Observations on the G.G. Smith Collection of Haworthia (1982)

G. G. Smith ‘s collection of Haworthia was donated to Kirstenbosch and the Compton Herbarium in 1950, together with an ostensible manuscript of a monograph, his basic collecting record, various catalogues of literature and odd notes. However, there was no indication of Smith’s overall view on the classification of Haworthia, or of any Intention he had for the genus at the time he abandoned work on it. On his death in February 1976, Dr M. Courtenay-Latimer obtained many remaining papers from his home. and also the Compton Herbarium became the repository on permanent loan of the entire collection belonging to the East London Museum. Among the papers Is an Immense number of detailed drawings by Dr Courtenay-Latimer of the kind which were used to illustrate Smith’s publications, as well as very detailed assessments of ‘species’. Smith accessioned all his plants individually and each plant was assessed on virtually every measurable character. It appears that Smith first considered whether a new taxon was indicated or not. and then made these numerical assessments against plants which either were, or were considered to be, existing taxa.

The papers show that Smith was in fact contemplating a whole new range of species and varieties. At the same time it is interesting to note his comment in a letter to the head of the Botanical Research Institute (as It is now named) in Pretoria. Here he says that trying to determine a species from one or two plants is a total waste of time. In a manuscript among his papers In which he concluded that the sections Obtusatae and Planifoliae were synonymous, he writes: ” In some cases with different plants from the same locality and even from the same cluster. it was possible to place some In each section.” This is a significant remark which collectors should note as even von Poellnitz described H. cymbiformis var. translucens and H. planifolla var. transiens from the same collection.

Smith seems to have been particularly Involved with the sections Trlfariae, Coarctatae, Obtusatae and Retusae as they then existed. In the section Obtusatae he had proposals for 13 new species, 18 varieties and two sub-varieties. All these are simply referred by the writer to H. cymbiformis (Haw.) Duval. In the Retusae he did not propose any new species but instead visualized 21 new varieties, two sub-varieties and a forma. In the case of H. nitidula v. Poelln. he had nine varieties in fact were drawn from the species H. mirabilis Haw., H. retusa (L.) Duval and H. emelyae v. Poelln. The accompanying illustrations show that H. emelyae v. Poelln, and H. mutica Haw. were both confused with H. pygmaea v. Poelln., while H. mutica and H. retusa were also confused.  In H. turgida Haw. Smith proposed seven new varieties. In the sections Fusiformes, Fenestratae, Loratae and Limipdae there were descriptions of one new variety in each; in the section Muticae that of one new species and two varieties, and in the Denticulatae one new species.

In the Trifariae there were proposals for four new species and 14 varieties in a species which is really not so particularly variable, i.e. H. viscosa (L.) Haw. It is in fact difficult to detect the differences in these supposed varieties from the photographs accompanying the descriptions. Finally in the Coarctatae there were descriptions of six new varieties of H. reinwardtii Haw., two of which actually belonging with H. coarctata Haw. This gives a grand total of 19 possible new species, 65 varieties, four sub-varieties and a forma.

Smith’s assessments involved detailed measurements and observations of as many as 56 different variables and should serve as a salutary lesson for any budding taxonomist. There is just no sense in arguing about trivia. The species are highly variable and in many cases are not clearly definable to the exclusion of other species. While each and every clone of Smith’s collection could ultimately have had a name involving three or four epithets, there is no justification for ridiculing this aspect of his work. Together with Dr Courtnay-Latimer, Smith left an herbarium record unrivalled in the Liliaceae and perhaps only by Dr L. Bolus’ equally invaluable contribution to a permanent record in the Mesembryanthemaceae.

Fig. 1 (top): GGS 2935 HAWORTHIA EMELYAE v. Poelln. From Uniondale – ‘H. pygmaea var. A. Smith’.
Fig. 2 (centre): GGS 3430 HAWORTHIA MUTICA Haw. From Bonnievale – ‘H. pygmaea var. B. Smith’.
Fig. 3 (bottom): GGS 3249 HAWORTHIA MUTICA Haw. From Stormsvlei – ‘H. retusa var K. Smith’.

Fig. 4 (top left): GGS 5061 HAWORTHIA MUTICA Haw. From Swellendam – ‘H. retusa var. J. Smith’.
Fig. 5 (bottom left): GGS 5377a HAWORTHIA RETUSA (L.) Duv. From E. Riversdale – ‘H. retusa var’. (H. geraldii Scott). A large clump.
Fig. 6 (top right): GGS 5377a HAWORTHIA RETUSA (L.) Duv.
Fig. 7 (bottom right) GGS 5377b HAWORTHIA RETUSA (L.) Duv. From E. Riversdale – ‘H. retusa var.’.

by M. B. Bayer
Photos by the author.
Nat. Cact. & Succ. J., Vol. 37/4 (1982) pp 105-106.

Just what do we do with names for Haworthia?

Previously published in BCSJl (Cactus World) 30.4:211(2012)

M B Bayer

Taxonomy always provokes differing views, and Haworthia in particular has been subject to years of vacillation. The author has long been a campaigner against the haphazard proliferation of new names for every new, morphologically different population or variant. He questions the vagueness of a conventional species concept and pleads for a more reason-based, logical and sensible, communal approach to understanding and classifying Haworthia species. He hopes in this article to convey a message which is relevant to whatever genera of plants you grow. Photography by the author.

In Haworthia, professional botanists have struggled with and avoided the group because it is so infused with amateurs whose interest in the genus far outweighs any knowledge of botany. So classification of Haworthia has muddled on with scant regard for the discipline of botany as a science. Whether that has changed, is not for me to say. I have personally been gathering information on distribution and variation for over 50 years and have very seriously tried to keep that in the context of the science I was trained in and present it in a manner that botanists can follow and hopefully accept.

What has developed is that academic and professional botanists have been working with the tools of molecular biology and the results of five independent studies have all pointed towards the same conclusion, which is that the species of Haworthia are elusive, and the related genera are also not adequately distinguishable in the DNA data. The best solution they can offer is to merge the genera back into a single genus, namely Aloe. My personal reaction is that this is not a new idea and also Gordon Rowley pointed this out as far back as the 1970’s. I have also said that the subgenus Haworthia does not sit comfortably with the other two subgenera. Had I been a true taxonomist I would have implemented that by separating Haworthia into three separate genera and that is what I really would like to see.  But the reality is that this does not solve the other problems that exist regarding Astroloba, Chortolirion, Poellnitzia, Chamaealoe, Leptaloe, Lomatophyllum, and the small Madagascan aloes. True botany alone can resolve the current and a new classification (still in manuscript form) has been proposed by a group of scientists that will really ‘rock the boat’ as far as collectors are concerned.

In Haworthiad (2012:4), I wrote about Haworthia mirabilis ‘submagnifica’. (Ed. note: The name in inverted commas, according to the author’s system indicates a variant name rather than a formal conventional variety, subspecies or form. It is his contention that there is no species definition and thus formal names have a large element of uncertainty.  Another option is to drop the use of any rank denotation at all). It is one of the first populations linked to von Poellnitz’ H. magnifica long before so much was learned about distribution and variation. I used the prefix “sub” because this means “somewhat”, “almost”, “slightly”, “partially”, and possibly a few other words that mean… it is, but it is not. The population concerned is Komserante (Figs 1-2) and this particular population has acquired the name H. vernalis (Figs. 3-4). But I think we need to start from scratch and drop all the ‘baggage’ of the years. I personally have learned so much since I wrote my revision in 1996 that I know it is not possible to properly backtrack and retrace the passage forward by the use of Latin names. Interfertility is the basis of the system we use to identify and describe species and my field experience was already proving that this cannot possibly apply in the way in which Haworthia has been, or is to be, classified.

It is quite evident that H. retusa and H. mirabilis, both of which I accept in a very much broader context, do hybridise and there are populations that fit between. But first let me just explain that I regard H. retusa now to include H. turgida and all the variants of that species (nomenclatural priority obviated the use of the name turgida to cover the greater body of populations for this species). In the same way I regard H. maraisii, H. magnifica, and H. heidelbergensis and whatever variants were attached to those, as H. mirabilis.  There are thus two species. My further observation is that H. pygmaea and H. mutica are segregates from the common gene pool of H. retusa and H. mirabilis. The Komserante population is the one in which that same gene pool is re-combining (Figs. 5-10). I am not in the least sure of all the intricacies but it seems to me that it is actually the group of populations that I recognize as H. retusa var. nigra that is pivotal in the relationship of all these species that I recognize. In this we discuss populations using names as prescribed by convention. This convention caters for chronology and authorship and not for evolutionary pathways. Both the names “retusa” and “turgida” precede the name “nigra”, but the populations that I now assign to H. retusa ‘nigra’ may better fit the concept of evolutionary origin.

The picture is complicated by the role of H. floribunda. This also hybridizes with both H. mirabilis and H. retusa as odd hybrids as well as at a population level. Just what are we to do? History has demonstrated all too well that a bevy of ill-assorted interested parties trying to impose a botanical classification is going to produce nothing but conflict and confusion. This has been going on now since the time that Smith, Von Poellnitz and Resende were simultaneously describing new species. How are we going to turn around and arrive at the understanding and stability of names that we seek?

In the past I have been extremely reluctant to make the following suggestion, and even now am a bit hesitant. What we need to do is turn to people who are employed to do this work. Herbaria and herbarium botanists are tasked and entrusted to classify and name plants. Perhaps it testifies to the complexity of the subject, or just its enormity, that these botanists have too often needed to defer to amateurs who have the interest, energy and enthusiasm and commitment to acquire field knowledge that a professional could never get the time or funds to do. The unfortunate part is that sometimes amateurs may not be able to relate their knowledge adequately to academic botany.

So what is the solution?  It is that the community leaders assume the responsibility for the establishment of a system of classification that is meaningful to the community they serve. By community, I mean initially the botanists who should be providing us with scientifically sound classifications, then editors who are familiar with what botanists do, next are the Societies with their memberships, and also opinion formers in those groups. Finally included are the reviewers and commentators who lead opinion in one direction or another. It is surely not that difficult to sit down together to discuss and arrive at a set of guidelines by which a decision can be reached as to what (not whose) system to accept. A solution does not belong to anyone. Latin names are assumed to refer to an entity called a “species”. Botany has indeed been very lax and remiss in not providing a definition and this is the prime reason why amateurs have had so much freedom in generating Latin names for the most frivolous reasons. Botanists themselves have often not been far behind.

I think it is time to change all this and must excuse myself from any decision making body or process because I have a vested interest in respect of all the words I have written on the subject.

  • Haworthia revisited. Umdaus Press, Hatfield. (1999)
  • Plants in my collection 7: H. mirabilismagnifica’. Haworthiad 26(1): 4-5 (2012)

Nomenclator (2013)

The Haworthia nomenclator: a list of accepted species with some guidelines for infraspecific names

M.B. Bayer* and J.C. Manning**

*PO Box 960, Kuilsriver 7579, South Africa
**South African National Biodiversity Institute, P/Bag X7, Claremont 7735, South Africa

7 October 2012
(revised 1 February 2013)

With the impending revision of the IOS Succulent Lexicon and a growing awareness that the current classification of the genus Haworthia is unnatural, the time is ripe to propose a list of species names that I (MB) consider worthy of recognition. This list is essentially the same as that published recently in Haworthia Update 7(4): 30–40 (2012), in which we formally published numerous new combinations and new synonyms. There are two changes from that list implemented here. New information prompts us to recognise H. marxii as a species distinct from H. emelyae, and we transfer var. livida from H. pubescens to H. maculata also on the basis of new information.

My considered opinion is that there are at most about 60 species in Haworthia and that a better and more critical treatment would reduce this still more. This contrasts markedly with Breuer (2010), who lists 368 ‘accepted’ species and reports the even more startling claim that Hayashi recognises 550! Some of this increase is due to the tendency for these authors to treat my varietal names as full species but they have also described many new species de novo. I am unable to accept all of their proposed taxa in the context of my extensive field knowledge of the genus and my practical experience of patterns of variation among wild populations.

Species concepts in the genus have always been idiosyncratic, driven primarily by a propensity to recognize variation over similarity and fostered by a general ignorance of the extent of intra-population variability in the wild. The recent almost exponential proliferation of names has succeeded in surrounded the genus with a thicket of nomenclatural twigs that is almost impossible to penetrate and which obscures rather than illuminates any real understanding of the genus. The very appeal of the genus is its almost infinite capacity to vary, and it is a tragedy that they are no longer appreciated for their individuality but are instead pushed into or pulled out of taxonomic boxes almost willynilly. It is very difficult not to suspect the motivation behind some of this bedlam.

While we in no way wish to proscribe anybody from expressing their opinions, we issue an urgent plea for restraint. The nomenclatural flood that has all but submerged the genus will only be exacerbated by floating additional formal names and combinations on the turbulent waters. In fact, we go so far as to recommend a moratorium on the publication of any new taxa in the genus that are proposed without an extensive survey of relevant variation patterns in the wild. Scientific journals reduce the chances that inadequately researched papers will see the light of day by sending all submissions to competent referees for comment and evaluation. Popular journals that transgress into the scientific arena by accepting descriptions of new taxa should do the same and the responsibility for this lies firmly with the editors.

Every scientific name that enters currency has to be accounted for by botanists in their lists and publications. To remove them from circulation requires a separate, formal act for each and every name. Dealing with the many dubious names in Haworthia is taxing task that can be ill afforded. Numerous invalidly published or illegitimate names have also entered circulation through non-adherence to the International Code of Botanical Nomenclature, which aims to regulate scientific names. This adds to the confusion and to the work.

What in fact is the primary purpose of these scientific names? Among botanical circles, species names carry a great deal of weight. In most instances they imply that individuals that share a name also share a common ancestry and can interbreed to produce viable seeds. Species with different names will not. Is this philosophy applied in Haworthia? The process of recognising species in botanical circles is generally top-down, with genera being first split into component species and the species then into subspecies or varieties acording to the particular patterns of variation shown by the constituent populations. This does not seem to apply in Haworthia. Here the process is largely bottom-up, with individuals or populations being given names and then shuffled into or among species. This is patently absurd.

In general terms, botanical names largely reflect similarities whereas horticultural names highlight differences. The two systems are thus not always congruent and little is to be served by confusing them. We therefore recommend that growers exploit the advantages of an informal system of nomeclature that will give them unlimited flexibility without clogging up the formal nomenclature any further. We also urge the Editors of popular journals to encourage the use of this system among their contributers. The great advantage of such an informal and non-ranked system is that it removes the hierarchical constraints that are inherent in the Linnaean system and that have already created problems with the placement of varieties and forms of Haworthia.

It could not be easier to implement and use: instead of worrying about the taxonomic level at which the variant is to be recognized (is it a subspecies, or a variety, or a form) the name appears in inverted commas without any indication of its rank. Such informal names can also be moved between species without any formal changes that are otherwise necessary. They are likely to be more descriptive and meaningful than a bare Latinised trivial epithet. As an example, should Mr Smith consider that the form of H. mirabilis var. sublineata from south of Bredasdorp with paler, attenuate leaves deserves special recognition, then he might usefully refer to those plants under the informal name H. mirabilis ‘Bredasdorp Pale’ Smith 2015. A typical illustration should be designated to fix the application of the name. Transferring of the variant to another species should follow the Zoological Code in carrying over the first author only (now in brackets) and not the transferring author as well. Thus: H. mirabilis ‘Bredasdorp Pale’ (Smith 2015). We are most grateful to Harry Mays, Editor of the Haworthia Update for his assistance and advice on this aspect.

THE LIST: All taxa that we accept are indicated in bold.Taxa that are not accepted at any rank are included as synonyms. Where possible we formally synonomise such names that have not yet been formally synonomised but many others (indicated with an asterisk *) do not appear in the International Plant Names Index (www.ipni.org) as of 20 January 2012 and are thus evidently unpublished or manuscript name. The publication of such names in the literature is irresponsible. Names that are separated by a full stop (.) are based on different types (heterotypic or taxonomic synonyms) whereas those separated by a colon (:) are based on the same type (homotypic or nomenclatural synonyms).

Haworthia Duval Pl. Succ. Horto. Alenc.: 7pp (1809). Baker in Jl. S. Afr. Bot. 18: 197(1880). Baker in Fl. cap. 6: 332 (1896). Berger in Das. Pfl. 4: 74 (1908). Bayer, New Haworthia Handb. (1982). Scott, The genus Haworthia (1985). Type species: H. arachnoidea (L.) Duval. [Typification largely by Breuer & Metzing in Taxon (1996)].

= Catevala Medik. (1786). Apicra Willd. (1811).

± 60 species, very variable and complex. The taxonomy of the genus is still unresolved. Species concepts used here largely follow Bayer’s (1976, 1982, 1997) treatments and are based on geographical distribution and co-occurrence.

NOTE: Recent phylogenetic analyses of nuclear and plastid DNA sequence data supports the view that the three subgenera comprise quite distinct lineages not immediately related to one another. They are thus as distinct as some of the other smaller genera and should thus logically be treated as separate genera. A more useful option is probably to include all of the alooid genera within Aloe.

Key to the subgenera

1. Flowers triangular or rounded-triangular at base; tube obclavate-curved; outer tepals free; style upcurved; seeds irregularly angled . . . subg. Haworthia

2. Flowers hexangular at base, gradually narrowing to junction with pedicel (substipitate); tube obcapitate-curved; outer tepals partly fused to inner; style straight; seeds irregularly angled . . . subg. Hexangulares

3. Flowers rounded at base and abruptly joined to pedicel (non-stipitate); petals partly fused; tube obcapitate-straight; style straight; seeds flattish . . . subg. Robustipedunculatae

I. Subgenus Haworthia. Type species: as for genus. ± 41 spp.

H. angustifolia Haw. in Philos. Mag. J. 66: 283 (1825). Neotype, designated by Breuer & Metzing (1997): Grahamstown to Alicedale, Bruyns 1653 (NBG).

= Aloe stenophylla Schult. & Schult.f. (1829). H. albanensis Shonl. (1912). H. angustifolia var. grandis Smith (1943).

H. angustifolia var. angustifolia

H. angustifolia var. altissima Bayer in Haw. Revis.: 26 (1999): H. altissima (Bayer) M.Hayashi in Haworthia Study 3: 13 (2000). Type: Riebeek East to Carlisle Bridge, Smith 5220 (NBG).

H. angustifolia var. baylissii (Scott) Bayer in Haw. Revis.: 27 (1999): H. baylissii Scott (1968). Type: Oudekraal, Zuurberg, Bayliss sub Scott 796 (PRE).

H. angustifolia var. paucifolia Smith in Jl. S. Afr. Bot. 14: 48 (1948): H. paucifolia (Smith) M.Hayashi in Haworthia Study 22: 11 (2010). Type: Frazers Camp, Smith 6819 (NBG).

H. arachnoidea (L.) Duval in Pl. Succ. Hort. Alenc.: 7 (1809): Aloe pumila var. arachnoidea L. (1753): Catevala arachnoidea (L.) Medik. (1786): Apicra arachnoidea (L.) Willd. (1811). Lectotype, designated by Scott (1977): Commelin, Praeludia Bot.: t. 27 (1703). Epitype, designated by Breuer & Metzing (1997): Buitenstekloof, Langvlei, Bayer 153 (NBG).

= H. arachnoidea var. minor Haw. (1819).

H. arachnoidea var. arachnoidea

= H. joubertii M.Hayashi in Haworthia Study 14: 16 (2005), nom. inval. H. laxa M.Hayashi in Haworthia Study 14: 14 (2005), nom. inval. H. limbata M.Hayashi in Haworthia Study 14: 16 (2005), nom. inval. *H. isomorpha *H. gilva

H. arachnoidea var. aranea (Berger) Bayer in Haw. Revis.: 30 (1999): H. bolusii var. aranea Berger (1908): H. aranea (Berger) Bayer (1976). Lectotype: Engler, Pflanzenr. 33: 114, f. 39 A–E (1908). Epitype, designated by Breuer & Metzing (1997): Robinson Pass, Moeras River Drift, Bolus 12372 (BOL).

H. arachnoidea var. namaquensis Bayer in Haw. Revis.: 31 (1999): H. namaquensis (Bayer) Breuer in Gen. Haworthia 1: 7 (2010). Type: Karrachabpoort, Richtersveld, Bayer 1674 (NBG).

H. arachnoidea var. nigricans (Haw.) Bayer in Haw. Revis.: 32 (1999): H. setata var. nigricans Haw. (1821). Neotype, designated by Bayer (1997): SW Vanwyksdorp, Bayer 2419 (NBG).

= H. helmiae V.Poelln. (1937): H. unicolor var. helmiae (V.Poelln.) Bayer (1976). H. venteri V.Poelln. (1939): H. unicolor var. venteri (V.Poelln.) Bayer (1976). H. scottii Breuer in Avonia 21: 55 (2003). H. nigrata M.Hayashi in Haworthia Study 15: 14 (2006). *H. apata *H. regens *H. formosa *H. kuromisa

H. arachnoidea var. scabrispina Bayer in Haw. Revis.: 34 (1999): H. scabrispina (Bayer) Breuer in Gen. Haworthia 1: 8 (2010). Type: Baviaans, Bayer 2105 (NBG) *H. matjiesta

H. arachnoidea var. setata (Haw.) Bayer in Haw. Revis.: 34 (1999): H. setata Haw. (1819). Iconotype: artist unknown, specimen received from Dr Mackrill ex Cape (K).

= H. setata var. media Haw. (1821). H. setata var. major Haw. (1821). Aloe setosa Schult. & Schult.f. (1829). H. gigas V.Poelln. (1932): H. setata var. gigas (V.Poelln.) V.Poelln. (1938). H. minima var. major V. Poelln. (1938): H. tenera var. major (V.Poelln.) Uitew. (1948). H. pectinis M.Hayashi in Haworthia Study 10: 13 (2003). H. tretyrensis Breuer in Avonia 21: 58 (2003). H. candida M.Hayashi in Haworthia Study 16: 16 (2006). H. cangoensis M.Hayashi in Haworthia Study 14: 13 (2005), nom. inval. H. angiras M.Hayashi in Haworthia Study 14: 13 (2005), nom. inval. H. kogmansensis M.Hayashi in Haworthia Study 14: 14 (2005), nom. inval.

H. aristata Haw. in Suppl. Pl. Succ.: 51 (1819). Iconotype: (K). Epitype: Deadman’s Gulch (Soutkloof), Smith 3550 (NBG).

= H. denticulata Haw. (1821). H. lapis Breuer & M.Hayashi in Alsterworthia Int. Special Issue 7: 6 (2004). H. rava M.Hayashi in Haworthia Study 14: 11 (2005), nom. inval.

H. bayeri Hammer & Venter in Cact. Succ. J (US) 69: 75 (1997). Type: S Uniondale, Stayner in KG164/69 (NBG).

= H. hayashii M.Hayashi in Haworthia Study 7: 14 (2002). H. laeta M.Hayashi in Haworthia Study 12: 13 (2004). H. indigoa M.Hayashi in Haworthia Study 12: 13 (2004). H. truterorum Breuer & Marx in Aloe 48: 54 (2011).

H. blackburniae Barker in J. S. Afr. Bot. 3:93 (1937). Type: Calitzdorp, Reynolds 1842 (NBG).

H. blackburniae var. blackburniae

H. blackburniae var. graminifolia (Smith) Bayer in Haw. Revis.: 42 (1999): H. graminifolia Smith (1942). Type: Schoemanspoort, M. Courtenay‑Latimer in Smith 5222 (NBG).

H. blackburniae var. derustensis Bayer in Haw. Revis.: 41 (1997): H. derustensis (Bayer) M.Hayashi in Haworthia Study 3: 13 (2000). Type: W. De Rust, Vlok sub Venter 93/24 (NBG).

H. bolusii Baker in J. Linn. Soc. Bot.:215 (1880). Type: Graaff-Reinet, Bolus 158 (K).

= H. odetteae Breuer in Avonia 21: 51 (2003). H. odyssei M.Hayashi in Haworthia Study 14: 11 (2005), nom. inval. H. capillaris M.Hayashi in Haworthia Study 16: 16 (2006).

H. bolusii var. bolusii

H. bolusii var. blackbeardiana (V. Poelln.) Bayer in Haw. Hand.: 31 (1976): H. blackbeardiana V.Poelln. (1932). Lectotype, designated by Breuer & Metzing (1997): ex cult. V.Poelln. 1932 (B).

= H. blackbeardiana var. major V.Poelln. (1937). H. inermis V.Poelln. (1932): H. altilinea var. inermis (V.Poelln.) V.Poelln. (1937): H. altilinea var. limpida f. inermis (V.Poelln.) V.Poelln. (1940). H. batteniae Scott (1979). H. calaensis Breuer in Alsterworthia Int. Special Issue 7: 5 (2004). H. specksii Breuer in Alsterworthia Int. Special Issue 7: 8 (2004).*H. hogsia *H. speciosa *H. malvina

H. bolusii var. pringlei (Scott) Bayer in Haworthiad 16: 62 (2002). H. decipiens var. pringlei (Scott) Bayer in Haw. Revis.: 67 (1999): H. pringlei Scott (Bradleya 12:103,1994). Type: Adelaide district, Scott s.n. PRE 8970 (PRE). H. hisui M.Hayashi in Haworthia Study 12: 10 (2004). H. lazulis M.Hayashi in Haworthia Study 14: 11 (2005), nom. inval. H. aquamarina M.Hayashi in Haworthia Study 10: 13 (2003). H. hastata M.Hayashi in Haworthia Study 12: 9 (2004).

H. chloracantha Haw. in Revis.:57 (1821): Aloe chlorocantha (Haw.) Scult. & Schult.f. (1829). Neotype, designated by Breuer & Metzing (1997): N Herbertsdale, Bayer KG411/75 (NBG).

H. chloracantha var. chloracantha

H. chloracantha var. denticulifera (V.Poelln.) Bayer in Haw. Hand.: 112 (1976): H. angustifolia var. denticulifera V.Poelln. (1937): H. denticulifera (V.Poelln.) M.Hayashi in Haworthia Study 3: 13 (2000). Type (icono.): (B).

= H. angustifolia var. lilliputana Uitew. (1953).

H. chloracantha var. subglauca V.Poelln. in Kakteenkunde 9:135 (1937): H. subglauca (V.Poelln.) M.Hayshi in Haworthia Study 3: 13 (2000). Neotype, designated by Breuer & Metzing (1997): Great Brak, Hurling & Neil (BOL).

H. cooperi Baker in Refug. Bot. 4: 233 (1871). Type: Cape, Cooper (K).

= H. vittata Baker (1871).

H. cooperi var. cooperi

= H. pallens Breuer & M.Hayashi in Alsterworthia Int. Special Issue 7: 7 (2004). *H. turcosa *H. elegans *H. foeda *H. yocans

H. cooperi var. dielsiana (V.Poelln.) Bayer in Haw. Revis.: 51 (1999): H. dielsiana V.Poelln. (1930): H. pilifera var. dielsiana (V.Poelln.) V.Poelln. (1940): H. obtusa var. dielsiana (V.Poelln.) Uitew. (1948). Neotype, designated by Bayer (1999): Sheldon, A.J. van der Merwe in Smith 1140 (NBG).

= H. joeyae Scott (1975).

H. cooperi var. doldii Bayer in Haworthiad 16: 65 (2002): H. doldii (Bayer) M.Hayashi in Haworthia Study 14: 11 (2005). Type: Chalumna, Dold 3961 (GRA).

H. cooperi var. gordoniana (V.Poelln.) Bayer in Haw. Revis.: 52 (1999): H. gordoniana V.Poelln. (1937): H. pilifera var. gordoniana (V.Poelln.) V.Poelln. (1938): H. obtusa var. gordoniana (V.Poelln.) Uitew. (1948). Neotype, designated by Bayer (1999): Patensie, Smith 3028 (NBG).

= H. harryi M.Hayashi in Haworthia Study 12: 9 (2004). H. jeffreis M.Hayashi in Haworthia Study 12: 10 (2004). H. pusilla M.Hayashi in Haworthia Study 12: 10 (2004). H. ligulata M.Hayashi in Haworthia Study 12: 6 (2004). H. venetia M.Hayashi in Haworthia Study 12: 6 (2004). *H. brandea *H. cineraria *H. compressa *H. gelatina *H. ionandra *H. neritica *H. silvicola *H. tomentosa

H. cooperi var. gracilis (V.Poelln.) Bayer in Haworthiad 16: 64 (2002): H. gracilis V.Poelln. (1929). Neotype, designated by Bayer (1999): Hellspoort, Britten (PRE).

= H. caerulea M.Hayashi & Breuer in Haworthia Study 12: 7 (2004).

H. cooperi var. isabellae (V.Poelln.) Bayer in Haworthiad 16: 62 (2002): H. gracilis var. isabellae (V.Poelln.) Bayer in Haw. Revis.: 77 (1999): H. isabellae V.Poelln. (1938). Neotype, designated by Bayer: Humansdorp, Gamtoos bridge, H. Hall sub NBG 68799 (NBG).

= H. azurea M.Hayashi in Haworthia Study 9: 12 (2003). H. arabesqua M.Hayashi in Haworthia Study 12: 7 (2004). H. bella M.Hayashi in Haworthia Study 12: 8 (2004). H. florens M.Hayashi in Haworthia Study 12: 11 (2004). H. pilosa M.Hayashi in Haworthia Study 12: 7 (2004). H. bathylis M.Hayashi in Haworthia Study 15: 116 (2006). H. lachnosa M.Hayashi in Haworthia Study 16: 16 (2006). H. ciliata M.Hayashi in Haworthia Study 14: 11(2005), nom. inval. *H. kromia. *H. patriae *H. cuprina *H. dasylis

H. cooperi var. leightonii (Smith) Bayer in Haw. Hand.: 128 (1976): H. leightonii Smith (1950). Type: Kayser’s Beach, Smith 6938 (NBG).

= Haworthia leightonii var. davidii Breuer in Avonia 21: 49 (2003).: Haworthia davidii (Breuer) M.Hayashi & Breuer (2005). Type: SW East London, Breuer 6970 (TUAT). *H. sabita?

H. cooperi var. minima (Bayer) Bayer (2012): H. minima Baker (1880) hom. illegit. non (Aiton) Haw. (1812): H. gracilis var. minima Bayer [as (Baker) Bayer] (1999). Iconotype: (K).

= H. tenera V.Poelln. (1932): H. translucens subsp. tenera (V.Poelln.) Bayer (1976): H. gracilis var. tenera (V.Poell.) Bayer (1999): H. cooperi var. tenera (V.Poelln.) Bayer (2002). H. cummingii Breuer & M.Hayashi in Haworthia Study 10: 4 (2003).

H. cooperi var. picturata (Bayer) Bayer in Haworthiad 16: 65 (2002): H. gracilis var. picturata Bayer (1999): H. picturata M.Hayashi (2000). Type: Enon, Thode 21507 (NBG).

= H. oculata M.Hayashi in Haworthia Study 12: 10 (2004). *H. florida *H. imperialis *H. kubusie

H. cooperi var. pilifera (Baker) Bayer in Haw. Revis.: 54 (1999): H. pilifera Baker (1871): H. obtusa var. pilifera (Baker) Uitew. (1948). Iconotype: Refug. Bot.: 234 (1871).

= H. stayneri V.Poelln. (1937): H. pilifera var. stayneri (V.Poelln.) V.Poelln. (1938): H. obtusa var. stayneri (V.Poelln.) Uitew. (1948). H. stayneri var. salina V.Poelln. (1937): H. pilifera var. salina (V.Poelln.) V.Poelln. (1938): H. obtusa var. salina (V.Poelln.) Uitew. (1948): H. salina (V.Poelln.) M.Hayashi (2010). H. pilifera var. dielsiana f. acuminata V.Poelln. (1940): H. obtusa var. dielsiana f. acuminata (V.Poelln.) Uitew. (1948). H. luri M.Hayashi in Haworthia Study 14:11 (2005), nom. inval. *H. sabrina

H. cooperi var. truncata (Jacobs.) Bayer in Haw. Rev.: 55 (1999): H. obtusa var. pilifera f. truncata Jacobs in Nat. Cact. Succ. J. 10: 81 (1955): H. ikra Breuer (2010). Neotype, designated by Bayet (1999): Runlets, Mgwali, Smith 5295 (NBG).

H. cooperi var. venusta (Scott) Bayer in Haw. Revis. (1999): H. venusta Scott in Bradleya 14:87 (1996). Type: NE Alexandria, Britten 781 (GRA).

H. cooperi var. viridis (Bayer) Bayer in Haworthiad 16: 65 (2002): H. gracilis var. viridis Bayer (1999). Type: Perdepoort, Smith 6867 (NBG).

= H. hamata M.Hayashi in Haworthia Study 10: 12 (2003). H. emeralda M.Hayashi in Haworthia Study 12: 11 (2004). H. subhamata M.Hayashi in Haworthia Study 12: 11 (2004). H. teres M.Hayashi in Haworthia Study 12: 7 (2004). *H. swannea

H. cymbiformis (Haw.) Duv. in Pl. Succ. Hort. Elenc.:7 (1809): Aloe cymbiformis Haw. (1804): H. concava Haw., nom. illegit. superfl. (1821). Neotype, designated by Breuer & Metzing (1997): Port Elizabeth, Walmer, Smith 2844 (NBG).

= H. planifolia Haw. (1825): H. cymbiformis var. planifolia (Haw.) Baker (1880): Aloe planifolia (Haw.) Salm-Dyck (1840). H. cymbiformis var. angustata V.Poelln. (1938): H. angustata (V.Poelln.) Breuer in Gen. Haw. 1: 7 (2010). H. cymbiformis var. angustata f. subarmata V.Poelln. (1938). H. cymbiformis var. compacta Triebn. (1938): H. compacta (Triebn.) Breuer in Gen. Haw. 1: 7 (2010). H. planifolia var. exulata V.Poelln. (1938). H. planifolia var. planifolia f. agavoides Triebn. & V.Poelln. (1938), et f. olivacea Triebn. & V.Poelln. (1938), et f. robusta Triebn. & V.Poelln. (1938), et var. incrassata V.Poell. (1938), et var. sublaevis V.Poelln. (1938), et var. longifolia Triebn. et V.Poelln. (1938), et var. longifolia f. calochlora Triebn. et V.Poelln. (1938). H. planifolia var. poellnitziana Resende (1943). H. lepida Smith (1944). *H. cana *H. ingens *H. plena *H. rosea

H. cymbiformis var. cymbiformis

H. cymbiformis var. incurvula (V.Poelln.) Bayer in Haw. Hand.: 124 (1976): H. incurvula V.Poelln. (1932). Neotype, designated by Breuer & Metzing (1997): Pluto’s Vale, Britten s.n. BOL71307 (BOL).

H. cymbiformis var. obtusa (Haw.) Baker in J. Linn. Soc. Bot. 18: 209 (1880). H. obtusa Haw. in Phil.Mag. 46: 282 (1825). Iconotype: (K).

= H. umbraticola V.Poelln. (1937): H. cymbiformis var. umbraticola (V.Poelln.) Bayer (1976). H. hilliana V.Poelln. (1937): H. umbraticola var. hilliana V.Poelln. (1938). H. obtusa var. pilifera f. truncata Jacobs. (1960). *H. blinkia

H. cymbiformis var. ramosa (Smith) Bayer in Haw. Revis.: 60 (1999): H. ramosa Smith (1940): H. cymbiformis f. ramosa (Smith) Bayer (1976). Type: Wooldridge, Smith 3168 (NBG).

H. cymbiformis var. setulifera (V.Poelln.) Bayer in Haw. Revis.: 62 (1999): H. planifolia var. setulifera V.Poelln. (1938): H. setulifera (V.Poelln.) Breuer (2010). Neotype, designated by Bayer (1999): Kwelegha Bridge, Smith 5257 (NBG). H. cymbiformis var. obesa V.Poelln. (1938): H. obesa (V.Poell.) Breuer. *H. sarcoidea

H. decipiens V.Poelln. in Repert. Spec. Nov. Regni. Veg. 28: 103 (1930). Neotype, designated by Breuer & Metzing (1997)): Prince Albert, Kleinsleutelfontein, Bayer 5157 (NBG).

= H. exilis M.Hayashi in Haworthia Study 10: 12 (2003). H. incrassa M.Hayashi in Haworthia Study 14: 12 (2005), nom. inval. *H. tooris

H. decipiens var. decipiens

H. decipiens var. cyanea Bayer in Haw. Revis.: 65 (1999): H. cyanea (Bayer) Hayashi (2000). Type: Fairview, W Jansenville, Bayer 4180 (NBG).

= H. amethysta M.Hayashi in Haworthia Study 10: 1 (2003). H. succinea M.Hayashi in Haworthia Study 10: 14 (2003). H. ianthina M.Hayashi in Haworthia Study 14: 12 (2005), nom. inval.*H. virginea

H. decipiens var. minor Bayer in Haw. Revis.: 66 (1999). Type: Kleinpoort, Smith 3588 (NBG). *H. tenmari

H. decipiens var. virella Bayer in Haworthiad 16: 63 (2002). Type: Ebenezer, Bayer 2070 (NBG).

= H. crinita M.Hayashi in Haworthia Study 10: 13 (2003). H. eminens M.Hayashi in Haworthia Study 10: 13 (2003). H. floccosa M.Hayashi in Haworthia Study 10: 13 (2003). H. kemari M.Hayashi in Haworthia Study 9: 11 (2003). H. fluffa M.Hayashi in Haworthia Study 12: 9 (2004). H. jansenvillensis Breuer in Alsterworthia Inst. 4: 16 (2004). H. pellucida M.Hayashi in Haworthia Study 14: 12 (2005), nom. inval. *H. delicata *H. ionides *H. lanceata *H. stewarta

H. decipiens var. xiphiophylla (Baker) Bayer in Haworthiad 16: 63 (2002). H. arachnoidea var. xiphiophylla (Baker) Bayer in Haw. Revis.: 36 (1999). Haworthia xiphiophylla Baker, Curtis’ Bot.Mag.: t. 7505 (1896). H. setata var. xiphiophylla (Baker) V. Poelln. (1938). Type: Uitenhage, Howlett (K).

= H. longiaristata V. Poelln. (1937). H. flavida M.Hayashi in Haworthia Study 10: 13 (2003). *H. kammaensis

H. emelyae V.Poelln. in Repert. Spec. Nov. Regni. Veg. 42: 271 (1937). Lectotype, designated by Breuer & Metzing (1997): [unpublished image] (B).

= H. blackburniae V.Poelln. (1937). H. correcta V.Poelln. (1938). H. picta V.Poelln. (1938). H. picta var. janvlokii Breuer in Avonia 21: 52 (2003). H. janvlokii (Breuer) Breuer (2010). H. breueri M.Hayashi in Haworthia Study 7: 14 (2002). H. picta var. tricolor Breuer in Avonia 21: 53 (2003).: H. tricolor ( Breuer ) M.Hayashi (2010).

 H. emelyae var. emelyae

H. emelyae var. comptoniana (Smith) Hammer and Venter in Cact. Succ. J. (US) 69: 77 (1997): H. comptoniana Smith (1945). Type: Georgida, Malherbe sub Smith 3433 (NBG).

H. emelyae var. major (Smith) Bayer in Haw. Revis.: 70 (1999): H. schuldtiana var. major Smith (1946): H. maraisii var. major (Smith) Bayer (1976): H. magnifica var. major (Smith) Bayer (1977). Type: Garcia’s Pass, Smith 5370 (NBG).

= H. wimii M.Hayashi in Haworthia Study 3: 13 (2000).

H. emelyae var. multifolia Bayer in Nat. Cact. Succ. J. 34:31 (1979): H. multifolia (Bayer) M.Hayashi (2000). Type: Riversdale, Springfontein, Bayer 1558 (NBG).

H. floribunda V.Poelln. in Repert. Spec. Nov. Regni Veg. 40: 149 (1936). Neotype, designated by Bayer (1982): [unpublished image] (B). Epitype, designated by Breuer & Metzing (1997): Blackdown, NE Heidelberg, Bayer 158 (NBG).*H. henda

H. floribunda var. floribunda

H. floribunda var. dentata Bayer in Haw. Revis.: 73 (1999): H. dentata (Bayer) M.Hayashi (2000), hom. illegit. non H.Jacobsen (1935). Type: W Riversdale, Dekenah 90 sub Smith 5502 (NBG).

H. floribunda var. major Bayer in Haw. Revis.: 74 (1999). Type: S Swellendam, De Kok (NBG).

= H. kondoi M.Hayashi in Haworthia Study 3: 13 (2000).

H. herbacea (Mill.) Stearn in Cactus J. 7: 40 (1938): Aloe herbacea Mill. (1768). Lectotype, designated by Bayer (1972): Illustration in Boerhaave, Index Alter Hort. Lugd.-Bat. 2: 130: t. 131 (1720). Epitype, designated by Breuer & Metzing (1997): N Ribbokkop, Bayer 161 (NBG).

= Aloe atrovirens DC. (1799): H. atrovirens (DC.) Haw. (1821). H. pumila (Willd.) Duval (1809). Aloe translucens Haw. (1804): H. translucens (Haw.) Haw. (1819): Aloe arachnoidea var. translucens (Haw.) Ker-G. (1811). H. pellucens Haw. (1812). H. pallida Haw. (1821). H. paynei V.Poelln. in Feddes Repert. 41: 206 (1937).: H. herbacea var. paynei (V.Poelln.) Bayer (1999). H. aegrota V.Poelln. (1939). H. submaculata V.Poelln. (1939). H. luteorosea Uitew. (1939).

H. herbacea var. herbacea

H. herbacea var. flaccida Bayer in Haw. Revis.: 86 (1999): H. flaccida (Bayer) Breuer (2010). Type: Worcester, Rooiberg, Bruyns (NBG).

H. herbacea var. lupula Bayer in Haw. Revis.: 86 (1999): H. lupula (Bayer) M.Hayashi (2000). Type: Villiersdorp, Boscheveld Mt., Wolfkloof, Esterhuysen (NBG).

H. lockwoodii Archibald in Fl. Pl. Africa 20: f. 792 (1940). Type: near Laingsburg, Lockwood-Hill 215 (GRA).

H. maculata (V.Poelln.) Bayer in Haw. Hand.: 130 (1976): H. schuldtiana var. maculata V.Poelln. (1940). Lectotype, designated by Breuer & Metzing (1997): Worcester, Venter 6 (BOL).

H. maculata var. maculata. *H. audens

H. maculata var. livida (Bayer) Bayer, comb. nov.: H. pubescens var. livida Bayer in Haw. Revis.: 134 (1999). Type: Worcester, Lemoenpoort, Bayer 1128 (NBG). *H. livida

H. marumiana Uitew. in Cact.Vetp. 6: 33 (1940). Type: Cape, Ladismith, ex hort. Stellenbosch sub 6610 (AMD).

= H. borealis M.Hayashi in Haworthia Study 15: 14 (2006). H. marmorata M.Hayashi in Haworthia Study 15: 14 (2006). H. tarkasia M.Hayashi in Haworthia Study 15: 14 (2006). *H. euchlora

H. marumiana var. marumiana

H. marumiana var. archeri (W.F.Barker ex Bayer) Bayer in Haw. Revis.: 104 (1999): H. archeri W.F.Barker ex Bayer (1981). Type: Whitehill, Archer s.n. NBG 68145 (NBG). *H. chibita *H. frazeri *H. nudata

H. marumiana var. batesiana (Uitew.) Bayer in Haw. Revis.: 105 (1999): H. batesiana Uitew. (1948). Type: Graaff-Reinet, Ferguson (AMD).

H. marumiana var. dimorpha (Bayer) Bayer in Haw. Revis.: 106 (1999): H. archeri var. dimorpha Bayer (1981): H. dimorpha (Bayer) M.Hayshi (2000). Type: Constable Station, W Laingsburg, Hall sub Smith 7418 (NBG).

H. marumiana var. reddii (Scott) Bayer (2012): H. cymbiformis var. reddii (Scott) Bayer (1999): H. reddii Scott in Cact. Succ. J. (US) 66:182 (1994). Type: Cathcart, Waterdown Dam, Scott 8968 (PRE). *H. boloensis *H. fatreddii

H. marumiana var. viridis Bayer in Haw. Revis.: 107 (1999). Type: S Prince Albert, Bayer 3620 (NBG). *H. viridis

H. marxii Gildenh. in Aloe 44: 4 (2007). Type: Western Cape, Rooinek Pass, Marx 605 (GRA, holo.).

H. mirabilis (Haw.) Haw. in Syn. Pl. Succ.: 95 (1812): Aloe mirabilis Haw. (1804). Neotype, designated by Bayer (1977): Illustration in Curtis’ Bot. Mag.: t. 1354 (1811). Epitype, designated by Breuer & Metzing (1997): Skuitsberg, between Caledon and Greyton, Bayer 2453 (NBG).

H. mirabilis var. mirabilis

H. mirabilis var. atrofusca (Smith) Bayer (2012): H. atrofusca Smith in Jl. S. Afr. Bot. 14:41 (1948): H. magnifica var. atrofusca (Smith) Bayer (1977). Type: Dekenah 225 sub Smith 6169 (NBG).

= H. enigma M.Hayashi in Haworthia Study 7: 14 (2002).

H. mirabilis var. badia (V.Poelln.) Bayer in Haw. Revis.: 109 (1999): H. badia V.Poelln. (1938): Haworthia mirabilis subsp. badia (V.Poelln.) Bayer (1976). Lectotype, designated by Bayer (1977): Illustration in Kakteenk. en Kakteenfr.: 76 (1938).

H. mirabilis var. beukmannii (V.Poelln.) Bayer in Haw. Revis.: 110 (1999): H. emelyae var. beukmannii V.Poelln. (1940): H. beukmannii (V.Poelln.) M.Hayashi (2000). Type: [unpublished image] (B). Epitype, designated by Bayer (1999): Caledon, Skuitsberg, Smith 3969 (NBG).

H. mirabilis var. consanguinea Bayer in Haw. Revis.: 111 (1999): H. consanguinea (Bayer) M.Hayashi (2000). Type: Die Galg, Bayer (NBG).

H. mirabilis var. heidelbergensis (Smith) Bayer (2012): H. heidelbergensis Smith in Jl. S. Afr. Bot. 14:42 (1948). Type: W Heidelberg, J. Dekenah 230 in Smith 6566 (NBG). *H. obscura?

H. mirabilis var. magnifica (V.Poelln.) Bayer (2012): Haworthia magnifica V.Poelln. in Repert. Spec. Nov. Regni Veg. 33: 240 (1933): H. maraisii var. magnifica (V.Poelln.) Bayer : 131 (1976). Lectotype, designated by Breuer & Metzing (1997): Riversdale, Ferguson (BOL).*H. vernalis

H. mirabilis var. maraisii (V.Poelln.) Bayer (2012): Haworthia maraisii V.Poelln. in Feddes Repert. 38:194 (1935): H. magnifica var. maraisii (V.Poelln.) Bayer (1977). Type (icono.): Swellendam, Marais in Swellendam 6410 (B).

= H. schuldtiana V.Poelln. (1937). H. schuldtiana var. robertsonensis V.Poelln. (1940). H. schuldtiana var. minor Triebn. et V.Poelln. (1940). H. schuldtiana var. subtuberculata V.Poelln. (1940). H. whitesloaneana V.Poelln. (1937): H. schuldtiana var. whitesloaneana (V.Poelln.) V.Poelln. (1940). H. schuldtiana var. sublaevis V.Poelln. (1940). H. schuldtiana var. simplicior V.Poelln. (1940). H. schuldtiana var. unilineata V.Poelln. (1940). H. sublimpidula V.Poelln. (1936). H. triebneriana var. diversicolor Triebn. et V.Poelln. (1939). H. angustifolia var. subfalcata V.Poelln. (1951), nom. inval. *H. calliantha

H. mirabilis var. meiringii (Bayer) Bayer (2012): H. maraisii var. meiringii Bayer in Haw. Hand.:134 (1976): H. magnifica var. meiringii (Bayer) Bayer (1977). Type: E of Bonnievale, Bayer in KG 224/70 (NBG). *H. meiringii

H. mirabilis var. mundula (Smith) Bayer (2012): H. mundula Smith in S. Afr. J. Bot. 12: 8 (1946): H. mirabilis subsp. mundula (Smith) Bayer (1976). Type: on Elim road, Smith 5479 (NBG).

H. mirabilis var. notabilis (V.Poelln.) Bayer (2012): H. notabilis V.Poelln. in Repert. Spec. Nov. Regni. Veg. 44: 134 (1938): H. maraisii. var. notabilis (V.Poelln.) Bayer (1976): H. magnifica var. notabilis Bayer (1977). Lectotype, designated by Breuer & Metzing (1997): [unpublished image] (B)..

= H. intermedia V.Poelln. in Kakteenk. 9: 133 (1937).: H. maculata var. ntermedia (V.Poelln.) Bayer (1999). H. schuldtiana var. erecta Triebn. & V.Poelln. (1940). H. nitidula var. opaca V.Poelln., nom. nud. (1948).

H. mirabilis var. paradoxa (V.Poelln.) Bayer in Haw. Revis.: 112 (1999): H. paradoxa V.Poelln. (1933): H. maraisii var. paradoxa (V.Poelln.) Bayer (1976): H. magnifica var. paradoxa (V.Poelln.) Bayer (1977). Neotype, designated by Breuer & Metzing (1997): Riversdale, Ferguson s.n. (BOL).

= H. jakubii Breuer in Alsterworthia Int. Sp. Is. 7: 10 (2004). *H. bobii

H. mirabilis var. scabra (Bayer) Bayer (2012): H. heidelbergensis var. scabra Bayer in Haw. Revis.: 82 (1999): H. scabrida Breuer (2010). Type: Drew, Leeurivier, Bayer 1700 (NBG).

H. mirabilis var. splendens (Hammer & Venter) Bayer (2012): H. magnifica var. splendens Hammer and Venter in Cact. Succ. J. (US) 70: 180 (1998): H. splendens (Hammer & Venter) M.Hayashi (2000). Type: W Albertinia, Venter (NBG).

H. mirabilis var. sublineata (V.Poelln.) Bayer in Haw. Revis.: 113 (1999): H. triebneriana var. sublineata V.Poelln. (1938): H. sublineata (V.Poelln.) Breuer (2010). Neotype, designated by Bayer (1999): S Bredasdorp, Smith 3966 (NBG).

H. mirabilis var. toonensis (Bayer) Bayer (2012): H. heidelbergensis var. toonensis Bayer in Haw. Revis.: 83 (1999): H. toonensis (Bayer) Breuer (2010). Type: Heidelberg, Matjestoon, Smith 6797 (NBG).

H. mirabilis var. triebneriana (V.Poelln.) Bayer in Haw. Revis.: 113 (1999): H. triebneriana V.Poelln. (1936). Lectotype, designated by Bayer (1999): [unpublished illustration] (B).

= H. willowmorensis V.Poelln. (1937). H. triebneriana var. depauperata V.Poelln. (1938): H. depauperata (V.Poelln.) Breuer (2010). H. triebneriana var. multituberculata V.Poelln. (1938). H. triebneriana var. rubrodentata Triebn. et V.Poelln. (1939). H. triebneriana var. napierensis Triebn. et V.Poelln. (1939). H. triebneriana var. turgida Triebn. (1939). H. triebneriana var. subtuberculata V.Poelln. (1939). H. triebneriana var. pulchra V.Poelln. (1940). H. rossouwii V.Poelln. (1938). H. nitidula V.Poelln. (1939). H. triebneriana var. diversicolor Triebner & V.Poelln. in Feddes Repert. 47: 9 (1939).: H. diversicolor (Triebner & V.Poelln.) M.Hayashi (2010).

H. monticola Fourcade in Trans. Roy. Soc. S. Africa 21:78 (1937). Type: George and Uniondale districts, Fourcade 2498 (K).

= H. divergens Bayer (1976).

H. monticola var. monticola

= H. bronkhorstii M.Hayahi in Haworthiad 15: 16 (2001). *H. baviens *H. glabella

H. monticola var. asema Bayer in Haw. Revis.: 117 (1999): H. asema (Bayer) M.Hayashi (2000). Type: Calitzdorp, Besemkop, Venter 12 (NBG).

H. mucronata Haw. in Suppl. Pl. Succ.: 50 (1819). Lectotype, designated by Bayer (1999): [unpublished illustration] (K).

= H unicolor V.Poelln. (1937): H. unicolor var. unicolor (V.Poelln.) Bayer (1982). H. mclarenii V.Poelln. (1939). H. tradouwensis Breuer in Avonia 21: 57 (2003). *H. armata *H. confluens *H. montagua

H. mucronata var. mucronata

H. mucronata var. habdomadis (V.Poelln.) Bayer in Haw. Revis.: 120 (1999): H. habdomadis V.Poelln. (1938): H. inconfluens var. habdomadis (V.Poelln.) Bayer (1976). Neotype, designated by Breuer & Metzing (1997): Seweweekspoort, Barker & Lewis s.n NBG2764/32 (BOL).

H. mucronata var. inconfluens (V.Poelln.) Bayer in Haw. Revis.: 121 (1999): H. altilinea var. limpida f. inconfluens V.Poelln. (1938): H. mucronata var. limpida f. inconfluens (V.Poelln.) V.Poelln. (1940): H. inconfluens (V.Poelln) Bayer (1976): H. habdomadis var. inconfluens (V.Poelln) Bayer (1977). Lectotype, designated by Breuer & Metzing (1997): [unpublished image] Triebner 1031 (B).

= H. bijliana var. joubertii V.Poelln. (1936). H. setata var. bijliana sv. joubertii (V.Poelln.) V.Poelln. (1938): H. setata var. joubertii (V.Poelln.) Jacobsen (1960). H. integra var. standeri Esterhuizen in Haworthiad 14: 21 (2000): H. standeri (Esterhuizen) M.Hayashi (2010). H. crystallina M.Hayashi in Haworthia Study 15: 116 (2006).*H. allomadis *H. calitzensis *H. rooibergensis *H. horrida *H. kotei

H. mucronata var. rycroftiana Bayer in Haw. Hand.: 54 (1976). Gouritz River between Vanwyksdorp and Herbertsdale, Bayer 1701 (NBG).

= H. integra V.Poelln. in Feddes Repert. 33: 239 (1933).

 H. mucronata var. morrisiae (V.Poelln.) V.Poelln. in Feddes Repert. 49: 29 (1940): H. altilinea var. morrisiae V.Poelln. (1938): H. inconfluens var. morrisiae (V.Poelln.) Bayer (1976): H. habdomadis var. morrisiae (V.Poelln.) Bayer (1977). Lectotype, designated by Breuer & Metzing (1997): [unpublished image] (B).

= H. sakai M.Hayashi in Haworthia Study 3: 13 (2000).

H. mutica Haw. in Revis.:55 (1821). Lectotype, designated by Bayer (1978): [image] (K; later published in Excelsa 8: 50 (1978). Epitype, designated by Breuer & Metzing (1997): NE Soetrivier Bridge, Bayer KG623/69 (NBG).

= H. otzenii Smith (1945). H. groenewaldii Breuer in Alsterworthia Int. 11: 15 (2011).

H. nortieri Smith in Jl. S. Afr. Bot. 12: 13 (1946). Type: Vanrhynsdorp, Smith 1676a (NBG).

= H. nortieri var. montana Smith (1950). H. nortieri var. giftbergensis Smith (1950): H. giftbergensis (Smith) Breuer (2010). H. agnis Battista in Alsterworthia Int. 2: 9 (2002). H. montana M.Hayashi in Haworthia Study 14: 14 (2005), nom. inval.

H. nortieri var. nortieri

H. nortieri var. albispina (M.Hayashi) Bayer (2012): H. albinspina M.Hayashi in Haworthia Study 8: 1 (2002). Type: E Laingsburg, Hayashi 02-48 (TUAT).

H. nortieri var. devriesii (Breuer) Bayer (2012): H. devriesii Breuer in Avonia 21: 47 (2003). Type: Prince Albert, Breuer 6930 (TUAT).

H. nortierii var. globosiflora (Smith) Bayer (1976): H. globosiflora Smith (1950). Type: Doornbosch, N Doorn River Bridge, Smith 7198 (NBG).

H. nortierii var. pehlemanniae (Scott) Bayer in Haw. Revis.: 129 (1999): H. pehlemanniae Scott (1982). Type: W Laingsburg, Scott 7450 (PRE).

H. outeniquensis Bayer in Haw. Revis.: 130 (1999). Type: Moerasriver, Venter 94/61 (NBG). *H. heroldia

H. parksiana V.Poelln. in Cactus J. 5: 34 (1936). Lectotype, designated by Breuer & Metzing (1997): [image, later published in Desert Pl. Life 10: 48 (1938)] (B).

H. pubescens Bayer in J. S. Afr. Bot. 38: 129 (1973). Type: Worcester, Sandberg Hills, Bayer 163 (NBG).

H. pulchella Bayer in J. S. Afr. Bot. 39: 232 (1973). Type: Touws River, Avondrust, Bayer 163 (NBG).

H. pulchella var. pulchella

H. pulchella var. globifera Bayer in Haw. Revis. :136 (1999): H. globifera (Bayer) M.Hayashi (2000). Type: SE Anysberg, Bruyns 7338 (NBG).

H. pygmaea V.Poelln. in Repert. Spec. Nov. Regni Veg. 27: 132 (1930). Neotype, designated by Breuer & Metzing (1997): hills E Great Brak, Fourcade 4759 (BOL).

= *H. asperata

H. pygmaea var. pygmaea

H. pygmaea var. acuminata (Bayer) Bayer (2012): H. retusa f. acuminata Bayer in Haw. Handb.: 53 (1976): H. retusa var. acuminata (Bayer) Bayer (1982): H. magnifica var. acuminata (Bayer) Bayer (1999). Type: N of Gouritzmond, Bayer in KG 311/7 (NBG). *H. acuminata.

H. pygmaea var. argenteo-maculosa (Smith) Bayer in Haw. Revis.: 138 (1999): H. dekenahii var. argenteo-maculosa Smith (1945): H. retusa f. argenteo-maculosa (Smith) Bayer (1976). Type: between Gouritz Bridge and Mossel Bay, Emett s.n. NBG68037 (NBG).

= H. silviae M.Hayashi in Haworthia Study 3: 13 (2000).

H. pygmaea var. dekenahii (Smith) Bayer (2012): H. dekenahii Smith in Jl. S. Afr. Bot. 10: 140 (1944): H. retusa var. dekenahii (Smith) Bayer (1982): H. magnifica var. dekenahii (Smith) Bayer (1999). Type: Farm Draaihoek, J. Dekenah 86 sub Smith 5489 (NBG).

H. pygmaea var. fusca (Breuer) Bayer (2012): H. fusca Breuer in Alsterworthia Int. Special Issue 7: 9 (2004). Type: W Albertinia, Breuer 8971 (GRA).

H. pygmaea var. esterhuizenii (M.Hayashi) Bayer (2013).  H. esterhuizenii M. Hayashi in Haworthia Study 7: 14 (2002). Type: Albertinia, Hayashi 96-6 (TUAT) H. pygmaea var. vincentii (Breuer) Bayer in Nomenclator (2012): H. vincentii Breuer in Alsterworthia Int. Special Issue 7: 11 (2004). H. vincentii Breuer in Alsterworthia Int. Special Issue 7: 11 (2004). Type: NE Albertinia, De Vries 071 (GRA).

H. reticulata (Haw.) Haw. in Syn. Pl. Succ.: 94 (1812): Aloe reticulata Haw. (1804). Neotype, designated by Bayer (1972): Illustration in Curtis’ Bot.Mag.: t. 1314 (1811). Epitype, designated by Breuert & Metzing (1997): SW Worcester, Ribokkkop, Bayer 160 (NBG).

= Aloe pumilio Jacq. (1804). H. reticulata var. acuminata (1938). H. hurlingii var. ambigua Triebn. & V.Poelln. (1938). H. guttata Uitew. (1947). H. intermedia V.Poelln. (1937), syn. nov: H. magnifica var. intermedia (V.Poelln.) Bayer (1999).

H. reticulata var. reticulata

H. reticulata var. attenuata Bayer in Haw. Revis.: 140 (1999). Type: S Bonnievale, Smith 3979 (NBG). *H. oxygona?

H. reticulata var. hurlingii (V.Poelln.) Bayer in New. Haw. Hand.: 52 (1982): H. hurlingii V.Poelln. (1936). Lectoptype, designated by Breuer & Metzing (1997): [image, later published in Desert Pl. Life 10: 125 (1938)] (B).

H. reticulata var. subregularis (Baker) Bayer in Haw. Revis.: 141 (1999): H. subregularis Baker (1870). Lectotype, designated by Bayer (1999): Illustration in Saund. Ref. Bot.: t. 232 (1870).

= H. haageana V.Poelln. (1930). H. haageana var. subreticulata V.Poelln. (1937).

H. retusa (L.) Duval in Pl. Succ. Hort. Alenc.: 7 (1809): Aloe retusa L. (1753). Lectotype, designated by Scott (1985): Illustration in Commelin, Horti Med. Amstelod. 2: t. 6 (1701). Epitype, designated by Breuer & Metzing (1997): Blikbonnie, E Riversdale, Dekenah s.n. NBG144772 (NBG).

= H. foucheii V.Poelln. (1940). H. retusa var. multilineata Smith (1946): H. multilineata (Smith) Scott (1985). H. retusa var. solitaria Smith (1946): H. solitaria (Smith) Scott (1973). H. retusa var. densiflora Smith (1946). H. geraldii Scott (1965). *H. subretusa

H. retusa var. retusa

H. retusa var. longibracteata (Smith) Bayer (2012): H. longibracteata Smith in Jl. S. Afr. Bot. 11: 75 (1945): H. turgida var. longibracteata (Smith) Bayer (1999). Type: near Stilbaai, Dekenah 18 sub Smith 5378 (NBG).

H. retusa var. nigra (Bayer) Bayer (2012): H. mutica var. nigra Bayer in Haw. Revis.: 126 (1999). Type: Kransriviermond, Smith 5753 (NBG). *H. quimutica *H. chromutica

H. retusa var. suberecta (V.Poelln.) Bayer(2012)H. turgida var. suberecta V.Poelln. in Repert. Spec. Nov. Regni Veg. 44: 134 (1938): H. suberecta (V.Poelln.) Breuer (2010). Neotype, designated by Bayer (1999): Brandwacht, Bayer s.n. KG631/69 (NBG).

= H. turgida var. subtuberculata V.Poelln. (1938). H. turgida var. pallidifolia Smith (1946): H. pallidifolia (Smith) Breuer (2010). *H. rodinii

H. retusa var. turgida (Haw) Bayer (2012)H. turgida Haw. in Suppl. Pl. Succ.: 52 (1819). Neotype, designated by Breuer & Metzing (1997): Swellendam, Breede River Bridge, Bayer 2420 (NBG).

= H. laetivirens Haw. (1819). H. caespitosa V.Poelln. (1936). H. caespitosa f. subplana V.Poell. (1938). H. caespitosa f. subproliferans V.Poelln. *H. pseuda *H. reflexa

H. rossouwii V.Poelln. in Kakteenk. 7: 75 (1938). Lectotype, designated here: [unpublished image] (B).

= H. serrata Bayer in Jl. S. Afr. Bot. 39: 249 (1973). Type: Heidelberg, Oudekraalkop, Bayer 166 (NBG).

H. rossouwii var. rossouwii

H. rossouwii var. calcarea (Bayer) Bayer (2012)H. mirabilis var. calcarea Bayer in Haw. Revis.: 110 (1999): H. calcarea (Bayer) M.Hayashi (2000). Type: Bredasdorp, De Hoop, Burgers 1648 (NBG).

H. rossouwii var. minor (Bayer) Bayer (2012)H. heidelbergensis var. minor Bayer in Haw. Revis.: 82 (1999): H. rooivleiensis Breuer (2010). Type: Bredasdorp, Rooivlei, Bayer sub KG 36/70 (NBG).

H. rossouwii var. petrophila (Bayer) Bayer (2012): H. variegata var. petrophila Bayer in Haw. Revis.: 159 (1999): H. petrophila (Bayer) M.Hayashi (2000). Type: Renosterfontein, Burgers 2158 (NBG).

H. rossouwii var. elizeae (Breuer) Bayer in Haworthia Update 2.2: 153 (2006): H. elizeae Breuer (2003). Type: W Swellendam, Breuer 6936 (TUAT).

H. semiviva (V.Poelln.) Bayer in Haw. Handb.: 153 (1976): H. bolusii var. semiviva V.Poelln. (1938). Lectotype, desigtnated by Breuer & Metzing (1997): [image, later published in Succulenta (Netherlands) 22: 25 (1940)] (B). *H. sphaeroidea *H. victoria

H. springbokvlakensis Scott in Jl. S. Afr. Bot. 36: 287 (1970). Type: Springbokvlakte, Scott 245 (PRE).

H. transiens (V.Poelln) Bayer in Haworthiad 16: 66 (2002): H. cymbiformis var. transiens (V.Poelln.) Bayer (1976): H. planifolia var. transiens V.Poelln. (1938). Lectotype, designated by Breuer & Metzing (1997): [unpublished image] (B).

= H. cymbiformis var. translucens Triebn. et V.Poelln. (1938). H. cymbiformis var. multifolia Triebn. (1938). H. cymbiformis var. brevifolia Triebn. et V.Poelln. (1938). *H. klipensis

H. truncata Schonland in Trans. Roy. Soc. S. Afr. 1: 391 (1910). Type: near Oudtshoorn, Britten (K).

= H. truncata f. tenuis V.Poelln. (1938): H. truncata var. tenuis (V.Poelln.) Bayer (1976). H. truncata f. crassa V.Poelln. (1938). H. truncata f. normalis V.Poelln. (1938). H. truncata var. minor Breuer in Avonia 21: 59 (2003).: H. papillaris Breuer (2010).

H. truncata var. truncata

H. truncata var. maughanii (V.Poelln.) Bayer in Haw. Revis.: 151 (1999). H. maughanii V.Poelln. (1932). Neotype, designated by Breuer & Metzing (1997): Calitzdorp, Malherbe s.n. NBG307/40 (NBG).

H. variegata Bolus in J. Bot. Soc. S. Afr.: 137 (1929). Type: Botterkloof, Mrs. E. Ferguson s.n. BOL18900 (BOL).

H. variegata var. variegata

H. variegata var. hemicrypta Bayer in Haw. Revis.: 158 (1999): H. hemicrypta (Bayer) M.Hayashi (2000). Type: NE lower slopes of Potberg, Burgers 2582 (NBG).

H. variegata var. modesta Bayer in Haw. Revis.: 159 (1999): H. modesta (Bayer) Hayashi (2000). Type: SW Kathoek, Bayer 2551 (NBG).

H. vlokii Bayer in Haw. Revis.: 160 (1999). Type: Swartberg Mts., Vlok sub Venter 91/2 (NBG).

H. wittebergensis Barker in Jl. S. Afr. Bot. 8: 245 (1942). Type : Witteberg, Pieterse sub NBG 68214 (NBG).

H. zantneriana V.Poelln. in Cactus J. 5: 35 (1936). Lectotype, designated by Breuer & Metzing (1997): [image, later published in Desert Pl. Life 9: 90 (1937)] (B).

H. zantneriana var. zantneriana

H. zantneriana var. minor Bayer in Haw. Revis.: 164 (1999): H. inspida Breuer (2010). Type: near Miller Station, Bayer 1702 (NBG).

II. Subgenus Hexangulares (Uitewaal) M.B.Bayer [as Uitewaal ex M.B.Bayer] in Haw. Handb.: 14 (1976). Type species: Haworthia coarctata Haw. [Lectotype, designated by Bayer (1976)]. ± 15 spp.

H. attenuata (Haw.) Haw. in Syn. Pl. Succ.: 92 (1812): Aloe attenuata Haw. (1804). Neotype, designated by Breuer & Metzing (1997): 20 km E Patensie, Sandland. Perry 660 (NBG).

= H. clariperla Haw. (1928): Aloe attenuata var. clariperla (Haw) Salm-Dyck (1834): H. attenuata var. clariperla (Haw.) Baker (1880): H. attenuata f. clariperla (Haw.) Bayer (1976). H. fasciata var. caespitosa Berger (1908). H. britteniana V.Poelln. (1937): H. attenuata var. britteniana (V.Poelln.) V.Poelln. (1937): H. attenuata f. britteniana [as britteniae] (V.Poelln.) Bayer (1976). H. attenuata var. odonoghueana et vars. linearis, uitewaaliana, deltoidea, minissima, inusitata Farden (1939).

H. attenuata var. attenuata

H. attenuata var. glabrata (Salm Dyck) Bayer (2012): Aloe glabrata Salm Dyck in Hort.Dyck.: 325 (1834): H. glabrata (Salm Dyck) Baker (1880). Neotype, designated by Smith & Greyling (1990): Illustration in Salm Dyck, Aloes Mesembr. 3: Aloe t. 7 [sect. 6: 13] (1840).

H. attenuata var. radula (Jacq.) Bayer in Haw. Revis.: 167 (1999): Aloe radula Jacq. (1804): H. radula (Jacq.) Haw. (1812). Type: Illustration in Jacq., Pl. Hort.Schoenbr. 4: t. 422 (1804). Epitype, designated by Breuer & Metzing (1997): 1.6 km from Hankey to Thornhill, Smith 3190 (NBG).

H. bruynsii Bayer in J. S. Afr. Bot. 47:789 (1981). Type: SE Steytlerville, Rossouw 456 (NBG).

H. coarctata Haw. in Philos.Mag. 64: 301 (1824). Neotype, designated by Breyer & Metzing (1997): 16 km from Grahamstown to Bathurst, Smith 7092 (NBG).

= H. chalwinii Marl.et Berg. (1906). H. reinwardtii var. conspicua V.Poelln. (1937). H. fallax V.Poelln. (1932): H. reinwardtii var. fallax V.Poelln. (1937). H. reinwardtii var. pseudocoarctata V.Poelln. (1940): H. coarctata var. haworthii f. pseudocoarctata (V.Poelln.) Resende (1943). H. coarctata var. haworthii Resende (1943). H. coarctata var. kraussii Resende (1943). H. reinwardtii var. committeesensis Smith (1943). H. reinwardtii var. huntsdriftensis Smith (1944). H. fulva Smith (1943). H. musculina Smith (1948). H. greenii var. silvicola Smith (1943).

H. coarctata var. coarctata

H. coarctata var. coarctata f. coarctata

H. coarctata var. coarctata f. greenii (Baker) Bayer in Haw. Revis.: 172 (1999): H. greenii Baker (1880): H. greenii subsp. coarctata var. greenii (Baker) Bayer (1973). Type: Cape, Cooper 1860 (K).

= H. peacockii Baker (1880). H. greenii f. bakeri Resende (1943). H. greenii f. minor Resende (1943).

H. coarctata var. adelaidensis (V.Poelln.) Bayer in Haw. Revis.: 172 (1999): H. reinwardtii var. adelaidensis V.Poelln. (1940): H. coarctata subsp. adelaidensis (V.Poelln.) Bayer (1973): H. adelaidensis (V.Poelln.) Breuer in Gen. Haw. 1: 7 (2010). Lectotype, designated by Breuer & Metzing 91997): [unpublished image] (B).

= H. reinwardtii var. riebeeckensis Smith (1944). H. reinwardtii var. bellula Smith (1945).

H. coarctata var. tenuis (Smith) Bayer in Haw. Revis.: 173 (1999): H. reinwardtii var. tenuis Smith (1948): H. coarctata ssp. coarctata var. tenuis (Smith) Bayer (1973): H. tenuis (Smith) Breuer (2010). Type: Cape, Alexandria Dist. Smith 3420 (NBG).

H. fasciata (Willd.) Haw. in Suppl. Pl. Succ.: 57 (1819): Apicra fasciata Willd. (1811): Aloe fasciata (Willd.) Salm Dyck (1937). Neotype, designated by Breuer & Metzing (1997): Hankey, Stayner s.n. NBG110360 (NBG).

= H. fasciata var. major Haw. (1819). Aloe fasciata var. major Salm Dyck (1837): H. fasciata var. major (Salm Dyck) V.Poelln. (1938). H. fasciata var. subconfluens V.Poelln. (1937): H. fasciata f. subconfluens (V.Poelln.) V.Poelln. (1938). H. fasciata f. ovatolanceolata V.Poelln. (1938). H. fasciata f. sparsa V.Poelln. (1938). H. fasciata f. variabilis V.Poelln. (1938). H. fasciata f. vanstaadenensis V.Poelln. (1938). H. browniana V.Poelln. (1937): H. fasciata f. browniana (V.Poelln.) Bayer (1976).

H. glauca Baker in J. Linn. Soc. Bot. 18:203 (1880). Type: Zuurberg Pass, Cooper (K).

= H. carrissoi Resende (1941).

H. glauca var. glauca

H. glauca var. herrei (V.Poelln.) Bayer in Haw. Hand.: 122 (1976): H. herrei V. Poelln. (1929). Neotype, designated by Breuer & Metzing (1997): Campherspoort, Barker 5069 (NBG).

= H. herrei var. depauperata V.Poelln. (1932). H. jacobseniana V.Poelln. (1937). H. eilyae V.Poelln. (1937). H. jonesiae V.Poelln. (1937). H. herrei var. poellnitzii Resende (1943). H. eilyae var. poellnitziana Resende (1943). H. eilyae var. zantneriana Resende (1943). H. armstrongii V.Poelln. (1937): H. glauca var. herrei f. armstrongii (V.Poelln.) Bayer (1976).

H. granulata Marloth in Trans. Ror. Soc. S. Afr. 2:39 (1910): H. venosa subsp. granulata (Marloth) Bayer (1976). Type: Verlatenkloof, Marloth 4217 (BOL).

= H. schoemanii M.Hayashi in Haworthia Study 9: 14 (2003).

H. koelmaniorum Oberm. & Hardy in Fl. Pl. Africa :f. 1502 (1967). Type: Groblersdal, Hardy & Mauve 2267 (PRE).

H. koelmaniorum var. koelmaniorum

H. koelmaniorum var. mcmurtryi (Scott) Bayer in Haw. Revis.: 181 (1999): Haworthia mcmurtryi Scott (1984). Type: Loskop, SW Dam, McMurtry 5247 (PRE).

H. limifolia Marloth in Trans. Roy. Soc. S. Africa 1: 409 (1908). Type: W Delagoa Bay, Marloth 4678 (PRE).

= H. limifolia var. diploidea Resende (1940). H. limifolia var. tetraploidea Resende (1940). H. limifolia f. marlothiana Resende (1941): H. limifolia var. marlothiana (Resende) Resende (1943). H. limifolia var. schuldtiana Resende (1940). H. limifolia var. stolonifera Resende (1940). H. limifolia var. stolonifera f. pimentelli Resende (1943). H. limifolia var. stolonifera f. major Resende (1943). H. limifolia var. keithii Smith (1950). *H. gideonii

H. limifolia var. limifolia

H. limifolia var. arcana G.F.Smith & N.R.Crouch in Bradleya 19: 119 (2001): H. arcana (G.F.Smith & N.R.Crouch) Breuer in Gen. Haw. 1: 7 (2010). Type: #

H. limifolia var. gigantea Bayer in Jl. S. Afr. Bot. 28: 215 (1962): H. gigantea (Bayer) M.Hayashi (2000). Type: Nongoma, Bayer 112 (PRE).

H. limifolia var. glaucophylla Bayer in Haworthia Update 2: 1 (2006): H. glaucophylla (Bayer) Breuer (2010). Type: Mpumalanga, Three Sisters, F. Venter 13700 (NBG).

H. limifolia var. ubomboensis (Verdoorn) Smith in Jl. S. Afr. Bot. 16: 3 (1950): H. ubomboensis Verdoorn (1941). Type: 16km S Stegi, Keith s.n. PRE26392 (PRE).

H. longiana V.Poelln. in Feddes Repert. 41: 203 (1937). Neotype, designated by Breuer & Metzing (1997): [unpublished image] (B).

= H. longiana var. albinota Smith (1948).

H. nigra (Haw.) Baker in J. Linn. Soc. Bot. 18: 203 (1880): Apicra nigra Haw. (1825). Neotype, designated by Breuer & Metzing (1997): Campherspoort, Barker 5099 (NBG).

= H. schmidtiana V.Poelln. (1929): H. nigra var. schmidtiana (V.Poelln.) Uitew. (1948). H. schmidtiana var. angustata V.Poelln. (1937): H. nigra var. angustata (V.Poelln.) Uitew. (1948). H. schmidtiana var. suberecta V.Poelln. (1937): H. nigra var. suberecta (V.Poelln.) Uitew. (1948). H. schmidtiana var. pusilla V.Poelln. (1938): H. nigra var. pusilla (V.Poelln.) Uitew. (1948). H. ryneveldii V.Poelln. (1939). *H. eonigra

H. nigra var. nigra

H. nigra var. diversifolia (V.Poelln.) Uitew. in Succulenta: 51 (1948): H. diversifolia V.Poelln. (1937): H. schmidtiana var. diversifolia (V.Poelln.) V.Poelln. (1938). Neotype, designated by Bayer (1999): Kruidfontein, Bruyns in KG435/75 (NBG).

= H. schmidtiana var. diversifolia f. nana V.Poelln. (1938): H. nigra var. diversifolia f. nana (V.Poelln.) Uitew. (1948).

H. nigra var. elongata (V.Poelln.) Uitew. in Succulenta: 51 (1948): H. schmidtiana var. elongata V.Poelln. (1938). Neotype, designated here: Slagtersnek, Van Jaarsveld & Marthinus 7913 (NBG).

H. pungens Bayer in Haw. Revis.:188 (1999). Type: Braamriver. Bruyns 7090 (NBG).

H. reinwardtii (Salm Dyck) Haw. in Saxifrag. Enum. 2: 53 (1821): Aloe reinwardtii Salm Dyck (1821). Neotype, designated by Scott (1981): Illustration in Salm Dyck, Aloes Mesembr. 1: Aloe t. 12 [sect. 6: 16] (1836). Epitype, designated by Breuer & Metzing (1997): hill above Ncera River Bridge, Smith 3563 (NBG).

= H. reinwardtii var. major Baker (1880). H. reinwardtii var. pulchra V.Poelln. (1937). H. reinwardtii var. archibaldiae V.Poelln. (1937). H. reinwardtii var. peddiensis Smith (1943). H. reinwardtii var. valida Smith (1943). H. reinwardtii var. grandicula Smith (1944). H. reinwardtii var. haworthii Resende (1943). H. reinwardtii var. triebneri Resende (1943).

H. reinwardtii var. reinwardtii

H. reinwardtii f. reinwardtii

H. reinwardtii f. chalumnensis (Smith) Bayer (1976): H. reinwardtii var. chalumnensis Smith (1943). Type: Chalumna, Smith 513 (NBG).

H. reinwardtii f. kaffirdriftensis (Smith) Bayer (1976): H. reinwardtii var. kaffirdriftensis Smith (1943). Type: Kaffirdrift, Smith 3364 (NBG).

H. reinwardtii f. olivacea (Smith) Bayer (1976): H. reinwardtii var. olivacea Smith (1944): H. olivacea (Smith) Breuer (2010). Type: Kaffirdrift, Smith 5260 (NBG).

H. reinwardtii f. zebrina (Smith) Bayer (1976): H. reinwardtii var. zebrina Smith (1944). Type: Kaffirdrift, Smith 5258 (NBG).

H. reinwardtii var. brevicula Smith in Jl. S. Afr. Bot. 10: 11 (1944): H. brevicula (Smith) Breuer in Gen. Haw. 1: 7 (2010). Type: Frazers Camp, Smith 3138 (NBG).

= H. reinwardtii var. diminuta Smith (1948).

H. scabra Haw. in Suppl. Pl. Succ.: 58 (1819). Lectotype, designated by Scott (1980): [illustration, later published in Cact. Succ. J. (Los Angeles) 52: 274 (1980)] (K).

= H. tuberculata V.Poelln. (1931). H. tuberculata var. acuminata V.Poelln. (1938). H. tuberculata var. sublaevis V.Poelln. (1938). H. tuberculata var. subexpansa V.Poelln. (1938). H. tuberculata var. angustata V.Poelln. (1940). H. scabra var. johanii M.Hayashi in Haworthiad 15: 16 (2001).: H. johanii (M.Hayashi) Breuer (2010).

H. scabra var. scabra

H. scabra var. lateganiae (V.Poelln.) Bayer in Haw. Revis.: 195 (1999): H starkiana var. lateganiae (V.Poelln.) Bayer (1976): H. lateganiae V.Poelln. (1937). Lectotype, designated by Breuer & Metzing (1997): [image, later published in Desert Pl. Life 9: 103 (1937): (B).

H. scabra var. morrisiae (V.Poelln.) Bayer in Haw. Hand.: 137 (1976): H. morrisiae V.Poelln. (1937). Lectotype, designated by Breuer & Metzing 91997): [image, later published in Kakteenk. & Kakteenfr. 1937: 132 (1937)] (B). *H. plettens

H. scabra var. starkiana (V.Poelln.) Bayer in Haw. Revis.: 197 (1999): H. starkiana V.Poelln. (1933). Lectotype, designated by Breuer & Metzing (1997): [unpublished image] (B).

= H. smitii V.Poelln. (1938).

H. sordida Haw. in Revis.: 51 (1821): Aloe sordida Schult. & Schult.f. (1829). Neotype, designated by Scott (1985): Illustration in Salm Dyck, Aloes Mesembr. 7: Aloe t. 1 [sect 7: 2] (1863).

= H. sordida var. agavoides (Zant. & V.Poelln.) Smith (1950): H. agavoides Zant. & V.Poelln. (1938).

H. sordida var. sordida

H. sordida var. lavranii Scott in Cact. Succ. J. (US) 53: 70 (1981): H. lavranii (Scott) Breuer (2010). Type: Perdehoek, Little Karoo, Hechter s.n. PRE61124 (PRE).

H. tessellata Haw. in Phil. Mag. 44: 300 (1824): . Aloe tessellata (Haw.) Schult. & Schult.f. (1829): H. venosa subsp. tessellata (Haw.) Bayer (1976). Lectotype, designated by Scott (1978): [illustration, later published in Cact. Succ. J. (Los Angeles) 50: 75 (1978) (K).

= H. parva Haw. (1824): Aloe parva (Haw.) Schult. & Schult.f. (1829): H. tessellata var. parva (Haw.) Baker (1880). H. tessellata var. inflexa Baker (1880). H. engleri Dint. (1914): H. tessellata var. engleri (Dint.) V.Poelln. (1938). H. pseudotessellata V.Poelln. (1929). H. tessellata var. tuberculata V.Poelln. (1936). H. minutissima V.Poelln. (1939): H. tessellata var. minutissima (V.Poelln.) Viveiros (194?). H. tessellata var. elongata Van Woerden (1940). H. tessellata var. simplex Resende & V.Poelln. (1942). H. tessellata var. stepheneana Resende & V.Poelln. (1942). H. tessellata var. luisierii Resende & V.Poelln. (1942). H. tessellata var. palhinhiae Resende & V.Poelln. (1942). H. tessellata var. velutina Resende & V.Poelln. (1942). H. tessellata var. coriacea Resende & V.Poelln. (1942): H. coriacea (Resende & V.Poelln) Breuer (2010). H. tessellata var. coriacea f. longior Resende & V.Poelln. (1942). H. tessellata var. coriacea f. brevior Resende & V.Poelln. (1942). H. tessellata var. obesa Resende & V.Poelln. (1942). H. venosa ssp. recurva sensu Bayer (1976). H. crousii [spahlm. crausii] M.Hayashi in Haworthiad 15: 16 (2001). *H. helensis *H. mediata

H. venosa (Lam.) Haw. in Saxifrag. Enum: 51 (1821): Aloe venosa Lam. (1873). Lectotype, designated by Scott (1978): Illustration in Commelin, Praeludia Bot.: t. 29 (1703). Epitype, desigtnated by Breuer & Metzing (1997): Swellendam, W of Breede River Bridge, Bayer 168 (NBG).

= Aloe tricolor Haw. (1804). = Aloe recurva Haw. (1804): H. recurva (Haw.) Haw. (1812). = H. distincta Brown (1876). = H. venosa var. oertendahlii Hjelmquist (1943). *H. irmiae

H. viscosa (L.) Haw. in Syn. Pl. Succ.: 90 (1812): Aloe viscosa L. (1753). Lectotype, designated by Scott (1981): Illustration in Commelin, Praeludia Bot.: t. 31 (1703). Epitype, designated by Breuer & Metzing (1997): Calitzdorp, Blackburn Valley, Barker 5073 (NBG).

= Aloe pseudotortuosa Salm Dyck (1817): H. pseudotortuosa (Salm Dyck) Haw. (1819): H. viscosa var. pseudotortuosa (Salm Dyck) Baker (1880). Aloe subtortuosa Salm Dyck (1836). Aloe tortuosa Haw. (1804): H. tortuosa (Haw.) Haw. (1812). H. concinna Haw. (1819): Aloe concinna (Haw.) Haw. (1829): H. viscosa var. concinna (Haw.) Baker (1880). Aloe tortuosa var. major Salm Dyck (1817). H. asperiuscula Haw. (1819): Aloe asperiuscula (Haw.) Salm Dyck (1836). H. cordifolia Haw. (1819): Aloe cordifolia (Haw.) Salm Dyck (1836). H. indurata Haw. (1821): Aloe viscosa var. indurata (Haw.) Salm Dyck (1836): H. viscosa var. indurata (Haw.) Baker (1880). H. viscosa var. major Haw. (1821). = H. viscosa var. minor Haw. (1821). H. viscosa var. parvifolia Haw. (1821). H. torquata Haw. (1827): Aloe torquata (Haw.) Salm Dyck (1836): H. viscosa var. torquata (Haw.) Baker (1880). H. viscosa var. subobtusa V.Poelln. (1938). H. viscosa var. caespitosa V.Poelln. (1938). H. beanii Smith (1945). H. beanii var. minor Smith (1945). H. viscosa var. cougaensis Smith (1945). H. viscosa var. viridissima Smith (1945). H. asperiuscula var. subintegra Smith (1945). H. asperiuscula var. patagiata Smith (1946). H. viscosa var. quaggaensis Smith (1948). H. viscosa var. variablis Breuer in Avonia 21: 61 (2003).: H. variabilis (Breuer) Breuer (2010).

H. woolleyi V.Poelln. in Repert. Spec. Nov. Regni Veg. 42: 269 (1937): H. venosa subsp. woolleyi (V.Poelln.) Bayer (1999). Lectotype, designated by Breuer & Metzing (1997): [image, later published in Cact. J. (Croydon) 7: 3 (1938) (B).

III. Subgenus Robustipedunculatae (Uitewaal) M.B.Bayer [as Robustipedunculares Uitewaal ex M.B.Bayer] in Haw. Handb.: 14 (1976). Type species: Haworthia margaritifera (L.) Haw. [lecto., designated by Bayer in Haw. Handb.: 14 (1976)]. 4 spp.

H. kingiana V.Poelln. in Cact. J. 5:31 (1936): H. subfasciata var. kingiana V.Poelln. (1938). Neotype, designated by Breuer & Metzing (1997): Great Brak, Dekenah 201 (NBG).

= H. zenigata M.Hayashi in Haworthiad 15: 20 (2001).

H. marginata (Lam.) Stearn in Cactus J. 12: 34 (1938): Aloe marginata Lam. (1783). Lectotype, designated by Scott (1985): Illustration in Commelin, Praeludia Bot.: t. 30 (1703).

= Aloe albicans Haw. (1804). H. albicans (Haw.) Haw. (1812). H. laevis Haw. (1821): H. marginata var. laevis (Haw.) Jacobson (1960). H. virescens Haw. (1821): H. albicans var. virescens (Haw.) Baker (1896): H. marginata var. virescens (Haw.) Uitew. (1939). H. ramifera Haw. (1821): H. marginata var. ramifera (Haw.) Jacobson (1960).

H. minima (Aiton) Haw. in Syn. Pl. Succ.: 92 (1812): A. margaritifera var. minima Ait. (1789). Lectotype, designated by Scott (1985): Illustration in Dillenius, Hort. Eltham: t. 16, f. 18 (1732).

= A. pumila var. margaritifera gamma L. (1753). Aloe margaritifera var minor Ait. (1789): Haworthia minor (Haw.) Duv. (1809). Apicra granata Willd. (1811): H. granata (Willd.) Haw. (1819): A. granata (Willd.) Schult. & Schult.f. (1829): H. margaritifera var. granata (Willd.) Baker (1880). A. margaritifera var. minor Ker‑G. (1811). A. erecta var. laetivirens Salm Dyck (1824). Aloe erecta Salm Dyck (1836). Aloe margaritifera var. major Ait. (1789): H. major (Ait.) Duv. (1809). A. margaritifera var media DC. (1799). H. brevis Haw. (1819): A. brevis (Haw.) Schult. & Schult.f. (1829). H. erecta Haw. (1819): A. erecta (Haw.) Schult. & Schult.f. (1829) [non A. erecta Salm Dyck (1836)]: H. margaritifera var. erecta (Haw.) Baker (1880). H. margaritifera var. corallina Baker (1880). H. mutabilis V.Poelln. (1938). H. opalina M.Hayashi in Haworthiad 15: 17 (2001). *H. flavens *H. obrata

H. minima var. minima

H. minima var. poellnitziana (Uitew.) Bayer in Haw. Revis.: 213 (1999): H. poellnitziana Uitew. (1939). Type: Drew, Meiring (AMD).

H. pumila (L.) Duval. (1809): Aloe pumila L. (1753): Aloe pumila var. margaritifera L. (1753): Aloe margaritifera (L) Burm.f (1768): H. margaritifera (L.) Haw. (1819). Lectotype, designated by Scott (1985): Illustration in Commelin, Horti Med. Amstelod.: t. 10 (1701).

= Aloe arachnoidea var. pumila Ait. (1789): A. pumila (Ait.) Haw. (1804), hom. illegit. non A. pumila L. (1753). Aloe margaritifera var. maxima Haw. (1804): H. maxima (Haw.) Duv. (1809): A. semimargaritifera var. maxima (Haw.) Salm Dyck (1817). H. margaritifera var. semimargaritifera (Salm Dyck) Baker (1880). A. papillosa Salm Dyck (1817): H. papillosa (Salm Dyck) Haw. (1819). *H. sparsa.

Hybrids
H. mortonii Breuer in Alsterworthia Int. 7: 22 (2007). *H. hammeri

The absurdity of taxonomy and nomenclature?

In Alsterworthia 13.1:6 (2013) there is yet another statement about the correct name for a species of Haworthia.  It reads …”The vexing matter of the correct name for Haworthia pumila has taxed some of the finest minds in botanical nomenclature”. The article then goes on to replace that name with H. margaritifera with an explanation so simple that it casts considerable doubt onto the quality of those minds that have examined the problem. There is of course also a difficulty in that the quoted sentence implies that H. pumila is the correct name, while the article goes on to dismiss it.

The fact is that Linnaeus listed four different things (varieties) under a single name Aloe pumila, and the only issue was about which of those four things ends up with that particular first name. It so happened that Burman in 1701 made a choice, and was followed by Aiton in 1789 who chose something else. So the name Aloe pumila stood but applied to two different things (species). Duval was unaware of the earlier Burman choice and used Aiton’s choice when he created the genus Haworthia. Dr L. A Codd, whom I would have accepted as a fine mind (and also as a very ethical man), advised C.L. Scott that Aiton’s choice was in fact illegitimate and hence also Duval’s usage in Haworthia. The opinion was that Burman’s choice was the first and also thus the legitimate one; and it could not be denied by the illegitimacy of the Aiton usage as a later action. So perhaps it was/is a question of rank or just an opinion that Aiton made up pumila as an entirely new name.

There is nothing complicated and mind boggling about this simple state of affairs. Or is that so? What on earth does the ICN as the product of presumably fine minds actually say about this? Does it take 50 years of debate to establish such a simple fact? The situation is further exacerbated in that the finest taxonomic minds are involved in an epic battle to either create a single alooid genus or many lesser genera. It appears that the latter option is winning ground although the war against single-species genera has surely not been abandoned. When the dust finally settles, it will be recognised that the taxon onto which this unfortunate species viz. Haworthia pumila/margaritifera resolves, will be a separate genus, probably Tulista, and then the truly correct name will be Tulista pumila. Or will it?

My personal opinion that however the case may truly be judged, the correct answer is the intent. Scott and Codd came to a workable end point way back in history and it has been my misfortune now to have defended that. I think there is a parallel in the case of Aloe bainesii. Put into use by Reynolds far back in history, it is found that the name barberae had page priority and thus preference. In what interest was the change made? Why does the code have a conservation facility for names? The fun seems to be in the argument rather than in usage.

The argument that I think L.A. Codd would have made is this. There are four varieties covered by the Linnaean epithet pumila. The first effective use of that epithet for one of the four was to the warty t10 of Commelin and that is how the name is formally typified. To use of that same epithet at any other time for any other of those four Linnaean varieties would be illegitimate. It is also not in the least certain that the name margaritifera is correctly typified by Wijnands on the same Commelin illustration t10. I aided Wijnands to this conclusion before myself stumbling on the fact that its correct typification would be on a Bradley illustration.

There is a curious twist to the issue and it is somewhat of an oversight that the persons involved never read the introduction to Haworthia Revisited. I explained the problem and also in respect to the correct application of the original name margaritifera to what we know as H. minima. I also cited the name H. pumila with the authors as (L.) Bayer to make it clear that I was not accepting the name with the authors (L.)Duval as Scott cited it. I thought at the time that it was a mistake on Scott’s part. I had also written to Dr Codd specifically about the issue and this is when he explained to me (as a professional taxonomist and fine mind) that the illegitimate use of the name pumila in Haworthia did not prevent the correct usage. It only strikes me now that he probably had advised Scott to the effect that the NAME as Duval had taken it through to Haworthia was correct, even if he had applied it to the wrong species. This whole issue has not been properly and fully aired. To argue that it is a new name seems to me just a piece of intellectual vanity that serves no purpose other than to demonstrate our collective failure to honour the intent of the code – or respect the dismay of interested person. A last point I make is that people can and will always find topics to disagree on, so this is an important trap to avoid and be mindful of. It is not particularly in the case of nomenclature that this seems to happen. I had no doubt at the time when I made the decision to accept Scott’s usage that no matter what my decision was, cause would be found to change it. If I had decided on either margaritifera (correctly typified) or maxima (as I. Breuer later did), this would also have been argued as wrong.

[-ed. There seems to be a number of taxonomic changes brewing. Time will tell whether pumila survives.]

References:

1. Haworthia margaritifera/pumila
Dr. John Manning. SANBI.
The vexing matter of the correct name for Haworthia pumila has taxed some of the finest minds in botanical nomenclature. Since I do not include myself among their company, I was not in the least surprised to find that I had misrepresented the situation. Thanks to expert input from Roy Mottram and Urs Eggli we can now put the matter to rights.

The issue of the correct name for Haworthia pumila starts with the fact that in his original publication of Aloe pumila, which forms the basis for this species, Linnaeus recognized several varieties, but without explicitly listing the typical variety, thus he did not list Aloe pumila L. var. pumila. Linnaeus’ Aloe pumila was subsequently effectively lectotypified by Burman f. (1701) [and later in enor by Scott (1978)] against the illustration in Commelin’s Horti medici Amstelodamensis, which is also the type of var. margarit!fera. This renders the name margaritifera homotypic with Aloe pumila L. (i.e. they share the same type). As the autonym (i.e. following automatically from the species name) for this species, pumila would normally have statutory priority over margarit(fera BUT, in the interim, the combination Haworthia pumila (Aiton) Haw. (1804) had been published, based on the name Aloe arachnoidea var. pumila Aiton, a quite different species that we know now as H herbacea. The publication of this combination renders Haworthia pumila (L.) Duval (1809) an illegitimate later homonym and thus not available for use in Haworthia. Because the combination Haworthia pumila cannot be used for Aloe pumila L. as a result of its prior usage for some other taxon it must be substituted with the next available valid and legitimate epithet, which is margaritifera. Note, however, that in any genus other than Haworthia the epithet pumila is the correct one to be used for this species.

The formal rendering of this situation is as follows:
Haworthia margaritifera (L.) Haw. (1819). Aloe pumila var. margaritifera L. (1753).  Aloe margaritifera (L.) Burm.f (1768).  Aloe pumila L. (1753). H pumila (L.) Duval. (1809), hom. illegit. non H pumila (Ait.) Haw. (1804). Lectotype, effectively designated by Burman f. in Prodromus florae Capensis: 10 (1768) [Superfluous lecotypification by Scott (1985)]: Illustration in Commelin, Horti medici Amstelodamensis, Pars altent: t.l 0 (1701): Aloe Afric: folio in summitate triangulari margaritifera, flore subviridi.

2. International Code of Nomenclature for algae, fungi, and plants (Melbourne Code)

3. Aloe pumila, Haworthia pumila; what or who is confused?  ISBN: 0-9534004-4-1 Bruce Bayer. Alsterworthia International Special Issue No.3. https://haworthiaupdates.org/aloe-pumila-haworthia-pumila-what-or-who-is-confused/

4. Commelin, Johannes, Horti medici amstelodamensis rariorum tam Orientalis, vol. 2: t. 10 (1701)
http://plantillustrations.org/illustration.php?id_illustration=122192
Commelin t10 1701 H. pumila

5. Commelin, Johannes, Horti medici amstelodamensis rariorum tam Orientalis, vol. 2: t. 11 (1701)
http://plantillustrations.org/illustration.php?id_illustration=122193&height=750
Commelin t11 1701 H. pumila

6. Curtis’s Botanical Magazine, vol. 33: t. 1360 (1811) [S.T. Edwards]
http://plantillustrations.org/illustration.php?id_illustration=8348
ST Edward 1811 Curtis Bot Mag v33 t.13608348

7. Moninckx, J., Moninckx atlas, vol. 3: t. 12 (1682-1709)
http://dpc.uba.uva.nl/cgi/i/image/image-idx?c=botanie;view=entry;cc=botanie;entryid=x-421058064 and http://plantillustrations.org/illustration.php?id_illustration=133655
Moninckx

8. History of Succulent Plants,  Bradley, Richard (t30) (1716)
http://www.botanicus.org/page/614136
Bradley t30

9. History of Succulent Plants,  Bradley, Richard (t21) (1716)
http://www.botanicus.org/page/614116
Bradley t21

Ed. – another …

10. J., Moninckx , Aloe Africana, folio in summitate triangulari / Margaritifera, Flore subviridi. / C: Commelin, Hort: Amst: Part: 2. pag: 19. Wijnands, D.O., The botany of the Commelins, Rotterdam 1983, p.134

http://dpc.uba.uva.nl/cgi/i/image/image-idx?c=botanie;view=entry;cc=botanie;entryid=x-421058064

The science (of plant names)

The debate arising from the announcement of Homo naledi, on what actually constitutes science is disturbing. It raises the question of science versus religion that is a horse flogged to death with no outcome but the death of the human soul. The argument should be scientism versus religion. Why?

Because there are two quite different ways of using the word “science”. Almost universally science is taken to be a function based solely on physical mensuration and on experiment and result gained from some sort of external physical observation i.e. scientism. This is a gross distortion because the word science is derived from the Latin word “scientea” that means “a KNOWING”. This knowing extends far beyond physical measurement and observation and is directly related to consciousness. Scientismists insist that consciousness is some sort of physical or chemical reaction that goes on in the nervous system. Absolute nonsense. Even the great palaeontologist gets it all wrong in his book “Rocks of ages” and his principle of non-overlapping magisteria.

Anyone can do true “science”. This is observation with sincerity of purpose, objectivity and a desire to know. Time I think will tell that the scientismic approach has been a deliberate distortion in which pursuit of knowledge has been directed away from the spiritual to the material. This is why the Dalai Lama and perhaps a few others have described the scientismic view of science as just another religion. The word science cannot be reduced to simple materialism as has been done. This is a distortion that has reduced man to the status of any other animal or plant.

So what about plant names?  In a way we have the same problem here. The sense and purpose of plant classification is to arrange plants in a hierarchy that reflects the orderly evolution from chaotic DNA and an original single life form, to that of more and more complex life forms with the human form as the pinnacle. It all started with study of physical characters and their imagined or studied development from one condition to another. The recently agreed truth, just like the belated acknowledgement of tectonic plate movement as the driver of continental drift, is that this dependence on simple physical characters is not satisfactory. The insights to DNA and the sequence analysis of the binding amino acids of the two strands of the nuclear protein structures have opened the window to a wholly different view of species and their relationships. 

But it should be noted that the argument is profound and the result actually not complete or perfect. The DNA sequencing is from limited access to many more millions of amino acid pairings each regarded now as a “character”. The statistical interpretation of the pairings and that presentation in a two-dimensional diagram is in my opinion a serious distortion.

Surprise after surprise is that the definition of what a species is, evades definition. Largely it is the zoological concept of non-interbreeding sets of life forms that constitute species that is followed in botany. But this is flawed. It is well known, especially in birds, that what may be seen to be two species in one place may not be true in another.  In plants that are position bound in respect of parentage and with less complex behavioural relationships, the position is considerably more confused. Because there is no true and secure definition and circumscription of what a species is, names have proliferated and abound where maybe there should be a lot less. Very few plant species have actually been grown for a study of their breeding relationships while conversely a great deal has been made of the variation within species, as well as of hybridization, for their use and benefit to man.

Estimates of the numbers of species of life vary.  These estimates are hardly useful without a real understanding of what a species is. Here in South Africa there are considered to be 24 000 to 25 000 species. Leaving this aside now, one has to look at the classification process and how plants are studied and organised. This is done in herbaria where dried specimens are assembled, mounted on sheets of cardboard and stored in herbaria. A name all begins in such a single (desirably more than one) specimen to which the name is attached. This is termed the “type specimen”. Theoretically all subsequent identifications should be confirmed by comparison with that single type. The system has worked incredibly well except for the problem of deviations that can be very misleading. Hence there is a constant revision as more and more specimens accumulate and things thought to be different are seen to be one and vice versa.

The next problem is that of personae. Not all individuals have equal skills or aptitudes and neither can any single person hope to acquire good enough knowledge of enough species and specimens to ensure any kind of consistency across the board. Unless species are actually cultivated from seed and the conditions of cultivation known to be non problematic, not enough is learned about variation to be really sure that something, say, with clubbed hairs on the leaves in one area, is not the same as something from another area that has simple hairs instead. Something as simple as this can lead to great argumentation about names. To top it all there is a huge element of personal achievement associated with the application of Latin names as well as an incentive to explorers to find and be associated with something new and different.

Still further confounding matters is that the type specimen may not be easily available to all and sundry and may not even be adequate for purposes of a good identification. This is because it is dried and pressed are sometimes out of recognition from the live state. Description is no easy matter and the original description may not even be accurate. The outcome is that herbaria acquire identifications of specimens based on those in other herbaria and these new identifications become the reference points for names.  They may be wrong. But the point is that a local use of a name becomes established and this may not be the same as that derived from the identification of another herbarium and its staff.

Public interest leads to the production of literature and things such as field guides and other reference works. A problem is that illustrating a single species and all its variants is just not physically possible. Firstly there is a problem that an author, however competent and skilled, may not even be familiar with all the variants even in his/her own special field of study. It is worth noting that in a genus such as Asparagus with only about 70 species in South Africa, there is simply not enough herbarium storage space to assemble just single specimens from across the distribution range. There is hardly one of these species for which a herbarium sheet is adequate to record a root system. How does one acquire and store all the information to report on the diversity and distribution of the respective group members?

Identifying from a field guide is thus problematic because there are things that look very similar and differences may either not be obvious to the inquirer but also species may be mentioned in discussion and not illustrated at all. For the average mind it is the picture that tells the story.

This primarily the reason for this site – to try and establish a local reference point so that an interest and awareness of a very special local creation becomes attainable.

24. Non-Linnaean Taxonomy

68. 2019.7.28 – Coming back to some sort of sensibility after 3 days in the field. Rogan Roth sent me these two pictures of tubeburcled mirabilis from the Swellendam area.

An extraordinary phenomenon. Ask me about it. We can identify 5-6 generations of Aloe ferox. The oldest single mother at a conservative 70 years of age based on the age of plants established at Karoo garden in 1946. The youngest seedlings are current year? I have seen a similar sequence from beyond Uniondale to west of Oudtshoorn.

69. 2019.7.30 – Rogan Roth kindly showed me this population east of Swellendam. It did not strike me as being the same as I had seen in that general area before and I also thought some of the plants could easily be slipped into the Rotterdam “groenewaldii” populations. With less rounding of the lead tips of course. Then it hit me that it appears I have been arguing “groenewaldii” in the context of a supposed discrete “mutica”. This sort of reasoning does not work in Haworthia. “Groenewaldii” is neither mutica, nor retusa, nor mirabilis and neither is it a species, subspecies or even variety of any of them. It is a discrete entity in a vast complex of Haworthias that could all be classed as H. retusa where each population is a discrete and significant part of that true species system. An added problem is that it is not clear where retusa stops. So the Linnaean system based on Darwinian evolution may be quite wrong. Genera and species are just human constructs – they aren’t real things. DNA sequencing may be telling us fairly accurately what the states are, and we are just not presenting or interpreting the product correctly? ♦

Taxonomy and Fieldwork

James Deacon asked Bruce Bayer, “What is this thing at Brandrivier?”

James – you have no idea how significant this picture is. It is an emelyae variant and I really need to know a lot more about precise whereabouts. Multifolia comes from a few km to the east and there was a very very rossouwii-like multifiolia on Brandrivier. It is pictured in Revisited. But it is not there anymore. What is there are plants like your picture indicate. Did you perhaps observe Tulista opalina?

Jakub Jilemicky added “This plant was described by Gerhard Marx as H. obserata. It occurs mainly at Brandrivier, but as well at Springfontein. It flowers with all the magnifica type plants, not with emelyae group.”

May 19 – 7888 Brandrivier. H. emelyae ‘obserrata’. It raises an interesting issue. Names may have to change every generation as the plants may change? It used to be ‘multifolia‘. Actually my species definition includes the matter of space and time. In which case the name ‘obserrata‘ is taxonomic malfeasance.

May 19 – 7846 Between Springfontein and Brandrivier. Flowering August. Surely the type loc for “H. obserrata” that I see as H. emelyae. But this is just a distraction. When you still have commentators making comparisons to the magnifica types and flowering times, you realize that the absurdity of Haworthia classification is going to continue for the next 80 years as well.

As a point of interest. There seem to be many different ideas of what species are. From the typological concept of things that look near identical, to a list of the species one thinks makes up a genus. In the latter case the genus is considered to be what is made up from the species one imagines. My own species concept is very well defined and my map (this spider web of colours) indicates the way factors of space and time are involved in only one small group of Haworthia.

Still paradoxa Vermaaklikheid but the first few were June and this is September.

Let me try this as no 3…What we have is a post of three pictures to show three “species” paradoxa, bobii and joleeniae and to ridicule Bayer for suggesting they are the same. Firstly those pictures are NOT the species. They are specimens taken to illustrate the species but by what is recognised in botanical taxonomy as the “typological concept”, i.e. a species consists of individuals that all look the same. I wish I could copy here what I wrote in the New Haworthia Handbook (1976) where I use the name H. magnifica var. paradoxa and discuss affinity with H. turgida, H. emelyae, H. retusa and H. mirabilis. I ended the discussion there with this… Consideration of the variability of this species and distribution of variants, is very helpful towards understanding variability in the genus as a whole. What I conclude is that the species are systems with any number of populations and individuals that vary enormously. The typological concept creates mayhem in the minds of critics, growers and collectors alike. So let us start with the paradoxa, but first dismiss H. magnifica as a species. That name is a total myth. The myth ghosts around probably a single plant I collected with J. Dekenah at the type locality. It proved very amenable in cultivation and plants ended up at Sheilam nursery to go world-wide. It is actually difficult to now find a clone quite the same at the original locality where there are several discrete “populations” in quite a small area – and countless variants. It is senseless to say that H. magnifica can be a species if in every aspect of such a decision it is topologically based, as is the unfortunate case. The name in SANBI is H. mirabilis. Paradoxa is a synonym. SANBI are not my friends or my clients. Some very bright and competent people are employed there. The element paradoxa is thus in my view a variant in the species H. mirabilis and illustrated here by three populations viz. at Vermaaklikheid, Osplaas and Koenserus.

Just get something clear about type specimens and the system. A specimen is only anchor for the name. It does not prove anything about where it comes from. It is just representative. A second point is in that the nomenclatural rules uphold chronological discovery (better still – description) over reality. This mad rule of priority totally confounds the prime aim of a classification that follows and explains the genetic history (phylogeny). If in fact evolutionary theory is even valid. Generally the rules provide fertile ground for confusion, argument and publication credits that do little to promote their purpose.

Two Vermaaklikheid picture sets have been posted. This is another. A cooler west facing outlook but also on those limestone rocks. I must confess to a bit of apprehension that some may claim this is a different species when my opinion will be a great deal more conservative in what lies ahead.

What is the problem? I suggest we have an antiquated, outdated, dysfunctional classification system so that our knowledge, philosophy and methodology does not allow explanation of groups like Haworthia. So I will try and demonstrate it like this…Gerhard posted pictures of paradoxa, bobii and joleeniae. One of each! So let us just see how this can be interpreted. Here are several pictures of ‘paradoxa‘ from Vermaaklikheid east of the village. I first saw it at a site north of the village.

There is so much still to explore. Here is a map just to indicate the scale that has to be exercised. Initially I was happy to stop every 50 miles to see what might be there. Now it is every 25meters! Just note an interesting phenomenon here. 3 species and as many populations as there are recorded habitats. M = mirabilis, R retusa and F floribunda. Yes we covered most of the ground between too.

Mukesh Vaid asked – What does these four digit numbers signify

Bruce Bayer – Just my collecting numbers. This map is only intended to show intensity of search to demonstrate anything. I did have a collecting permit strictly adhered to. Often, as I do now, I do my searching with camera!

Every collector should have an accession book to record what you record and find where and when. I idiotically did not get this right to start with. Even as an entomologist I did not keep proper numbers. When I started at Karoo Garden I used the garden accession system KG with number/year. No good. In the end it is the quality of accession record that indicates the credibility of the work! I did not have the luxury of digital camera or GPS that is essential nowadays. At one time it was enough to just say “collected between the Cape and the diamond fields! With plant theft and cadaverdog-like shadows, it is a bit stressful to even produce the maps that I show! Sometimes I have mentioned something and the next moment a new species is described directly connected??

Mukesh Vaid – Where is H. turgida in this?”

Bruce Bayer – This not actually about turgida but just to show level of search necessary. But let me take the opportunity to try and get this message/hypothesis across. There is a single gene pool (a system) that produces mirabilis, retusa, turgida, pygmaea, mutica and emelyae. It can be simplified if it recognised that retusa is really a offset of turgida in among 5 main lines. So let us try and get something else straight. Science (i.e. scientism actually) is a system of reductionism that supposes that everything can be explained by breaking things down to their smallest parts. So we mess up in Haworthia by thinking the smallest parts are species when in fact it is a system of many things. Does that help?

 

This is where I think Mukesh rightly has a problem. That bottom pink line should not be there. That is why I refer to them as intervals. These bureaucratic scientists lay down the law that this should be seen for what it is and call it an interval – because it is a break in distribution continuity e.g.. The Knysna interval is a serious break between SE coast flora and S Cape flora. That coast line area is not easily explored and the geology is limestone with a different vegetation. There may well be Haworthias there. There is a record of a mirabiloid(?) on the sea cliffs at St Sebastian west of the Breede River mouth.

There is a really weird intimation that bureaucrats have determined what species names apply on Haworthia! It is actually a very democratic process based on 4 tenets of science. Universal truth, communality – no secrets, no private gain, and organised scepticism. If you have the data and you have the facts, you are free to organise and present your case. I have no privileged access to anything and certainly no sycophantic following with commercial interests in mind. I often wonder that not a hair sticks up from the trenches of my defense when so much garbage is thrown on attack

On this map…. There is actually no known connection across from L = longebracteata (also a mirabiloid area), to P = paradoxa, to B = bobii. Historically the shore line has changed and there may have been. Variegata seems to have jumped the gaps. So now we have populations a = Buffelsfontein, b = Sandfontein, c = Sandhoogte and d = Infanta. A and b are in the De Hoop Reserve and it is quite difficult to access so I have not been there with a digital camera unfortunately. Buffelsfontein I owe to Chris Burgers, Sandfontein to Adam Harrower and Sandhoogte to Jakub Jelimicky. Infanta I owe to mesemb research and what “bob” had to do with it is anybody’s guess. Certainly I did not remotely think it was or is a new species, as excited as I was to first see it. The overall complexity of the spider web does not do justice for the problems of variability among the floribundoids, the variegatoids and the mirabiloids. Turgida seems to hold its own. Holistically I can conceive of only the one solution that excludes adding another few species to an impossibly and unrealistic list. It would be nice if the culprits owed up to the chain of events that led to “bobii” and a few other names. Including the authorization for collecting that is so uncomfortable and dehumanizing. I make no apology for suggesting the association of bobii and paradoxa , even beyond a greater issue of the mirabiloids. I do not doubt that it is a difficult “ask”. The two pictures are of ‘a’ and do not do justice to the plants in the field at all.

Arthur Dixon posted these .. Bruce Bayer replied “All ‘paradoxa’.”

These are the plants at ‘b’ where Adam Harrower recorded them. I named the place as Sandfontein or “Sandhoogte N”. Makes me long to go and drool over them again!

These are my pictures of ‘c’ in the ‘bobii’/paradoxa/joleeniae/mirabilis milieu. Funnily enough I really do sympathise with the doubters and unbelievers and am very apprehensive about further showing you what I think is the same. (remind me if I forget!). I have not mentioned “muticoid” in this lot where I say turgida is real. I suggest that mutica does come in to the picture and I will touch on that when I get to ‘joleeniae’.

Arthur posts…”It seems to me that endless discussions and reasoned arguments supported by habitat shots whilst life-affirming and endlessly enthralling are not advancing the discussion in any way as (returns to main point) WITHOUT that definition of ‘species’ the cycle continues to revolve (Personal point)”. Yes yes yes. It has been ongoing for the last 80 years. Like I said – I get credit for my great contribution to Haworthia while effectively been told I know nothing. I am happy to accept that, if some intelligence is put in place of what I have written over the years. Contrary to general belief, I do not like offending or hurting people. Therefore I am very limited in what I can actually say and tell. What we need is a dimensional shift in how we think, how we reason and in what we are really wanting to achieve. We have a societal crisis and we see it not!

Tony Brook wrote “My apologies Bruce I am not a Botanist but surely the definition and description of Bobbi should precluded the 2 plants which are relatively hairless. Otherwise many other Haworthia would be included in the “species”.”

Bruce Bayer replied “No Tony. this is essentially the problem. I did not consider bobii to be a species. H. mirabilissii the species and the best way of defining species at the moment is by DNA sequencing but rather also by what my definition of species requires. Viz a holistic view of its relationships, similarities whatever, with possible and probable relatives.”

Here is another ‘joleneae‘ population that demonstrates how observations can be slanted to re-enforce propaganda. Someone also sent me an article on Haworthiopsis that is a piece of real modern day journalism. Unable to tell left from right or right from wrong, the writer sits on the fence like a Fiscal Shrike impaling worms on the barbs, i.e. hoping to have his believers (us ordinary worms) accept him as an all-seeing eye of truth. This has plagued me all my writing life! No joleneae is not definitely and distinctly, always glabrous. Some of these pictures even show the mutica shiny speckled appearance those plants can have. Differences between populations are in my observation as much due to the skeletal soil differences (geology) as they are to spatial isolation. I think. Some amazing individuals here.

So let us move on because there are still surprises and unpalatable truths. While we have seen mirabilis ‘bobii‘ from the sandstones of the Potberg itself, we need to see what mirabilis does on the geological confoundment of the flats north of the Potberg. First there is Melkhoutfontein and I assume that this is included in the concept of “joleneae” (that I usually misspell). It really should be H. mirabilis ‘joleneae‘ and just forget formal process. It is not possible to regulate and manage the welter of names. An attempt was made to register Aloe cultivars, but if this is practical I doubt. It is senseless to argue there is no continuity from ‘bobii‘ to ‘joleneae‘. This just upholds a nonsensical humongous heap of formal binomials to argue about and ignores the many more things that attract either no aesthetic attention or commercial interest. Joleneae is on the terrace cobbly sandstone as a simply descriptor.

It occurs to me. Joleneae is claimed to be consistently glabrous. This comment disregards the electron microscopy “work” done by Dr. David Cutler of Kew that I reported on in Updates. It is obvious from these pictures that the plants are incipiently hairy or spinose whatever is correct. we simply cannot properly assess the real nature of individual characters like this. Just for recall – there was an amazing paper written on the cladistics of the Aloids published in Taxon (about 30 years ago). Whoever peer reviewed that paper prior to publication deserves serious censure. Barely a character state is correctly stated.

What it needs to is for the thought leaders, like editors, society committee members, media notaries etc. to get their act together and seriously consider what their role is in the mess of argument and infighting. I have suggested now a solution where at least in Haworthia we can (if we so choose) admit the spider web and set-out how to communicate about it. Perhaps we need to identify the mafia who have vested interest or are just too intellectually lazy or impractical to even want agreement.

Is this and that getting too much for you? Still ‘joleneae‘. It is a useful name, but not actually the issue. At this place Tulista minima (I am gobsmacked that some over zealous mind has decided it is actually T. minor – I suppose this name change in intended to avoid confusion!!! ) as does H. variegata ‘hemicrypta’. So I include hybrid pictures. The two species do not directly share habitat. Stoffelsriver.

Here is a map of the north Potberg area to highlight the significance of geology and its impact on floristics/vegetation/plant species. It is a complex situation with deposited materials overlying basic formations and erosional effects. The white material to the higher left are eroded and decayed shales that result in banks of white clay much like elsewhere towards Riversdale and Heidelberg. Is it surprising that the retusa/mirabiloids adjust and adapt accordingly. Why do these plants differ so much from joleneae/bobii/paradoxa and switch to resemble atrofusca and floribunda?

Snakes and ladders. Background noise! I have 206 folders for populations of which most are this unphotogenic ilk. Their lack of appeal and hidden nature is why H. heidelbergensis was spawned. The more conspicuous and bigger forms were H. maraisii and H. magnifica. The only attention I know they ever got from collectors was the complaint that they never could own or get a proper idea of what H. mirabilis looked like. Shades of the great doyen of Botanical Latin and plant taxonomy W.T. Stearn who destroyed the foundation of Haworthia taxonomy with his typification of the name Aloe atrovirens, spinis herbaceus numerosus ornata and choosing the herbaceus part for the epithet. H. atrovirens should be H. mirabilis! I do not think the name mirabilis was even used in von Poellnitz and Smith’s time? So I can see that my chances of putting Haworthia taxonomy to rest are zero. No herbarium can ever hope to hold a proper record of variation within a single population. Whoever wants to quarrel with me needs to now that their classification includes all the stuff I have tried to contend with! My pictures of this background noise are disappointing and I have none for stuff seen before ca. 2005 or so. Emoji of laughter or tears? And who wants to know what a species is anyway?

Nothospecies or notaspecies? That is the big question. Why bother to ask difficult questions, just call this H. mirabilisXmutica H. hammeri instead. It consists of one population occupying an area less than 500sqm among surrounding mirabilis and mutica populations. Will it ever be a system? (Nothospecies is coined for the offspring of two other species that in the absence of a definition become a new species. It really applies to readily seed propagating and readily dispersing plants – agriculture and horticulture!)

Here is my 2009 baby I think written in 2009 before DNA sequencing proved to us that there were 3 genera where we saw only 1. I said so when? First handbook 1976? The thing that really got me is that the results of the sequencing were actually fudged (again). The discussion and conclusions were written long before the introduction and methods, to ensure that there was a match up of results to hypothesis being tested.

Haworthia the problem child of taxonomy

Yes my favorite critic had something to say about this fishtail bud as well. Or at least the fact that I considered it at all. It is actually a feature of virtually all of the retusoid mirabiloids varying from zero in the east to nearly dramatic in the west. So herbacea and reticulata have the most exaggerated version. In these two systems the flower is nearly “regular” (as in pentagonal) hence reticulata ‘subregularis’. H. herbacea is characterised by the beige colouring while reticulata flower is pinkish. The Wolfkloof Villiersdorp herbacea has an enormous (close to 3cm long) very pink flower to fudge the issue. H. herbacea ‘paynei’ near McGregor has a bicoloured flower, hence ‘luteorosea’.

6509 H. mirabilis meiringii, W Bonnievale – Flowers are problematic because the flowers are not static things. They change by the day. In this case I pictured most open flowers on every single stem from 1-5 open.

6089 NW Potberg – some of the background noise to mirabilis. Many many populations of these small black things (“klein swartetjies” according to Michael Malherbe founder of Sheilam, in imitation of the Little Brown Jobs of bird-watching)). Not as enchanting as the larger and less common variants, they are not covered by popular classification.

H. mirabilis ‘notabilis’. This is a place in the mountains midway between Robertson and Worcester. Both arachnoidea and reticulata occur here as well in different habitats. There are shale, dolomite and sandstone formations. The countryside is formidable. How does one describe the plants here and link them adequately to a host of populations running all the way east to Ashton, and to the oddities of the NE Worcester area. Not only that. There are continuities southwards as well.

Lets try something. First the chaos formula imaging. Like a DNA seq. phylogram it is two dimensional and cannot adequately represent a spacetime issue (that species are whether evolutionary or independent creation of ‘species’. Secondly imagine a continuation of the fractal image with 6 species in a particular time frame continuing on to eventually end up as 3 species in a third frame? The frames are geographic space. The brackets demonstrate how species may overlap in distribution and/or characters. The chaos formula demonstrates overlap of characters in time or space but not in both as is needed. That is called linearity as opposed to actual reticulate reality? I am no intellectual wizard but am quite sure that plant taxonomy has got things WRONG.

Guan Tan-Amo Lim wrote “Haworthias are a little bit like domesticated dogs… they come in all shapes and sizes and can breed with each other readily. Yet dogs are all of one species. Could the many Haworthia species similarly be reduced to if not one species then to only a few? With many “breeds” corresponding to the natural populations in habitat?”

Bruce Bayer replied “Guan Yes. but we shift the problem from one level to another. I have a spider web of five species (turgida/retusa, emelyae, pygmaea, mutica, emelyae that could be one. But there is another spider web in the upper left of herbacea, reticulata, maculata and pubescens. So where do we stop? Things like wittebergensis, pulchella and marxii seem totally separate but there is chaos among all the other true Haworthia. Funny I was just browsing an article on a math issue that claims that there are things that are true but they cannot be proved to be true? Life is a conundrum.”

A fairly random lot? Actually no. This is a place a few km from ‘hammeri‘. Their is a rounded hill with small nondescript LBJs (little black jobs) most places, but at one spot quite large plants like this. Atrofuscoid? The floribunda-like leaf tip is common in the small mirabiloids. I should add… a note on fieldwork. Did I do field work? Walking around with nothing to measure and itemise but an eyeball assessment and some pictures.

6638 from NNE Bredasdorp. Mirabilis. This is a place where turgida also occurs, and with rossouwii and mutica within a few km. Also home to the ‘heidelbergensis minor’ that I suggest has rossouwii genetic material. One of these clones is very reminiscent of what I observed and considered a true hybrid between mutica and mirabilis where populations were in very close association. Does anyone really have problems with names used in an informal way like this rather than behind a facade of deep science and a degree of fraud?

From 6638 pictures. This weirdo strikes me as reminiscent of more obvious hybrids retusa/mirabilis or mutica/mirabilis where they are in close enough proximity to support a hybrid presumption. Turgida is an estimated 400m away from here.

Soumen Aditya comments “I didn’t see a features of natural hybrid … Most probably the polymorphic evolution…” Here is what IS most probably hybrid. Where mirabilis and mutica are in two populations meters apart. SO I think what would be features of a natural hybrid may just be a subjective opinion? I have mentioned before how problematic the issue of hybrids is and have often been asked – How do you tell it is a hybrid? Credibility in classification barely exists at the best of times.”

What do I ask? I once was in a meeting with a group of top managers discussing a topic they had been dealing with for over 20 years viz. rangeland production. I was suggesting a method of assessing potential. The group seemed so lukewarm to my suggestion that I felt the need to establish if they really did know what I was talking about. So I sent around a problem and asked if it could be solved using the available knowledge they had been debating for over the previous 20plus years. Deadly quiet. No wonder they were so indifferent. Now I feel exactly the same about Haworthia classification. People have been arguing and debating this since Herre’s time (1930). Here in SA nothing has changed. Perhaps I also do not know what I am talking about! The spider web for the retusoid/mirabiloid plants is a small part of the whole, and fairly straightforward compared to the bigger picture. But my suggestion for a systems approach is met with the same deadly quiet, especially from where it matters. What do I do next?

These are a few pictures of 30 from a population in a vast expanse of a no go area for any but the most intrepid. What is it? It is from an aloid sparse space and while I do have pictures for another 5 populations in the area they are not more informative. From my limited (is it that bad?) experience of mountains and the way succulent exploration has been done, I shudder to think how the Haworthia community, led as it is, is going to be able to digest what is still to be learned.

I mentioned that vast no-go area (6694). Here is one of the other 5 populations I know that happens to be only about 500m away (7994).

7994 Yes the flowers are significantly different. 7994 I attributed to maculata and the fishtail bud indicates that it is an extension of the retusa/mirabiloid web. The rounded bud tips of 6694 suggest arachnoidea or nortieri, as geographic candidates and the most probable system affinities.

June 4, 2021 – Something useful I can do is amplify H. mirabilis meiringii. I described this to draw attention to very herbacea like forms of mirabilis. This is in the Bonnievale area where the mirabilis variants seem like a system within a system, within a system. Westwards they are less spinescent and similarly eastwards. 6509. The name was not to honour someone so much as to record a time when plants were perhaps first harvested and sold from the field.

Silly me. I say these are the same (species)

H. mirabilis meiringii 7269

Mirabilis meiringii 7327

meiringii 7882

H. mirabilis Klipfontein

 ♦

Personal Names

Names of persons commemorated in Haworthia – and just what do those names mean? What motivated them? If you scratch my back I’ll scratch yours?

Browniana, dodsoniana, poellnitziana, resendeana, revendetii, batesiana, gordoniana, schuldteana, uitwaaliana, ryderiana, hammeri, bayeri, comptoniana, rycroftiana, rossouwii, geraldii, breueri, wimii, devriesii, davidii, cummingii, mortonii, bobii, groenewaldii, jakubii, marxii, joubertii, morrisiae, kingiana, longii, emelyae, zantneriana, fergusoniae, vlokii, bruynsii, tauteae, armstrongii, woolleyi, lateganae, eliseae, esterhuysenii, otzenii, koelmaniorum, marumiana, vincentii, dekenahii, beukmanii, fouchei, venteri, herrei, mcclarenii, meiringii, hurlingii, paynei, triebneriana, maraisii, scottii, joleneae, blackburniae, leightoniae, batteniae, stayneri, andriesii.

I am sure many more. How many of the collectors among them had permits or any sort of credentials modern times may demand, for the plants they collected and distributed (sometimes widely). In G.G.Smith’s time there were a hoard of collectors sending material from all over the country and even the world.

More personal names…walmsleyi, helmiae, engleri, hilliana, oertendalii, whitesloaneana, taylori, luisieri, tisleyi, stephaniana, palhiniae, starkiana, schoemanii, smitii, skinneri, bijliana, schmidtiana, rodinii, archibalbii, dielsiana, pearsonii, peacockii, nortieri, maughanii, lockwoodii, marlothiana, kraussi, krausiana, jonesiae, jacobseniana, haageana, greenii, carrissoi, chalwinii, beanii, baylissii, britteniae, o’donoghueana, archeri.

There are somewhere near 100 names, presumably these were all names for plants of some degree of interest. So we ask now the awkward question of conservation ex situ. Just how many of those names are still with us today and attached to a propagule of the originals. Oh come now! I worked for 18 years in a botanic garden dedicated to conservation, preservation and maintaining some sort of reference collection. Just to maintain the genetic diversity of say a group of 3 plants ex field is a monumental task. Within single figure years, the diversity is down to that of one clone no matter how hard or conscientiously the matter is pursued. ♦

DNA Sequencing

Do these pictures have any relevance for anyone?

Or these …

Aloe haworthioides and Aloiampelos striatula. What this has to do with Haworthia is demonstrate that DNA sequencing is highly suspect as a sure fire answer to classification problems. If we take Aloe haworthioides as an example, you will, or should have, read that piece out of Updates Vol 6. It explains the morphological oddity that it is. If you now refer to the paper by Manning et. al. that creates the aloid genera in Asphodelaceae for SANBI (South African Biodiversity Institute), a problem emerges. In the concatenation of the plastid region sequences, A. haworthioides is in the same clade as A. greatheadii, A. excelsa, A. de winteri and A. petricola. But with the nuclear region sequencing the clade includes A. lutescens, A. comosa, A. rupestris, A. munchi and Chortolirion angolense. In both cases, a more probable bunch of misfits you cannot imagine. Admittedly the statistical probabilities for the significance of the branching are poor. But this belies the extraordinary statement in the paper that evidence of a reticulated relationship as opposed to the evolutionary linear one, is obvious by its absence.

If we look at Aloiampelos (not Aloe anymore) striatula, the plastid sequencing places it with A. graciis, A. tenuior, A.ciliaris and A. commixta. With the nuclear sequence added, the arrangement stays the same. Seems OK until you consider, does the vegetative growth of A. striatula resemble that of the others? I do not think so. Furthermore it is geographically powerfully separated by its occurrence in the high mountains of the interior Eastern Cape, whereas the others are in the near coastal or lower lying areas. So what is the problem? Look at the flower of A. striatula. It is rather roughish but the remarkable thing is that instead of a petal/sepal arrangement in which there are the normal two upper outer sepals and one single lower outer sepal, with a single inner upper sepal and two inner lower ones, in A. striatula the situation is completely reversed. The flower is grossly different. The morphology of these two species in my opinion makes a mockery of sequencing as a sure-fire answer to classification. Add to this my experience with several sequencing projects, providing the material according to a pre-determined hypothesis and being ejected from the projects by questioning the results with new hypotheses written to fit; my confidence in science is fragmented.

Furthermore, examination of the Haworthia clades in both phyllograms of the Manning paper demonstrates very poor resolution. What there can be extracted is that the relationships are highly reticulate. This adds to my contention that any phyllogram (evolutionary tree) drawn in the two dimensions of the flat plane are totally misleading. This is obvious if you resort to a proper species definition of objects changing in geographic space and in time.

NOTE: I have to confess that I am a bit puzzled by the one picture of mine showing the end face of the flower that appears to show a single inner upper sepal. The cross-sections prove the odd arrangement. These pictures are from many years ago and my memory fails me. ♦