RESUMEN
Individuals that dare approach predators (predator inspection behaviour) may benefit by acquiring information regarding the potential threat of predation. Although information acquisition based on visual cues has been demonstrated for fish, it is unknown whether fish will inspect predators on the basis of chemical cues or whether such inspection behaviour results in information acquisition. Here, we first ascertained whether predator inspection behaviour can be mediated by chemical cues from predators by exposing groups of predator-naive glowlight tetras (Hemigrammus erythrozonus) to the chemical cues of a potential fish predator (convict cichlid Cichlasoma nigrofasciatum) that had been fed either tetras (which possess an alarm pheromone) or swordtails (Xiphophorus helleri, which lack Ostariophysan alarm pheromones). Tetras showed a significant increase in antipredator behaviour when exposed to the tetra-diet cue, but not when exposed to the swordtail-diet cue. Chemically mediated predator inspection behaviour was also affected. Both the latency to inspect and the minimum approach distance to the predator significantly increased, and the mean number of inspectors per predator inspection visit significantly decreased when tetras were exposed to the tetra-diet versus the swordtail-diet chemical cues. We then examined a potential benefit associated with chemically mediated predator inspection behaviour. Only tetras that were initially exposed to the tetra-diet cue and that had inspected the predator acquired the visual recognition of a convict cichlid as a predation threat. Our results thus demonstrate that (1) predator inspection behaviour in the glowlight tetra can be initiated by chemical cues, (2) chemically mediated inspection behaviour is affected by the presence of alarm pheromone, and (3) inspectors benefit by acquiring the recognition of novel predators. Copyright 1999 The Association for the Study of Animal Behaviour.
RESUMEN
Animals commonly approach (i.e. 'inspect') potential predators. Glowlight tetras, Hemigrammus erythrozonus, have previously been shown to inspect the combined chemical and visual cues originating from novel predators and to modify their inspection (approach) behaviour depending upon the predator's diet. We conducted two experiments to determine whether tetras would inspect the chemical cues of injured prey or the dietary cues of a novel predator in the absence of any visual cues. Shoals of glowlight tetras were exposed to either distilled water (control) or the skin extract of swordtail (lacking ostariophysan alarm pheromones) or the skin extract of tetra (with alarm pheromones). There was no significant difference in the frequency of predator inspection behaviour towards swordtail or tetra skin extract compared to the distilled water controls. In the second experiment, we exposed shoals of tetras to either distilled water or the odour of Jack Dempsey cichlids, Cichlasoma octofasciatum, which had been food deprived, or fed a diet of swordtails or tetras. There was no significant difference in the frequency of predator inspection behaviour towards the odour of the starved cichlids and the odour of the fed cichlids in either of the two diet treatments. However, when tetras were exposed to the odour of cichlids fed tetras, they took significantly longer to initiate an inspection visit, remained further from the source of the chemical cues and inspected in smaller groups, compared with the odour of a starved cichlid or a cichlid fed swordtails. These data strongly suggest that tetras will inspect chemical cues alone, but only if the cue contains information about the predator. Copyright 2000 The Association for the Study of Animal Behaviour.
RESUMEN
The products of aqueous Zn(II) sorption on high-surface-area alumina powders (Linde-A) have been studied using XAFS spectroscopy as a function of Zn(II) sorption density (Gamma=0.2 to 3.3 µmol/m(2)) at pH values of 7.0 to 8.2. Over equilibration times of 15-111 h, we find that at low sorption densities (Gamma=0.2-1.1 µmol/m(2)) Zn(II) forms predominantly inner-sphere bidentate surface complexes with AlO(6) polyhedra, whereas at higher sorption densities (Gamma=1.5 to 3.5 µmol/m(2)), we find evidence for the formation of a mixed-metal Zn(II)-Al(III) hydroxide coprecipitate with a hydrotalcite-type local structure. These conclusions are based on an analysis of first- and second-neighbor interatomic distances derived from EXAFS spectra collected under ambient conditions on wet samples. At low sorption densities the sorption mechanism involves a transformation from six-coordinated Zn-hexaaquo solution complexes (with an average Zn-O distance of 2.07 Å) to four-coordinated surface complexes (with an average Zn-O distance of 1.97 Å) as described by the reaction identical withAl(OH(a))(OH(b))+Zn (H(2)O)(6)(2+)--> identical withAl(OH(a)') (OH(b)')Zn(OH(c)')(OH(d)'+4H(2)O+zH(+), where identical withAl(OH(a))(OH(b)) represents edge-sharing sites of Al(O,OH,OH(2))(6) octahedra to which Zn(O,OH,OH(2))(4) bonds in a bidentate fashion. The proton release consistent with this reaction (z=a-a'+b-b'+4-c'-d'), and with bond valence analysis falls in the range of 0 to 2 H(+)/Zn(II) when hydrolysis of the adsorbed Zn(II) complex is neglected. This interpretation suggests that proton release is likely a strong function of the coordination chemistry of the surface hydroxyl groups. At higher sorption densities (1.5 to 3.5 µmol/m(2)), a high-amplitude, second-shell feature in the Fourier transform of the EXAFS spectra indicates the formation of a three-dimensional mixed-metal coprecipitate, with a hydrotalcite-like local structure. Nitrate anions presumably satisfy the positive layer charge of the Al(III)-Zn(II) hydroxide layers in which the Zn/Al ratio falls in the range of 1 : 1 to 2 : 1. Our results for the higher Gamma-value sorption samples suggest that Zn-hydrotalcite-like phases may be a significant sink for Zn(II) in natural or catalytic systems containing soluble alumina compounds. Copyright 2000 Academic Press.
RESUMEN
The uptake and release behavior of cobalt(II) was studied over thousands of hours in CO(2)-free aqueous suspensions of kaolinite under three pairs of total cobalt concentration (Co(T)) and near-neutral pH (7.5-7.8) conditions. Dissolved cobalt, aluminum, and silicon concentrations were monitored by ICPMS, and cobalt-containing products were identified by EXAFS spectroscopy. In each uptake experiment, cobalt sorbed to kaolinite as a mixture of surface-adsorbed monomers or polymers and hydrotalcite-like precipitates of the approximate composition Co(x)Al(OH)(2x+2)(A(n-))(1/n), where 2
RESUMEN
We have examined the molecular-scale details of aqueous Co(II) surface complexes and the types of surface sites to which these complexes bind on the (110) and (001) surfaces of single-crystal TiO(2) (rutile) using polarization-dependent grazing-incidence X-ray absorption fine structure (GI-XAFS) spectroscopy under ambient conditions in a humid atmosphere. On both surfaces, Co(II) adsorbs at sites corresponding to Ti-equivalent positions in an extension of the rutile structure. This result suggests that even if different crystallographic surfaces of metal oxides have strongly differing adsorption properties for gaseous species in ultra-high vacuum, they can have similar properties for adsorption of metal ions in aqueous solution, probably due to the tendency of liquid water to heal defects and satisfy the bonding requirements of coordinatively unsaturated surface atoms. Using a bond valence approach in combination with the XAFS results, we have proposed specific surface reactions for sorption of Co(II) on the (110) and (001) rutile surfaces as a function of pH and Co surface concentration. No evidence was found for well-ordered Co(II)-hydroxide-like precipitates that would show Co-Co pair correlations, or for Co-Ti pair correlations similar to those in anatase, as have been observed in other studies. These results demonstrate the utility of GI-XAFS spectroscopy on adsorbed metal ions at submonolayer surface coverages for determining the types of reactive sorption sites on metal oxide surfaces. Copyright 1999 Academic Press.
RESUMEN
Glowlight tetras, Hemigrammus erythrozonus, show a conspicuous visual display ('fin flicking') upon detecting a conspecific chemical alarm signal (alarm pheromone). We conducted laboratory studies to test two, nonmutually exclusive hypotheses regarding the function of this behaviour. To test the hypothesis that fin flicking acts as a visual alarm signal to conspecifics, we paired shoals of tetras with a stimulus tetra in an adjacent tank (separated by a one-way mirror) and exposed the stimulus tetras to conspecific skin extract (with alarm pheromone) or swordtail skin extract (which lacks ostariophysan alarm pheromone). Stimulus tetras significantly increased their frequency of fin flicking when exposed to conspecific skin extract, but not to the swordtail skin extract control. The test shoals showed a significant increase in antipredator behaviour in response to fin-flicking stimulus tetras, but not to stimulus tetras that did not fin-flick. To test the hypothesis that fin flicking serves as a predator deterrent, we paired predatory Jack Dempsey cichlids, Cichlasoma octofaciatum, with tetras in adjacent tanks and exposed the tetras to either conspecific or swordtail skin extract. Predators remained further away from the stimulus tetra, took longer to initiate a bite and displayed fewer bites towards tetras that fin-flicked compared with tetras that did not fin-flick. These results support our hypothesis that fin flicking in tetras serves as both a visual alarm signal to conspecifics and a deterring signal to predators, and suggest that individual tetras may reduce their risk of predation by fin flicking upon detecting a predation threat. Copyright 1999 The Association for the Study of Animal Behaviour.
RESUMEN
We have used X-ray absorption fine structure (XAFS) spectroscopy to investigate Cu(II) sorption complexes on high surface area amorphous silica (am-SiO2) and gamma-Al2O3. For Cu(II) on gamma-Al2O3, analysis of XAFS data collected after a solution-solid total contact time of 80-170 h showed that monomeric Cu(II) species predominate at surface coverages of 0.007 and 0.05 µmol m-2. Cu(II) on the gamma-Al2O3 surface has aluminum second neighbors at about 2.8 Å. Geometrical considerations indicate that this distance is consistent with models of Cu(II) binding to the gamma-Al2O3 surface in inner-sphere bidentate or monodentate modes on Al(O,OH)6 octahedra. For Cu(II) sorbed on am-SiO2, analysis of XAFS data collected after a solution-solid total contact time of 80-110 h showed that a dimeric Cu(II)-surface complex predominates, along with a minority monomeric Cu(II) surface species, at 0.03 and 0.05 µmol m-2. The XAFS-derived Cu-Si distance is in the range of 2.98 to 3.05 Å, suggesting that Cu(II) binds to am-SiO2 in an inner-sphere, monodentate fashion. XAFS spectra of Cu(II) sorbed on am-SiO2 collected after 20-30 h total contact time are quantitatively different from those collected after 80-90 h contact time. Analyses of these spectra indicate that the ratio of dimeric to monomeric Cu(II) surface complexes has increased with contact time. A discussion of the processes responsible for the different Cu(II) complexes on am-SiO2 and gamma-Al2O3 is presented. Copyright 1998 Academic Press.
RESUMEN
Surface precipitation is an important process in many areas of science and technology, including modeling contaminant segregation from groundwater to solid phases and dispersion of active phases on catalyst supports. XAFS, TEM, and XPS measurements of Co(II) sorbed on Al2O3 demonstrate that surface precipitates have formed from solutions that are undersaturated with respect to any known bulk solid phase. The precipitates have a structure similar to that of Co(OH)2(s), but are disordered and have a high concentration of Co vacancies. The data plus thermodynamic reasoning have been used to analyze the plausibility of various models for surface precipitation and to show that for Co(II)/Al2O3 it occurs by forming a double-hydroxide phase containing substrate-derived Al(III) ions. This idea was corroborated by mixing aqueous solutions of Al(III) and Co(II) at the pH and concentration of the sorption samples, forming a stable colloidal precipitate that is less soluble than either Al(OH)3 or Co(OH)2. The Co XAFS of this material was similar to that of the sorption samples. Successful quantitative models of metal ion transport in groundwater need to include the possibility of forming ternary and higher order precipitates that include ions derived from sparingly soluble solids. For catalyst impregnation, surface coprecipitation can prevent production of a well-dispersed precursor material.
RESUMEN
The structures and compositions of Pb(II) adsorption complexes and surface binding sites on alpha-Al2O3 (0001) and (1&1macr;02) surfaces were investigated in the presence of water using grazing-incidence X-ray absorption fine structure (GI-XAFS) spectroscopy. Pb(II) ions were found to adsorb in an inner-sphere mode on alpha-Al2O3 (1&1macr;02) but as outer-sphere complexes on alpha-Al2O3 (0001). The distance between the outer-sphere complexes and the surface places useful constraints on double-layer properties of water. A bond-valence model is described that relates the reactivities of surface functional groups and adsorption complexes to their molecular structures and compositions, and places constraints on the stoichiometries of adsorption reactions, including proton release. The EXAFS and modeling results suggest that Pb(II) and Co(II) ions bond to [AlAlAl-->O-1/2--> and [Al-OH+1/22] surface functional groups. In contrast, [AlAl > OH] groups complex Co(II) but not Pb(II). The results indicate the importance of using structurally defined surface sites to describe reactions at oxide-water interfaces.
RESUMEN
We have characterized the adsorption of Co(II) on the (0001) and (1102) surfaces of alpha-Al(2)O(3) single crystals under ambient conditions using polarization-dependent grazing-incidence X-ray absorption fine structure spectroscopy, in combination with bond valence modeling. Co(II) ions were found to be adsorbed on both surfaces in an inner-sphere fashion. Adions were found to adsorb dominantly in a tridentate fashion (i.e., bonded to three surface oxygens) on the (0001) surface and dominantly in a tetradentate fashion on the (1102) surface. Based on EXAFS results and bond valence analysis, plausible surface complexation reactions for Co(II) sorption on these two surfaces can be written as represent surface water molecules, hydroxyl groups, and oxygens bonded to one, two, and three Al cations, respectively. Copyright 1999 Academic Press.
RESUMEN
Thecomposition and mode of attachment of Cu(II) complexes at the gamma-Al(2)O(3)-water interface in suspensions containing a simple amino acid (glutamate) were characterized with EXAFS and FTIR spectroscopies. The spectroscopic results indicate that two types of Cu(II)-glutamate-alumina interactions are primarily responsible for Cu(II) and glutamate uptake between pH 4 and 9. In acidic suspensions of alumina, glutamate forms a bridge between Cu(II) ions and the (hydr)oxide surface (Type B complex). In this Type B surface complex, Cu(II) is bonded to amino acid headgroups (i.e., (+)H(3)NCHRCOO(-)) of two glutamate molecules. Spectroscopic and ionic strength dependent uptake results are combined to propose that the nonbonded side chain carboxylate groups of this complex are attracted to the oxide surface through long-range forces, leading to enhanced Cu(II) uptake relative to the glutamate-free system. In alkaline suspensions the relative amount of surface-bound Cu(II) complexed by glutamate decreases, and a direct Cu(II)-surface bond becomes the dominant mode of attachment (Type A complex). These surface complexes differ markedly from the species found in the alumina-free Cu(II)-glutamate aqueous system under similar solution conditions, where Cu(H(2)O)(2+)(6) and Cu(glutamate)(2-)(2) are the dominant species in acidic and alkaline solutions, respectively. Based on these spectroscopic results, surface complexation reactions are proposed for the Cu(II) and glutamate ternary interactions with the alumina surface in this system. Similarities between the results of this study and Cu(II) uptake behavior and complexation in the presence of natural organic material (NOM) indicate that Cu(II)-glutamate interactions mimic those in more complex Cu(II)-NOM-mineral-water systems. Copyright 1999 Academic Press.
RESUMEN
The physical and chemical properties of the hydrated alpha-Al(2)O(3) (0001) surface are important for understanding the reactivity of natural and synthetic aluminum-containing oxides. The structure of this surface was determined in the presence of water vapor at 300 kelvin by crystal truncation rod diffraction at a third-generation synchrotron x-ray source. The fully hydrated surface is oxygen terminated, with a 53% contracted double Al layer directly below. The structure is an intermediate between alpha-Al(2)O(3) and gamma-Al(OH)(3), a fully hydroxylated form of alumina. A semiordered oxygen layer about 2.3 angstroms above the terminal oxygen layer is interpreted as adsorbed water. The clean alpha-Al(2)O(3) (0001) surface, in contrast, is Al terminated and significantly relaxed relative to the bulk structure. These differences explain the different reactivities of the clean and hydroxylated surfaces.