天津近岸浮游植物群落对海洋酸化和硝酸盐加富的响应

为了评估海洋酸化和富营养化耦合作用对近海浮游生态环境的影响,本研究以天津市近岸海域浮游植物群落的生物地球化学指标为研究对象,分别采用一次性及连续培养的方式模拟自然水华及稳态条件,探究其对二氧化碳(CO₂)和硝酸盐浓度变化及二者耦合作用的响应。实验条件设置如下:1)对照:二氧化碳分压p(CO₂)40.53 Pa、无硝酸盐添加;2)酸化:p(CO₂)101.3 Pa、无硝酸盐添加;3)加N:p(CO₂)40.53 Pa、添加硝酸盐50 μmol·L^–1;4)酸化加N:p(CO₂)101.3 Pa、添加硝酸盐50 μmol·L^–1。实验结果表明,硝酸盐加富比酸化更加显著地促进浮游植物群落总叶绿素(Chl a)生物量及颗粒有机碳(POC)和颗粒有机氮(PON)积累,酸化和加N使浮游植物群落粒径大小升高。连续培养实验表明,酸化和N加富对Chl a、生物硅(BSi)、PON浓度、PON与颗粒有机磷(POP)比值(N/P)、POC与BSi比值(C/BSi)及沉降速率有协同交互作用,对POP和POC浓度及POC与PON比值(C/N)有拮抗性交互作用。在一次性培养后,酸化显著降低了浮游植物群落的沉降速率;而在连续培养后,酸化和N加富使浮游植物群落沉降速率显著升高。这些结果表明酸化和N加富对与近岸浮游植物相关的生物地球化学循环及在不同生长阶段的种群碳沉降存在不同的潜在影响及交互效应。     

Vulnerability of marine biodiversity to ocean acidification: A meta-analysis

The ocean captures a large part of the anthropogenic carbon dioxide emitted to the atmosphere. As a result of the increase in CO₂ partial pressure the ocean pH is lowered as compared to pre-industrial times and a further decline is expected. Ocean acidification has been proposed to pose a major threat for marine organisms, particularly shell-forming and calcifying organisms. Here we show, on the basis of meta-analysis of available experimental assessments, differences in organism responses to elevated pCO₂ and propose that marine biota may be more resistant to ocean acidification than expected. Calcification is most sensitive to ocean acidification while it is questionable if marine functional diversity is impacted significantly along the ranges of acidification predicted for the 21st century. Active biological processes and small-scale temporal and spatial variability in ocean pH may render marine biota far more resistant to ocean acidification than hitherto believed.     

CO2升高和阳光紫外辐射对坛紫菜生长和光合特性的耦合效应

大气CO₂持续升高,导致溶入海水中的CO₂增多,海水表层的H+浓度增加,从而引起海洋酸化。为了探讨近岸定生大型海藻对这种环境变化的响应,本文选择经济海藻坛紫菜为实验材料,研究海洋酸化与紫外辐射对藻体生长以及光合特性的影响。实验分两个CO₂处理,分别为正常空气水平(390 ppmv)和高CO₂水平(800 ppmv); 三种辐射处理,分别为全波长辐射(PAB)、滤除紫外线B(PA)和仅接受可见光处理(PAR)。研究结果表明,CO₂培养下的坛紫菜,在仅有可见光(P)或者同时有紫外线A(PA)存在的情况下,显著促进藻体的生长;但在全波长辐射处理下(PAB),这种作用不明显。高CO₂降低了藻体在P和PA处理下的光合作用速率,但对PAB处理作用不显著。高CO₂处理下的藻体,UV-B显著降低了全波长辐射下藻体紫外吸收物质的含量,但在正常CO₂水平下,紫外辐射的作用不显著。这表明高CO₂导致的生长优势被紫外辐射的负面效应所抵消,在全球变化的过程中,紫外辐射的进一步加强在海洋酸化的背景下甚至有可能降低坛紫菜的产量。     

Physiological Responses of the Mediterranean Subtidal Alga <Emphasis Type="Italic">Peyssonnelia squamaria</Emphasis> to Elevated CO<Subscript>2</Subscript>

The ecological consequences of ocean acidification are unclear due to varying physiological properties of macroalgae and species-specific responses. Therefore, in the present study, we used a laboratory culture experiment to analyse the eco-physiological responses of the Mediterranean subtidal red alga Peyssonnelia squamaria to CO₂-induced lower pH. Our results showed an increase in the photosynthetic performance and growth rate of P. squamaria, despite the reduction in CaCO₃ content in the low pH treatment. According to our results, we believe that samples exposed to elevated CO₂ could be regulated own nitrogen metabolism to support increased growth rate and it may be down-regulated nitrate uptake. As a result, we hypothesize that P. squamaria may benefit from ocean acidification.     

The SOLAS air-sea gas exchange experiment (SAGE) 2004

The SOLAS air-sea gas exchange experiment (SAGE) was a multiple-objective study investigating gas-transfer processes and the influence of iron fertilisation on biologically driven gas exchange in high-nitrate low-silicic acid low-chlorophyll (HNLSiLC) Sub-Antarctic waters characteristic of the expansive subpolar zone of the southern oceans. This paper provides a general introduction and summary of the main experimental findings. The release site was selected from a pre-voyage desktop study of environmental parameters to be in the south-west Bounty Trough (46.5°S 172.5°E) to the south-east of New Zealand and the experiment was conducted between mid-March and mid-April 2004. In common with other mesoscale iron addition experiments (FeAX’s), SAGE was designed as a Lagrangian study, quantifying key biological and physical drivers influencing the air-sea gas exchange processes of CO₂, DMS and other biogenic gases associated with an iron-induced phytoplankton bloom. A dual tracer SF₆/³He release enabled quantification of both the lateral evolution of a labelled volume (patch) of ocean and the air-sea tracer exchange at tenths of kilometer scale, in conjunction with the iron fertilisation. Estimates from the dual-tracer experiment found a quadratic dependency of the gas exchange coefficient on windspeed that is widely applicable and describe air-sea gas exchange in strong wind regimes. Within the patch, local and micrometeorological gas exchange process studies (100 m scale) and physical variables such as near-surface turbulence, temperature microstructure at the interface, wave properties and windspeed were quantified to further assist the development of gas exchange models for high-wind environments.There was a significant increase in the photosynthetic competence (F_v/F_m) of resident phytoplankton within the first day following iron addition, but in contrast to other FeAX’s, rates of net primary production and column-integrated chlorophyll a concentrations had only doubled relative to the unfertilised surrounding waters by the end of the experiment. After 15 days and four iron additions totalling 1.1 ton Fe²⁺, this was a very modest response compared to other mesoscale iron enrichment experiments. An investigation of the factors limiting bloom development considered co-limitation by light and other nutrients, the phytoplankton seed-stock and grazing regulation. Whilst incident light levels and the initial Si:N ratio were the lowest recorded in all FeAXs to date, there was only a small seed-stock of diatoms (less than 1% of biomass) and the main response to iron addition was by the picophytoplankton. A high rate of dilution of the fertilised patch relative to phytoplankton growth rate, the greater than expected depth of the surface mixed layer and microzooplankton grazing were all considered as factors that prevented significant biomass accumulation. In line with the limited response, the enhanced biological draw-down of pCO₂ was small and masked by a general increase in pCO₂ due to mixing with higher pCO₂ waters. The DMS precursor DMSP was kept in check through grazing activity and in contrast to most FeAX’s dissolved dimethylsulfide (DMS) concentration declined through the experiment. SAGE is an important low-end member in the range of responses to iron addition in FeAX’s. In the context of iron fertilisation as a geoengineering tool for atmospheric CO₂ removal, SAGE has clearly demonstrated that a significant proportion of the low iron ocean may not produce a phytoplankton bloom in response to iron addition.     

海洋酸化对浮游植物生理生态影响的研究进展

当前全球气候变化下的上层海洋变暖与酸化对以浮游植物为主的海洋生态系产生了重大影响，理解此背景下的海洋浮游植物生理生态响应，对我们理解和抑制全球气候变化具有重要意义。在全球大气二氧化碳分压（pCO₂）升高情景下，浮游植物通过光合作用、微生物循环等过程，通过不同功能群对海洋生源要素循环模式的改变，进而影响区域及全球海洋的生物地球化学循环。研究全球浮游植物对海洋酸化生理生态的响应使得我们对生物地球化学系统的认识更加全面、系统。     

Acidification at the Surface in the East Sea: A Coupled Climate-carbon Cycle Model Study

This modeling study investigates the impacts of increasing atmospheric CO₂ concentration on acidification in the East Sea. A historical simulation for the past three decades (1980 to 2010) was performed using the Hadley Centre Global Environmental Model (version 2), a coupled climate model with atmospheric, terrestrial and ocean cycles. As the atmospheric CO₂ concentration increased, acidification progressed in the surface waters of the marginal sea. The acidification was similar in magnitude to observations and models of acidification in the global ocean. However, in the global ocean, the acidification appears to be due to increased in-situ oceanic CO₂ uptake, whereas local processes had stronger effects in the East Sea. pH was lowered by surface warming and by the influx of water with higher dissolved inorganic carbon (DIC) from the northwestern Pacific. Due to the enhanced advection of DIC, the partial pressure of CO₂ increased faster than in the overlying air; consequently, the in-situ oceanic uptake of CO₂ decreased.     

The Interactive Effects of Elevated CO<Subscript>2</Subscript> and Ammonium Enrichment on the Physiological Performances of <Emphasis Type="Italic">Saccharina japonica</Emphasis> (Laminariales,Phaeophyta)

Environmental challenges such as ocean acidification and eutrophication influence the physiology of kelp species. We investigated their interactive effects on Saccharina japonica (Laminariales, Phaeophyta) under two pH conditions [Low, 7.50; High (control), 8.10] and three NH ₄ ⁺ concentrations (Low, 4; Medium, 60; High, 120 μM). The degree of variation of pH values in the culture medium and inhibition rate of photosynthetic oxygen evolution by acetazolamide were affected by pH treatments. Relative growth rates, carbon, nitrogen, and the C:N ratio in tissue samples were influenced by higher concentrations of NH ₄ ⁺ . Rates of photosynthetic oxygen evolution were enhanced under elevated CO₂ or NH ₄ ⁺ conditions, independently, but these two factors did not show an interactive effect. However, rates of NH ₄ ⁺ uptake were influenced by the interactive effect of increased CO₂ under elevated NH ₄ ⁺ treatment. Although ocean acidification and eutrophication states had an impact on physiological performance, chlorophyll fluorescence was not affected by those conditions. Our results indicated that the physiological reactions by this alga were influenced to some extent by a rise in the levels of CO₂ and NH ₄ ⁺ . Therefore, we expect that the biomass accumulation of S. japonica may well increase under future scenarios of ocean acidification and eutrophication.     

Spatial variability and temporal dynamics of surface water pCO2, ��O2/Ar and dimethylsulfide in the Ross Sea, Antarctica

We report results from two surveys of pCO₂, biological O₂ saturation (??O₂/Ar) and dimethylsulfide (DMS) in surface waters of the Ross Sea polynya. Measurements were made during early spring (November 2006-December 2006) and mid-summer (December 2005-January 2006) using ship-board membrane inlet mass spectrometry (MIMS) for high spatial resolution (i.e. sub-km) analysis. During the early spring survey, the polynya was in the initial stages of development and exhibited a rapid increase in open water area and phytoplankton biomass over the course of our ∼3 week occupation. We observed a rapid transition from a net heterotrophic ice-covered system (supersaturated pCO₂ and undersaturated O₂) to a high productivity regime associated with a Phaeocystis-dominated phytoplankton bloom. The timing of the early spring phytoplankton bloom was closely tied to increasing sea surface temperature across the polynya, as well as reduced wind speeds and ice cover, leading to enhanced vertical stratification. There was a strong correlation between pCO₂, ??O₂/Ar, DMS and chlorophyll a (Chl a) during the spring phytoplankton bloom, indicating a strong biological imprint on gas distributions. Box model calculations suggest that pCO₂ drawdown was largely attributable to net community production, while gas exchange and shoaling mixed layers also exerted a strong control on the re-equilibration of mixed layer ??₂ with the overlying atmosphere. DMS concentrations were closely coupled to Phaeocystis biomass across the early spring polynya, with maximum concentrations exceeding 100 nM.During the summer cruise, we sampled a large net autotrophic polynya, shortly after the seasonal peak in phytoplankton productivity. Both diatoms and Phaeocystis were abundant in the phytoplankton assemblages during this time. Minimum pCO₂ was less than 100 ppm, while ??O₂/Ar exceeded 30% in some regions. Mean DMS concentrations were ∼2-fold lower than during the spring, although the range of concentrations was similar between the two surveys. There was a significant correlation between pCO₂, ??O₂/Ar and Chl a across the summer polynya, but the strength of these correlations and the slope of O₂ vs. CO₂ relationship were significantly lower than during the early spring. Summertime DMS concentrations were not significantly correlated to phytoplankton biomass (Chl a), pCO₂ or ??O₂/Ar. In contrast to the early spring time, there were no clear temporal trends in summertime gas concentrations. Rather, small-scale spatial variability, likely resulting from mixing and localized sea-ice melt, was clearly evident in surface gas distributions across the polynya. Analysis of length-scale dependent variability demonstrated that much of the spatial variance in surface water gases occurred at scales of <20 km, suggesting that high resolution analysis is needed to fully capture biogeochemical heterogeneity in this system.     

Seasonal and inter-annual variability of air–sea CO2 fluxes and seawater carbonate chemistry in the Southern North Sea

A 3D coupled biogeochemical–hydrodynamic model (MIRO-CO₂&CO) is implemented in the English Channel (ECH) and the Southern Bight of the North Sea (SBNS) to estimate the present-day spatio-temporal distribution of air–sea CO₂ fluxes, surface water partial pressure of CO₂ (pCO₂) and other components of the carbonate system (pH, saturation state of calcite (Ω_ca) and of aragonite (Ω_ar)), and the main drivers of their variability. Over the 1994–2004 period, air–sea CO₂ fluxes show significant inter-annual variability, with oscillations between net annual CO₂ sinks and sources. The inter-annual variability of air–sea CO₂ fluxes simulated in the SBNS is controlled primarily by river loads and changes of biological activities (net autotrophy in spring and early summer, and net heterotrophy in winter and autumn), while in areas less influenced by river inputs such as the ECH, the inter-annual variations of air–sea CO₂ fluxes are mainly due to changes in sea surface temperature and in near-surface wind strength and direction. In the ECH, the decrease of pH, of Ω_ca and of Ω_ar follows the one expected from the increase of atmospheric CO₂ (ocean acidification), but the decrease of these quantities in the SBNS during the considered time period is faster than the one expected from ocean acidification alone. This seems to be related to a general pattern of decreasing nutrient river loads and net ecosystem production (NEP) in the SBNS. Annually, the combined effect of carbon and nutrient loads leads to an increase of the sink of CO₂ in the ECH and the SBNS, but the impact of the river loads varies spatially and is stronger in river plumes and nearshore waters than in offshore waters. The impact of organic and inorganic carbon (C) inputs is mainly confined to the coast and generates a source of CO₂ to the atmosphere and low pH, of Ω_ca and of Ω_ar values in estuarine plumes, while the impact of nutrient loads, highest than the effect of C inputs in coastal nearshore waters, also propagates offshore and, by stimulating primary production, drives a sink of atmospheric CO₂ and higher values of pH, of Ω_ca and of Ω_ar.     

Doubled CO2 impact on subarctic marine carbon cycle: a case study at Ocean Station P

Along with meteorological observations, complementary and systematic oceanographic observations of various physical, biological and chemical parameters have been made at Ocean Station P (OSP) (50°N, 145°W) since the early 1950s. These decadal time scale data have contributed to a better understanding of the physical, biological and chemical processes in the surface layer of the northeastern subarctic region of the Pacific Ocean. These data have demonstrated the importance of the North Pacific in the global carbon cycle and, in particular, the role of biological/chemical processes in the net exchange of CO₂ across the air–sea interface. Although we do not fully comprehend how climatic variations influence marine communities or marine biogeochemistry, previous studies have provided some basic understanding of the mechanisms controlling the seasonal and inter-annual variations of biological and chemical parameters (such as phytoplankton, bacteria, nitrate/ammonium concentration) at OSP, and how they affect the carbon cycling in the subarctic North Pacific. In this study, we investigate how these mechanisms might alter the seasonal variations of these parameters at OSP under a 2XCO₂ condition. We examine these influences using a new biological model calibrated by the climatological data from OSP. For the 2XCO₂ simulation, the biological model is driven off line (i.e., no feedback to the ocean/atmospheric model components) by the climatology plus 2XCO₂−1XCO₂ outputs from a global surface ocean model and the Canadian GCM. Under the 2XCO₂ condition, the upper layer ocean shows an increase in the entrainment rate at the bottom of the mixed layer for OSP during the late autumn and winter seasons, resulting in an increase in the f-ratio. Although there is an overall increase in the primary production (PP) by 3–18%, a decrease in the biomass of small phytoplankton and microzooplankton (due to mesozooplankton grazing) lowers the concentration of dissolved organic matter (DOM) by 4–25%. The model also predicts a significant increase in the concentrations of nitrate and ammonium, and in bacterial production during July and August. Doubling of the atmospheric CO₂ from 330 to 660 ppm forces the marine pCO₂ to increase by about 63%, much of which is driven by an increased flux of CO₂ from the atmosphere to the oceans.     

海洋酸化对海水青鳉胚胎骨骼发育的影响

本文在实验室模拟近期海洋酸化水平,对海洋酸化对海水青鳉鱼(Oryzia melastigma)胚胎骨骼发育的影响进行了初步研究。实验中,通过往实验水体中充入一定浓度CO2气体酸化海水。对照组CO2分压为450×10-6,两个处理组CO2浓度分别为1 160×10-6和1 783×10-6,对应的水体pH值分别为8.14,7.85和7.67。将海水青鳉鱼受精卵放入实验水体中至仔鱼孵化出膜,对初孵仔鱼经骨骼染色、显微拍照,挑取了仔鱼头部、躯干及尾部骨骼染色清晰的28个骨骼参数的长度进行了显微软件测量及数据统计分析。结果发现,酸化处理对实验鱼所测量的骨骼长度影响均不显著。因此推测,未来100~200年间海洋酸化对海水青鳉鱼的胚胎及初孵仔鱼的骨骼发育没有显著影响。     

Effects of seawater acidification by ocean CO<Subscript>2</Subscript> sequestration on bathypelagic prokaryote activities

We investigated the effects of seawater acidification induced by ocean CO₂ sequestration on bathypelagic prokaryotes. We simulated acidification conditions by bubbling high-CO₂ air or adding chemical buffer solutions to seawater samples in order to examine changes in total cell counts, heterotrophic production rate, direct viable cell count, and relative abundance of Bacteria and Archaea. Considerable suppression of prokaryotic activities was observed at pH 7.0 or lower, especially in samples enriched with organic matter. The relative abundance of Archaea increased with increasing CO₂ concentration. We found that seawater acidification can potentially alter heterotrophic activities and community structure of bathypelagic prokaryotes.     

CO2 outgassing off central Chile (31–30°S) and northern Chile (24–23°S) during austral summer 1997: the effect of wind intensity on the upwelling and ventilation of CO2-rich waters

The distribution of pH and alkalinity has been used to calculate the distribution of total inorganic carbon (TC) and fugacity of carbon dioxide (fCO₂) in the upper 200 m of the water column in coastal upwelling areas off northern Chile (23–24°S, near Antofagasta) and central Chile (30–31°S, near Coquimbo) during austral summer 1997. In these upwelling areas, colder surface waters were oxygen poor and strongly CO₂ supersaturated (100% near Antofagasta and 200% near Coquimbo), although below the pycnocline the CO₂ supersaturation invariably exceeded 200% in both areas. The larger surface CO₂ supersaturation and outgassing at 30°S were associated with stronger winds that promoted the upwelling of denser water (richer in CO₂) as well as a higher air–sea CO₂ transfer velocity. The consistent decrease in intensity of the southerly winds (as derived from NSCAT scatterometer data) from 30–31°S to 23–24°S suggests a corresponding decline in the intensity of the CO₂ outgassing due to upwelling. Additionally, we suggest here that the intensity of the local upwelling forcing (i.e. alongshore–equatorward winds) plays a role in determining the water mass composition and phytoplankton biomass of the coastal waters. Thus, while deep upwelling of salty and cold water resulted in high fCO₂ (up to 1000 μatm) and very low phytoplankton biomass (chlorophyll a concentration lower than 0.5 mg m⁻³), the shallow upwelling of less salty (e.g. salinity <34.5) and less CO₂-supersaturated water resulted in a higher phytoplankton biomass, which further reduced surface water fCO₂ by photosynthesis.     

Effects of CO<Subscript>2</Subscript> Enrichment on Marine Phytoplankton

Rising atmospheric CO₂ and deliberate CO₂ sequestration in the ocean change seawater carbonate chemistry in a similar way, lowering seawater pH, carbonate ion concentration and carbonate saturation state and increasing dissolved CO₂ concentration. These changes affect marine plankton in various ways. On the organismal level, a moderate increase in CO₂ facilitates photosynthetic carbon fixation of some phytoplankton groups. It also enhances the release of dissolved carbohydrates, most notably during the decline of nutrient-limited phytoplankton blooms. A decrease in the carbonate saturation state represses biogenic calcification of the predominant marine calcifying organisms, foraminifera and coccolithophorids. On the ecosystem level these responses influence phytoplankton species composition and succession, favouring algal species which predominantly rely on CO₂ utilization. Increased phytoplankton exudation promotes particle aggregation and marine snow formation, enhancing the vertical flux of biogenic material. A decrease in calcification may affect the competitive advantage of calcifying organisms, with possible impacts on their distribution and abundance. On the biogeochemical level, biological responses to CO₂ enrichment and the related changes in carbonate chemistry can strongly alter the cycling of carbon and other bio-active elements in the ocean. Both decreasing calcification and enhanced carbon overproduction due to release of extracellular carbohydrates have the potential to increase the CO₂ storage capacity of the ocean. Although the significance of such biological responses to CO₂ enrichment becomes increasingly evident, our ability to make reliable predictions of their future developments and to quantify their potential ecological and biogeochemical impacts is still in its infancy. This revised version was published online in July 2006 with corrections to the Cover Date.     

Global change ecotoxicology: Identification of early life history bottlenecks in marine invertebrates,variable species responses and variable experimental approaches

Climate change is a threat to marine biota because increased atmospheric CO₂ is causing ocean warming, acidification, hypercapnia and decreased carbonate saturation. These stressors have toxic effects on invertebrate development. The persistence and success of populations requires all ontogenetic stages be completed successfully and, due to their sensitivity to environmental stressors, developmental stages may be a population bottleneck in a changing ocean. Global change ecotoxicology is being used to identify the marine invertebrate developmental stages vulnerable to climate change. This overview of research, and the methodologies used, shows that most studies focus on acidification, with few studies on ocean warming, despite a long history of research on developmental thermotolerance. The interactive effects of stressors are poorly studied. Experimental approaches differ among studies. Fertilization in many species exhibits a broad tolerance to warming and/or acidification, although different methodologies confound inter-study comparisons. Early development is susceptible to warming and most calcifying larvae are sensitive to acidification/increased pCO₂. In multistressor studies moderate warming diminishes the negative impact of acidification on calcification in some species. Development of non-calcifying larvae appears resilient to near-future ocean change. Although differences in species sensitivities to ocean change stressors undoubtedly reflect different tolerance levels, inconsistent handling of gametes, embryos and larvae probably influences different research outcomes. Due to the integrative ‘developmental domino effect’, life history responses will be influenced by the ontogenetic stage at which experimental incubations are initiated. Exposure to climate change stressors from early development (fertilization where possible) in multistressor experiments is needed to identify ontogenetic sensitivities and this will be facilitated by more consistent methodologies.     

Strong CO2 outgassing from high nutrient low chlorophyll coastal waters off central Chile (30°S): The role of dissolved iron

Carbonate system parameters (pH and alkalinity) were used to estimate the coastal water CO₂ fluxes off central Chile (30°S) during September 2007. Coastal waters rich in nitrate and silicate were strongly CO₂ supersaturated and normally poor in chlorophyll a. MODIS satellite chlorophyll a data suggest that phytoplankton biomass remained particularly low during September 2007 although coastal waters were highly fertilized with nitrate and silicate. The phytoplankton gross primary productivity in macronutrient-rich waters was very low with the exception of shallow waters (e.g. within or near bays). Several iron-enrichment bottle experiments show that fCO₂ rapidly decreases during iron-enrichment treatments compared to controls. This suggests that iron limitation of phytoplankton growth (mainly diatoms) plays a role in maintaining high-CO₂ outgassing by preventing rapid interception of upwelled CO₂.     

Changes in deep-water CO2 concentrations over the last several decades determined from discrete pCO2measurements

Detection and attribution of hydrographic and biogeochemical changes in the deep ocean are challenging due to the small magnitude of their signals and to limitations in the accuracy of available data. However, there are indications that anthropogenic and climate change signals are starting to manifest at depth. The deep ocean below 2000 m comprises about 50% of the total ocean volume, and changes in the deep ocean should be followed over time to accurately assess the partitioning of anthropogenic carbon dioxide (CO₂) between the ocean, terrestrial biosphere, and atmosphere. Here we determine the changes in the interior deep-water inorganic carbon content by a novel means that uses the partial pressure of CO₂ measured at 20 °C, pCO₂(20), along three meridional transects in the Atlantic and Pacific oceans. These changes are measured on decadal time scales using observations from the World Ocean Circulation Experiment (WOCE)/World Hydrographic Program (WHP) of the 1980s and 1990s and the CLIVAR/CO₂ Repeat Hydrography Program of the past decade. The pCO₂(20) values show a consistent increase in deep water over the time period. Changes in total dissolved inorganic carbon (DIC) content in the deep interior are not significant or consistent, as most of the signal is below the level of analytical uncertainty. Using an approximate relationship between pCO₂(20) and DIC change, we infer DIC changes that are at the margin of detectability. However, when integrated on the basin scale, the increases range from 8–40% of the total specific water column changes over the past several decades. Patterns in chlorofluorocarbons (CFCs), along with output from an ocean model, suggest that the changes in pCO₂(20) and DIC are of anthropogenic origin.     

Linking phytoplankton community size composition with temperature, plankton food web structure and sea-air CO2 flux

Data collected at open water stations (depth>400 m) in all major ocean basins in 2006-2008 are used to examine the relationship between the size structure of the phytoplankton community (determined by size fractionated chlorophyll filtration), temperature and inorganic nutrient availability. A significant relationship (p<0.0005) was found between community size structure and temperature, with the importance of large cells in the community decreasing with increase in temperature. Although weaker than the temperature relationship, significant relationships were also noted between community cell size and DIN (nitrate, nitrite and ammonium: p=0.034) and phosphate (p=0.031) concentrations. When the data were divided into two groups of equal size, representing the samples with the highest and lowest DIN/phosphate concentrations, respectively, no difference could be identified between the slopes of the lines representing the relationship between size structure and temperature. There was, however, a difference in the intercepts between the two groups. If the relationship between size and temperature was only a response to nutrient availability, we would expect that the response would be the strongest in the groups with the lowest nutrient concentrations. These results suggest that, in addition to a nutrient effect, temperature may also directly influence the size structure of phytoplankton communities. The size structure of the phytoplankton community in this study correlated to the magnitude of primary production, export production (determined after Laws et al., 2000) and integrated water column chlorophyll. Significant relationships were also found between mesozooplankton production (determined using the proxy of calanoid+cyclopoid nauplii abundance as a percentage of the total number of these copepods) and both temperature and phytoplankton size, with production being the lowest in the warmest waters where phytoplankton were the smallest. In the North Atlantic, export production and community size structure appear to be related to ocean uptake of CO₂ from the atmosphere. The reported results suggest that ocean warming may directly alter plankton community structure. This, in turn, may alter the structure of marine food webs and impact the performance of the open ocean as a natural carbon sink.     

The contribution of atmospheric acid deposition to ocean acidification in the subtropical North Atlantic Ocean

The absorption of anthropogenic CO₂ and atmospheric deposition of acidity can both contribute to the acidification of the global ocean. Rainfall pH measurements and chemical compositions monitored on the island of Bermuda since 1980, and a long-term seawater CO₂ time-series (1983–2005) in the subtropical North Atlantic Ocean near Bermuda were used to evaluate the influence of acidic deposition on the acidification of oligotrophic waters of the North Atlantic Ocean and coastal waters of the coral reef ecosystem of Bermuda. Since the early 1980's, the average annual wet deposition of acidity at Bermuda was 15 ± 14 mmol m^− 2 year^− 1, while surface seawater pH decreased by 0.0017 ± 0.0001 pH units each year. The gradual acidification of subtropical gyre waters was primarily due to uptake of anthropogenic CO₂. We estimate that direct atmospheric acid deposition contributed 2% to the acidification of surface waters in the subtropical North Atlantic Ocean, although this value likely represents an upper limit. Acidifying deposition had negligible influence on seawater CO₂ chemistry of the Bermuda coral reef, with no evident impact on hard coral calcification.