Enigma 6. A change of title – predictiveness in science.

I get nowhere.

I started my talks in a recent visit to the USA with an amusing aside from Stephen Hammer.  I had asked him what the advertised title of my talks would be.  He said it did not matter because the titles of talks tend to mutate.  This new title and my old one viz. “The Haworthioid rocks of the Aspho Delay Sea” are however, one and the same through six different versions of this presentation.

John Rourke quoted to me  “The ship of many a taxonomist has been wrecked on the rocks of the Liliaceae”.  The thrust of my every presentation is that there is another sea which is incredibly and indescribably more turbulent and fraught with rocks, and shoals and perils of unbelievable magnitude.  This is the sea of human existence.  To quote some unknown philosopher “We are born in ignorance, we live in ignorance and we die in ignorance”.  The sea of human existence is a vast cradle of ignorance.

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Enigma 7. ICBN vs Larry C. Leach and Col. C.L. Scott.

No progress.

Abstract:
The presentation is intended to show that trial by the international botanical community has sentenced these two innocent people to death because they are INNOCENT of witchcraft (NOT guilty – to show this is clear and unambiguous as the ICBN may require).  M.B. Bayer is exempted only because he drew attention to this likely result in the case of Col. Scott, but simply stood aside and watched Leach trying to exonerate himself, and did nothing.

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Enigma 8. Does the ruling body of the ICBN know what it has done?

Abstract:
This presentation gives the answer to a rhetorical question asked as the title of a paper presented by Dr A. Cronquist (New York, 1988) to a conference of this august body:-

The question was ‘Do we know what we are doing?’
The answer is:-  ‘No.  Absolutely not.’  Because – To achieve nomenclatural stability, the strict implementation of the code requires a prophetic element beyond the reach of scientific prediction.  The code should be changed.

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Enigma 9. Does the ruling body of the ICBN know what it has done?

The text for this version is the same as for Version 8 with the addition of the following text:-

Literature cited:- The literature is practically that in:-
1998 Borgmann and Breuer, 12.3(79).

Add: 1986 Bayer, British Cactus and Succulent Journal 4.8:45.
1997 Smith, Bothalia 27.1:27.

The actual words to which I wish you to refer are:-

‘In later years Larry spent ‘far too much’ time on nomenclatural disputes………  Convinced that the International Code of Botanical Nomenclature could be improved, a number of proposals for amendation of parts of the code were unsuccessfully submitted.’
1997 Williamson, Aloe 34.1&2:30.

The actual first quotation from the work I use is this:-

‘Towards the last years of his life, he became bogged down in what APPEARED to be insoluble taxonomic problems.  His personal interpretation of the code led him into dark waters and he devoted much valuable time, that could have been more used more productively, to prolonged, stubborn argument.’

Enigma 10. Does the ruling body of the ICBN know what it has done?

The text for this version is the same as for Version 9 with the addition of the following text:-

MY CONTENTION IS:-
How ever real true professional do view and interpret the code, and the flexibility that it provides, this is not how it is seen and used by non-professional whether qualified academically or not.

Larry Leach was a perfectionist and hated being criticised rightly or wrongly for any mistake that he might have made – the code allows him to be criticised also for mistakes he did not make.  IS THAT FAIR?

Would he appreciate what these two friends of his who wrote his obituaries, have said there ?

I do not want this presentation on my behalf, but on behalf of these people whom I would like to see happy, alive or now gone.

Enigma 11. Titles of talks mutate – N+1

Abstract:
This presentation is to show that life is an everchanging mosaic (just like species), and if you are cast into the role of speaker at 2 weeks notice it may give you some problems.

Presentation:
The first title for my talk (i.e. Enigma N-1) was the “The Haworthiod rocks of the Liliaceae”.  This is based on what I thought my talk should be about, in terms of what the organisers would expect me to talk about, in terms of what the organisers would expect me to talk about.  It is what I might have talked about had I indicated my intention of attending the congress when it was mooted as far back as 1996.  I had no intention of being here, but by witchcraft or scientific prediction, I knew I would be.

Therefore I have a dilemma.  I have good reason not to give the talk expected of me and hence why I did not intend presenting one.  Therefore I have had to discover in my own mind, what are the pressures from within and without that bring me here.

I have come to know almost exactly what that pressure is through two weeks of blood, sweat and tears.  I accumulated some material for talks, which I think you as delegates should see, but I have already written or edited 10 versions of a presentation.

When I spoke recently in the USA, I was not sure what title I had submitted to the convention organisers at Omaha.  I asked Steven Hammer, and he said “Not to worry, the titles of talks tend to mutate”.  The title of my talk was given as “Haworthia – why controversy”.  I discovered in the 7 times I gave my talk, that it changed each time, but the title remained the same.  My talk about Haworthia and controversy could have been either the words of Steven’s advice, or my submitted title.  I discovered that both of them were equally relevant and apt.

In this case also I find I have given you a title for a talk and I would like to list other apt titles which I considered during preparation and after.  The following titles were considered on material available to me:-

1. Haworthia why controversy.
2. Astroloba corrugata – name game?

The following titles were a result of active preparation:-

1. Another open letter
2. The real enigma in Haworthia
3. The haworthioid rocks of the Aspho Delay Sea
4. The haworthioid rocks of the Aspho Della Sea
5. Cabbages and Kings
6. Predictiveness in science
7. ICBN vs Larry C. Leach and Col. C.L. Scott
8. Does the ruling body of the ICBN know what it has done?
9. Do. plus cited literature
10. Do. plus cited literature and postscript
N + 1. Titles of talks mutate – N+1
N + 2. (The presentation as on 31st August – unwritten)

At this point I now know that I should not give my talk at all

My talk is that I have nothing to say.

I have realised that I can now write what I must say.

I know why the congress organisers have invited me – they are people I respect and admire – I cannot say no to them.

BUT

I feel that there is a distinct body of delegates who do not know who I am, why I am here nor what is expected of me by the organiser.  I respect every one of those delegates too, known or unknown to me.

So I have come here to say nothing….BUT..PLEASE

SEE MY PAPER N + (N+1)

Enigma 12. N+(N+1) as the title of a presentation

Abstract:
In preparing for this talk in the short time allotted to me, I have tried to understand my own scientifically (intellectually) based prediction on why I am here, when I had no intention of being here.  In trying to write a presentation for you – out of my respect and liking for every single one of you – I have produced 11 (N) written versions.  In addition to this I have a presentation 12 (N+1).  In that final written version I will show that I have nothing to say, and that it may be pointles even saying it.  In reaching that point where I justify saying nothing, I see that I will never reach the end of N, and hence my title N+(N+1).

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Addendum 1. Haworthia – Where do we go from here?

(Written January 1986)

Col. C.L. Scott’s revision of Haworthia has recently appeared and I have seen three reviews of this book.  Both David Hardy (Aloe 23:52, 1986) and Michael Kimberley (Excelsa 12:107, 1986) quote Dr L.E. Codd’s introductory remarks to the book on Haworthia being a ‘complex and baffling genus’.  Infinitely more baffling is that, notwithstanding all the many words already written about Haworthia, we still remain so confused by them.  I did write a reply to Gordon Rowley’s Review (British.Cact.Succ.J. 3:?,1985) published in that same journal (4:45, 1986).  There is also an article in Excelsa (12:91, 1986) in which I touched on some of the attitudes that can be presented, and also complained that it is now barely possible to write about these plants without suggesting that someone is unsound.  Certainly that is not my intention and neither do I enjoy the suggestion that I am.

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Addendum 2. Notes of talk. Conference of the Mid-West Cactus and Succulent Society. Omaha June 1998.

I have not been very visible since 1983 and I need to try and explain why I am here.

It is by your invitation and at your expense, and frankly I wonder at my arrogance at assuming that I can meet the implications of this invitation.  I felt uncomfortable here (in USA) in 1981, especially at Albuquerque where my impression was that the audience wanted an entertainer and a performer.
I cannot fill that role.

Nevertheless, I am deeply conscious that I have some kind of debt and responsibility to you.  I am anxious to hold your respect and your affection – and to have some credibility when it comes to the real subject of my talk, hoping of course that it will impress itself upon your minds.

My role in Haworthia is this.  I grew up with J.R. Brown’s Succulents for the Amateur as my picture book.  I have been familiar with Haworthia since 1940 when I first started to grow them.  I tried to collect them seriously when I lived in Natal, but what I could obtain all looked very alike to me.  It is only when I landed up at the Karoo Botanic Garden that I began to understand the problem.

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Addendum 3. Haworthia – an approximation of a series of seven presentations given during the course of a short visit to USA June 1998, beginning at Omaha, Nebraska.

The title of the talk(s) was given as:-
Haworthia – why controversy.

As I was not sure if this title appeared on the Congress programme, I asked Steven Hammer prior to my departure for the States what title was advertised for my talk.  His reply was that I should not worry as the titles for talks of this kind tend to mutate.  In relation to my jaundiced view of Haworthia literature, I thought that this itself would make an equally good title for the subject of the talk.

I have come to the USA on invitation and the reasons I accepted this invitation are manifold.  Primarily I feel a sense of responsibility and duty to the subject; secondly I feel a sense of obligation as my interest in Haworthia owes much to the USA for the role J.R. Brown played in stimulating my interest in the genus, and thirdly I felt I ought to dispel the discomfort of the culture shock I had experienced in the USA when I visited it in 1982.

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Addendum 4. Salter’s revision of South African Oxalis (Oxalidaceae) and some new combinations from Herbertia 48 (1&2) – 1992

M.B. BAYER
Department of Agricultural Development
Winter Rainfall Region, Elsenburg (RSA).

ABSTRACT
The genus Oxalis, as it occurs in South Africa, is discussed generally in relation to the revision by T.M. Salter (1944).  A brief account is given of Salter’s collecting activities, the distribution and variability of the species, and the problems of classification.  Some new combinations are made.  Particular attention is paid to the section Pardales Salter, and all the 11 species recognised by Salter (many described by him) are combined in one species, namely Oxalis pardalis Jacq.  Two species, Oxalis dentata Jacq. and Oxalis lateriflora Jacq., are reduced under O. livida Jacq.  Similarly Oxalis urbaniana Schltr. and Oxalis callimarginata Weintr. are reduced under Oxalis goniorrhiza Eckl. & Zey.

Keywords: Oxalis, taxonomy, speciation.

Oxalis is particularly well represented in South America, and the species are also a very prominent component of the flora of the Mediterranean region of South Africa.  This region extends from Luderitz in Namibia, southeastwards to near East London on the southeast coast (Bayer, 1974).  Annual precipitation over this area varies enormously from as little as 100 to over 1400mm/annum.  The area is divided by Rutherford and Westfall (1986) into four distinct biomes on the basis of summer aridity, seasonal distribution of rainfall and on plant growth forms.  Both geology and topography vary enormously so that landscape heterogeneity and soil forms provide great habitat contrasts over short distances.  These factors, together with historical events, probably account for the richness of the Cape flora.  Despite the potential and realised weediness (for example: O. pes-caprae L. and O. caprina L.), many species are spectacularly colourful in autumn and winter and are useful and interesting as horticultural subjects.  T.M. Salter (1944) revised the genus on the basis of his own intensive collecting.  His interest in fact started in 1931, and, although he collected until 1957, serious attention to Oxalis continued only until 1942.

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Addendum 5. A harsh letter to Ingo Breuer

An edited copy of an unnecessarily harsh letter sent to Ingo Breuer, which includes a letter sent to Mr Harry Mays, editor of Haworthiad.  That letter commented on an article by Breuer published in Haworthiad and my reaction to it.  The comment was not for publication and was a request for assistance in countering bad and inaccurate writing.  I will make any apology for any offence and hurt I have caused by writing in this way, but I cannot apologise for anything which is true outside of my own thoughts:-

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Addendum 6. A review of the book ‘The world of Haworthias’ Vol.1 by Ingo Breuer, Niederzier, Germany,1998.

In my Haworthia Handbook (1976) I wrote “In the by now vast and inconsequential literature on Haworthia…”.  Breuer’s book is mostly an extraordinary and wonderful index of this literature and he advises us that “a hint on cultivation, caption or simple mention of a name” are excluded.  I did not fully realise how much trivial literature there was.  What I looked for in the book was its promise for Haworthia, and evidence that the author understood the literature he has so vigorously tracked.  In 1983 I took Haworthia as far as I could with the data and material that was available, and had some well-developed ideas as to what the next step was.  As it happened, Col. C.L. Scott’s book was published (1985) which inaugurated a tradition in Haworthia in which the scientific principle of organised scepticism is lost.  I wrote several articles trying to clear the cobwebs of uncertainty and confusion that this tradition embraced.  Apparently to no avail.  I am already aware of several articles which Breuer has authored and which have been the subject of some criticism.  For me they sow the seeds of concern for the future of Haworthia.

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Addendum 7. Is classification science or art?

A manuscript for the journal Asklepios.

Is classification science or art? Part 1.

The common reaction and assertion is that classification (of plants) is a matter of opinion.  It is also often stated to be an art, and even the late Prof.A. Cronquist in writing a book on the principles of plant taxonomy, describes it as ‘artful science’.  John Lavranos in a letter (1998), and an anonymous referee for SA Journal of Botany in an assessment of a manuscript, state that taxonomy is to a degree ‘art’.  It is necessary to examine this belief because it is intrinsic to our understanding of plants, the names we use for them and how we communicate about them.

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Addendum 8. A letter of disquiet to the Haworthia Society.

1999-10-21

The Chairperson
Haworthia Society
79 Osborne Road,
Sheffield
S11 9BA

Att.: Mrs Dorothy Minors.

Dear Mrs Minors,

Thank you for your very kind and considered reply to my letter of 22scd Sept.  My biggest regret is that I cannot put the names and faces together of all those real people that I met, and still meet, in my dealings with Haworthia.

I hope you have read the article I wrote which appeared in Asklepios recently.  Science is actually at a bit of a crossroads and this partly accounts for my own desperation and concern for what is true.  Science rests on classification.  Its fundamental weakness is its classification of creation into “conscious” and “unconscious”, and it deals only with the latter.  Science and materialism have become inseparable and falsely so.  Knowledge cannot be based on such a basic and false hypothesis that creation is a mindless chance event.  There is powerful evidence of an alternative hypothesis in a vast library of books and everywhere in human history.  What we presume to be science is materialism and there are profound cracks in the foundation.

During the last two years since I wrote Haworthia Revisited, I have done some very intensive revisiting and have some extraordinary material.  My problem is now to find an editor who is sympathetic to the position I find myself in.  Neither Aloe nor Haworthiad provide an environment in which I feel that I can write with diffidence and reservation; and that the audience is adequately and correctly informed to digest and judge what I have to say.  So it becomes pointless to say anything at all, and I am faced with the same problem that G G Smith ended up with i.e. invalidation.

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Addendum 9. Observations on cytology as a character source in Gasteria.

Introduction:-

The classification of Aloe, Haworthia, Gasteria, Astroloba and smaller related genera is in the public domain in the sense that there is an immense public interest in the collection and cultivation of these plants.  Unlike more general horticultural elements, succulents plants are of interest to collectors as natural “species”  and hence the taxonomy and nomenclature are central to the activity and communication which takes place in the collector citizenry.  Unfortunately the degree of interest and activity of competent (as opposed to trained) scientists (ie. botanists) has not reached the same degree and intensity.  The need for information and classification has by default passed to non-scientists/botanists.  A paper in respect of this topic is published in Asklepios (Bayer, Aug./Sept. 1999).  This particular article is written to further examine the nature of the data obtained by scientists and presented as such to the amateur community.  It is written particularly in the light of the conflict which has clouded the literature concerning Haworthia since at least 1947, and which continues unabated.

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Haworthia maculata ↔ Haworthia pubescens, MBB8002 Cilmor.

In Haworthia Update Vol 9 there is a report of a population MBB7997 identified as Haworthia pubescens from north of the Cilmor wine cellary. This is approximately 2-3km southwest of the type locality for the species.  I noted that the plants have less spinuliferous leaf surfaces and there is a degree of surface translucens and maculation (spotting). I also presented 3 pictures of MBB7271 of what I identified as H. maculata from south of the Cilmor cellar. When I first visited this locality I had no problem identifying the few plants I saw as H. maculata on account of their marked spotting.  However, on a recent visit we struggled to find plants at all and the few plants we found were too embedded in rock cracks to make any worthwhile identification.  So we revisited the site to explore more extensively and located a large number of plants higher up and slightly west of our first sightings.  These plants are illustrated here. They incline more to H. maculata than the plants at MB7997 and I have accessioned the population as MBB8002. There is the usual expected large variation in respect of superficial and observable characters. The plants can be proliferous and cluster, more so than at MBB7997. Similarly the leaves can have more translucens and even less spinuliferousness of the surfaces. Some plants have few and quite thick swollen leaves while others may have more and very slender pointed leaves. I have not observed the flowers and really do not expect them to make any difference to the problematic classification of populations that again are neither here nor there in a narrow concept of species. H. herbacea occurs at all four geographic positons at a radius of about 2km. At the brickfield to the northwest as well as just northeast of the Brandvlei Dam wall it is evident to me that there is a transition between H. maculata and H. herbacea. I did report the known distribution of H. maculata in Update 9.  While there is no suitable habitat between Die Nekkies hills at the Brandvlei Dam and the Audensburg or Kanetvlei, there is unexplored suitable habitat southwards to Moddergat and Hammansberg.  There is no evidence of H. maculata eastwards to where H. reticulata is known about 15km east on Ribbokkop.  Westwards no Haworthia is known although G.J. Payne did inform me that he had observed plants in the hills immediately southwest of the Dam at the now submerged hot spring in the Brandvlei prison area.

The submitted pictures include two views. View 1 is looking north of east across the Breede River to the Sandberg where H. pubescens occurs. Its full occurrence on those low hills is not known and this I will explore soon. View 2 is looking eastwards looking at a Dwyka Tillite hill across the river in the upper right. We found no Haworthia on that hill although both H. pumila and H. herbacea are present on the smaller rise to the right and behind it – also Dwyka.  H.herbacea is very abundant on a Dwyka tillite hill about 10km to the south. The corresponding hill on the left is Ribbokkop where H. herbaea, H. reticulata and hybrids are present, and H. arachnoidea also occurs. The limits of H. mirabilis are the higher hills in the background viz. Rooiberg, Gemsbokberg and those are Witteberg sandstones.

Addendum Haworthia pubescens MBB8011, SW Sandberg

Addendum.  H. pubescens MBB8011, SW Sandberg.

I need to point out that there is a still earlier article which covers Haworthia maculata (Haworthia maculata <–> Haworthia pubescens) that lays the basis for this discussion.  In that article I note the position of the Sandberg to Cilmor and DeWetsberg and intended to include the Sandberg H. pubescens in that article.  We could not get landowner contact and so that fell away.  However, this problem was overcome and we first explored a Dwyka Tillite outcrop southeast of Sandberg.  There is a vast accumulation of windblown sand on the first hill and we saw no Haworthia.  There is a smaller hill further to the southeast that is also Dwyka and erosion exceeds wind deposition so smaller non-geophytes do quite well.  We found both H. herbacea (see fig.1 MBB8014) and  H. pumila there.  From there we went to the southernmost point of the Sandberg.  A misjudgement landed our vehicle in mud and the drama to get out limited the time we had to explore.   We found a lone H. herbacea (fig. 2 MBB8012).  Returning a week later we approached the Sandberg from the southwest, and almost immediately on reaching the top we found H. pubescent.  Fig. 3 is a view towards Cilmor and DeWetsberg where the plants appear to be intermediate H. pubescens↔H. maculata.  The picture is useful to get some idea of the role of geographic and geological considerations.  The high mountains in the background are Table Mountain Sandstone and no Haworthia is known there.  I am not certain that this is true and G J Payne did tell me that he had seen plants on the extreme lower right and south of the Brandvlei Dam.  But also on the absolute distant and absolute left, is the Riviersonderend Mt.  That is also TMS.  The deep Wolfkloof Valley behind that is the locality for the much unexpected H. herbacea ‘lupula’.  (These inverted single commas are not entirely necessary but I use them to underscore my informal use of names that have less reality.  The var. lupula is real).  The mountains ahead of that last line are Hammansberg on the left and the Moddergat to the right.  Between there and DeWetsberg has not so far turned up Haworthia, but this is an exploration problem.  Behind the DeWetsberg is also underexplored.  H. herbacea does occur between DeWetsberg and behind the mountains on the low right just in the picture and also east of the brickfield out further right.  H. maculata is only known in this area along the Nekkies north (further to the right) of the Brandvlei Dam just visible in the picture.

Prior to this exploration H. pubescens was to me only known from the northern part of the Sandberg that lies south of a road going eastwards to Eilandia between Worcester and Robertson.  Here H. herbacea does occur on the lower northwest warm slopes.  H. pubescens seems to occur only on the upper two ridges and H. herbacea is not known to intermingle with it.  This is all Witteberg Sandstone that as a formation overlies Bokkeveld Shale and underlies TMS.

Coming back to the southwest corner of the Sandberg where we found H. pubescens.  The plants seem very similar to the species as it occurs to the north.  They were very cryptic and often in shady rock retreats where they were really hard to see.  It was mid- to late-morning when we were there and the plants were not going to be better exposed as the sun moved further west.  Although there was very suitable well-drained habitat lower down on the shaded east slopes, there were no plants and I speculate that this may be because the plants may need the cooling effect of wind movement up on the ridge.  The pictures tell the story of variability in respect of a whole range of leaf and rosette characters.

It is worth noting fig. 43 of the dead remains of a plant under a clump of restioid.  It seems that seedling survival is closely coupled to early protection giving rise to the concept of nurse-plants.  Plants are often very difficult to find because they are so hidden beneath accompanying vegetation.  But they do need light and the dynamics of vegetation growth and densification must have quite a big impact on the ageing and survival of plants.  It raises again the question of how long do the plants live?  For plants like Aloe ferox and A. dichotoma I do have a real experience of a lower limit of about 35 years and a top limit in the several hundred.  In  the field, the plants seem comfortably ageless.

The really interesting part is this.  While I was busy tediously cleaning a plant to photograph it, Daphne called to me to come and see a lighter green plant she had seen.  Moving in that direction I saw a plant that registered as H. herbacea but with some hesitation and doubt (see fig.4).  I then went to see what Daphne had observed.  They seemed less obviously H. herbacea but that seemed to be a logical and conservative opinion (see figs. 5-11).  That was until Daphne found two adjacent rosettes at the foot of a restioid clump that left me in no doubt that they were hybrid H. pubescens/maculate (see figs 9-12).  These were in bud whereas H. pubescens plants showed no sign of impending flowering.  Note the buds are less well developed than MBB8014 further east, even if possibly insignificant.  Going back to the other plants we confirmed my doubts.  They were a lighter colour and apparently softer texture that we would have expected in H. herbacea.  These were the only plants we saw in a space bridging the occurrences of plants of H. pubescens.

12-46 MBB8013 H. pubescens, SW Sandberg.

We did not explore the western slopes where habitat would have been more suitable for H. herbacea and I expect it does occur there.  What puzzles me is that so frequently have I found very distinctive hybrids between species in close proximity and very seldom where the species are some distance from one another.  I cannot say I have ever found a hybrid in the clear absence of both parents.  The example of Astroworthia bicarinata at Lemoenkloof, east of Barrydale, may be an exception where only Astroloba corrugata (syn A. muricata, A. aspera) is present but H. pumila apparently not.  Hybridization is thought to be an important element in the “evolution” of new species.  I doubt this as it is quite evident that separation into two species is a pre-requirement.  If new species have evolved in Haworthia by hybridization, how did they evolve as such in the first place?  The answer to me lies in the continuities between populations.  I observe, and have experienced of expected continuity between populations.  While the Cilmor populations are thought to be H. pubescensmaculata it cannot be said anymore that they are hybrid, or populations where the morph or drift to discrete elements has not reached a conclusion.  The latter is more likely.  As there is already apparent geographic continuity of H. maculata and H. herbacea, I was expecting some evidence of a similar relationship between H. herbacea and H. herbacea.  So here it is.  Hybridization as a factor in speciation in Haworthia does not seem to very likely.  It confirms for me that there is a fractal “chaotic” order to species in Haworthia and the reality is that a view of many truly discrete species is a fabrication and a very ill-considered view.

Acknowledgement:

We are always greeted with such kindness and helpfulness that we might have expected this from the Sandberg landowners too.  It came in no small measure.  Driaan Griesel was most enthusiastic and interested and also helped us with extracting our vehicle from the mud on the one occasion, and then jump-starting it after a flat battery on the second.  Our imposition did not so much as touch his view of the day.

(ed. – Bruce made another visit to Southwest Sandberg on 9 December 2012 and includes the following flower pictures.  He makes this comment; personal correspondence 27 December 2012.)

I am actually not sure at all about flowering time now.  I used to be quite sure of being able to collect seed of pubescens mid-Nov.  But I observed at Humansdorp that gordoniana peak flowering could be out by 6 weeks.  In  any case the plants can produce successive spikes so one can get delayed flowering and added to that energy in the first or the second flower set.  I know mirabilis at MacGregor can flower from Nov. thru to March while at Montagu mirabilis can flower as late as April/May.  Retusa and geraldii are quite happy to produce flowers in either Spring or Summer and Kobus observed that splendens did that too.  Maculata can flower from Sept. thru to late Dec.  And each population does its own thing.

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Genetic history – the place in Haworthia classification.

Preamble: Maybe the difficulties and strife in Haworthia classification is that we do not know what it is that taxonomists do. Taxonomy is the academic discipline of defining groups of biological organisms on the basis of shared characteristics and giving names to those groups. The scientists that do taxonomy are called taxonomists. The names taxonomists give to species don’t just tell us what they are called, but also tell us about how they are related to one another. In the following article Bruce Bayer shares his views that Haworthia taxonomy should be about more than identification and descriptions, rather the interpretation of the characters that reveal genetic relationships and evolutionary pathways. ~ Lawrence Loucka, 7 September 2012

Genetic  history – the place in Haworthia classification.

By M. B. Bayer

This is a huge subject and I cannot by aptitude or knowledge attempt to cover it fully.  However, it is so basic to plant classification and Latin naming that we all need to have some background understanding.  The entire object of classification boils down to arranging living (and once living things) in a scheme that follows the theory of an evolution from simple life forms to the present array of creatures.  This is because it is thought to be the logical way in which knowledge of the said creatures should be organised i.e. according to the way in which they traveled the creative way.  All classification is simply a way of organising information so that one can generalise from the singular to the plural.

Whether one believes in such a progressive process or in a spontaneous divine creative event does not matter.  All the evidence points to change of some kind and if we call it evolution does not alter anything.  It is argued that there is in fact no direct proof that, say, man evolved from a primitive primate.  That may well be so, but there are many fossil primates that are speculated to fill that gap. The case is that evolution is a scientific hypothesis and science does not, or cannot claim, that this is proven.  A scientific hypothesis simple stands as a possibility or probability of something known.  Such a hypothesis can only be proven untrue, and then it is replaced with a new hypothesis that stands as the accepted truth.

Whatever, the ultimate truth of the matter, classification in science is directed at reflecting how the different life forms are related to each other in respect of change?  In the acceptance of evolution the process of change is the genetic history of the organisms and is referred to as the phylogeny.  It is often depicted as a branching tree with the branches originating low on the trunk as ancient origin, to terminal branching for recent.

My experience with classification comes with education and qualification in entomology (insects).  It so happens in insects (and higher animals) that there are many characters and structures that can be used to examine the process of change and modification that might go with evolution (change).   The word “homology” is used.  So, say, the wing of a bird is likened to the forelegs of a dog – they are said to be homologous structures.  The change in structure from that of a segmented worm (eg. Onycophora) to say, a wasp, can be tracked through a whole range of insects.  The head of a wasp is seen to be derived from 6 primitive body segments, the thorax from three, and the abdomen from several.  There are muscles and nerve endings and sub-segments that are all evidence of these connections.  In entomology, there was a stage when a qualification in insect classification required the student to also present a phylogenetic scheme to explain relationships relative to an origin. This all based on morphological characters, their homology and their interpretation as primitive or advanced.  What is really odd is that too often a classification comes to deny the variability that a concept of selection and adaptation that evolution rests on, is denied.

In plants there is no luxury of musculature, or nervature or even detailed bone or segmented structure on which to base good homology.  Botanists are therefore very hard-pressed to properly derive phylogenies or explain this genetic history.  Nevertheless a very serious and honest effort is done to do this.  The process of cladistics was derived from entomology (Hennig) and became the standard for the student in botanical classification.  Students were required to evaluate characters on a basis of primitive and advanced, and construct cladograms that illustrated a hypothesized process of evolution.  The advantages of the method over conventional decision making were that it is said to be an objective way of arriving at a conclusion rather than personal subjective decision making.  With the complaints against my use of words and language, it is worth noting the remarks of a leading botanist who said that the methodology of cladistics was just the use of a new language that did nothing more than strain good-will.  Agreed.

With the arrival of DNA sequencing, a whole new ball-game was created with each amino-acid base pair representing a character.  So DNA sequencing has become the modern standard for the construction of phylogenies and genetic history – the phylograms.  So much so that the article in Taxon 56:645-648, 2007 by A.B. van Wyk argues that the phylogram represents the process of phylogeny as the genetic history as opposed to the cladogram that attempts to construct the genetic history.  I personally think that this is intellectual wizardry and the literature references in the Taxon article only expose the mystery that surrounds classification.  It takes classification wholly out of the reach of any but a polymath.  Basic to the whole issue is that scientists still have not reached any certainty about what a species is.  The theory of evolution is not disproved.  Van Wyk has said

Plant taxonomy, despite all its impressive achievements towards phylogenetic reconstruction, will then risk being denoted as yet another ivory tower science – a pursuit disconnected from the practical concerns and needs of everyday life, esoteric, over-specialized, its classifications of little practical use to the majority of end-users”. 

It sounds very impressive, but I weep for the fuel that it adds to the fire of ignorance.

What truly appears to be the case to me is this.  To construct a cladogram, the taxonomist needs to be very familiar with the plants and have a good understanding of the characters being used in the process; adjudging them according to some scale of advanced or primitive.  The DNA sequencing method requires no knowledge of the plants at all and a phyllogram simply follows a statistical analysis of equivalence of the base pairs.  What I see is DNA derived products that so far tell me no more than I already know about the genera, and nothing at all about the species other than some serious mismatches.

I argue for a species definition, not as some vague statement that species are things into which a genus can be divided, or simply a list of names under a Latin genus heading, or the zoological concept of closed breeding systems.  My definition drawn from a lifetime of interest, observation and experience in things material as well as esoteric, is that the creation is a conscious one.  This is not a new idea of mine.  The conflict between religion and science is that the one maintains that creationism followed some sort of seven day event as in the book of Genesis.  Whereas science (as we practice it today), has its origins in the quest for freedom from any such religious belief system.  Whether creation began as a big bang, and complete or incomplete does not matter to me.  We are faced with natural phenomena in the present that we can observe have changed and are changing.  I do not think either the cladogram or the phylogram is anywhere near good enough as an answer, because they are two-dimensional diagrams that do not adequately portray the realities of time and space.  Not only that, a three dimensional improved tree model will not show how fast things change within a time span.  My model of the species tree is a fractal model that suggests species in a process of “chaotic” order.  By the word fractal I mean the endless variation that seems to have no order.  While I insist that the concept of a species of Haworthia must mean the same as the concept of a species of insect or frog, or bird or mammal, I do not mean that each species of Haworthia has the same branch clarity on any tree depicting relationships.

What I do not know is how fast populations might change in the process of genetic drift i.e. move off in a direction determined just by the local genetic content.  Neither do I know how much nor how frequently interchanging of genetic material between populations occurs and how this is affected by distance between them.  In the field there is a very distinct flow of difference (or similarity) with geographic spread.   I have repeatedly found that with widely separated known populations, new populations between them are predictably intermediate.  It does not seem entirely rational that there are not more random isolated individuals.  My experience with hybrids is that they are very local to the mother plants while any populations tend to be very confined and local.  What is odd is that hybrids may be found despite great differences in flowering times of the parent species.

The reality in Haworthia, however we define species, is that there are populations that are neither one taxon nor another.  If the classification were to present a basic requirement that ALL populations known and unknown must fit the model, then definitely we have to consider that there are considerably less species than other writers are prepared to consider. One can continue building a classification from the top in which each new population is simply described as something new and given a Latin binomial. This process was suited to the origins of botanical exploration as well as nomenclature. It does make it a lot easier for collectors and the exciting process of always novelties for the collector.  Alternatively one can decide that classification is by this stage a fully predictive one and one that must primarily suit the requirements of botany. If only botanical classification was more professionally and rationally based.  Sampling is very extensive and a classification based on the known, is predictive.  Personally I am very comfortable that I have achieved this in large measure – not entirely, but close enough and a lot closer than some critics will concede.  With all that said and done, it is just a sad fact that formal classification is too often undertaken by people who have a need.  That need may satisfy them within the limits of their personal experience and knowledge, with an uncomfortable disregard for the depth of knowledge elsewhere.

Reference:  Readers can refer to the article in Haworthia Update Vol.2:149 (2006) “Nectar sugars in the Alooid minor genera and a need for another model”.  That article is also posted to the internet with much of my other writing in HaworthiaUpdates.org.

Haworthia mutica (groenewaldii) and its twisted leaves.

In this article Bruce Bayer responds to the notion that apparent leaf twist arrangement is a defining characteristic and further explains his disagreement in recognizing the Buffeljags plants as a new species.  (Also see Haworthia flowers – some comments as a character source, Volume 7, Chapter 4:- What is typical Haworthia mutica?, and Volume 7, Chapter 2:- Further exploration in Haworthia. Further to finale.)  The species definition Bayer uses is that populations are fractal and DNA is governed by mathematical non-linearity.  What does that mean?  We have space with two dimensions latitude and longitude, and we have time with two dimensions – calendar time, and the speed (instability) of the arrangement of the DNA base pairs.  At any moment in linear calendar time there will be an arrangement of the DNA depending on the stability of the DNA.  At one time there will be a clear set of ‘species’ and at another time a different set as the mix of characteristics continually change within and between the populations.  ~ Lawrence Loucka

Haworthia mutica (groenewaldii) and its twisted leaves.
By M.B. Bayer

There is some argument about the status of this population of plants at Buffeljags.  I have explained my opinion of it based on a species definition that I use.  I also have reported on three other populations a short way away at Rotterdam.  Furthermore I have discussed the flowers at length in a flower report.  These are all available free on Haworthiaupdates.org.  Gerhard Marx does not agree.  The disagreement first has its roots in what constitutes a species and Marx stays with the standard view that characters are what define species.  I opt for the view that species are systems related to geographic distribution and to all the elements that drive vegetation and change (evolution + equals change from some unknown initial condition).  I think these patterns of change and difference are fractal i.e. detailed pattern repeating itself.  Perhaps it would be more correct to say that the organization of pattern is according to a mathematical function which is non-linear.  This means that the end product has many different outcomes.  But this is complexity just of argument that none of us can deal with.

What comes into the geographic nature of species is also the nature of habitat.  What happens is that we have a set of apparent species in Haworthia with a known distribution range.  These species are primarily H. retusa and H. mirabilis.  There is clear evidence that H. pygmaea  and H. mutica emerge from a milieu of populations of those two and that H. floribunda is also involvedBuffeljags is geographically central to this arrangement and the habitat (wrongly described in the description of H. groenewaldii) is very unlike those where the named species generally occur.  It is thus no surprise that the plants appear different.  The Buffeljags population and its habitat also differ to a small degree from the west side of the river, but both are essentially geologically fairly recent river alluvial deposit.

Marx is insistent that the plants at Buffeljags are so different as to be a discrete species and I disagree.  My disagreement is based on my experience of characters in plants.  In Haworthia I think these are few and obscure.  Thus it is almost impossible to delineate or circumscribe a species by characters and no one has succeeded in producing an identification key that can work.  All the differences of opinion and argumentation about names come down to this issue of a species definition and the characters available to recognize them.

The essential points made for H. groenewaldii as a species is the shiny leaf surface and the flowering time.  H. mutica does flower four  months earlier – agreed.  But H. marginata in the same close area also flowers similarly out of synchronicity with H. marginata elsewhere, as H. minima was also observed to do.   In elaborating differences for H. groenewaldii, Marx offered the facts that the plants had fish-tail buds and that H. mutica did not.  Very soon after he stated that he did not actually know what the case was in H. mutica.

 Fig. 1 to 9, MBB7801 Haworthia mutica (groenewaldii), Buffeljags.

In addition he maintained that the leaves in H. groenewaldii were different as follows…”In terms of the angled newer leaves of H. groenewaldii, have a look at the plants again and you’ll see the young leaves are consistently twisted sideways.  A spiraling effect. This never shows up in H. mutica”.  I find this statement very odd because  such a structural difference would come down to a difference on the level of genus or even family. So I looked at the plants I have in my possession and provide illustrations here to demonstrate no significant deviation in respect of twisting.  I have even included a picture of a mature plant (fig. 10) of H. mirabilis to show the same “character”. The spiralling effect is universal in the aloids and is even visible in those species with distichous leaves.  In the retusoids, where H. mutica belongs, the leaves have been said to be 5-farious. More usually it is possible to see them as trifarious.  In young seedlings the leaves are bifarious as the very basic  spiral effect comes into play.

I do not think this is a character one can use to distinguish a species at all. There are many cases where it is fairly possible to characterize populations by a wide range of so-called characters. My opinion is that generally in the many species (by my definition) of Haworthia this can virtually only be done at individual plant level. The Buffeljags and Rotterdam populations are simply the western counterparts of populations around Albertinia (eg H. mirabilis ‘splendens’,  H. pygmaea ‘fusca’, H. pygmaea ‘esterhuizenii’) that emanate from the relationship of the prime species that I named above.

Comprehension and significance

My writing has been described in all kinds of terms, hermetic and pretentious being two of the adjectives used.  Recently Kris Tamayo also suggested that he had trouble understanding what I wrote or write.  The fact is that writing and expressing yourself is difficult.  But the first place is to be clear about what you want to say.  Or is that in fact the first place?

Writing is a means of communication and it really only should start when you are clear about what you think and what you want to say.  Then it requires that the listener is clear about what he/she wants to hear and has the common cultural heritage that permits communication and understanding to occur?

In writing and talking about plants I personally get very frustrated by the technical problems of definition and knowledge that mess up communication completely.  This is one of the obstacles in classification where there is no species definition and we do not actually know what species are.  There are a lot of other obstacles.  Recently someone wrote and implied that there were a lot of significant differences among Haworthia that could be used to arrive at a better classification (than any already available).  The point I would make is that this person has his own idiosyncratic view of what significance means.   This is not strange at all because a prominent scientist was once applying the statistical measure of standard deviation to two and three measured samples.  That measure probably cannot be used until many more measurements are made.   What is taken to be significant may be quite irrelevant to the actual question of whether there are more or less species.  This is why amateurs and collectors should keep clear of classification.  The professionals already have too many problems.

The characters we use to make identifications are important in that they may be of the yes and no kind i.e. present or absent, or they may be graded from vague to prominent.   So it is very easy to go to one end of the scale and take only the prominent or what happens to strike your eye.  This is exactly what happens.  Unless followers and interested parties realize the impact this sort of decision making affects what they may want to know and understand, there can never be any harmony and peace in the classification process.

Look at these flowers and see what you can glean from them…

 

These just happen to be the only three flowers I have of a few plants of Haworthia herbacea from recent sampling.  They are shown here in correct proportion to one another with the third being 18mm across at widest spread of the two upper outer petals.  So we have two things we can call characters i.e. size and colour that we could say in respect of this simple sample,  that they are significantly different.  No matter how many times or how we measured these two things, this fact would stay the same.  The plants happen to be from two populations and we can then ask if this is true for those populations.  I did ask such a question of both H. herbacea and H. reticulata, and ended up by learning that I needed a sample of about 200 flowers to arrive at a statistically true answer at a probability of 95%.  The thing is that I could go a little further south and sample another population and get a really pink flower with a spread of 25mm or more  that would nearly double the spread of my measurements.

There are several incidentals here.  One is the delineation of the mouth into the tube of the flower.  Why is it so clear in the third picture?  The second is that the first flower has not opened as flat across the face as the other two despite being at the same expected state in respect of time from opening.  The third is that the name “subregularis” was used in this genre of flowers because the petals are so equally spread; perhaps less-so in the middle picture.  Still a fourth curiosity is that in the southwestern species with the more extreme biarcuate bud with the fish-tail tip, is how the tips of the upper outer petals are “replicate” – i.e. the margins tend to fold together.  In the Worcester/Robertson Karoo particularly H. herbacea and H. reticulata have the “regular” flower shape.  But in H. mirabilis in this area, the upper outer petals may be held in a plane directly behind the inner outer petal and do not spread at all.  There the bud tip is still fish-tail and the upper outer petal tips very replicate.

 

 

Haworthia flowers – some comments as a character source, Appendix 5

Appendix 5.

Haworthia mutica, Sandrift, Drew MBB8018 = KG226/70 = JDV92/64

This is an unusual population in that it is the most northwestern one known although only about 15km from Klipport nearer Stormsvlei.  It is the source of the single plant that developed gross milkiness and for which I coined the name “Silver Widow”.   The population was first recorded by a Mr Meiring who worked as a nurseryman for the Bonnievale Nursery of Hurling and Neil in the years at least prior to World War 2.  There is a letter in the Compton Herbarium archive which records a transaction between Meiring and Triebner of 100 plants as 1s ea (i.e. = 10cents in today’s currency.).  I really struggled to find plants again in a very disturbed area  and eventually did so after I had placed “Silver Widow” there in her pot to see if the flowers would be pollinated in situ.  Indeed they were and then found about 20 plants in a very small area nearby.  This visit owes to the report by Jakub Jilemicky of still more plants a very short distance again from these.  Here there are about 80 plants in an area of about so many square meters.

Illustrations of the plants and flowers are given.  The only comment I can make is to repeat that I never ignored the flowers out of ignorance.  The fact is that we have a number of pretentious experts who have no concept of species other than an inherited vague notion that species have something to do with the capacity to interbreed.  The fact that Haworthia plants do so freely does not handicap their enthusiasm for new species either.  So this is a bit of irony.  My contention was that if you did consider flowers there would be a lot less species than even in my conservative approach.  In fact I am quite sure a competent professional taxonomist might well consider that I have been too generous with species and too kind to my critics.

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Die Nekkies Haworthia – A further visit and updated information

Bruce Bayer has now been back to Die Nekkies and returns with more detail to add to the broader Haworthia maculata picture, and considerable detail for H. maculata at its home range located north of the Brandvlei Dam on a low range of hills named Die Nekkies.  (See Haworthia Updates Volume 9, A myth corrected to – Haworthia maculata var. livida (Bayer) Bayer – and flowers ignored). These low hills extend for 10-12km east to west along the north shore of the Dam. They are geologically Witteberg Sandstone and H. maculata is not known off this formation except in the lower Hex River Pass where it is found in Table Mountain Sandstone.  H. herbacea (and H. reticulata) are more abundant on the Dwyka Tillite, and on Bokkeveld and Ecca shales. The Wiiteberg is sandwiched between Bokkeveld Shale and Dwyka Tillite, and Ecca Shale of the Karoo System overlies Dwyka Tillite.  Because of considerable faulting and folding the Cape Terrain is geologically and topographically very broken and there are a multitude of skeletal rocky habitats – the raw rock is very exposed and the surfaces are erosional. Haworthia are rarely found on depositional sites. The fact that there is also a stable and dependable winter rainfall also contributes greatly to the success of small succulents in situations that cannot maintain high biomass levels. This all drives home the fact that Darwin’s dictum that distribution is the lintel to understanding species is doubly true for Haworthia where morphological differences are minimal.

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Haworthia maculata leaf tips, faces and backs

Die Nekkies – a selection of Haworthia maculata plants with their leaf faces and backs showing variability over this extensive area.

I took the following photographs originally just to show how much the leaves varied in the species. The only locality data record was Die Nekkies with no differentiation into populations. The variability was firmly established and became apparent even within populations where the degree of variation surprised even me. It was also extrapolated across the genus.

As an afterthought, this turned my mind to Farden and Smith’s observation about the idiocy of trying to make varieties in Haworthia attenuata on the basis of leaf characters where the individual leaves varied so much that several varieties could be detected from the same plant. This is exactly what Breuer, Marx and Hayashi are actually doing when they get carried away by their justification for new species, drawing conclusions from single plants because of the inability of the mind to hold many images. This is exactly the way in which “H. magnifica” is maintained as a species when the imagery is based on the original single plant originally described. There can be no such thing as “H. magnifica” because the variation across the range of populations from Riversdale to Riviersonderend is so immense and complex.

The following photographs show a random selection of plants and their leaf faces and backs from Die Nekkies. These were taken some time ago when I did not record actual populations. They do record the variability of plants and leaves over this wide area which I classify as Haworthia maculata. For subsequently photographed plants I have recorded my population collection numbers which are indicated on the map found in Die Nekkies Haworthia – A further visit and updated information.

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Bontebok Park Haworthia floribunda and SW Klipport Haworthia mirabilis

I was at Bontebok Park south of Swellendam this week specifically to get another look at Haworthia floribunda there and why it is so different. On the way I did some exploring at Stormsvlei about 25km west of Swellendam where I know H. mutica Klipport in a shale environment, and a very odd H. mirabilis growing on a small patch of manganic conglomerate. But going south onto the northern slopes of the Bromberg we found three populations of H. mirabilis in sandstone that are again “different” in the sense that “H. groenewaldii” could be different from H. mutica. This is just a local geological phenomenon and fully sequential with H. mirabilis to all compass directions. If you extrapolate this to Swellendam you have to conclude that the Swellendam mix of H. floribunda, H. marginata, H. minima, H. floribunda, H. mutica and H. retusa is the way it is because of the unusual geology of the area. The Bontebok Park is a relatively massive area of tertiary gravel of mostly river origin and derived from Table Mountain Sandstone. Tertiary gravels east and south are derived from silcrete and ferricrete. I do not know the detail of the mineralogy but it most definitely forms the basis of the soils, vegetation and habitat across the Southern Cape. I specifically looked at H. marginata in the park and see that it was in seed i.e. September flowering with massive capsules and seed. Now if Marx can persuade someone that this is a different species, I accept that I am a monkey’s uncle and that the differences in H. marginata elsewhere e.g. Drew, Bredasdorp and Heidelberg or Riversdale, mean there are several similar species. Oh, I forget – that means H. floribunda would also be several species, and so is H. minima. But then H. mutica is of course several species and H. retusa several dozen. H. mirabilis several hundred.

This is 8017 from the Bontebok Park Swellendam. In some circles I am expected to get excited and see this as something new. In the context of the Haworthia in the wider area, this is a variant of H. floribunda. In my flower report it is evident that there is not much difference between the flowers or flowering time of this species and H. mirabilis. It hybridizes with H. retusa, H. retusa (turgida), and H. pygmaea despite differences in flowering time, and also with H. mirabilis. There are populations that I think are an older product of such hybridization (or failure to have ever separated).

Typical – an over-used comment. A white small glasss ball is found and named “Marble alba”. Then a red one is found and named “Marble rosea”. Then several other colours turn up and “rosea” is lumped under “Marble alba” as a variety. Automativally all the others become “Marble alba var alba” if they are not specifically named or not put under “rosea”. If “rosea” had started as “Marble alba var rosea”, there would automatically have been a “var alba”. All other glass marbles known and unknown would have been “var alba” even if no another white marble ever turned up. A type just establishes a name and the best way to determine how that name is used by an author is by ALL the illustrations and pictures he/she notes. A type that establishes a name may be an oddity or a single variant that does not easily establish a use. The advice handed to me by a group of taxonomists in 1972 was that it would be best to scrap all the old Haworthia names and start again from scratch. The group was led by Prof Schelpe, one of the few professors who as a taxonomist headed the department. He had explained this view in a published article in respect of Gasteria and why he rejected the idea of personally revising the genus. He had no solution for types and names that could not be directly linked to a set of herbarium specimens or similar evidence. Now substitute H. mirabilis for marbles alba and where the contrast of white and red is absent.

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Just what is the type form of H. mirabilis and what constitutes H. magnifica? That is the subject of my question about the way in which the typical variety is recognised. There are 4 populations of H. mirabilis in the Park and many to west, east and south. Imagining that there is also a “maraisii” is just crackpot even more so to say “magnifica”. There is quite definitely one system that you can see from many populations and that system inter-twines with two others also on the basis of many populations. At this stage of the available information on these populations there are a lot less species – see also the article Haworthia flowers – some comments as a character source published in Haworthia Updates Vol. 8 by Alsterworthia International. I also started off thinking that there was an H. maraisii and an H. magnifica but changed my mind quite early. In the last ten years I have come to see that both they and H. heidelbergensis are nothing but parts of one system viz H. mirabilis. Ask the authors who think otherwise to present some clear evidence based on good random sampling and statistics. See the Haworthia Updates Vol. 4 article Some variation in Haworthia mirabilis var. sublineata by Loucka and Bayer on the stats of H. mirabilis (sublineata).

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Klipport is a farm a bit off the beaten track on the north side of the Bromberg low range.  Bromberg is the eastern end of the Riviersonderend Mountains and is cut off from them by the Riviersonderend River that changes direction to the north to do so and then east again to join the Breede River.  Bokkeveld shale is strata-wise above the sandstone of this mountain range and a small amount of shale is present here on the south bank of the river.  At Klipport it is a narrow sloping stretch of about 500m long and about 75m wide with white gravel and clays.  The vegetation it totally different to the grassy fry Fynbos and renosterveld of the Bromberg and has karoid succulent vegetation with the endemic Gibbaeum esterhuysdeniae and a Brianhuntleya species.  The site is also home to a smoothish form of Haworthia pumila, and also to a range of  H. mutica variants that might have a name attached by now.  Another very interesting species there is Drosanthemum micans. This species has an extraordinary range of variation that parallels that of Haworthia and at Klipport is moving to another face as D. lavisii.  It would be very instructive if other Haworthia taxonomists could, or would, take note of this kind of parallel and recognize that there are significant clues to how Haworthia species and their variations are part of a larger pattern.

This small shaly area has a very patchy distribution of the species on it with patches of a restioid and Pteronia.  Through some weird quirk a German immigrant ploughed up a vast area of very marginal virginal  land and planted gums and pines that after 30 years are still far from harvestable.  I doubt if they will ever yield anything.  This happened under the eyes of Nature Conservation and the Dept of Agriculture that is supposed to manage land use.  The area on the river itself was paradoxically a source of timber in the early Cape days and is now severely infested with exotic gum and wattle.  It is this riverine growth that sustains the timber enterprise of the adjoining farm Vaandrigsdrift.  Not far away between the shale and the sandstone is a manganese deposit that is now being mined.  At the end of this deposit is a tiny set of large conglomerate-like rocks with a variant of H. mirabilis.  This species also occurs as an interesting ecotype a short way further east where the shale is less transformed along the sandstone interface.  In fact I do not know exactly what it it is that has driven this decay of Bokkeveld shale to kaolinic and bentonitic clays where it has been covered with Tertiary marine deposit at some stage in geological history.  Whatever it was, is certainly significant with respect to island-like habitats and “conserved” vegetation remnants.

MBB8028 H. mirabilis SW Klipport

MBB8030 H. mirabilis SW Klipport

MBB8031 H. mirabilis SW Klipport