A couple of posts ago, I explored the chemistry behind ocean acidification but did not touch on any of the implications on marine life. Hence, I will be covering this today, focusing mainly on calcification rates and acidosis. If you missed my explanation of ocean acidification, you can find it here.
Firstly, marine
calcifiers such as reef-forming corals, protozoans, molluscs, crustaceans, echinoderms and some algae are greatly affected by
the decrease in carbonate ions (CO32-) associated with
CO2 dissolution (Bijma et al., 2013). They use CO32-
to build and maintain their calcium carbonate shells and
skeletons, but this becomes increasingly difficult with falling CO32- concentrations. Consequently, many calcifiers have shown reduced rates of calcification in response to the increasing
partial pressure of CO2 (Fabry et al., 2008).
For tropical reef-building corals, it is predicted
that calcification rates will have reduced by 20-60% once CO2
concentrations reach double that of preindustrial levels. A change of this magnitude could
slow growth rates, making reefs much more vulnerable to erosion. Furthermore, with
the associated reductions in CO32- ions, it is likely
that much weaker skeletons will form and thus, allow erosional processes to
occur at quicker rates than previously (Guinotte and Fabry, 2008). A
report issued on Friday, following last year’s Third Symposium on the Ocean in a
High-CO2 World, delivers some extremely worrying facts. They state
with high confidence that ‘If CO2 emissions continue on the current
trajectory, coral reef erosion is likely to outpace reef building sometime this
century’. Take ocean warming into account and the prospect is even more dire – erosion could potentially outpace growth by mid-century, once CO2
levels reach 560 ppm. If this happens, there would be consequences for coral biodiversity, with many species losing their habitat (IGBP et al., 2013).
However, it is not all doom and gloom for tropical corals.
Fine and Tchernov found that two species of scleractinian corals
were able to survive under acidic conditions (pH values of 7.3-7.6) (2007). Initially,
their skeletons dissolved leaving the coral polyps exposed, but when pH
returned back to normal, the polyps were able to recalcify with no lasting effects. This offers a glimmer of hope for corals’ future in a high CO2
world. Still, we have to remain cautious as the study did not consider the
effects of predation on the naked polyps and there has been discrepancy about
its representativeness (Guinotte and Fabry, 2008).
As for cold-water corals, 70% will
experience unsaturated waters by 2100 (high confidence), with this beginning as
early as 2020 for some (IGBP et al., 2013).
As highly productive ecosystems with a rich biodiversity, this would impact the many deep-water organisms that rely on them as feeding grounds,
habitat and nursery areas (Guinotte and Fabry, 2008).
Many plankton and zooplankton species are also affected by
changes to the carbonate chemistry of the ocean (see Figure 1).
This is potentially detrimental considering they form integral components of
the marine food chain. Amongst those most sensitive to ocean acidification are
pteropods – the major planktonic producers of aragonite. In waters that are
unsaturated with respect to aragonite, it has been observed that pteropods are unable to maintain their shells and consequently, have begun dissolving (Orr et al., 2005). This is occurring in the
Southern Ocean today, impacting predators such as pink salmon (IGBP et al., 2013). The future for pteropods that are endemic
to polar regions depends on their ability to transition to lower latitudes,
where warmer, carbonate-rich waters await (Orr et al., 2005).
Figure 1. Photos showing scanning electron microscopy photographs of the coccolithophorid Gephyrocapsa oceanica under different carbon dioxide concentrations; normal in the top image (300 ppm) and elevated in the bottom (780-850 ppm). The distinct structural malformations can be clearly seen under higher carbon dioxide concentrations (Riebesell et al., 2000). |
However, once again, it is not all bad. Whilst the majority of marine calcifiers do see decreasing
calcification rates under acidic waters, some organisms actually benefit; these include some fleshy algae, seagrasses and phytoplankton groups (although
further research is still required to fully understand the underlying mechanisms) (IGBP et al., 2013). It appears that under higher CO2
concentrations, these experience increased photosynthesis and,
therefore, growth (Gattuso and Hansson, 2011).
Lastly, for many marine animals, including
invertebrates and some fish, the acidification of ocean waters can result in
acidosis. This is where high environmental CO2 levels cause an
increase in carbonic acid in the bloodstream. Consequently, the blood's pH is lowered, affecting many cellular processes. Acidosis can lead to
metabolic and behavioural depression, lowered resistance and asphyxiation (Howard et al., 2012). Compared to less
mobile organisms, fish appear to be more resistant to ocean acidification as
they do not have extensive calcium carbonate shells (IGBP et al., 2013). However, particularly in larval fish, acidic
seawater has led to impaired sensory performance, altered behaviour and
decreased growth rates, all of which impact predator-prey relationships (Howard et al., 2012). Overall though, this area remains insufficiently explored
and further research is required to fully understand the physiological
mechanisms behind individual animal responses to elevated CO2
levels.
To round things up, whilst a few organisms can tolerate or actually
benefit from acidic waters, many respond negatively to
ocean acidification. Survival, growth, abundance and
larval development for many organisms is reduced, alongside their ability to form
and maintain shells and skeletons. These impacts have repercussions on marine
food webs and biodiversity, which, in turn, ultimately affects society. It
has been suggested that over generations, acclimatization and evolutionary
adaption may occur that mitigates or even compensates for ocean acidification. To support this, there
are a few examples of limited adaption from the paleo-record,
but knowledge in this area remains patchy, not helped by the fact that every
species differs in its potential to adapt (Wittmann and Pörtner, 2013). What is
most problematic, however, is that the rate of ocean acidification today is
unprecedented; 30-100 times faster than at any point in the recent geological
past (Bijma et al., 2013). It is, therefore, hard
to imagine how marine life could possibly ever adapt quick enough to these
rapid changes in ocean chemistry.
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