I think you are alluding to lichens in your statement about 
Hi Aabir,

I think you are alluding to lichens in your statement about 
fungal/cyanobacterial neurotoxins, right? If so, I think you are referring to 
microcystins many species of Peltigera but they aren't "sit and wait" 
predators. Rather, the microcystins are hypothesized to function as an 
antiherbivory mechanism. 

I think lichens are a good example of what you are asking about, where 
association of two taxa creates new, unexpected functional traits that likely 
expans the fundamental niche of both taxa, although we usually only infer the 
niche expansion. Lichen growth forms are good example. They have a huge variety 
of surface area to mass ratios determined by their gross morphological form, 
which is strongly related to moisture regulation, as they are poikilohydric. At 
the same time, the photobionts ability to restart photosynthesis upon rewetting 
is controlled by the physiology of the photobiont. So, even if the lichen 
growth form allows quick rewetting, if the photobiont is cyanobacterial, the 
lichen will have a slower photosynthetic recovery in comparison to the same 
lichen with a green algal photobiont. This can be seen in what are called 
"photomorphs", where the same fungus switches between an green alga and 
cyanobacterial partner. The morphology is
 completely different, one looking like a dark, filamentous fruticose form 
(cyanobacterial) and the other a large, flat, leafy foliose form (green algal 
form). Many of the classical evolutionary patterns (eg. convergence) occur 
within these interplaying contraints to make similar functional traits (eg. 
Muggia, L., P. Nelson, T. Wheeler, L. S Yakovchenko, T. Tønsberg, and T. 
Spribille. “Convergent Evolution of a Symbiotic Duet: The Case of the Lichen 
Genus Polychidium (Peltigerales, Ascomycota).” American Journal of Botany98, 
no. 10 (2011): 1647–1656.).

-Peter
  


________________________________
 From: Aabir Banerji <[email protected]>
To: [email protected] 
Sent: Friday, September 6, 2013 8:55 AM
Subject: Re: [ECOLOG-L] "Emergent" functions contributing to the functional 
diversity of a community?
 

Hi, Jen.

Part of what inspired me to ask this question was a conversation I've had with 
some local microbiologists.  They, like the folks in Tamar's group, have 
apparently been doing comparative studies on microbial communities from 
different regions.  They had told me that a few of the communities lacked 
mercury-resistant species, based on there being no sign of the genes that are 
known to produce mercuric reductase in any of the samples.  This sounded to me 
like affirming the consequent, so I asked them if biofilms or consortia 
couldn't yield something equivalent to mercuric reductase.  The answer was no.

As you say, there's lots of literature on facilitation/symbiosis enabling 
species to survive and do stuff in places where they'd never be able to make it 
alone.  This is interesting and surprising enough, all by itself, and 
definitely contributes to communities being more than the sum of their parts.  
But my point is that, even if you only look at each partner separately, you 
would probably still have a guess as to what they can make happen in the 
community once they're there (e.g., photosynthesis, N-fixation).  You would not 
expect a cyanobacterium and a fungus to combine their respective enzymes into a 
neurotoxin and act like a sit-and-wait predator... yet perhaps less dramatic 
versions of this kind of thing happen often (and predictably) in complex 
communities.

~ Aabir


----- Original Message -----
From: Jenn Adams Krumins 
To: Aabir Banerji 
Sent: Fri, 06 Sep 2013 13:31:30 -0000 (UTC)
Subject: Re: [ECOLOG-L] "Emergent" functions contributing to the functional 
diversity of a community?







Hey Aabir,





I think you are looking for something very sophisticated when something very 
simple will do.  I the plant soil world - this kind of facilitation is 
everywhere.  Legumes...  mychorrhizae etc.  Look into that literature.  The 
presence of myccorrhizae does not only benefit the host plant.  there are  
networks - then it gets more interesting because one plant is paying with the 
others are reaping the rewards....







hope all is well for you over there - 


Jen







On Fri, Sep 6, 2013 at 5:57 AM, Aabir Banerji <[email protected]> 
wrote:





Hi, Martin.





Thank you... but this isn't quite what I'm looking for.  This is an (awesome) 
example of what I meant when I referred to a species gaining access to a new 
niche via the product/ability of another species (the parasite gaining the 
ability to lure in and feed on its definitive host by using its intermediate 
host as bait).  Even if the parasite happens to induce a novel morphology in 
its intermediate host, it won't generate a new process in the system or give us 
reason to reclassify the parasite into a new functional group.







Here's a potential example that I was sent yesterday: 
http://en.m.wikipedia.org/wiki/Anaerobic_oxidation_of_methane.  If the relevant 
microbes have to make a combination product to do the job, and neither can do 
so by itself, it means that AOM is an emergent function.







Another potential example (what I had in my head when I referred to 
neighborhood habitat amelioration) would be if dry-climate plants become 
drought-resistant by developing a water-retentive rooting pattern in 
mixed-species aggregates that they could not develop in monoculture.  In this 
case, drought-resistance is an emergent function.







I hope this is clearer.





Best regards,


Aabir





----- Original Message -----


From: Martin Meiss


To: Aabir Banerji


Cc: Ecological Society of America: grants, jobs, news


Sent: Thu, 05 Sep 2013 21:25:04 -0000 (UTC)


Subject: Re: [ECOLOG-L] "Emergent" functions contributing to the functional 
diversity of a community?











Would you consider this to be an example of what you're looking for: How about 
a parasite that needs an intermediate host before infecting its main host.  
Perhaps a worm that must live in a snail which must be eaten by a vertebrate 
before the parasite can enter the vertebrate to reach its adult form.













Martin M. Meiss














2013/9/5 Aabir Banerji <[email protected]>











Dear fellow ECOLOG users,

















The relationship between functional diversity and taxonomic diversity in 
ecological communities isn't always linear.  I imagine the simplest case of 
non-linearity is where there is a lot of functional redundancy among 
phylogenetically diverse taxa.  The opposite extreme (a depauperate community 
having a lot of functional diversity) is also possible... e.g., where 
generalist populations exhibit complex demographic structures or inducible 
polymorphisms.

























What I'd like to know, though, is if there is evidence of taxa fulfilling 
functions by associating with one another.  It's one thing for a species to 
enter a new niche by relying on the product or ability of a different species 
(such as a beneficial symbiont).  It's another for different species to combine 
complementary products or abilities to create/achieve something that no one 
species in the community is able to produce or achieve by itself (an "emergent" 
function).  This latter phenomenon would be something akin to neighborhood 
habitat amelioration... or, perhaps, something more general that includes 
neighborhood habitat amelioration.

























Would any of you happen to know of recent reviews or articles that address this 
topic?  Or some really good examples of it, perhaps?

















Thanks in advance!

















~ Aabir


























Dr. Aabir Banerji








Postdoctoral Associate








Institute of Evolutionary Biology and Environmental Studies








University of Zurich








[email protected]

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