体育消费的学理脉络、统计内容及其实施策略

采用文献资料法，依次从学理脉络、统计内容及其实施策略展开关于体育消费以及体育消费统计的讨论。认为：从学理上看，体育消费作为一个复杂概念，既牵涉宏观经济社会发展，也与文化意识形态紧密联系；而作为准确把握体育市场、把脉体育发展情况的基础性工作之一，体育消费统计则应该避免将体育消费概念泛化。应以体育政策为导向，面向人民的美好生活需要，对接国民经济统计制度，考虑建构以“体育教育与培训、体育文化与娱乐、体育保健与康复、体育传媒与信息、体育衣着耐用品、其他体育用品与服务、个人间接体育消费”为核心指标的统计框架，并通过长效工作方案的设计使体育消费统计工作制度化，通过统计调查制度的建构使体育消费统计执行有效化，通过统计数据的测算推算使体育消费统计结果精准化。     

The modernity of Dedekind’s anticipations contained in What are numbers and what are they good for?

Archive for History of Exact Sciences - We show that Dedekind, in his proof of the principle of definition by mathematical recursion, used implicitly both the concept of an inductive cone from an...     

Long-term increases in clutch size in common snapping turtles (Chelydra serpentina) and diamondback terrapins (Malaclemys terrapin)

Clutch size (CS) is a well-studied life history characteristic, and optimal egg size theory predicts that CS should correlate positively with reproductive investment. Turtles are good subjects for studies of reproductive strategies because few turtle species exhibit parental care; therefore quantifying their short-term reproductive investment is mostly limited to measuring egg size and number. Clutch size is usually reported as an average value for each turtle population, and where CS variation is noted, it is usually attributable to variation in adult body size. In two long-term studies of ecologically dissimilar species we detected a dramatic increase in CS in a common snapping turtle (Chelydra serpentina) population and in a diamondback terrapin (Malaclemys terrapin) population. It is unknown whether these changes are due to either variation in adult body size or resource availability; but the temporal patterns we observed have apparently never been reported previously. These trends remain unexplained and should be explored further.     

Whole genome sequencing as a means to assess pathogenic mutations in medical genetics and cancer

The past decade has seen the emergence of next-generation sequencing (NGS) technologies, which have revolutionized the field of human molecular genetics. With NGS, significant portions of the human genome can now be assessed by direct sequence analysis, highlighting normal and pathological variants of our DNA. Recent advances have also allowed the sequencing of complete genomes, by a method referred to as whole genome sequencing (WGS). In this work, we review the use of WGS in medical genetics, with specific emphasis on the benefits and the disadvantages of this technique for detecting genomic alterations leading to Mendelian human diseases and to cancer.