Synthesis of all-acrylic graft copolymers by grafting-through strategy in emulsion

In this paper, PnBA-g-PMMA brush-like and centipede multigraft copolymers were synthesized via DPE seeded emulsion polymerization and miniemulsion polymerization. PMMA macromonomers with single tail and double tails were prepared by DPE-technique in emulsion and Steglich esterification. Then PnBA-g-PMMA multigraft copolymers were obtained by miniemulsion copolymerization. The molecular weight and polydispersity indices of PMMA macromonomers and graft copolymers were characterized by GPC. The structural characteristics, weight content of PMMA and the number of grafting sites in brush-like and centipede multigraft copolymers were determined by ¹H NMR. The thermal performance of graft copolymers were analyzed by DSC and TGA. AFM confirmed microphase separation between PnBA block and PMMA block.     

A high molecular weight acrylonitrile copolymer prepared by mixed solvents polymerization: II. effect of DMSO/water ratios on polymerization and stabilization

A bifunctional comonomer β-methylhydrogen itaconate was synthesized to prepare high molecular weight poly [acrylonitrile-co-(β-methylhydrogen itaconate)] [P (AN-co-MHI)] by mixed solvents polymerization, which was used as carbon fiber precursor instead of acrylonitrile terpolymers. The effect of dimethyl sulfoxide (DMSO)/deionized water ratios on the polymerization, structure and stabilization of P (AN-co-MHI) was studied by elemental analysis, UV-Visible Spectroscopy, fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and differential scanning calorimetry (DSC). The highest viscosity-average molecular weight (76.72 × 10⁴ g/mol) of P(AN-co-MHI) was obtained in the mixed solvents of DMSO/deionized water = 10/90 (wt/wt) due to the zero chain transfer constant of deionized water for radical ~ ~ ~AN·, which is 10 times larger than that of P(AN-co-MHI) copolymers prepared in DMSO solution polymerization under the same conditions and is beneficial to improving the tensile strength of resulting carbon fiber. The composition of P(AN-co-MHI) was controlled by the ratio of DMSO/deionized water in the mixed solvents, it is attributed to the changes of AN/MHI ratio taking part in the polymerization reactions, which is caused by the different solubility of AN in the mixed solvents. From elemental analysis and FTIR studies, it can be found out that the content of MHI in P(AN-co-MHI) copolymer becomes larger with the increase of DMSO content in the mixed solvents. The FTIR, XRD and DSC results show that the stabilization of P(AN-co-MHI) copolymer was significantly improved by MHI compared with PAN homopolymer and poly (acrlonitrile-methyl acrylate-acrylic acid) terpolymer, such as larger extent of stabilization, lower initiation temperature and smaller E _a of cyclization, which is beneficial to preparing high performance carbon fiber.     

Novel amphiphilic temperature responsive graft copolymers PCL-<Emphasis Type="Italic">g</Emphasis>-P(MEO<Subscript>2</Subscript>MA-<Emphasis Type="Italic">co</Emphasis>-OEGMA) via a combination of ROP and ATRP: synthesis,characterization, and sol-gel transition

A series of well-defined novel amphiphilic temperature-responsive graft copolymers containing PCL analogues P(αClεCL-co-εCL) as the hydrophobic backbone, and the hydrophilic side-chain PEG analogues P(MEO₂MA-co-OEGMA), designated as P(αClεCL-co-εCL)-g-P(MEO₂MA-co-OEGMA) have been prepared via a combination of ring-opening polymerization (ROP) and atom transfer radical polymerization (ATRP). The composition and structure of these copolymers were characterized by ¹H NMR and GPC analyses. The self-assembly behaviors of these amphiphilic graft copolymers were investigated by UV transmittance, a fluorescence probe method, dynamic light scattering (DLS) and transmission electron microscopy (TEM) analyses. The results showed that the graft copolymers exhibited the good solubility in water, and was given the low critical temperature (LCST) at 35(±1) °C, which closed to human physiological temperature. The critical micelle concentrations (CMC) of P(αClεCL-co-εCL)-g-P(MEO₂MA-co-OEGMA) in aqueous solution were investigated to be 2.0 × 10^?3, 9.1 × 10^?4 and 1.5 × 10^?3 mg·mL^?1, respectively. The copolymer could self-assemble into sphere-like aggregates in aqueous solution with diverse sizes when changing the environmental temperature. The vial inversion test demonstrated that the graft copolymers could trigger the sol-gel transition which also depended on the temperature.     

Ultralow ppm <Emphasis Type="Italic">se</Emphasis>ATRP synthesis of PEO-<Emphasis Type="Italic">b</Emphasis>-PBA copolymers

Poly(ethylene oxide)-block-poly(butyl acrylate) copolymers were prepared via simplified electrochemically mediated atom transfer radical polymerization (seATRP) utilizing only 1 ppm of Cu^II complex, which is the limit of a successful well-controlled polymerization. The presented seATRP system works under potentiostatic and galvanostatic conditions. The polymerization results showed similar molecular weight evolution while maintaining a narrow molecular weight distribution throughout the reactions. ¹H NMR results confirm chemical structure of synthesized diblock copolymers. This ultralow ppm technique is promising candidate for polymerization from nanoparticles, flat surfaces, proteins, and DNA.     

Identification of Crepenynic Acid in the Seed Oil of <Emphasis Type="Italic">Atractylodes lancea</Emphasis> and <Emphasis Type="Italic">A. macrocephala</Emphasis>

Atractylodes rhizome is widely used in traditional Chinese herbal medicine. Although the chemical composition of the root has been studied in detail, the oil content and fatty acid composition of the seeds of Atractylodes species have not been reported. Fatty acyl composition of seeds from Atractylodes lancea and A. macrocephala was determined by gas chromatography and mass spectrometry of fatty acid methyl esters and 3-pyridylcarbinol esters. The predominant fatty acid in the seeds of both species was linolenic acid, but the unusual acetylenic fatty acid, crepenynic acid (cis-9-octadecen-12-ynoic acid), was also observed at levels of 18% in A. lancea and 13–15% in A. macrocephala. Fatty acid content was 24% for the samples of A. lancea and 16–17% for samples from A. macrocephala. sn-1,3 regioselective lipase digestion of seed lipids revealed that crepenynic acid was absent from the sn-2 position of the seed triacylglycerol. Crepenynic acid was also found in the seed oil of Jurinea mollis at 24% and was not present in the sn-2 position of the TAG. A contrasting distribution of crepenynic acid was found in the oil of Crepis rubra, suggesting differences in crepenynic acid synthesis or TAG assembly between these species.     

Thermal behavior of layered perovskite-like compounds in the Bi<Subscript>4</Subscript>Ti<Subscript>3</Subscript>O<Subscript>12</Subscript>-BiFeO<Subscript>3</Subscript> system

The thermal properties of compounds of the general formula Bi _{m + 1} Fe _{m ? 3} Ti₃O_{3m + 3}, which are layered perovskite-like phases of the Aurivillius type, are investigated as a function of their composition. It is demonstrated that the temperature of decomposition of the Bi _{m + 1} Fe _{m ? 3} Ti₃O_{3m + 3} compounds decreases with an increase in the thickness of perovskite-like layers alternating in the structure and that the composition dependence of the temperature of the structural transition observed in these compounds exhibits a more complex behavior. The linear thermal expansion coefficients of all the compounds under investigation are found to be virtually independent of the composition.     

Acetoacetoxy functionalized natural rubber latex capable of forming cross-linkable film under ambient conditions

This work demonstrates that natural rubber (NR) latex particles containing acetoacetoxy (AcAc) groups are able to undergo cross-linking upon film formation at ambient temperature by reaction with glutaraldehyde (GTA). Natural rubber latex grafted with poly(acetoacetoxyethyl methacrylate) (NR-g-PAAEM) was synthesized by seeded emulsion polymerization, using benzoyl peroxide (BPO) as an initiator in free radical polymerization. The degree of grafting of PAAEM in the graft copolymers was evaluated by ¹H NMR technique. Transmission electron microscope (TEM) was used for investigation the particle morphology of the grafted NR latex. Since the AcAc groups are intentionally attached to the NR particles providing sites of cross-linking at ambient temperature, the cross-linking ability of these sites by reaction with GTA was then investigated. The results revealed that the latex film of NR-g-PAAEM with the addition of GTA had a much higher tensile strength in comparison with the film without GTA. The surface morphology of the NR-g-PAAEM latex film formed in the absence and presence of the GTA cross-linker was also investigated using atomic force microscopy (AFM). By GTA addition into the NR-g-PAAEM latex before film formation, an increase in the root-mean-square (RMS) roughness of the surface of the latex film was observed. Moreover, it was also observed that the NR-g-PAAEM films with the addition of GTA had higher activation energy for thermal degradation than that without the cross-linker. This confirms that the cross-linking reaction took place in the NR-g-PAAEM latex film as a result of its reaction with the GTA.     

Simulation of the composition and proportions of anions in polymerized silicate melts

A new statistical model is proposed for describing an equilibrium structure of polymer complexes in a silicate melt. The model makes it possible to calculate the molecular-mass distributions of polyanions of the general formula (Si _i O_{3i + 1 ? j} )^{2(i + 1 ? j} )^?, where i is the number of silicon atoms and j is the number of intramolecular closures of bridging bonds. The proposed model is implemented as the STRUCTON computer program (version 1.1, 2006) intended for calculating the composition and proportions of polyanions at different degrees of polymerization of the system. The executable code is implemented on personal computers. The distributions of Q ⁿ structons, which are obtained experimentally from Raman and NMR spectroscopic data or evaluated theoretically, are used as input parameters for the computer program. The testing calculations are performed with the STRUCTON program for three arbitrary distributions of Q ⁿ particles corresponding to different degrees of polymerization 0.25 ≤ α ≤ 0.49 for the model system containing 104 initial structons. The results of the statistical simulation have demonstrated that a limited ensemble of polymer complexes is formed in the system, so that the mean number of different types of complexes varies from 46 to 141. This result correlates with an increase in the mean size of anions from 1.87 to 8.60 and with a decrease in the total number of polymer particles from 5320 to 1166 in the aforementioned range of degrees of polymerization α.     

Optimization of controlled ring-opening polymerization of <Emphasis Type="SmallCaps">l</Emphasis>-lactide to hydroxyl terminated polylactides using zinc acetate catalyst

Hydroxyl terminated polylactide polymers with number of average molecular weights (M _n ) varying from 1625 to 3459 g mol^?1 were synthesized by ring opening bulk polymerization of lactide in the presence of zinc acetate being a potent catalyst. The use of 1,4 butanediol (BDO) initiator leads to hydroxyl terminated polylactides, thus excellent precursors for shape-memory biodegradable polyurethanes. Different reaction conditions employed for the synthesis of hydroxyl terminated polylactide polymers via activated monomer mechanism may result in differences in M _n , percentage mass conversion and percentage degree of crystallinity (%χ _c ) of the product. Influence of process parameters, i.e. catalyst concentration, initiator concentration, reaction temperature and time on characteristics of hydroxyl terminated polylactides was studied. These polymers were characterized by Nuclear Magnetic Resonance (¹H-NMR) spectroscopy, Fourier transforms infrared (FTIR) spectroscopy, gel permeation chromatography (GPC) and X-ray diffraction (XRD) techniques. FTIR and ¹H-NMR confirmed the formation of hydroxyl terminated polylactides. M _n was determined by ¹H-NMR, GPC and end group analysis. %χ _c was calculated from XRD spectra. Maximum mass conversion, M _n and %χ _c were observed at 5 mol% SnOct₂ and 5 mol% BDO concentration. At optimum temperature of 145 °C, these characteristics improved linearly with polymerization time up to 6 h and declined thereafter.     

Sexual Deception in the <Emphasis Type="Italic">Eucera</Emphasis>-Pollinated <Emphasis Type="Italic">Ophrys leochroma</Emphasis>: A Chemical Intermediate between Wasp- and <Emphasis Type="Italic">Andrena-</Emphasis>Pollinated Species

Ophrys flowers mimic sex pheromones of attractive females of their pollinators and attract males, which attempt to copulate with the flower and thereby pollinate it. Virgin females and orchid flowers are known to use the same chemical compounds in order to attract males. The composition of the sex pheromone and its floral analogue, however, vary between pollinator genera. Wasp-pollinated Ophrys species attract their pollinators by using polar hydroxy acids, whereas Andrena-pollinated species use a mixture of non-polar hydrocarbons. The phylogeny of Ophrys shows that its evolution was marked by episodes of rapid diversification coinciding with shifts to different pollinator groups: from wasps to Eucera and consequently to Andrena and other bees. To gain further insights, we studied pollinator attraction in O. leochroma in the context of intra- and inter-generic pollinator shifts, radiation, and diversification in the genus Ophrys. Our model species, O. leochroma, is pollinated by Eucera kullenbergi males and lies in the phylogeny between the wasp and Andrena-pollinated species; therefore, it is a remarkable point to understand pollinator shifts. We collected surface extracts of attractive E. kullenbergi females and labellum extracts of O. leochroma and analyzed them by using gas chromatography with electroantennographic detection (GC-EAD) and gas chromatography coupled with mass spectrometry (GC-MS). We also performed field bioassays. Our results show that O. leochroma mimics the sex pheromone of its pollinator’s female by using aldehydes, alcohols, fatty acids, and non-polar compounds (hydrocarbons). Therefore, in terms of the chemistry of pollinator attraction, Eucera-pollinated Ophrys species might represent an intermediate stage between wasp- and Andrena-pollinated orchid species.     

Raman spectra and surface structure of CaO-Fe<Subscript>2</Subscript>O<Subscript>3</Subscript>-Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-SiO<Subscript>2</Subscript> glass leached in potassium hydroxide solutions

It is difficult to research on the surface structure of amorphous phase in fly ash during leaching reaction due to crystalline phase and complex structure. In the present work, in order to reveal the effects of leaching reaction on the surface structure of amorphous phase in fly ash, the modelling CaO-Fe₂O₃-Al₂O₃-SiO₂ glass was prepared by the traditional melting methods. The leaching reaction of CaO-Fe₂O₃-Al₂O₃-SiO₂ glass with 7.5 M KOH was investigated by spectroscopy, spectrophotometer and wet chemical method. The results show that the content of Q ¹, Q ², Q ³ and Q ⁴ of glass without corrosion was 4.21, 9.51, 23.03 and 52.55%, respectively, which shows that the network polymerization of glass is compact. The leaching reaction of glass can be described by the following equation: dS/dt = k/(r + S ₀). Leaching in KOH for various times induces the content of Q ⁴ and Q ¹ to be decreased, and Q ² and Q ³ increased, resulted in the depolymerization of network and the surface glass dissolved in alkaline solution to form a gel phase. In stage one of leaching reaction, the rate of iron ion leached from glass surface was slow, which resulted in the small slope of straight-line relationship of leaching curve. In the following stage, the leaching rate of iron ion increased with the prolongation of time.     

Attraction of Three Mirid Predators to Tomato Infested by Both the Tomato Leaf Mining Moth <Emphasis Type="Italic">Tuta absoluta</Emphasis> and the Whitefly <Emphasis Type="Italic">Bemisia tabaci</Emphasis>

Plants emit volatile compounds in response to insect herbivory, which may play multiple roles as defensive compounds and mediators of interactions with other plants, microorganisms and animals. Herbivore-induced plant volatiles (HIPVs) may act as indirect plant defenses by attracting natural enemies of the attacking herbivore. We report here the first evidence of the attraction of three Neotropical mirid predators (Macrolophus basicornis, Engytatus varians and Campyloneuropsis infumatus) toward plants emitting volatiles induced upon feeding by two tomato pests, the leaf miner Tuta absoluta and the phloem feeder Bemisia tabaci, in olfactometer bioassays. Subsequently, we compared the composition of volatile blends emitted by insect-infested tomato plants by collecting headspace samples and analyzing them with GC-FID and GC-MS. Egg deposition by T. absoluta did not make tomato plants more attractive to the mirid predators than uninfested tomato plants. Macrolophus basicornis is attracted to tomato plants infested with either T. absoluta larvae or by a mixture of B. tabaci eggs, nymphs and adults. Engytatus varians and C. infumatus responded to volatile blends released by tomato plants infested with T. absoluta larvae over uninfested plants. Also, multiple herbivory by T. absoluta and B. tabaci did not increase the attraction of the mirids compared to infestation with T. absoluta alone. Terpenoids represented the most important class of compounds in the volatile blends and there were significant differences between the volatile blends emitted by tomato plants in response to attack by T. absoluta, B. tabaci, or by both insects. We, therefore, conclude that all three mirids use tomato plant volatiles to find T. absoluta larvae. Multiple herbivory did neither increase, nor decrease attraction of C. infumatus, E. varians and M. basicornis. By breeding for higher rates of emission of selected terpenes, increased attractiveness of tomato plants to natural enemies may improve the effectiveness of biological control.     

Cluster Self-Organization of Intermetallic Systems: Two-Layer Quasi-Spherical Nanocluster Precursors K69 and K26 in the Crystal Structure of Li<Subscript>26</Subscript>Na<Subscript>58</Subscript>Ba<Subscript>38</Subscript> (<Emphasis Type="Italic">cF</Emphasis>488)

The geometric and topological analysis of the crystal structure of intermetallic Li₂₆Na₅₈Ba₃₈ (cF488, a = 27.335 Å, V = 20 424 ų, F-43m) is carried out using computer methods (ToposPro software package). The analysis method is based on determining the chemical composition and structure of an intermetallic cluster precursor and constructing a basic 3D network of the structure in the form of a graph whose nodes correspond to the position of their centers of gravity. Using the method of the complete decomposition of the 3D factor graph of the crystal structure into cluster substructures, we find two types of framework-forming nanoclusters, namely, K69 of the 1@16@52 composition and K26 of the 0@4@22 composition with point symmetry g =–43m. The symmetric and topological code of self-assembly of 3D structures from nanocluster precursors is reconstructed in the following form: primary chain → microlayer → microframework. Clusters Ba5, Na₆(Na₄), and Na₂В are determined as spacers occupying voids in the 3D framework of nanoclusters K69 and K26.     

Density and microhardness of glasses in the SrO-B<Subscript>2</Subscript>O<Subscript>3</Subscript>-SiO<Subscript>2</Subscript> system

The density d at a temperature of 25°C is measured by the hydrostatic weighing method, the Vickers microhardness H _V is determined, and the fluctuation free volume fraction f _g is calculated for glasses in the SrO-B₂O₃-SiO₂ system with a constant strontium oxide content in the range from 35 to 45 mol %. It is demonstrated that the quantities H _V and f _g decrease and the density d increases with an increase in the SrO content.     

<Emphasis Type="Italic">m</Emphasis>-Cresol-substituted triethyl aluminum/MoCl<Subscript>5</Subscript>/TBP catalytic system for coordination polymerization of butadiene

Coordination polymerization of butadiene was initiated by a catalyst system consisting of tributyl phosphate (TBP) as ligand, molybdenum pentachloride as primary catalyst and triethyl aluminum substituted by m-cresol as co-catalyst. The effects of the substitution of m-cresol on the activity of the catalyst system, molecular weight and molecular weight distribution, intrinsic viscosity and microstructures of the resulting polymers were investigated in details. The molecular weight and molecular weight distribution of the polymerization products were determined by GPC. The microstructure of the polymerization products was characterized by FTIR, ¹³C NMR and DSC techniques. The experimental results indicated that the polymerization activity of the reaction system and the molecular weight of the polymerization products gradually increased with the increase of the substitution content of m-cresol, namely, Al(OPhCH₃)₂Et?>?Al(OPhCH₃)Et₂?>?Al(OPhCH₃)_0.5Et_2.5>AlEt₃. The 1,2-structure contents of the polymerization products could be adjusted between 89 and 91% through the control of the substitution of m-cresol, and there was minute quantities of crystalline structures in the resulting polymers due to the increasing content of the syndiotactic 1,2-polybutadiene. In a word, the existence and increase of steric hindrance of m-cresol made it easier for polymerization products to form interdisciplinary 1,2-structure.     

Stingless Bees: Chemical Differences and Potential Functions in <Emphasis Type="Italic">Nannotrigona testaceicornis</Emphasis> and <Emphasis Type="Italic">Plebeia droryana</Emphasis> Males and Workers

Cuticular wax, abdominal and cephalic extracts of foraging workers and males of Nannotrigona testaceicornis and Plebeia droryana, from the “Aretuzina” farm in São Simão, SP, Brazil, were analyzed by GC-MS. The principal constituents were hydrocarbons, terpenes, aldehydes, esters, steroids, alcohols, and fatty acids. Interspecific differences for both cuticular wax and cephalic extracts were found. The composition of cuticular wax and cephalic extracts was similar at the intraspecific level, with minor component differences between males and workers. Abdominal extracts differentiated sexes (male and worker) at the intraspecific and interspecific levels. The main chemical components in abdominal extracts of N. testaceicornis workers and males were geranylgeranyl acetate and (Z)-9-nonacosene, respectively. The principal components of abdominal extracts from P. droryana workers and males were tetradecanal and unsaturated fatty acids (linoleic and linolenic acids), respectively. A secondary alcohol, (S)-2-nonanol, was detected in Plebeia droryana males only, but not in workers. Preliminary field experiments showed that (S)-(+)-2-heptanol and (S)-(+)-2-heptanol/ (S)-(+)-2-nonanol (1:1) attracted workers of P. droryana, N. testaceicornis, and Frieseomelitta silvestrii. However, males did not respond suggesting that these compounds do not function as alarm or recruitment pheromones . In addition, racemic mixtures were inactive.     

SHS of Y<Subscript>2</Subscript>Ti<Subscript>2</Subscript>O<Subscript>7</Subscript>-based mineral-like ceramics: Influence of green density

Explored was the influence of compacting pressure (P) and green density (ρ) on the properties of Zr-doped mineral-like pyrochlore ceramics Y₂(Ti_{1 – x} Zr _x )₂O₇ (x ≤ 0.3) prepared by SHS method. The optimal ρ values that provide minimal porosity and maximal mechanical strength of synthesized ceramics were found. An increase in ρ was found to decrease combustion temperature and increase pyrochlore lattice parameter a. Green density was also found to affect phase composition of the SHS-produced ceramics under study.     

Parameters of luminescence and the local structure of Eu<Superscript>3+</Superscript> centers in fluorogermanate glasses

The influence of the chemical nature of the local environment of Eu³⁺ ions on the parameters of luminescence of these centers in glasses of the (BaGeO₃)_{1 ? x ? y} (Al₂O₃) _x (0.45CaF₂ · 0.55MgF₂) _y (x = 0.25, y = 0; x = 0.17, y = 0.17; x = 0.15, y = 0.22; x = 0.07, y = 37.00; x = 0, y = 0.45) system is investigated. The oxidation state of europium atoms and the degree of homogeneity of their local environment in the glasses are determined using ¹⁵¹Eu Mössbauer spectroscopy.     

Identification of the Unsaturated Heptadecyl Fatty Acids in the Seed Oils of <Emphasis Type="Italic">Thespesia populnea</Emphasis> and <Emphasis Type="Italic">Gossypium hirsutum</Emphasis>

The fatty acid composition of the seed oils of Thespesia populnea and cotton variety SG-747 (Gossypium hirsutum) were studied to identity their 17-carbon fatty acids. With a combination of chemical derivatization, gas chromatography, and mass spectrometry, 8-heptadecenoic acid, 9-heptadecenoic acid, and 8,11-heptadecadienoic acids were identified in both oils. Additionally, traces of 10-heptadecenoic acid were identified in the T. populnea oil. Although these odd-carbon number fatty acids are present in only minor amounts in cottonseed oil, they make up about ~2 % of the fatty acids in T. populnea seed oil. The identification of these acids indicates that fatty acid α-oxidation is not restricted to cyclopropene fatty acids in these plants, but also occurs with unsaturated fatty acids. Combined with malvalic acid (generally accepted as being formed by α-oxidation of sterculic acid), ~7 % of the fatty acids in T. populnea seed have under gone α-oxidization. The results should help clarify the composition of T. populnea seed oil, which has been reported inconsistently in the literature.     

Fall Composition of Storage Lipids is Associated with the Overwintering Strategy of <Emphasis Type="Italic">Daphnia</Emphasis>

Diapause, which occurs through the production of dormant eggs, is a strategy used by some zooplankton to avoid winter months of persistent low temperatures and low food availability. However, reports of active zooplankton under the ice indicate that other strategies also exist. This study was aimed at evaluating whether the composition of storage lipids in the fall differs between diapausing and active overwintering Daphnia. We assessed the quantity of storage lipids and fatty acid (FA) composition of Daphnia species, along with FA content of seston, in six boreal, alpine and subarctic lakes at the onset of winter, and evaluated the association between storage lipids and Daphnia overwintering strategy. We found that active overwintering Daphnia had >55% body fat and the highest FA concentrations. Polyunsaturated FA, especially stearidonic acid (18:4n-3; SDA) and high ratios of n-3:n-6, were preferentially retained to a greater extent in active overwintering Daphnia than in those that entered diapause. Daphnia FA composition was independent of that of the seston diet, indicating that Daphnia adjusted their storage lipids according to the physiological requirements of a given overwintering strategy. The occurrence of an active overwintering strategy has consequences for zooplankton community structure, and can have important implications for the transfer of high-quality energy at higher trophic levels.