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  • 1
    ISSN: 1573-1561
    Keywords: Acer rubrum ; Adirondacks ; aspen ; beaver ; Castor canadensis ; feeding inhibition ; Populus tremuloides ; red maple
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract At many beaver (Castor canadensis) sites at Allegany State Park in New York State, red maple (Acer rubrum) is the only or one of the few tree species left standing at the ponds' edges. The relative palatability of red maple (RM) was studied in three ways. (1) At seven beaver sites, the available and utilized trees were recorded and an electivity index (E) computed. Of 15 tree species, RM ranked second or fourth lowest. (2) In experiment I, RM, sugar maple (A. saccharum, SM), and quaking aspen (Populus tremuloides) logs were presented cafeteria style at 10 colonies. RM was the least preferred. (3) Bark of RM was extracted with solvents. Aspen logs were painted (experiment II) or soaked (experiment III) with this RM extract and presented to beaver cafeteria-style, along with aspen and RM controls. This treatment rendered aspen logs less palatable, indicating that a chemical factor had been transferred.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-1561
    Keywords: Castor canadensis ; beaver ; castoreum ; communication ; social odors ; phenolic compounds ; neutral compounds ; territorial behavior ; response measures
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract North American beaver (Castor canadensis) mark their territories with castoreum, a chemically complex secretion from their castor sacs. The phenolic and neutral fractions of castoreum have been shown to elicit specific behavioral responses from beavers in a field setting. Our objective was to identify compounds/mixtures that evoked responses similar to those stimulated by castoreum. We assayed recently identified phenolic compounds, some phenolics that had been determined to be biologically active in previous studies, the neutral compound borneol, and combinations of phenolic compounds, neutral compounds, and the two combined. Biological activity was measured by the elicitation and extent of specific responses and their strength (duration, frequency, and proportion of beavers responding). Generally, single compounds stimulated fewer responses than mixtures. A 26-compound mixture of phenolic and neutral compounds elicited responses in a similar proportion of trials as castoreum. However, responses to castoreum were stronger than to any synthetic sample. Further investigation of different measures of response, namely, elicitation, completeness, and strength, are deemed necessary to fully decipher the design of social odors.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 15 (1989), S. 887-893 
    ISSN: 1573-1561
    Keywords: Adirondacks ; beaver ; Castor canadensis ; castoreum ; nuisance beaver ; odors ; pheromone ; repellent ; scent marking ; territory ; wildlife damage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Unoccupied beaver (Castor canadensis) sites in New York State were for two years experimentally scented with a mixture of beaver castoreum and anal gland secretion. These sites were colonized less often than unscented control sites. The beaver is the first mammal to have been shown experimentally to use intraspecific odor cues when settling in vacant habitat. Territorial pheromones may be useful as repellents for beaver or other rodents.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 21 (1995), S. 1745-1762 
    ISSN: 1573-1561
    Keywords: beaver ; Castor canadensis ; castoreum ; neutral compounds ; monoterpenes ; co-injection ; fractionation ; identification ; synthesis ; territory marking
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract North American beavers (Castor canadensis) mark their territories with castoreum, the strong-smelling paste in their castor sacs. In their own territories, beavers respond with scent marking to experimental scent marks that consist of strange castoreum (or selected components). In part, the unique odor of castoreum is due to large amounts of phenolic compounds and neutral compounds. Purified neutral compounds were analyzed by GC. GC-MS, and NMR; identities of the neutral compounds were confirmed by comparing the properties of authentic compounds with those of the isolated compounds. We identified 13 neutral compounds that had not been reported before for castoreum. Most of these are oxygen-containing monoterpenes. Of the nine neutral compounds reported by Lederer (1949), only three are confirmed in our analysis; the other six neutral compounds are either absent or are not volatile enough to be detected by our methods. Eight compounds—6-methyl-l-heptanol, 4,6-dimethyl-l-heptanol, isopinocamphone, pinocamphone, two linalool oxides, and their acetates—were synthesized for structure identification and bioassays.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 21 (1995), S. 1349-1364 
    ISSN: 1573-1561
    Keywords: Adirondacks ; Allegany State Park ; allopatric ; aspen ; beaver ; Castor canadensis ; feeding inhibition ; Populus tremuloides ; predator odor ; repellent ; sympatric
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Free-ranging beaver (Castor canadensis) in two different beaver populations in New York State were exposed to predator chemicals to test feeding inhibition. Solvent extracts of feces were applied to stem sections of aspen, the preferred food tree of beavers, permitting smelling and tasting the samples. Predator odors were from wolf (Canis lupus), coyote (Canis latrans), dog (Canis familiaris), black bear (Ursus americanus), river otter (Lutra canadensis), lynx (Lynx canadensis), and African lion (Panthera leo). The experiment was repeated. The predator odors reduced feeding compared to untreated or solvent-treated controls. One population consumed 17.0% of the samples with predator odor and 27.0% of the controls in summer, and 48.4% and 60.0%, respectively, in autumn. The other population accepted 3.15% of the predator odor samples and 11.05% of the controls in summer. Coyote, lynx, and river otter odors had the strongest effects. Diesel oil and bitter-tasting neem extract had weaker effects. Predator odors are promising as feeding repellents for beaver.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0009-2940
    Keywords: Aldehydes ; Ketones ; Titanium complexes ; Niobium complexes ; Tantalum complexes ; Phosphonium chlorides ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Transition Metal-Activated Organic Compounds, XXXVII[1].  -  A Novel Reaction of Aldehydes and Ketones: Synthesis and Spectroscopic Investigation of α1-Phosphonioalkoxy Transition Metal ComplexesHerrn Professor Ulrich Schöllkopf zum 65. Geburtstag gewidmet.By treatment of aldehydes and ketones with one mole equivalent of a Lewis acid (TiCl4, NbCl5, TaCl5) and one mole equivalent of PPh3, or in one case of Ph2PCH2CH2PPh2, the aldehyde derivates [R1CH(P+Ph2R2)-OMCln]Cl- (4-8; M=Ti, Nb, Ta; R2=Ph or CH2CH2PPh2) and the ketone derivatives [R1R2C(P+Ph3)-ONbCl4]Cl- (9-10) were prepared. Complexes 4-10 were isolated as air-and water-sensitive solids. According to the NMR spectra some of the obtained aldehyde derivatives 4-8 exist in solution as a mixture of isomers or oligomers, whereas the ketone derivatives 9 and 10 form in solution an equilibrium with the free ketone and the complex NbCl5 · PPh3. The chloride ion of 4-10 is perhaps coordinated to the metal.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 701-704 
    ISSN: 0009-2940
    Keywords: N-Silyl amides ; Precursor ; 14N-NMR ; Titanium ; Tungsten ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of hexachlorodisilazanyllithium (Cl3Si)2NLi (1), with TiCl4 leads selectively to the novel fully chlorinated amides (Cl3Si)2NTiCl3 (2) or [(Cl3Si)2N]2 TiCl2 (3), respectively, depending on the molar ratio of the starting materials. The analogous reaction of 1 with WCl6 yielded the amide imide Cl3SiN=W(Cl3)N(SiCl3)2 (5) by elimination of SiCl4. The relative amounts of the starting materials had no effect on the formation of 5. 14/15N- and 29Si-NMR data on the starting materials and products show significantly different effects, when compared with those of analogous N-trimethylsilyl derivatives, due to the lower energy of the electrons in the N—Si and N—M ß bonds. The crystal structure of 5 (triclinic, space group P1) was determined by X-ray structure analysis.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0009-2940
    Keywords: Chemoselectivity ; Titanium complexes ; Niobium complexes ; Tantalum complexes ; Methylation of aldehydes and ketones ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Transition Metal-Activated Organic Compounds, XXXVIII[1].  -  Chemoselective Nucleophilic Methylation Reactions by In-Situ-Blocking of Aldehyde Groups by α1-Phosphonioalkoxide FormationHerrn Professor Ulrich Schöllkopf zum 65. Geburtstag gewidmet.For the selective methylation of a keto group in the presence of an aldehyde group the complex MeTiCl3·PPh3 and especially the reagent system [TiC]4·PPh3 + 0.5 Me2Zn] proved to be favourable. For instance, 6-oxoheptanal (8) was methylated by [TiCl4·PPh3 + 0.5 Me2Zn] at the keto group with 89% yield and 99:1 selectivity, whereas it was methylated by [TiCl4 + 0.5 Me2Zn] at the aldehyde group with 81% yield and 96:4 selectivity. A selective methylation of benzaldehyde in the presence of heptanal was achieved with MeNbCl4·PPh3 or [NbCl5·PPh3 + 0.75 Me2Zn] to give (1-chloroethyl)benzene (14; yield 92 or 53%; selectivity in each case 93:7) or with [TaCl5·PPh3 + 1.5 Me2Zn] to give mainly 1-phenylethanol (15) besides 16. A 96:4-selective benzylation (yield 74%) of a ketone in the presence of an aliphatic aldehyde was possible with [TiCl4·PPh3 + 1 PhCH2MgBr].  -  The high chemoselectivity is caused by irreversible blocking of aliphatic aldehyde groups by α1-phosphonioalkoxide formation[1], whilst the corresponding reaction of keto groups[1] and of benzaldehyde is reversible.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 17 (1991), S. 715-734 
    ISSN: 1573-1561
    Keywords: Adirondacks ; beaver ; bioassay ; Castor canadensis ; castoreum ; field study ; New York ; phenols ; pheromone ; scent marks ; territorial marking
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Behavioral activity of single components of beaver castoreum was demonstrated for the first time. In four experiments samples were presented to free-ranging beaver in their family territories. First, responses to whole castoreum and anal gland secretion (AGS) from males and females were tested. Second, 24 compounds, known to be constituents of beaver castoreum, were individually screened for activity. Four of these consistently released immediate responses during the observation periods. These are the phenols 4-ethylphenol and 1,2-dihydroxybenzene and the ketones acetophenone and 3-hydroxyacetophenone. In the most complete responses, the beaver sniffed from the water, were attracted to the odor, swam toward its source, went on land, and then approached, sniffed, pawed, and scent-marked the artificial scent mound. 4-Ethoxyphenol, a compound not yet found in castoreum, also released these responses. Five additional compounds resulted in a few delayed visits to the samples during the night following the observations, as evidenced by destroyed scent mounds. These are 4-methyl-1,2-dihydroxybenzene, 4-methoxyacetophenone, 5-methoxysalicylic acid, salicylaldehyde, and 3-hydroxybenzoic acid. Third, mixtures of 24 and six compounds were tested. Responses to these mixtures could be as strong as those to whole castoreum. Fourth, the four regularly active compounds were tested in two additional beaver populations and proved to be active there, too. The response was strongest in the densest beaver population.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 13 (1971), S. 151-155 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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