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Plectranthus (see Appendix). Anecdotal evidence, publications by Goldblatt & Manning<br />

(1999, 2000) and confirmation by pollen collected from voucher specimens <strong>of</strong> S.<br />

wiedemanni, extended the Guild to members <strong>of</strong> other plant families (Acanthaceae,<br />

Orchidaceae, Balsaminaceae, Gesneriaceae and Iridaceae) that occur in forested<br />

habitat along the Eastern seaboard <strong>of</strong> southern Africa.<br />

A study on pollination systems in Brownleea (Larsen et al. 2008) confirmed that in a<br />

Grahamstown population (EC, South Africa), B. coerulea is pollinated by S.<br />

wiedemanni, with flies at this site also visiting stands <strong>of</strong> Hypoestes aristata (Vahl) Sol.<br />

ex. Roem & Schult. (Acanthaceae) which may act as a magnet species; this species<br />

was included in the S. wiedemanni guild by Potgieter & Edwards (2005). Interestingly,<br />

B. coerulea at Umtamvuna was rather found to be pollinated by a tabanid fly, Ph.<br />

aethiopica, with P. ciliatus creating a possible magnet effect at the study site which was<br />

a forest patch situated next to grassland (Larsen et al. 2008).<br />

This type <strong>of</strong> habitat is similar to that occupied by succulent forms <strong>of</strong> P. saccatus with<br />

short, white flowers that have blue speckling on the corolla limbs, which superficially<br />

resemble the speckled nectar guides <strong>of</strong> P. ciliatus (and that <strong>of</strong> B. coerulea). A few<br />

plants <strong>of</strong> B. coerulea were seen amongst the population <strong>of</strong> P. saccatus studied at<br />

Beacon Hill, Umtamvuna NR, but for which no pollinator data was recorded. It is<br />

possible that Ph. aethiopica pollinates this form <strong>of</strong> P. saccatus at Umtamvuna NR,<br />

since the average proboscis length (8.9 mm) listed in Table 2 <strong>of</strong> Larsen et al. (2008)<br />

corresponds favourably to the 5 – 7 mm tube length <strong>of</strong> P. saccatus at this site. It is,<br />

however, also possible for acrocerid flies or anthophorine bees to be the pollinators <strong>of</strong><br />

this Plectranthus species (see Appendix, P. saccatus). The month <strong>of</strong> observation <strong>of</strong> B.<br />

coerulea at Umtamvuna NR is not given by Larsen et al. (2008), but it is likely that S.<br />

wiedemanni had not yet emerged at that site at the time <strong>of</strong> the study, since the fly<br />

species has been recorded from forests at that site (C. Potgieter unpubl. data). At the<br />

Kologha Forest study site where P. ciliatus was observed for pollinators in the current<br />

Plectranthus study (near Stutterheim, EC), B. coerulea was seen to be pollinated by S.<br />

wiedemanni, with a voucher carrying pollinaria <strong>of</strong> the orchid (Potgieter & Edwards<br />

2005).<br />

Stenobasipteron wiedemanni is responsible for the evolution <strong>of</strong> specialised long-tubed<br />

corollas in four species (or forms) <strong>of</strong> Plectranthus, three <strong>of</strong> which are endemic to the<br />

Pondoland Centre <strong>of</strong> Endemism. The long-tubed form <strong>of</strong> P. saccatus that occurs on<br />

Chapter 8/ 106

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