Haworthia Revisited – 56. Haworthia venosa

56. Haworthia venosa (Lam.) Haw., Revis. :51(1821).  Bayer :166(1976).  Scott, Cact.Succ.J(U.S.) 50:74(1978).  Bayer :76(1982).  Scott :35(1985).  Aloe venosa Lam. Encycl. 1:89(1873).  Type: icon, 80:t29, Commelin, Prael.Bot. (1703).  Epitype (B&M): Swellendam, Bayer 168 (NBG):  Aloe tricolor Haw., Trans.Linn.Soc. 7:25(1804).  Type: as for H. venosa:   H. recurva Haw. Syn.Pl.Succ. :94(1812).  Haw., Revis. :51(1821).  Aloe recurva Haw., Trans.Linn.Soc. 7:10(1804).  Simms Bot.Mag. :t.1353(1811).  Salm Dyck, Monogr. 7:f3(1836).  Type: Cape, Masson.  Not preserved.  Neotype (designated here): icon, f3, Salm Dyck loc.cit.:  H. distincta N.E. Brown, Gard.Chron. 6:130(1876).  Type: Cape, Graaff Reinet, Bolus (K):  H. venosa var. oertendahlii Hjelmquist in Bot.Notiser :233(1943).  Type: Not known.

venosa: veined.

Rosette usually stemless, slowly proliferous by off-set or stolons, to 30mm tall.  Leaves to 100 X 15mm, spreading to recurved, ovate-deltoid, upper surfaces smooth reticulate, lower surfaces usually slightly scabrid.  Inflorescence sparsely branched, lax.  Flowers tepals fused, tube straight, lower inner tepals revolute.

1982 – Originally the writer concluded that the name ‘recurva’ should be applied to what was generally known as H. tessellata.  Scott (1978) insists on recognising three discrete species in this context and rejects the name ‘recurva’ as insufficiently known.  After propagating H. venosa ssp. venosa from seed and seeing the extraordinary resemblance of the seedlings to the illustration in Simms Botanical Magazine of H. recurva, the writer is prepared to accept Salm‑Dyck’s statement that H. recurva was in fact grown from seed of H. venosa.  The writer cannot accept Scott’s arguments regarding the status of the three subspecies listed above.  Firstly the ssp. granulata is not confined to Verlatenkloof.  It occurs at various points in the Ceres Karoo and there is a considerable variation in caulescence, leaf markings, and growth form.  These variants do thoroughly confuse the issue as it is impossible to lay down definite criteria to consistently separate the subspecies.  The ssp. venosa occurs in the Breede river valley and the variation here is also great.  In the northern population the plants may have leaves up to 120mm long whereas a population (since destroyed) has been observed in the south with leaves less than 30mm long.  In the field the leaves of the plants are invariably erect, whereas in cultivation they tend to recurve.  The ssp. tessellata is extremely widespread occurring in South West Africa, the southern Orange Free State and at high altitudes near New England and Barkly East in the north‑eastern Cape.  There is no cytological evidence available to suggest that the subspecies are discrete.  Most chromosome counts are for ssp. tessellata, which does include polyploids, one count is available for ssp. venosa and none for ssp. granulata.  Recent chromosome counts by Brandham (unpublished), confirm that normal diploids occur in all three subspecies.  There is such a grey area of indeterminate forms that it is considered wiser to adopt a concept of subspecies for this group.  The essential differences are that in ssp. venosa, the leaf surfaces are obscurely or lightly reticulate on the leaf faces, in ssp. tessellata the reticulation is pronounced, and in ssp. granulata the plants are caulescent and the leaf faces both scabrous and obscurely reticulate.  Cultivation does not pose any particular problems.  The ssp. granulata is from one of the driest areas in South Africa bordering on the winter rainfall area.  It is very slow growing and also slowly proliferous by off‑sets.  The ssp. venosa occurs in a dry area of the winter rainfall area and, while acaulescent, does form small clumps.  Ssp. tessellata is very variable.  It occurs primarily in the summer rainfall area and may be vigorously proliferous and also stoloniferous, or only slowly proliferous by offsets.

1999 – No changes are suggested here except to concede to repeated suggestions that H. woolleyi also be included in this species.  There is an interesting record of Dr J. Muir of Riversdale from the Albertinia area which suggests that the ssp. venosa occurs in the Gouritz River valley.  Scott considers that H. distincta did not originate from Graaff- Reinet as N.E. Brown maintained.  This may be correct but it is rather ironic that the pressure to include ssp. venosa and ssp. tessellata under one species arose from repeated comments on the similarity of forms of the latter at Graaff-Reinet to the Breede River subspecies.

a. ssp. venosa.

Distribution: 3420 (Bredasdorp): Swellendam (‑AB), Bayer 168 (NBG); Bontebok Park (-AB), Bayer 3453 (NBG); Breede River (-AB), Fouche 60 (PRE); Malgas (-BC), Bayer 2670 (NBG).

Inadequately located: Swellendam, Theunissen (BOL); Albertinia, Muir (BOL).

b. ssp. granulata (Marl.) Bayer :120(1976).  Bayer :120(1976).  H. granulata Marl., Trans.R.Soc.S.Afr. 2:39(1910).  Scott, Cact.Succ. J(U.S.) 50:74(1978).  Scott :9(1985).  Type: Cape, Verlatenkloof, Marloth 4217 (BOL).

granulata: granulate.

This subspecies occurs virtually around the perimeter of the dry Ceres Karoo both in the higher rocky mountainous areas as well as on the flats among spiny Mesembryanthemaceae.  It is usually caulescent and the stemless forms seem to be more scabrid.

Distribution: 3219 (Wuppertal): Skitterykloof (-DC), Bayer 4669 (NBG).  3319 (Worcester): N. Karooport (-BA), Hall in NBG827/54.  3220 (Sutherland): Ganagas Pass (-AA), Bruyns 274 (NBG).  Ouberg Pass (-AD), Bruyns 2750 (BOL); Bantamsfontein (-CC), Bayer 5750 (NBG); Verlatenkloof (‑DA), Marloth 4217, 9632 (BOL), Scott 2200 (PRE), Hall 3168 (NBG), Stayner in KG309/68 (NBG); 60km N. Matjiesfontein (-DA), Scott 2201 (PRE).  3320 (Montagu): Touwsriver, Avondrust (-AC), Bayer 4668 (NBG); Witbergsrivier (-BD), Joffe 964 (PRE).

Inadequately located: Roggeveld, Logan (BOL); Wakloof (-BB), Hardy 2467 (PRE).

c. ssp. tessellata (Haw.) Bayer.  Bayer :149 (1976).  Bayer :76 (1982).  H. tessellata Haw., Phil.Mag. 44:300 (1824).  Scott, Cact.Succ.J. (U.S.) 50:74(1978).  Scott :37(1985).  Aloe tessellata (Haw.) Roem.et Schultes, Syst.Veg. 7:653 (1829).  Salm Dyck, Monogr. 8:t1 (1836).  Lecotype (Scott, 1985): icon (K):  H. parva Haw., Phil.Mag. 44:301 (1824).  H. tessellata var. parva (Haw.) Baker, JLinn.Soc.Bot. 18:211(1880).  Aloe parva Roem.et Schultes, Syst.Veg. 7:763(1829).  Salm Dyck, Monogr. 8:t2 (1836).  Type: Not preserved.  Neotype (designated here): Icon. :t2 Salm Dyck, Monogr.:  H. tessellata var. inflexa Baker JLinn.Soc.Bot. 18:211 (1880).  Type: ex hort, Kew.  Not preserved:  H. engleri Dint., Neu.Pfl.D.S.W.Afr. :31(1914).  H. tessellata var. engleri (Dint.) V.Poelln., Feddes Repert.Spec.Nov. 44:202(1938).  Type: S.W.Africa, Ussis-Schulucht, Engler in Dinter 3156:  H. pseudotessellata V.Poelln., Feddes Repert.Spec.Nov. 27:133(1929).  Type: Cape, Kruidfontein Rail, Mrs van der Bijl.  Not preserved:  H. tessellata var. tuberculata V.Poelln., Cact.Succ.J(U.S.).5:33(1936).  Type: Cape, DeRust, Mrs Helm.  Not preserved:  H. minutissima V.Poelln., Des.Pl.Life 11:193 (1939). H. tessellata var. minutissima (V.Poelln.) Viveiros (1949).  Type: Cape, Cradock, Fouche in Triebn. 1212.  Not preserved:  Neotype (B&M) icon, Des.Pl.Life 10:193 (1939): H. tessellata var. elongata Van Woerden, Succ. 22:37 (1940).  Type: Namibia, Pevelberg, Graesner in Dresden 2205.  Not preserved: Lectotype (B&M): icon in Succ:38 H. tessellata var. simplex Resende et V.Poelln., Broteria 11:49(1942).  Type: ex hort Coimbra.  Not preserved:  H. tessellata var. stepheneana Resende ibid. :50.  Type: Cape.  Not preserved:  H. tessellata var. luisierii Resende ibid. :51.  Type: Cape, Queenstown, Triebn. 1207.  Not preserved:  H. tessellata var. palhinhiae Resende ibid. :51.  Type: ex hort Dahlem.  Not preserved:  H. tessellata var. velutina Resende ibid. :52.  Type: ex hort Hamburg.  Not preserved:  H. tessellata var. coriacea Resende ibid. :52.  Type: Cape, Port Elizabeth, Long.  Not preserved:  H. tessellata var. coriacea fa longior Resende ibid.  Type: Cape, Long.  Not preserved:  H. tessellata var. coriacea fa brevior idem. :53.  Type: Cape, Long.  Not preserved:  H. tessellata var. obesa Resende ibid. 54.  Type: ex hort Dahlem.  Not preserved.:  H. venosa subsp. recurva (Haw.) sensu Bayer :149 (1976).

tessellata: square patterned.

This is one of the most widespread and also abundant of the haworthias.  It is extremely variable, which is usually the case with any of the less localised species.  Motohashi et al. have examined chromosome numbers in this species and found polyploidy to be common.  Hexaploids and octaploids appear to dominate the northeast, while tetraploids do so in the northwest and southeast.  The number of chromosomes does not materially affect the appearance of the plants.

Distribution: 2623 (Vryburg): Vryburg (-DC), Vermeulen in KG108/60 (NBG).  2716 (Rosh Pinah): Schwarzekuppe, Aurus (-CB), Bruyns 3198 (NBG); Namuskluft (-DD), Bruyns 3926 (BOL), Bruyns 3171 (NBG).  2723 (Kuruman): Matlaring River (-AB), Acocks 2510 (BOL,PRE).  2724 (Taung): Buxton (-DB), Brueckner 1207 (PRE); Klein Boetsap (-CD), Pocock (BOL).  2816 (Alexander Bay): Hellskloof (-BD), Leighton 2333 (BOL). Augrabies (-CB), Marloth 12525 (PRE).  2817 (Vioolsdrift): Helskloof (-CD), Smith 6814 (NBG); NE. Eksteenfontein (-CD), Littlewood in KG955/62 (NBG); Kouefontein (-CD), Bayer 1661 (NBG).  2818 (Witputz): (-CA), Smith 7506 (NBG).  2820 (Aughrabies): Aughrabies (-CB), Leipoldt (BOL); Kakamas (-DB), Fuller 134 (BOL).  2821 (Upington): Wegdraai (-DD), Smith 2342 (NBG).  2917 (Springbok): Gunhill, Anenous (-BA), Barker 8966 (NBG); Arabees (-BB), Smith 1680, 1686 (NBG); (-BC), Meyer (BOL); Kinderle (-BD), Smith 7276a, 7277 (NBG).  2918(Aggenys): Aggenys (-BB), Oliver, Tolken & Venter 55 (PRE).  2922 (Prieska): Marydale (-AA), Smith 1677 (NBG); Prieska (-DB), Bryant 576 (PRE).  2923 (Douglas): Mazelsfontein (-BA), (BOL). 3.6km NW. Campbell (-DC), Leistner 902 (PRE).  2924 (Luckhoff): Belmont (-AD), Lang 6854 (PRE); (-DB), Freund 44 (BOL).  2925 (Fauresmith): Jagersfontein (-CB), Smith 7486 (NBG); Koppies (-CB), Henrici 1956 (PRE); Veld Reserve (-CB), Marloth 13104 (PRE); Veld Reserve (-CB), C.A.Smith 536 (PRE); Veld Reserve (-CB), C.A. Smith 5208 (PRE); Koppie (-CB), Verdoorn 2372 (PRE).  3019 (Loeriesfontein): Jaagvlakte (-BD), Bruyns 3037 (BOL).  3022 (Carnarvon): Vaalhoek (-CC), Bruyns 3034 (NBG).  3023(Britstown): Omdraaisvlei (-AA), Smith 2343 (NBG); Brakfontein (-CB), Smith 7280 (NBG); Twyfelhoek -DA), Bruyns 3021 (NBG); Vloekpoort (-DD), Bruyns 3018 (NBG).  3024 (Philipstown): (-AD), Battenhauser (BOL); De Aar (-CA), C.A. Smith 2809 (PRE).  3025 (Colesburg): Philipolis (-AD), Smith 7478 (NBG); Bethulie (-BD), Smith 5182 (NBG).  3026 (Aliwal North): Kraairivier (-AB), Smith 6063 (NBG); Tussen Riviere (-AC), Roberts 5570 (PRE); Murraysville (-CD), Smith 7412 (NBG); Doctors Drift (-DA), Gerstner 58 (PRE).  3027 (Zastron): Vegkop 11km W. Zastron (-AC), Fouche in PRE 34871; Karnmelksrivier (-CA), Smith 5669 (NBG).  3119 (Calvinia): Ezelskop (-AA), Bruyns 6841 (NBG); Koppieskraal (-AB), Pearson 4887 (BOL); Vanrhyns Pass (-AC), Bolus 1206/32 (NBG), Smith 3943 (NBG).  3120(Williston): Hamberg, Syter (-AD), Branch 333 (NBG).  3123(Richmond): Victoria West (-AC), James in NBG925/13 (BOL); Nuwerus (-CD), Bayer 4677 (NBG).  3124(Hanover): Cypherwater (-AD), Bruyns 3007 (BOL); Tweedale, Noupoort (-BB), Branch 38 (NBG).  3125 (Steynsburg): Flouker (-AC), Branch 39 (NBG); Rooispruit (-AD), Smith 6056 (NBG); Schoombie (-AD), Smith 3639 (NBG); Thebus (‑BC), Latimer in NBG 69408, Smith 610, 3636, 3637 (NBG).  3221 (Merweville): Aarfontein (-AD), Bruyns 6276b (BOL).  3222 (Beaufort West): Karoo Park (-BA), Branch 34 (NBG); E. Molteno Pass (-BC), Bayer 2372 (NBG); Road to Loxton (-BC), Scott 350 (PRE); Stolshoek (-BD), Bruyns 3383 (BOL).  3223 (Rietbron): Nelspoort (-AA), Bayer 2385 (NBG), Stayner in KG767/60 (NBG); Redcliffe (-BA), Bruyns 7055 (BOL).  3224 (Graaff-Reinet): Aberdeen Road (-CD), C.A. Smith in PRE 8888.  3225 (Somerset East): Mt. Zebra Park (-AD), Branch 33, 40 (NBG); Halesowen (-BA), Bayer 4667 (NBG), Reynolds in NBG2552/33 (NBG), Smith 2240 (NBG).  3326 (Grahamstown): Committees (-BB), Dyer 2172 (PRE).

Inadequately located: Sunnyside, Beaufort West, Esterhuysen (BOL); Aliwal North, Reynolds 112, in NBG2399/32, in NBG 2401 (BOL); Graaff Reinet, Bolus 794 (BOL); Aberdeen, Ferguson (BOL); Ex hort., Van Nouhuys in PRE 34853 (PRE).

d. ssp. woolleyi (V.Poelln.) Bayer comb.nov.  H. woolleyii V.Poelln., Feddes Repert.Spec.Nov. 42:269(1938).  Bayer :168(1976).  Bayer :79(1982).  Scott :40(1985).  Type: Cape, Springbokflats, Woolley in Long 440.  Not preserved.  Lectotype: icon (B).

woolleyi: after C.H.T. Woolley.

1982 – When evaluating species rarity, H. woolleyi is seldom called to mind.  However, there are only two recorded instances of its ever having been collected.  The writer’s own record is of a single large clump growing completely hidden within a spiny shrub on the northern face of a rocky outcrop.  The relationship is obviously with H. venosa but it has many more leaves per rosette.  These are inserted closely on the stem so that the plant form is very like that of say H. attenuata.  The leaves are obscurely tesselate and also long and slender (up to 60mm long.).  Cultivation appears to be difficult and growth extraordinarily slow.  Although a clump‑forming species, offsetting is very slow and it is as quick to propagate this species from seed as from offset.

1999 – There are still very few records for this subspecies and this may either reflect its rarity or the general lack of systematic and conscientious recording.  There is no doubt that many collectors have roamed the area to the chagrin and annoyance of the local farmers.  The population known to me was very sound up to at least 1980 when I recorded at least six large proliferous clones.  Soon after this an attempt was made to protect the area by changing the fence-lines.  This appears to have been a total disaster as the new fence either placed the plants within the farmer’s grazing camp, or concentrated stock against the fence just where the plants existed.  Whoever may have been so cloddishly stupid to have been able and willing to eradicate (by collecting) the proliferous clones that I knew, is inconsequential now.  The moving of the fence, coupled with overgrazing (using the term to mean exerting grazing pressure to the extent that gross erosion ensues), or perhaps only the latter, has resulted in total destruction of the habitat.  The site is overgrown with weedy Mesembryanthemaceae and Atriplex lindleyi.  Also where there was a small but healthy number of H. sordida and some hybrids with H. woolleyi in a stable, vegetated ravine, there are now just erosion gullies and weeds.

Distribution: 3324 (Steytlerville): Springbok Flats (-BD), Woolley in NBG 1990/37 (BOL), Long 1442 (PRE); Kleinpoort (‑BD), Bayer 167 (NBG).

Volume 5, Chapter 11:- What is Haworthia schoemanii?

Among a plethora of new names, are two really interesting items.

Firstly there is a really useful formalization of a host of old names by Gordon Rowley. This is something that I understood to be taken as unwritten truth and logic. While so sensible and practical it almost widens the gulf between the ordinary way we use names to communicate, and the unreal world of formal taxonomy. I will just give the one example to demonstrate this viz. H. coarctata subsp. coarctata, var. grandicula ‘Baccata’, or H. coarctata subsp. coarctata ‘Grandicula’ ‘Baccata’. This is a probable botanical truth where in the end there is a population (yet to be formally identified) in which all the plants despite any variability are ‘grandicula’ and something in cultivation (and not wholly improbably in some similar incidences, two quite different clones) that on the available evidence seems to have been drawn from the same population, which is ‘baccata’.

The second item is the name H. schoemanii.  Described by M. Hayashi in Haworthia Study (9:14, 2003), it was said to have one of two close allies viz. H. woolleyii and an H. crausii. This latter ‘species’ I did not know, or of. Gerhard Marx kindly sent me the picture that appears in Haworthia Study (4:8, 2000) and I really do not know why this is compared with H. woolleyii. I would say that it also collapses in the same way and into the same place as ‘Schoemanii’. Most of the other new names I have been able to assign with very little stress into my own understanding of the system of plants that falls in Haworthia. However, the illustration of this plant and the comparison with H. woolleyii, again stretches the limits of credibility. It was said to have been collected on a hill near Dwyka Station. I must confess that the report that Hayashi found this species by himself is one I find very hard to accredit, being familiar with his modus operandi and field familiarity. When I was at Dwyka station myself I was under the impression that the plants had been collected by Paul Schoeman for whom it is named. Had I known the facts I would have been even more skeptical that it had in fact been collected there. It is said to have thinner and shorter leaves than H. woolleyii and the stem not to elongate as in H. granulata. I consider this to be fairly threadbare stuff in as much as the number of leaves is not brought into the equation and neither is the variability of H. granulata. At Skitterykloof, Avondrust and Karooport, the plants do not form stems as they do in Verlatenkloof or the Koedoesberg. At Patatsriver the plants are stemless too and the leaves are fairly thin and erect (This may be the source of ‘Crausii’). A Harry Hall collection from Skitterykloof was of stemless plants with very long and thin leaves. I would not say that H. woolleyii makes dense clumps by rhizomes as Hayashi states. But it does have many long thin leaves broadening of course at the base. It does cluster, but by offsetting aboveground and very close to the crown of the plant as does H. attenuata for one. This can barely be stated to be rhizomatous, which implies an elongated self-rooting horizontal stem with food storage. The term stoloniferous is applicable to the underground trailing stems or even root-like structures that eventually manifest as new rosettes and that occur in several Haworthia species. Plants with elongated stems can also be found in H. venosa subsp. tessellata and stoloniferous forms are also common.

Anyone else who really and genuinely wants to understand plants in the context of relationships and a realistic classification is now faced with the same problem as myself and one of some magnitude. That magnitude is of course only measurable in terms of individual knowledge and experience of the South African vegetation and geographical reality.

Where now is Dwyka Station? It is between Beaufort West and Laingsburg and centre to an area that barely raises a blip in the context of the species rich South African flora. What happens there geologically, geographically, historically, botanically? I am not going to attempt to answer the question in any detail except to comment that there is absolutely nothing in my own database to suggest that there could be any new species of Haworthia there – of any kind, – let alone one that looks so like ‘woolleyii’ by author statement and by my own imaging of the illustration.

Firstly one has to consider that ‘woolleyii’ occurs as a single known population east of Springbokvlakte far to the east and south. It has other species associations there. Secondly it is vested in the classification of H. venosa for the very reason that it has an uncomfortable resemblance to the subsp. ‘tessellata’ (the fact that this classification of subspecies is in doubt is irrelevant and is only as valuable as the ‘looks like…’ observation).

Now I did not find anything in my very brief visit to Dwyka Station itself except to confirm my view that there is absolutely nothing there to suggest an environment in which something as fundamental as a different Haworthia species could ever have evolved or survived in terms of vegetation and historical changes. Hayashi writes that he found five clones on “the mountain slope near Dwyka station”. The slope at Dwyka Station barely passes mention as that of any mountain and is mostly contained in rail reserve that is severely impacted on. I should add that we could only identify Dwyka station by virtue of the abandoned ganger’s cottages and there is a possibility that Hayashi was referring to the power substation about a kilometer away where we also looked. There may be a few plants there at either place but it was extremely dry and the absence of any other vegetation of any interest at all discouraged anything else but a fairly brief but intensive search by the three of us. In my experience, Haworthias never occur in such depauperate environments. So we went a little further west to near Koup Station, rather than spend time trying to access ownerships and nearby hillsides that could have been more fruitful than immediately Dwyka Station. Koup is of course the location for H. arachnoidea var. scabrispina, fig. 6, and also for H. nortieri (Oh dear!) var. pehlemanniae ‘Albispina’ (?) or should I have written H. nortieri var. globosiflora ‘Pehlemanniae’ ‘Albispina’. Remember that H. nortieri ‘deVriesii’ (in the bounds of a more realistic language) occurs at Prince Albert to the southeast.

I was accompanied by my wife Daphne, whom I mention extremely reluctantly in the crucible of a fairly dubious lot of writers, literature and connotation. She has a mind and eye uncluttered by taxonomic perturbations and has developed a vegetation penetrating and interference defying Haworthia locating radar. So at Oskopvlakte west of Koup she found plants that must surely explain H. schoemanii. What is as unpeculiar about Oskopvlakte and Dwyka Station is that they are on the boundary of the winter rainfall biome and the edge of the Succulent Karoo domain within that. (I deliberately correct the formal botanical concept of the biome status of the Succulent Karoo where history and causation seem to be confused). While Daphne was finding haworthias I was looking at Conophytums, Pelargoniums (the obligate winter rainfall growers) figs. 6-7, as well as other species familiar to me such as Astroloba bullulata, and thinking “Yes, this is Tanqua Karoo stuff”. Then Daphne called me. What is the plant she found? Wholly reminiscent of  H. venosa subsp. granulata, figs 1-5, that is known to me from only about 12 widely scattered populations on the periphery (refugial and mountaineous) of the Tanqua Karoo. The nearest populations to Koup (Oskopvlakte) east of Laingsburg are at Avondrust southeast of Touws River, and Patatsriver WNW of Matjesfontein. Distance can be said to be a factor, but not in view of the overall distribution of H. venosa and its allies in any taxonomic dispensation. To my jaundiced eye ‘Crausii’ could equally easily be explained by these Oskopvlakte plants.

So for the collector I would suggest the label as simply H. ‘Schoemanii’, without the ‘H’ and even without the capital ‘S’, and most importantly of all, without any derogation of the late Paul Schoeman who was well known to me and against whom I have no ill-will of any kind. My only complaint is that his name has been dragged into the realm of botanical reality in the way that it has.

I actually have no interest whatsoever in taxonomy and nomenclature apart from their evil necessity. I just felt it was incumbent on me to make known some of the obvious problems of identification and use of names in the sphere of plants that I like. So this foray out of retirement is simply necessitated by an original motivation that can never go away any more than that the name ‘schoemanii’ will, and this is reasonably so in terms of human interest.

Acknowledgement
Dr. Gerrit Visser, who made this excursion possible, Daphne whose company I value, Mr. Adriaan Botes of Oskopvlakte, who so graciously and kindly gave us access to his farm. Gerhard Marx kindly sent me the copied description of ‘Schoemanii’ and ‘Crausii’ (The latter wholly in Japanese). He also kindly commented and offered some corrections to the manuscript. ♦

Volume 5, Chapter 12:- More on Haworthia venosa ‘granulata’

I wrote “What is Haworthia schoemanii? in reference to the statements I have made that I did not want to write any more. But also kind of intimating that really we need to find some sense in all this “namenklutter”, while at the same time I am drifting away from the community that controls it and isolated from that which generates most of it. My note was about the names ‘schoemanii’ and ‘crausii’; and their perceived improbable existence as biological systems. This is then ust a very short note to elaborate on a record of mine of H. venosa subsp. granulata that I gave as from Patatsriver Road. This was partly because I did not want to advertise too openly where the site was and because I was not even sure of the farm name. Nowadays, while I fully appreciate there are some not very nice people who do and will abuse the situation; I do not believe there is any merit whatsoever in secrecy. It seems to me that this simply exacerbates the whole situation just as does the insistence that conservation laws that so effectively exclude people from participation, contribute to conservation.

When I transferred to the Department of Agriculture in 1987, I became involved in vegetation regeneration. This had been initiated in the Western Cape as early as 1936.  Without a single indication of success I was tasked with the job of continuing the great work. The department had used a site at Bantamsfontein in the southeastern Tanqua Karoo that is accessed via the Patatsriver Road that links Ceres by a country road directly with Matjesfontein that is on the main highway Cape Town to Laingsburg and on to the north. The site can best be described as a rather homogenous stand of Ruschia spinosa on a low-lying and flat area with very little surface rock. It had been used for a reseeding experiment. The only present evidence, after nearly 30years is a few scattered plants of Atriplex nummularia outside the treated plots. Our visit in 1988 was to attempt sowing of Osteospermumj sinuatum into the Ruschia as nurse plants using a rather inventive handseeder. I am sure it could only have been this close attention to those nurse plants that drew my attention to the very cryptic plants of ‘granulata’. (I must mention here the abhorrence that has been expressed at this violation of some sort of ethic that requires the use of virtual the full Latin set of epithets for every mention. I strongly suspect that this is only to vindicate a wholly false belief in a reality that the names seldom have).

The plants I saw were seldom stemmed and what I grew and propagated were smallish stemless plants generated by rhizome (underground shoot). The habitat is/was quite unlike the high rocky slopes that I would have expected to find these plants in and I often wondered about this issue. Unfortunately my activities in vegetation ecology, while allowing me so much time in the field, required me to be where the animal action was and focused on general vegetation rather than the sort of exploration and observation I would have liked to do in terms of my own interest. The consequence is that I learned very little about Haworthia in those years.

After my recent experience with ‘schoemanii’ and Steven Hammer’s expressed interest in Conophytum distribution, I took the opportunity of going back to Bantamsfontein. The farm is owned by Jan du Toit, a leading light in the fruit farming industry of the Koue Bokkeveld in the Ceres District. The farmers there traditionally also owned farms in the Tanqua/Ceres Karoo, and stock would be driven, or later transported, there for grazing during the winter months. Production has declined dramatically over the last 60 years and many farms are now owned by people who have “invested in a seaside cottage in the Karoo”. Mr. Du Toit does still continue there with sheep though his business is 98% fruit. The vegetation is in excellent condition.

Daphne and I started searching in the old experimental site and quickly found plants, few and scarce as they were. Our usual response in a situation like this is to ask “Now where are they really?” In other words, to try and establish where the preferred habitat actually was. We crossed to the west side of the road and walked a long way without finding any more plants. We only saw a few H. arachnoideatanqua’. Then we drove a short distance northwards to a rocky ridge that looked more probable, and as surely there were the plants in abundance. Mr. Du Toit was our host for the night and the next day we searched south of the farm house, finding ‘granulata’ and ‘arachnoidea’ over a wide area.

The pictures will illustrate the variation. The plants may be stemless or stemmed and propagate by short offsets or by longish rhizome. The leaves may be quite slender and acuminate or short and squat; unmarked on the inner upper surface or plain.

I have tried to understand the geology of the area and get some idea of the significance of parent materials in relation to soils and the distribution of plant species. I am quite convinced that this is really important, but I just cannot formulate why this is. Just as the SW Cape area from George to Caledon can be seen to vary from east to west, so is it that the Karoo is divided. In the latter case it is more easily explained by the fact that the parent sediments of the Karoo Supergroup come from essentially two different sources. The smaller southwestern area was fed in the times of Gondwanaland by fairly large particle

sediments from what is now South America (the Parana basin), while the larger northwest was fed by finer turbidites from northern and western (the Karoo Basin). Dwyka Tillite of earlier glacial origin is exposed on the western and southern boundaries, Dolerites of later origin dominate the north while the eastern boundary of the Tanqua karoo is contemporary deposition. In skeletal soils it seems obvious that source material strongly dictates mineralogy, derived soil texture and consequently vegetation. Overriding this geology is topographical feature and climate pattern.

I find it very odd, considering the short span of human life, that those events from as long ago as 545m years may be so relevant to the present and to plant species whose history seems to be so recent. It is also very odd, for me at least, to understand why so many of the Tanqua Karoo endemics are in the oldest formation of the Ecca Geological Group i.e. Tierberg Formation, and not in the overlying three.

Acknowledgement
Mr. Jan du Toit for gracious hospitality and kindness. Dr. De Ville Wickens for information on the geology of the Tanqua Karoo. ♦