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991.
Lisa Filippi Mantaro Hironaka Shintaro Nomakuchi 《Ethology : formerly Zeitschrift fur Tierpsychologie》2012,118(5):503-510
Females of the subsocial shield bug Parastrachia japonensis (Heteroptera: Parastrachiidae) incorporate trophic eggs (nutritive eggs) into their egg mass. Considerable variation occurs among females in trophic egg number and the proportion of an egg mass that is composed of trophic eggs. Because trophic eggs are essential to the development and survival of young, this variation could significantly impact female fitness. We tested the hypothesis that trophic egg abundance is induced by maternal phenotype (weight, body size) and resource exposure. We predicted that resource limitations would cause females to produce fewer fertile eggs and more trophic eggs and that larger and heavier females would produce more of each egg type. Females ovipositing early in the season are exposed to different resource conditions than those that oviposit late. Thus, we compared egg production patterns between these two groups and several other factors related to nesting. No correlation was seen between body size and trophic egg abundance, or, indeed, egg production, overall; however, heavier females produced heavier egg masses. Counter to our prediction, late females, which had greater access to food, produced significantly more total eggs, fewer fertile eggs, and more trophic eggs than early females. A binomial generalized linear model analysis indicated that the factors most correlated with the percentage of an egg mass destined to become trophic eggs were resource abundance, resulting from early or late oviposition, and distance of the nest from the host tree, with closer females producing more trophic eggs. The findings support our hypothesis that resource availability and, to a lesser extent, maternal phenotype affect trophic egg abundance. 相似文献
992.
Click chemistries have been investigated for use in numerous biomaterials applications, including drug delivery, tissue engineering, and cell culture. In particular, light-mediated click reactions, such as photoinitiated thiol−ene and thiol−yne reactions, afford spatiotemporal control over material properties and allow the design of systems with a high degree of user-directed property control. Fabrication and modification of hydrogel-based biomaterials using the precision afforded by light and the versatility offered by these thiol−X photoclick chemistries are of growing interest, particularly for the culture of cells within well-defined, biomimetic microenvironments. Here, we describe methods for the photoencapsulation of cells and subsequent photopatterning of biochemical cues within hydrogel matrices using versatile and modular building blocks polymerized by a thiol−ene photoclick reaction. Specifically, an approach is presented for constructing hydrogels from allyloxycarbonyl (Alloc)-functionalized peptide crosslinks and pendant peptide moieties and thiol-functionalized poly(ethylene glycol) (PEG) that rapidly polymerize in the presence of lithium acylphosphinate photoinitiator and cytocompatible doses of long wavelength ultraviolet (UV) light. Facile techniques to visualize photopatterning and quantify the concentration of peptides added are described. Additionally, methods are established for encapsulating cells, specifically human mesenchymal stem cells, and determining their viability and activity. While the formation and initial patterning of thiol-alloc hydrogels are shown here, these techniques broadly may be applied to a number of other light and radical-initiated material systems (e.g., thiol-norbornene, thiol-acrylate) to generate patterned substrates. 相似文献
993.
994.
Solar radiation and functional traits explain the decline of forest primary productivity along a tropical elevation gradient 下载免费PDF全文
Nikolaos M. Fyllas Lisa Patrick Bentley Alexander Shenkin Gregory P. Asner Owen K. Atkin Sandra Díaz Brian J. Enquist William Farfan‐Rios Emanuel Gloor Rossella Guerrieri Walter Huaraca Huasco Yoko Ishida Roberta E. Martin Patrick Meir Oliver Phillips Norma Salinas Miles Silman Lasantha K Weerasinghe Joana Zaragoza‐Castells Yadvinder Malhi 《Ecology letters》2017,20(6):730-740
One of the major challenges in ecology is to understand how ecosystems respond to changes in environmental conditions, and how taxonomic and functional diversity mediate these changes. In this study, we use a trait‐spectra and individual‐based model, to analyse variation in forest primary productivity along a 3.3 km elevation gradient in the Amazon‐Andes. The model accurately predicted the magnitude and trends in forest productivity with elevation, with solar radiation and plant functional traits (leaf dry mass per area, leaf nitrogen and phosphorus concentration, and wood density) collectively accounting for productivity variation. Remarkably, explicit representation of temperature variation with elevation was not required to achieve accurate predictions of forest productivity, as trait variation driven by species turnover appears to capture the effect of temperature. Our semi‐mechanistic model suggests that spatial variation in traits can potentially be used to estimate spatial variation in productivity at the landscape scale. 相似文献
995.
Lisa M. Durso Gregory P. Harhay Timothy P. L. Smith James L. Bono Todd Z. DeSantis Dayna M. Harhay Gary L. Andersen James E. Keen William W. Laegreid Michael L. Clawson 《Applied and environmental microbiology》2010,76(14):4858-4862
The intestinal microbiota of beef cattle are important for animal health, food safety, and methane emissions. This full-length sequencing survey of 11,171 16S rRNA genes reveals animal-to-animal variation in communities that cannot be attributed to breed, gender, diet, age, or weather. Beef communities differ from those of dairy. Core bovine taxa are identified.The gastrointestinal tracts (GIT) of beef cattle are colonized by microorganisms that profoundly impact animal physiology, nutrition, health, and productivity (5). The GIT microbiota potentially impact food safety via pathogen shedding (13) by interacting with organisms such as Salmonella and competing for resources in the GIT. Cattle intestinal microbiota also play an important role in methane emissions, with U.S. beef cattle alone contributing an estimated 3.87 million metric tons of methane into the environment each year, both from rumen and large-intestine fermentations (7). Although the bovine fecal microbiota have been well characterized using culture-based methods, these techniques are necessarily limited to characterizing bacteria that can be grown in the laboratory. Culture-independent methods can reveal community members that are recalcitrant to culture. Only a handful of deep-sequencing studies have been done using culture-independent 16S rRNA-based methods (1, 11, 12, 14), all with dairy cattle, which have a fundamentally different diet and metabolism from beef cattle. Despite the potential contributions of the beef cattle GIT microbiota to animal health, food safety, and global warming, these communities remain poorly characterized. With the advent of pyrosequencing technology, researchers now have the tools to characterize these important communities. Pyrosequencing will allow rapid characterization of large-sample data sets (1). However, the taxonomic information generated by rapid sequencing is approximate by necessity (9), and full-length 16S-rRNA sequencing remains the “gold standard” method. Accordingly, we have characterized fecal bacteria from six feedlot cattle by full-length capillary sequence analysis of 11,171 16S rRNA gene clones (Fig. (Fig.11).Open in a separate windowFIG. 1.Bacterial diversity of six feedlot beef cattle. Gray bars represent the percentages of all 16S sequences that were assigned to each taxonomy. Colored dots represent the percentages of 16S sequences from each library that were assigned to each taxonomic group. Asterisks indicate unclassified members of the named taxon. Panel A shows the data for the first 99% of all the sequences. Panel B shows the data for the remaining 1% of sequences. Note differences in scales for panels A and B.Rectal grab fecal samples (n = 6) were collected according to institutional animal care guidelines. All animals were female cross-bred MARCIII beef heifers, 6 to 8 months of age, 214 to 241 kg, housed in the same feedlot pen for 2 months prior to fecal collection, and fed the same typical feedlot beef production growing rations consisting of 61.6% corn silage (41.3% dry matter), 15.2% alfalfa hay, 20.9% corn, and 2.3% liquid supplement.Total fecal DNA was isolated from homogenized samples using MoBio UltraClean fecal kit (Carlsbad, CA). PCR was performed using 27F and 1392R primers (11). Amplification consisted of 25 cycles, with an annealing temperature of 55°C. Amplicons from three reactions per sample were pooled (8), cloned using the Invitrogen TOPO TA cloning kit (Carlsbad, CA), and sequenced bidirectionally with M13 primers using an ABI 3700 sequencer (17). Low-quality and chimeric sequences (6) were excluded from further analysis. Distance matrices were compiled from ClustalW alignments (18) in PHYLIP (4). Pairwise estimates of shared richness were calculated using EstimateS, version 8.2 (R. K. Colwell; http://purl.oclc.org/estimates). DOTUR (16) was used to identify operational taxonomic units (OTUs) and to generate rarefaction curves (Fig. (Fig.2),2), richness and evenness estimates, and Shannon''s and Simpson''s diversity indices (Table (Table1).1). A 97% similarity cutoff and an 85% similarity cutoff for estimating OTUs were used to approximate species and class-level designations (15). Taxonomies were assigned to one member of each OTU using the RDP “classifier” tool (19), and the RDP taxonomic information was used for Fig. Fig.11 and and3.3. Common bovine taxa were identified based on inclusion in all three U.S. culture-independent studies (this study and references 1 and 11).Open in a separate windowFIG. 2.Rarefaction curves for six feedlot beef cattle. OTUs were assigned at the 85% DNA sequence similarity level. For comparison purposes, all six curves were truncated after 1,321 sequences.Open in a separate windowFIG. 3.Phylum-level distribution of bacterial sequences from six beef feedlot cattle. Asterisks indicate unclassified members of the named taxon.
Open in a separate windowaCI, confidence interval.The GIT community of beef feedlot cattle characterized in this study was found to share many taxa with the bovine GIT community described for dairy cattle (1, 11, 14), although the relative abundances of the major bacterial groups differed considerably. The fecal microbiota of beef cattle were dominated by members of the Firmicutes, with 62.8% of the OTUs belonging to this taxonomic group (Fig. (Fig.3).3). Bacteroidetes (29.5% of the OTUs) and Proteobacteria (4.4% of the OTUs) were also represented in feces (Fig. (Fig.3).3). A total of seven phyla were found in our six animals.Total estimated species richness values (Chao) for each of the six animals were 372, 600, 1,393, 526, 612, and 320 (Table (Table1).1). These cattle richness numbers are higher than those observed for three human subjects (164, 332, and 297) (2). The mean of Chao pairwise estimates of shared richness between any two of the six cattle fecal libraries was 230.Our findings, in addition to those from pyrosequencing studies (1), identify a core set of bovine GIT bacterial taxa, including the Bacteroidetes Prevotella and Bacteroides; the Firmicutes Faecalibacterium, Ruminococcus, Roseburia, and Clostridium; and the proteobacterium Succinovibrio (Fig. (Fig.1).1). These genera are consistently identified in bovine feces and likely compose part of the bovine resident microbiota. Although the potential exists for culture-independent methods to reveal minority microbial community members, 16S rRNA gene sequencing in dairy (1, 11) and beef cattle supports the list of core taxa identified using culture-based methods.Comparisons between our data set and recent studies done with dairy cattle (1, 11, 12) suggest that although beef and dairy cattle share many of the same major bacterial groups, the relative abundances of these groups in beef and dairy cattle may differ, and there may be differences between the two groups in the compositions of minority community members. The most common genus in beef cattle from our study was Prevotella, representing 24% of the total number of sequences evaluated. In comparison, Dowd et al. (1) found that Prevotella spp. represented only 5.5% of the total 16S genes sequenced from 20 dairy cattle, and Prevotella was not listed in the top 10 most frequently occurring OTUs in either of the studies from McGarvey et al. (11, 12). Likewise, Clostridium represented only 1.5% of the total beef sequences but 19% of the dairy pyrosequences (1). There were a number of bacterial sequences present in the beef cattle sequences but not reported in the dairy sequences, including Arthrobacter, Asteroleplasma, Bifidobacterium, Collinsella, Delftia, Eggerthella, Lactobacillus, Mitsuokella, Olsenella, and Propionibacterium (1, 11), although a number of these genera have been cultured from dairy animals in the past. It must be noted that all of these sequencing studies examined only a small number of animals, and each method has limitations which affect interpretation of the results. The full-length sequencing performed as part of this beef cattle study and two dairy studies (11, 12) relies on a PCR step which can potentially affect the relative numbers of each taxon observed due to PCR bias, while the pyrosequeincg method used in the 20-animal dairy study suffers from artifacts that potentially affect taxonomic assignment and richness estimates due to short read lengths and potential biases in evenness (how many of each group) due to primer and template mismatches (3). Nonetheless, these studies indicate that there may be fundamental differences between the gastrointestinal communities of beef and dairy cattle, they provide a comprehensive examination of the communities present in the specific animals tested, and they serve to provide important baseline information for further studies examining various factors which can impact cattle gastrointestinal communities.The taxonomic information generated by deep sequencing of beef cattle feces revealed considerable animal-to-animal variation in the operational taxonomic unit (OTU) composition of the individual libraries (Fig. (Fig.1).1). The OTU designation facilitates an analysis of the community data without forcing the assignment of sequences into an incomplete and imperfect bacterial taxonomic system. It relies on DNA sequence similarity to assign sequences to a particular OTU defined by the level of DNA sequence similarity. In total, 1,906 OTUs (97% OTU designation) were identified in the six libraries. Of these, only 24 OTUs (1.2%) (comprising 1,253 [11.2%] of sequences) were present in all six libraries, while 1,348 OTUs (69%) were found only in individual libraries. Of these, 1,064 OTUs (77%) were unique, represented by a solitary clone (range of 3% to 29% of the total clones from each individual animal). These data hint at considerable animal-to-animal variation in bacterial community structure at the species level that cannot be readily attributed to breed, gender, age, macroecologic factors such as weather conditions, or diet, given that the animals in this study were controlled for these variables, and support the conclusions of Manter et al. (10) that pooling samples can obscure rare phylotypes.Our results from beef cattle suggest that there may be differences in the bacterial community members present in the GIT of each individual animal that cannot be attributed to diet, breed, gender, age, or macroecologic factors such as weather and suggest the need for the high-resolution community sequencing of much larger numbers of animals before “core” minority community members can be identified. Considering the limited nature of the community surveys to date and all of the genetic, management, geographic, and temporal factors that can contribute to the composition of GIT microbiota, much work remains before we are able to understand and predict the community composition of any individual animal. 相似文献
TABLE 1.
Richness and diversity indices for 6 beef feedlot cattleLibrary and animal (n) | No. of OTUs observed | Species richness (CI)a by: | Diversity (CI) by: | ||
---|---|---|---|---|---|
Chao | ACE | Shannon''s index | Simpson''s index | ||
97% DNA sequence similarity | |||||
Animal 1 (2,485) | 198 | 372 (294-515) | 329 (280-408) | 3.89 (3.83-3.95) | 0.0422 |
Animal 2 (2,084) | 416 | 600 (538-694) | 604 (552-675) | 5.40 (5.35-5.45) | 0.0066 |
Animal 3 (1,710) | 696 | 1,393 (1,224-1,615) | 1,418 (1,327-1,523) | 6.13 (6.08-6.18) | 0.0027 |
Animal 4 (1,512) | 294 | 526 (439-665) | 483 (425-566) | 4.71 (4.63-4.78) | 0.0237 |
Animal 5 (2,059) | 314 | 612 (495-805) | 488 (434-566) | 4.93 (4.88-4.99) | 0.0126 |
Animal 6 (1,321) | 174 | 320 (252-447) | 289 (244-361) | 4.18 (4.11-4.25) | 0.0286 |
85% DNA sequence similarity | |||||
Animal 1 (2,485) | 48 | 61 (51-99) | 62 (52-90) | 2.64 (2.59-2.68) | 0.1056 |
Animal 2 (2,084) | 77 | 107 (87-165) | 102 (87-139) | 3.38 (3.34-3.43) | 0.0505 |
Animal 3 (1,710) | 130 | 153 (139-186) | 151 (140-174) | 4.07 (4.02-4.12) | 0.0254 |
Animal 4 (1,512) | 66 | 75 (68-98) | 77 (70-96) | 2.71 (2.64-2.78) | 0.0931 |
Animal 5 (2,059) | 69 | 80 (72-109) | 84 (75-110) | 3.31 (3.26-3.36) | 0.0545 |
Animal 6 (1,321) | 54 | 65 (57-102) | 61 (56-76) | 2.90 (2.83-2.97) | 0.0939 |
996.
Brian C. Shook Stefanie Rassnick Daniel Hall Kenneth C. Rupert Geoffrey R. Heintzelman Kristen Hansen Devraj Chakravarty James L. Bullington Robert H. Scannevin Brian Magliaro Lori Westover Karen Carroll Lisa Lampron Ronald Russell Shawn Branum Kenneth Wells Sandra Damon Scott Youells Xun Li Mel Osbourne Paul F. Jackson 《Bioorganic & medicinal chemistry letters》2010,20(9):2864-2867
A novel series of arylindenopyrimidines were identified as A2A and A1 receptor antagonists. The series was optimized for in vitro activity by substituting the 8- and 9-positions with methylene amine substituents. The compounds show excellent activity in mouse models of Parkinson’s disease when dosed orally. 相似文献
997.
Jason Jones Christine E. Gibb Susanne C. Millard Jennifer J. Barg† M. Katharine Girvan‡ M. Lisa Veit§ Vicki L. Friesen Raleigh J. Robertson 《Journal of Biogeography》2005,32(10):1827-1833
Aim Bergmann's rule, the tendency for body size to be positively correlated with latitude, is widely accepted but the mechanisms behind the patterns are still debated. Bergmann's originally conceived mechanism was based on heat conservation; other proposed mechanisms invoke phylogeny, migration distance and resource seasonality. With the goal of examining these mechanisms, we quantified morphological variation across the breeding range of a Neotropical migratory songbird, the cerulean warbler (Dendroica cerulea). Location Deciduous forests of eastern North America. Methods We sampled nine cerulean warbler populations, spanning the species’ breeding range. We captured 156 males using targeted playback and model presentation, and included 127 adult males in our analyses of morphological variation. We used an information‐theoretical approach to identify climatic variables associated with geographical variation in body size. Results Cerulean warbler body size adheres to Bergmann's rule: individuals in northern populations are larger than those in southern populations. Variation in body size is best explained by variation in dry and wet‐bulb temperature and actual evapotranspiration. Main conclusions Adherence to Bergmann's rule by the cerulean warbler appears to be linked to thermodynamics (heat conservation in the north, evaporative cooling in the south) and resource seasonality. Multiple selection pressures can interact to generate a single axis of morphological geographical variation, and even subtle fluctuations in climatic variables can exert significant selection pressures. We suggest that the influence of selection pressures on migrants might be enhanced by migratory connectivity, providing further support for the important role played by this phenomenon in the ecology, evolution and population dynamics of migratory songbirds. 相似文献
998.
999.
The fluid dynamics of sperm motility near both rigid and elastic walls is studied using the immersed boundary method. Simulations
of both single and interacting organisms are presented. In particular, we find that nearby organisms originally undulating
with a 90° phase shift may adjust their relative swimming velocities and phase-lock. Comparisons with previous analytical
results are also discussed. The tendency of a near-wall to attract organisms is demonstrated. 相似文献
1000.