Quantum correlations in a cluster-like system

We discuss a cluster-like 1D system with triplet interaction. We study the topological properties of this system. We find that the degeneracy depends on the topology of the system, and well protected against external local perturbations. All these facts show that the system is topologically ordered. We also find a string order parameter to characterize the quantum phase transition. Besides, we investigate two-site correlations including entanglement, quantum discord and mutual information. We study the different divergency behaviour of the correlations. The quantum correlation decays exponentially in both topological and magnetic phases, and diverges in reversed power law at the critical point. And we find that in TQPT systems, the global difference of topology induced by dimension can be reflected in local quantum correlations.Comment: 7 pages, 6 figure

South Asian summer monsoon projections constrained by the Intedacadal Pacific Oscillation

A reliable projection of future South Asian summer monsoon (SASM) benefits a large population in Asia. Using a 100-member ensemble of simulations by the Max Planck Institute Earth System Model (MPI-ESM) and a 50-member ensemble of simulations by the Canadian Earth System Model (CanESM2), we find that internal variability can overshadow the forced SASM rainfall trend, leading to large projection uncertainties for the next 15 to 30 years. We further identify that the Interdecadal Pacific Oscillation (IPO) is, in part, responsible for the uncertainties. Removing the IPO-related rainfall variations reduces the uncertainties in the near-term projection of the SASM rainfall by 13 to 15% and 26 to 30% in the MPI-ESM and CanESM2 ensembles, respectively. Our results demonstrate that the uncertainties in near-term projections of the SASM rainfall can be reduced by improving prediction of near-future IPO and other internal modes of climate variabilit

Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinosis associated with a novel mutation of the highly conserved leucine residue 116 of Claudin 16 in a Chinese patient with a delayed diagnosis: A case report

Background: Sixty mutations of claudin 16 coding gene have been reported in familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) patients. Recent investigations revealed that a highly conserved glycine-leucine-tryptophan (115G-L-W117) motif in the first extracellular segment (ESC1) of claudin 16 might be essential for stabilization of the appropriately folded ECS1 structure and conservation of normal claudin 16 function. However, neither missense nor nonsense mutation has ever been described in this motif. Our study aimed at identifying mutations in a Chinese patient with FHHNC and exploring the association between genotype and phenotype. Case presentation: A 33-year-old female presented with 4 years history of recurrent acute pyelonephritis without other notable past medical history. Her healthy parents, who aged 56 and 53 respectively, were second cousins, and her only sibling died from renal failure without definite cause at age 25. Renal ultrasound imaging demonstrated atrophic kidneys and bilateral nephrocalcinosis. The laboratory workup revealed impaired renal function (Stage CKD IV), hypocalcemia and mild hypomagnesemia, accompanied with marked renal loss of magnesium and hypercalciuria. During the follow-up, treatment with calcitriol and calcium but not with magnesium was difficult to achieve normal serum calcium levels, whereas her serum magnesium concentration fluctuated within normal ranges. In the end, the patient unavoidably reached ESRD at 36 years old. The clinical features and family history suggested the diagnosis of FHHNC. To make a definite diagnosis, we use whole-exome sequencing to identify the disease-causing mutations and Sanger sequencing to confirm the mutation co-segregation in the family. As a result, a novel homozygous mutation (c.346C > G, p.Leu116Val) in115G-L-W117motif of claudin 16 was identified. Her parents, grandmother and one of her cousins carried heterozygous p.Leu116Val, whereas 200 unrelated controls did not carry this mutation. Conclusions: We described a delayed diagnosis patient with FHHNC in the Chinese population and identified a novel missense mutation in the highly conserved115G-L-W117motif of claudin 16 for the first time. According to the reported data and the information deduced from 3D modeling, we speculate that this mutation probably reserve partial residual function which might be related to the slight phenotype of the patient

Answering Complex Questions by Joining Multi-Document Evidence with Quasi Knowledge Graphs

Direct answering of questions that involve multiple entities and relations is a challenge for text-based QA. This problem is most pronounced when answers can be found only by joining evidence from multiple documents. Curated knowledge graphs (KGs) may yield good answers, but are limited by their inherent incompleteness and potential staleness. This paper presents QUEST, a method that can answer complex questions directly from textual sources on-the-fly, by computing similarity joins over partial results from different documents. Our method is completely unsupervised, avoiding training-data bottlenecks and being able to cope with rapidly evolving ad hoc topics and formulation style in user questions. QUEST builds a noisy quasi KG with node and edge weights, consisting of dynamically retrieved entity names and relational phrases. It augments this graph with types and semantic alignments, and computes the best answers by an algorithm for Group Steiner Trees. We evaluate QUEST on benchmarks of complex questions, and show that it substantially outperforms state-of-the-art baselines