Volume 5, Acknowledgements

In some cases acknowledgement has already been made in respect of some of the populations discussed in these chapters.  New acknowledgements are Mr. Artho Saayman of Platkop, Mr. and Mrs. Wilhelm Zietsman of Kruis Rivier, Mr and Mrs. Coetzee Uys of Morning Star, Messrs Chris and Pieter van Deventer of Kransriviermond, Johan Groenewald of Buffeljags, Clive and Duprecia Stramrood of Kadies Landing, the Uys brothers  of Sandfontein and Meerlus, the Steenkamps of Appelbos,  Annatjie and Jaap Viljoen of Swellendam, Hector Odendaal of Dankbaar, Ryno Stander of KomseRandte, Tineke Kraaij and Carli Venter of Bontebok National Park, Anne Lise Vlok and Rhet Hisemann of W Cape Nature Conservation Board, Stiaan Conradie of Lower Breede Conservancy.  Others such as to Mr. and Mrs. Anna and Arno Steenkamp of Anna’s Farm (Oudekraalkop) for their generosity and hospitality, Mr. and Mrs. Hennie van Deventer of Koppies, Mr. Dirk Papendorp of Voorstekop and Uitvlugt,  Mr.  Uys Willemse of Goedverwagting, need repeating.  We are most grateful to Dr. Paul Taylor for an albeit failed excursion to the west bank of the Duiwenhoks River and similarly to Nico DeJager of Victoriasdale for an interesting but fruitless search of the Wankoe Randte and a little more success on Klipheuwel, Mr. H. Eksteen of Grootkloof and Mr.  M. Dippenaar of Diptka for so kindly allowing us access to their properties.  There are many other landowners and people we contacted with less significance in respect of places actually visited or in terms of plants found but no less in respect of  the universal kindness and helpfulness of landowners.

There are many other peripheral and significant contributions from people (not necessarily agreeing with what I say nor how) such as Prof. Richard Cowling, Dr. Syd Rhamdani, Diederik van den Abbeele and even people who have no connection to Haworthia, but who share the same passion for nature and for plants … Mrs. Hettie Conradie of Worcester who makes us feel as though it is we who own her home and Mrs. Anso LeRoux who may both be housewives, but biologists by nature.  Gordon Rowley has demonstrated the value of humour in a field where there seems naught else to do but tear hair out.  Etwin Aslander in his quiet and effective way has been a great friend.

Then there is Gerhard Marx, whose dogged refusal to blindly accept anything at face value, has been most helpful in so many respects.  Kobus Venter has always been a great friend and mentor in relation to the ways of the world and I am extraordinarily grateful for his unwavering support and kinship.  He and Mirna, in graciously allowing us the use of their holiday home at Stilbaai facilitated this work.  Steven Hammer has been another remarkable personage in my life and I am most grateful for him being the sensitive, perceptive, empathic and remarkable man he is.

Lastly where I have used the term “we” I have included my wife, Daphne.  This is actually with great reluctance because anything to do with taxonomy and nomenclature brings with it a cloud of derogation and negativity – what to say of the negative attitudes that surround the word “collection”.  It seems that in past civilizations there was great respect for nature and many of the rites and rituals were an appeasement to nature for the benefits she bestowed in terms of what she provided in the way of food, clothes and shelter – the basic needs of man.  Daphne has provided me with the trust and support of a true companion and I regard her very dearly.  There is no need for her to remind me, as she seldom does, that few other housewives would traipse so blithely and happily through the wilderness with someone who does not seem to know where he is going or what he is doing next.

I feel a need to explain again that I became a taxonomist by default where there are also systematists and nomenclaturalists and I would not wish to be any of these.  We as individuals are all inclined to make bold and general statements based only on what we know and ignore the very much greater body that we do not know at all.  I would say that it is depressingly sad that information is processed and distributed as knowledge often from a very limited experience and limited data base.  After 45 years of this I actually am painfully aware that there is still a lot that I do not know about.  I make no apologies for a revision that is precisely the sort of product that comes from constant testing of a hypothesis.  I take it very remiss of a publisher that did not honour the integral part of a contract to further research and validate the work.  I am extremely grateful to Harry Mays for publishing a vast series of articles that were originally intended for a home based publication but mindlessly lost in a mire of conflicting interests.

 

Volume 6, Introduction

It is a matter of considerable concern to me that the lack of “adequatio” for the understanding of Haworthia is so conspicuous by its absence.  Three reviews appeared for 5 small essays published as a supplement to Haworthiad and also as a portion of Haworthia Update Vol. 5.  To suggest that these reviews are anything but some sort of myopia is an understatement and I find it difficult to try and explain why.  My reason is simply that many criticisms simply arise out of the fact that the reviewers are not familiar with my writing and have no basis for assuming that they are up to the task of reviewing what I have written.  Nothing is being learnt from history where the same old arguments about opinions hardly differ from those voiced 60 years ago.

The real issue is that there is confusion in the minds of collectors as the user public, about the uses and application of Latin names in the pursuit of their interests.  Professional botany offers no assistance and any numbers of poorly equipped authors of necessity, invent and re-invent types, the interpretation of names and then their application.  This does nothing to assist the collector.  The reviews of that small segment of my writing do not help either and certainly do not generate a climate that encourages me to write any further.  One review calls for a revision when the message is that a formal revision might just be intellectual vanity when a practical list of names and explanation is presented to add to an existing Revision.  A second review seems to tout a mistaken belief that self fertility and polyploidy may be explanations for the intractable problems that we have in the self-sterile non-polyploid haworthias.  A third review is seemingly facetious comment that may obscure my opinions as those of the reviewer and acceptable as such, but not if seen to be mine.  None of these reviews will be helpful to anyone who may need to decide what set of names makes more sense than another.  There is no common voice and any reader is left to make up his own mind in the absence of any good authority.  Perhaps this is something I should be personally grateful for because there are noises emanating from various sources that my opinions also threaten understanding rather than enhancing it.  I have to accept that it may be difficult for anyone to agree with me who has not had the same exposure to the intractability of biological systems that seems to have been my lot in life.

I regret that I did not, prior to publication, see the forward to Vol. 2 that I hoped would generate “common voice”.  It, unfortunately, is just a bit of personalized chitchat about the writer.  It can hardly generate any confidence in what he may have written about and does not attempt to do so.

My revision in 1996 (published 1999) admits the problems of typification and my attempt to stay within the historically recognized interpretations and applications of names.  A revision is fundamentally a reconciliation of new information and new “collections” and the Update Volumes have been an ongoing reporting of new finds and observations.  More than one reviewer seems to think that a change of mind is indicative of weak argument rather than a product of new and better information.

Update Vol. 1 (2001), published by Umdaus Press includes one essay regarding Haworthia mucronata and five others dealing almost wholly with Haworthia cooperi and its variants.

Subsequent volumes were published by Alsterworthia. Update Vol. 2 appeared in 2006 in two parts comprising a total of 17 chapters and a list of Bayer accessions.  Update Vol. 3 was published in 2007, also in two parts and comprising 15 essays.  Update Vol. 4 was also published in 2007 in one part comprising 10 essays of which two were intended to close the saga.  However, a surge of inquiry and energy made me decide to have a last serious effort to try an answer some outstanding questions in my own mind.  So Update Vol. 5 was published in 2009 and comprises 16 essays.  Perhaps, if nothing else, these essays just demonstrate how much there is out there in the field that has escaped attention.

Update Vol. 6 is simply a small set of essays that address some loose ends of which there are still many. One essay in particular will remain unwritten because, while I have some information, it is not enough to base any conclusions on.  This concerns the area between Oudtshoorn and Uniondale.  It is also not the only gap in my experience and knowledge. The chapters in Update Vol. 2 should demonstrate just how intensively the field has to be explored to get to grips with the possible dynamics of the plants.  This view should be re-enforced by the subsequent volumes.  While I have tried to hold to a belief in “species” and names relevant to some sort of system, it seems to me that as a society we are denied the freedom to really know what the meaning and purpose of creation is.  Science itself seems to insist that there is none and botanists largely view the observance of nomenclatural rules as the primary criterion in the application of names.

My experience and observation now suggest to me that creation is purposeful and meaningful.  Life is manifested in various distinctive forms and these forms are manifested according to their DNA.  This DNA may be the fundamental stuff of consciousness in living things too; flowing from and responsive to the energy fields of physical bodies such as the galaxy and the solar system.  Life on earth is driven by catastrophic events of varying degree and varying intervals, so that species simply represent those sets of living things as they come, change and go with successive events.  We do not only need to consider what species might be and mean, but also when.  Who knows?

———-

Printed edition of Haworthia Update Volume 6 can be obtained from

Harry Mays
Woodsleigh, Moss Lane, St Michaels on Wyre, Preston, PR3 0TY, UK.
hmays@freenetname.co.uk
http://www.cactus-mall.com/alsterworthia/

Volume 6, Chapter 1:- Haworthia and Chameleons

There is a very curious parallel in the problems and aspects of classification and identification of haworthias and chameleons that I personally find a bit mystifying.  Classification of succulent plants and especially Haworthia is often done outside of mainstream science, which means that it is not done by trained professional botanists, who can stand in the intellectual arena with academics and degreed intellectuals.  It has been pointed out to me that this is the problem in Haworthia and also why professionals do not want to attempt to resolve the issue because the nomenclature has been so confused and complicated by all the bungling that has taken place.  Having been on the fringes, and indeed even failed attempting to cross the bridge into academia, I find it very difficult indeed to reconcile my life experience in the amateur arena with what I encounter from the professional one.  This is because I have observed an ever widening gap between the perceptions of the non-science individual compared to that of the professional. My interest in chameleons is simply another aspect of my interest and passion for living things and I am distressed that the knowledge and understanding of these fascinating animals, as with Haworthia, is so clouded by ignorance and confusion.

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Volume 6, Chapter 2:- Towerlands. Haworthia retusa ‘turgida’

In Haworthia Update 4 I wrote an essay about the haworthias east of Albertinia in which I discussed their relation to H. retusa  and H. mirabilis, while generally lumping them largely in H. pygmaea.  There are of course real ‘turgida’ populations as far east as near Mossel Bay, so I argued the case for an interplay of the two former species that over the whole distribution range generated two ‘species’ in the east viz. H. pygmaea and H. retusa (to include ‘turgida’), and three ‘species’ in the west adding H. mutica to H. mirabilis and H. retusa.

Recently I had the pleasure of meeting Gregory Nicholson who is studying botany at University, Cape Town.  He surprised me by telling me that there was a Haworthia on his parent’s property west of Herbertsdale.  It was not in fact so much surprising as confirmation of the belief I formed on a trip a short while before that there must be haworthias in the very suitable terrain of the Jakkals River valley 6km west of Herberstdale.  The surprise came when Greg indicated the position of the plants much deeper into the mountains.

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Volume 6, Chapter 3:- Still more about Haworthia on Kaboega

Part 1.
Kaboega is a set of farms on the northeast of the Zuurberg Mountain range, north of Kirkwood and off the Addo National Park. I wrote about the haworthias that occur there in Haworthia Update Vol.1. There is also an article in Aloe 40:10 (2003) in which there is a discussion of the variation of those haworthias as related to geology and topography. My wife and I frequently visit Kaboega to renew relationships with Ian and Sandy Ritchie who live there. Each time we go we try to explore some different area. We generally end-up with something that is notably new.
There is a real problem in trying to reconcile the populations we see with the names that are available and the way in which I have tried to formalize them myself. The problem is that Kaboega seems to occupy some sort of central and neutral position and it is by no means easy to arrive at any clean rational classification. Three of my species are involved, and I have to say they are “mine” because other authors are in strong disagreement. The three species I see are H. cymbiformis, H. cooperi, and H. aristata. It is firstly necessary to explain that I interpret the name H. aristata in Haworthia Revisited quite differently from what I might have done earlier; and quite differently from other authors who have simply taken the easy route and associated the name with Little Karoo elements for which I use the name H. mucronata. My interpretation of the name will be quite evident from my writings and from the pictures submitted with this article. The use of the name H. cymbiformis with respect to Kaboega is a major problem for someone like myself who is firmly convinced that geographical relationships are foremost in the recognition of species as living systems. On Kaboega, plants that look like H. cymbiformis seem to proceed out of a complex that is surely H. cooperi. If one properly considers all the populations that I ascribe to H. aristata one is seriously confronted with the reality that it is also a geographic variant of H. cooperi.

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Volume 6, Chapter 4:- Haworthia emelyae and some of its variants

Where are we?  Geography plays such a critical role in my perception of the species that it is important to try to understand why and how it touches on the issue.  The Langeberg Mountains is a Table Mountain Sandstone about 10km wide and 1500m high running east-west and separating the inland Little Karoo from the Lowland Renosterveld of the southern Cape.  There are five main travel routes through those mountains of which two are via river gorges viz. Cogmanskloof, Tradouw, and then there is also the Gouritz River Gorge where there is no road.  Haworthia is not generally considered a sandstone and high mountain species because, firstly, there are few records to suggest that and, secondly, because they are averse to the higher moisture levels.  However, there are many records in the low and close foothills.  H. retusa ‘turgida’ is recorded in the higher areas and in the vegetation associated with the sandstone viz. the Fynbos.  Fig. 1 is a view taken looking eastwards from Kleindoorn (Kleindoornrivier). This is about 16km east of Barrydale that sits at the northern end of the Tradouw Pass.  The next farm is Brandrivier (B) and beyond that is Springfontein.  Muiskraal is marked with an “M” and this is at the northern end of Garcia Pass from Riversdale to Ladismith.  The “O” marks Oskop which is beyond Zandkraal and about 15km beyond Muiskraal.  Another 10km will take you past Waterval and bring you to Aasvoelvallei at the confluence of the Grootriver with the Gouritz..  The last stretch is another 10km over the Cloete’s Pass to Herbertsdale from where one travels back westward 7km to Towerlands.

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Volume 6, Chapter 5:- Haworthia emelyae ‘major’ and multifolia. New populations.

1a.View from above Onverwacht North Westward to Ladismith

1b. View looking south west over Muiskraal to Garcia Pass

 

There used to be a regular bus service between Riversdale and Ladismith and J. Dekenah made use of this for his excursions into the Little Karoo to find plants for G.G. Smith.  He thus discovered H. emelyae ‘major’ at the northern mouth of Garcia Pass.  He also submitted a single specimen of a plant collected from the karoid veld a little further north.  It is that record that suggested to me that ‘major’  was linked to H. emelyae further east and north as well as to ‘multifolia’ to the west.  Etwin Aslander found what I regarded as the equivalent of ‘multifolia’  (see figs 2a-i) on a low plateau north of Garcia pass on the farm Muiskraal that is at the foot of the mountains north of Garcia Pass.

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Volume 6, Chapter 6:- Die Nekkies and Biomes and Haworthia maculata.

1. Looking down the north face Die Nekkies east to west

It is always assumed that botanists have a good grip of their subject, as one supposes for the scientists in other disciplines. Any science is the advance of knowledge by observation, hypothesis and testing by systematic enumeration and experiment. This is furthered by replication and review by other scientists.  Botany is far behind the exact sciences, because of the very nature and complexity of living things and systems, and also behind because zoology where animal life is obviously more organized than is the case with plants and where more attention is focused.

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Volume 6, Chapter 7:- Taking Haworthia cooperi further – Kliprivier.

It is very difficult to write about particular plants when one has to contend with the fact that one is not sure what Latin names may mean to the reader.  I wrote a piece with closure in mind and thought I would send it to a non-taxonomist botanist whom I think is a tribute to the profession.  Extracts from his response are “I am an ardent supporter of your species concept and couldn’t agree more strongly with your statement that without variation, there would be no evolution…I do agree that the pervasive species concepts force us to ignore the most interesting and productive research avenue: documenting and understanding variation in the field.”

It is worth considering what he has said about “pervasive species concepts” and just what he might mean when he says they force us to ignore documentation and understanding of variation in the field.  It seems to me that the converse is the truth.  Failure to properly understand and document variation has contributed to the pervasiveness of false concepts which fly in the face of science.  I keep harping away at this question of lack of definition, because it is not apparent to me that any reader appreciates my point of view.  To my mind a key issue is made of nomenclature and the rules that govern it, and very little attention at all is given to whether these Latin names help our understanding at all. I feel that my contribution contributes mostly to documentation of variation and that I cannot do much in respect of understanding.  This short article should explain why.

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Volume 6, Chapter 8:- A fleeting look at Haworthia arachnoidea

How did this start?  Is it possible to see anything with such a quick peek?

Somewhere in my memory bank is my stated opinion that understanding H. arachnoidea would assist any botanist towards a better understanding of classification. This was long before I came to see that this is a lot more necessary than I thought then. It is not just botanists who seem dumbed down to the reality of a diversity that is necessary for response to change and largely denied by the nomenclatural code and how it is practiced.  We have not understood change or what changes can occur.  During perhaps only the last 15 to 20 years has it become apparent that changes are cataclysmic and frequent.  I will skip the fact that the violence of catastrophe, or the drivers of catastrophe, may also induce change at even a cellular level.

I usually go into the field with a specific goal while also carrying a host of peripheral questions in my mind.  While exploring the problem of H. schoemanii, I was thus also thinking of Conophytum.  After photographing a species seen at Laingsburg, I mentioned to Steven Hammer that I had also seen it in the southeastern Tanqua Karoo (Bakoven).  This was news to him and so in my wish to re-establish the reality of H. venosa subsp. granulata recorded at Patasriver (actually Patatsriver road and that is another story that will be told) as well as the Conophytum for Steven, I undertook an expedition to the Tanqua.

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Volume 6, Chapter 9:- Interesting nursery plants

I have become increasingly concerned about the poor relations that exist between collectors and the authority of Nature Conservation.  The argument that collectors threaten and despoil natural populations is very real and I do not dispute at all that Conservation authorities have a very valid complaint. They have a function to perform. On the other hand there is an interaction between human beings and nature in all its forms that should be fostered to the benefit of both sides.

Nurseries, traders and collectors are as much of the picture as are conservationists, institutions, researchers and landowners.  It is unfortunate that there is no non-government party that lobbies for the rights and activities of the former group,  but it is not my intention nor within my competence to argue all the aspects of the case.

I strongly believe that people have the right of access to nature in all its forms and the issue is one of individual responsibility and proper consideration of consequences. An appreciation of and sensitivity to nature should be reflected in whatever we do in our lives. My own collecting impulses led me to institutional employment where I could exercise my interest to what I thought were efforts more worthy than my personal interests.  From that position I also did try to share and extend privileges to a wider circle.  It is  in this way that I became involved with Sheilam Nursery.  It was not my wish or intention that my collection should have come to be housed there. However, Sheilam has succeeded over a period of nearly 40 years to maintain a fairly true record of my collections obtained as propagated material from the Karoo Garden at Worcester.  My offer of permitted collections dating from my revision of Haworthia in 1966 to the Karoo Garden was rejected and for a while resided with Etwin Aslander at Brackenfell.  It has since passed to Garth Schwegman at Sheilam who has taken a particular interest in the maintenance and propagation of that collection.

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Volume 6, Chapter 10:- Non-pilose "pilosa"

When I was at the Karoo Garden I became a bit befuddled by the way botanists referred to the Cape Floral Kingdom.  It seemed to me that they used the term for the vegetation that was on the Table Mountain sandstones and conveniently excluded that which was not.  Thus the “Fynbos” vegetation, characterized by its Ericaceae, Proteaceae and Restionacea, was synonymous with this floral kingdom.  An official document was published at the time which purported to classify the Southern African vegetation into biomes as major floral assemblages with very broad boundaries.  It did not make sense to me because my observations were that the “fynbos”, however different in terms of historical origin, was essentially a flora of the sandstones, and that there was rather a winter rainfall biome which included karoid (Succulent Karoo mainly) flora.  The role of geological substrate and skeletal soils seemed to me to be pivotal as there are places where one can virtually take a single step from one vegetation assemblage into another.

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Volume 6, Chapter 11:- North and Northwest of the Potberg

In an earlier article I described how Haworthia floribunda (at B on map) transmutes eastwards to H. variegata (at A on map) between the localities Klipfontein and Kleinberg, which are north of the Potberg Mountain. This is despite the fact that they both occur in close proximity at the northwestern end of the mountain. Difficulties now arise in the immediate vicinity to the west (at point W) and this extends northwestwards (to points C and D on the map).  While we can confidently ascribe names to floribunda and variegata at those particular sites, the plants to the west and northwest are confounding.  They fall into a no-man’s-land of these two species with H. mirabilis, H. maraisii, H. heidelbergensis and even H. mutica thrown in.

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Volume 6, Chapter 12:- A look at Aloe haworthioides

Aloe haworthioides was described by Baker in 1887, moved to a unispecies genus Aloinella by Lemée in 1939 and then into Lemeea by Heath in 1993.  This was wisely all undone by G. F Smith et al in 1995.  This taxonomic dance is one of those events which probably bring taxonomy into disrepute in the minds of people otherwise respectful of scientific process.

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Volume 7, Chapter 1:- Haworthia retusa ‘nigra’ – Another grand finale.

Introduction
I wonder.  I have written so many words purporting to be my last that my credibility here too must be under stress.  Two very recent articles of mine in Alsterworthia deal essentially with that issue, although they also cover the discovery of Haworthia mutica (Buffeljags) (= H. groenewaldii Breuer).  They do not cover my subsequent thoughts on actually reading the description of this new “species” by Breuer, Marx and Groenewald.  I hope that the present manuscript will explain why I reject this as a Latin binomial although anyone who is in the least familiar with my writing should already know.  Spurred on by that discovery, I instigated a search in another area of the Buffeljags valley adjoining the Bontebok Park accompanied by Jannie Groenewald who informed me of what he had found in still another area I had long wanted to explore.  So I instigated another search there too and again with Jannie.  A discussion of these new finds is submitted to Cactus and Succulent Journal where I trust it will be published.  The essence is already in Alsterworthia and this article is written to widen the readership, submit more pictures and maintain continuity with the 6 volumes of Haworthia Update that Harry Mays has been so conscientiously and determinedly publishing.  This is all writing that may not otherwise have seen the light of day.  I am personally extremely grateful for that as I have had a mania since writing my revision Haworthia Revisited and Update Vol. 1 (both Umdaus), to set the record straight and explore all the unknowns, or at least some of them.

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Volume 7, Chapter 2:- Further exploration in Haworthia. Further to finale.

The writing of my grand finale was inspired by several things. One of these was another item of a mind-numbing foray into the classification of Haworthia. So I asked that deep thinker and observer, Gerhard Marx, for a devil’s advocate (abbrev. DA) point of view which he has done with the same competence he has as an artist. I have many times in my writing addressed the issue of a species definition and produced one too. Not surprisingly the first thing the DA does is dismiss my definition without producing one of his own. Simply being able to say that an indeterminate number of plants from some population are sufficiently different in respect of a character or two from other haworthias, is motivation enough for the generation of a new name?

The case of H. groenewaldii Breuer, described in an article authored in Alsterworthia 2.2:15-20 by Breuer, Marx and Groenewald is the case in point. It presents the description of this supposed new species from Buffeljags east of Swellendam. The article is written in the first person (Breuer) who quotes extensively from Gerhard’s e-mails, and includes a piece by Jannie Groenewald under the heading “Description of the Vegetation type and distribution”. The overall impression is of an article that conforms to the style of a forgotten era and it is not possible or sensible to attempt a rational dismissal.  Who is actually responsible for the article and how does one correct misleading statements without giving offence?

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Volume 7, Chapter 3:- A field trip to the Potberg area.

Introduction:
These field trips are always made with some objective in mind in respect of new exploration.  In this case I wanted to get more pictures of H. mutica as it is a species that I have few digital images of.  There were also localities that I remembered from the days when I was sweeping the countryside at a fairly coarse scale and was not much bothered by detail.  I confidently expected the number of real species conforming to that in other fields of botany and zoology, to be in the region of 33.  I never dreamed that such divergent views would, or even could, arise from less information than even then available to me.  So while 450 names were whittled down to the mid-hundreds by me, students of the genus have in recent years pushed that up to the 600 mark.  My opinions have been couched in quite conservative terms but it is a problem of the nomenclatural system that an identification in respect of a Latin name evokes a reality that does not exist.  I maintain that the problems we experience in Haworthia are no different to that which exists in many animal and plant genera.  I think that primarily this is because of the absence of insight into, and understanding of, the actual nature of species and the two dimensional model we use to relate them.  Species are very variable systems because they have to be to survive the constantly changing world they occupy.  In this article I am just going to present images of plants within populations of four different species viz. H. variegata, H. minima, H. mirabilis and H. mutica.

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Volume 7, Chapter 4:- What is typical Haworthia mutica?

A supposed new species of Haworthia viz. H.groenewaldii Breuer, is described in an article authored in Alsterworthia 11.2:13-17 by Breuer, Marx and Groenewald.  It presents the description of this supposed new species from Buffeljags east of Swellendam that I would simply have identified as another variant of H. mutica.  This is not because I am confounded by the variability among the plants in the genus, or even in any one species.  I recognize the species as systems of populations in which the individuals vary from one another as one would expect in any group of living things that maintains the flexibility to adapt to constantly changing world conditions.  In this even time becomes a variable.  I think species are very important elements if the whole of creation and not just for taxonomist and collector activity.  Other people have other ideas of what species are, so my disagreement is hopefully forgivable..

Although H. mutica was described by Haworth in 1821 it was not allied to a South African field population until recognized by Col Scott in 1985.  G.G. Smith had failed to recognize it when he described his H. otzenii in 1945.   The type by which the name is supported is a Kew illustration reproduced here as Fig. 1.  This then is what one would expect a typical representative of the species to look alike.  Now the ever present problem in Haworthia, is that no two plants in a population may look quite the same.  Hence my problem with the description in which the word “typical” is rather bandied about.  It falls into the first aspect of taxonomy.

Firstly a plant is illustrated on the front cover of the respective Alsterworthia that, presumably the authors, state is a typical specimen of H. groenewaldii.  Secondly, Marx is quoted as saying that the “typical H. mutica” grows only 20km west at the farm Dankbaar.   Statements like these are used to strengthen and support opinions and generate a reality that Latin binomials sadly lack.  It so happens that I know both these populations quite well and these statements are news to me.   I do not think the specimen on the front cover is by any means typical of the population at Buffeljags, and certainly not at three sites recently discovered nearby.  The plants at Dankbaar also do not in my opinion fully meet the imputed similarity to fig.1.  See fig 2. for an image of a plant representative of the Dankbaar population.  I would be very hesitant to say that this is typical of Dankbaar plants.

There is a curious problem here in that Scott does not use the type illustration in his Revision and does not state any origin of the plant he uses to illustrate the species i.e. H. mutica.  As far as I am aware the type of a synonym that G G Smith described viz. H. otzenii , came from east of Riviersonderend, but this is for an Otzen collection no. 6.  The type was cited by Scott as Otzen 10 but this is not in the Compton herbarium where it should be.  So I am not sure offhand where that came from.  However, this is not really relevant to the discussion.  I just want to state that finding a plant that matches the type is no mean feat and that it was by sheer chance that in 1969 I came across a population of plants at Hasiesdrift that did.  See fig. 4 and 5.  I selected one image and then realized that it did not have round enough leaf tips to meet need, so I selected another.  In the first picture the leaves tend to have a “mucro” – a small point to the leaf that looks different to a well developed end-awn (bristle) that the leaves can also have.

Another issue is that Gerhard Marx once argued with me that the mooted H. groenewaldii was much nearer to H. mirabilis than to H. mutica as I had suggested.  What he luckily is able to ignore is my observation of the similarity of some plants of H. mutica to H. mirabilis see figs 5 and 6.  I never saw a plant quite like fig. 5 in all my exploration at Buffeljags but Jannie Groenewald collected this one there.  Fig. 6 is not typical of the population either and I used this same figure somewhere else in my writing to comment on the similarity to H. mirabilis ‘badia’ variants at Sandfontein (east of the “typical”).  Gerhard is still more fortunate to be able to ignore the similarity of H. mutica to H. retusa see figs 7 and 8.  I even surprised myself when in looking for a suitable picture, from many, I picked this fig. 7 and find it is also Hasiesdrift albeit a cultivated version.  (There is such an interesting story around the Hasiesdrift site).   Fig. 8 is a representive of H. retusa from Pienaarsriver pictures and I feel sure that readers will agree that the names could be switched.  It was very difficult to ignore pictures from Pienaarsriver that I could have used with figs 5 and 6 in the context of H. mirabilis.

It becomes still more interesting (I would have said complicated but my critics maintain that this variation confuses me and it is actually possible to get it all tidy and neat) when one further compares a plant of H. retusa ‘nigra’ ( fig. 9) with both H. mutica (fig. 7); and then H. retusa ‘nigra’ (fig. 10) with H. retusa (fig. 11).  The latter is in fact from the population where the variant ‘geraldii’  originates.

A last point I can make is that the leaf flecks said to characterize “H. groenewaldii” do occur in H. mutica at Klipport (see figs 12 & 13). One cannot simply ignore the extraordinary chain of similarities that extends across the entire distribution area producing only a slightly different situation at either extreme.

Floral difference is a great issue that is misused to force an opinion.  The flower is extremely difficult to study because the differences across the entire subgenus are so small.  There are complications where, as an example, flowers of H. pulchella ‘globifera’ are indistinguishable from those of H. cymbifomis var. incurvula.  In the subg. Hexangulares there is an incredible problem where floral differences within species exceeds that between species e.g. a flower of a plant of H. limifolia may more closely resemble that of H. coarctata rather than that of another plant of H. limifolia.  It is easy to draw conclusions from small samples of a few flowers from a few populations but one very soon finds that with increasing sample size the most carefully constructed table of differences becomes senseless.  Just when is an ever-aging flower on a stalk at the precise same stage of a flower you want to compare it with?  How many flowers from how many plants are needed to make a valid statement?  Do not forget that the observations must be made on plants on the basis of random selection too.  This is a requirement mostly totally ignored when the more serious question of a species difference is being debated.  That of course brings us back to this casual use of the word “typical” and its intractability.

The hardest problem to deal with is that of flowering time and on the face of it a winter flowering time versus a summer flowering time can be taken to suggest significant difference.  Yet if one considers that a species needs to harbour genetic variation to ensure adaptation to any kind of environmental change and so survival, a different flowering time may be an extremely useful resource.  Then we do have the reality of hybrids between species that do flower at these different times.  So obviously and self-evidently populations of species may exist that has arisen from such hybridization between plants that flower at different seasons.  The capacity of plants and animals to synchronize breeding periodicity is well-known.

I close with my observation that H. mutica is an assorted group of plants that seem to fall in some middle zone between H. mirabilis and H. retusa.  Hence in the west we have H. mirabilis/ H. mutica/H. retusa ‘nigra’, while in the east we have H. pygmaea (=H. mirabilis+H.retusa ‘retusa’) and H. retusa ‘turgida’.  In the area between there is vast variation of H. mirabilis and H. retusa that get a bit of H. floribunda thrown in too.

So am I confused, or have I confused you?  As Steven kindly put it…’it’s almost as if you were being blamed for nature’s complexities’.  Of course the ultimate reality is that we each have our own idea of what “species” are, and here I have used my version!

Volume 7, Chapter 5:- Still more Haworthia mutica and Haworthia mirabilis

It so happens.  Heidi Hartmann first visited the Karoo Garden more than 35 years ago and it has been very difficult for me to pay attention both to her mesembs and all my other plant interests.  In the last few years she has been working on Acrodon.  This is a small genus of only 5 to 6 species that occurs in the Southern Cape with much the same distribution and habitat requirements as Haworthia.  She had had some second thoughts on a species she had described as Acrodon calcicola and intimated that she needed photographs to show what proves to be detaching fruits (capsules).  So off we went to get that northeast of Bredasdorp at Rooivlei.  But Nick Helme had about a year before sent me an intriguing picture of a greenish soft looking plant from near the DeHoop Reserve entrance road to the east.  I had considered that it might be an equivalent of the H. muticaXmirabilis population at Die Kop (MBB7500) that Ingo Breuer usefully described as H. hammeri .  I use the name with great trepidation because to say what is correct usage is difficult.  It could pass as a cultivar name, a varietal name or a form name.  I am quite sure it has its origins in the interaction of two species and that is what a botanical name should reflect that; thus H. muticaXmirabilis or however else the nomenclaturists may require.  So these journeys are never without distractions as Rooivlei itself is a remarkable site.  I find that I have few images of the populations of Haworthia that occur there.  The product is nearly all pictures/images.

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Volume 7, Chapter 6:- Field trip to Van Reenens Crest and Niekerkshek.

M B Bayer, PO Box 960, Kuilsriver 7579, RSA.

The objective was to explore some likely habitats previously observed at Van Reenens Crest and nearby.   We extended the scope to include further exploration for Haworthia mutica as I am still questioning the place of this species in the greater scheme of things.  Thus here are four sets of populations that I report on viz. H. mirabilis, H. retusa ‘nigra’, H. floribunda and H. mutica.  See maps Figs 1 and 2 for geographical position.

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Volume 7, Chapter 7:- More on Haworthia mirabilis and H. mutica from east of Bredasdorp.

More on Haworthia mirabilis and H. mutica from east of Bredasdorp.

M B Bayer, PO Box 960, Kuilsriver 7579, RSA

The area concerned is the long and wide contact zone between the Limestone stretching from Bredasdorp to Potberg, and the Bokkeveld shale north of that.  The soils and vegetation of the two areas are grossly different.  The limestones are agriculturally almost useless, while the shales are prime wheat and pasturage producing soils although relatively low yielding.  The vegetation of the shales is Renosterveld and there are very few patches left.  Large areas resemble ecological deserts with nothing of the original surface intact.  Here and there are shale banks and associated quartz outcrops and also some remnants of tertiary deposits that overlie the shale.  Under this deposit layer the shale has decomposed to kaolin and in places there are gravel sheets of fine quartz on white clay.  The skeletal nature of these remnants is the saving grace but it is unbelievable to what lengths farmers must have gone to make fields arable.  Enormous amounts of stone that have been carted away and dumped to make cultivated lands.  Sadly the stone is often dumped on exposed rock and prime Haworthia habitat.  The remnants are still under threat and a mindset that has developed in the road construction and maintenance arena is that roads must be clean and scraped fence to fence.  Similarly there are farmers who want every square inch under control and in subservience to their production needs.  Dense vegetation is abhorred and burnt to control predation of sheep by jackal and lynx.  Vegetation adjoining crops is treated with weedkiller to minimize crop contamination.  Crops are also grown in conjunction with animal production.  When crops are in, the animals are on fallow land and on whatever is left of natural vegetation.   It is the harsh reality of conservation.

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Haworthia flowers – some comments as a character source, part 1

Haworthia flowers – some comments as a character source.

M B Bayer, PO Box 960, Kuilsriver 7579, RSA

Introduction:

The object of this essay is to discuss where we are now with respect to classification of Haworthia. Despite my comments and observations stretching over 50 years, there are still taxonomists writing and arguing on the basis of method and practice that generated the anarchy of names that existed at the start of my involvement. This method is what is probably referred to as “typological” i.e. there is a single herbarium specimen and anything that departs from this in some mind catching way is a different and thus needs a new name. At the generic level, recent DNA studies show that Haworthia is indeed three separate entities (the subgenera), and that these cannot be rationally separated from the aloid genera. Formal classification requires that Haworthia thus be subsumed in Aloe (see Treutlein et al, Rhamdani et al and Daru et al). This is both incomprehensible and anathema to writers and collectors locked into method that does not rest on any insight to what the problem of species actually is, let alone take proper cognizance of the problems that exists at generic level.

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Haworthia flowers – some comments as a character source, part 2

2. THE RACEME. Figures Set 2 show the bases of the peduncles in several collections to again show how variable they are and not only because of plant vigor and current growth conditions. Diameter can vary by a factor of three. Color is variable and the bract spacing and size of bracts as variables must be noted. Fig 6 is simply a robust spike in a population where the flowers were sparsely spaced on the stem with approximately 15-20 flowers per stem, whereas this raceme had nearly 30 flowers. The number can drop to as low as three. In 7917 we noted a single plant with an inflorescence of over 600mm where the average was below 300. Similarly at 7818 there was one colossal inflorescence of 800mm where again the average was between 300 and 400mm. There is a real problem in that the typological attitude is often adopted when making comparisons like this. An extreme example would be to take H. retusa south of Riversdale as typical of the species. These are massive plants (source of ‘Jolly Green Giant’) and the inflorescences are huge with many flowers. This is not typical for the species and especially so if one takes the mountain cliff populations (H. turgida) to be the same species (as I do) where the plants are proliferous and the inflorescences many and reduced. Plants in poor niches and even poor habitats, flower weakly and the inflorescences are reduced. Figs 7 shows varying capsule positions on the stem. Figs 8 and 9 show a distichous and a secund inflorescence and figs 10 to 15 demonstrate the varied spacing of the flowers that is observable even in any one population although the images are for two different accessions. In Fig. 8 the middle flowers are in a single plane and I regret not having observed the leaf arrangement in that specific plant, because this is a distichous arrangement as the low Fibonacci number of a spiral arrangement of the flowers. This may have been reflected in the leaf arrangement too. The spacing and arrangement of the flowers is also a variable and the number of flowers may also vary. Figs 16 to 18 show bud arrangement and the way in which the fish-tail buds have upturned tips. Although the peduncle does continue to lengthen, most of the lengthening takes place in the flower producing area and towards the upper end of the raceme. The peduncle does not always stay straight and may bend slightly at each floret. The number and distance of the flowers along the peduncle may affect bud packing just as peduncle formation in the rosette results in the appearance of a groove on the leaf face. This is a secondary physical phenomenon and is not an inherent “character”. The leaf keel for example may also be influenced just by physical leaf-packing. A peduncle of a flower from the centre of a plant will have a many angled base, but one arising from a leaf axel only 2-angled. Generally the raceme is indeterminate, meaning that it does not end in a pedicel and flower. But I have seen an individual raceme of H. floribunda with a terminal flower. This exemplifies our problem where characters one might think could be used to determine even genera, are variables at species level.

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Haworthia flowers – some comments as a character source, part 3

6. THE CAPSULES. Figs 6.1 first size differences that can be found within individual inflorescences. The remaining images show 8 capsules per population for a few populations to show variation in size and shape. The way the capsule ripens and splits is very variable. In some cases the capsule is pinched near the end but the locule tips flare outwards. This has the effect of seeds being retained in the capsule. In others the locules flare regularly and symmetrically from the base and the seed is all easily released. In the Van Reenen Crest populations the capsules were inclined to be a reddish hue. But colour can vary depending on the ripening process and they also bleach with time. Fig.6.4 7978 shows this in capsules drying after the peduncle was taken, and retaining their greenish colour. In H. floribunda the capsules are smaller and it appears that they may flare at the tips more in splitting and be coarsely crispate. This is not always the case but it is a tendency in the smaller capsules to do this. Fig. 6.7 is of capsules in 7910 H. floribunda, Rietkuil; compared against 7913 H. mirabilis also Rietkuil east of Swellendam. It is quite evident that even a capsule structure as apparently characteristic as in H. floribunda, is replicated in a different species. Fig. 6.8 is of 7955 Van Reenens Crest, and 7262 south of Greyton. I thought the capsules of 7955 were smaller, reddish coloured and slightly rougher than those of 7262. But the capsule structure in the entire genus is very similar to those shown on this figure and it is just not conceivable that some feature will stand out and resolve issues that exist in respect of the entire group.

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Haworthia marxii and H. truteriorum in relation to rational classification.

Explanatory note: In a rationalized list of names I wrote and had published in Haworthia Update Vol 7. I made two decisions. On of these was in respect of H. marxii and the other in respect of H. truteriorum. In the case of H. marxi I included it under H. emelyae. In the case of H. truteriorum, I placed this under H. bayeri. In neither case did I have good evidence for doing so, much other than my conviction that a classification is intended to reflect origins and relationships. In formalizing names one perforce is pressured into making decisions that you are not informed enough to make. My main defense is that the authors of the two species were not adequately informed either. I think their account of H. mutica (their H. groenewaldii) at Buffeljags demonstrates this. H. marxii presents particular problems that I simply do not have any substantial data that I can process.  In the case of H. truteriorum I did have some to which I can now add. This suggests as Breuer and Marx indirectly indicate, that H. truteriorum relates to my concept of H. mirabilis.   I concede that I may be quite wrong in attributing it to H. bayeri. I find it very difficult to see the decision to describe it as a distinct species as a logical scientific action. This article does not extol any imagined virtues or skills of mine. It is only intended to further project my opinion that we urgently need to work towards a classification that does satisfy scientific principle and not novelty or commercial ends. It is also a counter to some very negative opinion aimed in my direction.

At a level above classification lies respect for people and their feelings.  Therefore this writing should not be seen as anything but a commentary on the classification process and not how this can also denigrate people as much as honor them. H. marxii is described by Sean Geldenhuys in ALOE 44.1:5, 2007 from apparently 2 populations in a confined area in the north and east of the Little Karoo. Placing it with H. emelyae simply reflects doubts that need to be expressed about how this oddity has come about, and respect lost for reasons not necessary to explain. H. truteriorum is described by Ingo Breuer and Gerhard Marx in ALOE 48.3:54, 2012 and refers to a single population of plants southeast of Oudtshoorn. That this latter population is singular and extremely interesting goes without question except for how it is explained. Despite much correspondence with both authors and after reading their published works, I am not aware that either has a concept of what a species is any different than what may have been held by either K. Von Poellnitz or G.G. Smith. Ingo Breuer particularly has published what he refers to as a species concept of Haworthia. This is nothing more than a long list of Latin binomials and we have to assume that this is then also a list of real species whatever they might be.  Gerhard Marx maintains that my attempt at a species definition is so broad as to be meaningless.  He has not supplied an alternative definition and I am left with the impression that he makes the same assumptions that “character” differences equate species as does the ordinary uninformed mortal.

H. truteriorum is described in a popular journal (Aloe) that has been approached by at least one botanist not to publish new species as there is no official review process. However, the response was that the journal does have its own in-house authorities that cover the possibilities of scientific lapse.  I note that the article is specifically foot-noted to indicate an editorial review and I perforce do not see this as a check on the scientific content.  There are some lapses that I will deal with but recognizing that these might not be the same ones that a properly qualified botanist (a minimum of a recognized 4-year degree course), nor those that an experienced and knowledgeable botanical taxonomist may have corrected.  More important though is the population itself and where it fits into the overall Haworthia picture.

The most substantial gain that we can make is to arrive at a species definition.  It is evident to me that species are complex systems in which there are variations that have arisen from to earth differences and must continue to exist to facilitate response. If there is evolution and thus adaptation and selection, then there has to be something to work with.   The phylogenetic idiom was “specialization is precursor to extinction”.   Geological and habitat diversity result in plant diversity.  This diversity is necessary for survival as the habitat changes. Therefore a species will have a geographic distribution across which individuals and populations will vary and be different from one another. Geology and geomorphology will be strong factors influencing plants like Haworthia that are associated with skeletal soils and rocky habitats. This means that we have to look for associations in respect of distributions and the driving forces that affect even vegetation. Thus in the case of H. marxii (known from 2 populations in a small area south of Laingsburg) the vegetative appearance of the plants cannot be seen in any other species geographically closer than H. emelyae, which is quite a long distance away southwards. The presence of H. pumila in the same area as H. marxii suggests that the Haworthia presence there could extend from the Worcester/Robertson Karoo. Hence H. mirabilis, also present in the Montagu area, cannot be ruled out in seeking a relation to H. marxii. There is much more to this issue of H. mirabilis in respect of its variability and its distribution into the Little Karoo that impacts directly on this suggestion. It also impacts on the real identity of H. truteriorum.

Where I see a real problem with H. marxii is in floral morphology. I gather that the flower very much resembles that of H. marumiana dimorpha. In the same way that the flower of H. pulchella globifera is identical to that of H. cymbiformis incurvula at Plutos Vale, there is a massive problem in drawing conclusions from flowers as a character for the level at which all role players are trying to identify species. But so-much for H. marxii and I do not seriously question it.

The case of H. truteriorum is more manageable. I have been speculating for a long time that H. mirabilis and H. emelaye may in fact be the same species. This may be the proper level at which we should be recognizing species as systems. I extend the argument even to say that it is not inconceivable that H retusa and H. mirabilis are one species. This means that I have to bury my long-held objection to the view that “Haworthia is a genus in a state of active evolution”. My objection being that this is an obvious aspect and that in any case all species are faced with the inevitable need for change and adaptation. But this does not weaken my view that species are chaotic fractal systems that vary around a point of attraction according to the stability of their genetic bases and mutating rate. How strong I am on the technicalities of DNA and evolutionary theory may be problematic, but there is no evidence that other authors even contemplate the issues.

Gerhard Marx is a remarkable observer and I have huge respect for his many skills. Breuer is a really competent compiler too. I do not question what they say about the characters of the plants and their observations.  What I question is their knowledge and insight into broader botany and the distribution and variation in Haworthia however much more they know than the above average collector.

My prime objection is that the description involves a single localized population. This in itself creates huge doubts in my mind because on this basis, Breuer’s several hundred species is conservative. I will only dwell on three other points. The one is their very trite “Never before have retusoid type Haworthias been found growing in shale in the Little Karoo”. The second point is the habitat description in relation to geology. The third is the flower and flowering time. The fourth is about the illustrations and the art work.

Haworthia mirabilis was recorded in shale at Barrydale by Smith prior to 1947. It was recorded at two places in shale or shale derived soils prior to 1999 and I can add that I have seen it at two new locations in shale in the Montagu area since. The second point is the description where it is referred to H. bayeri and H. emelyae occurring in quartzite and quartzite conglomerates. As in the description of H. groenewaldii, this is simply a very crude and inaccurate account of a very important issue. I am no geologist but I do know what quartz is and that it occurs in both shale and sandstone formations. Furthermore, I do know that the Oudtshoorn area has an incredible geology with ancient and recent geological formations adjoining as a consequence of faulting and folding. Quartz is Silicon Oxide and is apparently soluble in water at high temperature and pressure formation so that it can accumulate in fissures and bands in parent rock. In both sandstone and shale the quartz varies in purity, and the crystals in size. South of the Langeberg the shales are covered in an extensive layer of tertiary gravels that are far less extensive north of the mountains. But the main point is that the vast quartz patches of the Little Karoo are actually associated with quartz existent in the Bokkeveld shale. The “species” need to be properly looked at in their relation to that complex geology that exists there.  Marx and Breuer mention the differences north and south of the Outeniqua Mountains. But the Outeniqua Mountains are just an eastern extension of the Langeberg from the Gouritz River gorge. The geology north of that area is quite different from that west of the Gouritz. This suggests an ignorance of geography added to that displayed for the geology.

Checking my own knowledge and experience of the habitats of the species involved (viz. bayeri and emelyae – with the name picta an anomalous insertion), it is very clear that the statement “quartzite and quartzite conglomerates” is erroneous. There are four geological formations involved and these are the Table Mountain Sandstones, Bokkeveld Shales, and then Enon and Tertiary deposits. In the Heimersriver where the H. bayeriH. emelyae and “H. truteriorum” are reported, lacks Enon presences. The report of the plants in unfragmented, unweathered upright shale (Bokkeveld) needs to note that the quartz patches in the area are the result of fragmented and weathered shale.

Marx and Breuer perhaps should also take account of H. outeniquensis not a great deal further south in an area that I believe is still unexplored. There is also the mystery of a plant found by Avril Schein in that close area that remains unexplained.

We know from the H. retusa /H. mirabilis interaction that flowering time is no barrier to hybridization and that flowering time may not be indicative of a completed speciation process.  Ignoring the fact that we can only guess, on the basis of the scientific paradigm, that we are interpreting and trying to understand an evolutionary process. Breuer has attempted to jump this issue by the recognition of “aggregates” and the two authors use the fob of “the mirabilis/maraisii/magnifica complex. This complex I presume is explained as a list of names only. This I do think emanates from a mis- understanding of a real knowledge of field botany generally and of Haworthia in particular. I say this with great emphasis and conviction because it is something I am still working towards. I have just completed a very thorough look at a the flowers of a very small fragment of populations driven by the expressed opinions of both these authors in diverse places, that flowers are significant with the import that I have ignored them. The fact is that if the flowers are considered then we have a bigger problem than before – not a solution. The flowering time of H. truteriorum that Breuer and Marx cite is very possibly an indicator of behavior rather than a species differentiator. Why they emphasize it is most probably, as J Manning pointed out, most observers (taxonomists) have a subconscious belief that species are things that do not interbreed and so flowering time is seen as such a great barrier to interbreeding that it MUST be a major species indicator. My observation is that this is not true and that species are inherently highly variable systems with great capacity to respond to environmental drama that may threaten their continued existence. The nature of the problem is very well illustrated in the case of H. retusa and H.mirabilis where I contend that a fully developed view of the genus may require that they be seen as one species. Thus the importance of flower and flowering time is part of the myth of a non-existent species definition and is confounded by the concept Breuer and Marx have of the nature of Haworthia species.

There is a very good description of the flower and its character, but the illustration and the art work is weak. The photograph of the flower is of a single dissected flower to show an internal structure that could be of any species in the subgenus and is hardly helpful. That flower does not look to me like the perhaps longer narrower flower of H. mirabilis (real) which is largely recognizable on the arrangement of the petal tips in the bud-stage.  This ‘mirabilis’ character should be apparent in the way the petal tips display and we have only a painting to judge this by. Despite Marx’s craftsmanship I am not sure if his flower picture is a true image. I do have an observation on with his outstanding art. Many years ago, photography was a bit of a handicap when it came to illustration of floral and other plant detail. Historically artists were used to capture detail that could not be described or otherwise illustrated. In the present age this is a bit of a myth and it lives on simply because of the skill that is involved in the production of a good piece of botanical art. Marx’s art is up there with the very best.  But good art does not equate to good science? Or does it?  Botanical art is perhaps not the same as pure art and the intent of either may be quite different.  With pure art one could surely be trying to achieve the same goal as science and there must be some trick to understanding the similarity.

My conclusion is to plead for more rational classification and better attention to those things that matter. The fragmentation of a genus by Latin binomials just because of collector and novelty interests, aggravated by commercial implications however slight, is a disservice to all of us.