Catálogo de publicaciones - revistas

Compartir en
redes sociales


Nature

Resumen/Descripción – provisto por la editorial en inglés
Nature is a weekly international journal publishing the finest peer-reviewed research in all fields of science and technology on the basis of its originality, importance, interdisciplinary interest, timeliness, accessibility, elegance and surprising conclusions. Nature also provides rapid, authoritative, insightful and arresting news and interpretation of topical and coming trends affecting science, scientists and the wider public.
Palabras clave – provistas por la editorial

No disponibles.

Disponibilidad
Institución detectada Período Navegá Descargá Solicitá
No detectada desde jul. 2012 / hasta dic. 2023 Nature.com
No detectada desde jul. 2006 / hasta ago. 2012 Ovid

Información

Tipo de recurso:

revistas

ISSN impreso

0028-0836

ISSN electrónico

1476-4687

Editor responsable

Springer Nature

País de edición

Reino Unido

Fecha de publicación

Tabla de contenidos

Experimental quantum key distribution certified by Bell's theorem

D. P. NadlingerORCID; P. Drmota; B. C. Nichol; G. Araneda; D. Main; R. Srinivas; D. M. Lucas; C. J. BallanceORCID; K. IvanovORCID; E. Y.-Z. TanORCID; P. SekatskiORCID; R. L. Urbanke; R. RennerORCID; N. SangouardORCID; J.-D. BancalORCID

Palabras clave: Multidisciplinary.

Pp. 682-686

A device-independent quantum key distribution system for distant users

Wei ZhangORCID; Tim van LeentORCID; Kai Redeker; Robert Garthoff; René Schwonnek; Florian Fertig; Sebastian Eppelt; Wenjamin Rosenfeld; Valerio Scarani; Charles C.-W. LimORCID; Harald Weinfurter

<jats:title>Abstract</jats:title><jats:p>Device-independent quantum key distribution (DIQKD) enables the generation of secret keys over an untrusted channel using uncharacterized and potentially untrusted devices<jats:sup>1–9</jats:sup>. The proper and secure functioning of the devices can be certified by a statistical test using a Bell inequality<jats:sup>10–12</jats:sup>. This test originates from the foundations of quantum physics and also ensures robustness against implementation loopholes<jats:sup>13</jats:sup>, thereby leaving only the integrity of the users’ locations to be guaranteed by other means. The realization of DIQKD, however, is extremely challenging—mainly because it is difficult to establish high-quality entangled states between two remote locations with high detection efficiency. Here we present an experimental system that enables for DIQKD between two distant users. The experiment is based on the generation and analysis of event-ready entanglement between two independently trapped single rubidium atoms located in buildings 400 metre apart<jats:sup>14</jats:sup>. By achieving an entanglement fidelity of <jats:inline-formula><jats:alternatives><jats:tex-math>$$ {\mathcal F} \,\ge 0.892(23)$$</jats:tex-math><mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:mrow> <mml:mi>ℱ</mml:mi> <mml:mspace /> <mml:mo>≥</mml:mo> <mml:mn>0.892</mml:mn> <mml:mrow> <mml:mo>(</mml:mo> <mml:mrow> <mml:mn>23</mml:mn> </mml:mrow> <mml:mo>)</mml:mo> </mml:mrow> </mml:mrow> </mml:math></jats:alternatives></jats:inline-formula> and implementing a DIQKD protocol with random key basis<jats:sup>15</jats:sup>, we observe a significant violation of a Bell inequality of <jats:italic>S</jats:italic> = 2.578(75)—above the classical limit of 2—and a quantum bit error rate of only 0.078(9). For the protocol, this results in a secret key rate of 0.07 bits per entanglement generation event in the asymptotic limit, and thus demonstrates the system’s capability to generate secret keys. Our results of secure key exchange with potentially untrusted devices pave the way to the ultimate form of quantum secure communications in future quantum networks.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 687-691

Magnetic memory and spontaneous vortices in a van der Waals superconductor

Eylon PerskyORCID; Anders V. Bjørlig; Irena Feldman; Avior Almoalem; Ehud Altman; Erez BergORCID; Itamar Kimchi; Jonathan Ruhman; Amit Kanigel; Beena KaliskyORCID

Palabras clave: Multidisciplinary.

Pp. 692-696

Exceptional-point-based accelerometers with enhanced signal-to-noise ratio

Rodion KononchukORCID; Jizhe CaiORCID; Fred Ellis; Ramathasan ThevamaranORCID; Tsampikos KottosORCID

Palabras clave: Multidisciplinary.

Pp. 697-702

Atomic imaging of zeolite-confined single molecules by electron microscopy

Boyuan ShenORCID; Huiqiu WangORCID; Hao XiongORCID; Xiao ChenORCID; Eric G. T. Bosch; Ivan Lazić; Weizhong Qian; Fei WeiORCID

Palabras clave: Multidisciplinary.

Pp. 703-707

Dislocation-induced stop-and-go kinetics of interfacial transformations

Xianhu SunORCID; Dongxiang Wu; Lianfeng Zou; Stephen D. House; Xiaobo ChenORCID; Meng LiORCID; Dmitri N. Zakharov; Judith C. Yang; Guangwen ZhouORCID

Palabras clave: Multidisciplinary.

Pp. 708-713

Threshold response to melt drives large-scale bed weakening in Greenland

Nathan MaierORCID; Florent GimbertORCID; Fabien Gillet-Chaulet

Palabras clave: Multidisciplinary.

Pp. 714-720

Competition for pollinators destabilizes plant coexistence

Christopher A. JohnsonORCID; Proneet Dutt; Jonathan M. Levine

Palabras clave: Multidisciplinary.

Pp. 721-725

Inner ear biomechanics reveals a Late Triassic origin for mammalian endothermy

Ricardo AraújoORCID; Romain DavidORCID; Julien BenoitORCID; Jacqueline K. Lungmus; Alexander Stoessel; Paul M. BarrettORCID; Jessica A. Maisano; Eric Ekdale; Maëva Orliac; Zhe-Xi LuoORCID; Agustín G. MartinelliORCID; Eva A. Hoffman; Christian A. Sidor; Rui M. S. MartinsORCID; Fred SpoorORCID; Kenneth D. AngielczykORCID

Palabras clave: Multidisciplinary.

Pp. 726-731

The sequences of 150,119 genomes in the UK Biobank

Bjarni V. HalldorssonORCID; Hannes P. EggertssonORCID; Kristjan H. S. Moore; Hannes Hauswedell; Ogmundur EirikssonORCID; Magnus O. Ulfarsson; Gunnar PalssonORCID; Marteinn T. Hardarson; Asmundur OddssonORCID; Brynjar O. JenssonORCID; Snaedis Kristmundsdottir; Brynja D. Sigurpalsdottir; Olafur A. StefanssonORCID; Doruk BeyterORCID; Guillaume Holley; Vinicius Tragante; Arnaldur Gylfason; Pall I. Olason; Florian Zink; Margret Asgeirsdottir; Sverrir T. Sverrisson; Brynjar Sigurdsson; Sigurjon A. Gudjonsson; Gunnar T. Sigurdsson; Gisli H. HalldorssonORCID; Gardar Sveinbjornsson; Kristjan Norland; Unnur StyrkarsdottirORCID; Droplaug N. Magnusdottir; Steinunn Snorradottir; Kari Kristinsson; Emilia Sobech; Helgi Jonsson; Arni J. Geirsson; Isleifur Olafsson; Palmi Jonsson; Ole Birger PedersenORCID; Christian ErikstrupORCID; Søren BrunakORCID; Sisse Rye OstrowskiORCID; Steffen Andersen; Karina Banasik; Kristoffer Burgdorf; Maria Didriksen; Khoa Manh Dinh; Christian Erikstrup; Daniel Gudbjartsson; Thomas Folkmann Hansen; Henrik Hjalgrim; Gregor Jemec; Poul Jennum; Pär Ingemar Johansson; Margit Anita Hørup Larsen; Susan Mikkelsen; Kasper Rene Nielsen; Mette Nyegaard; Sisse Rye Ostrowski; Susanne Sækmose; Erik Sørensen; Unnur Thorsteinsdottir; Mie Topholm Brun; Henrik Ullum; Thomas Werge; Gudmar Thorleifsson; Frosti Jonsson; Pall Melsted; Ingileif JonsdottirORCID; Thorunn RafnarORCID; Hilma HolmORCID; Hreinn Stefansson; Jona Saemundsdottir; Daniel F. GudbjartssonORCID; Olafur T. Magnusson; Gisli Masson; Unnur Thorsteinsdottir; Agnar Helgason; Hakon JonssonORCID; Patrick SulemORCID; Kari Stefansson;

<jats:title>Abstract</jats:title><jats:p>Detailed knowledge of how diversity in the sequence of the human genome affects phenotypic diversity depends on a comprehensive and reliable characterization of both sequences and phenotypic variation. Over the past decade, insights into this relationship have been obtained from whole-exome sequencing or whole-genome sequencing of large cohorts with rich phenotypic data<jats:sup>1,2</jats:sup>. Here we describe the analysis of whole-genome sequencing of 150,119 individuals from the UK Biobank<jats:sup>3</jats:sup>. This constitutes a set of high-quality variants, including 585,040,410 single-nucleotide polymorphisms, representing 7.0% of all possible human single-nucleotide polymorphisms, and 58,707,036 indels. This large set of variants allows us to characterize selection based on sequence variation within a population through a depletion rank score of windows along the genome. Depletion rank analysis shows that coding exons represent a small fraction of regions in the genome subject to strong sequence conservation. We define three cohorts within the UK Biobank: a large British Irish cohort, a smaller African cohort and a South Asian cohort. A haplotype reference panel is provided that allows reliable imputation of most variants carried by three or more sequenced individuals. We identified 895,055 structural variants and 2,536,688 microsatellites, groups of variants typically excluded from large-scale whole-genome sequencing studies. Using this formidable new resource, we provide several examples of trait associations for rare variants with large effects not found previously through studies based on whole-exome sequencing and/or imputation.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 732-740