Abstract
Ocean acidification doesn’t just erode calcium carbonate shells. It can also slow the rate of diatoms to build their beautiful, intricate silica cell walls. Thinner walls mean lighter diatoms making the algae less able to transport carbon to the deep ocean. Diatoms are a key group of non-calcifying marine phytoplankton, responsible for ~40% of ocean productivity. Growth, cell size, and silica content are strong determinants of diatom resilience and sinking velocity; therefore, the effect of diatom species on ocean biogeochemistry is a function of its growth strategy, size, and frustule thickness. In natural environments, pH directly affects the diatom’s growth rate and therefore the timing and abundance of species. Consequently, understanding impacts of ocean acidification on diatom community structure is crucial for evaluating the sensitivity of biogeochemical cycles and ecosystem services in the world’s oceans.
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5.1 Introduction
Ocean acidification is a global threat to the world’s oceans, estuaries, and rivers. It is projected to grow as carbon dioxide (CO2) and continues to be emitted into the atmosphere at record-high levels. The oceans take up CO2 from the atmosphere and are responsible for absorbing around a third of the CO2 emitted by fossil fuel burning, deforestation, and cement production since the industrial revolution (Sabine et al. 2004). While this is beneficial in terms of limiting the rise in atmospheric CO2 concentrations and hence greenhouse warming due to this CO2, there are direct consequences for ocean chemistry. Ocean acidification describes the lowering of seawater pH and carbonate saturation that result from increasing atmospheric CO2 concentrations. There are also indirect and potentially adverse biological and ecological consequences of the chemical changes taking place in the ocean now and as projected into the future (Ridgwell and Schmidt 2010).
Climate affects diatoms in complex ways. As the planet warms due to the increase in carbon dioxide, scientists predict that diatoms will decrease compared to other planktons such as coccolithophores and cyanobacteria (Tatters et al. 2013). In lakes and rivers, a changing climate alters river flow in many parts of the world. The frequency and severity of droughts and floods is changing, which influences diatom species and where they grow. Furthermore, climate controls circulation patterns and thermal stratification of lakes and oceans, which alter diatom species composition (Bach and Taucher 2019). Diatoms affect climate on a global scale. As diatoms photosynthesize, they absorb carbon dioxide from the atmosphere and release oxygen. Although diatoms are very small, they live in the vast oceans, the world over. The effect of fixation of carbon by diatoms and release of oxygen alters the chemistry of the atmosphere. It is well-known that diatoms play a vital role in pelagic food webs and elemental cycling in the oceans (Smetacek et al. 2012). Therefore, understanding the effects of global warming on diatom community structure is essential for considering the sensitivity of biogeochemical cycles and ecosystem services in the world oceans.
5.2 Ocean Acidification
Ocean acidification is the ongoing decrease in the pH value of the Earth’s oceans, caused by the uptake of CO2 from the atmosphere. Friedlingstein et al. (2020) stated that the rate of atmospheric CO2 levels has persisted to increase and nearly tripled between the 1960s and 2010s. Oceans have mitigated this growth by absorbing about a quarter of CO2 emissions between 1850 and 2019. As the amount of carbon dioxide in the atmosphere increases, the amount of carbon dioxide absorbed by the ocean also increases. This leads to a series of chemical reactions in the seawater which has a negative impact on marine life and ecosystem functioning (Vargas et al. 2022). As the ocean acidifies, the concentration of carbonate ions decreases. Calcifying organisms such as mussels, corals, and various plankton species need exactly these molecules to build their shells and skeletons (Fig. 5.1). Also, other marine organisms that do not have calcium carbonate shells or skeletons need to spend more energy to regulate their bodily functions in acidifying waters.
5.3 Effects of Ocean Acidification on Marine Diatoms Community
Diatoms are among the most important and prolific microalgae in terms of both abundance and ecological functionality in the ocean. They are within the division of Bacillariophyta and serve directly or indirectly as food for many animals with an assessed contribution of almost 25% to global primary production (Tréguer and De La Rocha 2013). There are at least 30,000 of diatom species which differ in size and ranging from below 3 μm up to a few millimeters (Mann and Vanormelingen 2013). Diatoms are found as single cells or in chains in pelagic and/or benthic habitats and take free-living, surface-attached, symbiotic, or parasitic lifestyles (Mann and Vanormelingen 2013).
Diatom community composition could be affected by different environmental stressors in different ocean areas due to their massive relevance for the Earth system (Tréguer et al. 2018). There have been a number of research articles (Table 5.1) that studied the effects of future CO2 on marine diatom communities in short-term incubations (Bach et al. 2019; Feng et al. 2009, 2010; Hare et al. 2007; Kim et al. 2006; Tortell et al. 2002, 2008). Also, short-term ocean acidification experiments were done with single species of cultured diatoms (Chen and Gao 2003; Li et al. 2012; Sobrino et al. 2008; Sun et al. 2011; Wu et al. 2010). Few others (Crawfurd et al. 2011; Tatters et al. 2012) have used experimental plans in which isolated diatoms were exposed to different CO2 conditions for longer periods (more than three months). Most studies indicated that elevated CO2 led to a measurable increase in phytoplankton productivity, promoting the growth of larger chain-forming diatom. Future studies will be required to evaluate whether this is also the case for other types of algal communities from other marine systems (Table 5.1).
5.4 Impacts of Ocean Acidification on the Growth of Diatoms
Diatoms in different waters suffer from variations of light and temperature as well as fluctuations in seawater carbonate chemistry. It is predictable that the growing partial pressure of CO2 (pCO2) in seawater due to ocean acidification will reduce the cellular requirement of diatoms for energy and resources, therefore stimulating diatom growth and carbon (C) fixation (Tortell et al. 2008). Diatoms show diversified responses to ocean acidification; higher CO2 concentrations are displayed to enhance (Gao et al. 2012b; Kim et al. 2006; King et al. 2011), have no effect (Boelen et al. 2011) or even inhibit (Li and Campbell 2013; Low-Décarie et al. 2011; McCarthy et al. 2012; Sugie and Yoshimura 2013) growth rates of diatom species. However, raised CO2 in the ocean increases its availability to algae; the reduced pH can affect the acid-base balance of cells (Flynn et al. 2012). In addition, the higher CO2 and reduced pH levels can interact with solar radiation and temperature, showing synergistic, antagonistic, or balanced effects (Gao et al. 2012a). Therefore, the mechanisms involved in the responses to ocean acidification of diatoms need to be further explored.
5.5 The Physiological Response of Marine Diatoms to Ocean Acidification
The responses of marine diatoms to ocean acidification are highly variable and species-specific as shown in Table 5.2. Diatoms work greatly efficient CO2 concentrating mechanisms (CCMs) to reach a high ratio of carboxylation to oxygenation (Raven et al. 2011). They are resistant to high levels of UV radiation (Wu et al. 2012), preferable a low sensitivity to photoinactivation of PSII compared with other phytoplanktons (Key et al. 2010 and Wu et al. 2011), and positively exploit variable light (Lavaud et al. 2007).
Li et al. (2012) estimated the combined effects of ocean acidification, UV radiation, and temperature on the diatom Phaeodactylum tricornutum and grew it under two CO2 concentrations (390 and 1000 μatm); growth at the higher CO2 concentration increased non-photochemical quenching (NPQ) of cells and partially responded the damage to PS II (photosystem II) produced by UV-A and UV-B. The ratio of repair to UV-B-induced damage decreased with increased NPQ, reflecting induction of NPQ when repair dropped behind the damage, and it was higher under the ocean acidification condition, showing that the increased pCO2 and lowered pH counteracted UV-B-induced harm. As for photosynthetic carbon fixation rate which increased with increasing temperature from 15 to 25 °C, the elevated CO2 and temperature levels synergistically interacted to reduce the inhibition caused by UV-B and thus increase the carbon fixation.
5.6 Conclusions and Future Perspectives
Ocean acidification is known to reduce calcification of many calcifying organisms. Different diatom species may have entirely diverse responses to ocean acidification, mostly because of variances in species or phenotypes. The ocean acidification made changes in diatom competitiveness, and assemblage structure may change key ecosystem services; therefore, monitoring community abundance of diatoms over longer timescales is important to gain information on their responses to environmental changes.
References
Bach LT, Taucher J (2019) CO2 effects on diatoms: a synthesis of more than a decade of ocean acidification experiments with natural communities. Ocean Sci 15:1159–1175. https://doi.org/10.5194/os-15-1159-2019
Bach LT, Hernández-Hernández N, Taucher J, Spisla C, Sforna C, Riebesell U, Arístegui J (2019) Effects of elevated CO2 on a natural diatom community in the subtropical NE Atlantic. Front Mar Sci 6:75. https://doi.org/10.3389/fmars.2019.00075
Boelen P, van de Poll WH, van der Strate HJ, Neven IA, Beardall J et al (2011) Neither elevated nor reduced CO2 affects the photophysiological performance of the marine antarctic diatom Chaetoceros brevis. J Exp Mar Biol Ecol 406:38–45
Chen X, Gao K (2003) Effect of CO2 concentrations on the activity of photosynthetic CO2 fixation and extracellular carbonic anhydrase in the marine diatom Skeletonema costatum. Chin Sci Bull 48:2616–2620. https://doi.org/10.1360/03wc0084
Crawfurd KJ, Raven JA, Wheeler GL, Baxter EJ, Joint I (2011) The response of Thalassiosira pseudonana to long-term exposure to increased CO2 and decreased pH. PLoS One 6:e26695
Feng Y et al (2009) The effects of increased pCO2 and temperature on the North Atlantic spring bloom. I. The phytoplankton community and biogeochemical response. Mar Ecol Prog Ser 388:13–25. https://doi.org/10.3354/meps08133
Feng Y et al (2010) Interactive effects of iron, irradiance and CO2 on Ross Sea phytoplankton. Deep-Sea Res 57:368–383. https://doi.org/10.1016/j.dsr.2009.10.013
Flynn KJ, Blankford JC, Baird ME, Raven JA, Clark DR et al (2012) Changes in pH at the exterior surface of plankton with ocean acidification. Nat Clim Chang 2:510–513
Friedlingstein P, O’Sullivan M, Jones MW, Andrew RM, Hauck J, Olsen A, Peters et al (2020) Global carbon budget 2020. Earth Syst Sci Data 12:3269–3340. https://doi.org/10.5194/essd-12-3269-2020
Gao K, Helbling EW, Hader DP, Hutchins DA (2012a) Responses of marine primary producers to interactions between ocean acidification, solar radiation, and warming. Mar Ecol Prog Ser 470:167–189
Gao K, Xu JT, Gao G, Li YH, Hutchins DA et al (2012b) Rising CO2 and increased light exposure synergistically reduce marine primary productivity. Nat Clim Chang 2:519–523
Hare CE, Leblanc K, DiTullio GR, Kudela RM, Zhang Y, Lee PA, Riseman S, Tortell PD, Hutchins DA (2007) Consequences of increased temperature and CO2 for algal community structure and biogeochemistry in the Bering Sea. Mar Ecol Prog Ser 352:9–16. https://doi.org/10.3354/meps07182
Hong H, Li D, Lin W, Li W, Shi D (2017) Nitrogen nutritional condition affects the response of energy metabolism in diatoms to elevated carbon dioxide. Mar Ecol Prog Ser 567:41–56
Key T, Mccarthy A, Campbell D, Six C, Roy S, Finkel Z (2010) Cell size tradeoffs govern light exploitation strategies in marine phytoplankton. Environ Microbiol 12:95–104. https://doi.org/10.1111/j.1462-2920.2009.02046.x
Kim JM, Lee K, Shin K, Kang JH, Lee HW (2006) The effect of seawater CO2 concentration on growth of a natural phytoplankton assemblage in a controlled mesocosm experiment. Limnol Oceanogr 51(4):1629–1636
King AL, Sanudo-Wilhelmy SA, Leblanc K, Hutchins DA, Fu F (2011) CO2 and vitamin B12 interactions determine bioactive trace metal requirements of a subarctic pacific diatom. ISME J 5:1388–1396
Lavaud J, Strzepek RF, Kroth PG (2007) Photoprotection capacity differs among diatoms: possible consequences on the spatial distribution of diatoms related to fluctuations in the underwater light climate. Limnol Oceanogr 52:1188–1194. https://doi.org/10.4319/lo.2007.52.3.1188
Li G, Campbell DA (2013) Rising CO2 interacts with growth light and growth rate to alter photosystem II photoinactivation of the coastal diatom Thalassiosira pseudonana. PLoS One 8:e55562
Li Y, Gao K, Villafane V, Helbling EW (2012) Ocean acidification mediates photosynthetic response to UV radiation and temperature increase in the diatom Phaeodactylum tricornutum. Biogeosciences 9:3931–3942. https://doi.org/10.5194/bg-9-3931-2012
Low-Décarie E, Fussmann GF, Bell G (2011) The effect of elevated CO2 on growth and competition in experimental phytoplankton communities. Glob Chang Biol 17:2525–2535
Mann DG, Vanormelingen P (2013) An inordinate fondness? The number, distributions, and origins of diatom species. J Eukaryot Microbiol 60:414–420. https://doi.org/10.1111/jeu.12047
McCarthy A, Rogers SP, Duffy SJ, Campbell DA (2012) Elevated carbon dioxide differentially alters the photophysiology of Thalassiosira pseudonana (Bacillariophyceae) and Emiliania huxleyi (Haptophyta). J Phycol 48(3):635–646
Mejía LM, Isensee K, Méndez-Vicente A, Pisonero J, Shimizu N, González C, Monteleone B, Stoll H (2013) B content and Si/C ratios from cultured diatoms (Thalassiosira pseudonana and Thalassiosira weissflogii): Relationship to seawater pH and diatom carbon acquisition. Geochim Cosmochim Acta 123:322–337. https://doi.org/10.1016/j.gca.2013.06.011
Raven JA, Giordano M, Beardall J, Maberly SC (2011) Algal and aquatic plant carbon concentrating mechanisms in relation to environmental change. Photosynth Res 109:281–296. https://doi.org/10.1007/s11120-011-9632-6
Ridgwell A, Schmidt DN (2010) Past constraints on the vulnerability of marine calcifiers to massive carbon dioxide release. Nat Geosci 3:196–200
Riebesell U, Wolf-Gladrow DA, Smetacek V (1993) Carbon dioxide limitation of marine phytoplankton growth rates. Nature 361:249–251. https://doi.org/10.1038/361249a0
Sabine CL, Feely RA, Gruber N et al (2004) The oceanic sink for anthropogenic CO2. Science 305:367–371
Shi D, Li W, Hopkinson BM, Hong H, Li D, Kao SJ, Lin W (2015) Interactive effects of light, nitrogen source, and carbon dioxide on energy metabolism in the diatom Thalassiosira pseudonana. Limnol Oceanogr 60:1805–1822
Shi D, Hong H, Su X, Liao L, Chang S, Lin W (2019) Physiological response of marine diatoms to ocean acidification: differential roles of seawater pCO2 and pH. J Phycol 55:521–533
Smetacek V, Klaas C, Strass VH, Assmy P, Montresor M et al (2012) Deep carbon export from a Southern Ocean iron-fertilized diatom bloom. Nature 487:313–319. https://doi.org/10.1038/nature11229
Sobrino C, Ward ML, Neale PJ (2008) Acclimation toelevated carbon dioxide and ultraviolet radiation in the diatom Thalassiosira pseudonana: effects on growth, photosynthesis, and spectral sensitivity photo inhibition. Limnol Oceanogr 53:494–505. https://doi.org/10.4319/lo.2008.53.2.0494
Sugie K, Yoshimura T (2013) Effects of pCO2 and iron on the elemental composition and cell geometry of the marine diatom Pseudo-nitzschia pseudodelicatissima (Bacillariophyceae). J Phycol 49:475–488
Sun J, Hutchins DA, Feng Y, Seubert EL, Caron DA, Fu FX (2011) Effects of changing pCO2 and phosphate availability on domoic acid production and physiology of the marine harmful bloom diatom Pseudo-nitzschia multiseries. Limnol Oceanogr 56:829–840. https://doi.org/10.4319/lo.2011.56.3.0829
Tatters AO, Fu FX, Hutchins DA (2012) High CO2 and silicate limitation synergistically increase the toxicity of Pseudo-nitzschia fraudulenta. PLoS One 7:e32116. https://doi.org/10.1371/journal.pone.0032116
Tatters AO, Roleda MY, Schnetzer A, Fu F, Hurd CL, Boyd PW, Caron DA, Lie AAY, Hoffmann LJ, Hutchins DA (2013) Short- and long-term conditioning of a temperate marine diatom community to acidification and warming. Philos Trans R Soc B 368:20120437. https://doi.org/10.1098/rstb.2012.0437
Torstensson A, Chierici M, Wulff A (2012) The influence of increased temperature and carbon dioxide levels on the benthic/sea ice diatom Navicula directa. Polar Biol 35:205–214. https://doi.org/10.1007/s00300-011-1056-4
Tortell PD, DiTullio GR, Sigman DM, Morel FMM (2002) CO2 effects on taxonomic composition and nutrient utilization in an equatorial Pacific phytoplankton assemblage. Mar Ecol Prog Ser 236:37–43. https://doi.org/10.3354/meps236037
Tortell PD et al (2008) CO2 sensitivity of Southern Ocean phytoplankton. Geophys Res Lett 35:L04605. https://doi.org/10.1029/2007GL032583
Tréguer PJ, De La Rocha CL (2013) The world ocean silica cycle. Annu Rev Mar Sci 5:477–501. https://doi.org/10.1146/annurev-marine-121211-172346
Tréguer P, Bowler C, Moriceau B, Dutkiewicz S, Gehlen M, Aumont O et al (2018) Influence of diatom diversity on the ocean biological carbon pump. Nat Geosci 11:27–37. https://doi.org/10.1038/s41561-017-0028-x
Vargas CA, Cuevas LA, Broitman BR et al (2022) Upper environmental pCO2 drives sensitivity to ocean acidification in marine invertebrates. Nat Clim Chang 12:200–207. https://doi.org/10.1038/s41558-021-01269-2
Wu Y, Gao K, Riebesell U (2010) CO2-induced seawater acidification affects physiological performance of the marine diatom Phaeodactylum tricornutum. Biogeosciences 7:2915–2923
Wu H, Cockshutt AM, McCarthy A, Campbell DA (2011) Distinctive photosystem II photo inactivation and protein dynamics in marine diatoms. Plant Physiol 156:2184–2195. https://doi.org/10.1104/pp.111.178772
Wu X, Gao G, Giordano M, Gao K (2012) Growth and photosynthesis of a diatom grown under elevated CO2; in the presence of solar UV radiation. Fundam Appl Limnol/Arch Hydrobiol 180:279–290
Wu Y, Campbell DA, Irwin AJ, Suggett DJ, Finkel ZV (2014) Ocean acidification enhances the growth rate of larger diatoms. Limnol Oceanogr 59:1027–1034
Yang GY, Gao K (2012) Physiological responses of the marine diatom Thalassiosira pseudonana to increased pCO2 and seawater acidity. Mar Environ Res 79:142–151
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Rashedy, S.H. (2023). Ocean Acidification Conditions and Marine Diatoms. In: Srivastava, P., Khan, A.S., Verma, J., Dhyani, S. (eds) Insights into the World of Diatoms: From Essentials to Applications. Plant Life and Environment Dynamics. Springer, Singapore. https://doi.org/10.1007/978-981-19-5920-2_5
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