Factors driving bumble bee (Hymenoptera: Apidae: Bombus) and butterfly (Lepidoptera: Rhopalocera) use of sheared shrubland and young forest communities of the western Great Lakes.

In the northern Great Lakes region, the creation and maintenance of early-successional woody communities as wildlife habitat have increasingly become a conservation priority. The extent to which insect pollinators use these systems remains largely anecdotal. In summer (June-August) of 2021, we surveyed 49 early-successional sites in the western Great Lakes region treated with either shrub-shearing or silviculture (young forest) for bumble bees, butterflies, and habitat components (i.

A novel SNP assay reveals increased genetic variability and abundance following translocations to a remnant Allegheny woodrat population.

Background: Allegheny woodrats (Neotoma magister) are found in metapopulations distributed throughout the Interior Highlands and Appalachia. Historically these metapopulations persisted as relatively fluid networks, enabling gene flow between subpopulations and recolonization of formerly extirpated regions. However, over the past 45 years, the abundance of Allegheny woodrats has declined throughout the species' range due to a combination of habitat destruction, declining hard mast availability, and roundworm parasitism.

Relative Efficiency of Drag Fabrics for Collection of Blacklegged Tick (Acari: Ixodidae) Larvae, Nymphs, and Adults.

The blacklegged tick (Ixodes scapularis Say) vectors several bacterial, protozoan, and viral human pathogens. The known distribution, abundance, and phenology of I. scapularis within its estimated range are incomplete.

Lyme Disease Risk of Exposure to Blacklegged Ticks (Acari: Ixodidae) Infected with Borrelia burgdorferi (Spirochaetales: Spirochaetaceae) in Pittsburgh Regional Parks.

Lyme disease is the most commonly reported vector-borne illness and sixth most commonly reported notifiable infectious disease in the United States. The majority of cases occur in the Northeast and upper-Midwest, and the number and geographic distribution of cases is steadily increasing. The blacklegged tick (Ixodes scapularis Say) is the principal vector of the Lyme disease spirochete (Borrelia burgdorferi sensu stricto) in eastern North America.

Isolation and Crystallographic Characterization of Two, Nonisolated Pentagon Endohedral Fullerenes: Ho N@C (22010)-C and Tb N@C (22010)-C.

Purified samples of Ho N@C (22010)-C and Tb N@C (22010)-C have been isolated by two distinct processes from the rich array of fullerenes and endohedral fullerenes present in carbon soot from graphite rods doped with Ho O or Tb O . Crystallographic analysis of the endohedral fullerenes as cocrystals with Ni(OEP) (in which OEP is the dianion of octaethylporphyrin) shows that both molecules contain the chiral C (22010)-C cage. This cage does not obey the isolated pentagon rule (IPR) but has two sites where two pentagons share a common C-C bond.

High Blocking Temperature of Magnetization and Giant Coercivity in the Azafullerene Tb @C N with a Single-Electron Terbium-Terbium Bond.

The azafullerene Tb @C N is found to be a single-molecule magnet with a high 100-s blocking temperature of magnetization of 24 K and large coercivity. Tb magnetic moments with an easy-axis single-ion magnetic anisotropy are strongly coupled by the unpaired spin of the single-electron Tb-Tb bond. Relaxation of magnetization in Tb @C N below 15 K proceeds via quantum tunneling of magnetization with the characteristic time τ =16 462±1230 s.

Mitochondrial genome of an Allegheny Woodrat ().

The Allegheny woodrat () is endemic to the eastern United States. Population numbers have decreased rapidly over the last four decades due to habitat fragmentation, disease-related mortality, genetic isolation and inbreeding depression; however, effective management is hampered by limited genetic resources. To begin addressing this need, we sequenced and assembled the entire Allegheny woodrat mitochondrial genome.

Nanoscale fullerene compression of an yttrium carbide cluster.

The nanoscale parameters of metal clusters and lattices have a crucial influence on the macroscopic properties of materials. Herein, we provide a detailed study on the size and shape of isolated yttrium carbide clusters in different fullerene cages. A family of diyttrium endohedral metallofullerenes with the general formula of Y(2)C(2n) (n = 40-59) are reported.

Acoustic, piezoelectric, and dielectric nonlinearities of AlN in coupled resonator filters for high RF power levels.

Coupled resonator filters (CRFs) are the new generation of BAW filters recently designed for the front-end modules of mobile transmission systems. Looking for designers' requirements, CRF devices have been characterized and modeled. The model based on equivalent circuits relies on material constants such as stiffness and electro-coupling coefficients, and works only for linear-mode propagation.

Encapsulation of a radiolabeled cluster inside a fullerene cage, (177)Lu(x)Lu((3-x))N@C(80): an interleukin-13-conjugated radiolabeled metallofullerene platform.

In this communication, we describe the successful encapsulation of (177)Lu into the endohedral metallofullerene (177)Lu(x)Lu(3-x)N@C(80) (x = 1-3) starting with (177)LuCl(3) in a modified quartz Kraschmer-Huffman electric generator. We demonstrate that the (177)Lu (beta-emitter) in this fullerene cage is not significantly released for a period of up to at least one-half-life (6.7 days).

Preparation and structural characterization of the Ih and the D5h isomers of the endohedral fullerenes Tm3N@C80: icosahedral C80 cage encapsulation of a trimetallic nitride magnetic cluster with three uncoupled Tm3+ ions.

We report an efficient method for the preparation and purification of the Ih and the D5h isomers of Tm3N@C80. Following preparation in a Kratschmer-Huffman electric-arc generator, the Tm3N@C80 isomers were obtained by a chemical separation process followed by a one-stage isomer selective chromatographic high-performance liquid chromatography (HPLC) separation (pyrenyl, 5PYE column). The HPLC chromatographic retention behavior on a pentabromobenzyl (5PBB) column suggests a charge transfer of approximately 6 electrons; [M3N] 6+@C80(6-) and the chromatographic retention mechanisms of the Ih and the D5h isomers of Tm3N@C80 on both 5PBB and 5PYE columns are discussed.

Nitroxide/substrate weak hydrogen bonding: attitude and dynamics of collisions in solution.

The study of intermolecular collisions and bonding interactions in solutions is of critical importance in understanding and predicting solute/solvent properties. Previous work has established that stable paramagnetic nitroxide molecules are excellent probes of intermolecular interactions for hydrogen bonding in polar solvents. In this study, 1H, 2H, 13C, 15N NMR and liquid/liquid intermolecular transfer dynamic nuclear polarization (L2IT DNP) results are obtained for the paramagnetic probe molecule, TEMPO, interacting with the common aprotic and protic polar solvents, CH3CN and CH3CONH2, yielding a profile of both dipolar and scalar interactions.

[Clinical and posturographic comparison of patients with recent total hip arthroplasty].

Purpose Of The Study: To highlight the congruence of clinical and posturographic tests in patients undergoing hip arthroplasty.

Material And Methods: Ten patients (six males and four females) were included in this study and tested when at admission and discharge from the rehabilitation department (12 and 27 days after surgery respectively). The patients were asked to stand undisturbed in the upright position, eyes closed on a system composed of two force platforms.

Isolation and structural characterization of a family of endohedral fullerenes including the large, chiral cage fullerenes Tb(3)N@C(88) and Tb(3)N@C(86) as well as the I(h) and D(5)(h) isomers of Tb(3)N@C(80).

The recent finding that isomer 2 of Tb(3)N@C(84) uses one of the 51,568 possible nonisolated pentagon rule (non-IPR) structures for the C(84) cage rather than one of the 24 cage isomers that do obey the IPR suggests that further experimental work on the structure of larger endohedrals is needed to observe the utility of the IPR rule in this uncharted territory. The structures of the newly synthesized endohedral fullerenes--Tb(3)N@C(88), Tb(3)N@C(86), and the Ih and D(5)(h) isomers of Tb(3)N@C(80)--have been determined by single-crystal X-ray diffraction on samples cocrystallized with NiII(octaethylporphyrin). In contrast to the situation for isomer 2 of Tb(3)N@C(84), the structures of Tb(3)N@C(88) and Tb(3)N@C(86) do conform to the IPR.

In vitro and in vivo imaging studies of a new endohedral metallofullerene nanoparticle.

Purpose: To evaluate the effectiveness of a functionalized trimetallic nitride endohedral metallofullerene nanoparticle as a magnetic resonance (MR) imaging proton relaxation agent and to follow its distribution for in vitro agarose gel infusions and in vivo infusions in rat brain.

Materials And Methods: The animal study was approved by the animal care and use committee. Gd(3)N@C(80) was functionalized with poly(ethylene glycol) units, and the carbon cage was hydroxylated to provide improved water solubility and biodistribution.

Preparation and structure of CeSc2N@C80: an icosahedral carbon cage enclosing an acentric CeSc2N unit with buried f electron spin.

Herein, we report the preparation, purification, and characterization of a mixed trimetallic nitride endohedral metallofullerene, CeSc(2)N@C(80). Single-crystal X-ray diffraction shows that CeSc(2)N@C(80) consists of a four-atom asymmetric top (CeSc(2)N) inside a C(80) (I(h)()) carbon cage. Unlike the situation in most endohedrals of the M(3)N@C(2)(n)() type, the nitride ion is not located at the center of the carbon cage but is offset by 0.

Purification of endohedral trimetallic nitride fullerenes in a single, facile step.

A major hurdle hampering the development of fullerenes, endohedral metallofullerenes, and nanotubes has been the difficulty of obtaining high purity samples. Soots prepared in the usual manner via a Krätschmer-Huffman electric-arc generator consist of mixtures of insoluble carbonaceous materials and soluble fullerenes: C60, C70, C76, C78, C84, etc. When metals are introduced as endohedral species the complexity of the resultant soot is even greater because of the presence of multiple isomers of both the empty fullerenes and the endohedral metallofullerenes.

NMR chemical shifts. Substituted acetylenes.

The MPW1PW91/6-311+G(2d,p) and MP2/6-311+G(2d,p) GIAO nuclear shieldings for a series of monosubstituted acetylenes have been calculated using the MP2/6-311G(2d,p) geometries. Axially symmetric substituents such as fluorine may lead to large changes in the isotropic shielding but have little effect on the tensor component (zz) about the C[triple bond]C bond axis. On the other hand, substituents such as vinyl and aldehyde groups lead to essentially no difference in the isotropic shielding but are calculated to give a large zz paramagnetic shift to the terminal carbon of the acetylene group, without having much effect on the inner carbon.

Crystallographic characterization and structural analysis of the first organic functionalization product of the endohedral fullerene Sc(3)N@C(80).

The structure of Sc3N@C80-C10H12O2, a Diels-Alder cycloadduct of Sc3N@C80, has been determined. The crystallographic data shows that cycloaddition occurs at a C-C bond of 6:5 ring junction, and that the fullerene C1-C2 bond is elongated and pulled out from the fullerene. The Sc3N unit is well-ordered within the C80 cage and positioned away from the site of addition.

A symmetric derivative of the trimetallic nitride endohedral metallofullerene, Sc3N@C80.

The reaction of Sc3N@C80 with 6,7-dimethoxyisochroman-3-one (13C labeled) provides the first functionalized derivative of the trimetallic nitride template (TNT) endohedral metallofullerene family. The reaction mixture is dominated by a single 13C labeled monoadduct product that was purified by HPLC. The 13C labeled monoadduct was characterized by 1H NMR, 13C NMR, and MALDI-TOF mass spectrometry.