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At least 19 recordsLinked to original sources
PubMed2026

Shifts of antibiotic resistance genes across an estuarine meandering bend and dissemination risks to offshore oceans.

Meandering is a fundamental geomorphic feature of rivers that plays a critical role in regulating pollutant attenuation. To elucidate its impact on antibiotic resistance genes (ARGs) distribution in estuarine intertidal sediments, samples were collected from both the landward side (freshwater-dominated) and the seaward side (tide-dominated) of a meander bend during ebb and flood tides. The total relative abundance of ARGs was approximately 2.7 times higher on the landward side, peaking during the ebb tide. Microbial composition analysis showed that genera Acinetobacter and Pseudomonas were dominant at the landward sites, while halophilic genera such as Marinobacter and Exiguobacterium were abundant at the seaward sites. Further analysis of metagenome-assembled genomes (MAGs) demonstrated that the dominant landward genus Acinetobacter acted as a key host of ARGs, with two of four MAGs encoding more than ten ARGs. Notably, the total relative abundance of mobile genetic elements was high but consistent between sides and tidal cycles (p > 0.05). Given this high dissemination risk, we further forecasted the ARGs transfer scenarios to oceanic settings based on a set of offshore MAGs (n = 3626). Three ARGs, i.e., acrA, vanSL, and AAC(2')-Ia, were inferred to have transfer potential, supported by neighboring MGEs detected in marine microorganisms. Analysis of the genomes of predicted recipients in the SRA database confirmed the predicted mobilizations. Together, this study highlights that the meandering planform may serve as a significant barrier, attenuating the discharge of ARGs from terrestrial sources into the marine environment.

Estuaries↗
PubMed1991

Genetic mapping of meander tail, a mouse mutation affecting cerebellar development.

The meander tail mouse harbors a recessive mutation on chromosome 4 that affects the anterior lobes of the cerebellum and the caudal vertebrae. Examination of the mea/mea cerebellum reveals that the complete disorganization of all cell types seen in the anterior lobes is separated by a sharp and consistent boundary from the normal cytoarchitecture of the posterior lobes. In the absence of any biochemical information regarding the affected gene product, attempts to clone the gene must rely on the strategy of reverse genetics. As an initial step in this process we have constructed a genetic linkage map spanning 68 cM of chromosome 4 using an intersubspecific phenotypic backcross. The loci included in this analysis are Calb, Ggtb, Lv, b, Ifa, mea, D4Rp1, Glut-1, Lck, Lmyc-1, and Eno-1. This analysis positions the mea phenotypic locus in the interval between Ifa and Glut1. These results also further define regions of homology between mouse chromosome 4 and human chromosomes 8, 1, and 9. This linkage map provides the means to evaluate candidate genes, and to identify tightly linked markers useful for cloning the meander tail locus.

Animals↗
PubMed1990

Meander tail reveals a discrete developmental unit in the mouse cerebellum.

Analyses of phenotypic mutations with altered patterns of cellular organization in invertebrate systems have lead to the identification of genes important to histogenesis. Efforts to identify genes defining segments or compartments in mammalian systems and demonstrate a role for such genes in the establishment of the cellular architectonics of the brain have been hampered by the absence of phenotypic mutations that reveal compartments. Evidence is presented that in the cerebellum of the mutant mouse, meander tail, there is an abrupt transition from the normal cytoarchitecture seen in the posterior lobes to a severely disorganized cellular pattern. Thus, in the anterior lobes the Purkinje cells are positioned randomly throughout the cortex, and other cellular layers, including the internal granule cell layer, do not form. In addition, radial Bergmann glial processes are virtually absent. One explanation for the discrete boundary of the affected area in the anterior portion of this mutant cerebellar cortex is that the meander tail gene influences compartmental cellular organization in mammalian brain.

Animals↗
PubMed1991

Modeling gamma absorbed dose due to meandering plumes.

A theory was developed to predict the average gamma absorbed dose rates due to a continuous Gaussian plume that meanders due to variations in the wind's direction caused by large-scale eddies. Such meandering often occurs under very stable, low-wind conditions. The theory is based on Gifford's fluctuating Gaussian plume model. Approximate calculations based on this theory were compared to traditional approaches based on an average concentration distribution.

Accidents↗
PubMed1991

Spinocerebellar projection in the meander tail mutant mouse: organization in the granular posterior lobe and the agranular anterior lobe.

The cerebellum of the mutant mouse, meander tail, is characterized by normal cytoarchitecture posteriorly and abnormal, agranular cortex anteriorly. Anterograde WGA-HRP tracing analysis of the spinocerebellar projection reveals typical mossy fiber labeling posteriorly in lobule VIII. However, in the anterior cortex, a finer, more diffuse pattern of labeling is seen, unlike the distinct banded pattern of mossy fiber rosettes which characterizes the spinocerebellar projection in the normal animal.

Animals↗
PubMed1992

Expression of the Purkinje cell specific zebrin antigens in the cerebellum of the meander tail mutant mouse.

The cerebellum of the meander tail mutant mouse is characterized by normal cytoarchitecture in the posterior lobe and agranular, abnormal cytoarchitecture in the anterior lobe. The Purkinje cells form a monolayer in the posterior lobe but are dispersed throughout the cortex of the anterior lobe. Examination of these cells with the zebrin antibodies demonstrates that in spite of the morphologic and laminar disorganization of these cells in the anterior lobe, they are organized into the appropriate number of correctly positioned immunopositive zebrin clusters.

Animals↗
PubMedDate not supplied

Meander tail: a recessive mutant located in chromosome 4 of the mouse.

A variable kinked-tail mutant was found in 1974 in a moderately inbred stock of mice at Iowa State University, Ames. It was named meander tail and was shown to be completely recessive. Study 8 alizarin-stained skeletons showed all degrees of ankylosis or fusions of tail vertebrae and occasionally other vertebrae. Extreme examples had great reduction in number of tail vertebrae. Affected mice over 2 weeks old commonly also show some unsteadiness, presumably a pleiotropic effect of the mutant. Less commonly, one or both hind legs showed some paralysis. Linkage tests of the mutant, symbolized mea, place it fairly close to brown, b, in chromosome 4, and apparently in the small segment between Ps and Pt.

Animals↗
PubMed1992

On the convergent cell movements of gastrulation in Fundulus.

Mainly because of its transparency, the Fundulus gastrula constitutes ideal material for direct study of morphogenetic cell movements in vivo. Marking studies show that deep cells of the germ ring converge toward and enter the embryonic shield, where they undergo extension. Those close to the shield move faster. Analysis of videotapes reveals that all deep cells of the dorsal germ ring move toward the shield. But none moves in a direct line. All meander considerably. Germ ring cells nearer the shield move toward it at a higher net rate than those farther away because they meander less. This suggests that exogenous factors promote their directionality. Cells in the prospective yolk sac adjacent to the germ ring also show net convergence, but they meander more. Directional forces are apparently stronger in the germ ring. Converging deep cells move both by filolamellipodia and, less frequently, by blebs. However, there is very little individual cell movement; all cells are almost always in adhesive contact with other cells in moving cell clusters. Clusters vary constantly in size, continually aggregating with other cells and other clusters and splitting. Filolamellipodial cells show contact inhibition of cell movement. Nevertheless, they move and do so directionally, presumably in part because, as members of cell clusters, much of their movement is passive. They also show intercalation or invasive activity, but, consistent with their contact-inhibiting properties, only when neighboring cells separate and provide free space. Cells moving by blebbing locomotion are non-contact inhibiting and intercalate readily. Cell division continues during convergence. Although this temporarily arrests their movement, the daughter cells soon join in the mass convergent movement.

Animals↗
PubMed1992

Can we really walk straight?

Twenty healthy men were asked to walk as straight as possible to a target 60 m away at normal speed. A series of footprints was recorded for each subject by having him wear socks soaked with red ink and walk on white paper fixed flat to the floor. Fourier analysis was applied to determine whether the subjects actually were able to walk straight, and the results revealed that all walked in a sinuous line rather than a straight line. Periodicity and amplitude of the meandering differed from subject to subject. These facts suggest that none of us can walk in a strictly straight line; rather, we meander, primarily due to a slight structural or functional imbalance of our limbs, which produces a gait asymmetry, and secondarily due to feedback from our sense of sight, which acts to correct the shifted walking course.

Adult↗
PubMed1985

Afferent innervation of extraocular muscles in the rat studied by retrograde and anterograde horseradish peroxidase transport.

After injection of horseradish peroxidase (HRP) into extraocular muscles of rat perikarya were labeled mainly along the medial edge of the ophthalmic subdivision of the trigeminal ganglion but not in the mesencephalic nucleus of the trigeminal nerve. Injections of HRP into the trigeminal ganglion labeled simple as well as branching and meandering free fiber endings in extraocular muscles. No evidence for muscle spindles was found, but the meandering endings may be considered as candidates for stretch receptors.

Animals↗
PubMed1991

Metabolic heterogeneity in human calf muscle during maximal exercise.

Human skeletal muscle is composed of various muscle fiber types. We hypothesized that differences in metabolism between fiber types could be detected noninvasively with 31P nuclear magnetic resonance spectroscopy during maximal exercise. This assumes that during maximal exercise all fiber types are recruited and all vary in the amount of acidosis. The calf muscles of seven subjects were studied. Two different coils were applied: an 11-cm-diameter surface coil and a five-segment meander coil. The meander coil was used to localize the 31P signal to either the medial or the lateral gastrocnemius. Maximal exercise, consisting of rapid plantar flexions, resulted in an 83.7% +/- 7.8% decrease of the phosphocreatine pool and an 8-fold increase of the inorganic phosphate (Pi) pool. At rest the Pi pool was observed as a single resonance (pH 7.0). Toward the end of the first minute of exercise, three subjects showed three distinct Pi peaks. During the second minute of exercise the pH values stabilized at 7.12 +/- 0.12, 6.63 +/- 0.15, and 6.27 +/- 0.23. The same pattern was seen when the signal was collected from the medial or lateral gastrocnemius. In four subjects only two distinct Pi peaks were observed. The Pi peaks had differing relative areas in different subjects, but they were reproducible in each individual. This method allowed us to study the appearance and disappearance of the different Pi peaks, together with the changes in pH. Because multiple Pi peaks were seen in single muscles they most likely identify different muscle fiber types.

Adenine Nucleotides↗
PubMed1990

[Observations on Demodex folliculorum by scanning electron microscopy].

Additional observations on some fine structures of Demodex folliculorum under SEM were presented in this paper, including supracoxal spines, hypostome, palpal claws, male and female podosomal setae, leg claw-basal spur, femoral spur, etc. The supracoxal spines were rivet-shaped and the hypostome was pearshaped. The claws on the tarsal coxa of the pulpus meander to the ventral side instead of meandering to the dorsal side. Based on these structural characteristics, it was inferred that podosomal seta may be a sensilla and claw-basal spur as well as femoral spur can protect mites against being expelled from follicules.

Animals↗
PubMed1987

Collateral mesenteric circulation.

The origins of historical terms, such as "Arc of Riolan" and "marginal artery of Drummond" are traced herein with emphasis on the inherent confusion caused when these terms are used. Basic mesenteric anatomy is briefly mentioned and pathologic anatomy with its altered direction of blood flow induced by atherosclerosis is stressed. The significance of the meandering mesenteric artery as the main collateral vessel between the superior and inferior mesenteric artery is emphasized along with preoperative and intraoperative ways to ascertain whether or not the origin of this latter vessel can be safely ligated. Specific operations, such as abdominal aortic aneurysmorrhaphy and sigmoid colectomy, which can potentially interfere with blood flow in the meandering mesenteric artery, are discussed in an attempt to prevent postoperative necrosis of any portion of the intestine that may have deficient mesenteric blood flow.

Blood Vessel Prosthesis↗
PubMed1985

Effects of age on Meissner corpuscles: a study of silver-impregnated neurites in mouse digital pads.

Investigation focused on finding qualitative and quantitative evidence of age-changes in the quantity of neural surface within Meissner corpuscles. These mechanoreceptors were studied in 53 mice (nine age-groups) ranging from 1.7 to 24 months old. Forepaw digital pads were formalin-fixed and frozen-sectioned parallel to each digit and perpendicular to the skin. Serial sections were then silver-impregnated to allow light microscopic examination of the neurites (axons) in corpuscles. From young (1.7-7 months) to middle age (9-15 months), neurites became more coarse, tortuous, ramified, varicose, and thus more complex. At old age (18-24 months), neurites seemed attenuated and showed more of an irregular winding, twisted, or tangled pattern with less parallel orientation to the skin surface than the regular spiraled, looped, or arched pattern typical at young and middle ages. Corpuscle size appeared greatest at middle age, smallest at young age. Dermal papillae not occupied by corpuscular neurites were most abundant at old age. The number of corpuscles per area and neurites per corpuscle decreased significantly with age, whereas the number of neurite bifurcations per corpuscle increased significantly. Morphometric analysis of neurites projected by a camera lucida onto a planimeter showed that the length of neurites meandering through a fixed interval of tissue increased significantly until age 12 months-evidence of increased tortuosity; the area of neurites measured within the same fixed interval, and the area of neurite terminals changed significantly as inverse parabolic functions of age-evidence of increased volume until middle age, which decreased thereafter. The general trend of these changes implied growth at young age and atrophy at old age.(ABSTRACT TRUNCATED AT 250 WORDS)

Aging↗