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264 Annals <strong>of</strong> the<br />
Missouri Botanical Garden<br />
these may allow exploitation by bees. Other species<br />
in the Guild (with shorter corolla tubes) are not<br />
solely visited by S. wiedemanni, but still need to<br />
be included since the fly provides an efficient pollination<br />
service (Potgieter et al., 1999).<br />
DISCUSSION BY FAMILY<br />
LAMIACEAE<br />
Pollination <strong>of</strong> Plectranthus hilliardiae, P. reflexus,<br />
P. ambiguus, and long-tubed forms <strong>of</strong> P. saccatus<br />
has previously been discussed in Potgieter et<br />
al. (1999) and Potgieter and Edwards (2001). In<br />
most areas where Stenobasipteron wiedemanni has<br />
been observed, Plectranthus species (long- or shorttubed)<br />
tend to form a major component <strong>of</strong> the forest<br />
understory. Orthosiphon tubiformis occurs in different<br />
habitat to forest understory Plectranthus species<br />
and has been discussed by Goldblatt and Manning<br />
(2000).<br />
ACANTHACEAE<br />
Honeybees collect pollen from Isoglossa hypoestiflora,<br />
but the long, narrow corolla tube prohibits<br />
nectar access. Honeybees would not contribute to<br />
significant pollen carryover over large distances,<br />
since pollen is groomed into the scopae before the<br />
worker bees return to their hives. Isoglossa cooperi<br />
closely resembles I. hypoestiflora in floral shape<br />
and size, differing only in the presence <strong>of</strong> glandular<br />
hairs on the calyx and bracts. The species are <strong>of</strong>ten<br />
sympatric (Fig. 4A). From a pollination perspective,<br />
these two species are very similar and fit the Stenobasipteron<br />
wiedemanni pollination Guild. They occur<br />
in afromontane and scarp forest and are generically<br />
anomalous with respect to flower color and<br />
corolla morphology. Most Isoglossa Oerst. species<br />
in South Africa are hymenophilous (pers. obs.),<br />
with creamy white flowers and short corolla tubes<br />
(mostly less than 10 mm in length). These creamy<br />
white species are common in savanna and tropical<br />
and subtropical forests.<br />
The observation <strong>of</strong> visits to Hypoestes aristata<br />
shows that Stenobasipteron wiedemanni may form<br />
part <strong>of</strong> a more generalized suite <strong>of</strong> pollinators in<br />
species with shorter floral tubes. As in shortertubed<br />
Plectranthus species, the fly still contributes<br />
to pollen carryover, since the elongate anther filaments<br />
deposit pollen on the body <strong>of</strong> the fly and the<br />
elongate style is able to remove pollen from this<br />
position. A similar situation exists in Barleria obtusa,<br />
where long-proboscid bees can also access<br />
nectar by crawling into the widened distal part <strong>of</strong><br />
the corolla tube.<br />
ORCHIDACEAE<br />
The record for long-proboscid fly pollination in<br />
Brownleea Harv. ex Lindl. (Goldblatt & Manning,<br />
2000) highlights the disjunction between grasslandand<br />
forest-growing species. Brownleea macroceras<br />
Sond. is pollinated by Prosoeca ganglbaueri (Johnson<br />
& Steiner, 1995), which occurs in montane<br />
grassland at high altitudes. By contrast, B. coerulea<br />
is a forest margin species <strong>of</strong> lower altitudes and is<br />
pollinated by Stenobasipteron wiedemanni. Brownleea<br />
coerulea is a widespread species (Fig. 3C) that<br />
also occurs in Madagascar, where its pollination has<br />
not been studied.<br />
BALSAMINACEAE<br />
The floral visits by Stenobasipteron wiedemanni<br />
to Impatiens hochstetteri subsp. hochstetteri are the<br />
first published records <strong>of</strong> nemestrinid fly pollination<br />
in the Balsaminaceae. This plant species is<br />
widespread across Africa, but the distribution <strong>of</strong> S.<br />
wiedemanni elsewhere in Africa is not known.<br />
Grey-Wilson (1980) recorded butterflies as pollinators<br />
<strong>of</strong> the ‘‘flat type’’ flowers in the section to<br />
which I. hochstetteri subsp. hochstetteri belongs, yet<br />
little information is available on the pollination <strong>of</strong><br />
specific Impatiens L. (Grey-Wilson, 1980). We have<br />
observed papilionoid butterfly visits to I. hochstetteri<br />
subsp. hochstetteri at Ferncliffe Nature Reserve<br />
in Pietermaritzburg (KZN) confirming the above.<br />
The distribution <strong>of</strong> Impatiens hochstetteri subsp.<br />
hochstetteri in southern Africa (Fig. 3D) shows a<br />
number <strong>of</strong> plots outside forested areas. This species<br />
relies on moist forest habitats and may occur in<br />
scrub forest patches that are below the resolution<br />
<strong>of</strong> our Geographic Information System that was<br />
used for mapping.<br />
GESNERIACEAE<br />
Very little is known about pollination in Streptocarpus<br />
(Hilliard & Burtt, 1971), and it is likely<br />
that Stenobasipteron wiedemanni is the pollinator <strong>of</strong><br />
a number <strong>of</strong> Streptocarpus species that conform to<br />
the floral morphology <strong>of</strong> S. formosus.<br />
IRIDACEAE<br />
The genus Hesperantha comprises many scented,<br />
pale species with crepuscular anthesis that are<br />
thought to be pollinated by moths (Goldblatt, 1984).<br />
Contrary to this pattern, H. huttonii is odorless, has<br />
diurnal anthesis and colored flowers—attributes<br />
suited to nemestrinid fly pollination. Long-proboscid<br />
fly pollination <strong>of</strong> day-flowering species <strong>of</strong> Hesperantha<br />
is not uncommon. Hesperantha latifolia<br />
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