Egg dispersion in codling moth: Influence of egg extract and of its fatty acid constituents

Codling moth females (Cydia pomonella, Lepidoptera: Tortricidae) (CM) usually lay single eggs and have a tendency to disperse. In a first experiment we observed that single females exposed to 20 apples distribute their eggs regularly among apples, suggesting a dispersive oviposition behavior. In a dual-choice situation, isolated females avoided oviposition on areas of cardboard treated with a methylene dichloride egg extract at the dose of ca. 1.0 egg equivalent/cm². A strong avoidance was obtained in response to a 20-fold dose, which was accompanied by a significant reduction of total oviposition. Seven major compounds found by GC analyses in the methylene dichloride extract of 2 to 3-day-old eggs were saturated or unsaturated C₁₄-C₁₈ straight-chain fatty acids: myristic acid, palmitic acid, palmitoleic acid, stearic acid, oleic acid, linoleic acid, and linolenic acid. This was confirmed by GC-MS analysis of an extract made by ethyl ether. Smaller amounts of three methyl esters were also identified as methyl myristate, methyl palmitate, and methyl stearate. A blend of the seven fatty acids (FA) mimicked rather well the avoidance provoked by the extract, and this avoidance was confirmed by choice between treated and untreated fruits by single females. The treatment of apples with the 7FA mixture induced an aggregative distribution of the eggs among apples. We also found that the amounts of fatty acids harvested in the extract depend on the egg age. Amounts of fatty acids increased until eggs were 4 days old and then decreased before hatching. In this paper we discuss the possible role of simple molecules, such as fatty acids and their esters, as semiochemicals indicative of juvenile tissues.     

Fatty acid biosynthesis during embryogenesis in the amphibianBufo arenarum Hensel

The fatty acid composition and biosynthesis of fatty acids were studied during early embryogenesis of the toadBufo arenarum Hensel. The ova and stages up to the 6 1/2 day embryo have similar fatty acid compositions, with ca. 70% unsaturated acids. The eggs and embryo were permeable to acetate and impermeable to palmitic, linoleic, and eicosa-8,11,14-trienoic acid. Labeled acetate was incorporated by the eggs into the saturated acids-lauric, myristic, palmitic, stearic, arachidic, and behenic-and into the unsaturated acids-myristoleic, palmitoleic, oleic, and eicosaenoic acids. During segmentation and gastrulation, de novo biosynthesis of fatty acids increased, desaturation to myristoleic, palmitoleic, and oleic acids was enhanced; and fatty acids were esterified to triglycerides, phosphatidyl choline, and phosphatidyl ethanolamine. The feeding embryo (11 days) changed the pattern of incorporation to less incorporation into triglycerides.     

Chemical Composition and Characteristics of <Emphasis Type="Italic">Commiphora wightii</Emphasis> (Arnott) Bhandari Seed Oil

The seeds of Commiphora wightii (Arnott) Bhandari contain 9.8 ± 0.7% oil. The fatty acid composition and chemical properties of the extracted oil were determined. Gas liquid chromatography of the methyl esters of the fatty acids shows the presence of 46.62% saturated fatty acids and 51.40% unsaturated fatty acids. The fatty acid composition is as follows: capric acid 3.50%, myristic acid 14.51%, palmitic acid 6.68%, stearic acid 4.70%, arachidic acid 3.18%, behenic acid 14.05%, myristoleic acid 1.34%, palmitoleic acid 12.07%, oleic acid 14.15%, eicosenoic acid 0.11%, linoleic acid 22.34% and alpha linoleic acid 1.37%.     

Chemical investigation ofSolanum khasianum seed fat

The seeds ofSolanum khasianum contain 14.5% of a fatty oil. The component fatty acids were found by gas liquid chromatography analysis to be 0.2% myristic, 14.2% palmitic, 0.9% palmitoleic, 4.4% stearic, 15% oleic, and 62.6% linoleic acids.     

Fatty acid composition of rice lipids by gas-liquid chromatography

Gas-liquid Chromatographic analysis of the methyl ester of lipids of four rice varieties showed that bran lipids had significantly higher mean contents of linoleic and linolenic acids, but lower contents of myristic, palmitic, palmitoleic, and stearic acids than milled rice lipids. Nine fatty acids were detected. The principal components were oleic, linoleic, and palmitic, which also was confirmed by thin-layer chromatography of the esters. Issued as I.R.R.I. Journal Series No. 12     

Fatty acid composition of lymphocytes and macrophages from rats fed fiber-rich diets: A comparison between oat bran- and wheat bran-enriched diets

The effect of oat bran-(OBD) and wheat bran-enriched diets (WBD) on fatty acid composition of neutral lipids and phospholipids of rat lymphocytes and macrophages was investigated. In neutral lipids of lymphocytes, OBD reduced the proportion of palmitoleic acid (48%), whereas WBD reduced by 43% palmitoleic acid and raised oleic (18%), linoleic (52%), and arachidonic (2.5-fold) acids. In neutral lipids of macrophages, OBD increased palmitic (16%) and linoleic (29%) acids and slightly decreased oleic acid (15%). The effect of WBD, however, was more pronounced: It reduced myristic (60%), stearic (24%) and arachidonic (63%) acids, and it raised palmitic (30%) and linoleic (2.3-fold) acids. Neither OBD nor WBD modified the composition of fatty acids in phospholipids of lymphocytes. In contrast, both diets had a marked effect on composition of fatty acids in macrophage phospholipids. OBD raised the proportion of myristic (42%) and linoleic (2,4-fold) acids and decreased that of lauric (31%), palmitoleic (43%), and arachidonic (29%) acids. WBD increased palmitic (18%) and stearic (23%) acids and lowered palmitoleic (35%) and arachidonic (78%) acids. Of both cells, macrophages were more responsive to the effect of the fiber-rich diets on fatty aicd composition of phospholipids. The high turnover of fatty acids in macrophage membranes may explain the differences between both cells. The modifications observed due to the effects of both diets were similar in few cases: an increase in palmitic and linoleic acids of total neutral lipids occurred and a decrease in palmitoleic and arachidonic acids of phospholipid. Therefore, the mechanism involved in the effect of both diets might be different.     

Analysis of Albizzia lebbeck Flower Oil

The oil of Albizzia lebbeck flowers was analysed. Saponifiable lipid contains capric, lauric, myristic, palmitic, palmitoleic, stearic, oleic, linoleic, arachidic and behenic acids. Unsaponifiable lipid was found to contain aliphatic alcohols, taraxerol, β-amyrin, cycloartenol, lupeol, 24-methylene cycloartanol, campesterol, sitosterol and four unidentified components.     

金银花浸膏挥发性成分分析及在卷烟中的应用

采用气相色谱-质谱分析技术(GC-MS)分析了金银花浸膏的挥发性成分和相对含量进行了分析,共鉴定出67种成分,主要为亚油酸甲酯、棕榈酸、十八碳烯酸甲酯、棕榈酸甲酯、亚麻酸甲酯、芳樟醇、棕榈酸乙酯、亚油酸乙酯、亚油酸、肉豆蔻酸、亚麻酸乙酯等。对金银花浸膏在卷烟中进行了添加实验,发现添加了金银花浸膏的卷烟刺激性明显得到降低、烟香更加柔和、具有更好的抽吸口感。     

HBr-Reactive acids ofMalva sylvestris seed oil

Malva sylvestris seed oil contained 5.6% sterculic, 11.0% malvalic, 1.6% vernolic, 15.6% lauric, 6.6% myristic, 26.6% palmitic, 5.6% palmitoleic, a trace of stearic, 23.0% oleic and 4.0% linoleic acids. The co-occurrence of malvalic and sterculic acids was established by gas liquid chromatography (GLC) of the silver nitrate-methanol treated esters usingSterculia foetida esters as the reference standard. Co-occurrence of epoxy acid (vernolic acid) was confirmed withVernonia anthelmintica as the lipid standard.     

The fatty acid composition of small and large naturally occurring milk fat globules

Native milk fat globules of various mean diameters, ranging from d₄₃ = 1.5 to 7.3 μm, were obtained using microfiltration of raw whole milk acquired in winter and spring. After total lipid extraction, fatty acid composition was characterized by methyl and butyl ester analysis using gas chromatography. The oleic and linoleic acid content of milk obtained in winter increased with fat globule size, whereas myristic and palmitic acid decreased. There was significantly more lauric, myristic and palmitoleic acid, and less stearic acid in small fat globules compared to large fat globules in milk obtained in both winter and spring. The relative content of oleic and linoleic acids were found to depend on fat globule size and season. Results are interpreted on the basis of the relative content of milk fat globule membrane depending on fat globule size, and on consequences of compositional variations on milk fat globule melting behavior.     

Component fatty acids ofAspergillus terreus fat

The component fatty acids of the fat elaborated byAspergillus terreus Thom, which was found to be a promising mold for the production of fat, have been studied. The fat has, based on gas liquid chromatographic evidence, 0.1% lauric, 1.9% myristic, 23.4% palmitic, 0.1% palmitoleic, 0.3% stearic, 14.1% oleic, 39.4% linoleic and 20.7% linolenic acids. The presence of large proportions of linoleic and linolenic acids suggests technological interest for the fat.     

Separation of Oleic Acid from Fatty Acid Impurities

Abstract

A method of oleic acid purification is described. The method consists of the following five steps: 1) cooling of the sample to 4°C for a partial separation of palmitic acid by crystallization, 2) distillation at reduced pressure (0.8 mmHg) for removal of lauric and myristic acids, 3) crystallization of stearic and palmitic acids from acetone at -25°C, 4) separation of oleic acid from palmitoleic and linoleic acids by oleic acid crystallization from aqueous methanol solutions at ?10°C, 5) reduced pressure (0.5 mmHg) distillation of the resulting oleic acid sample for removal of water and methanol. By utilizing the procedure described above, a sample containing only 82% oleic acid was refined to a product containing 98.7–98.9% oleic acid.     

Studies on Apocynacea Seed Oils

The fatty acid composition of three seed oils of Apocynaceae has been studied in this investigation. The seed oils of Apocynaceae were examined for their component acids and were found to contain the following acids: Rauwolfia serpentina, Benth, (wt.%) lauric 0.2 %, myristic 0.8 %, palmitic 17.7%, stearic 4.9 %, arachidic 0.9 %, behenic 0.6 %, oleic 34.4 %, and linoleic 40.5 %. Rauwolfia tetraphylla, Linn. syn. Rauwolfia canescens, Linn., Rauwolfia heterophylla, Roem and Schult, (wt.%) lauric 0.9 %, myristic 3.4 %, palmitic 25.7 %, stearic 10.3%, arachidic 1.6%, behenic 1.4%, oleic 36.5 %, and linoleic 20.2 %. Vinca rosea Linn syn. Lochnera rosea, Linn. (wt.%) lauric 0.2%, myristic 1.0%, palmitic 1.4 %, stearic 6.8 %, arachidic 1.3 %, behenic 0.6 %, oleic 73.6 %, and linoleic 15.1 %.     

The lipids of the common house cricket,Acheta domesticus L. I. Lipid classes and fatty acid distribution

The lipids of the common house cricket,Acheta domesticus L., have been examined with the following results. The fatty acids associated with the lipid extracts do not change significantly from the third through the eleventh week of the crickets' postembryonic life. The major fatty acids are linoleic (30–40%), oleic (23–27%), palmitic (24–30%), and stearic acids (7–11%). There are smaller amounts of palmitoleic (3–4%), myristic (∼1%), and linolenic acids (<1%). The fatty acid composition of the cricket lipids reflects but is not identical to the fatty acids of the dietary lipids: linoleic (53%), oleic (24%), palmitic (15%), stearic (3%), myristic (2%), and linolenic acid (2%). The amount of triglycerides present in the crickets increases steadily from the second through the seventh or eighth week of postembryonic life, then drops sharply. Other lipid classes, such as hydrocarbons, simple esters, diglycerides, monoglycerides, sterols, and free fatty acids remain about constant. The composition of the fatty acids associated with the tri-, di-, and monoglycerides and the free fatty acid fraction are all about the same. The fatty acids associated with the simple esters are high in stearic acid. Postdoctoral Research Associate, Department of Chemistry, University of Michigan, 1965–1967.     

Ant repellent effect of the sternal gland secretion ofPolistes dominulus (Christ) andP. sulcifer (Zimmermann). (Hymenoptera: Vespidae)

The long-chain carboxylic acids identified in the sternal gland secretion ofPolistes dominulus andP. sulcifer females were tested individually on three species of ants,Crematogaster scutellaris, Formica cunicularia, andLasius sp., in order to verify if they have a repellent effect. The unsaturated acids (palmitoleic, linoleic, and oleic) act as repellents of all three ant species, while the saturated acids (lauric, myristic, palmitic, and stearic) have no effect. The mixture reproducing the secretion of the sternal glands ofP. dominulus maintained its repellency for at least four days.     

Site-specific differences in the fatty acid composition of human adipose tissue

The fatty acid composition of triacylglycerols from fifteen distinct adipose depots taken from each of seven adult male human subjects was compared. Oleic, palmitic, linoleic, stearic, myristic, palmitoleic and vaccenic acids accounted for more than 90% of the triacylglycerol fatty acids in all sites from all subjects; a number of other fatty acids were also identified and quantified. There were large differences in theaverage fatty acid composition between individual subjects. There were no site-specific differences in the proportions of myristic (3.8–4.7% of triacylglycerol fatty acids), palmitic (23–29%), linoleic (6.7–9.8%) or vaccenic (4.1–4.7%) acids or in the proportions of any of the less abundant fatty acids. There were some significant site-specific differences in the proportions of palmitoleic, oleic and stearic acids. The calf depot contained more palmitoleic acid (6.41±1.09%) than the trapezius (3.12±0.55%), perirenal (3.59±0.50%) and mesenteric (3.70±0.43%) depots, more oleic acid (42.13±1.27%) than the trapezius (36.03±2.18%), perirenal (36.50±1.56%) and breast (37.13±1.55%) depots and less stearic acid (5.18±0.89%) than the trapezius (8.57±0.97%), perirenal (8.49±0.75%), mesenteric (7.87±0.42%), breast (8.02±0.75%) and clavicular (8.34±0.78%) depots. The buttock depot contained less stearic acid (6.06±0.65%) than the perirenal, mesenteric and clavicular depots, while the anterior thigh depot contained less stearic acid (6.07±0.70%) than the perirenal depot. These findings indicate that, while most human adipose depots differ little in fatty acid composition, some sites, in particular the calf, perirenal, trapezius and mesenteric depots, have site-specific properties.     

Fatty acid composition of Iranian citrus seed oils

Fatty acid compositions of seed oils from eight Iranian citrus fruits were determined. The ranges of values for major fatty acids were 21.8–29.4% palmitic, 3.1–7.60% stearic, 0.3–1.3% palmitoleic, 23.5–32.3% oleic, 33.5–39.8% linoleic, and 3.1–7.6% linolenic. Low amounts (up to 0.1%) of myristic and arachidic acids and traces of a few unidentified ones constituted minor fatty acids.     

Egg yolk lipids and maternal diet in the nutrition of turkey embryo

Turkey hens were fed diets containing no added fat nor diets supplemented with soybean oil or neatsfoot oil. The composition of neutral and polar lipid fatty acids present in the unincubated turkey egg yolk was compared with that of those present in the yolk sac of the developing turkey embryo at different stages of development. Comparisons were made of the fatty acid fractions in the entire embryo homogenates, except liver and heart, which were analyzed separately. Changes in the relative amounts of the fatty acids are reported as affected by age of the embryo and by dietary lipids. The fatty acids from both the neutral and polar lipids which were utilized to the greatest extent for embryonic development were palmitoleic, oleic, linoleic, and linolenic, regardless of the dietary supplements. Arachidonic, tetracosenoic, and docosahexaenoic acids also were metabolized by the embryo. Saturated fatty acids, used by the embryo as development progressed, were palmitic, stearic, and arachidic acids. Analyses of the liver fatty acids showed that the C16∶0 C16∶1, C18∶0, C18∶1, and C20∶4 acids in the neutral and polar lipids decreased with embryonic development and varied with the type of diet. The heart contained low levels of myristic, palmitic, stearic, arachidic, and arachidonic acids in the neutral lipids and palmitoleic and oleic acids in the polar lipids.     

Cyclopropenoid and Fatty Acid Composition of Kydia calycina Seed Oil

The seed oil of Kydia calycina is found to contain the following acids (Wt%): Lauric 3.7, myristic 6.0, palmitic 4.9, stearic 11.4, arachidic 2.8, behenic 2.5, oleic 60.6, linoleic 5.3, and cyclopropenoid fatty acid content 2.9.     

Chemical composition and characteristics ofMoringa peregrina seeds and seeds oil

TheMoringa peregrina kernel contains 1.8% moisture, 54.3% oil, 22.1% protein, 3.6% fiber, 15.3% carbohydrate and 2.5% ash. The composition and characteristics of the extracted oil were determined. Gas liquid chromatography of methyl esters of the fatty acids shows the presence of 14.7% saturated fatty acids and 84.7% unsaturated fatty acids. The fatty acid composition is as follows: palmitic 9.3%, palmitoleic 2.4%, stearic 3.5%, oleic 78.0%, linoleic 0.6%, linolenic 1.6%, arachidic 1.8% and behenic 2.6%.