Cottonmouth Moccasins: Adapting to the Beach and Beyond

Could some pit vipers evolve the capacity to invade the world’s oceans?


Last Thursday, while doing some fieldwork in Levy County, I came across this Florida cottonmouth as it was sunning itself after an early morning swim:

The warning behavior being demonstrated in the last photo is how the ‘cottonmouth’ earned its common name; trespassers and would be predators can be caught off-guard and intimidated when the snake curtly flashes the white interior of its mouth. The warning was certainly well received by me – I’ll take being startled over enduring a venomous bite any day of the week!

The Florida cottonmouth Agkistrodon piscivorus conanti is one of three subspecies of water moccasin native to the United States; the other two varieties include the Eastern cottonmouth (Agkistrodon piscivorus piscivorus) and the Western cottonmouth (Agkistrodon piscivorus leucostoma). These three subspecies of semi-aquatic pit vipers are renowned for their exceptional swimming ability and their associated preference for habitats in and around the freshwater lakes, streams and swamps of the Southeast U.S. They have adapted to be masters of wetlands; well, masters of freshwater wetlands anyway…

Even though their preferred range places them in proximity to the Atlantic Ocean and the Gulf of Mexico, the conquest of marine ecosystems by the cottonmouths has been - as it has with most aquatically inclined reptiles - blockaded. The physiological demands of maintaining adequate hydration in a high-saline environment has constrained the Agkistrodon genus to a landward life. But things could change.

Could cottonmouths evolve to live in the sea, like kraits or sea snakes?

As mentioned previously, the above images show a cottonmouth from Levy County, Florida. Levy County is located in West Central Florida and boasts an impressive coastline along the Gulf of Mexico. The coastline even has barrier islands. In fact, one such barrier island, called Seahorse Key, has its very own population of cottonmouths - cottonmouths that have found a niche in the intertidal zone.

Generally considered opportunistic carnivores, the bulk of the average cottonmouth’s diet is derived through consumption of its wetland neighbors - frogs and fish - however, they have been known to occasionally snack on insects, lizards, birds, rats, or even other moccasins. The cottonmouths of Seahorse Key have taken their tastes for fish from the freshwater to the saltwater; there they eat marine fish scavenged from the intertidal zone or haphazardly dropped from the Key’s bird rookeries. In addition to marine fish, the cottonmouths of Seahorse Key will even eat SEAWEED if it has the odor of fish on its leaves.

So, the cottonmouths of Seahorse Key have a proven ability to eat, digest and process marine food resources. They posses elongate lungs to provide buoyancy and streamlined bodies capable of eel-like swimming locomotion. As with other pit vipers they have venom to aid in capture of fast moving fish. And, in regards to reproduction, cottonmouths give birth to live young, so there’s no need to go to shore to lay eggs…

It seems that the only other major factor restricting the cottonmouths’ sea-ward invasion is a limited tolerance for high-salinity…

If only there was a selective pressure for improved salt water tolerance; for instance, a selective pressure something like being stuck on an island that is subject to rising sea levels. What are the chances of that happening?

The behavioral and physiological adaptations required in order for a land animal to successfully undertake a conquest of the sea are undoubtedly both varied and numerous; but, with sufficient selection pressure, ample time, and an incremental, step-wise process it can and has happened.

For example, consider all of the behavioral and physiological changes that must have occurred in order for a few Devonian lobe-finned fish to find their way to shore as fully terrestrial tetrapods! Or, viewing the scenario in reverse, imagine the adaptations that permitted Eocene land mammals to re-enter the sea as a line of cetaceans!

Subtle cumulative changes over time can alter a lineage’s dietary preferences, reproductive rituals and even bodily mechanics.

Lillywhite, H., Sheehy, C., & Zaidan, F. (2008). Pitviper Scavenging at the Intertidal Zone: An Evolutionary Scenario for Invasion of the Sea BioScience, 58 (10) DOI: 10.1641/B581008

What Spider is this?

Anyone know which species of spider this is?

It was in west central Florida - near Crystal River, Levy County.

I'm guessing Gea heptagon, but haven't seen one quite like this one - with so many numerous huge spines...

Awesome Picture: Florida Panthers in the Picayune

I was just emailed this picture of a mama panther and her cubs:

The email (from a reliable source) advises that the photo was recently taken during a fly-over of the Picayune Strand near Naples in South Florida.

Looks like three wild Florida panthers - cool!

Also pictured are what looks like a recently cleared road and stands of noxious Melaleuca – could be better! (As a matter of fact it is getting better - click here for info).

In addition to dealing with us ecosystem-altering and land-lusting apes, Florida panthers must also cope with other parasites – including highly specialized trematodes that have evolved a fancy for fare of the feline sort...

Trematodes are flukes of nature (sorry, couldn’t resist) in that they've evolved an astonishing, almost incomprehensible level of developmental plasticity. Most have evolved the ability to subtly manipulate their growth rates and sexual maturation to track the resources available in their environment. For parasitic nematodes, their environment is manifested by the internal chemistry of their victims. Id est, the digestive enzymes, hormones and antibodies expressed through the physiology of their hosts help the trematodes gauge the probability of reproductive success and to tune their own developmental process accordingly. This fantastic capacity for flexibility is of survival benefit because should a trematode happen to find itself immersed in the body of an unsuitable host, it can induce a state of arrested development and shift its metabolism to complete dormancy while awaiting transmission to a more favorable chemical climate. As a natural corollary, if the trematode succeeds in locating its target host (aka, its 'definitive host') it can quickly push development into overdrive and achieve reproductive adulthood in short order, thereby maximizing the opportunity to its individual advantage. Being unrestrained by the ticking-clock of reproductive efficacy, trematodes can migrate from host-to-host and even between species with relative ease. As a case study, consider the misadventures undertaken by the trematode species named Alaria marcianae.


Alaria marcianae is a fascinating organism known to target, as definitive hosts, the kittens of the Florida Panther (Puma concolor couguar). The Florida Panther holds a critically endangered status and, as the common name strongly suggests, resides in the state of Florida. The tawny colored Florida Panther is one variety of a widely recognized group of felids that are also known by the names cougar, mountain lion and puma. The panther-intersecting life cycle of Alaria marcianae is complex with several possible vectors of transmission, but in choosing an arbitrary starting point for the purpose of description, we can assume that its convoluted journey begins within the intestines of an adult panther.

Having recently been deposited in the intestinal tract of an adult feline, members of Alaria marcianae start their lifecycle as eggs. The eggs, unembryonated germ cells, intermix with the partially digested remnants of raccoons, armadillos and other common delicacies found in the panther's system, and are then excreted with the animal's feces. On being submerged in the inundated wetlands for which south Florida – and the Picayune Strand - is renowned, water stimulates the eggs to internally develop embryos. Once these embryos have achieved sufficient maturation, sunlight triggers the eggs to hatch free swimming, cilia-driven, paramecium-looking critters called miracidia.

The miracidia are not adult Alaria marcianae, rather they represent a sexually immature stage of development that is specialized for seeking out a very specific (obligate) intermediate host. To ultimately succeed in stalking a panther, the miracidia of Alaria marcianae must first locate and infect a ram's horn snail of the genus Helisoma.

On locating a ram's horn, the miracidium attaches itself to the soft exposed flesh of the snail, and by excreting tissue-degrading enzymes, it parts ways with its cilia-bearing outer layer. It then penetrates into the snail's body cavity. Shedding its ciliated epithelium, the miracidium becomes an immature sporocyst. Although sporocysts still lack the ability to reproduce sexually, by embedding in the snail's nutrient rich organs they acquire the power to produce additional replicates of themselves - clones called 'daughter sporocysts.'


Further advancing on the panther, the new daughters promptly leave their mother's side and venture to the snail's gonads. Mollusk hormones produced by the gonads fuel special cells within the daughters as they morph into tailed, tadpole-looking larval forms called cercariae. The cercariae swim to, and exit from, the snail's shell-producing mantle. From there, they return once again to the open water as free-swimmers.

Leaving the snail behind, the cercariae swim to the water's surface and hunt down the true tadpoles of the leopard frog (Rana pipiens) - their second intermediate host. Hijacking the leopard frog's tadpoles for transport, the cercariae drop their own tail and burrow into the tadpole's skin. There's no need for self-propulsion when riding inside a tadpole. Once inside the developing frog, Alaria marcianae, then at a stage where they're referred to as mesocercaria, cease further development and undergo another round of asexual cloning. As numbers continue to multiply, they patiently rest, waiting for the tadpoles to carry them landward as adult leopard frogs.

In time, the mesocercaria-bearing tadpoles grow into leopard frogs and move their parasitic cargo to land. On terra firma the leopard frogs are hunted by a wide range of predators; occasionally falling prey to yet another preferred host (aka, a 'paratenic host') of Alaria marcianae, the raccoon. After catching an infested frog, the raccoon's digestive enzymes make short work of the frog's flesh - in the process releasing the mesocercaria. As with its previous host, the mesocercaria multiply in the raccoon, but continue to maintain a state of arrested development - they are not yet adults.

Did I mention that raccoons in south Florida happen to be a favorite prey item of the endangered panther?

Utilizing methods similar to those during the frog-to-raccoon transmission, Alaria marcianae find their way into adult panthers by contaminating raccoons - panther prey. During the process of raccoon digestion, mesocercaria are liberated from tissue and enter the bloodstream by penetrating the intestinal wall.

Now, if the panther they find themselves parasitizing, by chance, turns out to be a lactating female, her hormones will stir the mesocercaria into migrating to her mammary glands where they will transmit (trans-mammary) to the digestive system of her kittens'. The term used to describe the situation in which a mother acts as a paratenic host to her own offspring is called 'amphiparatenesis.'

Here, amphiparatenesis results in the imbibing of mesocercaria-laden milk by the kittens. As with the mesocercaria residing within their mother, the parasites in the kittens will penetrate the intestinal wall and enter the blood stream. They'll surf the blood stream until reaching the lungs where they become metacercaria; as metacercaria they harden the surrounding lung tissue forming protective cysts. Having profitably acquired housing in their definitive host, the cysts in the lungs will eventually be coughed-up the trachea and then promptly swallowed into the esophagus. Once back in the intestines, Alaria marcianae accelerates its developmental process, achieves sexually reproductive adulthood (as sequential hermaphrodites), and deposits the next generation of eggs in the intestine.

Thus the cycle comes full circle.




Reference:
Foster, G., Kinsella, J., Sheppard, B., & Cunningham, M. (2009). Transmammary Infection of Free-Ranging Florida Panther Neonates by Alaria marcianae (Trematoda: Diplostomatidae) Journal of Parasitology, 95 (1), 238-239 DOI: 10.1645/GE-1749.1

Douglas Adams on Lemurs, Dolphins and other Wildlife

Cool just found this at TED - funny!

It's From back in 2001.

Douglas Adams' close encounters with these rare and unusual animals reveal that evolution, ever ingenious, can be fickle too -- in a University of California talk that sparkles with his trademark satiric wit.

Breaking News: Footprints challenge theory of evolution

Footprints challenge theory of evolution

At least according to a paper in Arizona, which proclaims that “Research by UA assistant anthropology professor David Raichlen and his colleagues provide evidence suggesting that 3.6 billion years ago, hominins walked with the same upright gait that humans do today...”

Link: Arizona Daily Wildcat

Really, upright hominins 3.6 BILLION years ago??? Bipedal locomotion is one thing, but upright walking during the Archean that’s impressive - especially considering the lack of oxygen.


Incidentally, the mentioned research actually makes an argument for hominin bipedalism first occurring around 3.6 MILLION years ago. And the research is not a challenge to evolution; in fact, it fully endorses it.

The research is available at PloS; here’s the abstract:
Background
Debates over the evolution of hominin bipedalism, a defining human characteristic, revolve around whether early bipeds walked more like humans, with energetically efficient extended hind limbs, or more like apes with flexed hind limbs. The 3.6 million year old hominin footprints at Laetoli, Tanzania represent the earliest direct evidence of hominin bipedalism. Determining the kinematics of Laetoli hominins will allow us to understand whether selection acted to decrease energy costs of bipedalism by 3.6 Ma.

Methodology/Principal Findings
Using an experimental design, we show that the Laetoli hominins walked with weight transfer most similar to the economical extended limb bipedalism of humans. Humans walked through a sand trackway using both extended limb bipedalism, and more flexed limb bipedalism. Footprint morphology from extended limb trials matches weight distribution patterns found in the Laetoli footprints.

Conclusions
These results provide us with the earliest direct evidence of kinematically human-like bipedalism currently known, and show that extended limb bipedalism evolved long before the appearance of the genus Homo. Since extended-limb bipedalism is more energetically economical than ape-like bipedalism, energy expenditure was likely an important selection pressure on hominin bipeds by 3.6 Ma.



Raichlen, D., Gordon, A., Harcourt-Smith, W., Foster, A., & Haas, W. (2010). Laetoli Footprints Preserve Earliest Direct Evidence of Human-Like Bipedal Biomechanics PLoS ONE, 5 (3) DOI: 10.1371/journal.pone.0009769

The Views of Biology Teachers towards Teaching Evolution

In discussing Marco Rubio’s anti-science perspectives during the previous post, I mentioned Florida’s miserable (though improving) track record in regards to the teaching of evolution. As it turns out, the National Association of Biology Teachers has recently published the results of a survey which focused on the attitudes held by Florida’s biology teachers towards the teaching of evolution.

The survey’s data was derived from the responses of 353 Florida biology teachers; 28% of which taught biology in kindergarten through the fifth grade, 24% instructed biology in grades six through eight and 48% taught biology at the high school level (grades 9–12).


A Few of the Findings:
20% of Florida’s biology teachers are NOT COMFORTABLE with even INCLUDING evolution as a required science standard


17% of the teachers felt that biology COULD be taught and understood WITHOUT teaching evolution


17% DISAGREED that the earth is at least 4 billion years old (34% of those that disagreed believed that the earth is only between 4,000 and 40,000 years old)


34% felt that believing in God MEANS rejecting evolution


72% of the respondents reported that they HAD NEVER BEEN criticized by other teachers or school administrators in regards to HOW they taught evolution


44% of the teachers indicated that their teaching of evolution HAS BEEN criticized by students or parents


If the above numbers seem frightening consider this: The study’s respondents were solicited from the Building a Presence in Science (BaP) program of the National Science Teachers Association. Therefore, the numbers could be biased towards the "pro" science education end of the spectrum!!!


FOWLER and MEISELS (2010). Florida Teachers’ Attitudes about
Teaching Evolution The American Biology Teacher, 72 (2), 96-99 : 10.1525/abt.2010.72.2.8

Tadpole Tails and Predator Induced Plasticity

Last Wednesday, while doing field work near Goethe State Forest, I happened onto the paths of a couple pinewoods tree frogs (Hyla femoralis). One frog was observed practicing evasive acrobatic skills between the leaves of a saw-palmetto dominated groundcover; the second frog, taking a more leisurely approach to the day, was found lazily stretched out on mid-swamp tree branch. Because of a recent environmentally-induced neglect of this blog on my part, I thought that the two frogs would serve as a good model for a post on how tadpoles can alter their developmental physiology in response to local ecological conditions.

Like many other frogs, the pinewoods tree frog undergoes a complex life cycle which carries them from the ephemeral waters of ponds, swamps and puddles to an adulthood existence in the trees. In response to the variability of selective pressures expressed by their environments, natural selection has shaped Hyla femoralis in such away as to be flexible. One example of this flexibility is the way in which their tadpoles can alter phenotype – their morphology - in response to the presence of predators. As opposed to their developmental processes rigidly rendering tadpoles displaying uniform and unchanging morphologies, the DNA of flatwoods tree frogs has been programmed to make size, growth rate and coloration malleable characteristics. The ability of an organism to change its physical characteristics to better fit local conditions is called ‘developmental plasticity.’

In addition to normal variations encountered at the regional level, or within individual populations, the colors and shapes exhibited by tadpole tails can differ from one location to another; this is because tail characteristics can be changed in response to cues in the environment. In waters lacking abundant predators, Hyla femoralis tadpole tails are generally colorless, or are of a dull brownish-red color. In contrast to relatively safer waters, the tadpoles hosted by puddles with abundant predators (predators like dragon fly larvae, for example) are often found bearing tails with distinct red-spot markings and an enhanced, taller shape and muscular robustness. Increased tail muscle provides greater propulsion, allowing the tadpoles to employ accelerated speeds as part of their predator evasion tactics. Though, it’s still an area for inquiry, changes in the pattern and coloration of tails may provide a crypsis function by either providing improved camouflage, or by directing predatory attacks tail-ward, away from the tadpoles’ main body mass – improved survival through either concealing or revealing.

The chemical signals that switch tail enhancement into overdrive include those compounds released by other tadpoles as warning pheromones during predatory attack and those molecules discharged by the predator while digesting prey-tadpole tissues. So, in other words, a predator’s attack and digestion of a conspecific tad liberates chemicals into the water that are received by other tadpoles during development; as a result, resources are directed away from ‘normal’ growth processes and are directed to tail augmentation.

Cool stuff!

A couple quick notes:

Pinewoods tree frogs display distinct orange or yellow spots on their inner side of their thighs, while in the field these spots help distinguish Hyla femoralis from other species with similar body color patterns. Though not pictured here, the leg spots were observed during the frogs’ recent attempts at evading a certain species of primate paparazzi. Their tadpole stage lasts for about two months, and the breeding season begins in March and runs through the summer months.

Although cypress swamps and pine flatwoods are distinct natural community types, they are both occupied by the pinewoods tree frog. The first snapshot above shows one Hyla femoralis precariously perched on the stem of a saw palmetto plant just a few inches off the ground in a well-drained upland flatwoods area. The second shows another individual leisurely laying on a tree branch about five feet above the surface waters of a swamp. In Florida, these communities are often directly adjacent to each other:

LaFiandra, E., & Babbitt, K. (2004). Predator induced phenotypic plasticity in the pinewoods tree frog, Hyla femoralis : necessary cues and the cost of development Oecologia, 138 (3), 350-359 DOI: 10.1007/s00442-003-1412-3

Evolving from Promiscuity to Monogamy

New research has revealed how the process of evolution can result in sexually promiscuous animals undergoing adaptation for monogamy.


Reproduction is an expensive endeavor. Tremendous time and resources are invested in seeking-out healthy partners, in consummating relationships, and in rearing the resultant offspring. Luckily, evolution has resulted in life being programmed to strive for resource efficiency; to work towards maximum reproductive benefit at minimum personal expense. In regards to pair-bonding between the sexes, this biological imperative for reproductive economy has made promiscuity the rule and monogamy the exception. However, despite the fact that promiscuous mating systems are the prevailing strategy in nature, environmental factors can push typically promiscuous species towards monogamy.

As a case in point, a report published in the April issue of The American Naturalist details how the ‘mimic poison dart frog’ (Ranitomeya imitator) parted ways with promiscuity to adapt a lifestyle as the first scientifically recognized genetically monogamous amphibian.

Like other frog species, poison dart frogs incur a certain amount of risk by laying their eggs in water. Although water is a biological prerequisite for frog survival, ponds, lakes and puddles also house predatory fish and other animals that prey on vulnerable eggs and tadpoles. During its evolutionary past, the menace of predation pushed the mimic poison dart frogs away from larger, riskier ponds to the considerably smaller, but safer, pools held by leaves of large bromeliad plants. Unfortunately, although the tree-top bromeliads decreased the rate of frog young predation, the movement from the big ponds raised a separate issue – nutrient limitation.

The big ponds definitely had more predators; but, they also had substantially more food. In fact, the ponds had so much food that a single frog-parent (in this case the male) was able to handle the tadpoles all by himself – a single parent family arrangement was all that was necessary to raise the next generation. In contrast, the waters held by the bromeliads averaged only about 24 milliliters in volume, far too little to hold ample provisions for a startup tadpole. In order to maintain their newly acquired safe housing, the mimic dart frogs had to adapt a new tactic.

Male mimic dart frogs had previously evolved the capacity to both transport and guard young tadpoles, but having moved to the suburbs, the females needed to help-out with feeding; rearing had become too difficult a task for the males to handle on their own. If they were to ensure the survival of their young, the days of leaving dad to care for the kids were over – monogamy was the best option. Unlike males, female mimic darts have the ability to produce eggs. To do their part, mom frogs adopted a strategy called trophic egg feeding, a practice in which they lay unfertilized eggs in the bromeliad pools for the tadpoles to eat.

An absolutely amazing video of this monogamous behavior was recorded by the BBC during the dissertation work of Jason Brown. Jason was the lead author of the cited paper, and the mimic dart footage was included in the David Attenborough narrated documentary “Life in Cold Blood.”

This is awesome footage:





Brown, J., Morales, V., & Summers, K. (2010). A Key Ecological Trait Drove the Evolution of Biparental Care and Monogamy in an Amphibian The American Naturalist, 175 (4), 436-446 DOI: 10.1086/650727

Ecographica is a Finalist: Conservation or Geosciences

I just received an email from Research Blogging requesting my votes for 2010’s best blog awards…

Working through the nominees, I was surprised to discover that Ecographica was selected as a finalist in the Conservation and Geosciences category – I had no idea!

My thanks to the readers and judges for supporting this blog!!!!


Since January of 2009, Ecographica has contributed 109 research related posts to Research Blogging. Vertebrate Proxies of Climate Change has been the most popular of the research postings; it reviews/summarizes some of the ways in which vertebrates can be used to study shifting climates.


Thanks again!

How Enticing Viruses Manipulate Animals

Viruses are ubiquitous to life; they infect everything from the smallest of bacterial cells to the largest of whales. And though these these miniscule pathogens often bring illness, they do not contaminate our bodies out of malice or spite, rather they do so out of necessity. Lacking the prerequisite internal anatomy for self-reproduction, viruses invade the cells of the living as a means of insuring their posterity. They splice their DNA (or RNA) into the nucleus of the host’s cells and effectively subvert its cellular mechanics to meet viral reproductive ends. Hijacked cells are re-programmed by the viruses and become factories dedicated to the task of manufacturing more viruses; viruses which ultimately move on to other victims. In addition to hacking programming codes for the building of replicates, viruses often include sub-routines, or additional programming hacks, that facilitate their journey to new hosts.

By undermining the normal life-processes of the host’s cells, viruses are detriments to health; however, more than just illness can remain in the wake of a virus’s biological sabotage. Sometimes included with the observable symptoms of an ailment are other characteristics of viral infection that serve to promote the spread of disease. The genes that viruses splice into a host cell’s mainframe can code for phenotypes that manipulate unwitting vectors into exposing themselves – purely for the benefit of the virus.

For example, recent work out of Penn State University has shown that a virus common to the squash group of plants does more than just hack a virus-building program into the cells of its vegetative victims - it also includes a program that attracts insects. The cucumber mosaic virus (CMV) infects plants with a gene that causes the plant to synthesize and release chemicals that draw-in hungry aphids. Normally, aphids use their capacity to chemically sense plants as a way to zero-in on healthy and nutritious foodstuffs essential to their survival. By manipulating the aphids’ chemo-sense, the virus’s genes trick the insects into locating and then taking a bite from the diseased leaves of an infected plant. Even though the plant may emit a ‘delicious smell,’ because it has been subjected to disease, it lacks the nutrients needed by the aphids. Luckily for the aphids, after just one bite their tasting-sense overrides their smelling-sense and they’ll bugger-off in search of better food. Unfortunately for other squash plants, the aphids now have a mouthful of CMV virus! Thus, the virus spreads.

The genes of the cucumber mosaic virus can integrate into the DNA of a plant, causing it to produce a chemical compound that manipulates aphids into volunteering their time and services as vectors of disease. This scenario isn’t unique to viruses, plants and insects. Other studies have shown that a similar pathogen to chemo-attractant dynamic exists between sandflies and hamsters; the parasitic protozoa Leishmania causes infected hamsters to produce chemicals that attract sandflies as vectors. And in humans, there is some evidence that Plasmodium falciparum causes more than just malaria, it also hijacks human bodies to produce chemicals that attract more mosquitoes.


Mauck, K., De Moraes, C., & Mescher, M. (2010). Deceptive chemical signals induced by a plant virus attract insect vectors to inferior hosts Proceedings of the National Academy of Sciences DOI: 10.1073/pnas.0907191107

Communicating Science: Blogs and the Media

As newspapers and cable news cut science coverage, where can the science-curious get reliable science and technology news? Ira Flatow and guests discuss how the Internet — including blogs and social media — is filling the coverage gap.

Great conversation - Listen to the Audio!

Go to the NPR webpage and click on Communicating Science in the Recent Episodes column: Here

From NPR's Science Friday

How to Study Invasive Species, a Conservation and Ecological Imperative

The January edition of The American Midland Naturalist includes an essay by Daniel Simberloff (University of Tennessee) that bears the questioning title “Invasions of Plant Communities – More of the Same, Something Very Different, or Both?” As alluded to by the interrogative title, the central theme of the piece is whether or not the ecological characteristics displayed by invasive plant species are similar to those demonstrated by native plants during the natural succession of a vegetative community. In other words, do the strategies and tactics employed by invasives during the conquest of new habitats follow similar patterns of recruitment and regeneration as those exhibited by native plants in moving a community towards maturation? Or, in contrast to natural succession patterns, do invasive species have unique biological or demographic qualities that require a novel or specialized approach to studying their dynamics?

Daniel poses great questions, because, recognizing that we live in a world of mass travel and shifting climates, the study of invasive dynamics is of critical importance to the conservation of biodiversity – protecting natural habitats and native species. In addition to conservation, by researching the interplay of native and non-native species during the establishment of ecosystems we will undoubtedly gain a wealth of knowledge in regards to the feedbacks between evolution and ecology (i.e. how do those species lacking a shared co-evolutionary history come to achieve a stable strategy for survival?).

So, with that in mind, here’s my answer to Daniel’s question: Both!


Cause’ in a nutshell: Although invasive species will exhibit some life-history strategies comparable to those of plants from the newly invaded habitat (growth pattern, time to reproductive maturity, etc…) they will also be subject to environmental factors of a temporal nature that do not influence the natives (at least to the same extent).

Said differently, because the growth, reproductive habits and resource needs of an invasive likely mirror those of at least one native plant, the invasive could theoretically replace the native with little ill effect to the ecosystem; the invasive could fill the niche left void by the out-competed native plant without disrupting the energetics of the plant community as a whole. BUT, at the same time, a newly arrived invasive species may have a distinct advantage over a native transient because it is completely foreign to the ecosystem. For example, being unrecognized by its new environment the invasive may, for a period of time, be buffered against attack by herbivores, parasites and other stressors that may be actively reducing the fitness of the locals.

Similar to the above potential advantages, the invasive could also be subject to the detrimental affects of being an outsider - brought about by a lack of co-evolved pollinators, ect…

I would also argue that the above temporal effects associated with being a novel addition to an ecosystem, though only short-lived, can be magnified greatly by stochastic events. I would suggest this because – generally – variability in initial survival rates contributes greatly to ultimate establishment; often more so than reproductive strategy, which is subject to greater phylogenetic constraint (i.e. initial survival is more important than in choosing to produce many low-quality seeds when young, or to conserve energy and produce fewer higher-quality seeds when older).


Daniel’s essay is a great read and offers plenty of real-world case studies to emphasize his points; definitely check it out!


Simberloff, D. (2010). Invasions of Plant Communities – More of the Same, Something Very Different, or Both? The American Midland Naturalist, 163 (1), 220-233 DOI: 10.1674/0003-0031-163.1.220