Catasetinae seedling behaviour question and few more things to discuss
In my garden I saw much but much more than once, a strange behaviour on Catasetinae (both Cycnoches and Catasetum), and since both genera represent the two phylogenetic branches of subtribe Catasetinae (one with Cycnoches-mormodes and basal Dresseleria, and the other with Catasetum-Clowesia), I have the felling all genera inside this subtribe shares the same odd thing...
The strange behaviour I am talking about is that sometimes the new born seedlings on my palms and rotten wood at my house don't develop their first pseudobulb were the seed rest, but on the contrary, the seed first develop a very thin but long rhizome that sometimes grows for more than a meter long before "stops" and develop the first pseudobulb. People that are following me knows that this early rhizome could be more white chlorophyll-less or green (with chlorophyll an even small speudo-leaves) depending if is growing inside the media or at open space.
This odd behaviour obviously is a response to seek and "find" a better place to grow, for example, once I followed for months the trail of one of those "early rhizomes" developing inside a dry palm petiole base, and the seedling rhizome at various points had "carved" the dry petiole to find a way to light and open air, and them "decided" that the point wasn't "correct" and buried again into the inner-petiole surface just to appear more downstairs until at some point, the rhizome "decided" to develop the pseudobulb at last. That behaviour is even possible to see on in vitro culture, as I saw on Brunos place.
my question is the following
this behaviour have a name?????
can someone can talk a little bit more about it????
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Another question I have (not related to seedlings) are the secondary "roots" that looks like "clustered upward filaments" (Holst call it pneumatophores) on adult plants. The thing is that in nature it is obvious that the early morning dry-season dew/myst concentrate on those filaments and them by gravitation it goes to the roots... Tthem.... why Holst says those filaments are pneumatophores?????...
Pneomatophores (like the word pneuma implies) are roots with "air supply" function like we find on mangrove and other swamp and damped areas plants... True pneumatophore roots are alive, and in Catasetinae this filaments are quite dead. Even if they weren't dead at all (which is not the case), those "roots" lack velamen, something quite necessary for photosynthesis on orchids roots (Vandas on the contrary have pneumatophores in the true sense on the word)
Since Holst is a smart guy much more informed on Catasetinae than me, I have the feeling that I misunderstood him because of his decision to use the word "pneumatophore" instead of another "technical" word for those modified radicular system... and for them my question in this matter is the following...could it be that Holst is not talking about air-aid absorption but about some sort of odd system that increase the velocity of air passing trough the filaments????... I mean, could it be that Holst have the idea that in this way Catasetums encourage somehow air circulation and for them avoid damp conditions fatal to the roots???
Since I am not in to aerodynamics, I really cant tell if the later could be the case... and about my observation about the dew collector system, it is based on observation only.
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The last question is why in the name of Jesus Christ Cyrtopodium and Galeandra are clustered outside the Catasetinae subtribe and clustered with less similar genera like Cymbidium and a large etc...
I am not botanist, nether I know Cymbidieae taxonomic clues for systematic and nether known almost anything about resent phylogenetic studies on the subject, but I like to learn and for them I ask.... someone can explain to me please why in this case a "Lion" shares more affinity with "Lynx" than "panthers"?... It have to be a reason that explain this """parallel evolution"""
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Jan
Last edited by Jan Pahl; 10-22-2009 at 05:11 PM..
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