Nature is resilient, animals can adapt to change

We are always puzzled by the widespread belief amongst native plant advocates that native animals are dependent upon native plants and the corollary argument that non-native plants are invasive because they have no predators.  We suspect that one of many reasons for this assumption is a lack of understanding about evolution.  That is, if you believe that animals are unable to adapt to new plant species, then you probably assume that the new plant species are not useful nor are they prey to native animals.  

The Gallup Poll tracks the opinions of Americans regarding evolution.  In 2010 a surprisingly small percentage of Americans (16%) believed in the evolution of man unguided by God.  Even amongst those who believe in evolution, it is often seen as an historical process that moves too slowly to be perceived.  Science has only recently found living examples of on-going evolution:

“A growing appreciation that organic evolution, like mountain building, is an ongoing rather than simply historical process has stimulated an infusion of evolutionary thinking into mainstream ecology.”(1)

The Soapberry Bug

Soapberry bug on balloon vine. Scott Carroll, UC Davis

The soapberry bug (Jadera haematoloma) is an example of a native insect that has changed genetically in less than 100 generations over a period of 20 to 50 years in response to a new non-native plant host. 

The soapberry bug is named for the plant upon which it depends for both food and reproduction, the Sapindaceae family (‘Soapberry’ family).  In southern Florida, the native host plant of the soapberry bug was the balloon vine (Cardiospermum corindum).  As its name suggests, its seed is large and round.  The soapberry bug that feeds on that seed has a large jaw–up to about 70% of its body length–that enables it to get the seed into its mouth. 

In the 1950s a new member of the Sapindaceae family of plants was introduced to southern Florida, the Chinese flametree (Koelrueleria elegans) as an ornamental.  Its seed is much smaller than the seed of the balloon vine.  The soapberry bug quickly made a transition to its new host and over time it evolved several adaptations to it.  The jaw of the soapberry bug that feeds on the flametree is much smaller, as little as 50% of its body length. 

The life cycle of the soapberry bug has also changed and is better suited to the brief, simultaneous availability of seeds of its new host, the flametree:  “The flametree-specialized race [of soapberry bug] has a briefer development time (and thus an earlier age at first reproduction), greater fecundity, and exhibits greater expenditure of effort towards reproduction than the balloon vine race of J. haematoloma from which they originated.”(2)

In south Florida, the soapberry bug now has two genetically distinct races that are suited to their specific hosts–one native, one not.  The original race has not changed where its host is the native balloon vine.  The soapberry bug is not very mobile, so these two populations are physically separated.  This is an example of increased genetic biodiversity in response to an introduced plant. 

There are 400 genera and 1,500 species of plants in the Sapindaceae family all over the world(3), so we should not be surprised to find many other examples in the scientific literature of insect hosts that are adapted to them, whether they are native or introduced plants, as well as differences in those insects that are suited to the specific plants and/or their locations.  The soapberry bug isn’t an isolated example of an insect that has rapidly evolved to adapt to new hosts.  On the other hand, science cautions us against generalizing to all insects. 

We offer our readers three sources of information, depending upon their scientific knowledge.  The National Public Radio story about soapberry bug evolution is addressed to the layman.  At the opposite extreme, the citation in our footnotes is addressed to scientists with expertise in genetics.  The middle ground, from which we drew most heavily, is a website about soapberry bugs

Cheerful conclusion

As we often do, we conclude cheerfully that nature is remarkably resilient.  Although nature is less fragile than native plant advocates believe it to be, we don’t take that as an invitation to abuse it.  We treat nature with respect, and that includes taking care of what is here, whether it is native or non-native.  


(1) Carroll, Scott P., et. al., “Genetic architecture of adaptive differentiation in evolving host races of the soapberry bug, Jadera haematoloma,” Genetica, 112-113: 257-272, 2001

Evolution didn’t stop in 1492

One of the most appealing of the many arguments used by native plant advocates in support of their ideology is the evolutionary concept of “co-evolution.”  Co-evolution is defined by Forgotten Pollinators(1) as “The idea in evolutionary ecology that certain mutualistic organisms have directed or redirected each other’s evolutionary trajectory.”  The implication of this theory is that plants and animals that have evolved together are interdependent and that loss of a particular plant will result in the loss of the animals with which it evolved.  Native plant advocates sometimes describe these relationships as “a lock and key,” implying that native plants and animals fit together in a mutually beneficial relationship which is exclusive. 

Those who believe this theory are obviously deeply committed to saving all native plants because they believe the loss of any single plant would inevitably lead to the loss of the animals that are dependent upon it.  Likewise, non-native animals are often exterminated based on the assumption that they compete with native animals and that loss of native animals will lead to the loss of native plants.

There are three problems with this theory. First, while there are some examples of truly exclusive co-evolved relationships in which both species cannot survive without the presence of the other, the number of such relationships is quite small.  Second, even these relationships are not immutable because evolution has not stopped, and therefore other species may develop mutualistic relationships with the prior exclusively mutualistic species.  And third, organisms are opportunistic and are quick to take advantage of any new opportunities, meaning that many interactions observed between species in the wild are not co-evolved at all.  For example, the honeybee pollinates hundreds of species of North American plants and it didn’t evolve with any of them (since honeybees were introduced into North America from Europe, which had introduced them from Africa).

Why is “co-evolution” rare in nature?

When defining “co-evolution” Forgotten Pollinators adds this caveat, “Good examples of truly reciprocal coevolution are difficult to find.”  Although the concept of “co-evolution” has a certain logical appeal, the explanation for why it is rare in nature is even more logical:  it is a risky survival strategy in a world that is constantly changing.  If, for example, the specific plant upon which a specific animal depends doesn’t bloom or doesn’t return from its dormant phase because of a sudden, even temporary, change in the climate, the animal that is dependent upon that plant is out of luck.  Since such fluctuations of environmental conditions are common, natural selection does not favor the animal that is restricted to a single plant for which there is no substitute.  Such exclusive relationships therefore do not persist in nature.

Nature provides “back-ups” that will enable plants and animals to respond to fluctuating environmental conditions.  For example, few plants have a single pollinator.  Most have several, usually of several different types.  One bee may be a particularly effective pollinator of a particular plant, but that plant is probably also visited by a fly, a butterfly, a bird, a beetle, etc.  As humans do, plants and animals don’t just give up when conditions change.  We all look for and usually find other alternatives. 

Native bumblebee gathering nectar and/or pollen from non-native cotoneaster. Albany Bulb, Albany, California

“Evolution right under our nose”

The Science Section of yesterday’s New York Times features an article about evolution of animals in New York City In the most densely populated city in the country, founded nearly 400 years ago, 74% of the native plant species that existed when the city was founded in 1624, still exist there.(2)  San Francisco has an even lower rate of extirpation of its native plants since it was founded in 1850.  Ninety-seven percent of the 714 plant species known to exist in San Francisco in 1850 are still found in San Francisco

Midtown Manhattan as seen from the Empire State Building. Creative Commons Attribution Share Alike

The fascinating article in the New York Times reports that the ability of animals to evolve in response to changing environmental conditions has enabled their survival in the urban environment. 

The white-footed mouse is an example of a native animal that is thriving in New York City.  The urban environment creates isolated urban islands, such as parks.  Scientists find that virtually every park in New York City has a population of genetically unique white-footed mice.  In fact, “The amount of [genetic] differences you see among populations of mice in the same borough is similar to what you’d see across the whole southeastern United States,” according to the scientist studying this mouse in New York City.

It’s difficult to imagine a more altered, artificial environment than the road medians on Broadway on the Upper West Side of Manhattan, which are composed of landfill used to cover the subway tunnel.  However, scientists have found 13 species of ants living in some of these medians.  Nine of the thirteen species are native. 

Nature is opportunistic and resilient.  It isn’t necessary to eradicate non-native plants and animals to ensure the survival of native plants and animals.  What greater laboratory to illustrate the resilience of nature than New York City? 


(1) Buchmann and Nabhan, The Forgotten Pollinators, Island Press, 1996

(2) Duncan et al, “Plant traits and extinction in urban areas:  a meta-analysis of 11 cities,” Global Ecology and Biogeography, July 2011