kristian, Greg (and the
Smithsonian) have most generously provided free copies of around the world
& at vast expense.

There is a lot to digest, but at present I need help on one small aspect. I
do not understand the parapodial distinctions -  'with similar rami,'
'spioniform' (aha - we might know a priori who have those!), 'with
projecting neuropodia.'

In particular I am unclear how for example a nereid (grouped as 
'projecting neuropodia') could not have 'similar rami.' Although Fauchald
and Rouse claim (p105) that nereid notopodia are shorter 'in most taxa,'
this is not my experience.  So it is subjective (thus agreeing with F&R on
p81), and in any case not something that is so clear-cut as to be of
fundamental significance.   And one might also say that a spioniform has
similar rami or that a spionid may, in other places, be without postsetal
lobes and thus have  tori (another parapodial classification) - unless one
defines a torus as only having uncini - but that is dealt with under setae
and would eliminate the example arenicolids (getting messy here).

Given that they are short-hand for (I hope) much more complex 
decision-making than those simple titles imply, I am not sure that we are
finally told enough to be convinced those groups are well-defined and
mutually exclusive (they are permitted to overlap in the analysis, but have
not been overlapped, I think, in the coding).

Perhaps it does not matter in the overall context - &  I look forward to
the enlightenment from the list that will dispel my current faint
discontent with the R&F parapodial classification.

PS: I assume Capitellidae singled out as having _uncini_ (p88) is not true
since this character is not listed in its family review  or in the matrix? 


--
  Geoff Read <g.read@niwa.cri.nz>


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From daemon  Sat Feb 21 13:14:43 1998
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To: annelida@net.bio.net
From: "sashka" <sashka@com2com.ru>
Reply-To: annelida@net.bio.net
Subject:       Spirorbid bibliography
Date:          Sat, 21 Feb 1998 18:01:49 +0300

Dear all,

If you interest spirorbid's bibliography, you can find it on the Lena
Kupriyanova's homepage http://rav.sio.rssi.ru/~lena/spir-lit.html
(Spirorbidae bibliography) ; http://rav.sio.rssi.ru/~lena/ (Lena
Kupriyanova's homepage).

This bibliography is still under preparing, but I hope it may be useful
for you. This is complete up to 95 % for recent and  40 % for fossil
species. I will greatly appreciate for any additions and remarks. My
e-mail sashka@com2com.ru, my ICQ # 7715265

Alexander Rzhavsky


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From daemon  Mon Feb 23 02:21:11 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id CAA02843
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To: annelida@net.bio.net
Date:          Mon, 23 Feb 1998 10:01:07 +1100
Reply-To: annelida@net.bio.net
From: Greg Rouse <gregr@bio.usyd.edu>
Subject:       Re: With similar rami

Dear Geoff et al.,


<smaller>Please feel free to inform me or Kristian of any other
discrepancies and errors in F&R (1997) and R&F (1997)</smaller>;
revisions are of course inevitable. Regarding your posting:


"Perhaps it does not matter in the overall context - &  I look forward
to the enlightenment from the list that will dispel my current faint
discontent with the R&F parapodial classification."

(snip)


Consultation of the Appendix in Rouse and Fauchald (1997: 194) will 
show you the following regarding the Nereididae:

"<smaller>44-55. Parapodial structures. Though often of equal size the
results of Fitzhugh (1987) suggest that projecting neuropodia is the
plesiomorphic condition in the family. Dorsal and ventral cirri are
present.</smaller>"


"PS: I assume Capitellidae singled out as having _uncini_ (p88) is not
true since this character is not listed in its family review  or in the
matrix?"

(snip)


<smaller>An error is an error so thanks for pointing it out and sorry
for any confusion. But </smaller>note the caveat in Rouse and Fauchald
(1997: 141): 

<smaller>"Appendix IV provides the basis for all the scoring in the
matrices (Appendix II) and is to be taken as the primary source if
there are any discrepancies with Fauchald & Rouse (1997)."


greg

</smaller>
Greg Rouse

School of Biological Sciences A08

University of Sydney

N.S.W. 2006

Australia

Tel.     (02) 9351 5571

Fax     (02) 9351 4119

International: 61 2 replaces 02

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From daemon  Mon Feb 23 22:10:01 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id WAA06352
Message-Id: <199802240610.WAA06352@net.bio.net>
To: annelida@net.bio.net
From: "Geoff Read" <g.read@niwa.cri.nz>
Reply-To: annelida@net.bio.net
Organization:  NIWA (Nat. Inst. Water & Atmos. Research)
Date:          Tue, 24 Feb 1998 18:53:04 +1100
Subject:       Re: With similar rami


> results of Fitzhugh (1987) suggest that projecting neuropodia is the
> plesiomorphic condition in the family [Nereididae].

It is interesting that A/P character 46 - projecting neuropodia, and
character 47 - tori, seem to be unrewarding as they both display multiple
transformations. Character 49 - spiomorph, however, appears solid. 

With 20/20 hindsight I think I would have preferred to see the comparison
of noto/neuro dispensed with (In the Aciculata only Nephtyidae and
Amphinomidae have 'similar rami' - but we know the parapodia of this pair
are very different!). Rather it should be possible to characterize a 
notopodial ramus relative only to all other notopodial rami types, and a 
neuropodium likewise.

My 2 cents, as they say.

--
  Geoff Read <g.read@niwa.cri.nz>

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From daemon  Tue Feb 24 17:36:31 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id RAA12349
Message-Id: <199802250136.RAA12349@net.bio.net>
To: annelida@net.bio.net
From: "Geoff Read" <g.read@niwa.cri.nz>
Reply-To: annelida@net.bio.net
Organization:  NIWA (Nat. Inst. Water & Atmos. Research)
Date:          Wed, 25 Feb 1998 14:25:37 +1100
Subject:       Re: Spirorbid bibliography


> If you interest spirorbid's bibliography, you can find it on the Lena
> Kupriyanova's homepage http://rav.sio.rssi.ru/~lena/spir-lit.html
> (Spirorbidae bibliography) ; http://rav.sio.rssi.ru/~lena/ (Lena
> Kupriyanova's homepage).

The file is 137Kb at present. The _extreme_ slowness of this link may try
the patience of some - go and have a cup of coffee - have two cups -  but
eventually it will arrive!

However, if Alexander Rzhavsky gives me permission, I can put  a 
'mirror' copy on the USA-based biodiversity.uno.edu site as well. 

The same offer applies to anyone with a large bibliography, or dataset, or
image, or document for circulation. 

--
  Geoff Read <g.read@niwa.cri.nz>

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From daemon  Tue Feb 24 20:43:28 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id UAA04594
Message-Id: <199802250443.UAA04594@net.bio.net>
To: annelida@net.bio.net
From: "Geoff Read" <g.read@niwa.cri.nz>
Reply-To: annelida@net.bio.net
Organization:  NIWA (Nat. Inst. Water & Atmos. Research)
Date:          Wed, 25 Feb 1998 17:32:46 +1100
Subject:       The most eurythermal metazoan

The most eurythermal metazoan? 

It is a polychaete.

According to:

Cary,SC; Shank,T; Stein,J (1998): Worms bask in extreme temperatures.
Nature 391(6667), 545-546 (5 Feb issue. Scientific correspondence).

In situ temperature records in tubes of Alvinella pompejana living on
sides of hydrothermal vent chimneys show an average of 68 deg C, with 
spikes exceeding 81, whereas tube opening (on outside of chimney) temp is 
22 deg C. This makes Alvinella the most thermotolerant and eurythermal 
metazoan known. 

(The authors also refer to  Pierre Chevaldonne's & D. Desbruyeres' 1992
note in Nature.)

--
  Geoff Read <g.read@niwa.cri.nz>

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From daemon  Thu Feb 26 16:02:47 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id QAA10258
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To: annelida@net.bio.net
From: "Geoff Read" <g.read@niwa.cri.nz>
Reply-To: annelida@net.bio.net
Organization:  NIWA (Nat. Inst. Water & Atmos. Research)
Date:          Fri, 27 Feb 1998 12:26:43 +1100
Subject:       Re: Spirorbid bibliography


> However, if Alexander Rzhavsky gives me permission, I can put  a 
> 'mirror' copy on the USA-based biodiversity.uno.edu site as well. 

He did. 

The link is from the page:

http://biodiversity.uno.edu/~worms/bib-list.html

--
  Geoff Read <g.read@niwa.cri.nz>

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From daemon  Thu Feb 26 16:33:14 1998
Received: (from daemon@localhost) by net.bio.net (8.6.12-r-beta/8.6.6) id QAA14118
Message-Id: <199802270033.QAA14118@net.bio.net>
To: annelida@net.bio.net
From: "Geoff Read" <g.read@niwa.cri.nz>
Reply-To: annelida@net.bio.net
Organization:  NIWA (Nat. Inst. Water & Atmos. Research)
Date:          Fri, 27 Feb 1998 13:16:25 +1100
Subject:       Re: With similar rami

Geoff Read wrote:

> It is interesting that ...

<silence>

Come on folks. This is supposedly an informal discussion group. Is
there nothing in F&R, R&F that you would like to express a comment on or
ask about? 

How depressing if true. That's not the case though ... is it? 

--
  Geoff Read <g.read@niwa.cri.nz>

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From daemon  Fri Feb 27 13:55:43 1998
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To: annelida@net.bio.net
Date:          Fri, 27 Feb 1998 09:11:43 -0100
Reply-To: annelida@net.bio.net
From: Peter Wirtz <peter@dop.uac.pt>
Subject:       Lygdamis

Dear Colleagues,

as you probably know, Dr. Dave Kirtley died a few months ago. At the time
of his death, he was preparing a description of a new species of Lygdamis
(Sabellariidae), which is quite common at Madeira. In a paper on Madeiran
inverts and in my book on marine inverts of Madeira, the Canary Islands
and the Azores, I have called this species L. murata (an identification
confirmed by another polychaetologist prior to publication).

Who is working on Lygdamis/ Sabellariidae and would be willing to
describe this new species in a reasonable time (within no more than a
year) ? I would be willing to dig out a few more, even though this can be
several hours work under water.

Peter

Dr. Peter Wirtz
currently at U of Azores,
back at U of Madeira after 27 March and email then again
biomar@dragoeiro.uma.pt


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