多棘扁甲轮在中国的新记录及对扁甲轮属的评论

正相对于西方而言,古北区的东侧,轮虫的研究资料非常缺乏~([3])。中国现存的很多轮虫资料也已经非常陈旧~([4—6]),当然,近年也有一些论文相继报道了这一淡水系统中非常重要的浮游动物类群~([7—12]),其中不乏涉及分子方法研究轮虫分类~([13])和轮虫的生态研究~([14])。但是从已有的资料可以发现,很多已知的轮虫分布大多集中在武汉、海南、洞庭湖、西藏等地,我们可以看到一个很显然的现象,即只有中国的这些地方被较为详细地研究过,     

The macroecology of infectious diseases: a new perspective on global‐scale drivers of pathogen distributions and impacts

Identifying drivers of infectious disease patterns and impacts at the broadest scales of organisation is one of the most crucial challenges for modern science, yet answers to many fundamental questions remain elusive. These include what factors commonly facilitate transmission of pathogens to novel host species, what drives variation in immune investment among host species, and more generally what drives global patterns of parasite diversity and distribution? Here we consider how the perspectives and tools of macroecology, a field that investigates patterns and processes at broad spatial, temporal and taxonomic scales, are expanding scientific understanding of global infectious disease ecology. In particular, emerging approaches are providing new insights about scaling properties across all living taxa, and new strategies for mapping pathogen biodiversity and infection risk. Ultimately, macroecology is establishing a framework to more accurately predict global patterns of infectious disease distribution and emergence.     

A high‐throughput capillary isoelectric focusing immunoassay for fingerprinting protein sialylation

The serum half‐life, biological activity, and solubility of many recombinant glycoproteins depend on their sialylation. Monitoring glycoprotein sialylation during cell culture manufacturing is, therefore, critical to ensure product efficacy and safety. Here a high‐throughput method for semi‐quantitative fingerprinting of glycoprotein sialylation using capillary isoelectric focusing immunoassay on NanoPro (Protein Simple) platform was developed. The method was specific, sensitive, precise, and robust. It could analyze 2 μL of crude cell culture samples without protein purification, and could automatically analyze from 8 samples in 4 h to 96 samples in 14 h without analyst supervision. Furthermore, its capability to detect various changes in sialylation fingerprints during cell culture manufacturing process was indispensable to ensure process robustness and consistency. Moreover, the changes in the sialylation fingerprints analyzed by this method showed strong correlations with intact mass analysis using liquid chromatography and mass spectrometry. © 2015 American Institute of Chemical Engineers Biotechnol. Prog., 32:235–241, 2016     

Impacts of dust on plant health,survivorship and plant communities in semi‐arid environments

There is a general perception that dust accumulation on plant surfaces causes negative impacts to plants. Consequently, it is common for environmental regulatory agencies to apply vegetation monitoring requirements to oil, gas and mining developments. We use two independent, medium‐term monitoring studies in semi‐arid Australia to examine this relationship at two scales: plant health and survivorship of a threatened subspecies (Tetratheca paynterae paynterae: Elaeocarpaceae) at Windarling Range between 2003 and 2014; and changes in plant health and floristic composition on Barrow Island between 2009 and 2014. Accumulation of dust decreased rapidly with distance from source. At Windarling Range, even at the site with the highest dust load, there was no significant impact on Tetratheca paynterae paynterae compared with the less dusty sites for 10 years. Similarly, there was no significant effect between distance from the source of dust and floristic composition on Barrow Island for 5 years. The probability of plants transitioning to a lower health condition between one year and the next did not appear to be related to dust load. This is further supported by comparing the same site before and after paving the road (removal of dust source), which showed no clear trends. Trends in plant health are likely to be driven more by the variability of cumulative rainfall in the preceding 5 months than dust load. The observed temporal variation in the mean dust load may also be related to variation in rainfall. In conclusion, in these case studies from semi‐arid Australia, we find no evidence to support the perception that, under the observed climatic condition and dust deposition rates up to 20 or 77 g m^?2 per month at Windarling Range and Barrow Island, respectively, dust accumulation on plants causes negative impacts.     

Underwater acoustic behavior of bearded seals (Erignathus barbatus) in the northeastern Chukchi Sea, 2007–2010

Bearded seal (Erignathus barbatus) calls were recorded using autonomous passive acoustic recorders deployed in the northeastern Chukchi Sea between October 2007 and October 2010. Continuous acoustic data were acquired during summer (August to mid‐October), and overwinter data (mid‐October through July) were acquired on a duty cycle of 40/48 min every 4 h. We investigated the spatio‐temporal distribution and acoustic behavior of vocalizing bearded seals in this multiyear data set. Peaks in calling occurred in spring, coinciding with the mating period, and calls stopped abruptly in late June/early July. Fewer calls were detected in summer, and the vocal presence of seals increased with the formation of pack ice in winter. Vocal activity was higher at night than during the day, with a peak around 0400 (AKST). Monthly patterns in proportional use of each call type and call duration were examined for the first time. The proportion and duration of AL1(T) and AL2(T) call types increased during the mating period, suggesting that males advertise their breeding condition by producing those specific longer trills. The observed seasonal and diel trends were consistent between years. These results improve our understanding of occurrence and acoustic behavior of bearded seals across the northeastern Chukchi Sea.     

Estimates of forest floor litter frog communities: A comparison of two methods

Estimates of forest leaf litter frog density, mass, richness and diversity given by the widely used 8 m × 8 m large plot method (LPM) were compared with estimates obtained by a newly proposed method (small 2 m × 1 m plots with leaf removal; SPLR). The study site was an undisturbed area of the Atlantic Rainforest of Ilha Grande, an island located in the south of Rio de Janeiro State, Brazil. Twenty‐four LPM (totalling 1536 m² of forest floor) and 90 SPLR (totalling 180 m² of forest floor) were performed. The estimates obtained by the two methods differed markedly, indicating that even using a much smaller sampling area (11.7% of that of LPM), SPLR gave frog density estimates six times higher, and frog mass estimates approximately 2.5 times higher than estimates provided by LPM. The species richness and diversity obtained by the two methods were similar, despite the fact that the total area sampled with SPLR was much smaller. These data suggest that LPM may underestimate the abundance and biomass of leaf litter frogs in a given area.     

Plant Conservation in the Caribbean Island Biodiversity Hotspot

While the Caribbean is a recognized “biodiversity hotspot”, plant conservation has not received adequate attention; particularly, given the high levels of endemism in many plant groups. Besides establishing protected areas, there needs to be a sustained effort to study the taxonomy, systematics and ecology of the flora. Recent phylogenetic studies have shown high levels of endemism and conservation studies indicate a large propotion of the flora is threatened with extinction. Eight recommendations are given for plant conservation in the region.     

Characterization of <Emphasis Type="Italic">Penicillium</Emphasis> Species by Ribosomal DNA Sequencing and BOX,ERIC and REP-PCR Analysis

The genus Penicillium is one of the largest and widely distributed fungal genera described to date. As a result, its taxonomic classification and species discrimination within this genus has become complicated. In this study, 52 isolates that belonged to the Penicillum genus and other related genera were characterized using two DNA-based methods: (i) analysis of the nucleotide sequences of internal transcribed spacers in ribosomal DNA and (ii) analysis of DNA fingerprints that were generated by polymerase chain reactions with specific primers for enterobacterial repetitive intergenic consensus (ERIC) and repetitive extragenic palindromic (REP) sequences, and BOX elements. Using both methods, Penicillium species were discriminated from other fungal genera. Furthermore, Penicillium species that include strains which are used as biocontrol agents, such as P. glabrum, P. purpurogenum, and P. oxalicum, could be distinguished from other Penicillium species using these techniques. Based on our findings, we propose that a polyphasic approach that includes analysis of the nucleotide sequences of ribosomal DNA and detecting the presence of highly conserved, repeated nucleotide sequences can be used to determine the genetic relationships between different Penicillium species. Furthermore, we propose that our results can be used as a start point to develop a strategy to monitor the environmental presence of particular strains of Penicillium species when they are used as biocontrol agents.     

Analytical platform for verification and quantitation of target peptides in human serum: application to cathelicidin

A selective and sensitive, fully automated platform for verification and quantitative determination of target peptides in biofluids is proposed and then validated by development of a method for analysis of cathelicidin in human serum. The method is based on the on-line coupling of solid-phase extraction (SPE) and tandem mass spectrometry with direct infusion. Mass spectrometry analysis was carried out by multiple reaction monitoring using three transitions (one for quantitative analysis and two for qualitative analysis), all them confirmed by in silico fragmentation of the target peptide. Samples were prepared in the SPE workstation on a polymeric divinylbenzene resin by preconcentration, deproteinization, and cleanup, removing salts and interferences after direct injection of human serum. The analytical process required 12 min. The limits of detection and quantitation were 2.5 and 8.25 μg/L, respectively (0.20 and 0.66 pg on column). Repeatability and within-laboratory reproducibility were 2.4% and 2.7%, respectively. A dual-cartridge configuration was used to test recovery of cathelicidin in serum, resulting in 80%. Because quantitative retention in the cartridge was assessed, determination of cathelicidin was validated without using synthetic peptides labeled with stable isotopes. The hyphenated system allows full automation, thereby improving reproducibility and accuracy, as demanded by clinical analysis.