RESUMO
The assimilation of inorganic nutrients by phytoplankton strongly depends on environmental conditions such as the availability of nitrogen and temperature, especially warming. The acclimation or adaptation of different species to such changes remains poorly understood. Here, we used a multimethod approach to study the viability and physiological and biochemical responses of the marine diatom Chaetoceros pseudocurvisetus to different temperatures (15, 25, and 30 °C) and different N:P ratios. Nitrogen limitation had a greater effect than high temperature on cell growth and reproduction, leading to a marked elongation of setae, decreased phosphorus assimilation, increased lipid accumulation, and decreased protein synthesis. The elongation of setae observed under these conditions may serve to increase the surface area available for the uptake of inorganic and/or organic nitrogen. In contrast, high temperatures (30 °C) had a stronger effect than nitrogen deficiency on cell death, nitrogen assimilation, chlorophyll a accumulation, the cessation of setae formation, and cell lipid remodelling. Significant changes in thylakoid lipids were observed in cells maintained at 30 °C, with increased levels of digalactosyldiacylglycerol and sulfoquinovosyldiacylglycerol. These changes may be explained by the role of galactolipids in thylakoid membrane stabilization during heat stress.
Assuntos
Diatomáceas , Clorofila A/metabolismo , Diatomáceas/metabolismo , Lipídeos , Nitrogênio/metabolismo , TemperaturaRESUMO
This conference report describes the training activities that took place in the frame of the Integrated in Situ Chemical MApping probe (SCHeMA) summer school organized from the 14th to the 16th of June 2016 in Bilbao (Spain).
Assuntos
Ecologia/educação , Monitoramento Ambiental/métodos , Técnicas Biossensoriais/métodos , Ciclo do Carbono , Metais/análise , Compostos Orgânicos Voláteis/análiseRESUMO
It is still unclear how the chemical speciation of Cu in surface seawater is impacted by aerosols from various sources deposited on the sea surface, which is surprising, considering the environmental importance of Cu. Therefore, we used voltammetry to investigate Cu complexing capacity (CuCC) in the sea surface microlayer (SML) and in the underlying water (ULW) of the oligotrophic middle Adriatic Sea during February-July 2019. The focus was on the impacts of specific atmospheric processes such as open-fire biomass burning (BB), pollination season and Saharan dust intrusion. The presence of ligand class L2 (19.9-392.0, average 63.8, median 43.1) nM; log K2 (8.3-10.2, average 9.6, median 9.6) was observed in all samples, while ligand class L1 (40.5-76.1, average 53.6, median 48.9) nM; log K1 (10.3-11.1, average 10.6, median 10.5) was found in only 25% of SML samples. Throughout the period, the SML was enriched with organic ligands by a factor of up to 9.1 compared to the ULW, mainly due to the high sensitivity of the SML to specific atmospheric depositions. In addition, measurements with corresponding specific model aerosols were conducted to analyse their impacts on CuCC. Pollen directly affected CuCC in the SML by increasing the concentration of allochthonous ligands such as proteins. The deposition of BB aerosols rich in nutrients and trace metals stimulated the biological production of organic ligands, showing an indirect effect on CuCC delayed by up to two weeks. Finally, Saharan dust had a negligible impact on CuCC. This study illustrates the susceptibility of oligotrophic coastal area to the effects of pollen and open-fire BB aerosols in altering the Cu-binding organic ligands in the SML.
Assuntos
Água do Mar , Água , Ligantes , Aerossóis/análise , Poeira/análiseRESUMO
The global importance of abiotic oceanic production of volatile organic compounds (VOCs) still presents a source of high uncertainties related to secondary organic aerosol (SOA) formation. A better understanding of the photochemistry occurring at the ocean-atmosphere interface is particularly important in that regard, as it covers >70% of the Earth's surface. In this work, we focused on the photochemical VOCs production at the air-water interface containing organic material from authentic culture of marine diatom Chaetoceros pseudocurvisetus. Abiotic VOCs production upon irradiation of material originating from total phytoplankton culture as well as the fraction containing only dissolved material was monitored by means of PTR-ToF-MS. Furthermore, isolated dissolved lipid fraction was investigated after its deposition at the air-water interface. All samples acted as a source of VOCs, producing saturated oxygenated compounds such as aldehydes and ketones, as well as unsaturated and functionalized compounds. Additionally, a significant increase in surfactant activity following irradiation experiments observed for all samples implied biogenic material photo-transformation at the air-water interface. The highest VOCs flux normalized per gram of carbon originated from lipid material, and the produced VOCs were introduced into an atmospheric simulation chamber, where particle formation was observed after its gas-phase ozonolysis. This work clearly demonstrates abiotic production of VOCs from phytoplankton derived organic material upon irradiation, facilitated by its presence at the air/water interface, with significant potential for affecting the global climate as a precursor of particle formation.
Assuntos
Poluentes Atmosféricos , Diatomáceas , Compostos Orgânicos Voláteis , Compostos Orgânicos Voláteis/análise , Atmosfera/química , Água , Aerossóis/análise , Lipídeos , Poluentes Atmosféricos/análiseRESUMO
Atmospheric deposition (AD) of nutrients and its impact on the sea surface requires consideration of interfacial processes within the sea surface microlayer (SML), the ocean-atmosphere boundary layer of major importance for many global biogeochemical and climate-related processes. This study comprised a comprehensive dataset, including dissolved NO3-, NH4+ and PO43- in ambient aerosol particles, wet deposition and sea surface samples collected from February to July 2019 at a central Adriatic coastal site. The aerosol mean concentration of dissolved nitrogen (DIN = NO3- + NH4+) and PO43- were 48.8 ± 82.8 µmol m-3 and 0.8 ± 0.6 µmol m-3, respectively, while their total fluxes (dry + wet) ranged from 24.2 to 212.3 µmol m-2 d-1 (mean 123.2 ± 53.2 µmol m-2 d-1) and from 1.2 to 2.1 µmol m-2 d-1 (mean 1.5 ± 0.3 µmol m-2 d-1), respectively. Intensive local episodes of open biomass burning (BB) significantly increased aerosol DIN concentrations as well as DIN deposition fluxes, particularly altering the molar DIN/PO43- ratio of atmospheric samples. The DIN temporal patterns showed high variability in the SML (range 0.2-24.6 µmol L-1, mean 5.0 ± 7.1 µmol L-1) in contrast to the underlying water samples (range 0.5-4.2 µmol L-1, mean 1.9 ± 1.2 µmol L-1), with significant increases during BB periods. Variability in abundance of heterotrophic bacteria and autotrophs in the SML along with concentrations of bulk dissolved and particulate organic carbon as well as dissolved and particulate lipids and carbohydrates, gel particles and surfactants followed DIN enhancements with a two-week delay. This study showed that AD can affect the short-term scale enrichments of organic matter in the SML, especially when accompanied by BB emissions typical of the overall Mediterranean coastal environment. This could have strong implications for global air-sea exchange processes, including those of climate relevant gases, mediated by the SML.
Assuntos
Atmosfera , Água do Mar , Aerossóis/análise , Poeira , Monitoramento Ambiental , Nitrogênio/análise , Água do Mar/químicaRESUMO
Aerosol (PM10), bulk deposition, sea surface microlayer (SML) and underlying water (ULW) samples were collected simultaneously during a field campaign at the middle Adriatic coastal site between February and July 2019, to assess the impact of atmospheric deposition (AD) of biologically relevant trace metals (TM) (Zn, Cu, Co, Ni, Cd and Pb) on the sea surface responses in an oligotrophic coastal region. Anthropogenic emissions from continental Europe, alongside local/regional domestic heating, likely affected the concentrations of Zn, Cd and Pb in aerosols during winter-early spring, while traffic emissions during the tourist season impacted Ni, Co and Cu aerosol concentrations. Additionally, open-fire biomass burning (BB) episodes caused considerable TM concentration increases, while Saharan dust intrusion in spring led to a 10-fold increase in Co concentrations in PM10 samples. These intensive episodes significantly affected the bulk deposition fluxes of TMs, showing that a small number of such extreme events, common to Mediterranean coastal areas, could be responsible for most of the AD. Enrichments and concentrations of total TMs in SML samples collected following BB events indicated that such events, along with high precipitation, influenced TM partitioning in surface water layers. We estimated that AD represents a significant source of TM to the shallow middle Adriatic coastal area, highlighting the need to further explore the atmosphere-sea surface links, to expand our understanding of the biogeochemistry of these important micronutrients and pollutants, including their impact on the aquatic community.
Assuntos
Poluentes Atmosféricos , Oligoelementos , Aerossóis/análise , Poluentes Atmosféricos/análise , Atmosfera , Monitoramento Ambiental , Oligoelementos/análiseRESUMO
We demonstrate improved power of Iatroscan thin layer chromatography/flame ionization detection (TLC-FID) technique for analysis of complex marine lipid mixture by developing protocol for the separation and analysis of glycolipids including sulfoquinovosyldiacylglycerols (SQDG), monogalactosyldiacylglycerols (MGDG) and digalactosyldiacylglycerols (DGDG). We have modified the common protocol used so far for the analysis of lipid classes by replacing the elution step which uses pure acetone for the elution of acetone mobile polar lipids, with the elution step containing chloroform-acetone (72:28, v:v) for separation of MGDG and DGDG. To separate SQDG from the complex lipid matrix we introduced solvent mixture acetone-chloroform-methanol-formic acid (33:33:33:0.6, v:v:v:v). Quantification of glycolipid classes was performed after calibration with glycolipid standards for the masses between 0.2 and 2.7-5.0µg. With this new protocol we have successfully separated three glycolipids from the complex particulate lipid mixture of the seawater samples. Such an approach extends the power of existing protocol for the analysis of lipids which altogether ensure detection and quantification of 18 lipid classes what was demonstrated on seawater samples. This enables to gain a very broad system overview of the particularly complex environments as are seas, oceans and freshwaters.
Assuntos
Glicolipídeos/análise , Poluentes Químicos da Água/análise , Cromatografia em Camada Fina/métodos , Ionização de Chama , Galactolipídeos/análise , Água do Mar/químicaRESUMO
A systematic investigation of non-phosphorus containing glycolipids (GL) was conducted in the northern Adriatic Sea during two years at two stations with different nutrient loads. GL concentration varied both spatially and temporally, with values of 1.1-21.5 µg/L and 0.4-44.7 µg/L in the particulate and the dissolved fraction, respectively. The highest concentrations were measured during summer in surface waters and at the more oligotrophic station, where GL yields (% of total lipids) were often higher than 20% and 50% in the particulate and dissolved fractions, respectively. To obtain more insight into factors governing GL accumulation autotrophic plankton community structure (pico-, nano- and microplankton fractions), chlorophyll a, heterotrophic bacteria and nutrient concentrations were measured together with hydrographic parameters and sunlight intensity. During the investigated period smaller autotrophic plankton cells (pico- and followed by nanoplankton) prevailed in abundance over larger cells (microplankton), which were found in large numbers in freshened surface samples. Several major findings resulted from the study. Firstly, during PO4 limitation, particularly at the oligotrophic station, enhanced glycolipid instead of phospholipid accumulation takes place, representing an effective phosphate-conserving mechanism. Secondly, results suggest that at seawater temperatures >19 °C autotrophic plankton considerably accumulate GL, probably to achieve thermal stability. Thirdly, high sunlight intensities seem to influence increased GL accumulation; GL possibly plays a role in cell mechanisms that prevent/mitigate photooxidation. And finally, substantial accumulation of GL detected in the dissolved fraction could be related to the fact that GL do not contain biologically relevant elements, like phosphorus, which makes them an unattractive substrate for enzyme activity. Therefore, substantial portion of CO2 could be removed from the atmosphere in P-limited regions during summer via its capture by plankton and conversion to GL.