Sunlit Environments Research Articles

Initial stomatal conductance increases photosynthetic induction of trees leaves more from sunlit than from shaded environments: a meta-analysis.

It has long been held that tree species/leaves from shaded environments show faster rate of photosynthetic induction than species/leaves from sunlit environments, but the evidence so far is conflicting and the underlying mechanisms are still under debate. To address the debate, we compiled a dataset for 87 tree species and compared the initial increasing slope during the first 2-min induction (SA) and stomatal and biochemical characteristics between sun and shade species from the same study, and those between sun and shade leaves within the same species. In 77% of between-species comparisons, the species with high steady-state photosynthetic rate in the high light (Af) exhibited a larger SA than the species with low Af. In 67% within-species comparisons, the sun leaves exhibited a larger SA than the shade leaves. However, in only a few instances did the sun species/leaves more rapidly achieve 50% of full induction, with an even smaller SA, than the shade species/leaves. At both the species and leaf level, SA increased with increasing initial stomatal conductance before induction (gsi). Despite exhibiting reduced intrinsic water-use efficiency in low light, a large SA proportionally enhances photosynthetic carbon gain during the first 2-min induction in the sun species and leaves. Thus, in terms of the increase in absolute rate of photosynthesis, tree species/leaves from sunlit environments display faster photosynthetic induction responses than those from shaded environments. Our results call for re-consideration of contrasting photosynthetic strategies in photosynthetic adaption/acclimation to dynamic light environments across species.

Effects of organic additives on spectroscopic and molecular-level features of photo-induced dissolved organic matter from microplastics

The environmental occurrence and impact of dissolved organic matter leached from microplastics (MP-DOM) has been the subject of increased research interest. Commercial plastics, which typically contain additives, are subject to natural weathering processes and can eventually lose their additives. However, the effects of organic additives in commercial microplastics (MPs) on the release of MP-DOM under UV irradiation remain poorly understood. In this study, four polymer MPs (polyethylene; PE, polypropylene; PP, polystyrene; PS, polyvinylchloride; PVC) and four commercial MPs, including a PE zip bag, a PP facial mask, a PVC sheet, Styrofoam, were subjected to leaching under UV irradiation, and the MP-DOM was characterized using Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS) and fluorescence excitation emission matrix-parallel factor analysis (EEM-PARAFAC). Although UV light promoted the leaching of MP-DOM from both MP groups, the amount released was more pronounced for the polymer MPs than for the commercial MPs. The commercial MP-DOM was characterized by a prominent protein/phenol-like component (C1), while a humic-like component (C2) prevailed in the polymer MPs. FT-ICR-MS identified a higher number of unique molecular formulas for the commercial than for the polymer MP-DOM. The unique molecular formulas of commercial MP-DOM included known organic additives and other breakdown products, while the polymer MP-DOM featured more pronounced unsaturated carbon structures in its identified unique formulas. Several molecular-level parameters showed significant correlations with fluorescence properties, such as CHO formulas (%) with C1 and condensed aromatic structure (CAS-like, %) with C2, suggesting the potential application of fluorescent components as an optical descriptor for the complex molecular-level composition. This study also revealed the possible high environmental reactivity of both polymer MPs and fully weathered plastics due to the unsaturated structures generated in sunlit environments.

Design and Experimental Evaluation of Composite Magnesium Phosphate Cement-Based Coating with High Cooling Effect

The application of surface heat reflective coatings is one of the effective measures to solve the temperature disease of concrete structures in sunlit environments. To achieve strong bonding, high durability, and good cooling characteristics, a novel inorganic reflective thermal insulation coating was prepared using magnesium phosphate cement (MPC) as the binder and reflective matrix, and titanium dioxide and glass beads as the reflective thermal insulation reinforcement functional additives. The optimum ratio of the new reflective thermal insulation coating was preferred through laboratory irradiation test, thermal conductivity test, and spectral reflectance test. The results show that MPC itself was a good reflection cooling material, and the surface and internal temperatures of concrete blocks were reduced by 7.6 °C and 6.6 °C, respectively, after using MPC as the cooling coating. When 2% titanium dioxide was added to MPC, the surface and internal temperatures were further reduced by 6.0 °C and 4.9 °C, respectively. On top of this, the surface and internal temperatures of the concrete were reduced by a further 3.9 °C and 2.2 °C when 8% glass beads were added. The bond strength of the MPCTG coating to the concrete matrix reached 2.1 MPa. Finally, the microscopic characteristics and the reflective thermal insulation mechanism of the MPCTG coating were investigated with the aid of SEM, thermo gravimetric analysis, and XRD analysis. The results show that the MPC in the MPCTG coating was well hydrated, and a large number of hydration products encapsulated the unreacted MgO particles, titanium dioxide, and glass beads, forming a dense whole with high reflection and low thermal conductivity, and the coating effectively prevented the entry of radiant heat. At the same time, the MPCTG coating was thermally stable below 70 °C. The magnesium phosphate cement-based reflective thermal insulation coating developed in this study has potential application prospects in concrete structure cooling coatings.

Saccharibacteria harness light energy using type-1 rhodopsins that may rely on retinal sourced from microbial hosts

Microbial rhodopsins are a family of photoreceptive membrane proteins with a wide distribution across the Tree of Life. Within the candidate phyla radiation (CPR), a diverse group of putatively episymbiotic bacteria, the genetic potential to produce rhodopsins appears to be confined to a small clade of organisms from sunlit environments. Here, we characterize the metabolic context and biophysical features of Saccharibacteria Type-1 rhodopsin sequences derived from metagenomic surveys and show that these proteins function as outward proton pumps. This provides one of the only known mechanisms by which CPR can generate a proton gradient for ATP synthesis. These Saccharibacteria do not encode the genetic machinery to produce all-trans-retinal, the chromophore essential for rhodopsin function, but their rhodopsins are able to rapidly uptake this cofactor when provided in experimental assays. We found consistent evidence for the capacity to produce retinal from β-carotene in microorganisms co-occurring with Saccharibacteria, and this genetic potential was dominated by members of the Actinobacteria, which are known hosts of Saccharibacteria in other habitats. If Actinobacteria serve as hosts for Saccharibacteria in freshwater environments, exchange of retinal for use by rhodopsin may be a feature of their associations.

PixelEngineTM All-in-One: a Printable Pixel-Driver MicroIC with Three-Dimensionally Integrated Red, Green, and Blue MicroLEDs

Displays that utilize millions of tiny microLEDs promise a future generation of phones, computers and televisions that are bright enough for sunlit environments yet consume less power. The microLEDs are made using wafer-level semiconductor processes, and key to manufacturing displays is the capability to assemble billions of microLEDs onto panels. Elastomer stamp transfer printing is a mass transfer technology with the yield, accuracy, speed, and scalability required to meet the demands of display manufacturing. The versatility of elastomer stamp transfer leads to further innovations for displays, these include the ability to integrate miniature integrated circuits, called microICs, for advanced backplanes and strategies where microLEDs are combined into PixelEngine packages on intermediate substrates before final assembly to the display panel. This paper reviews how transfer printing has been applied to microLED display development to date and describes a pixel-driver microIC with vertically integrated microLEDs, called PixelEngineAll-in-One, that performs all pixel functions and is designed to enable displays realized through assembly onto passive wiring panels.

Photosynthetic activity in Devonian Foraminifera

Abstract. Photosynthetically active foraminifera are prolific carbonate producers in warm, sunlit, surface waters of the oceans. Foraminifera have repeatedly developed mixotrophic strategies (i.e., the ability of an organism or holobiont to both feed and photosynthesize) by facultative or obligate endosymbiosis with microalgae or by sequestering plastids (kleptoplasts) of ingested algae. Mixotrophy provides access to essential nutrients (e.g., N, P) through feeding while providing carbohydrates and lipids produced through photosynthesis, resulting in substantial energetic advantage in warm, sunlit environments where food and dissolved nutrients are scarce. Our morphological as well as stable carbon isotope data provide, as of now, the earliest (Mid-Devonian) evidence for photosynthetic activity in the first advanced, multichambered, calcareous foraminifera, Semitextularia, from the tropical shelf of the Laurussia paleocontinent. This adaptation likely influenced the evolutionary radiation of calcareous Foraminifera in the Devonian (“Givetian revolution”), one of the most important evolutionary events in foraminiferal history, that coincided with the worldwide development of diverse calcifying marine communities inhabiting shelf environments linked with Devonian stromatoporoid coral reefs.

Millimeter-sized smart sensors reveal that a solar refuge protects tree snail Partula hyalina from extirpation

Pacific Island land snails are highly endangered due in part to misguided biological control programs employing the alien predator Euglandina rosea. Its victims include the fabled Society Island partulid tree snail fauna, but a few members have avoided extirpation in the wild, including the distinctly white-shelled Partula hyalina. High albedo shell coloration can facilitate land snail survival in open, sunlit environments and we hypothesized that P. hyalina has a solar refuge from the predator. We developed a 2.2 × 4.8 × 2.4 mm smart solar sensor to test this hypothesis and found that extant P. hyalina populations on Tahiti are restricted to forest edge habitats, where they are routinely exposed to significantly higher solar radiation levels than those endured by the predator. Long-term survival of this species on Tahiti may require proactive conservation of its forest edge solar refugia and our study demonstrates the utility of miniaturized smart sensors in invertebrate ecology and conservation.

PH-dependent photochemical transformation of arsenic sulfide sludge catalyzed by Fe ions under visible light irradiation

Arsenic sulfide sludge (ASS) is a typical precipitation product of acid smelting wastewater. Previous study reported that when exposed to sunlight, the release and oxidation of As(III) in ASS were markedly accelerated. However, the key factor to trigger the photocatalytic transformation of ASS is still unclear. Herein, we revealed that the coexisting Fe(II)/Fe(III) ions were critical to promote the photo-oxidation of released As(III) under visible light. We further validated that Fe(II)-stimulated photo-oxidation mechanism of As(III) in ASS was pH-dependent. In acid conditions, OH and SO4− were promoted by Fe(II)/Fe(III) cycling catalysis with the assistance of the reductive sulfur species from ASS, e.g. S2− and SO32−, and thus accelerated the oxidation of As(III). While in neutral conditions, the nascent ferric hydroxide colloids enhanced the oxidation rate of As(III) via photo-induced ligand-to-metal-charge transfer (LMCT) mechanism. These findings help in predicting and controlling the fate of real arsenic-containing sludge in sunlit environments.

Photochemistry after fire: Structural transformations of pyrogenic dissolved organic matter elucidated by advanced analytical techniques

Pyrogenic organic matter (pyOM) is the solid residue left after pyrolysis of organic matter, a process occurring in nature during forest fires. Upon rain events, pyrogenic dissolved organic matter (pyDOM) leaches into the rain water and is transferred to the aquatic environment where it has been identified as an important component of the global carbon cycle. Overall, pyDOM consists of highly condensed aromatic compounds (ConAC) and poorly characterized aliphatic molecules. While the ConAC are thought to be persistent in the environment, a large ConAC accumulation that would match the calculated fluxes of pyDOM formation and export has not been observed. Photo-degradation has been identified as a major pyDOM sink, and it can potentially account for the discrepancy in the global mass balance of pyDOM.Photochemistry of pyDOM has been studied to a certain extent, but neither the structural transformation pathways of pyDOM nor how they relate to pyrolysis temperature and parent feedstocks are well understood. In response to this need, we have examined the products after photo-irradiation of pyDOM derived from a temperature series (250, 400, 525, 650 °C) of oak biochars made under controlled laboratory conditions, which can be considered model pyrogenic substances. Ultrahigh resolution mass spectrometry (FT-ICR-MS), one-dimensional 1H NMR, and two-dimensional 1H-1H total correlation spectroscopy (TOCSY) NMR were used to evaluate the compositional changes that occurred with photo-irradiation.In agreement with previous studies, pyDOM aryl groups were the most photo-labile, and alkyl and O-alkyl groups were photo-produced. A new finding is that polysubstituted olefinic moieties of pyDOM were also photo-degraded. Using TOCSY we identified several small molecular weight compounds whose abundances changed non-linearly across the combustion continuum which suggests that different radical processes occur in the different char leachates. Using mass spectrometric data we observed that pyDOM from oak chars made at lower temperatures (250 and 400 °C), as well as pyDOM from a grass char prepared at 650 °C, photo-transformed to a more hydrogenated and oxygenated composition. In contrast, pyDOM from higher temperature char leachates (525 and 650 °C) transformed predominantly into smaller aliphatic compounds. To explain these differences, we propose a photo-transformation mechanism for ConAC which includes oxygenation of ConAC, ring-opening reactions, and sequential decarboxylation yielding small aliphatic N-rich molecules (marine-like composition). These structures could be further polymerized by reactive oxygen species to form straight-chain alkanes if not consumed by microorganisms. Results from these controlled experiments reveal that the extent of photo-transformation appears to be a function of production temperature and parent feedstock. This study enhances our understanding of ConAC and pyDOM, their terrestrial-to-marine transfers, geochemical stability, and eventual fate in sunlit environments. Here we also show the value of structural characterization of pyDOM, and reveal the many unknowns left to be answered for this complex and analytically challenging type of organic matter.

Fe(II)-Catalyzed Ligand-Controlled Dissolution of Iron(hydr)oxides.

Dissolution of iron(III)phases is a key process in soils, surface waters, and the ocean. Previous studies found that traces of Fe(II) can greatly increase ligand controlled dissolution rates at acidic pH, but the extent that this also occurs at circumneutral pH and what mechanisms are involved are not known. We addressed these questions with infrared spectroscopy and 57Fe isotope exchange experiments with lepidocrocite (Lp) and 50 μM ethylenediaminetetraacetate (EDTA) at pH 6 and 7. Addition of 0.2-10 μM Fe(II) led to an acceleration of the dissolution rates by factors of 7-31. Similar effects were observed after irradiation with 365 nm UV light. The catalytic effect persisted under anoxic conditions, but decreased as soon as air or phenanthroline was introduced. Isotope exchange experiments showed that added 57Fe remained in solution, or quickly reappeared in solution when EDTA was added after 57Fe(II), suggesting that catalyzed dissolution occurred at or near the site of 57Fe incorporation at the mineral surface. Infrared spectra indicated no change in the bulk, but changes in the spectra of adsorbed EDTA after addition of Fe(II) were observed. A kinetic model shows that the catalytic effect can be explained by electron transfer to surface Fe(III) sites and rapid detachment of Fe(III)EDTA due to the weaker bonds to reduced sites. We conclude that the catalytic effect of Fe(II) on dissolution of Fe(III)(hydr)oxides is likely important under circumneutral anoxic conditions and in sunlit environments.

Morphometric and behavioural changes in the early life stages of the sea cucumber Cucumaria frondosa

The present study examined morphological and behavioural development in post-settled juveniles of the commercial sea cucumber Cucumaria frondosa, in an effort to assist captive breeding and conservation initiatives. Juveniles developed all 10 tentacles within 16 months; they had 9 podia and measured 4.6 mm in length after 21 months. Scaling between body length and number of podia was isometric, whereas dorsal tentacle metrics showed negative allometric scaling, indicating that growth was accompanied by a decreasing tentacle to body size ratio. Dorsally-oriented tentacles developed and ramified faster, showing 6 ramifications after 21 months, when ventrally-oriented tentacles only displayed one. This asynchrony underlines the distinctive roles of dorsal vs. ventral tentacles during the early months. The former were strictly used to capture plankton from the water column; whereas the latter were used for anchorage and feeding on deposited material. Ossicles of the body wall increased in length and thickness, and became slightly curved and rounded in older juveniles. Light intensity and water flow tolerance increased with age; from 25 lx and 5 cm s−1 in 1-month-old individuals, to >50 lx and 10 cm s−1 in 6, 12, and 21-month-old individuals, consistent with migration from sheltered to more exposed locations. Moreover, 1 and 6-month-old juveniles preferred rock substrates and black or red background colours; whereas 12 and 21-monthd-old individuals favoured substrates of coralline algae and a red background, also indicative of increasing affinity with sunlit environments and a shift from benthic to planktonic feeding. Juveniles of all age classes were feeding (i.e. had deployed tentacles) 24 h a day and commonly sought vertical surfaces. Together, the findings shed light on the early juvenile ecology of this cold-water suspension-feeding sea cucumber. Considering the expansion of sea cucumber fisheries and growing interest in the aquaculture of C. frondosa, this work also provides a framework for improved stock management and culture protocols.

Solar-panel and parasol strategies shape the proteorhodopsin distribution pattern in marine Flavobacteriia

Proteorhodopsin (PR) is a light-driven proton pump that is found in diverse bacteria and archaea species, and is widespread in marine microbial ecosystems. To date, many studies have suggested the advantage of PR for microorganisms in sunlit environments. The ecophysiological significance of PR is still not fully understood however, including the drivers of PR gene gain, retention, and loss in different marine microbial species. To explore this question we sequenced 21 marine Flavobacteriia genomes of polyphyletic origin, which encompassed both PR-possessing as well as PR-lacking strains. Here, we show that the possession or alternatively the lack of PR genes reflects one of two fundamental adaptive strategies in marine bacteria. Specifically, while PR-possessing bacteria utilize light energy (“solar-panel strategy”), PR-lacking bacteria exclusively possess UV-screening pigment synthesis genes to avoid UV damage and would adapt to microaerobic environment (“parasol strategy”), which also helps explain why PR-possessing bacteria have smaller genomes than those of PR-lacking bacteria. Collectively, our results highlight the different strategies of dealing with light, DNA repair, and oxygen availability that relate to the presence or absence of PR phototrophy.

Plant physiological changes along an encroachment gradient: an assessment of US Mid-Atlantic serpentine barrens

Serpentine barrens of the Mid-Atlantic United States are globally rare, grass-dominated ecosystems thought to exclude C₃ species and characterized by unique soil composition. However, like many grassland ecosystems globally, these sites are presently facing encroachment by surrounding forest. In this ecosystem, the tendril climbing vine, Smilax rotundifolia, forms dense thickets around barrens that typically precede forest encroachment. While numerous factors speculatively initiate and promote encroachment in these systems, few studies have examined photosynthetic responses of serpentine grasses to changes in resource availability initiated by encroachers or physiological ability of encroaching S. rotundifolia to colonize high-light barren environments. We sought to understand both environmental and physiological dynamics of encroachment along an irradiance gradient in these systems. At three serpentine barren sites in southeastern Pennsylvania, physiological responses of the native grasses Sorghastrum nutans and Schizachyrium scoparium to increased shading by S. rotundifolia were examined. Additionally, the physiological performance of S. rotundifolia in the forest understory was compared to that in sunlit barrens environments. Light-saturated photosynthesis (Aₛₐₜ), stomatal conductance (gₛ), instantaneous transpiration efficiency (ITE), maximum efficiency of photosystem II (Fᵥ/Fₘ), midday leaf water potential (ψₗₑₐf) and specific leaf area (SLA) were measured for all species over the course of the 2014 growing season. Two-way analyses of variance were used to assess changes in these parameters across growing environments, as well as seasonally for each species. Multiple regression analyses were also performed to investigate the influence of vapor pressure deficit (D) and leaf temperature (Tₗₑₐf) on Aₛₐₜ and ITE. Light-saturated photosynthesis was significantly greater in S. rotundifolia growing in sun than in the shade (P < 0.001) and early in the season (P = 0.012). Sun S. rotundifolia had up to 27% greater Aₛₐₜ than shaded plants. Even with reduced ψₗₑₐf in the barrens, S. rotundifolia maintained high gₛ though Aₛₐₜ was limited by high D later in the growing season. These data are in agreement with recent research suggesting that plants are not subject to water limitation in Mid-Atlantic barrens. Unexpectedly, shaded grasses at the encroachment interface did not exhibit any significant reduction in Aₛₐₜ. Declines in grass photosynthesis do not likely occur until S. rotundifolia rhizomes transition into monotypic thickets, completely excluding grasses. Encroachment by S. rotundifolia appears to be primarily facilitated by its ability to capitalize on light resources early on in the summer growing season, when environmental conditions are less stressful.

Iron Isotope Fractionation during Fe(II) Oxidation Mediated by the Oxygen-Producing Marine Cyanobacterium Synechococcus PCC 7002.

In this study, we couple iron isotope analysis to microscopic and mineralogical investigation of iron speciation during circumneutral Fe(II) oxidation and Fe(III) precipitation with photosynthetically produced oxygen. In the presence of the cyanobacterium Synechococcus PCC 7002, aqueous Fe(II) (Fe(II)aq) is oxidized and precipitated as amorphous Fe(III) oxyhydroxide minerals (iron precipitates, Feppt), with distinct isotopic fractionation (ε56Fe) values determined from fitting the δ56Fe(II)aq (1.79‰ and 2.15‰) and the δ56Feppt (2.44‰ and 2.98‰) data trends from two replicate experiments. Additional Fe(II) and Fe(III) phases were detected using microscopy and chemical extractions and likely represent Fe(II) and Fe(III) sorbed to minerals and cells. The iron desorbed with sodium acetate (FeNaAc) yielded heavier δ56Fe compositions than Fe(II)aq. Modeling of the fractionation during Fe(III) sorption to cells and Fe(II) sorption to Feppt, combined with equilibration of sorbed iron and with Fe(II)aq using published fractionation factors, is consistent with our resulting δ56FeNaAc. The δ56Feppt data trend is inconsistent with complete equilibrium exchange with Fe(II)aq. Because of this and our detection of microbially excreted organics (e.g., exopolysaccharides) coating Feppt in our microscopic analysis, we suggest that electron and atom exchange is partially suppressed in this system by biologically produced organics. These results indicate that cyanobacteria influence the fate and composition of iron in sunlit environments via their role in Fe(II) oxidation through O2 production, the capacity of their cell surfaces to sorb iron, and the interaction of secreted organics with Fe(III) minerals.

Ultraviolet photo-oxidation of polyvinylpyrrolidone (PVP) coatings on gold nanoparticles.

Polymeric coatings are commonly applied to impart functionality and colloidal stability to engineered nanoparticles. In natural environments, transformations of the coating can modify the particle transport behavior, but the mechanisms and outcomes of these transformations have not yet been thoroughly evaluated. This study investigates the photo-transformations of polyvinylpyrrolidone (PVP) coatings on gold nanoparticles (AuNPs) under ultraviolet (UV) irradiation, representing light exposure in surface waters or other sunlit environments, and the impact on the AuNP colloidal stability. Multiple orthogonal characterization methods were applied to interrogate UV-induced transformations and their consequences. Rapid oxidation of the PVP coating occurred upon UV exposure. The transformed PVP largely persisted on the AuNP surface, albeit in a collapsed polymer layer around the AuNP surface. This transformation resulted in drastically diminished colloidal stability of the AuNPs, consistent with loss of steric stabilization. While the residual coating modified the interaction of the AuNPs with calcium counterions, it did not prevent subsequent stabilization by humic acid. This study demonstrates the importance of both chemical and physical coating transformations on nanoparticles, and hence the need for orthogonal and complementary characterization methods to fully characterize the coating transformations. Finally, the specific transformations of the PVP-coated AuNPs investigated here are discussed more broadly with respect to generalizability to other polymer-coated NPs and the implications for their fate in sunlit or other reactive environments.

Photochemical transformations of thiolated polyethylene glycol coatings on gold nanoparticles.

Photochemical reactions can cause significant transformations of manufactured nanomaterials in sunlit environments. While transformations of inorganic nanoparticles (NPs) have been investigated extensively, less attention has been focused on the direct impact of aqueous photochemical reactions on adsorbed organic macromolecules that form the NP corona and strongly influence the surface interactions and reactivity that affect NP transport, fate, and toxicity. Here, we assess the transformations of methoxy polyethylene glycol thiol (mPEGSH) coatings on gold NPs (AuNPs) under controlled UV irradiation. A decrease in the adsorbed layer thickness of polymer was observed within 24 h of UV irradiation, resulting in increased susceptibility of the transformed NPs to aggregation. Surface chemistry analyses, including X-ray photoelectron spectroscopy (XPS), showed loss of the ether groups but persistence of reduced S on the AuNP surface, indicative of a chain scission mechanism yielding different NP surface properties from that of either the initial PEGylated AuNP or the citrate-stabilized AuNP prior to coating with mPEGSH. The transformation of the chemisorbed polymer was compared to that of dissolved mPEGSH in the presence and absence of the Au NPs, as evaluated by liquid chromatography - mass spectrometry (LC-MS). In contrast to the NP-adsorbed coating, the primary observed transformation of the dissolved mPEGSH was thiol oxidation to disulfides without extensive chain scission. This study demonstrates that transformations of adsorbed macromolecular coatings must be considered to accurately predict NP attachment behavior, and hence transport, in environmental systems. Because the corona transformation was not predictable from that of the dissolved polymer, direct NP surface characterization is required to discern the fundamental reactions involved in the photochemical transformation of coatings after sorption to the NP surface.

Sunlight inactivation of fecal indicator bacteria in open-water unit process treatment wetlands: Modeling endogenous and exogenous inactivation rates

A pilot-scale open-water unit process wetland was monitored for one year and found to be effective in enhancing sunlight inactivation of fecal indicator bacteria (FIB). The removal of Escherichia coli and enterococci in the open-water wetland receiving non-disinfected secondary municipal wastewater reached 3 logs and 2 logs in summer time, respectively. Pigmented enterococci were shown to be significantly more resistant to sunlight inactivation than non-pigmented enterococci. A model was developed to predict the inactivation of E. coli, and pigmented and non-pigmented enterococci that accounts for endogenous and exogenous sunlight inactivation mechanisms and dark processes. Endogenous inactivation rates were modeled using the sum of UVA and UVB irradiance. Exogenous inactivation was only significant for enterococci, and was modeled as a function of steady-state singlet oxygen concentration. The rate constants were determined from lab experiments and an empirical correction factor was used to account for differences between lab and field conditions. The model was used to predict removal rate constants for FIB in the pilot-scale wetland; considering the variability of the monitoring data, there was general agreement between the modeled values and those determined from measurements. Using the model, we estimate that open-water wetlands at 40° latitude with practical sizes can achieve 3-log (99.9%) removal of E. coli and non-pigmented enterococci throughout the year [5.5 ha and 7.0 ha per million gallons of wastewater effluent per day (MGD), respectively]. Differences in sunlight inactivation rates observed between pigmented and non-pigmented enterococci, as well as between lab-cultured and indigenous wastewater bacteria highlight the challenges of using FIB as model organisms for actual pathogens in natural sunlit environments.

Into the light: diurnality has evolved multiple times in geckos

Geckos are the only major lizard group consisting mostly of nocturnal species. Nocturnality is presumed to have evolved early in gecko evolution and geckos possess numerous adaptations to functioning in low light and at low temperatures. However, not all gecko species are nocturnal and most diurnal geckos have their own distinct adaptations to living in warmer, sunlit environments. We reconstructed the evolution of gecko activity patterns using a newly generated time-calibrated phylogeny. Our results provide the first phylogenetic analysis of temporal activity patterns in geckos and confirm an ancient origin of nocturnality at the root of the gecko tree. We identify multiple transitions to diurnality at a variety of evolutionary time scales and transitions back to nocturnality occur in several predominantly diurnal clades. The scenario presented here will be useful in reinterpreting existing hypotheses of how geckos have adapted to varying thermal and light environments. These results can also inform future research of gecko ecology, physiology, morphology and vision as it relates to changes in temporal activity patterns. © 2015 The Linnean Society of London, Biological Journal of the Linnean Society, 2015, ●●, ●●–●●.

Effect of Light on Biodegradation of Estrone, 17β‐Estradiol, and 17α‐Ethinylestradiol in Stream Sediment

AbstractBiodegradation of [A‐ring 14C] Estrone (E1), 17β‐estradiol (E2), and 17α‐ethinylestradiol (EE2) to 14CO2 was investigated under light and dark conditions in microcosms containing epilithon or sediment collected from Boulder Creek, Colorado. Mineralization of the estrogen A‐ring was observed in all sediment treatments, but not epilithon treatments. No difference in net mineralization between light and dark treatments was observed for 14C‐E2. Net mineralization of 14C‐E1 and 14C‐EE2 was enhanced in light treatments. Extents of 14CO2 accumulation and rates of mineralization were significantly greater for E2 than E1 under dark conditions, but were comparable under light conditions. These results indicate substantial differences in the uptake and metabolism of E1 and E2 in the environment and suggest biorecalcitrance of E1 relative to E2 in light‐limited environments. The extent of 14CO2 accumulation and rate of mineralization for EE2 in dark treatments were less than half of that observed for E2 and generally lower than for E1, consistent with previous reports of EE2 biorecalcitrance. However, 14CO2 accumulation and rates of mineralization were comparable for EE2, E2, and E1 under light conditions. These results indicate photoactivation and/or phototransformation/photodegradation processes can substantially enhance heterotrophic biodegradation of estrogens in sunlit environments and may play an important role in estrogen transport and attenuation.

Indirect Photolysis of Perfluorochemicals: Hydroxyl Radical-Initiated Oxidation of N-Ethyl Perfluorooctane Sulfonamido Acetate (N-EtFOSAA) and Other Perfluoroalkanesulfonamides

Selected perfluorinated surfactants were irradiated in aqueous hydrogen peroxide solutions using artificial sunlight to study transformation under aquatic environmental conditions. Indirect photolysis mediated by hydroxyl radical was observed for N-ethyl perfluorooctane sulfonamidoethanol (N-EtFOSE), N-ethyl perfluorooctane sulfonamido acetate (N-EtFOSAA), N-ethyl perfluorooctane sulfonamide (N-EtFOSA), and perfluorooctane sulfonamide acetate (FOSAA). An upper limitforthe bimolecular reaction rate constant for reaction of *OH and N-EtFOSAA was determined to be (1.7 +/- 0.7) x 10(9) M(-1)s(-1). A proposed reaction pathwayfor degradation of the parent perfluorochemical, N-EtFOSE, to the other perfluoroalkanesulfonamides and perfluorooctanoate (PFOA) was developed and includes oxidation and N-dealkylation steps. As they did not undergo additional degradation, perfluorooctane sulfonamide (FOSA) and PFOA were the final degradation products of hydroxyl radical-initiated oxidation. UV-visible absorption spectra for the perfluorochemicals, showing absorbance in the UV region below the range of natural sunlight are also reported. In sunlit environments, indirect photolysis of perfluorochemicals is likely to be important in the determination of their environmental fate given the slow rates expected for biotransformation and weak sorption. Photolytic conversion of perfluorochemicals into refractory perfluorinated acids, mainly PFOA, could mean that a significant fraction of these compounds will accumulate in the world's oceans.