Selection on spur shape in Impatiens capensis.

Rapid speciation within some plant families has been attributed to the evolution of floral spurs and to the effect of spur length on plant reproductive success. The flowers of Impatiens capensis (jewelweed) possess a long, curved spur in which nectar is produced and stored. Spur length and curvature varies among plants within one population. Here I document that spur shape is variable in natural populations, variation within plants is less than variation among plants, and spur shape is correlated with components of female and male reproductive success. The apparent natural selection is weakly directional in 1 of 2 years, with greatest seed production and pollen removal occurring in flowers with the greatest spur curvature. Bee pollinator visit length is longest at flowers with highly curved spurs, and they leave less nectar in these spurs than in flowers with straighter spurs. Spur angle evolution may be limited, at least in part, by opposing selection by nectar-robbers who prefer to visit flowers with greater spur curvature. Other factors that might contribute to the maintenance of spur angle variation are temporal variation in the strength of selection and potential genetic correlations of spur shape with other traits under selection.

Foraging behavior affects pollen removal and deposition in Impatiens capensis (Balsaminaceae).

Flowers of most plant species are visited by a variety of animals. Some of these visitors are effective pollinators while others remove resources without transferring pollen. Studies comparing the effectiveness of different visitors as pollinators often compare taxa without considering variation in behavior within a taxon. Wilson and Thomson (Ecology 72: 1503-1507, 1991) documented the effects of honey bees and bumble bees on the pollination dynamics of Impatiens capensis. They found that pollen-collecting honey bees removed large numbers of pollen grains from anthers but deposited little of it on stigmas; bumble bees, which sought nectar, removed less pollen but deposited more of it on stigmas. It is unclear whether the low pollen transfer efficiencies of honey bees are explained by their morphology or by their pollen-collecting behavior. We repeated the work of Wilson and Thomson at a site where honey bees were foraging for nectar, not pollen. We measured the quantity of pollen remaining in anthers, the number of pollen grains deposited on stigmas, and seed production after single visits by honey bees and bumble bees. The differences between the taxa disappeared when they were foraging in a similar manner. Our results clearly demonstrate the importance of foraging behavior on the pollination effectiveness of floral visitors.

Diurnal and nocturnal pollination of Silene alba (Caryophyllaceae).

Flowers that are open for >12 h may be visited by both diurnal and nocturnal pollinators. I compared the effectiveness (measured as seed production and pollen movement distance) of diurnal and nocturnal pollinators of Silene alba, a species whose flowers open in evening but close by midmorning the following day. By bagging flowers either during evening hours or during daylight hours or both day and night, I compared seed production caused by diurnal and nocturnal pollinators. Flowers exposed only to nocturnal visitors (mostly sphingid and noctuid moths) produced significantly more seeds than flowers exposed only to diurnal visitors (bees, flies, and wasps). Fluorescent dye applied to anthers moved significantly further and to more stigmas at night than during the day. In both measures of pollination effectiveness, nocturnal-visiting moths are better pollinators of S. alba than are the diurnal-visiting bees, flies, and wasps. These data support the hypothesis that floral phenology is an adaptation to expose flowers to the most effective pollinators.

The effects of stigma age on receptivity in Silene alba (Caryophyllaceae).

Silene alba, a perennial, dioecious plant, produces flowers that open in the evening and can remain open and receptive to pollination for up to 5 d, though in hot and dry conditions the flowers will wilt during the day only to reopen night after night. In the field, it is visited by two different kinds of pollinators with differential success: moths visit the flowers at night, and their movements result in broad pollen dispersal and large seed production, whereas bees, wasps, and flies visit the flowers in the mornings and have decreased pollination effectiveness. However, this differential success may be due to a decrease in stigmatic receptivity soon after the flowers open. We performed controlled pollinations to determine the effect of stigma age on pollen germination and seed set. We pollinated flowers at 12-h intervals up to 120 h and divided these into two sets: from one set, we removed stigmas 24 h after pollination to examine percentage of pollen germination. The second set of flowers was allowed to produce fruits, and the seeds were counted and weighed. Pollen germination declined significantly with stigma age, but there was no significant effect of stigma age at pollination on the number or mass of resulting seeds. Thus, the decreased pollination success of bees is not due to a decrease in stigmatic receptivity but is most likely a result of pollinator inefficiency.

CONSEQUENCES OF FLORAL VARIATION FOR MALE AND FEMALE REPRODUCTION IN EXPERIMENTAL POPULATIONS OF WILD RADISH, RAPHANUS SATIVUS L.

We documented effects of floral variation on seed paternity and maternal fecundity in a series of small experimental populations of wild radish, R. sativus. Each population was composed of two competing pollen donor groups with contrasting floral morphologies and several designated maternal plants. Progeny testing with electrophoretic markers allowed us to measure paternal success. Realized fecundity by each maternal plant and the fraction of those seeds attributable to each pollen donor group were used as outcome variables in path analysis to explore relationships between floral characters (petal size, pollen grain number per flower, and modal pollen grain size), pollinator visitation patterns, and reproductive success. A wide range of pollinator taxa visited the experimental populations, and patterns of discrimination appeared to vary among them. The impact of visitation on male and female reproduction also varied among taxa; visits of small native bees significantly increased paternal success, while those of honey bees reduced male fitness. Only visits by large native bees had discernible effects on recipient fecundity, and, overall, fecundity was not limited by visitation. Maternal plants bearing large-petalled flowers produced fewer flowers during the experiment, reducing their total seed production. In these small populations, postpollination processes (at least in part, compatibility) significantly influenced male and female reproductive success. Variation in pollinator pools occurring on both spatial and temporal scales may act to preserve genetic variation for floral traits in this species.

Local distribution of C3 and C4 grasses in sites of overlap on Mount Kenya.

A zone of C3-C4 grass overlap has been identified on the northern slopes of Mount Kenya at elevations of 2,800-3,200 m. At higher elevations, C3 grasses predominate; below, C4 grasses predominate. At each of three elevational sites of overlap, a series of transects was surveyed for C4 and C3 grass composition. All transects were located in structurally similar vegetation (high elevation grassland) within 150 m of each other. Transects were run in a variety of topographic situations. Within each transect, several environmental parameters were measured. Both unweighted (species presence/absence) and weighted (by frequency) measures of %C4 composition were significantly correlated with dry season soil moisture. Drier transects contain significantly more C4 species, in greater frequency, than wetter transects. Other correlations of C4 composition (e.g. factors which tend to parallel soil moisture) were also found. This local trend parallels the larger scale tendency of C3 grasses to replace C4 grasses with increasing elevation. Finer scale habitat partitioning may account for C3-C4 overlap within transects.