三江源国家公园草地地上生物量时空动态及其气候影响

三江源区位于青藏高原腹地,作为长江、黄河、澜沧江三大河流的发源地,是我国重要的生态安全屏障。基于三江源区域草地AGB的野外调查数据,本研究采用多种机器学习算法集成分析的方式构建模型,实现了高精度的三江源国家公园草地AGB时空估算。基于AGB时空模拟结果,分析了近19年(2000—2018年)三江源国家公园区域草地AGB的时空动态变化。研究结果显示：(1)通过多种机器学习结合贝叶斯平均模型,草地AGB模拟值与实测值的r为0.88,RMSE为71.60g/m²,表明多模型集成分析的方式对草地AGB估算获得了较好的模拟效果。(2)三江源国家公园区域草地AGB的空间分布具有明显的空间异质性,呈从东南向西北递减的趋势。(3)2000—2018年长江源国家公园、黄河源国家公园和澜沧江国家公园区域草地AGB多年平均值分别为82.96 g/m²、117.54g/m²和168.39 g/m²。(4)近19年间,在黄河和长江源园区受到温度上升的影响草地AGB呈现出非显著性上升趋势;澜沧江区域,由于2015和2016年的...     

Revision of the genus Acrochordiceras Hyatt, 1877 (Ammonoidea,Middle Triassic): morphology,biometry, biostratigraphy and intra‐specific variability

Abstract: The family Acrochordiceratidae Arthaber, 1911 ranges in age from latest Spathian to the middle/late Anisian boundary, and it represents a major component of ammonoid faunas during that time. The middle Anisian genus Acrochordiceras Hyatt, 1877 is the most widespread taxon of the family and occurs abundantly worldwide within the low paleolatitude belt. However, there is a profusion of species names available for Acrochordiceras. This excessive diversity at the species level essentially results from the fact that sufficiently large samples were not available, thus leading to a typological approach to its taxonomy. Based on new extensive collections obtained from the Anisian (Middle Triassic) Fossil Hill Member (Star Peak Group, north‐west Nevada) for which a high resolution biostratigraphic frame is available, the taxonomy and biostratigraphy of the genus Acrochordiceras Hyatt, 1877 is herein revised with respect to its intra‐specific variation. Morphological and biometric studies (c. 550 bedrock‐controlled specimens were measured) show that only one species occurs in each stratigraphic level. Continuous ranges of intra‐specific variation of studied specimens enable us to synonymize Haydenites Diener, 1907, Silesiacrochordiceras Diener, 1916 and Epacrochordiceras Spath, 1934 with Acrochordiceras Hyatt, 1877. Three stratigraphically successive species are herein recognized in the low paleolatitude middle Anisian faunas from Nevada: A. hatschekii (Diener, 1907), A. hyatti Meek, 1877 and A. carolinae Mojsisovics, 1882. Moreover, an assessment of intra‐specific variation of the adult size range does not support recognition of a dimorphic pair (Acrochordiceras and Epacrochordiceras) as previously suggested by other workers (Epacrochordiceras is the compressed and weakly ornamented end‐member variant of Acrochordiceras). The successive middle Anisian species of Acrochordiceras form an anagenetic lineage characterized by increasing involution, adult size and intra‐specific variation. This taxonomic revision based on new bedrock‐controlled collections is thus an important prerequisite before studying the evolution of the group.     

From transects to transcripts: Teasing apart the architecture of reproductive isolation

Understanding the processes underlying speciation has long been a challenge to evolutionary biologists. This spurs from difficulties teasing apart the various mechanisms that contribute to the evolution of barriers to reproduction. The study by Rafati et al. ( 2018 ) in this issue of Molecular Ecology combines spatially explicit whole‐genome resequencing with evaluation of differential gene expression across individuals with mixed ancestry to associate the genomic architecture of reproductive barriers with expression of reproductive incompatibilities. In a natural hybrid zone between rabbit subspecies, Oryctolagus cuniculus cuniculus and O. c. algirus (Figure  1 ), Rafati et al. ( 2018 ) use landscape‐level patterns of allele frequency variation to identify potential candidate regions of the genome associated with reproductive isolation. These candidate regions are used to test predictions associated with the genomic architecture of reproductive barriers, including the role of structural rearrangements, enrichment of functional categories associated with incompatibilities, and the contribution of protein‐coding versus regulatory changes. A lack of structural rearrangements and limited protein‐coding changes in candidate regions point towards the importance of regulatory variation as major contributors to genetic incompatibilities, while functional enrichments indicate overrepresentation of genes associated with male infertility. To quantify phenotypic expression of proposed incompatibilities, the authors assess gene expression of experimental crosses. Extensive misregulation of gene expression within the testes of backcross hybrids relative to F1 and parental individuals provides an important link between genotype and phenotype, validating hypotheses developed from assessment of genomic architectures. Together, this work shows how pairing natural hybrid zones with experimental crosses can be used to link observations in nature to mechanistic underpinnings that may be tested experimentally.     

Evidence that presynaptic changes are involved in the expression of LTP and LTD of NMDA receptor-mediated EPSCs in area CA1 of the hippocampus

Plasticity of NMDA receptor-mediated synaptic transmission was studied in the CA1 region of the hippocampus utilising whole cell patch-clamp recording techniques. LTP was associated with a decrease in CV whereas LTD was accompanied by an increase in CV and a decrease in Pr. These data are consistent with LTP and LTD being an opposite expression of the same fundamental process.     

Craniodental body mass estimators in the dwarf bushbaby (Galagoides)

This study reports data on 17 craniodental body mass estimators in a sample (n = 38) of dwarf galagos (Galagoides). Correlation coefficients (r) range from a high of 0.64 for bizygomatic breadth and body mass to a low of 0.10 for M(3) length and body mass. Of the 17 variables studied, 7 exhibit significant (P < 0.05) correlation coefficients, with 5 of the 7 being multitooth (i.e., tooth row) or cranial variables. In contrast to the correlation coefficients of greater than 0.90 (e.g., Martin [1980] Z Morphol Anthropol 71:115-124; Steudel [1981] Int J Primatol 2:81-90; Gingerich et al. [1982] Am J Phys Anthropol 58:81-100; Conroy [1987] Int J Primatol 8:115-137) published for higher taxonomic level analyses (i.e., all-primate or prosimian) for many of the same variables studied here, the current data indicate weaker relationships when analyzed at the generic level. Possible explanations for the contrast in correlation coefficients between the current and many previous studies include the following: 1) individual variation due to a geographically dispersed sample, 2) individual body mass fluctuations due to seasonal food availability, and 3) individual variation within the sample due to variation in life-history parameters. Because the overall size range of the individuals in a specific or generic level analysis is smaller than that in an ordinal or subordinal sample, the individual variation normally masked when using species means represents a larger proportion of the total variation in a more limited sample. This may then be a cause of these weaker correlations.     

August Weismann on Germ-Plasm Variation

August Weismann is famous for having argued against the inheritance of acquired characters. However, an analysis of his work indicates that Weismann always held that changes in external conditions, acting during development, were the necessary causes of variation in the hereditary material. For much of his career he held that acquired germ-plasm variation was inherited. An irony, which is in tension with much of the standard twentieth-century history of biology, thus exists – Weismann was not a Weismannian. I distinguish three claims regarding the germ-plasm: (1) its continuity,(2) its morphological sequestration, and (3) its variational sequestration. With respect to changes in Weismann's views on the cause of variation, I divide his career into four stages. For each stage I analyze his beliefs on the relative importance of changes in external conditions and sexual reproduction as causes ofvariation in the hereditary material. Weismann believed, and Weismannism denies, that variation, heredity, and development were deeply intertwined processes. This article is part of a larger project comparing commitments regarding variation during the latter half of the nineteenth century. This revised version was published online in July 2006 with corrections to the Cover Date.     

Many amino acid substitution variants identified in DNA repair genes during human population screenings are predicted to impact protein function

Over 520 different amino acid substitution variants have been previously identified in the systematic screening of 91 human DNA repair genes for sequence variation. Two algorithms were employed to predict the impact of these amino acid substitutions on protein activity. Sorting Intolerant from Tolerant (SIFT) classified 226 of 508 variants (44%) as "Intolerant." Polymorphism Phenotyping (PolyPhen) classed 165 of 489 amino acid substitutions (34%) as "Probably or possibly damaging." Another 9-15% of the variants were classed as "Potentially intolerant or damaging." The results from the two algorithms are highly associated, with concordance in predicted impact observed for approximately 62% of the variants. Twenty-one to thirty-one percent of the variant proteins are predicted to exhibit reduced activity by both algorithms. These variants occur at slightly lower individual allele frequency than do the variants classified as "Tolerant" or "Benign." Both algorithms correctly predicted the impact of 26 functionally characterized amino acid substitutions in the APE1 protein on biochemical activity, with one exception. It is concluded that a substantial fraction of the missense variants observed in the general human population are functionally relevant. These variants are expected to be the molecular genetic and biochemical basis for the associations of reduced DNA repair capacity phenotypes with elevated cancer risk.     

Phylogeography of the component species of broad-leaved evergreen forests in Japan,based on chloroplast DNA variation

In order to elucidate the past distribution and colonization routes of broad-leaved evergreen (lucidophyllous) forests, we investigated the intraspecific phylogeographic patterns of lucidophyllous forests in Japan and surrounding areas. We selected 6 component species with a similar geographic distributions growing in Castanopsis-dominant forests. We defined possible important refugia during the glacial periods as the regions rich in rare haplotypes (with a frequency of 5% or less), or as regions rich in the number of common haplotypes (with a frequency of more than 5%). We then located the sites of refuge by comparing the intraspecific phylogeographic patterns among 6 component species of lucidophyllous forests with respect to these two parameters (i.e., haplotype uniqueness and the number of haplotypes). The following results were obtained during the course of this study: (1) rare haplotypes were distributed among islands around the main islands of Japan; (2) rare subtypes and the greatest numbers of common haplotypes were observed in Kyushu, a finding which agreed with fossilized pollen data demonstrative of the past existence of refugia in southern Kyushu; and (3) rare haplotypes were found on the Muroto Peninsula, and the second greatest numbers of common haplotypes were observed on the Kii Peninsula, a finding which suggested the existence of additional important refugia along the Pacific coast of Japan during the glacial ages.     

Clerodane-type diterpenoids from Nannoglottis ravida

Chemical investigation of the roots of Nannoglottis ravida resulted in the characterization of two 5alpha,10alpha-cis-clerodane-type diterpenoides, ravidin A and B. Their structures and stereochemistry were established by spectroscopic methods, including X-ray crystallographic diffraction analysis of ravidin A. Their significance in terms of the chemotaxonomy of Nannoglottis is discussed.     

Fine Spatial Structure of Atlantic Hake (<Emphasis Type="Italic">Merluccius merluccius</Emphasis>) Stocks Revealed by Variation at Microsatellite Loci

Genetic variation at 5 microsatellite loci was analyzed for European hake Merluccius merluccius sampled from 9 different regions in the Atlantic Ocean and the Mediterranean Sea. Significant genetic differentiation was found between samples, suggesting a fine subdivision of Atlantic and Mediterranean hake stocks. These results are discussed in the context of the decline of demersal fish species, probably due to overfishing.