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FIGURE 35.— Known distribution o f A loe neilcrouchii.

Additional specimen exam ined

KWAZULU-NATAL.— 2930 (Durban): between New Hanover and Dalton, (-B C ), 2010-01-05, N.R. Crouch. G.F. Smith <£ /. Johnson

1260 (PRE).

ACKNOWLEDGEMENTS

The authors would like to thank the following people: Ms Isabel Johnson, KwaZulu-Natal National Botani­ cal Garden, South African National Biodiversity Insti­ tute (SANBI), for providing transport, and facilitating access to the site; Ms Hester Steyn, National Herbarium, SANBI. Pretoria, for producing the distribution map; Dr Otto Leistner for providing the Latin diagnosis; Ms Gill Condy, SANBI, Pretoria, for the line drawing; two ref­ erees for suggesting improvements to the manuscript.

REFERENCES

BERGER. A. 1908. Liliaceae-Asphodeloideae-Aloineae. 8. Aloe L. In A. Engler & K. Prantl, Das Pflanzenreich IV, 38, III, II (Heft 33): 159-326, 329, 330. Engelmann, Leipzig.

CRAIB, C. 2005. Grass aloes o f the South African veld. Umdaus Press, Hatfield, Pretoria.

GLEN, H.F. & HARDY. D.S. 2000. Aloaceae (first part): Aloe. In G. Germishuizen, Flora o f southern Africa, vol. 5, part I, fascicle 1: 1-159. National Botanical Institute, Pretoria.

KLOPPER, R.R., CHATELAIN, C., BANNINGER, V., HABASHI, C\, STEYN, H.M., DE WET, B.C., ARNOLD, T.H., GAUTIER. L., SMITH, G.F. & SPICHIGER, R. 2006. Checklist o f the flo w er­

ing plants o f sub-Saharan Africa. An index o f accepted names and synonyms. Southern African Botanical Diversity Network

Report No. 42: 1-892. SABONET. Pretoria.

LAUBSCHER. N.F. 1973. Aantekeninge oor die Suid-Afrikaanse

Graminialoe Reynolds en Leptoaloe Berger. Aloe 11,1: 4 -9 .

MUCINA, L. & RUTHERFORD, M.C. (eds). 2006. The vegetation o f South Africa, Lesotho and Swaziland. Strelitzia 19. South Afri­ can National Biodiversity Institute, Pretoria.

REYNOLDS, G.W. 1950. Aloes o f South Africa. Aloes o f South Africa Book Fund, Johannesburg.

SMITH, G.F. 2003. Aloe craibii Gideon F.Sm. (Asphodelaceae: Alooi-deae): a new species o f grass aloe from the Barberton Centre o f Endemism, Mpumalanga, South Africa. Bradleya 21: 2 5 -2 8 . SMITH, G.F. 2005. The fascinating world o f the grass aloes o f South

Africa. In C. Craib, Grass aloes o f the South African veld: v iii-ix. Umdaus Press, Hatfield, Pretoria.

VAN JAARSVELD, E.J. & VAN WYK, A.E. 2006. Aloe challisii, a new cliff-dwelling aloe from Mpumalanga, and a checklist o f the obligate cliff-dwelling aloes in South Africa and Namibia.

Aloe 43: 3 6-41.

VAN WYK, B-E. & SMITH, G.F. 2004. Guide to the aloes o f South

Africa, edn 2. Briza Publications, Pretoria.

R.R. KLOPPER* and G.F. SMITH*

* Biosystematics Research and Biodiversity Collections Division, South African National Biodiversity Institute, Private Bag X 10I, 0001 Pretor­ ia. E-mail: R.KIopper(a sanbi.org.za; G .S m ith s sanbi.org.za.

Acocks Chair, H.G.W.J. Schweickerdt Herbarium, Department o f Plant Science, Univ ersity o f Pretoria, 0002 Pretoria.

MS. received: 2009-09-17.

BRUNIACEAE

NEW SPECIES OF THAMXEA AND BRUNIA FROM W ESTERN CAPE, SOUTH AFRICA

The Bruniaceae is one o f the 33 ‘Cape floral clades’ (Linder 2003) mainly distributed in the Western Cape, South Africa. Since the revision published by Pillans (1947), much work has been done to understand the inter­ generic relationships and biology o f the family (ClaBen- Bockhoff, in press). Based on molecular and morphologi­ cal data, a new classification has been proposed accepting

six o f the formerly 12 genera (ClaBen-Bockhoflf et al. in

press). With the two newly described species in the present paper, there are currently 79 species in the family.

Thamnea matroosbergensis A. V.Hall, sp. nov.

Fruticulus humilis usque ad 0.3 m altus; foliis 0 .8 -1.0 (-l .2) mm longis spiraliter insertis ellipticis sessilibus, pagina laterali paulo discoidea pagina abaxiali profunde carinata castanea. Inflorescentia flore solitario sessili ad apicem ramorum principalium vel in ramis lateralibus. Flores bracteis 6-10 usque ad 2 mm longis: sepalis libe- ris 1.7-2.1 mm longis; petalis ± 25 mm longis, albidis.

limbis late obovatis obtusis patentibus; staminibus 1.5- 2.1 mm longis, antheris 0.9 mm longis; nectario annu- lari viridi 0.1 mm alto; ovario uniloculari. placenta libera centrali, ovulis 4 -8 pendulis; stylo supeme contracto; fructu 1.8 mm longo, ellipsoideo, castaneo, tholo umbo- nato longo terminanti.

TYPE.— Western Cape, 3319 (Worcester): Worces­ ter Dist.; SE slopes o f Matroosberg, (-B C ), 5000-6000'

[1 520-1 830 m], 18 November 1962, Esterhuysen

29877 (BOL, holo.). Figure 36.

Sprawling shrublets, up to 0.3 m high; no coppice shoots or lignotuber recorded; distal branching dense to diffuse, main lateral branches spreading rather widely from main axis, fairly evenly dispersed along it; leaves obscuring more densely branched stems; young stems

ridged, glabrous, older stems almost smooth. Leaves spi­

rally arranged, elliptic, 0.8— 1.0( — 1.2) mm long, sessile

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Bothalia 40,1 (2010) 97

FIGURE 36.— H olotype o f Thamnea m atm osbergen sis, Esterhuvsen

2 9 8 7 7 { BOL).

rather discoid with base curving abruptly into stem, abax- ial surface strongly keeled (Figure 37B), flat or slightly channelled between keel and leaf margin, surfaces glossy brown, glabrous; margins hyaline; stipules absent; stomata

on abaxial side only (Figure 37A, B). B ud le a f colleter

incurved, broadly triangular-acute (Figure 37B), semi- terete, 0.1 mm long, dark brown, lost from older leaves.

Inflorescence: flowers solitary (Figure 38A), sessile at ends o f main branches, some on 1-22 mm long side branches no different from leafy vegetative stems, terminal flower opening from before to later than those on side branches;

old receptacles and bracts not persistent. Involucral bracts

6-1 0 , up to 2 mm long, lower leaf-like but with a rapid transition distally to w ider laminae, upper ovate, obtuse but with a dark apiculus, rather hard-textured, distally

shortly ciliate. Floral receptacle ± 0.2 mm long, glabrous,

finely ribbed, transition to calyx with a slight indentation

(Figure 37C). Sepals free, lanceolate, 1.7-2.1 mm long,

acute, imbricate, keeled, term inating in a hyaline to brown

tip, distally ciliate. Petals ± 2.5 mm long, white, weakly

clawed; limb broadly obovate obtuse, spreading; 2 narrow ridges along the prom inent m idrib near base o f adaxial

surface. Stamens 1.5-2.1 mm long; anthers 0.9 mm long

(Figure 37C), distally lunate; pollen 3-colporate (Figure

37E). Flower scent not recorded. Nectarostomata present

around upper edge o f ovary (Figure 37D). O vary 2/3 infe­

rior, 1-locular with free central axile placenta bearing 4 -8 pendulous ovules at apex; style 0.6-0.9 times as long as

sepals, tapering; stigma capitate (Figure 37C). Fruit ellip­

soid, 1.8 mm long, distal end with short umbonate dome, red-brown, shallowly sulcate, glabrous; style-base persist­

ent, broadly convex. Flowering tim e: Novem ber to April.

D iagnostic fe a tu re s: Thamnea matroosbergensis is

sim ilar to T. thesioides D um m er and T. uniflora (L.) Sol.

ex Brongn., both belonging to different subclades within the genus (Q uint & ClaGen-Bockhoff 2006). It differs

from T. thesioides in having a longer style (1 .3 -1 .6 mm

long vs 0.7 mm long in T. thesioides); stam ens alm ost

as long as the sepals; a style o f alm ost double the length

(1 .3 -1 .6 mm vs 0.7 mm in T. thesioides) and a convex

dom e at the fruit apex. It differs from T. uniflora in hav­

ing longer sepals (1.7-2.1 mm vs 1.2-1.4 mm in T. uni­

flora); a sem i-inferior instead o f an inferior ovary and in lacking a hairy fruit with a nectary rim on its top. The m aterial is clearly distinct enough to w arrant recognition at species level, although the extrem ely small size o f the m ain organs will require careful analysis for identifica­ tion. It is rem arkably constant in the three collections from the site except that one shoot is taller and more dif­ fuse, but in other respects they are identical.

D istribution a n d ecology: Thamnea m atroosbergen­

sis has seldom been collected and is known from a sin­

gle area, the steep, rocky southeast-facing slopes o f the M atroosberg in the Hex River M ountains, from 1 500 to 1 800 m (Figure 39). This site lies 35 km east from

the locality o f T. thesioides in the Ceres area, but is at a

rather higher altitude.

A dditional m aterial exam ined

W ESTERN CAPE.— 3319 (Worcester): Matroosberg, amongst boulders, S side o f ‘Coat o f A rm s’ Rock, ± 6000' [1 830 m], 19-01-1959, E sterhuvsen 2 8 1 5 0 (BOL); ibid., rocks on SE slope, 5 0 0 0 -6000' [1 5 20-1 830 m], 7-04-1959, Esterhuysen 277 1 0 (BOL).

B ru n ia c o m p a c ts A. V H all, sp. nov.

Frutex patens usque ad ± 0.5 m altus basiram ifer, ram ificatio distali densa; foliis 2 .7 -3 .2 mm longis, usque ad 4.8 mm longis in sirculis rapide crescentibus, lanceo- latis acutis, sessilibus, abrupte ex caulibus crescentibus; abaxialiter villosis m inus adaxialiter. Inflorescentia flori- bus in capitulis densis term inalibus, 3 -4 mm latis, race- m osis; axe principali per anthesin non crescendi, axibus ulterioribus novis sym podialibus. Flores bractea 0 .6-0.8 mm longa, arete appressa, ovata, dense villosa; bracteo- lis dense villosis; receptaculis florum 0 .6 -0 .8 mm longis; sepalis ± 1 .1 mm longis, anguste deltoideis acum inatis, abaxialiter villosis, dense ciliatis; corolla alba, petalis liberis 0 .6 -1 .2 mm longis, ellipticis, abaxialiter villosis; stam inibus ± 0.8 mm longis, distaliter incurvatis; ovario sem i-infero, ± 0.7 mm longo, biloculari, utroque loculo ovulo unico pendulo; nectario absenti; stylis duobus 0 .9

-1.3 mm longis, leviter connatis, distaliter recurvatis.

TY PE.— Western Cape, 3219 (Clanw illiam ): Ceres Dist., G ideon’s Kop, S Cederberg, Sandfontein area, ( -

CB), 4 5 0 0 -5 0 0 0 ’ [1 370-1 520 m], 25 Oct. 1966, Ester­

huysen 31628 (BOL, holo.). Figure 40.

Shrubs spreading, up to 0.5 m high, branched at base.

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cop-Bothalia 40,1 (2010)

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Bothalia 40,1 (2010) 99

;

m

.

I

FIGURE 38.— Flowering branchlets. A, Thamnea m atroosber­ gensis; B, Brunia com pacta.

Scale bars: 1 mm. Artist: D. Franke, Mainz).

pice shoots. D istal branching dense, lateral branches close

to main axis, somewhat clustered at nodal zones with

fewer branches in between. Young stems usually hidden by

leaves, lacking decurrent ridges, tomentose distally, with older shoots pale brown when dried; old leafless stems dark grey-brown, smooth, with scattered leaf scars; stip­

ules absent. Leaves lanceolate (Figure 41 A, B), 2.7-3.2

mm long, up to 4.8 mm in fast-growing coppice shoots, acute, sessile, appearing abruptly from stem, lamina from side basally appressed to stem then gradually curving slightly away, increasingly so throughout its length; adax­ ial surface slightly concave and basally keeled, abaxial surface smoothly rounded, abaxially villous (Figure 41 B), adaxially less so (Figure 41 A), older leaves glabrescent, in coppice shoots more densely villous; stomata only on

adaxial surface (Figure 41C). B ud le a f colleter as a brown,

erect papilla 0.2 mm long, soon broadening slightly and

darkening to form a black deltoid apiculus shrinking to

a minute patch in older leaves. Inflorescence with 6-1 0

flowers in terminal, dense clusters (Figure 38B), 3—4 mm wide, main axis not continuing growth during anthesis,

TYPE

FIGURE 39.— Known distribution o f Thamnea m atroosbergensis, • ; FIGURE 4 0.— H olotypc o f Brunia com pacta, Esterhuvsen 31628

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Bothalia 40,1 (2010)

101

further branching sym podial with one new dom inant shoot, old inflorescence peduncles persistent as braete-

ate, villous structures am ong older branches. Bract sub­

tending each flow er closely appressed, ovate, 0.6 -0.8 mm long, m idrib not visible, densely villous, with a black apiculus; bracteoles 2, oblanceolate, navicular,

black-tipped, densely villous. F loral receptacle 0.6 0.8

mm long, with transition to calyx lacking a constric­

tion. ( alyx tube vestigial, segm ents narrow ly deltoid, ±

1.1 mm long, acum inate, separated by a broadly obtuse gap. abaxially villous, densely ciliate, lacking a m idrib,

hyaline with m inute dark apiculus. Corolla white, pet­

als tree from stam ens, elliptic, 0.6 1.2 mm long, erect to spreading, abaxially villous, adaxial surface with a thick

cushion-like sw elling lying against top o f ovary. Sta­

mens ± 0.8 mm long, distally incurved; anthers 0.2 111111

long, lobes parted and slightly divergent below ; pollen

(4)5-colporate (F igure 4 IF). O vary ha If-inferior, ± 0.7

mm long, top villous w ith single nectarostom ata (Figure 41 D, E); locules 2, wall betw een com plete at anthesis, each bearing a pendulous ovule on one o f tw o placentas in each loculus; styles 0.9—1.3 m m long, slightly adnate, distally curved to point term inal stigm as into a lateral

position. F ruit with enlarged receptacle and shrivelled

flow er parts attached; seed ovoid, 1.3 x 0.8 111111, brow n,

transversely w rinkled, lacking an elaiosom e. F low ering

tim e: January, A pril. May, A ugust and O ctober.

D iagnostic features'. B runia co m p a cta differs from B. sacculata (K irchner ex Pi I Ians) C lass.-B ockh. & E.G.H.

Oliv. in having hairs on the adaxial le a f side, from B.

m icrophylla Tliunb. in having larger leaves (2 .4 -2 .8 111111

instead o f 1.2 2.4 mm in B. m icrophylla) and from B.

squalida E.Mey. ex Sond. in having distally recurved instead o f erect styles. W ith the second group it shares the very short petals (sh o rter than 1.5 m m ) appearing in

all species so far included in this group. H erein, B. co m ­

pacta is very sim ilar to B. hullata (Schltr.) C lass.-B ockh. & E.G.H.Oliv. differing in having 6 10 instead o f only 1 ( 3 ) flowers per inflorescence. T hough the relationships are not clear, the species is p relim inarily grouped under

Brunia subgen. M niotham nea.

The species varies w ithin the collections in having fast-growing coppice shoots am ong the norm al ones,

as in Esterhuvsen 3 2 /6 0 (B O F ). T hese have longer and

more densely villous leaves, and less profuse branching.

D istribution a n d ecology: Brunia compacta has been collected in the southern Cedarberg and Cold Bokkeveld M ountains, north o f Ceres, at altitudes from 1 200 to

1 500 111 (Figure 39). At one o f its localities it is recorded

as not com m on but widespread in the area (Apollo Peak,

southern Cedarberg: Esterhuvsen 32160). The shrubs

occur am ong rocks, large boulders and cliffs on upper slopes. After fires the species reproduces from seedlings.

Note: this new species was at first recorded as one

belonging in the genus Raspalia Brongn., but according

to the new classification o f the family (ClaBen-Bockhoff

et al. in press), it must be placed in the genus Brunia Lam.

under which Raspalia is being placed in synonymy based

on m olecular analyses (Quint & ClaBen-Bockhoff 2006).

A dditional m aterial exam ined

WEST LRN CAPE.— 3219 (Clanwilliam): Clanwilliam, Apollo Peak, S Cederberg, on S side at hase o f massive rock or cl ill's, 4000-5000' [1 520 m], (-C A ), 17-05-1%9, Esterhuvsen 32160 (BOL); Clanwil­ liam. Kaffirkop [KatYerskop], suurvlakte, S Cederberg, amongst boulders on upper slopes, (-C A ), 17-04-1976, Esterhuvsen 34250 (BOL); Ceres, central peak o f Schurweberg above ‘Excelsior’ N o f Bokkeveld Tafel-berg, amongst rocks on SW side o f rocky summit, 4X00' (?) [1 460 m], ( - ( D ) , 15-08-1971, Esterhuvsen 32619 (BOL); Ceres, Schurweberg Peak (between Bokkeveld Sneeuberg and Bokkeveld Tafelberg) amongst rocks, 4500’ [1 370 m], (-C D ), 1-01-1962, Esterhuvsen 29432 (BOL).

REFERENCES

CLABEN-BOCKHOFF, R. in press. Bruniaceae. In J.W. Kadereit & V. Bittrich. The fam ilies a n d gen era o f vascular plan ts, vol. 10. CLABEN-BOCKHOFF, R„ OLIVER, E.G.H., HALL, A.V. & QUINT,

M. in press. N ew classification o f the Bruniaceae based on molecular and morphological data. Taxon.

LINDER, IIP. 2003. The radiation o f the Cape flora, southern Africa.

B iological R eview 78: 59 7 -6 3 8 .

PI LI. A N S, N.S. 1947. A revision o f Bruniaceae. Journal o f South Afri­

can Botany 13: 121-206.

QUINT, M. & CLABEN-BOCKHOFF, R. 2006. Phylogeny o f Bru­ niaceae based on m atK and ITS sequence data. International

Jou rn al o f P lan t Science 167: 135-146.

A.V. HALL*. E.G.H. OLIVER** and R. CLABEN-BOCKHOFF***

* Formerly: Bolus Herbarium, University o f Cape Town. Present ad­ dress: Helderberg Village, Private Bag X 19, 7125 Somerset West. ** Department o f Botany & Zoology, Stellenbosch University, Private Bag X I, 7602 Matieland, Stellenbosch.

*** Institut fur Spezielle Botanik, Johannes Gutenberg-Universitat, M ain/, Germany.

MS. received: 2008-10-16.

PTER ID O PH Y TA : POLYPODIACEAE

THE STATUS OF x P L E O P O D IU M IN AFRICA

A widepread central and southern A frican taxon almost

intermediate between Pleopeltis m acrocarpa (Bory ex

Willd.) K aulf and Pleopeltis polypodioides (L.) E.G.

Andrews & W indham subsp. ecklonii (K unze) J.P.Roux

was shown convincingly by A nthony & Schelpe (1985) to arise from the hybridization o f these two polypods. As

at that time, Pleopeltis polypodioides subsp. ecklonii was

referred to the genus P olypodium I... these authors neces­

sarily established the hybrid genus x Pleopodium Schelpe

& N.C.A nthony to accom m odate their putative hybrid, x Pleopodium sim ianum Schelpe & N.C.Anthony. Roux

(2001) estimated that ± 10 such x Pleopodium taxa are

known from the neotropics, with only one recorded for Africa (Roux 2009). We have been able to trace only five

validly published x Pleopodium taxa worldwide (Anthony

& Schelpe 1985; Mickel & Beitel 1987).

Follow ing the transfer in Windham (1993) o f the typi­

cal (neotropical) subspecies o f Polvpodium polypodioi­

des (L.) Watt to Pleopeltis Humb. & Bonpl. ex Willd.,

Roux (2009) provided a new com bination for the Afri­

References

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