I’d like to go back to the discovery of a complex calcium signaling toolkit in the single-celled organism, Monosiga brevicollis. The researcher who discovered this toolkit in this protozoan, Xinjiang Ca, wisely raised the following question:
We conclude that an extensive Ca2+ signaling ‘toolkit’ exists in the unicellular choanoflagellates, preceding the origins of animals (Metazoa). The current hypothesis of Ca2+ signaling acquires new dimensions in light of this novel discovery. Why does such an apparently simple unicellular organism need a complex Ca2+ signaling machinery?
Yes, why does such an apparently simple unicellular organism need such complex Ca2+ signaling machinery? And it’s not just the calcium toolkit, as the same unicellular organism has a toolkit of tyrosine kinases that is “more elaborate and diverse than found in any multicellular organism.”
Because I think there may something very significant here, let me refer to this state as Needless Complexity (NC). This is not to say that this is functionless complexity, as I am willing to bet all this complexity plays a role in the lifecyle of Monosiga brevicollis. I suspect that out in the wild, these creatures live rather complex lives, and both the calcium and tyrosine kinase systems are involved in control and adaptation that are involved with the every day life of these creatures (for example, I would expect different systems may come into play in response to different environmental conditions and time of day).
This complexity is needless in the sense that it is not required for unicellular, eukaryotic life. That is, other species of protozoa are able to survive just fine without the elaborate calcium and kinase systems. Such complexity is therefore not needed for unicellular life, but will become needed for complex, metazoan life. NC is thus a feature that is recognized from a relativistic perspective.
I plan to expand in much more depth about Needless Complexity and its role as part of a mechanism for front-loading evolution.