Pollinator-mediated selection in a specialized hummingbird-Heliconia system in the Eastern Caribbean.

Phenotypic matches between plants and their pollinators often are interpreted as examples of reciprocal selection and adaptation. For the two co-occurring plant species, Heliconia bihai and H. caribaea in the Eastern Caribbean, we evaluated for five populations over 2 years the strength and direction of natural selection on corolla length and number of bracts per inflorescence. These plant traits correspond closely to the bill lengths and body masses of their primary pollinators, female or male purple-throated carib hummingbirds (Eulampis jugularis). In H. bihai, directional selection for longer corollas was always significant with the exception of one population in 1 year, whereas selection on bract numbers was rare and found only in one population in 1 year. In contrast, significant directional selection for more bracts per inflorescence occurred in all three populations of the yellow morph and in two populations of the red morph of H. caribaea, whereas significant directional selection on corolla length occurred in only one population of the red morph and one population of the yellow morph. Selection for longer corollas in H. bihai may result from better mechanical fit, and hence pollination, by the long bills of female E. jugularis, their sole pollinator. In contrast, competition between males of E. jugularis for territories may drive selection for more bracts in H. caribaea. Competitive exclusion of female E. jugularis by territorial males also implicates pollinator competition as a possible ecological mechanism for trait diversification in these plants.

Evidence for ecological causation of sexual dimorphism in a hummingbird.

Unambiguous examples of ecological causes of animal sexual dimorphism are rare. Here we present evidence for ecological causation of sexual dimorphism in the bill morphology of a hummingbird, the purple-throated carib. This hummingbird is the sole pollinator of two Heliconia species whose flowers correspond to the bills of either males or females. Each sex feeds most quickly at the flower species approximating its bill dimensions, which supports the hypothesis that floral specialization has driven the evolution of bill dimorphism. Further evidence for ecological causation of sexual dimorphism was provided by a geographic replacement of one Heliconia species by the other and the subsequent development of a floral dimorphism, with one floral morph matching the bills of males and the other of females.

Effect of floral orifice width and shape on hummingbird-flower interactions.

Nectar guides are common among insect-pollinated plants, yet are thought to be rare or absent among hummingbird-pollinated plants. We hypothesize that the lower lips and trumpet-shaped orifices of many hummingbird flowers act as nectar guides to direct hummingbirds to the flowers' nectar and orient the birds for pollination. To test this hypothesis we conducted laboratory experiments using flowers of Monarda didyma (bee balm) and M. fistulosa (wild bergamot), which have orifice widths of about 4 mm and 2 mm, respectively, and latex flowers with orifice widths of 4 mm and 2 mm and three orifice shapes (trumpet, lipped, and lipless). Rubythroated hummingbirds (Archilochus colubris) made fewer errors during bill insertion and spent a smaller proportion of their feeding visit in error at M. didyma flowers than at M. fistulosa flowers, and at unaltered flowers of both species than at flowers with lower lips removed. Handling times were longer at both lipped and lipless flowers of M. didyma than at those of M. fistulosa, and at lipped than at lipless flowers of M. didyma. The average duration of contact between a hummingbird and a flower's anthers and stigma was longer at M. didyma than at M. fistulosa for both lipped and lipless flowers, and at lipped than at lipless M. didyma flowers. Hummingbirds missed the openings of latex flowers with their bills more frequently and spent a greater percentage of their total feeding visit in error at (i) 2-mm than at 4-mm flowers of all three shapes, (ii) lipless flowers than at trumpet or lipped flowers, and (iii) lipped flowers than at trumpet flowers of both widths. The duration of hummingbird/anther contact was longer at (i) 2-mm than at 4-mm flowers of all shapes, (ii) lipped than at trumpet or lipless flowers, and (iii) lipless than at trumpet flowers for both widths. No significant differences in handling times of hummingbirds were observed among any of the latex flower shapes or widths. Our results demonstrate that orifice shapes can act as guides by reducing the frequency of feeding errors by visiting hummingbirds, and that effects of orifice shape on pollination must be considered in conjunction with flower widths and locations of anthers and stigmas.

Foraging ability of rufous hummingbirds on hummingbird flowers and hawkmoth flowers.

We examine the suitability of ornithophilous flowers and sphingophilous flowers in Ipompsis and Aquilegia for nectar foraging by the hummingbird Selasphorus rufus. In S. rufus, bill length averages 18.9 mm in females and 17.3 mm in males. Maximal tongue extension approximates bill length, suggesting that birds can feed from floral tubes up to 33.5 mm in length. However, their ability to do so is limited by two factors. First, the maximal depth at which S. rufus can extract nectar decreases with the width of the floral tube. Second, feeding time is shortest in short floral tubes and progressively increases as the tubes lengthen because of increased time required for tongue extension and retraction. Hence, nectar foraging occurs with optimal efficiency in moderately broad floral tubes with lengths that do not exceed or only slightly exceed the bill length plus

The evolution of sexual dimorphism in animals: Hypotheses and tests.

Three major hypotheses, based upon mechanisms of sexual selection, intersexual food competition and reproductive role division, have been advanced to explain the evolution of sexual dimorphism in body size and morphology of animals. Genetic models suggest that all of the hypotheses are plausible, and empirical studies demonstrate that each of the three mechanisms operates in natural populations. However, problems arise in testing hypotheses for the evolution of sexual dimorphism: more than one mechanism may be operating simultaneously, and the demonstrated occurrence of a mechanism does not indicate that it actually results in selection for dimorphism. A recent statistical technique offers a solution to these problems and provides a promising new approach to the study of sexual dimorphism, in which researchers can assess the relative importance of each mechanism in present-day selection for sexual dimorphism within a species.

The relative importance of prey availability and intruder pressure in feeding territory size regulation by harriers, Circus cyaneus.

The relative importance of prey availability and intruder pressure in the regulation of harrier (Circus cyaneus) territory size was investigated over two years using analytical methods chosen to permit comparison with Myers et al. (1979) study of sanderlings (Calidris alba). Relationships between territory area and two variables, prey type (mice; large, medium, and small birds) and intruder type (conspecific neighbors, conspecific floaters, and heterospecific floaters), and the consistency of these relationships between years, also were examined. Individual harrier territory areas were highly variable, ranging from 7.8 to 1249 ha in 1984/1985, and 3.9 to 71.3 ha in 1985/1986. Of the prey variables, only mouse availability was significantly inversely correlated with territory area in both years, and slopes resulting from correlations between the logarithms of these two variables did not differ significantly from - 1, the expected result if harriers were adjusting mouse availabilities. The abundance of mice in conjunction with their greater ease of capture relative to birds made them functionally more available, and hence harriers' primary prey. This may explain why mice, rather than birds, were apparently the defended resource. Of the intruder variables, neighbor variables were most strongly inversely cortelatd with territory area. Partial correlation analyses to determine the relative importance of intruder pressure and prey availability in regulating territory size revealed that in 1984/1985, mouse availability and intruder pressure were relatively independent and each explained some variation in territory area, whereas in 1985/1986, mouse availability, rather than intruder pressure, significantly explained all variation in territory area. Possible explanations for why territory sizes of harriers appear to be regulated more closely by food density, whereas territory sizes of sanderlings appear to be regulated more closely by intruder pressure, are based upon differences in 1) neighbor effects, 2) environmental ronmental variability, and 3) accuracy of resource assessment by intruders. The variation in intruder rates and prey availabilities observed between years suggests the need to conduct studies over several years in order to assess accurately the relative importance of these variables in territory-size regulation.