Re: Re: squalens, sambucina etc (a bit long) (was Iris pallida cultivars & nomenclatural question)
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- Subject: Re: [iris-species] Re: squalens, sambucina etc (a bit long) (was Iris pallida cultivars & nomenclatural question)
- From: &* A* M* <n*@charter.net>
- Date: Wed, 30 Jun 2004 13:44:50 -0400
- References: <20040630134612.31971.qmail@web80001.mail.yahoo.com>
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From: r*@sbcglobal.net
To: i*@yahoogroups.com
Sent: Wednesday, June 30, 2004 9:46 AM
Subject: Re: [iris-species] Re: squalens, sambucina etc (a bit
long) (was Iris pallida cultivars & nomenclatural question)
"First off the top of my head many early whites were the result of Iris
kashmiriana breeding. I seem to remember that it was believed to be more
dominant that what had existed before but my memeory is fuzzy on that. I am not
even sure anymore that I really know what kashmiriana is. We have discussed this
before."
Bob, even though this was addressed to Dave, please
let me comment on some specifics involving whites--from tetraploid experience
mostly.
The early dominant whites of the 'Purissima' sort
derive their genetic pattern primarily from 'Kashmir White' which is of
uncertain origin. It *may* be from a white form of *Iris
kashmiriana.* What is certain, however, is that the same dominant
inhibitor of *pallida* blue can be inherited either from the non-blue
44-chromosome sterile IB sorts derived from *lutescens*
(Lam.1789) on the rare occasions tetraploid offspring can
be obtained. More recent SDB's from TB x *pumila* origin
sometimes also contain the factor hidden behind the pumila anthocyanin pigment,
so advanced generation hybrids into TB stock can introduce the dominant
inhibitor. On this basis some have speculated that 'Kashmir White' may owe
its inhibitor to dwarf ancestry.
In support of this interpretation I might
mention a cross of 'Garnet Treasure,' an early red-violet SDB
from 'Minnie Colquitt,' X a blue Suiter seedling from (Sun Lakes x
'hoogiana,' a blue form I believe) which yielded half odd pale
blue near-whites with no pumila fall spot, and half medium violets with the
spot. There were about thirty seedlings bloomed from the cross. The
simplest and most probable interpretation is that the violet SDB brought one
dose of the inhibitor into the array. Since the seedlings were
unbalanced sterile IB "arilmeds" the interpretation could not be
tested.
There appears to have been demonstrated
in TB's at least two different whites of recessive origin in addition
to the "glaciata" type, which, when crossed, do not yield
all whites. One of the whites is exemplified by Melvina Suiter's
'White Satin,' a sib to 'Sun Lakes,' a blue from blue parents. 'White
Satin' was registered in 1950 and is from (Blue Champagne x Sylvia
Murray). 'Sun Lakes,' due to an oversight, does not appear in the registry
until the *Iris Check List* 1979, but is from the same time period. A cross
reported by Vallette of 'White Satin' with 'Matterhorn,' a glaciata,
yielded a variety of anthocyanin color types and a couple of plicatas
and whites. There are other
derivitives of 'Gloriole' of the same type white as exemplified by 'White
Satin.'
The other recessive, non-glaciata, white is
typified by 'Dayspring.' The *aphylla* clone 'Ostry White' may be
the same as one or the other of these, or be of a third type. A post to
"Iris-talk" some months ago mentioned a cross of a white with 'Ostry White'
which did not produce whites. I cannot for the moment recall with
certainty whether the post originated with Harald Mathes or what was the
identity of the other white.
There is a discussion of the question of various
whites (rather, non-blues), in TWOI on pp. 401-403 and ff., probably
authored by Keith Keppel. He is one who can speak with authority on this
matter, incidentally, and probably can point one to the taxonomic data you
seek.
I have assumed the whites of the 'White Satin' type
to have derived their genetic white type from *Iris pallida,* although I know of
no simple way to test that assumption.
On a related matter to the above, I might
comment that the karyotypes I've seen published for *Iris variegata,* *pallida,*
and *kashmiriana* are very similar, suggesting that these Eupogons, and probably
many other of the Asiatic tetraploids, are of very close evolutionary
relationships. An exception might be *Iris trojana,* which has some
characteristics of a rather distinct sort. The clone I had from L. F.
Randolph resembled a more primitive 'Blue Rhythm,' with the same deep
branching and very similar form. It would not surprise me if part of the
unknown part of the ancestry of 'Blue Rhythm' did not include one or more
inclusions of *trojana.* Other than this exception, it would surprise me
if all the other collected tetraploids were not actually variants of the
same species, even though they originated from areas as remote from one another
as Afghanistan, Turkey and the European mainland.
I am in the hope that the molecular studies you
mentioned recently can eventually untangle the nomenclature and affinities of
the various collected tetraploid Eupogons and their relationship(s) to the
*pallida/variegata* complex. Even though many of the actual
species clones are no longer extant, their first generation hybrids are, and
might possibly be useful in determining the relationships..
Neil Mogensen z 7 western
NC
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