μM Phosphate Research Articles

Role of manganese oxides and oxyhydroxides in phosphate sequestration in natural aquatic environments

Excessive inputs of phosphorus (P) to aquatic environments can lead to eutrophication. Adsorption of phosphate on Fe oxides is one of the main process that can limit P availability. Oxidized forms of Mn have also been suggested to play a role in P trapping. However, although a considerable number of studies have shown the relationships between the geochemistry of Fe and that of phosphates, few studies have attempted to show the direct links between Mn and P. In the present study, we studied the adsorption of phosphate on synthetized Mn(III) and Mn(IV) oxides placed under natural conditions. The aim was to compare the role of Fe and Mn oxides in phosphate adsorption. Two muddy sediments were collected in a river bed at the edge of a large agricultural area. A sandy sediment was collected downstream. A muddy and a sandy sample were taken in a coastal environment. The experiments on phosphate adsorption by sediment and Mn oxides were carried out in slurries containing in situ waters spiked with 10 μM phosphate. Control experiments without Mn-oxide addition showed that the natural sediments tested still had the capacity to adsorb phosphate, in particular due to the presence of reactive Fe(III) oxides, extractable by an ascorbate solution. The addition of Mn(III) and Mn(IV) oxides in much larger quantities than the initial quantity of Fe oxides had little impact on the rate of phosphate adsorption. For both Mn(III) and Mn(IV) oxides, the Mn/P ratio between added particulate Mn and adsorbed P was very high, with values between 260 and 1000. The Fe/P ratio of the iron oxides contained in the slurries was between 6 and 20. On average, the P adsorption capacity of the Fe oxides was 50 times greater than that of the Mn oxides. Manganese oxides are generally less abundant than iron oxides in natural environments. Mn oxides therefore play a minor role in P sequestration compared with Fe oxides. Even if there are environments where Mn oxides can concentrate, the reduction of Mn oxides and subsequent liberation of adsorbed P does not represent a major risk for eutrophication of aquatic ecosystems.

Assessing the nitrate and phosphate uptake kinetics potential and growth performance of Gracilaria corticata var. cylindrica in shrimp farm water (SFW)

Gracilaria corticata var. cylindrica (GCC) was studied as a biofilter in shrimp farm water (SFW) and its growth and biochemical attributes in the medium were evaluated. GCC showed significant nutrient absorption from SFW, with maximum nitrate and phosphate uptake observed after the first 48 h. Nitrate depletion happened faster than phosphate, thus showing a higher affinity for nitrate uptake (78.4% removal) by GCC. Nutrient uptake kinetics followed the Michaelis–Menten curve, with Vmax values of 43.16 μM g dw−1 h−1 for nitrate and 67.50 μM g dw−1 h−1 for phosphate. Also, GCC’s low Km values (12.53 µM for nitrate, 1.91 µM for phosphate) indicated efficient nutrient utilization. GCC showed rapid growth in SFW, with a daily growth rate of 2.93 ± 0.19% d−1, comparable to the commercial MP1 media (3.54 ± 0.19% d−1) and greater to seawater (2.23 ± 0.13% d−1). Proximate analysis revealed consistent biochemical compositions across all three media, with carbohydrate and protein contents of 2.24 ± 0.41% and 0.76 ± 0.12%, respectively, in SFW. Pigment analysis revealed that pigment concentrations varied, with SFW having the greatest R-PE concentration (182.25 ± 32.77 µg g−1), followed by MP1 media and saltwater. R-PC concentrations followed a similar pattern, with SFW having the greatest concentration (85.73 ± 19.33 µg g−1). These findings highlight GCC’s potential as an efficient biofilter for reducing nitrate and phosphate levels in SFW, therefore offering a sustainable solution for aquaculture effluent management and the potential integration of GCC into shrimp farming practices.

Fluorescein@NH2-UiO-66 Probe for Ratiometric Fluorescence Sensing of Trace Phosphate in Water

Phosphate pollution leads to deterioration in water quality, posing a serious threat to human health. Therefore, it is important to develop a highly selective and sensitive fluorescent probe for phosphate detection. Here, we report a novel ratiometric fluorescent probe, Fluorescein@NH2-UiO-66 (denoted as Flu@NH2-UiO-66), for the trace detection of phosphate in water. Specifically, during the in situ solvothermal synthesis of Flu@NH2-UiO-66, fluorescein molecules were encapsulated into the cavities of the metal-organic framework. Furthermore, the encapsulation amount of fluorescein was controlled by adjusting the acidity of the system. The Flu@NH2-UiO-66 (60 H+) sample, prepared with a 60:1 molar ratio of acetic acid to the metal center exhibited distinct dual fluorescence signal peaks. The probe showed a highly selective fluorescence response to phosphate. Within a range of 0–20 μM phosphate concentration, the probe demonstrated excellent linear detection capability with a detection limit of 0.37 μM. Moreover, the mechanism of fluorescence enhancement can be attributed to the addition of phosphate, which greatly increases the UV absorbance of the probe. This study developed a novel ratiometric fluorescent probe capable of rapid, sensitive, and stable detection of trace phosphate, which is of great significance for environmental management.

Emodin suppresses alkali burn-induced corneal inflammation and neovascularization by the vascular endothelial growth factor receptor 2 signaling pathway.

To investigate the effects of emodin on alkali burn-induced corneal inflammation and neovascularization. The ability of emodin to target vascular endothelial growth factor receptor 2 (VEGFR2) was predicted by molecular docking. The effects of emodin on the invasion, migration, and proliferation of human umbilical vein endothelial cells (HUVEC) were determined by cell counting kit-8, Transwell, and tube formation assays. Analysis of apoptosis was performed by flow cytometry. CD31 levels were examined by immunofluorescence. The abundance and phosphorylation state of VEGFR2, protein kinase B (Akt), signal transducer and activator of transcription 3 (STAT3), and P38 were examined by immunoblot analysis. Corneal alkali burn was performed on 40 mice. Animals were divided randomly into two groups, and the alkali-burned eyes were then treated with drops of either 10 μM emodin or phosphate buffered saline (PBS) four times a day. Slit-lamp microscopy was used to evaluate inflammation and corneal neovascularization (CNV) in all eyes on Days 0, 7, 10, and 14. The mice were killed humanely 14 d after the alkali burn, and their corneas were removed and preserved at －80 ℃ until histological study or protein extraction. Molecular docking confirmed that emodin was able to target VEGFR2. The findings revealed that emodin decreased the invasion, migration, angiogenesis, and proliferation of HUVEC in a dose-dependent manner. In mice, emodin suppressed corneal inflammatory cell infiltration and inhibited the development of corneal neovascularization induced by alkali burn. Compared to those of the PBS-treated group, lower VEGFR2 expression and CD31 levels were found in the emodin-treated group. Emodin dramatically decreased the expression of VEGFR2, p-VEGFR2, p-Akt, p-STAT3, and p-P38 in VEGF-treated HUVEC. This study provides a new avenue for evaluating the molecular mechanisms underlying corneal inflammation and neovascularization. Emodin might be a promising new therapeutic option for corneal alkali burns.

Distribution and biogeochemical perspectives of nutrients in the Eastern Equatorial Indian Ocean

The seasonal reversal of ocean circulation associated with seasonal change in the direction of prevailing winds and the occurrence of several anomalous events in the Eastern Equatorial Indian Ocean (EEIO) make this region dynamic and complex in terms of its biogeochemical characteristics. Two multidisciplinary cruises were conducted to measure nutrients and associated physicochemical parameters across the water column (up to 1000 m) of the EEIO during boreal summer and winter monsoons to understand the distribution of nutrients and their spatio-temporal variability from a biogeochemical perspective. The seasonality in the thermohaline structure of the region is indistinct except for surface salinity drop during summer monsoon due to more precipitation on-site and in adjoining areas. Low concentrations of chlorophyll at the surface and in the deep chlorophyll maxima represent the oligotrophic nature of this region. Surface water was found nutrient-depleted (0.03–0.4 µM Nitrate, 0.02–0.13 µM Phosphate). The maxima of vertical profiles of nitrate and phosphate were recorded at a shallower depth (150–200 m) when compared to its maxima in usual oceanic conditions, but a silicate maximum was recorded in deeper water. In the surface and upper mixed layer paucity of nutrients resulted in low N:P and N:Si ratios. Therefore, nitrogen limitation is evident. The overall ratio of N:P yielded a mean value of 15.33 and matched with the representative literature value for the Indian Ocean. The minimum oxygen values (<50 µM) in the deep water (150–200 m) indicated a hypoxic condition. No signature of denitrification and a moderate nitrate deficit were observed in deep waters. The negative values of Nitrate anomaly (N-tracer) at 50–100 m depth were attributed to a Watermass influenced by denitrification. The prevailing oligotrophic condition caused limited synthesis of organic matter and subsequently little decomposition in deep water. The maxima in the apparent oxygen utilization (AOU) profile are confined to 150 to 200 m depth and represent the most active zone for regeneration that is limited to shallow depth. Regenerated nutrients reached maxima at shallower depth and primarily control material cycling in this region. Supply of nitrate to the surface water based on the preformed values of prevailing water mass was primarily by Bay of Bengal water. According to the findings of this study, preformed nitrate concentrations between 100 and 200 metres below the surface were found very low, indicating that Indonesian Through Flow (ITF) has little impact on the distribution of nutrients in this area.

Methionine application at low phosphate level promotes root-to-shoot cadmium translocation by mobilizing weakly bound apoplastic cadmium in valerian (Valeriana officinalis L.)

Controlling the uptake and translocation of heavy metals in medicinal plants is crucial due to its strong impact on the safety and quality of derived medicinal plant products. This study investigated the effects of phosphate and methionine on the distribution and chemical forms of Cd in valerian (Valeriana officinalis L.) roots and shoots. Seedlings were grown for two weeks in a Cd-free nutrient solution containing either 400 or 1200 μM phosphate and then exposed for 10 days to 10 μM Cd either in combination with 400 μM or no methionine in the nutrient solution. Root Cd was partitioned into a symplastic and an apoplastic Cd fraction using a desorption procedure with EDTA. A sequential extraction method was applied to determine chemical forms in which Cd was retained in both roots and shoots. “Pectate- and protein-bound Cd” and HAc-soluble “Cd phosphates” were the dominant Cd forms in sequential extractions of both roots and shoots. Phosphate increased the HAc-soluble “Cd phosphate fraction” in the roots, but not in the shoots. Methionine did not affect this fraction, but strongly increased ethanol- and water-soluble Cd in roots and shoots. While it also increased the “pectate- and protein-bound Cd fraction” in the shoots, it decreased this fraction and the share of apoplastic Cd in the roots. The phosphate treatment reduced Zn accumulation in the roots but had no effect on Zn accumulation in the shoots, whereas Met increased shoot Zn. The results indicate that methionine induced root-to-shoot Cd translocation primarily by mobilizing weakly bound Cd to root cell walls at the low phosphate level. This could help limit Cd accumulation in valerian roots grown for medicinal use.

Lab-on-Chip for In Situ Analysis of Nutrients in the Deep Sea

Microfluidic reagent-based nutrient sensors offer a promising technology to address the global undersampling of ocean chemistry but have so far not been shown to operate in the deep sea (>200 m). We report a new family of miniaturized lab-on-chip (LOC) colorimetric analyzers making in situ nitrate and phosphate measurements from the surface ocean to the deep sea (>4800 m). This new technology gives users a new low-cost, high-performance tool for measuring chemistry in hyperbaric environments. Using a combination of laboratory verification and field-based tests, we demonstrate that the analyzers are capable of in situ measurements during profiling that are comparable to laboratory-based analyses. The sensors feature a novel and efficient inertial-flow mixer that increases the mixing efficiency and reduces the back pressure and flushing time compared to a previously used serpentine mixing channel. Four separate replicate units of the nitrate and phosphate sensor were calibrated in the laboratory and showed an average limit of detection of 0.03 μM for nitrate and 0.016 μM for phosphate. Three on-chip optical absorption cell lengths provide a large linear range (to >750 μM (10.5 mg/L-N) for nitrate and >15 μM (0.47 mg/L-P) for phosphate), making the instruments suitable for typical concentrations in both ocean and freshwater aquatic environments. The LOC systems automatically collected a series of deep-sea nitrate and phosphate profiles in the northeast Atlantic while attached to a conductivity temperature depth (CTD) rosette, and the LOC nitrate sensor was attached to a PROVOR profiling float to conduct automated nitrate profiles in the Mediterranean Sea.

Assessment of Water Quality and Phytoplankton Structure of Eight Alexandria Beaches, Southeastern Mediterranean Sea, Egypt

This study aims to investigate the abundance, community, and structure of phytoplankton, physicochemical parameters, and some eutrophication state indices, to estimate the water quality of eight selected beaches along the Alexandria Coast, in the southeast of the Mediterranean Sea. The samples were collected monthly from 2019 to 2020. Nutrient values ranged from 1.54 to 33.21 µM for nitrate, 0.01 to 1.98 µM for nitrite, 0.12 to 9.45 µM for ammonia, 0.01 to 1.54 µM for phosphate, and 0.67 to 29.53 µM for silicate. Phytoplankton biomass was characterized by chlorophyll-a concentration, which fluctuated between 0.12 and 12.31 µg L−1. The annual phytoplankton average was 63.85 ± 17.83 × 103 cells L−1. Phytoplankton was highly diversified (228 taxa), and the most diversified group was diatoms (136 taxa), followed by a remarkably low number of Dinophyta (36 taxa). Diatoms reached maximum abundance in December. Meanwhile, a dense bloom of microalga Chlorella marina occurred in June on some beaches. High temperature, high dissolved inorganic nitrogen, and less-saline waters have supported green algal proliferation. The Shannon–Wiener diversity index (H’) showed that there was a qualitative seasonal difference in the composition of the phytoplankton community. Waters of beaches 1–3 were classified as between clean and moderately polluted; and beaches 4–8 varied between moderately and heavily polluted. The study revealed that human activities might have triggered the algal bloom and may be responsible for alterations in the Alexandria coast ecosystem.

Marine Water Quality at Diego Garcia: A Preliminary Study of Pollution Levels in Coastal and Lagoon Waters

Diego Garcia is the largest atoll within the Chagos Archipelago in the Indian Ocean. Since the 1960s it has been a military base, populated only by military and support personnel. Infrastructure includes sewage treatment works, a waste disposal facility and an airbase. Lagoon use includes boating and large vessel anchorage. Current pollution levels by inorganic nutrients and other contaminants are unknown. A field study was undertaken in March 2019 to obtain baseline information on key environmental parameters and pollutants for assessing the state of marine water quality. Outside the atoll, three stations were sampled where human impacts were likely to be lowest (two off the north coast, considered as ‘near-pristine’; one on the east coast); one station was sampled in the lagoon mouth; 10 stations were sampled downstream from two sewage outflows. Inside the lagoon, 10 stations were sampled at near-shore sites likely to be directly impacted by activities such as boating and waste management; six stations were sampled in the central or eastern lagoon. In situ sensors were used to estimate temperature, salinity, chlorophyll (as fluorescence) and dissolved oxygen. Discrete water samples were analyzed for nutrients, chemical contaminants, heavy metals and fecal indicator bacteria. Sea surface temperatures were highest (29.5–35 °C) inside the lagoon; salinities were generally higher (&amp;gt; 34.1) outside the lagoon (vs 33.8–34.1 inside). Surface nutrient concentrations at near-pristine stations were undetectable for nitrate and phosphate and averaged 1.39 μM for dissolved inorganic nitrogen (DIN) and 1.73 μM for silicate. Concentrations were higher at most other stations (maximum 5.7 μM DIN, 0.38 μM phosphate, and 9.93 μM silicate), with ammonium contributing most to DIN. In the lagoon, chlorophyll concentrations were relatively low (0.3 – 0.6 μg chl l–1) near the surface and higher (max 0.9 μg chl l–1) at depth. Results suggested low levels of pollution overall. However, levels of nutrients, oxygen deficiency, chemical contaminants (e.g., solvents and DEET) and heavy metals (cadmium, nickel, zinc and copper) at some sites inside the lagoon are a concern due to slow flushing rates and will be used to inform future monitoring and assessment of environmental health at Diego Garcia.

On-site electrochemical determination of phosphate with high sensitivity and anti-interference ability in turbid coastal waters

Phosphate is considered to be an important biogenic element and responsible for eutrophication in aquatic ecosystems, existing in both dissolved and absorbed forms. Due to the complex matrix of coastal seawater, a high sensitivity and anti-interference method for phosphate detection is required for environmental protection. In this study, a novel electrochemical method was proposed based on reduced graphene oxide-ordered mesoporous carbon screen-printed electrode (rGO-OMC/SPE) analysis, allowing sensitivity and reliable determination of phosphate in turbid coastal waters. Combining the good absorption capacity of OMC with the excellent electroconductivity of rGO, the fabricated electrode exhibits improved signal responses, enhanced by up to 43-fold. The platform was evaluated using turbidity interference test with good recovery percentages comprised between 96% and 105% in different phosphate concentration, and salinity interference test between 92% and 105%, respectively. A linear range from 0.2 to 150 μM phosphate was achieved, with a detection limit of 0.05 μM (s/n = 3). The fabricated platform was successfully used for on-site analysis of phosphate in turbid coastal waters. This reliable and effective method for the analysis of phosphate in turbid coastal waters allows for sensitivity and anti-interference determination, while also representing a significant step towards comprehensive and convenient analysis of phosphorus species.

Phosphate hinders the complexation of dissolved organic matter with copper in lake waters.

The properties of phosphate in lakes and their ability to cause eutrophication have been well studied; however, the effects of phosphate on the environmental behavior of other substances in lakes have been ignored. Dissolved organic matter (DOM) and heavy metals may coexist with phosphate in lakes. Herein, the mechanisms underlying the influence of phosphate on heavy metals complexation with DOM were investigated using multi-spectroscopic tools. Overall, the amount of DOM-bound Cu(Ⅱ) decreased with the increasing phosphate content. Furthermore, the fluorescence excitation and emission matrix results combined with parallel factor analysis showed that when the Cu(Ⅱ) concentration increased from 0 to 5mg/L and 50μM phosphate to the reaction of DOM and copper, the fluorescence intensity of tyrosine (component 1), humic-like (component 2) and tryptophan (component 3) decreased by 36.46%, 57.34%, and 74.70% compared with the treatment with no phosphate addition, respectively. This finding indicates that the binding of different fluorescent components to Cu(Ⅱ) was restricted by phosphate. Furthermore, different functional groups responded differently to Cu(Ⅱ) under different phosphate concentrations. The binding sequence of different functional groups under high concentration of phosphate (phenolic hydroxyl group＞amide (Ⅰ) ＞carbohydrates) was completely opposite to that with no phosphate. These results demonstrated that phosphate could restrict the binding affinity of heavy metals with different fluorescent substances or organic ligands of DOM, suggesting that the comigration of DOM-bound heavy metals in lakes is hindered by phosphate and the risk of heavy metal poisoning in aquatic organisms is therefore diminished.

Microalga Scenedesmus bijugus: Biomass, lipid profile, and carotenoids production in vitro

Manipulating specific nutrients in growth media to boost production of lipids or carotenoids in microalgae is a widespread practice; however, it decreases overall biomass productivity, an important consideration for viable production of biofuels. In the present study, maximum productivity of lipids (117.01 mg/L/d) and biomass (249.60 mg/L/d) was obtained on day 13 in Bold's basal medium (BBM) modified by adding 25 mM NaCl and 20 μM phosphate. Lutein and astaxanthin productivity was, however, only slightly different from that in the standard medium, namely blue-green-11 (BG-11). The lipids profile was dominated by C16:0 and C 18:1 fatty acids ranging from 26.69 to 39.32% and 10.8–35.31% (palmitic and oleic acids) in all the five variants of the culture medium. These results indicate that the highest proportion of saturated fatty acids (SFA; 61.02%) was obtained in BG-11 whereas that of monounsaturated fatty acids (MUFA; 37.34%) was obtained in BBM supplemented with NaCl (50 mM) and phosphate (20 μM). All the five variants led to lipids suitable for biodiesel production, marked by a lipid profile dominated by the two fatty acids. It is concluded that making the culture medium more saline and enriching it with phosphates increased lipid and biomass productivity and the synthesis of fatty acids methyl esters (FAME).

Isolation and Characterization of Molybdenum-reducing Pseudomonas sp. from Agricultural Land in Northwest-Nigeria

Microbial heavy metals reduction has an important role in the biological system and in environmental metals recycling to remove its toxic effects in soil and wastewater. A molybdenum-reducing bacterium with the potential to reduce toxic hexavalent molybdenum to colloidal molybdenum blue (Mo-blue) was isolated from agricultural land in Northwest-Nigeria. The Gram’s stain and microscopic examination reveal that the isolate is a Gram-negative, however, phylogenetic analysis of the 16S rRNA identifies the isolate as Pseudomonas sp. Molybdenum reduction in this bacterium is optimally supported by glucose at 1.0% (w/v). The optimum phosphate and molybdate concentrations supporting molybdate reduction were between 3.5 and 7.5 mM for phosphate and 100 mM molybdate. Molybdate reduction is optimum at 37 ᵒC and pH between 6.5 and 7.5. The capacity of this isolate to reduce toxic molybdenum to a less toxic form is novel and makes the bacterium an important instrument for bioremediation of this pollutant.

Direct 3D-printing of phosphate glass by fused deposition modeling

Additive manufacturing of oxide glass enables on-demand, low-cost manufacturing of complex optical components for numerous applications, opening new opportunities to explore functionalities inaccessible otherwise. Here, we report a straightforward extrusion-based 3D-printing approach, deploying the fused deposition modeling (FDM) process, to produce optically transparent phosphate glasses with complex geometries and preserved structural and photoluminescence properties. Using a customized entry-level FDM desktop printer with a layer resolution of 100 μm, highly dense and transparent europium-doped phosphate glass structures can be fabricated from glass filaments pulled using a fiber-drawing tower from the parent glass preform. Combined with the suggested strategies for performance and quality improvement, professional-grade FDM printers can offer better layer resolutions. This direct approach for 3D-printing phosphate glass may open up new horizons not only for developing cutting-edge optical components but also for promoting new biomedical solutions upon making use of alternative biocompatible phosphate compositions.

Arsenolipids in Cultured Picocystis Strain ML and Their Occurrence in Biota and Sediment from Mono Lake, California.

Primary production in Mono Lake, a hypersaline soda lake rich in dissolved inorganic arsenic, is dominated by Picocystis strain ML. We set out to determine if this photoautotrophic picoplankter could metabolize inorganic arsenic and in doing so form unusual arsenolipids (e.g., arsenic bound to 2-O-methyl ribosides) as reported in other saline ecosystems and by halophilic algae. We cultivated Picocystis strain ML on a seawater-based medium with either low (37 µM) or high (1000 µM) phosphate in the presence of arsenite (400 µM), arsenate (800 µM), or without arsenic additions (ca 0.025 µM). Cultivars formed a variety of organoarsenic compounds, including a phytyl 2-O-methyl arsenosugar, depending upon the cultivation conditions and arsenic exposure. When the cells were grown at low P, the organoarsenicals they produced when exposed to both arsenite and arsenate were primarily arsenolipids (~88%) with only a modest content of water-soluble organoarsenic compounds (e.g., arsenosugars). When grown at high P, sequestration shifted to primarily water-soluble, simple methylated arsenicals such as dimethylarsinate; arsenolipids still constituted ~32% of organoarsenic incorporated into cells exposed to arsenate but < 1% when exposed to arsenite. Curiously, Picocystis strain ML grown at low P and exposed to arsenate sequestered huge amounts of arsenic into the cells accounting for 13.3% of the dry biomass; cells grown at low P and arsenite exposure sequestered much lower amounts, equivalent to 0.35% of dry biomass. Extraction of a resistant phase with trifluoroacetate recovered most of the sequestered arsenic in the form of arsenate. Uptake of arsenate into low P-cultivated cells was confirmed by X-ray fluorescence, while XANES/EXAFS spectra indicated the sequestered arsenic was retained as an inorganic iron precipitate, similar to scorodite, rather than as an As-containing macromolecule. Samples from Mono Lake demonstrated the presence of a wide variety of organoarsenic compounds, including arsenosugar phospholipids, most prevalent in zooplankton (Artemia) and phytoplankton samples, with much lower amounts detected in the bottom sediments. These observations suggest a trophic transfer of organoarsenicals from the phytoplankton (Picocystis) to the zooplankton (Artemia) community, with efficient bacterial mineralization of any lysis-released organoarsenicals back to inorganic oxyanions before they sink to the sediments.

Stability-Indicating HPLC method for estimation of omarigliptin in tablets – Oxidative and photolytic kinetics and degradation products formed under oxidative conditions

After the development and validation of a stability indicating analytical method for omarigliptin (OMG) using the HPLC method, a study of oxidative and photolytic degradation kinetics and identification of the main degradation products obtained after stress testing under oxidative conditions of this substance and the degradation pathway, was proposed. The separations were performed using an Agilent ZORBAX C8 250 × 4.6 mm column and the mobile phase consisted of 10 µM phosphate buffer and methanol 45:55 (v/v) with 230 nm wavelength detection. The HPLC method was validated according to official guides. It showed to be sensitive, accurate, precise, linear, robust and specific and was successfully used to determine the drug in its pharmaceutical formulation, to investigate the degradation kinetics of omarigliptin in the oxidative and photolytic medium and to get to know the reaction rate. Mass spectrometry was useful to identify the main oxidative degradation products and chemical analysis was used as a proposal to estimate the degradation routes of OMG.

Symbiont transmission and reproductive mode influence responses of three Hawaiian coral larvae to elevated temperature and nutrients

Elevated temperatures and nutrients are degrading coral reef ecosystems, but the understanding of how early life stages of reef corals respond to these stressors remains limited. Here, we test the impact of temperature (mean ~ 27 °C vs. ~ 29 °C) and nitrate and phosphate enrichment (ambient, + 5 µM nitrate, + 1 µM phosphate and combined + 5 µM nitrate with 1 µM phosphate) on coral larvae using three Hawaiian coral species with different modes of symbiont transmission and reproduction: Lobactis scutaria (horizontal, gonochoric broadcast spawner), Pocillopora acuta (vertical, hermaphroditic brooder) and Montipora capitata (vertical, hermaphroditic broadcast spawner). Temperature and nutrient effects were species specific and appear antagonistic for L. scutaria and M. capitata, but not for P. acuta. Larvae survivorship in all species was lowest under nitrate enrichment at 27 °C. M. capitata and L. scutaria survivorship increased at 29 °C. However, positive effects of warming on survivorship were lost under high nitrate, but phosphate attenuated nitrate effects when N/P ratios were balanced. P. acuta larvae exhibited high survivorship (> 91%) in all treatments and showed little change in larval size, but lower respiration rates at 29 °C. Elevated nutrients (+N+P) led to the greatest loss in larvae size for aposymbiotic L. scutaria, while positive growth in symbiotic M. capitata larvae was reduced under warming and highest in +N+P treatments. Overall, we report a greater sensitivity of broadcast spawners to warming and nutrient changes compared to a brooding coral species. These results suggest variability in biological responses to warming and nutrient enrichment is influenced by life-history traits, including the presence of symbionts (vertical transmission), in addition to nutrient type and nutrient stoichiometry.

A terbium(III)-functionalized zinc(II)-organic framework for fluorometric determination of phosphate.

A terbium(III)-functionalized zinc(II)-organic framework (Tb-MOF-Zn) is shown to be a viable fluorescent probe for phosphate. The organic ligands 4,4',4″-[((2,4,6-trimethylbenzene-1,3,5-triyl)tris(methylene))tris(oxy)]tribenzoic acid (H3L3) contains multiple carboxyl groups that canreact with zinc(II) to yield tubular MOF-Zn. The MOF-Zn was further functionalized with Tb(III) to produce a lanthanide composite of type Tb-MOF-Zn which displays strong fluorescence with excitation/emission maxima at 285/544nm. Fluorescence is quenched by phosphate because of the specific interaction with Tb(III) in Tb-MOF-Zn. The concentration of Tb-MOF-Zn, reaction time and pH value of the solution were optimized. Fluorescence drops linearly in the 0.01 to 200.0μM phosphate concentration range, and the detection limit is 4.0nM. The fluorescent probe was also used to prepare a microdot array on a glass slide for visual detection of phosphate under illumination with UV light. Graphical abstractA terbium(III) functionalized zinc(II)-organic framework was synthesized and used as fluorescent probe for determination of phosphate ions.

Production of quality seaweed biomass through nutrient optimization for the sustainable land-based cultivation

The Ulva fasciata Delile is a rapidly growing intertidal green marine macroalga and is a potential source of numerous value-added products such as mineral salts, ulvan, cellulose, and proteins. It is among the edible seaweeds that can bring down the pressure on to the terrestrial crop farming. The cultivation of such economically valuable species presents two major advantages: their higher photosynthetic efficiency that leads to the higher level of atmospheric CO2 sequestration and the biomass produced can effectively be employed in food formulations to combat the food security issues. In this study, the optimum concentration of nutrients namely, nitrate and phosphate were estimated to maximize the biomass production to achieve higher growth rates with the best biochemical contents. The optimization of nutrient regimes resulted in the modulation of algal cell-cycle as evidenced by the highly varying growth rates (ranging from 6% to 56%) as well as dynamic nutrient uptake kinetics. The biochemical analysis of biomass grown in optimized nutrient combination (N2: 60 μM nitrate; 6 μM phosphate) contained proteins 9.3 ± 0.32%, carbohydrates 20.2 ± 2.51% and lipids 6.28 ± 0.84% on dry weight basis. Further, the cultures with the optimized nutrient combination were found to have healthy green leaf-like thallus with reduced or no incidence of deterioration of biomass. The findings reported in this study would be useful for the sustainable production of Ulva in land-based systems.

Caribbean gorgonian octocorals cope with nutrient enrichment

Corals inhabit oligotrophic waters, thriving amidst limited nutrients such as nitrogen and phosphorous. When nutrient levels increase, usually due to human activity, the symbiosis of dinoflagellates (family Symbiodiniaceae) with scleractinian corals can break down. Although gorgonian corals dominate many Caribbean reefs, the impact of enrichment on them and their algae is understudied. We exposed two gorgonian species, Pseudoplexaura porosa and Eunicea tourneforti, to elevated concentrations of either ammonium (10 μM or 50 μM) or phosphate (4 μM). Enrichment with 10 μM ammonium increased chlorophyll content and algal density in both species, whereas the host biochemical composition was unaffected. Exposure to 50 μM ammonium only reduced the quantum yield in P. porosa and mitotic indices in both species. Conversely, algal carbon and nitrogen content within E. tourneforti increased with 4 μM phosphate exposure. These gorgonian species coped with short-term nutrient enrichment, furthering our understanding of the success of Caribbean gorgonians.