Darwin predicted that flowers and pollinators are engaged in an evolutionary arms race. But that’s not always the case. In a group called columbines, evolution happened in a stop-start ‘punctuated’ way, as the flowers encountered new pollinators with increasingly long tongues.
Charles Darwin was a visionary in more ways than one. In 1862, Darwin was studying a Malagasy orchid called Angraecum sesquipedale, whose nectar stores lie inaccessibly at the bottom of a 30cm long spur (tube). Darwin predicted that the flower was pollinated by a moth with tongue long enough to raid the spur.
Few people believed him, but in 1903, zoologists discovered Darwin’s predicted moth, Xanthopan morgani praedicta, and it did indeed have a very long tongue. Darwin’s accurately predicted the extraordinary but matching lengths of moth tongue and orchid spur, but his explanation for them is another story.
The arms race model
He suggested that the two species were locked in an ‘evolutionary arms race’. Orchids and pollinators gradually co-evolved over time, lengthening both tongues and spurs in response to each other.
Orchids with the longest spurs have an advantage. Their nectar stores are only just within reach of pollinators, so they are tempting but don’t sacrifice too much valuable nectar. For pollinators, the advantage belongs to those with the longest tongues because they have access to the most food.
The arms race model has become widespread and popular since Darwin’s time. It helps to explain relationships between predators and prey, parasites and hosts and even males and females. But its original function – to explain the relationship between flowers and pollinators – has just been called into question.
Justen Whittall and Scott Hodges from the University of California, Santa Barbara, tested the arms race theory by looking at another long-spurred flowering plants – the columbines (Aquilegia sp). In these flowers, every petal carries its own elongated nectar spur and the advent of these spurs coincided with the recent and rapid diversification of this group.
Whittall and Hodges charted the evolutionary relationships between the 25 North American columbine species, whose spurs range form barely a centimetre in length, to just over twelve. They found that this great variety of lengths was driven by changes in pollinators, rather than gradual races against a single one.
The flowers with the shortest spurs were pollinated by short-tongued bumblebees. Hummingbirds, whose tongues are longer, pollinate columbines with longer spurs, while hawk-moths, with the longest tongues of all, carry the pollen of the longest-spurred flowers.
There is no overlap between these three groups and once a lineage switches pollinator it doesn’t go back. Over the course of their evolution, the columbine lineages went from bumblebees to hummingbirds, and then to hawkmoths, lengthening their spurs with every jump.
The ‘pollinator shift’ model
Based on these observations, Whittall and Hodges put forward an alternative to Darwin’s arms race model. They imagined a columbine ancestor that was well adapted to the tongue length of a specific pollinator (say, a bumblebee).
In part of its range, the flower started to be visited by a second pollinator (say, a hummingbird) with a much longer tongue. In this area, the plant rapidly evolved a longer spur in response to its new partner and over time, this led to two species with different spur lengths and different pollinators.
In this model, the columbines’ spurs evolved in a ‘punctuated’ stop-start way, very different to Darwin’s model of gradual change. Each pollinator shift triggered a large evolutionary rush, as the species lengthened their spurs in response to the longer tongues of their new partners. In between these shifts, the pace of evolution slowed down considerably.
But Darwin’s arms race idea isn’t out for the count yet. Whittall points out that columbines that are pollinated by hawkmoths have a great variety of spur lengths themselves that were most likely the result of an arms race. And the moths themselves evolved long before the columbines did, so the variations in their tongue lengths must have evolved in relationships with other plants.
An adaptive valley
The stop-start model also explains a difference between columbines around the world. Those in Europe and Asia have a much smaller range of spur lengths than their North American cousins, and none of them are pollinated by hawkmoths. Whittall and Hodges have an answer for this too – it’s because Eurasia has no hummingbirds.
Imagine if flowers tried to make the evolutionary leap from bumblebee to hawkmoth without the intermediate stepping stone of hummingbirds. At the intermediate spur length, the flower would have excluded its old pollinator, whose tongues would now be too short to reach any nectar. But it would have no advantage over its new pollinator, whose amply long tongues could drink the flowers dry.
Between bumblebee and hawkmoth lies an ‘adaptive valley’, where intermediate-length flowers have no advantage and are ignored by natural selection. In Eurasia, there is not enough impetus for a species to cross it. But North America, the hummingbirds act as a stepping stone that allowed the columbines to ford this gap and evolve even more extreme flowers.
Reference: Whittall & Hodges. 2007. Pollinator shifts drive increasingly long nectar spurs in columbine flowers. Nature 447: 706-709.
Technorati Tags: Justen Whittell, Scott Hodges, orchids, columbines, nectar spurs, flower evolution, evolutionary arms races, punctuatedevolution, hawkmoths, pollinators, science
Images: Moth from MSN Encarta, columbine montage from Justen Whittall’s website.
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Filed under: Animal evolution, Animal kingdom, Evolution, Evolutionary arms race, Plants | 5 Comments »