Symbiodinium dinoflagellates
establish symbiont relationships with a variety of hosts, including, Cnidarian
coral. Symbiodinium can be free
living in the water column or can be attained through symbiont acquisition. 85%
of Cnidarian species host Symbiodinium through
indirect transmission (Fournier, 2013) and Symbiodinium
clades establish non-random relationships with a host species. This paper
highlights there is little knowledge on how corals first acquire their
symbionts, they look into the growing field of the ecology of free-living Symbiodinium types and those symbioses
with juvenile corals to the benthos.
In order to fully appreciate this paper it is important to
note the two modes of transmission for the uptake of Symbiodinium which can occur in cnidarian species; horizontal and vertical.
This paper focuses mainly on horizontal transmission (indirect, from the water
column), however vertical (Direct, from parent) is spoken about for comparison.
Evidence for vertical transmission of Symbiodinium
cells may not be a ‘closed’ circuit and corals using vertical transmission
may uptake exogenous Symbiodinium cells
may successfully colonise on adult hosts.
Nitschke et al used three species
of newly settled aposymbiotic (symbiont-free) corals (Acropora millepora, Acropora selago and Isopora palifera) in an open aquarium system containing; (i)
sterilised sediment and adult coral fragments combined; (ii) adult coral
fragments alone; (iii) sterilised sediments alone or (iv) seawater at Heron
Island, GBR. The colonies were placed within aquariums and monitored at Heron
Island Research Station. The settlement for juvenile corals of the Acropora species were tested with filtered seawater to remove particulates and
sediment before distribution in the aquaria. Symbiont acquisition was
investigated through visual counting, with the aid of a light microscope, at
six time points within a 12 day period. Days counted were determined based on
which coral spp. was used, between Acropora
spp and Isopora palifera.
Scleractinian corals expel photosynthetically active
symbionts at a constant rate and in large quantities. Results found similar
patterns of symbiont transmission across the two broadcasting coral species: A. millepora and A. selago. Symbiodinium was
expelled originally in the coral alone treatment after 7days, after this symbiont
acquision continued at a rapid rate.
Results showed that in seawater alone juvenille corals
acquired Symbiodinium cells by the
end of the experiment; A. millepora (19%), A. selago (14%) and I. palifera (18%).
This suggests that seawater alone could be a potential source of Symbiodinium, however as the % values
show there is low abundance of recruitment. Graham et al (2008) demonstrated
that aposymbiotic coral larvae can survive in the water column for 200 days in
vitro, showing that recruits may survive for extended periods without Symbiodinium cells. Other research
concluded that Symbiodinium can
colonise in sediment, this could show that sediment may provide another habitat
for the symbionts to grow and survive until taken up by a juvenile host,
although, it is important to understand if these colonies are clade specific.
It is understood that some scleractinian, reef-building
corals inhibit nutrient poor waters, highlighting the importance of
understanding horizontal transmission of Symbiodinium
cells between adult and juvenile corals, as this symbiosis is necessary for
nutrient recycling in oligotrophic waters. The knowledge in this area could be
improved by further understanding into the density of Symbiodinium in the water column and to investigate their free
living nature until chemotaxis occurs.
Paper reviewed:
Nitschke, M.R., Davy, S.K. and
Ward, S., 2016. Horizontal transmission of Symbiodinium cells between adult and
juvenile corals is aided by benthic sediment. Coral
Reefs, 35(1), pp.335-344.
References:
Fournier, A. (2013) The story of
symbiosis with zooxanthellae, or how they enable their host to thrive
in a nutrient poor environment. BioSciences Master Reviews, 1-8.
Graham EM, Baird AH, Connolly SR (2008). Survival synamics of scleractinian coral larvae and implications for dispersal. Coral Reefs 27:529-539
Graham EM, Baird AH, Connolly SR (2008). Survival synamics of scleractinian coral larvae and implications for dispersal. Coral Reefs 27:529-539
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