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2.
Sci Adv ; 8(22): eabn6749, 2022 Jun 03.
Article in English | MEDLINE | ID: mdl-35648865

ABSTRACT

Basalts and mantle peridotites of mid-ocean ridges are thought to sample Earth's upper mantle. Osmium isotopes of abyssal peridotites uniquely preserve melt extraction events throughout Earth history, but existing records only indicate ages up to ~2 billion years (Ga) ago. Thus, the memory of the suspected large volumes of mantle lithosphere that existed in Archean time (>2.5 Ga) has apparently been lost somehow. We report abyssal peridotites with melt-depletion ages up to 2.8 Ga, documented by extremely unradiogenic 187Os/188Os ratios (to as low as 0.1095) and refractory major elements that compositionally resemble the deep keels of Archean cratons. These oceanic rocks were thus derived from the once-extensive Archean continental keels that have been dislodged and recycled back into the mantle, the feasibility of which we confirm with numerical modeling. This unexpected connection between young oceanic and ancient continental lithosphere indicates an underappreciated degree of compositional recycling over time.

3.
Sci Rep ; 11(1): 4123, 2021 Feb 18.
Article in English | MEDLINE | ID: mdl-33603040

ABSTRACT

Two-thirds of the Earth is covered by mid-ocean ridge basalts, which form along a network of divergent plate margins. Basalts along these margins display a chemical diversity, which is consequent to a complex interplay of partial mantle melting in the upper mantle and magmatic differentiation processes in lower crustal levels. Igneous differentiation (crystal fractionation, partial melting) and source heterogeneity, in general, are key drivers creating variable chemistry in mid-ocean ridge basalts. This variability is reflected in iron isotope systematics (expressed as δ57Fe), showing a total range of 0.2 ‰ from δ57Fe = + 0.05 to + 0.25 ‰. Respective contributions of source heterogeneity and magma differentiation leading to this diversity, however, remain elusive. This study investigates the iron isotope systematics in basalts from the ultraslow spreading Gakkel Ridge in the Arctic Ocean and compares them to existing data from the fast spreading East Pacific Rise ridge. Results indicate that Gakkel lavas are driven to heavier iron isotope compositions through partial melting processes, whereas effects of igneous differentiation are minor. This is in stark contrast to fast spreading ridges showing reversed effects of near negligible partial melting effects followed by large isotope fractionation along the liquid line of descent. Gakkel lavas further reveal mantle heterogeneity that is superimposed on the igneous differentiation effects, showing that upper mantle Fe isotope heterogeneity can be transmitted into erupting basalts in the absence of homogenisation processes in sub-oceanic magma chambers.

4.
Sci Adv ; 6(44)2020 Oct.
Article in English | MEDLINE | ID: mdl-33127673

ABSTRACT

Earth's upper mantle, as sampled by mid-ocean ridge basalts (MORBs) at oceanic spreading centers, has developed chemical and isotopic heterogeneity over billions of years through focused melt extraction and re-enrichment by recycled crustal components. Chemical and isotopic heterogeneity of MORB is dwarfed by the large compositional spectrum of lavas at convergent margins, identifying subduction zones as the major site for crustal recycling into and modification of the mantle. The fate of subduction-modified mantle and if this heterogeneity transmits into MORB chemistry remains elusive. Here, we investigate the origin of upper mantle chemical heterogeneity underneath the Western Gakkel Ridge region in the Arctic Ocean through MORB geochemistry and tectonic plate reconstruction. We find that seafloor lavas from the Western Gakkel Ridge region mirror geochemical signatures of an Early Cretaceous, paleo-subduction zone, and conclude that the upper mantle can preserve a long-lived, stationary geochemical memory of past geodynamic processes.

5.
Nature ; 579(7798): 250-255, 2020 03.
Article in English | MEDLINE | ID: mdl-32161389

ABSTRACT

The lithified lower oceanic crust is one of Earth's last biological frontiers as it is difficult to access. It is challenging for microbiota that live in marine subsurface sediments or igneous basement to obtain sufficient carbon resources and energy to support growth1-3 or to meet basal power requirements4 during periods of resource scarcity. Here we show how limited and unpredictable sources of carbon and energy dictate survival strategies used by low-biomass microbial communities that live 10-750 m below the seafloor at Atlantis Bank, Indian Ocean, where Earth's lower crust is exposed at the seafloor. Assays of enzyme activities, lipid biomarkers, marker genes and microscopy indicate heterogeneously distributed and viable biomass with ultralow cell densities (fewer than 2,000 cells per cm3). Expression of genes involved in unexpected heterotrophic processes includes those with a role in the degradation of polyaromatic hydrocarbons, use of polyhydroxyalkanoates as carbon-storage molecules and recycling of amino acids to produce compounds that can participate in redox reactions and energy production. Our study provides insights into how microorganisms in the plutonic crust are able to survive within fractures or porous substrates by coupling sources of energy to organic and inorganic carbon resources that are probably delivered through the circulation of subseafloor fluids or seawater.


Subject(s)
Aquatic Organisms/genetics , Aquatic Organisms/metabolism , Energy Metabolism/genetics , Geologic Sediments/microbiology , Microbiota/genetics , Oceans and Seas , Carbon Cycle/genetics , Gene Expression Profiling
6.
Talanta ; 205: 120160, 2019 Dec 01.
Article in English | MEDLINE | ID: mdl-31450451

ABSTRACT

Simple data processing and unattended calibration are achieved in automated standard dilution analysis (aSDA) using two internal standards and an inline lab-made mixing chamber furnished from a common plastic syringe. Only two calibration solutions are required per sample, which minimizes reagent consumption and waste generation. Solution 1 contains 50% sample and 50% of a standard containing the analytes and internal standard 1 (IS1). Solution 2 has 50% sample and 50% of a blank containing internal standard 2 (IS2). The concentration of analyte in the sample is calculated from (i) the slope and intercept of an analyte vs. IS1 plot, (ii) the concentration of analyte in the standard added to Solution 1, and (iii) the intercept of a second plot with IS1vs. IS2. The aSDA method was used to determine Cd, Co, Cr, Cu, Pb and Zn in tap and creek water, beer, cola soft drink, mouthwash, cough syrup and cachaça by ICP OES. Addition/recovery experiments involving these same samples and other challenging matrices (i.e. 40% v/v HNO3, and 1% m/v Na, Ca or C) were performed to evaluate the method's accuracy. The results were compared with values obtained with external standard calibration (EC), internal standardization (IS) and standard additions (SA). Considering all samples and analytes evaluated, aSDA provided the best accuracy, with an average absolute error (ε‾=|analytepercentrecovery-100|) of 4% (EC, IS and SA had 13%, 9% and 7% errors, respectively). The aSDA strategy is a simple and inexpensive alternative to traditional methods. It has great potential for broad implementation with existing ICP OES instrumentation, as it requires little modification to systems already in place in routine laboratories.

7.
Nature ; 494(7436): 195-200, 2013 Feb 14.
Article in English | MEDLINE | ID: mdl-23389441

ABSTRACT

The global ridge system is dominated by oceanic rises reflecting large variations in axial depth associated with mantle hotspots. The little-studied Marion Rise is as large as the Icelandic Rise, considering both length and depth, but has an axial rift (rather than a high) nearly its entire length. Uniquely along the Southwest Indian Ridge systematic sampling allows direct examination of crustal architecture over its full length. Here we show that, unlike the Icelandic Rise, peridotites are extensively exposed high on the rise, revealing that the crust is generally thin, and often missing, over a rifted rise. Therefore the Marion Rise must be largely an isostatic response to ancient melting events that created low-density depleted mantle beneath the Southwest Indian Ridge rather than thickened crust or a large thermal anomaly. The origin of this depleted mantle is probably the mantle emplaced into the African asthenosphere during the Karoo and Madagascar flood basalt events.

8.
Spinal Cord ; 50(9): 655-60, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22641257

ABSTRACT

OBJECTIVE: Nontraumatic spinal epidural hematoma (SEH) during pregnancy is rare. Therefore, appropriate management of this occurrence is not well defined. The aim of this study was to extensively review the literature on this subject, to propose some novel treatment guidelines. METHODS: Electronic databases, manual reviews and conference proceedings up to December 2011 were systematically reviewed. Articles were deemed eligible for inclusion in this study if they dealt with nontraumatic SEH during pregnancy. Search protocols and data were independently assessed by two authors. RESULTS: In all, 23 case reports were found to be appropriate for review. The mean patient age was 28 years and gestational age was 33.2 weeks. Thirteen cases presented with acute interscapular pain. The clinical picture consisted of paraplegia, which occurred approximately 63 h after pain onset. Spinal cord decompression was performed within an average time of 20 h after neurological deficit onset. Fifteen patients had cesarean deliveries, even when the gestational age was less than 36 weeks. CONCLUSION: This review failed to identify articles, other than case reports, which could assist in the formation of new guidelines to treat SEH in pregnancy. However, we believe that SEH may be managed neurosurgically, without requiring prior, premature, cesarean section.


Subject(s)
Hematoma, Epidural, Spinal/diagnosis , Hematoma, Epidural, Spinal/surgery , Pregnancy Complications/diagnosis , Pregnancy Complications/surgery , Decompression, Surgical/methods , Disease Management , Female , Humans , Infant, Newborn , Pregnancy
9.
J Pediatr Ophthalmol Strabismus ; 47(6): 338-46, 2010.
Article in English | MEDLINE | ID: mdl-20210280

ABSTRACT

BACKGROUND: This study estimated when it is safe to stop follow-up visits after cessation of amblyopia treatment and to identify factors associated with deterioration of visual acuity. METHODS: Study patients included 282 patients aged 7 to 13 years who were monitored for deterioration after cessation of amblyopia treatment (median follow-up: 3.9 years). RESULTS: Six (2.1%) patients lost 2 or more logarithm of the minimum angle of resolution levels of visual acuity and 77 (27.3%) patients lost 1 or more Snellen lines of visual acuity. Good compliance with re-treatment stopped further deterioration and lost visual acuity was regained (average follow-up after re-treatment: 3.3 years). Life table analysis indicated that 95% of the cases that deteriorated occurred within 24 months after cessation of treatment. Multivariable analysis corrected for duration of treatment uncovered factors independently associated with deterioration. CONCLUSION: A clinically important risk of deterioration of visual acuity was found during the first 2 years after cessation of amblyopia treatment. Follow-up time longer than 2 years is recommended in the presence of a developing risk factor such as increasing anisometropia. With prompt re-treatment and good compliance, deterioration can be stopped and visual acuity can be restored.


Subject(s)
Amblyopia/therapy , Continuity of Patient Care , Office Visits , Withholding Treatment , Adolescent , Amblyopia/diagnosis , Amblyopia/physiopathology , Child , Female , Follow-Up Studies , Humans , Life Tables , Male , Monitoring, Physiologic , Risk Factors , Secondary Prevention , Sensory Deprivation , Time Factors , Treatment Outcome , Visual Acuity/physiology
10.
Science ; 310(5748): 654-7, 2005 Oct 28.
Article in English | MEDLINE | ID: mdl-16254183

ABSTRACT

Nineteen uranium-lead zircon ages of lower crustal gabbros from Atlantis Bank, Southwest Indian Ridge, constrain the growth and construction of oceanic crust at this slow-spreading midocean ridge. Approximately 75% of the gabbros accreted within error of the predicted seafloor magnetic age, whereas approximately 25% are significantly older. These anomalously old samples suggest either spatially varying stochastic intrusion at the ridge axis or, more likely, crystallization of older gabbros at depths of approximately 5 to 18 kilometers below the base of crust in the cold, axial lithosphere, which were uplifted and intruded by shallow-level magmas during the creation of Atlantis Bank.

11.
Nature ; 426(6965): 405-12, 2003 Nov 27.
Article in English | MEDLINE | ID: mdl-14647373

ABSTRACT

New investigations of the Southwest Indian and Arctic ridges reveal an ultraslow-spreading class of ocean ridge that is characterized by intermittent volcanism and a lack of transform faults. We find that the mantle beneath such ridges is emplaced continuously to the seafloor over large regions. The differences between ultraslow- and slow-spreading ridges are as great as those between slow- and fast-spreading ridges. The ultraslow-spreading ridges usually form at full spreading rates less than about 12 mm yr(-1), though their characteristics are commonly found at rates up to approximately 20 mm yr(-1). The ultraslow-spreading ridges consist of linked magmatic and amagmatic accretionary ridge segments. The amagmatic segments are a previously unrecognized class of accretionary plate boundary structure and can assume any orientation, with angles relative to the spreading direction ranging from orthogonal to acute. These amagmatic segments sometimes coexist with magmatic ridge segments for millions of years to form stable plate boundaries, or may displace or be displaced by transforms and magmatic ridge segments as spreading rate, mantle thermal structure and ridge geometry change.

12.
Nature ; 418(6893): 68-72, 2002 Jul 04.
Article in English | MEDLINE | ID: mdl-12097907

ABSTRACT

Inferring the melting process at mid-ocean ridges, and the physical conditions under which melting takes place, usually relies on the assumption of compositional similarity between all mid-ocean-ridge basalt sources. Models of mantle melting therefore tend to be restricted to those that consider the presence of only one lithology in the mantle, peridotite. Evidence from xenoliths and peridotite massifs show that after peridotite, pyroxenite and eclogite are the most abundant rock types in the mantle. But at mid-ocean ridges, where most of the melting takes place, and in ophiolites, pyroxenite is rarely found. Here we present neodymium isotopic compositions of abyssal peridotites to investigate whether peridotite can indeed be the sole source for mid-ocean-ridge basalts. By comparing the isotopic compositions of basalts and peridotites at two segments of the southwest Indian ridge, we show that a component other than peridotite is required to explain the low end of the (143)Nd/(144)Nd variations of the basalts. This component is likely to have a lower melting temperature than peridotite, such as pyroxenite or eclogite, which could explain why it is not observed at mid-ocean ridges.

13.
J Clin Apher ; 14(1): 35-41, 1999.
Article in English | MEDLINE | ID: mdl-10355662

ABSTRACT

The collection of peripheral blood progenitor cells (PBPC) requires the combined efforts of the Transfusion Medicine/Hemapheresis and Hematology/Oncology services and HLA/Progenitor Cell and Immunology laboratories. Coordination and communication among these different services and laboratories are key to attaining an optimal collection in a timely manner for the patient undergoing PBPC collection. In an effort to improve patient care by same-day decision to cease or continue collections avoiding unnecessary collections, needless patient trips to the hospital and ultimately increasing patient satisfaction, a flow chart was used to capture the sequence of events. The flow chart served as a powerful tracking tool that defined system process and steps to attain enumeration of CD34+ cells the same day of collection. It provided documentation of work flow from each of the independent operations involved in progenitor cell collection and enumeration turn-around-time including attending and staff time involvement. By using the flow chart, potential and actual problem areas were demonstrated and this allowed for creative thinking and problem solving by individual sections rather than recriminations. Finally, it focused all the staff involved in the common goal of a shorter turn-around-time for CD34+ cell enumeration the same day of collection. This allowed a prompt decision for subsequent leukapheresis as improved service to oncology patients and their physicians.


Subject(s)
Blood Banks/organization & administration , Case Management/organization & administration , Hematopoietic Stem Cell Transplantation , Hospitals, University/organization & administration , Leukapheresis/methods , Medical Records Systems, Computerized , Software Design , Time and Motion Studies , Adult , Ambulatory Care/organization & administration , Ambulatory Care/statistics & numerical data , Anticoagulants/adverse effects , Appointments and Schedules , Child , Citric Acid/adverse effects , Efficiency , Hematopoietic Stem Cell Transplantation/nursing , Hematopoietic Stem Cell Transplantation/statistics & numerical data , Hospitals, University/statistics & numerical data , Humans , Leukapheresis/nursing , Leukocyte Count , Neoplasms/therapy , New York , Patient Care Team , Phlebotomy/nursing , Problem Solving , Time Factors , Time Management
15.
Clin Lab Med ; 14(3): 459-71, 1994 Sep.
Article in English | MEDLINE | ID: mdl-7805341

ABSTRACT

Technological changes in the clinical laboratory are usually driven by the goal of patient care optimization. In the last decade, the trend appeared to be directed at clinical laboratory decentralization. A new generation of analytical instruments, the biosensors, is redirecting laboratory testing closer to the patient, at the bedside, in the physician's office, and by the patient at home. These miniaturized biosensors are easy to operate, require small specimen size, and provide reliable results with rapid TAT. Thus far, bedside testing using biosensor technology appears to offer unique opportunities for earlier availability of clinical laboratory data, decision making, and more specific diagnosis, and faster and more frequent monitoring; these may translate into improved patient care and reduced hospital costs. It is likely that this trend will continue into the twenty-first century. Electrochemical sensors (e.g., for electrolytes, glucose, urea, and hematocrit) and pulse oximetry, having gained clinical acceptance, will probably be the leading instrumentation for bedside testing. Continuous monitoring either by near-infrared sensing technology or with an implantable sensor is valuable in the care of the critically ill patient. Acceptance for clinical use will depend on complete data integration and a favorable cost-benefit ratio.


Subject(s)
Biosensing Techniques , Laboratories/trends , Medical Laboratory Science/trends , Clinical Laboratory Techniques/trends , Diagnostic Tests, Routine/trends , Humans , Laboratories, Hospital/trends , Monitoring, Physiologic/methods , Oximetry , Spectrophotometry, Infrared , United States
16.
Am J Clin Pathol ; 100(6): 599-605, 1993 Dec.
Article in English | MEDLINE | ID: mdl-8249905

ABSTRACT

A recently available portable clinical analyzer (PCA), which examines sodium, potassium, chloride, glucose, urea nitrogen, and hematocrit levels on 60 microL of blood and calculates hemoglobin and osmolality levels within 2 minutes, was evaluated. Blood from 574 patients was drawn by emergency department staff, who immediately tested the samples with the PCA and transported them for plasma analysis on a reference analyzer in the clinical laboratory. Correlations between the PCA and the reference analyzer were as follows: R2 = 0.987 for urea nitrogen; R2 = 0.97, glucose; R2 = 0.937, K;R2 = 0.79, hematocrit; R2 = 0.751, sodium; and R2 = 0.689 for chloride. With its rapid turnaround, small sample requirement, and ease of operation, the PCA is most useful in an emergency department setting, where immediate access to clinically relevant laboratory testing is required in support of urgent clinical decision-making.


Subject(s)
Blood Chemical Analysis/instrumentation , Emergency Medical Services/methods , Pathology, Clinical/instrumentation , Blood Chemical Analysis/economics , Blood Chemical Analysis/trends , Cost-Benefit Analysis , Humans , Pathology, Clinical/economics , Pathology, Clinical/trends , Sensitivity and Specificity
20.
Am J Obstet Gynecol ; 167(6): 1672-8, 1992 Dec.
Article in English | MEDLINE | ID: mdl-1471685

ABSTRACT

OBJECTIVE: The differential vasoactive effects of hydralazine on the uteroplacental vascular bed were studied. STUDY DESIGN: After control measurements were taken, near-term chronically prepared pregnant sheep were continuously infused with angiotensin II. Maternal arterial pressure was increased by 32 mm Hg. Hydralazine was then administered; the effects on regional resistance and blood flow were evaluated with a radionuclide-labeled microsphere technique. Analysis of variance for repeated measures was used to compare observations. RESULTS: When compared with the hypertensive state, hydralazine caused the following changes by 40 minutes (mean +/- SEM): Although maternal blood pressure fell 31% +/- 5% (p = 0.0005), placental blood flow was unchanged, total uteroplacental blood flow increased 24% +/- 8% (p = 0.03), total uteroplacental resistance decreased 43% +/- 4% (p = 0.0002), placental resistance decreased 19% +/- 9% (p = 0.01), myoendometrial blood flow increased 390% +/- 82% (p = 0.0005), and myoendometrial resistance decreased 82% +/- 4% (p = 0.0005). CONCLUSIONS: In angiotensin II-induced hypertensive ewes, hydralazine is an effective dilator of the uteroplacental vascular bed and can maintain placental blood flow while blood pressure.


Subject(s)
Endometrium/blood supply , Hydralazine/pharmacology , Hypertension/physiopathology , Myometrium/blood supply , Adrenal Glands/blood supply , Angiotensin II/pharmacology , Animals , Female , Injections, Intravenous , Microspheres , Placenta/blood supply , Pregnancy , Regional Blood Flow/drug effects , Renal Circulation/drug effects , Sheep , Vascular Resistance/drug effects
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