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Institución detectada Período Navegá Descargá Solicitá
No detectada desde mar. 1997 / hasta dic. 2023 Science Journals

Información

Tipo de recurso:

revistas

ISSN impreso

0036-8075

ISSN electrónico

1095-9203

Editor responsable

American Association for the Advancement of Science (AAAS)

País de edición

Estados Unidos

Fecha de publicación

Cobertura temática

Tabla de contenidos

Forgotten books: The application of unseen species models to the survival of culture

Mike KestemontORCID; Folgert KarsdorpORCID; Elisabeth de BruijnORCID; Matthew DriscollORCID; Katarzyna A. KapitanORCID; Pádraig Ó MacháinORCID; Daniel SawyerORCID; Remco SleiderinkORCID; Anne ChaoORCID

<jats:p>The study of ancient cultures is hindered by the incomplete survival of material artifacts, so we commonly underestimate the diversity of cultural production in historic societies. To correct this survivorship bias, we applied unseen species models from ecology to gauge the loss of narratives from medieval Europe, such as the romances about King Arthur. The estimates obtained are compatible with the scant historic evidence. In addition to events such as library fires, we identified the original evenness of cultural populations as an overlooked factor in these assemblages’ stability in the face of immaterial loss. We link the elevated evenness in island literatures to analogous accounts of ecological and cultural diversity in insular communities. These analyses call for a wider application of these methods across the heritage sciences.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 765-769

Biomimetic fracture model of lizard tail autotomy

Navajit S BabanORCID; Ajymurat OrozalievORCID; Sebastian KirchhofORCID; Christopher J Stubbs; Yong-Ak SongORCID

<jats:p>Lizard tail autotomy is an antipredator strategy consisting of sturdy attachment at regular times but quick detachment during need. We propose a biomimetic fracture model of lizard tail autotomy using multiscale hierarchical structures. The structures consist of uniformly distributed micropillars with nanoporous tops, which recapitulate the high-density mushroom-shaped microstructures found on the lizard tail’s muscle fracture plane. The biomimetic experiments showed adhesion enhancement when combining nanoporous interfacial surfaces with flexible micropillars in tensile and peel modes. The fracture modeling identified micro- and nanostructure-based toughening mechanisms as the critical factor. Under wet conditions, capillarity-assisted energy dissipation pertaining to liquid-filled microgaps and nanopores further increased the adhesion performance. This research presents insights on lizard tail autotomy and provides new biomimetic ideas to solve adhesion problems.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 770-774

Isospin magnetism and spin-polarized superconductivity in Bernal bilayer graphene

Haoxin ZhouORCID; Ludwig HolleisORCID; Yu SaitoORCID; Liam CohenORCID; William Huynh; Caitlin L. Patterson; Fangyuan Yang; Takashi TaniguchiORCID; Kenji WatanabeORCID; Andrea F. YoungORCID

<jats:p> In conventional superconductors, Cooper pairing occurs between electrons of opposite spin. We observe spin-polarized superconductivity in Bernal bilayer graphene when doped to a saddle-point van Hove singularity generated by a large applied perpendicular electric field. We observe a cascade of electrostatic gate-tuned transitions between electronic phases distinguished by their polarization within the isospin space defined by the combination of the spin and momentum-space valley degrees of freedom. Although all of these phases are metallic at zero magnetic field, we observe a transition to a superconducting state at finite magnetic field <jats:italic>B</jats:italic> <jats:sub>‖</jats:sub> ≈ 150 milliteslas applied parallel to the two-dimensional sheet. Superconductivity occurs near a symmetry-breaking transition and exists exclusively above the <jats:italic>B</jats:italic> <jats:sub>‖</jats:sub> limit expected of a paramagnetic superconductor with the observed transition critical temperature <jats:italic>T</jats:italic> <jats:sub>C</jats:sub> ≈ 30 millikelvins, consistent with a spin-triplet order parameter. </jats:p>

Palabras clave: Multidisciplinary.

Pp. 774-778

Demographic implications of lead poisoning for eagles across North America

Vincent A. SlabeORCID; James T. AndersonORCID; Brian A. Millsap; Jeffrey L. Cooper; Alan R. HarmataORCID; Marco Restani; Ross H. Crandall; Barbara Bodenstein; Peter H. Bloom; Travis BoomsORCID; John BuchweitzORCID; Renee CulverORCID; Kim Dickerson; Robert Domenech; Ernesto Dominguez-VillegasORCID; Daniel DriscollORCID; Brian W. Smith; Michael J. Lockhart; David McRuerORCID; Tricia A. MillerORCID; Patricia A. OrtizORCID; Krysta Rogers; Matt Schwarz; Natalie TurleyORCID; Brian Woodbridge; Myra E. Finkelstein; Christian A. TrianaORCID; Christopher R. DeSorboORCID; Todd E. KatznerORCID

<jats:p>Lead poisoning occurs worldwide in populations of predatory birds, but exposure rates and population impacts are known only from regional studies. We evaluated the lead exposure of 1210 bald and golden eagles from 38 US states across North America, including 620 live eagles. We detected unexpectedly high frequencies of lead poisoning of eagles, both chronic (46 to 47% of bald and golden eagles, as measured in bone) and acute (27 to 33% of bald eagles and 7 to 35% of golden eagles, as measured in liver, blood, and feathers). Frequency of lead poisoning was influenced by age and, for bald eagles, by region and season. Continent-wide demographic modeling suggests that poisoning at this level suppresses population growth rates for bald eagles by 3.8% (95% confidence interval: 2.5%, 5.4%) and for golden eagles by 0.8% (0.7%, 0.9%). Lead poisoning is an underappreciated but important constraint on continent-wide populations of these iconic protected species.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 779-782

SARS-CoV-2 Beta variant infection elicits potent lineage-specific and cross-reactive antibodies

S. Momsen ReinckeORCID; Meng YuanORCID; Hans-Christian KornauORCID; Victor M. CormanORCID; Scott van HoofORCID; Elisa Sánchez-Sendin; Melanie RambergerORCID; Wenli YuORCID; Yuanzi Hua; Henry TienORCID; Marie Luisa Schmidt; Tatjana SchwarzORCID; Lara Maria JeworowskiORCID; Sarah E. Brandl; Helle Foverskov RasmussenORCID; Marie A. HomeyerORCID; Laura StöfflerORCID; Martin BarnerORCID; Désirée KunkelORCID; Shufan HuoORCID; Johannes Horler; Niels von WardenburgORCID; Inge Kroidl; Tabea M. EserORCID; Andreas Wieser; Christof Geldmacher; Michael HoelscherORCID; Hannes GänzerORCID; Günter WeissORCID; Dietmar Schmitz; Christian DrostenORCID; Harald PrüssORCID; Ian A. WilsonORCID; Jakob KreyeORCID

<jats:p>Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Beta variant of concern (VOC) resists neutralization by major classes of antibodies from COVID-19 patients and vaccinated individuals. In this study, serum of Beta-infected patients revealed reduced cross-neutralization of wild-type virus. From these patients, we isolated Beta-specific and cross-reactive receptor-binding domain (RBD) antibodies. The Beta-specificity results from recruitment of VOC-specific clonotypes and accommodation of mutations present in Beta and Omicron into a major antibody class that is normally sensitive to these mutations. The Beta-elicited cross-reactive antibodies share genetic and structural features with wild type–elicited antibodies, including a public VH1-58 clonotype that targets the RBD ridge. These findings advance our understanding of the antibody response to SARS-CoV-2 shaped by antigenic drift, with implications for design of next-generation vaccines and therapeutics.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 782-787

The debt trap

Erika Moore

Palabras clave: Multidisciplinary.

Pp. 790-790

A unified genealogy of modern and ancient genomes

Anthony Wilder WohnsORCID; Yan WongORCID; Ben JefferyORCID; Ali AkbariORCID; Swapan MallickORCID; Ron PinhasiORCID; Nick PattersonORCID; David ReichORCID; Jerome KelleherORCID; Gil McVeanORCID

<jats:p>The sequencing of modern and ancient genomes from around the world has revolutionized our understanding of human history and evolution. However, the problem of how best to characterize ancestral relationships from the totality of human genomic variation remains unsolved. Here, we address this challenge with nonparametric methods that enable us to infer a unified genealogy of modern and ancient humans. This compact representation of multiple datasets explores the challenges of missing and erroneous data and uses ancient samples to constrain and date relationships. We demonstrate the power of the method to recover relationships between individuals and populations as well as to identify descendants of ancient samples. Finally, we introduce a simple nonparametric estimator of the geographical location of ancestors that recapitulates key events in human history.</jats:p>

Palabras clave: Multidisciplinary.

Pp. No disponible

A framework for scintillation in nanophotonics

Charles Roques-CarmesORCID; Nicholas RiveraORCID; Ali Ghorashi; Steven E. KooiORCID; Yi YangORCID; Zin Lin; Justin BerozORCID; Aviram MassudaORCID; Jamison Sloan; Nicolas RomeoORCID; Yang YuORCID; John D. JoannopoulosORCID; Ido KaminerORCID; Steven G. JohnsonORCID; Marin SoljačićORCID

<jats:p>Bombardment of materials by high-energy particles often leads to light emission in a process known as scintillation. Scintillation has widespread applications in medical imaging, x-ray nondestructive inspection, electron microscopy, and high-energy particle detectors. Most research focuses on finding materials with brighter, faster, and more controlled scintillation. We developed a unified theory of nanophotonic scintillators that accounts for the key aspects of scintillation: energy loss by high-energy particles, and light emission by non-equilibrium electrons in nanostructured optical systems. We then devised an approach based on integrating nanophotonic structures into scintillators to enhance their emission, obtaining nearly an order-of-magnitude enhancement in both electron-induced and x-ray–induced scintillation. Our framework should enable the development of a new class of brighter, faster, and higher-resolution scintillators with tailored and optimized performance.</jats:p>

Palabras clave: Multidisciplinary.

Pp. No disponible

Rethinking the A cation in halide perovskites

Jin-Wook LeeORCID; Shaun TanORCID; Sang Il SeokORCID; Yang YangORCID; Nam-Gyu ParkORCID

<jats:p> The A cation in ABX <jats:sub>3</jats:sub> organic-inorganic lead halide perovskites (OLHPs) was conventionally believed to hardly affect their optoelectronic properties. However, more recent developments have unraveled the critical role of the A cation in the regulation of the physicochemical and optoelectronic properties of OLHPs. We review the important breakthroughs enabled by the versatility of the A cation and highlight potential opportunities and unanswered questions related to the A cation in OLHPs. </jats:p>

Palabras clave: Multidisciplinary.

Pp. No disponible

Hyperexcitable arousal circuits drive sleep instability during aging

Shi-Bin LiORCID; Valentina Martinez DamonteORCID; Chong ChenORCID; Gordon X. WangORCID; Justus M. KebschullORCID; Hiroshi YamaguchiORCID; Wen-Jie BianORCID; Carolin PurmannORCID; Reenal PattniORCID; Alexander Eckehart UrbanORCID; Philippe MourrainORCID; Julie A. KauerORCID; Grégory ScherrerORCID; Luis de LeceaORCID

<jats:p> Sleep quality declines with age; however, the underlying mechanisms remain elusive. We found that hyperexcitable hypocretin/orexin (Hcrt/OX) neurons drive sleep fragmentation during aging. In aged mice, Hcrt neurons exhibited more frequent neuronal activity epochs driving wake bouts, and optogenetic activation of Hcrt neurons elicited more prolonged wakefulness. Aged Hcrt neurons showed hyperexcitability with lower KCNQ2 expression and impaired M-current, mediated by KCNQ2/3 channels. Single-nucleus RNA-sequencing revealed adaptive changes to Hcrt neuron loss in the aging brain. Disruption of <jats:italic>Kcnq2/3</jats:italic> genes in Hcrt neurons of young mice destabilized sleep, mimicking aging-associated sleep fragmentation, whereas the KCNQ-selective activator flupirtine hyperpolarized Hcrt neurons and rejuvenated sleep architecture in aged mice. Our findings demonstrate a mechanism underlying sleep instability during aging and a strategy to improve sleep continuity. </jats:p>

Palabras clave: Multidisciplinary.

Pp. No disponible