ABSTRACT
In aquatic ecosystems, unicellular algae form the basis of the food webs. Theoretical and experimental studies have demonstrated that one of the mechanisms that maintain high diversity of ...phytoplankton is through predation and the consequent evolution of defence mechanisms. Proposed defence mechanisms in phytoplankton are diverse and include physiological (e.g. toxicity, bioluminescence), morphological (e.g. silica shell, colony formation), and behavioural (e.g. escape response) traits. However, the function of many of the proposed defence mechanisms remains elusive, and the costs and benefits (trade‐offs) are often unquantified or undocumented. Here, we provide an overview of suggested phytoplankton defensive traits and review their experimental support. Wherever possible we quantify the trade‐offs from experimental evidence and theoretical considerations. In many instances, experimental evidence suggests that defences are costless. However, we argue that (i) some costs materialize only under natural conditions, for example, sinking losses, or dependency on the availability of specific nutrients, and (ii) other costs become evident only under resource‐deficient conditions where a rivalry for limiting resources between growth and defence occurs. Based on these findings, we suggest two strategies for quantifying the costs of defence mechanisms in phytoplankton: (i) for the evaluation of defence costs that are realized under natural conditions, a mechanistic understanding of the hypothesized component processes is required; and (ii) the magnitude of the costs (i.e. growth reduction) must be assessed under conditions of resource limitation.
Silicified cell walls as a defensive trait in diatoms Pančić, Marina; Torres, Rocio Rodriguez; Almeda, Rodrigo ...
Proceedings - Royal Society. Biological sciences/Proceedings - Royal Society. Biological Sciences,
04/2019, Letnik:
286, Številka:
1901
Journal Article
Recenzirano
Odprti dostop
Diatoms contribute nearly half of the marine primary production. These microalgae differ from other phytoplankton groups in having a silicified cell wall, which is the strongest known biological ...material relative to its density. While it has been suggested that a siliceous wall may have evolved as a mechanical protection against grazing, empirical evidence of its defensive role is limited. Here, we experimentally demonstrate that grazing by adult copepods and nauplii on diatoms is approximately inversely proportional to their silica content, both within and among diatom species. While a sixfold increase in silica content leads to a fourfold decrease in copepod grazing, silicification provides no protection against protozoan grazers that directly engulf their prey. We also found that the wall provides limited protection to cells ingested by copepods, since less than 1% of consumed cells were alive in the faecal pellets. Moreover, silica deposition in diatoms decreases with increasing growth rates, suggesting a possible cost of defence. Overall, our results demonstrate that thickening of silica walls is an effective defence strategy against copepods. This suggests that the plasticity of silicification in diatoms may have evolved as a response to copepod grazing pressure, whose specialized tools to break silicified walls have coevolved with diatoms.
Many species of phytoplankton produce toxins that may provide protection from grazing. In that case one would expect toxin production to be costly; else all species would evolve toxicity. However, ...experiments have consistently failed to show any costs. Here, we show that costs of toxin production are environment dependent but can be high. We develop a fitness optimization model to estimate rate, costs, and benefits of toxin production, using PST (paralytic shellfish toxin) producing dinoflagellates as an example. Costs include energy and material (nitrogen) costs estimated from well-established biochemistry of PSTs, and benefits are estimated from relationship between toxin content and grazing mortality. The model reproduces all known features of PST production: inducibility in the presence of grazer cues, low toxicity of nitrogen-starved cells, but high toxicity of P-limited and light-limited cells. The model predicts negligible reduction in cell division rate in nitrogen replete cells, consistent with observations, but >20% reduction when nitrogen is limiting and abundance of grazers high. Such situation is characteristic of coastal and oceanic waters during summer when blooms of toxic algae typically develop. The investment in defense is warranted, since the net growth rate is always higher in defended than in undefended cells.
The amphibious plant species Sagittaria sagittifolia and Ranunculus lingua here serve as model systems to study differences in leaf optical properties of different leaf types that develop in aquatic ...and terrestrial environments. We aimed to determine leaf traits that explain most of the variability in the reflectance and transmittance spectra in the range from 280 to 880 nm. Comparisons of leaves of the same form revealed marked differences in their structures and particularly in the content of total methanol-soluble UV-absorbing compounds. Submerged leaves transmit radiation over the whole range measured, but emerged leaves transmit only at wavelengths from 500 to 650 nm, and above 690 nm. Redundancy analysis shows that biochemical leaf traits, namely the UV-absorbing compounds chlorophyll a and b, together with the specific leaf area (SLA), significantly affect the reflectance spectra, explaining 60% of the spectra variability. Pigment levels negatively affect reflectance, while the effect of SLA is positive. Physical traits like thickness of the palisade mesophyll, SLA, and thickness of the lower and upper epidermis, along with anthocyanin content, explain 62% of the transmittance spectra variability. This study provides new insight into the understanding of data collected for aquatic and semi-aquatic plants based on spectral analyses.
We studied how exposure to oil spill response technologies affect marine microorganisms during Arctic winter and spring. Microorganisms were exposed to chemically dispersed oil (DISP), in situ burnt ...oil (ISB), and natural attenuated oil (NATT) in mesocosms from February to May. We subsampled the mesocosms and studied the effects of oil in laboratory incubations as changes in biomass of the major functional groups: bacteria, heterotrophic-nanoflagellates, dinoflagellates, ciliates, pico- and nanophytoplankton, and diatoms over two 14-day periods. In winter, the majority of polycyclic aromatic hydrocarbons (PAHs) remained encapsulated in the ice, and the low concentrations of PAHs in water led to minute changes in biomass of the investigated groups. In spring, however, when the PAHs were partially released from the melting ice, the biomass of many functional groups in DISP and NATT decreased significantly, while the changes in ISB were less pronounced. The overall biomass reduction, as observed in this study, could lead to a disrupted transfer of energy from the primary producers to the higher trophic levels in oil affected areas.
•Oil remediation tools enhance growth of bacteria and heterotrophic nanoflagellates.•In situ burning has the least harmful effects on microbial community structure.•Chemical dispersant and oil weathering reduce microbial community biomass by 50%.
Grazers can induce toxin (domoic acid, DA) production in diatoms. The toxic response has been observed in two species of Pseudo-nitzschia and was induced by Calanus copepods. In this study, ...interactions between diatoms and copepods were further explored using different species of diatoms and copepods. All herbivorous copepods induced toxin production, whereas exposure to carnivorous copepods did not. In line with this, increasing the number of herbivorous copepods resulted in even higher toxin production. The induced response is thus only elicited by copepods that pose a real threat to the responding cells, which supports that the induced toxin production in diatoms evolved as an inducible defense.
The cellular toxin content in Pseudo-nitzschia was positively correlated to the concentration of a group of specific polar lipids called copepodamides that are excreted by the copepods. This suggests that copepodamides are the chemical cues responsible for triggering the toxin production. Carnivorous copepods were found to produce less or no copepodamides.
Among the diatoms exposed to grazing herbivorous copepods, only two of six species of Pseudo-nitzschia and none of the Nitzschia or Fragilariopsis strains responded by producing DA, indicating that not all Pseudo-nitzschia species/strains are able to produce DA, and that different diatom species might have different strategies for coping with grazing pressure. Growth rate was negatively correlated to cellular domoic acid content indicating an allocation cost associated with toxin production. Long-term grazing experiments showed higher mortality rates of grazers fed toxic diatoms, supporting the hypothesis that DA production is an induced defense mechanism.
Diatoms of the genus Pseudo-nitzschia produce domoic acid (DA), a toxin that is vectored in the marine food web, thus causing serious problems for marine organisms and humans. In spite of this, ...knowledge of interactions between grazing zooplankton and diatoms is restricted. In this study, we examined the interactions between Calanus copepodites and toxin producing Pseudo-nitzschia. The copepodites were fed with different concentrations of toxic P. seriata and a strain of P. obtusa that previously was tested to be non-toxic. The ingestion rates did not differ among the diets (P. seriata, P. obtusa, a mixture of both species), and they accumulated 6%-16% of ingested DA (up to 420 µg per dry weight copepodite). When P. seriata was exposed to the copepodites, either through physical contact with the grazers or separated by a membrane, the toxicity of P. seriata increased (up to 3300%) suggesting the response to be chemically mediated. The induced response was also triggered when copepodites grazed on another diatom, supporting the hypothesis that the cues originate from the copepodite. Neither pH nor nutrient concentrations explained the induced DA production. Unexpectedly, P. obtusa also produced DA when exposed to grazing copepodites, thus representing the second reported toxic polar diatom.
Silicified cell walls as a defensive trait in diatoms Pančić, Marina; Torres, Rocio Rodriguez; Almeda, Rodrigo ...
Proceedings of the Royal Society. B, Biological sciences,
04/2019, Letnik:
286, Številka:
1901
Journal Article
Recenzirano
Diatoms contribute nearly half of the marine primary production. These microalgae differ from other phytoplankton groups in having a silicified cell wall, which is the strongest known biological ...material relative to its density. While it has been suggested that a siliceous wall may have evolved as a mechanical protection against grazing, empirical evidence of its defensive role is limited. Here, we experimentally demonstrate that grazing by adult copepods and nauplii on diatoms is approximately inversely proportional to their silica content, both within and among diatom species. While a sixfold increase in silica content leads to a fourfold decrease in copepod grazing, silicification provides no protection against protozoan grazers that directly engulf their prey. We also found that the wall provides limited protection to cells ingested by copepods, since less than 1% of consumed cells were alive in the faecal pellets. Moreover, silica deposition in diatoms decreases with increasing growth rates, suggesting a possible cost of defence. Overall, our results demonstrate that thickening of silica walls is an effective defence strategy against copepods. This suggests that the plasticity of silicification in diatoms may have evolved as a response to copepod grazing pressure, whose specialized tools to break silicified walls have coevolved with diatoms.
•Mesocosm study of effects of oil spill response technologies on Artic copepods.•Dispersed oil led to highest PAH release compared to other technologies.•PAH concentrations under the sea ice remain ...low throughout winter and spring.•Physiology of Calanus glacialis females were unaffected by the PAH exposure levels.•Dispersion of oil in sea ice reduce nauplii survival and increase deformity.
A mesocosm study with oil in ice was performed in Van Mijenfjorden in Svalbard to compare effects of the oil spill responses (OSR) in situ burning, chemical dispersion and natural attenuation on the physiological performance of the Arctic copepod Calanus glacialis. Seawater collected from the mesocosms in winter and spring was used in laboratory incubation experiments, where effects on fecal pellet production, egg production and hatching success were investigated over a period of 14 days. Polycyclic aromatic hydrocarbon (PAH) seawater concentrations were lowest in winter. Brine channel formation in spring resulted in an 18 times increase in PAH concentration in the chemical dispersion treatment (1.67 μg L−1), and a 3 fold increase in the natural attenuation (0.36 μg L−1) and in situ burning (0.04 μg L−1) treatments. The physiological performance of female C. glacialis was unaffected by the PAH seawater concentrations. However, a higher mortality and deformity of nauplii was observed in the chemical dispersion treatment, highlighting the importance of considering secondary effects on next generation in future environmental risk assessment of OSR. This study shows that during the ice-covered period, chemical dispersion of oil spills leads to higher PAH exposure than natural attenuation and in situ burning, with potential consequences for recruitment of Arctic copepods.
Seasonal strategies in the world’s oceans Visser, André W.; Brun, Philipp; Chakraborty, Subhendu ...
Progress in oceanography,
November-December 2020, 2020-11-00, Letnik:
189
Journal Article
Recenzirano
•Life history of marine organisms is strongly influenced by their size and seasonality.•Resting stages and dormancy are used by small organisms (bacteria to small copepods).•Energy reserves and ...vertical migration are used by medium sized organisms (larger copepods).•Latitudinal migration is used by large organisms (forage fish to whales).•Organisms with lifespans of around 1 year employ a combination of strategies.
Throughout much of the world’s oceans, life is organized around seasonal cycles of feast and famine. Here we seek to understand the life-history strategies by which marine organisms contend with seasonal variations through a range of adaptations and traits, including overwintering stages, dormancy, investment in reserves, and migration. Our perspective is broad, spanning across marine food webs, from unicellular plankton to whales, and covering all latitudes, from the equator to the poles. The analysis is organized around a simple mechanistic life history optimization model. The model generates several general hypotheses: (i) small organisms should cope with winters by making resting stages or by dormancy; (ii) medium-sized organisms should build reserves and perform seasonal vertical migration to reduce predation; (iii) large organisms should primarily employ latitudinal migrations to follow seasonal peaks in production. Subsequently, these hypotheses are tested against a large assemblage of observations and data reported in the literature. Body size, trophic level, and the intensity and duration of seasonal highs and lows appear to be closely related to seasonal strategies. Some, but not all of these hypotheses are borne out by our analysis of data. In particular, we find that organisms with a lifespan on the order of the seasonal length employ a multitude of strategies.
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