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We investigate the reorientation dynamics of four octanol isomers with very different characteristics regarding the formation of hydrogen-bonded structures by means of photon-correlation spectroscopy (PCS) and broadband dielectric spectroscopy. PCS is largely insensitive to orientational cross-correlations and straightforwardly probes the α-process dynamics, thus allowing us to disentangle the complex dielectric relaxation spectra. The analysis reveals an additional dielectric relaxation contribution on time scales between the structural α-process and the Debye process. In line with nuclear magnetic resonance results from the literature and recent findings from rheology experiments, we attribute this intermediate contribution to the dielectric signature of the O–H bond reorientation. Due to being incorporated into hydrogen-bonded suprastructures, the O–H bond dynamically decouples from the rest of the molecule. The relative relaxation strength of the resulting intermediate contribution depends on the respective position of the hydroxy group within the molecule and seems to vanish at sufficiently high temperatures, i.e., exactly when the overall tendency to form hydrogen bonded structures decreases. Furthermore, the fact that different octanol isomers share the same dipole density allows us to perform an in-depth analysis of how dipolar cross-correlations appear in dielectric loss spectra. We find that dipolar cross-correlations are not solely manifested by the presence of the slow Debye process but also scale the relaxation strength of the self-correlation contribution depending on the Kirkwood factor. [ABSTRACT FROM AUTHOR]

Genetic relationships were examined among wild-caught southern flying squirrels (Glaucomys volans) sharing the same natural nest cavity. Under natural conditions, typically 75-80% of southern flying squirrel nest groups comprise adult-aged individuals. The remainder nest in family-based groups or are solitary. The coefficient of relatedness within nest groups of adult individuals and family-based nest groups was examined through microsatellite DNA analysis. Family or adult nest groups were identified from the age class of individual group members determined through a discriminant function analysis based on body mass. From this information, nest groups were categorized as family-based groups comprising a single adult female with nestlings, adult groups comprising adult aged-individuals, or subadult nest groups. The average coefficient of relatedness was determined in each nest group. Within the putative family groups, most individuals were 1st-order relatives. In the adult nest groups, the coefficient of relatedness was low, indicating that these individuals were unrelated. The relationships within the subadult nest groups were intermediate. This is the 1st study to show that adult nestmate southern flying squirrels typically are unrelated and do not nest in family-based groups. Key words: coefficient of relatedness, discriminant function analysis, group nesting, microsatellite DNA

Prey capture in owls and hawks is largely dependent on the biomechanics of the hindlimbs, and both limb size and grip forces potentially determine the size of prey that can be captured and the extent of possible resource partitioning among sympatric species. Morphological study of six species of sympatric raptors--the owls Otus asio, Strix varia, and Bubo virginianus; and the hawks commonly considered their diurnal 'ecological equivalents,' Falco sparverius, Buteo lineatus, and Buteo jamaicensis--revealed that, in both groups, talon closure is effected by two discrete mechanisms that function together in a potentially additive or alternative fashion. Grip force measurements obtained from live owls and hawks using 'hydraulic' perches showed that grip force increases exponentially with body size and that owls produce greater forces than hawks. That finding is consistent with the distinctive osteology and myology of their hindlimbs and with their hunting behavior. These data provide some understanding of the different demands of diurnal and nocturnal hunting as well as the mechanism of coexistence for those six species in eastern woodlands.

Southern Appalachian grass balds pose both an ecological mystery and a conservation dilemma. Two schools of thought are patronized for the persistence of the treeless expanses: natural and anthropogenic. The existence of rare, endemic plants and northern relicts supports the former, therefore warranting preservation of such special natural communities.

We suggest a way to disentangle self- from cross-correlation contributions in the dielectric spectra of glycerol. Recently it was demonstrated for monohydroxy alcohols that a detailed comparison of the dynamic susceptibilities of photon correlation and broadband dielectric spectroscopy allows to unambiguously disentangle a collective relaxation mode known as the Debye process, which arises due to supramolecular structures, and the α-relaxation, which proves to be identical in both methods. In the present paper, we apply the same idea and analysis to the paradigmatic glass former glycerol. For that purpose we present new light scattering data from photon correlation spectroscopy measurements and combine these with literature data to obtain a data set covering a dynamic range from 10−4–1013 Hz. Then we apply the above mentioned analysis by comparing this data set with a corresponding set of broadband dielectric data. Our finding is that even in a polyalcohol self- and cross-correlation contributions can approximately be disentangled in that way and that the emerging picture is very similar to that in monohydroxy alcohols. This is further supported by comparing the data with fast field cycling NMR measurements and dynamic shear relaxation data from the literature, and it turns out that, within the described approach, the α-process appears very similar in all methods, while the pronounced differences observed in the spectral density are due to a different expression of the slow collective relaxational contribution. In the dielectric spectra the strength of this peak is reasonably well estimated by the Kirkwood correlation factor, which supports the view that it arises due to dynamic cross-correlations, which were previously often assumed to be negligible in dielectric measurements. [ABSTRACT FROM AUTHOR]

We have developed a flexible experimental setup to conduct triplet solvation dynamics (TSD) experiments. The setup is capable of exciting dyes at 355, 320 and 266 nm. Phosphorescence spectra can be recorded up to a 10 ns-resolution usually covering three decades using a grating spectrograph and a CCD camera. In this contribution, we describe the experimental setup as well as first investigations on water-alcohol mixtures, microemulsions and new dyes for TSD, i.e. naphthalene derivates, which take full advantage of this experimental method sensitive to the local environment of the dyes. [ABSTRACT FROM AUTHOR]