Contrasting accumulation biokinetics and distribution of Am, Co, Cs, Mn and Zn during the whole development time of the eggs of the common cuttlefish, Sepia officinalis

Cuttlefish eggs were exposed to ²⁴¹Am, Co, Cs, Mn and Zn for different periods of time during the 50-d of the embryonic development at 17 °C. Exposures were carried out using background dissolved concentrations of the metals, using the corresponding γ-emitting radiotracers (²⁴¹Am, ⁵⁷Co, ¹³⁴Cs, ⁵⁴Mn and ⁶⁵Zn). Eggs were then placed in non-contaminating conditions. Experiments allowed assessing 1) the uptake and depuration kinetics of the selected elements and 2) their distribution among the different egg compartments (i.e. eggshell, vitellus, peri-vitelline fluid and embryo). ²⁴¹Am, Co and Zn were accumulated continuously by the eggs all along the development time, whereas Mn reached saturation after one month of exposure. Interestingly, the uptake kinetics of Cs tightly followed the weight variation of the eggs, mainly because of water influx/outflux. During the first month of the embryonic life, ²⁴¹Am, Co, Cs, Mn and Zn remained associated with the eggshell, indicating that the latter acted as an efficient shield against their penetration. Nevertheless, from this time onwards, Co, Cs, Mn and Zn accumulated more or less efficiently in the embryo according to the following order: Cs > Zn > Mn > Co. ²⁴¹Am was the only element tested that did not cross the eggshell all along the exposure time. The depuration kinetics revealed that the retention capacity of the eggs varied during the embryonic life. The contrasting accumulation biokinetics are discussed in terms of chemical and biological processes occurring during the cuttlefish egg development.     

Temperature and pCO2 effect on the bioaccumulation of radionuclides and trace elements in the eggs of the common cuttlefish,Sepia officinalis

The increasing release of CO₂ by human activities leads to ocean acidification and global warming. Both those consequences (i.e., increase in seawater pCO₂ and temperature) may drastically affect the physiology of marine organisms. The effects of low pH and elevated temperature on the bioaccumulation of radionuclides (²⁴¹Am, ¹³⁴Cs) and trace elements (⁶⁰Co, ⁵⁴Mn or ⁷⁵Se) were studied during the embryonic development of the common cuttlefish Sepia officinalis. The lowered accumulation of essential ⁶⁰Co and ⁵⁴Mn with decreasing pH was larger at 16 °C than at 19 °C. Se was not detected in the embryo whereas it penetrated through the eggshell, suggesting that an alternative pathway ensures the supply of this essential metal for the embryo. ²⁴¹Am was totally retained by the eggshell irrespective of pH and temperature. Finally, the amount of Cs found in the peri-vitelline fluid increased with decreasing pH likely because of an enhanced swelling of the cuttlefish egg under elevated CO₂.     

Adsorption of Radionuclides (134Cs, 85Sr, 226Ra, 241Am) by Extracted Biomasses of Cyanobacteria (Nostoc Carneum, N. Insulare, Oscillatoria Geminata and Spirulina Laxis-Sima) and Phaeophyceae (Laminaria Digitata and L. Japonica; Waste Products from Alginate Production) at Different pH

The extracted biomasses of four cyanobacteria (Nostoc carneum, Nostoc insulare, Oscillatoria geminata, and Spirulina laxissima) grown in axenic mass cultures, and of four samples of Laminaria obtained from different locations (L. digitata I and II, France; L. japonica I and II, China; all waste products from alginate production) were tested for their ability to adsorb four radionuclides (¹³⁴Cs, ⁸⁵Sr, ²²⁶Ra, and ²⁴¹Am) under different pH regimes. In addition, two of the cyanobacterial biomasses (N. carneum. and O. geminata) and the four Laminaria biomasses were phosphorylated before being tested as radionuclide adsorbers. The non-phosphorylated cyanobacterial biomasses showed very low adsorption of ¹³⁴Cs but substantially higher removal of ⁸⁵Sr and ²²⁶Ra, which increased with increasing pH. ²⁴¹Am was almost completely removed from the solution at low pH, but less at higher pH. After phosphorylation, removal of ¹³⁴Cs, ⁸⁵Sr and ²²⁶Ra by the cyanobacterial biomasses was improved, particularly at lower pH, but there was almost no adsorption of ²⁴¹Am. The non-phosphorylated Laminaria biomasses showed good removal of ¹³⁴Cs and very good adsorption of ⁸⁵Sr and ²²⁶Ra. Removal of ²⁴¹Am was high at low pH but decreased with increasing pH. After phosphorylation, adsorption of ¹³⁴Cs by Laminaria samples was slightly improved; removal of ⁸⁵Sr and ²²⁶Ra was increased at low pH with a tendency towards decrease in adsorption with increasing pH; but almost no ²⁴¹Am was adsorbed. The origin of the cyanobacterial and Laminaria materials appeared to have little effect on the adsorption of the radionuclides.     

Long-term development of the radionuclide exposure of murine rodent populations in Belarus after the Chernobyl accident

As a determinant of the associated health risks, the behavior of radionuclides in natural ecosystems needs to be better understood. Therefore, the activity concentration of various long-lived radionuclides released due to the Chernobyl accident, and the corresponding contributions to the whole-body dose rate, was studied as a function of time in mammalian indicator species inhabiting the natural forest ecosystems of Belarus, the bank vole (Clethrionomys glareolus) and the yellow-necked mouse (Apodemus flavicollus). The activity concentrations of ¹³⁷Cs, ¹³⁴Cs, ⁹⁰Sr, ²³⁸Pu, ^239,240Pu, ²⁴¹Pu and ²⁴¹Am in soil and in animals were measured at five monitoring sites with different ground deposition of radionuclides at different distances from the destroyed reactor. The observed temporal pattern of the radionuclide activity concentration in the studied animal populations reflects the changes in biological availability of these isotopes for biota, mostly due to fuel particle destruction and appearance of dissolved and exchangeable forms of radionuclides. The time course of ^134+137Cs activity concentrations in animal populations appeared as a sequence of increase, peak and decrease. Maximal levels of radiocesium occurred 1–2 years after deposition, followed by an exponential decrease. Concentrations of incorporated ⁹⁰Sr increased up to the tenth year after deposition. The activity concentrations of transuranic elements (²³⁸Pu, ^239,240Pu, ²⁴¹Pu and ²⁴¹Am) were much lower than those of the other radionuclides, in the studied animals. A considerable activity of ²⁴¹Am in animals from areas with high levels of contamination was firstly detected 5 years after deposition, it increased up to the tenth year and is expected to increase further in the future. Maximal values of the whole-body absorbed dose rates occurred during the year of deposition, followed by a decrease in the subsequent period. Generally, this decrease was monotonic, mainly determined by the decrease of the external γ-ray dose rate, but there were exceptions due to the delayed maximum of internal exposure. The inter-individual distributions of radionuclide concentrations and lifetime whole-body absorbed doses were asymmetric and close to log-normal, including concentrations and doses considerably higher than the population mean values.     

Vertical Distribution and Estimated Doses from Artificial Radionuclides in Soil Samples around the Chernobyl Nuclear Power Plant and the Semipalatinsk Nuclear Testing Site

For the current on-site evaluation of the environmental contamination and contributory external exposure after the accident at the Chernobyl Nuclear Power Plant (CNPP) and the nuclear tests at the Semipalatinsk Nuclear Testing Site (SNTS), the concentrations of artificial radionuclides in soil samples from each area were analyzed by gamma spectrometry. Four artificial radionuclides (²⁴¹Am, ¹³⁴Cs, ¹³⁷Cs, and ⁶⁰Co) were detected in surface soil around CNPP, whereas seven artificial radionuclides (²⁴¹Am, ⁵⁷Co, ¹³⁷Cs, ⁹⁵Zr, ⁹⁵Nb, ⁵⁸Co, and ⁶⁰Co) were detected in surface soil around SNTS. Effective doses around CNPP were over the public dose limit of 1 mSv/y (International Commission on Radiological Protection, 1991). These levels in a contaminated area 12 km from Unit 4 were high, whereas levels in a decontaminated area 12 km from Unit 4 and another contaminated area 15 km from Unit 4 were comparatively low. On the other hand, the effective doses around SNTS were below the public dose limit. These findings suggest that the environmental contamination and effective doses on the ground definitely decrease with decontamination such as removing surface soil, although the effective doses of the sampling points around CNPP in the present study were all over the public dose limit. Thus, the remediation of soil as a countermeasure could be an extremely effective method not only for areas around CNPP and SNTS but also for areas around the Fukushima Dai-ichi Nuclear Power Plant (FNPP), and external exposure levels will be certainly reduced. Long-term follow-up of environmental monitoring around CNPP, SNTS, and FNPP, as well as evaluation of the health effects in the population residing around these areas, could contribute to radiation safety and reduce unnecessary exposure to the public.     

Distribution and tissue retention of cesium-134 and cobalt-6o in the nile catfish clarias lazera (cuv. & val.)

The Nile catfish, Clarias lazera was found to concentrate radioactive cesium-134 and cobalt-6o from the aquatic environment. For cesium-134 the rate of uptake increased by increase of exposure time, while for cobalt-6o maximum uptake occurred after one day of exposure. The corresponding concentration factors at maximum uptake levels were 0.37 and 0.36 for cesium and cobalt respectively.The internal distribution of these radionuclides in the different tissues and organs of the fish due to uptake from the aquatic environment followed the decreasing order:For ¹³⁴Cs: muscle, bone, gills, stomach, kidneys, intestine and liver.For ⁶⁰Co: bone, muscle, gills, intestine, kidneys, stomach and liver.The internal distribution due to ingestion of these radionuclides followed nearly the same order as was found in case of uptake from the aquatic environment.     

Solubility of airborne radioactive fuel particles from the Chernobyl reactor and implication to dose

Airborne particles of nuclear fuel from the Chernobyl reactor that had been collected on air filters and stored, were characterised using in vitro dissolution tests to assess effective doses after their inhalation. As solvent, the Gamble biological fluid was used to simulate lung fluid. The solubility of the measured radionuclides decreased in the order ¹³⁷Cs>⁹⁰Sr>>²⁴¹Am^239+240Pu in the simulated lung fluid. The dissolution rate constant of e.g. ^239+249Pu ranged from 0.72 to 5.4×10^–6 g·cm^–2 d^–1 and decreased (for all nuclides) with increasing particle size as predicted from theoretical considerations. Considering the inhalation dose, decreasing dose with size and increasing doses with lower solubility may partly counterbalance each other for ¹³⁷Cs and ⁹⁰Sr. On the other hand, for ²³⁹Pu and ²⁴¹Am larger particles and associated lower solubility both change the resulting dose in the same direction towards lower values. The comparison of the experimentally determined dose coefficients with ICRP values indicates that nuclear fuel particles closely resemble type M material characteristics for ¹³⁷Cs and ⁹⁰Sr and type S material characteristics for ²³⁹Pu and ²⁴¹Am.     

241Am dating of lake sediments

²⁴¹Am derived from decay of fallout ²⁴¹Pu is now frequently detected in analyses of lake sediments by low-background gamma assay, and offers an alternative to weapons test ¹³⁷Cs in dating recent sediments at those sites where the ¹³⁷Cs record has been degraded by post-depositional mobility or obliterated by Chernobyl fallout. Calculations of the in-growth of ²⁴¹Am from ²⁴¹Pu indicate a nominal distribution broadly similar to that of ¹³⁷Cs, with the maximum ²⁴¹Am activity occuring in fallout dating from 1963. Results from a number of sites suggest that ²⁴¹Am is significantly less mobile in lake sediments than ¹³⁷Cs, and that its distribution in cores reflects more closely the fallout record. Since further decay of existing weapons debris will increase ²⁴¹Am concentrations by about 24% over the next 40 years, ²⁴¹Am is likely to play an increasingly important role in assessing the validity of ²¹⁰Pb dates at sites with varying sediment accumulation rates.     

Age-dependent accumulation of <Superscript>137</Superscript>Cs by pike <Emphasis Type="Italic">Esox lucius</Emphasis> in the Yenisei River

Age-dependent accumulation of ¹³⁷Cs in the muscles and bodies of the pike Esox lucius (aged two to seven years) inhabiting a section of the Yenisei River polluted with artificial radionuclides has been studied. The content of ¹³⁷Cs in muscles varied from 0.5 to 7.0 Bq/kg of fresh weight. The maximum content of the radionuclide has been found in juveniles. The content of ¹³⁷Cs in pike muscles and body decreased considerably with age. The high content of ¹³⁷Cs in the muscles of juveniles is probably a consequence of their higher intensity of feeding as compared to older individuals, which is due to the intense growth of juveniles.     

Effect of biotite,zeolite, heavy clay,bentonite and apatite on the uptake of radiocesium by grass from peat soil

Biotite is a potassium rich mineral, which is used as a fertilizer in organic farming and as a soil amendment in conventional farming. Its ability to reduce ¹³⁴Cs uptake by ryegrass from peat soil was studied in pot experiments and compared with zeolite, heavy clay, bentonite and apatite. In addition, the long-term effect of biotite on ¹³⁷Cs uptake from peat soil was studied in the peat field. In the pot experiments in the first cut of ryegrass, the minerals decreased ¹³⁴Cs uptake by plants in the following order: zeolite > heavy clay > bentonite > biotite > apatite. Apatite did not have any effect on the plant ¹³⁴Cs level. In the later cuts, the uptake of ¹³⁴Cs from biotite-treated soil decreased further while that from soils treated with other minerals remained unchanged or even increased. In general, ¹³⁴Cs uptake by plants decreased with increasing mineral level. The decrease of ¹³⁴Cs uptake became more efficient, especially at the early growth stage, by mixing small amounts of zeolite in biotite. The results of the field experiment indicated the long-term effect of biotite on reducing ¹³⁴Cs uptake by plants. Biotite application rate was 30 t ha-1. The five-year mean of the plant/soil concentration ratio of ¹³⁷Cs was 0.05 for biotite-treated soil, in contrast to 0.14 for the control soil. On the whole, biotite reduced considerably the ¹³⁷Cs level of plants on peat soil and this effect was long-lasting. For an effective reduction of plant radiocesium a great quantity of biotite is needed and therefore it is most suitable for greenhouse cultivation where contaminated slightly decomposed peat is used as a growing medium.     

Radioecological indexes of fallout measurements from the Fukushima nuclear accident

Fallout from the Fukushima nuclear accident has been monitored for about 1 month in Thessaloniki, Northern Greece. Three different radionuclides, one short-lived, one relatively long-lived and one long-lived fission product were identified in air, grass and milk samples. The ¹³¹I, ¹³⁷Cs and ¹³⁴Cs activity concentrations in air reached 497, 145 and 126 μBq m⁻³, respectively on 4 April, 2011. These radionuclides are of particular concern regarding their transfer from the environment to population through the ingestion pathways for the assessment of the Fukushima accident consequences. Radioecological indexes (eco-indexes) of fallout measurements in the air–grass–cow-milk–man pathway for ¹³¹I were determined, as they are related to radiological impact of the Fukushima derived radionuclides on the public and environment.     

Testicular steroidogenesis is not altered by 137 cesium Chernobyl fallout,following in utero or post-natal chronic exposure

The testis is especially sensitive to pollutants, including radionuclides. Following the Chernobyl nuclear power plant accident, several of these radionuclides were emitted and spread in the environment. Subsequently, children presented some disruptions of the endocrine system. To determine whether these disruptions were due to 137 cesium (¹³⁷Cs) exposure, the effects of chronic contamination with low doses of ¹³⁷Cs in utero or from birth on testicular steroidogenesis in rats were studied. Contamination was continued for 9 months. No modification was observed in circulating level of hormones (17β-estradiol, testosterone, follicle-stimulating hormone, luteinizing hormone) following in utero or post-natal contamination. Expression of several genes involved in testicular steroidogenesis was affected (cyp19a1, fxr, sf-1), without modification of protein expression or activity. Our results suggest that growing organisms may be affected at the molecular level by ¹³⁷Cs contamination at this post-accidental dose.     

Interaction of Cd and Zn during uptake and loss in the polychaete Capitella capitata: Whole body and subcellular perspectives

The interaction between Cd and Zn in aquatic organisms is known to be highly variable. The purpose of this study was to use a subcellular compartmentalization approach to examine Cd and Zn interactions in the deposit-feeding polychaete Capitella capitata (sp. I). Laboratory-reared C. capitata were co-exposed to Cd (background or 50 μg Cd l^− 1) and Zn (background or 86 μg Zn l^− 1) with ¹⁰⁹Cd and ⁶⁵Zn as radiotracers for 1 week. After the 1-week uptake period, subsets of worms were allowed to depurate accumulated metals for an additional 1 week. Worms from both phases (uptake and loss) were then subjected to subcellular fractionation to determine the compartmentalization of metals as metal-sensitive fractions [MSF — organelles and heat-denaturable proteins (HDP)] and biologically detoxified metals [BDM — heat-stable proteins (HSP) and metal-rich granules (MRG)]. Uptake and loss of Cd and Zn in C. capitata at the whole body level were similar at bkgd-Cd/bkgd-Zn, with worms depurating the majority of accumulated metal (∼ 75% Cd and ∼ 64% Zn). When exposure of Zn or Cd was increased (bkgd-Cd/86-Zn; bkgd-Zn/50-Cd), uptake of background levels of Cd or Zn, respectively, was suppressed by ∼ 50%. These accumulated metals, however, were retained during the loss phase resulting in ∼ 40-50% greater Cd and Zn whole body tissue burdens than those of bkgd-Cd/bkgd-Zn worms. Beyond exhibiting similar patterns of uptake and loss at the whole body level, Cd and Zn behaved similarly at the subcellular level. Under background levels (bkgd-Cd/bkgd-Zn), after uptake, worms partitioned a majority of Cd (∼ 65%) and Zn (∼ 55%) to the HSP and organelles fractions. The HDP and MRG fractions contained less than ∼ 6% of both metals. Following depuration, at bkgd-Cd/bkgd-Zn, Cd and Zn were lost from all subcellular fractions; loss from HSP was the greatest contributor to whole body loss. When exposed to elevated concentrations of Zn or Cd, the suppression in uptake of bkgd-Cd or bkgd-Zn observed in whole body uptake was largely due to suppressions in the storage of Cd and Zn to HSP. These results suggest that Cd-Zn interactions reduce partitioning of both Cd and Zn to HSP, indicating that metal-binding proteins such as metallothioneins play a key role in these interactions.     

Thermal tolerance of Litopenaeus vannamei (Crustacea: Penaeidae) acclimated to four temperatures

Critical thermal minima (CTMin) and maxima (CTMax) values were determined for the Pacific white shrimp Litopenaeus vannamei post-larvae and juveniles at four different acclimation temperatures (15, 20, 25, and 30 °C). The CTMin of shrimp at these acclimation temperatures were 7.82, 8.95, 9.80, and 10.96 °C for post-larvae and 7.50, 8.20, 10.20, and 10.80 °C for juveniles, respectively, at 1 °C h⁻¹ cooling rate. The CTMax values were 35.65, 38.13, 39.91, and 42.00 °C for post-larvae and 35.94, 38.65, 40.30, and 42.20 °C for juveniles at the respective acclimation temperatures. Both acclimation temperature and size of the shrimp affected CTMin values of L. vannamei (P<0.01). Overall, juveniles displayed significantly lower CTMin values than the post-larvae (P<0.0001). However, the CTMax response by post-larvae and juveniles were not significantly different from each other and no interaction was determined between the acclimation temperature and development stage (P>0.01). The area of the thermal tolerance polygon over four acclimation temperatures (15, 20, 25, and 30 °C) for the post-larvae of L. vannamei was calculated to be 434.94 °C². The acclimation response ratio (ARR) values were high ranging from 0.35 to 0.44 for both post-larvae and juveniles. L. vannamei appears to be more sensitive to low temperatures than other penaeid species and its cold tolerance zone ranged from 7.5 to 11 °C. In successful aquaculture temperature must never fall below 12 °C to prevent mortalities. Upper thermal tolerance is less of a problem as in most subtropical regions maximum water temperature rarely exceeds 34 °C, but care should be given if shallow ponds with low water renewal rate are being used.     

Estimated Dietary Intake of Radionuclides and Health Risks for the Citizens of Fukushima City,Tokyo, and Osaka after the 2011 Nuclear Accident

The radionuclides released from the Fukushima Daiichi nuclear power plant in 2011 pose a health risk. In this study, we estimated the 1st-year average doses resulting from the intake of iodine 131 (¹³¹I) and cesium 134 and 137 (¹³⁴Cs and ¹³⁷Cs) in drinking water and food ingested by citizens of Fukushima City (∼50 km from the nuclear power plant; outside the evacuation zone), Tokyo (∼230 km), and Osaka (∼580 km) after the accident. For citizens in Fukushima City, we considered two scenarios: Case 1, citizens consumed vegetables bought from markets; Case 2, citizens consumed vegetables grown locally (conservative scenario). The estimated effective doses of ¹³⁴Cs and ¹³⁷Cs agreed well with those estimated through market basket and food-duplicate surveys. The average thyroid equivalent doses due to ingestion of ¹³¹I for adults were 840 µSv (Case 1) and 2700 µSv (Case 2) in Fukushima City, 370 µSv in Tokyo, and 16 µSv in Osaka. The average effective doses due to ¹³⁴Cs and ¹³⁷Cs were 19, 120, 6.1, and 1.9 µSv, respectively. The doses estimated in this study were much lower than values reported by the World Health Organization and the United Nations Scientific Committee on the Effects of Atomic Radiation, whose assessments lacked validation and full consideration of regional trade in foods, highlighting the importance of including regional trade. The 95th percentile effective doses were 2–3 times the average values. Lifetime attributable risks (LARs) of thyroid cancers due to ingestion were 2.3–39×10⁻⁶ (Case 1) and 10–98×10⁻⁶ (Case 2) in Fukushima City, 0.95–14×10⁻⁶ in Tokyo, and 0.11–1.3×10⁻⁶ in Osaka. The contributions of LARs of thyroid cancers due to ingestion were 7.5%–12% of all exposure (Case 1) and 12%–30% (Case 2) in Fukushima City.     

Concentration of Strontium-90 at Selected Hot Spots in Japan

This study is dedicated to the environmental monitoring of radionuclides released in the course of the Fukushima nuclear accident. The activity concentrations of β⁻ -emitting ⁹⁰Sr and β⁻/γ-emitting ¹³⁴Cs and ¹³⁷Cs from several hot spots in Japan were determined in soil and vegetation samples. The ⁹⁰Sr contamination levels of the samples were relatively low and did not exceed the Bq⋅g⁻¹ range. They were up four orders of magnitude lower than the respective ¹³⁷Cs levels. This study, therefore, experimentally confirms previous predictions indicating a low release of ⁹⁰Sr from the Fukushima reactors, due to its low volatility. The radiocesium contamination could be clearly attributed to the Fukushima nuclear accident via its activity ratio fingerprint (¹³⁴Cs/¹³⁷Cs). Although the correlation between ⁹⁰Sr and ¹³⁷Cs is relatively weak, the data set suggests an intrinsic coexistence of both radionuclides in the contaminations caused by the Fukushima nuclear accident. This observation is of great importance not only for remediation campaigns but also for the current food monitoring campaigns, which currently rely on the assumption that the activity concentrations of β⁻-emitting ⁹⁰Sr (which is relatively laborious to determine) is not higher than 10% of the level of γ-emitting ¹³⁷Cs (which can be measured quickly). This assumption could be confirmed for the samples investigated herein.     

Retention of radionuclides by some aquatic fresh water plants

The uptake of radionuclides ⁶⁰Co, ³²P and ¹³⁴Cs by some aquatic plants (Lemna gibba, Ceratophyllum demersum and Potamogeton crispus) present in the Ismailia Canal at different pH values and for different contamination periods was studied. The experimental results showed that the uptake generally decreases as the water pH increased. The tested macrophytes proved to be reliable biological indicators.     

Uptake and translocation of 134Cs by maize roots as affected by heterogeneous distribution of 134Cs

Structure-induced non-uniform water flow induces a heterogeneous distribution of surface-applied radionuclides in the soil profile. This study was conducted to assess the amount of ¹³⁴Cs which can be taken up by a single root growing in an area enriched in ¹³⁴Cs relative to the total amount of ¹³⁴Cs that can be taken up by the whole root system growing in an area homogeneously contaminated with ¹³⁴Cs. A split-root experiment was used to simulate the heterogeneous distribution of ¹³⁴Cs and roots. Seedlings of maize (Zea mays L. cv Corso) were grown for 14 days in solution culture and then transferred to a two-compartment pot system, where a single root was grown in a ¹³⁴Cs contaminated compartment while the rest of the root system was grown in an uncontaminated compartment. Plants with the whole root system growing in a solution contaminated with ¹³⁴Cs were used as control. We tested the effect of the competition between Cs and K on the uptake and translocation of ¹³⁴Cs by using two K concentrations, 0.2 and 1.05 mM. At the K concentration of the nutrient solution of 0.2 mM the single root representing 21% of the total root weight was able to take up 47% of the ¹³⁴Cs taken up by the entire root system, while at 1.05 mM the single root, representing 15% of the total root weight, took up 15% of the ¹³⁴Cs taken up by the entire root system. The translocation of ¹³⁴Cs from the root to the shoots did not depend on the external K concentration in the nutrient solution, but it was lower in the split root treatment than in the control treatment at both K concentrations. Section Editor: R. W. Bell     

Impact of Light and Temperature on the Uptake of Algal Symbionts by Coral Juveniles

The effects of temperature and light on the breakdown of the coral-Symbiodinium symbiosis are well documented but current understanding of their roles during initial uptake and establishment of symbiosis is limited. In this study, we investigate how temperature and light affect the uptake of the algal symbionts, ITS1 types C1 and D, by juveniles of the broadcast-spawning corals Acropora tenuis and A. millepora. Elevated temperatures had a strong negative effect on Symbiodinium uptake in both coral species, with corals at 31°C showing as little as 8% uptake compared to 87% at 28°C. Juveniles in high light treatments (390 µmol photons m⁻² s⁻¹) had lower cell counts across all temperatures, emphasizing the importance of the light environment during the initial uptake phase. The proportions of the two Symbiodinium types taken up, as quantified by a real time PCR assay using clade C- and D-specific primers, were also influenced by temperature, although variation in uptake dynamics between the two coral species indicates a host effect. At 28°C, A. tenuis juveniles were dominated by C1 Symbiodinium, and while the number of D Symbiodinium cells increased at 31°C, they never exceeded the number of C1 cells. In contrast, juveniles of A. millepora had approximately equal numbers of C1 and D cells at 28°C, but were dominated by D at 30°C and 31°C. This study highlights the significant role that environmental factors play in the establishment of coral-Symbiodinium symbiosis and provides insights into how potentially competing Symbiodinium types take up residence in coral juveniles.     

Nitrilotris(methylenephosphonates) in aqueous solution and solid state - dilatometric, potentiometric and NMR investigations

Dissociation and alkali complex formation equilibria of nitrilotris(methylenephosphonic acid) (NTMP, H₆L) have been studied by dilatometric, potentiometric and ³¹P NMR-controlled titrations. Dilatometry indicated the formation of alkali complexes ML (M=Li, Na, K, Rb, Cs) at high pH with a stability decreasing from Li to Cs. An efficient combination of potentiometric and NMR methods confirmed two types of alkali metal complexes MHL and ML. Stability constants for the equilibria following M⁺ + HL⁵⁻ ? MHL⁴⁻ and M⁺ + L⁶⁻ ? ML⁵⁻, respectively, were determined: logK_NaHL=1.08(0.07), logK_KHL=0.86(0.08), logK_NaL=2.24(0.03). Systematic errors are introduced by using alkali metal hydroxides as titrants for routine potentiometric determinations of dissociation constants pK_a5^app and pK_a6^app. Correction formulae were derived to convert actual dissociation constants pK_a into apparent dissociation constants pK_a^app (or vice versa). The actual dissociation constants were found: pK_a5(H₂L⁴⁻ ? H⁺ + HL⁵⁻)=7.47(0.03) and pK_a6(HL⁵⁻ ? H⁺ + L⁶⁻)=14.1(0.1). The anisotropy of ³¹P chemical shifts of salts M_nH_6 − nL (M=Li, Na, n=0-5) is more sensitive towards titration (n) than isotropic solution state chemical shifts.