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Category Archives: Transhuman News
DNA barcoding to monitor marine mammal genetic diversity
Posted: December 30, 2013 at 12:43 pm
PUBLIC RELEASE DATE:
30-Dec-2013
Contact: Jean-Luc Jung jung@univ-brest.fr Pensoft Publishers
Marine mammals are flagship and charismatic species, very attractive for the general public. Nowadays, they are also considered as highly relevant sentinel of the marine realm. Their presence and their welfare in an area is thought to indicate the health of the place, whereas their disappearance, their displacement, or a decrease in their abundance or health could reflect negative environmental changes, whether of anthropogenic origin or not.
Monitoring marine mammal biodiversity is often difficult to perform. If some species can be easily observed, others are more difficult to detect, because for instance, of their scarcity or their discrete behavior. One of the solution suggested by scientists is based on the organization of stranding networks, listing and recording marine mammal strandings, which represent a cost-effective means to follow the marine mammal biodiversity.
Researchers from Ocanopolis and from the Laboratory BioGeMME (Biologie et Gntique des Mammifres Marins dans leur Environnement) of the University of Brest, in collaboration with the Parc naturel marin d'Iroise and PELAGIS, have evaluated the usefulness of DNA barcoding in the monitoring of marine mammal biodiversity. They confirmed the species identifications performed by field correspondents, identified degraded carcasses or parts of carcasses, and examined intraspecific genetic variations for the harbour porpoise and the grey seal, undetectable by visual observation.
The conclusions of their study, published in a special issue of the open access journal Zookeys dedicated to DNA barcoding (DNA barcoding: a practical tool for fundamental and applied biodiversity research), are that the use of DNA barcoding in conjunction with a stranding network will clearly increase the accuracy of the monitoring of marine mammal biodiversity. Global climate change, as well as more localized environmental changes (some of which are caused by humans), has impacts on the marine realm. A routine use of DNA barcoding to monitor marine mammal biodiversity will clearly increase our capacity to detect such impacts, which is a necessary first step to take appropriate conservation measures.
In France, the French marine mammal stranding recording program has been created at the beginning of the 70s by the CRMM (Centre de Recherche sur les Mammifres Marins, La Rochelle, presently the Joint Service Unit PELAGIS, UMS 3462, University of La Rochelle- CNRS). The network comprises about 260 field correspondents, members of organizations or volunteers (Peltier et al. 2013, PloS One, e62180).
In Brittany (a region located at the northwest of France), the network is coordinated by Ocanopolis in Brest. In this area, and all species included, an average of 150 animals strand each year, representing, in the last ten years, 14 species of cetaceans and five species of pinnipeds. These species include for instance, common and bottlenose dolphins, harbour porpoises, but also larger animals like minke whales and fin whales. Some rare stranding events include deep-diving or exotic species, such as arctic seals.
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THE LUCIFER GENOME – Video
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THE LUCIFER GENOME
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Eczema Free Forever Book + Get Discount – Video
Posted: at 12:43 pm
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Eczema Free Forever Free Download + Get Discount – Video
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Eczema Free Forever By Rachel Anderson + Get Discount – Video
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Facial Eczema Treatment – Review to Facial Eczema Treatment – Video
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Facial Eczema Treatment - Review to Facial Eczema Treatment
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Atopic eczema, atopic dermatitis. DermNet NZ
Posted: at 12:43 pm
Facts about the skin from DermNet New Zealand Trust. Topic index: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Atopic eczema is a chronic, itchy skin condition that is very common in children but may occur at any age. It is also known as eczema, atopic dermatitis and neurodermatitis. It is the most common form of dermatitis.
Atopic eczema usually occurs in people who have an 'atopic tendency'. This means they may develop any or all of three closely linked conditions; atopic eczema, asthma and hay fever (allergic rhinitis). Often these conditions run within families with a parent, child or sibling also affected. A family history of asthma, eczema or hay fever is particularly useful in diagnosing atopic eczema in infants.
Atopic eczema is not contagious! It arises because of a complex interaction of genetic and environmental factors. These include defects in skin barrier function making the skin more susceptible to irritation by soap and other contact irritants, the weather, temperature and non-specific triggers: see Causes of atopic eczema.
There is quite a variation in the appearance of atopic eczema between individuals. From time to time, most people have acute flares with inflamed, red, sometimes blistered and weepy patches. In between flares, the skin may appear normal or suffer from chronic eczema with dry, thickened and itchy areas.
The presence of infection or an additional skin condition, the creams applied, the age of the person, their ethnic origin and other factors can alter the way eczema looks and feels.
There are however some general patterns to where the eczema is found on the body according to the age of the affected person.
More images of atopic eczema and flexural dermatitis.
Atopic eczema affects 15-20% of children but only 1-2% of adults. It is impossible to predict whether eczema will improve by itself or not in an individual.
It is unusual for an infant to be affected with atopic eczema before the age of four months but they may suffer from infantile seborrhoeic dermatitis or other rashes prior to this. The onset of atopic eczema is usually before two years of age although it can manifest itself in older people for the first time.
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Atopic eczema, atopic dermatitis. DermNet NZ
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7 Helpful Treatments for Eczema and Dry, Itchy and Sensitive Skin – Video
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7 Helpful Treatments for Eczema and Dry, Itchy and Sensitive Skin
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Psoriasis Free For Life 2014 (legit review instant access) – Video
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Gene that influences the ability to remember faces identified
Posted: at 12:42 pm
Dec. 23, 2013 New findings suggest the oxytocin receptor, a gene known to influence mother-infant bonding and pair bonding in monogamous species, also plays a special role in the ability to remember faces. This research has important implications for disorders in which social information processing is disrupted, including autism spectrum disorder. In addition, the finding may lead to new strategies for improving social cognition in several psychiatric disorders.
A team of researchers from Yerkes National Primate Research Center at Emory University in Atlanta, the University College London in the United Kingdom and University of Tampere in Finland made the discovery, which will be published in an online Early Edition of Proceedings of the National Academy of Sciences.
According to author Larry Young, PhD, of Yerkes, the Department of Psychiatry in Emory's School of Medicine and Emory's Center for Translational Social Neuroscience (CTSN), this is the first study to demonstrate that variation in the oxytocin receptor gene influences face recognition skills. He and co-author David Skuse point out the implication that oxytocin plays an important role in promoting our ability to recognize one another, yet about one-third of the population possesses only the genetic variant that negatively impacts that ability. They say this finding may help explain why a few people remember almost everyone they have met while others have difficulty recognizing members of their own family.
Skuse is with the Institute of Child Health, University College London, and the Great Ormond Street Hospital for Children, NHS Foundation Trust, London.
Young, Skuse and their research team studied 198 families with a single autistic child because these families were known to show a wide range of variability in facial recognition skills; two-thirds of the families were from the United Kingdom, and the remainder from Finland.
The Emory researchers previously found the oxytocin receptor is essential for olfactory-based social recognition in rodents, like mice and voles, and wondered whether the same gene could also be involved in human face recognition. They examined the influence of subtle differences in oxytocin receptor gene structure on face memory competence in the parents, non-autistic siblings and autistic child, and discovered a single change in the DNA of the oxytocin receptor had a big impact on face memory skills in the families. According to Young, this finding implies that oxytocin likely plays an important role more generally in social information processing, which is disrupted in disorders such as autism.
Additionally, this study is remarkable for its evolutionary aspect. Rodents use odors for social recognition while humans use visual facial cues. This suggests an ancient conservation in genetic and neural architectures involved in social information processing that transcends the sensory modalities used from mouse to man.
Skuse credits Young's previous research that found mice with a mutated oxytocin receptor failed to recognize mice they previously encountered. "This led us to pursue more information about facial recognition and the implications for disorders in which social information processing is disrupted." Young adds the team will continue working together to pursue strategies for improving social cognition in psychiatric disorders based on the current findings.
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