Joshua trees at LiveScience

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Over at LiveScience, my collaborator Chris Smith describes the research we’ve done so far on the interaction between Joshua trees and their pollinators:

First, the match between the Joshua tree flowers and the moths’ ovipositors suggested that coevolution might have molded the relationship between the plant and the pollinator. Second, because the plants are completely dependent on the moths for reproduction, the differences in the flowers might have caused Joshua trees to split into two different species.


Yucca brevifolia in Tikaboo Valley, Nevada. Photo by jby.

Pollination before flowers

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ResearchBlogging.orgWhich came first, the pollinator or the pollinated? An article in this week’s Science suggests that a diverse group of insects may have been drinking nectar and pollinating plants millions of years before the appearance of modern flowering plants [$-a].



Panorpis communis, a modern scorpionfly species, and a sketch of ancient, pollinating scorpionflies. Photo by JR Guillaumin; sketch from Ollerton and Coulthard (2009).

Prior to the origins of modern flowering plants, or angiosperms, in the early-middle Cretaceous period, most of the diversity of land plants were gymnosperms. These plants are characterized by “naked seeds” — reproductive organs exposed to the air, where the wind can catch pollen and carry it from one plant to fertilize the ovules of another. In a world dominated by gymnosperms, the thinking used to be, animal pollinators were mostly unnecessary.

The new paper by Ren et al. challenges this idea with the description of a set of fossilized scorpionflies, all of which have strikingly long probosces that are clearly suited to sucking up liquid. The earliest of these fossils are from the Jurassic, tens of millions of years before the flowering plants began to diversify. In modern insects, sucking mouthparts like the ones described are associated with two kinds of feeding: drinking pollen, and drinking blood. To determine which was most likely in this case, Ren et al. performed energy-dispersive spectroscopy on the best-preserved fossil, and found no sign of the elevated levels of iron in the proboscis that would result from the residue of blood meals. This suggests that the scorpionflies were drinking nectar, or something like it.

Nectar has one major function in plants: to attract insects. Ant-protected plants reward their ants with nectar, and flowering plants use nectar to lure animal pollinators close enough to pick up or drop off pollen. If these ancient scorpionflies were, in fact, living on nectar, Ren et al. reason they were probably pollinating contemporary plants, which were all gymnosperms. The authors identify a diverse list of candidate host plants, including seed ferns and a relative of the modern ginkgo, whose reproductive structures were (1) too well-sheltered for efficient wind pollination or (2) included tubular structures similar to those that modern plants use to guide nectar-feeding pollinators. Finally, the authors point out, many modern gymnosperms produce “ovular secretions” that are very similar to the nectar produced by angiosperms.

As a neontologist, I’m often amazed how much can be told from million-years-old fossils — who knew there was a way to test for residual blood in a fossilized proboscis? At the same time, Ren et al. connect some mighty scattered dots to build their hypothesis. The real clincher is that it seems mighty unlikely that animal pollination would be rare in a world that already has both flying insects and pollen-producing plants. Animal pollination is much more efficient than wind pollination, and if there’s one constant in evolutionary history, it’s that living things rarely miss an opportunity like that.

References

Ollerton, J., & Coulthard, E. (2009). Evolution of animal pollination. Science, 326 (5954), 808-9 DOI: 10.1126/science.1181154

Ren, D., Labandeira, C., Santiago-Blay, J., Rasnitsyn, A., Shih, C., Bashkuev, A., Logan, M., Hotton, C., & Dilcher, D. (2009). A probable pollination mode before angiosperms: Eurasian, long-proboscid scorpionflies. Science, 326 (5954), 840-7 DOI: 10.1126/science.1178338

Invasive species not so bad?

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Over on Slate, Rebecca Tuhus-Dubrow says some conservation biologists are starting to question the importance of preventing species invasions:

Certainly, they say, non-native plants and critters can be terribly destructive—the tree-killing gypsy moth comes to mind. Yet natives such as the Southern Pine Beetle can cause similar harm. The effects of exotics on biodiversity are mixed. Their entry into a region may reduce indigenous populations, but they’re not likely to cause any extinctions (at least on continents and in oceans—lakes and islands are more vulnerable). Since the arrival of Europeans in the New World, hundreds of imports have flourished in their new environments.

Tuhus-Dubrow cites the case of Tamarisk in the U.S. Southwest — an aggressive introduced shrub that has also ended up providing important nesting sites for the endangered southwestern willow flycatcher.

The fact of the matter is that human-introduced species can eventually integrate into an ecological community; once they do it’s hard to get them out, and problematic as to whether it’s a good idea. In Australia, dingoes helped extirpate many other large predators when they were introduced by the first humans to arrive on that continent — and now they’re critical to controlling other, later-introduced mammal species.

(Thanks to Ephraim Zimmerman for point this one out to me!)


Invasive pest, or critical flycatcher habitat? Maybe both. Photo by Anita363.

Defense, or Social Security?

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Mike Konczal considers the effect of breaking Defense Department spending out as a separate line item on pay stub tax witholding statements, alongside Social Security and Medicare. If citizens saw a number for military alongside social spending, they might make more informed choices about the relative values of each.

How much of your two weeks work cycle would you like to spend working to keep a global military hegemony going? I’d probably want to clock it out around my first coffee break on Monday (which is fairly early), but that’s me.

Some pacifists withhold a portion (or all) of their Federal taxes in protest against military spending, and there’s even a campaign to let people opt out of funding the military on their tax forms. Maybe Konczal’s idea would be a good alternative?

“France’s answer to James Bond”

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Shades of Clouseau, but this still looks like I’d enjoy it way too much.

DVD on Amazon

Carnival of Evolution #17 at Adaptive Complexity

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Over at Adaptive Complexity, Michael White has just compiled the 17th monthly Carnival of Evolution. Marking the 150th anniversary of the publication of The Origin of Species (November, 1859), Michael structures submitted posts into a “virtual voyage of the Beagle.” Topics range from the sexual habits of our ape-like ancestors* to a highly optimistic study predicting that the frequency of the creationist meme in the United States will drop to 0% by 2050.

* Which habits might, I think, explain why we never invite them round to tea.

Berry Go Round #21 at Beetles in the Bush

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Ted MacRae has a fine round-up* for the 21st monthly Berry Go Round, the bontanical blog carnival. And he notes that BGR needs a badge. Must … resist … urge … to spend afternoon futzing with Inkscape.


Photo by jby.

*Including a set of nested footnotes that would make David Foster Wallace blush.

I want to teach this course

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Via io9: BIOL 103, “Biology in Science Fiction”, at Kenyon College. Sure, the lesson on tribbles is probably just about density-dependent population growth. But it’s a lesson on tribbles.

Endless forms: Oral sex by fruit bats

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ResearchBlogging.orgOne of those scientific papers that seems to have been written with the blogosphere in mind: biologists have just published records of fellatio by the fruit bat Cynopterus sphinx. Apparently C. sphinx females are pretty flexible — they lick their mate’s penis during copulation, which evidently induces him to stay in longer (see the graph below, with drawing). The authors offer a handful of non-mutually-exclusive hypotheses for the adaptive benefit of the behavior, ranging from lubrication to increased fertilization efficiency. The full text is available for free at PLoS ONE, if you’re up for some hot-and-heavy behavioral observations.


Graph from Tan et al. (2009), Figure 3.

Update: In a more in-depth post over at Boing-Boing, Maggie Koerth-Baker wonders why there needs to be an adaptive purpose for a pleasurable behavior (there doesn’t, as far as I’m concerned), and points out that there’s also a video in the supporting information. Which video has some totally unscientific background music.

Reference

Tan, M., Jones, G., Zhu, G., Ye, J., Hong, T., Zhou, S., Zhang, S., & Zhang, L. (2009). Fellatio by fruit bats prolongs copulation time PLoS ONE, 4 (10) DOI: 10.1371/journal.pone.0007595

How to synchronize flowering without really trying

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This post was chosen as an Editor's Selection for ResearchBlogging.orgOne way plants can gain an advantage in their dealings with pollinators, seed dispersers, or herbivores is to act collectively. For instance, when oak trees husband their resources for an extra-big crop of acorns every few years instead of spreading them out, acorn-eating rodents are overwhelmed by the bumper crop, and more likely to miss some, or even forget some of the nuts they cache. These benefits of synchronized mass seed production, or “masting,” are straightforward, but how it happens is less clear. A paper in the latest issue of Ecology Letters has an answer — synchronization happens accidentally [$-a].


Bumper acorn crops ensure that squirrels miss a few. Photo by douglas.earl.

When Dan Janzen first described masting as an adaptation in plants’ coevolution with seed predators, he proposed that “an internal physiological system” [$-a] acted as a timer between masting events, with masting ultimately triggered by weather conditions. However, mathematical models have suggested a different possibility, the “resource-budget hypothesis:” that masting synchronization arises through an interaction of resource and pollen limitation [$-a].

Resource limitation works in concert with pollen limitation by catching plants at two stages of the seed-production process. First, if the resources required for seed production are more than can be accumulated in a single year, or if the availability of resources varies from year to year, then some years will be spent building up reserves instead of producing flowers. When reserves are built up, seed production is limited by the availability of pollen to fertilize flowers. Plants that flower when most of the rest of the population doesn’t will fail to set much seed, so they’ll have reserves to make seeds in the next year. This doesn’t require Janzen’s “internal physiological system” for the plants to synchronize, although such a system might evolve to reduce the likelihood of wasting resources by flowering out of synch.

The new paper tests this model in populations of a western U.S. wildflower, Astralagus scaphoides, which flowers at high frequency every alternate year. The authors prevented seed production in the plants by removing their flowers, either in a “press” of three years in a row or in a single “pulse” during one high-flowering year. The plants’ response to these treatments would reveal the role of resource and pollen limitation in synchronizing seed production.

If resource depletion after fruit set prevents reproduction in successive years, we predicted that ‘press’ plants would flower more than control plants every year, as they were never allowed to set fruit. We predicted that ‘pulse’ plants would flower again in 2006, but not set fruit due to density-dependent pollen limitation in a low-flowering year.

The authors also measured the sugars stored in the roots of plants collected before and after flowering in a high-flowering year.


Seed predator in action. Photo by tombream07.

The resource-budget hypothesis worked. Plants prevented from setting seed were forced out of synch with the rest of the population. “Pulse” plants flowered the year after treatment, but because few other plants did, they received little pollen and set little seed. They then had resources to flower yet another year, with the rest of the population this time, and set much more seed, depleting their reserves and bringing them back into synch. “Press” plants continued to flower at high rates each year, as long as they were prevented from setting any seed. Sugar levels built up in the tested roots during non-flowering years, and dropped after high-flowering years.

So masting arises as an emergent result of two limitations acting on plants — the resources needed to make seed, and good access to pollen. A couple of simple rules lead, undirected, to an ordered system that affects entire natural communities.

References

Crone, E., Miller, E., & Sala, A. (2009). How do plants know when other plants are flowering? Resource depletion, pollen limitation and mast-seeding in a perennial wildflower. Ecology Letters, 12 (11), 1119-26 DOI: 10.1111/j.1461-0248.2009.01365.x

Janzen, D. (1971). Seed predation by animals Ann. Rev. Ecol. Syst., 2 (1), 465-92 DOI: 10.1146/annurev.es.02.110171.002341

Janzen, D. (1976). Why bamboos wait so long to flower Ann. Rev. Ecol. Syst., 7 (1), 347-91 DOI: 10.1146/annurev.es.07.110176.002023

Satake, A., & Iwasa, Y. (2000). Pollen coupling of forest trees: Forming synchronized and periodic reproduction out of chaos. J. Theoretical Biol., 203 (2), 63-84 DOI: 10.1006/jtbi.1999.1066