Explore the vast range of titles available.

Reproductive success of many plant species declines in fragmented habitat, but this effect is little studied in trees of tropical rain forest understorey. Paypayrola blanchetiana (Violaceae) is a continuous-flowering treelet endemic to the Atlantic rain forest of north-east Brazil. Plants are distributed in localized patches. Flower, fruit and seed production of a total of 86 trees was quantified in six forest fragments, each belonging to one of two categories of size (> 300 ha vs. < 50 ha) and fragmentation history (isolated for c. 25–30 y vs. at least c. 50 y). Relative fruit set (fruits/flower) and seed set (seeds/ovule) were calculated for a spatial (total fruit set of tree individuals) and a temporal analysis (combined month-by-month fruit set in patches in response to different flowering intensities). Fruit set (1%) and seed set (0.6%) were very low, but variable among trees. Plants in large fragments had significantly higher fruit set and seed set than plants in small fragments. Trees in older fragments, however, displayed similar fruit and seed set to those in recently created ones. We found no interaction effect on seed set of fragment size and isolation time. Seed set was a negative function of patch flower density. Possible drivers of the observed patterns are discussed.

The main aims of the study were: (1) to investigate the effect of fragment age in relation to other patch- and landscape-scale measures of forest fragmentation, and (2) to assess the relative importance of fragmentation, habitat degradation (i.e. degradation caused by selective logging and past shifting cultivation) and putative pre-existing species turnover in structuring current land-snail assemblages. South-western Sri Lanka. The land-snail fauna was sampled using standardized belt transects. Fifty-seven transects were sampled in 21 lowland rain forest fragments (c. 1-33,000 ha). The spatial arrangement of fragments in the study area was explicitly considered in an effort to take into account the non-random nature of fragmentation and degradation and the possibility that current species composition may reflect patterns of species turnover that existed prior to fragmentation. The data set of 57 land-snail species and 28 environmental and spatial variables was analysed using canonical correspondence analysis and partial canonical correspondence analysis. Fragment age, mean shape complexity (i.e. a landscape-scale measure of shape complexity), altitude, and the spatial variables x (longitude), y (latitude) and y² explained significant variation in land-snail species composition. None of the three nominal variables quantifying habitat degradation was significantly correlated with variation in species composition. The independent effects of fragment age and mean shape complexity were similar. The combined effect of the spatial variables alone was larger than the independent effects of fragment age, mean shape complexity or altitude, but was of the same order of magnitude. The total variation explained by the spatial variables was comparable to the total non-spatial variation accounted for by fragment age, mean shape complexity and altitude. Fragment age was found to be one of only two key determinants (the other was shape complexity at the landscape scale) driving fragmentation-related changes in community composition. The influence of pre-fragmentation patterns of species turnover on assemblage structure can be stronger than the effects of fragmentation measures, such as age, and may override the effects of forest degradation. Thus, strong patterns of pre-existing turnover may potentially confound interpretation of the effects of forest fragmentation and degradation.

Question: What is the relative importance of area- and edge-effects on woody seedling diversity in old Afromontane forest fragments? Location: Mistbelt Afromontane forests, KwaZulu-Natal midlands, South Africa. Methods: Woody seedling abundance and species richness in 590 1-m2 plots were sampled at the forest edge (< 10 m from the edge) and interior in 31 old (> 60 a) Afromontane forest fragments (0.05 – 328.5 ha) with closed edges in an ancient grassland matrix. Results: Unlike young (< 20 a) Amazonian fragments, there was no edge- or area-effect on sample plot seedling density and species richness, although these increased significantly with increasing herb cover (less disturbance). Seedling density, but not species richness, declined significantly with herbivory of seedlings, regardless of forest size or plot location. Seedling community composition and richness did not differ significantly between the edge and interior of forests across the range of forest sizes (i.e. no edge-effect). Community composition was nested with small forests retaining a subset of the seedling flora of larger forests. Overall, cumulative seedling species richness increased with forest area (i.e. area-effect). Conclusions: Holocene climatic extinction filtering events and area-dependent species relaxation have potentially selected for tree species with convergent life histories adapted to local fragmentation-effects. Stable environmental conditions at old edges in these naturally fragmented forests cause similar regeneration conditions and seedling species composition between edge and interior. Consequently, seedling density and species richness are controlled more by response to gradients of local disturbance (habitat area, herb cover, herbivory) than by proximity to the edge. Large patches (> 50 ha) with intact edges had the highest tree seedling diversity and are a conservation priority. Although small patches contain no unique species they preserve landscape processes, have conservation value, and require protection. Conservation principles derived from recently created Amazonian fragments and that emphasize edge-effects, require critical evaluation for application to old Afromontane patches. Nomenclature: Arnold & de Wet (1993).

Several pottery sherds from the Svilengrad-Brantiite site, Bulgaria, were mineralogically and petrographically analyzed. The aim was to add information to the very scarce material data available for Early Bronze Age pottery in the southeastern Thrace plain, Bulgaria, in order to examine a possible raw-material source of the pottery. The characterization techniques applied were optical microscopy (OM), petrographic microscopy (PM), scanning electron microscopy coupled with energy dispersive X-ray spectroscopy (SEM-EDS), X-ray fluorescence (XRF) spectroscopy, and X-ray diffraction (XRD). The pottery samples consisted of two typological groups: a local-made type and a cord-impressed decoration type influenced by foreign cultures. All of the samples were produced from fine clay pastes that had a quite similar composition, with abundant mineral grains of similar mineral composition and fragments of metamorphic and granitic rocks. The chemical compositions of each mineral in the grains and fragments were almost identical, and consistent with those from metamorphic and granitic rocks from the Sakar-Strandja Mountains near the study site. The clay paste compositions corresponded to those of illite/smectite mixed-layer clay minerals or mixtures of illite and smectite, and the clay-mineral species were consistent with those in Miocene–Pleistocene or Holocene sediments surrounding the site.

This trial compared once-weekly dulaglutide, a GLP-1 receptor agonist, with placebo for glycemic control in youths with type 2 diabetes who may have been receiving metformin or basal insulin. Dulaglutide was superior at 26 weeks.

Three different glucagon-like peptide-1 (GLP-1) receptor agonists reduce cardiovascular outcomes in people with type 2 diabetes at high cardiovascular risk with high glycated haemoglobin A1c (HbA1c) concentrations. We assessed the effect of the GLP-1 receptor agonist dulaglutide on major adverse cardiovascular events when added to the existing antihyperglycaemic regimens of individuals with type 2 diabetes with and without previous cardiovascular disease and a wide range of glycaemic control. This multicentre, randomised, double-blind, placebo-controlled trial was done at 371 sites in 24 countries. Men and women aged at least 50 years with type 2 diabetes who had either a previous cardiovascular event or cardiovascular risk factors were randomly assigned (1:1) to either weekly subcutaneous injection of dulaglutide (1·5 mg) or placebo. Randomisation was done by a computer-generated random code with stratification by site. All investigators and participants were masked to treatment assignment. Participants were followed up at least every 6 months for incident cardiovascular and other serious clinical outcomes. The primary outcome was the first occurrence of the composite endpoint of non-fatal myocardial infarction, non-fatal stroke, or death from cardiovascular causes (including unknown causes), which was assessed in the intention-to-treat population. This study is registered with ClinicalTrials.gov, number NCT01394952. Between Aug 18, 2011, and Aug 14, 2013, 9901 participants (mean age 66·2 years [SD 6·5], median HbA1c 7·2% [IQR 6·6–8·1], 4589 [46·3%] women) were enrolled and randomly assigned to receive dulaglutide (n=4949) or placebo (n=4952). During a median follow-up of 5·4 years (IQR 5·1–5·9), the primary composite outcome occurred in 594 (12·0%) participants at an incidence rate of 2·4 per 100 person-years in the dulaglutide group and in 663 (13·4%) participants at an incidence rate of 2·7 per 100 person-years in the placebo group (hazard ratio [HR] 0·88, 95% CI 0·79–0·99; p=0·026). All-cause mortality did not differ between groups (536 [10·8%] in the dulaglutide group vs 592 [12·0%] in the placebo group; HR 0·90, 95% CI 0·80–1·01; p=0·067). 2347 (47·4%) participants assigned to dulaglutide reported a gastrointestinal adverse event during follow-up compared with 1687 (34·1%) participants assigned to placebo (p<0·0001). Dulaglutide could be considered for the management of glycaemic control in middle-aged and older people with type 2 diabetes with either previous cardiovascular disease or cardiovascular risk factors. Eli Lilly and Company.

Little is known about the response of arbuscular mycorrhizal fungal communities to ecosystem development. We use a long‐term soil chronosequence that includes ecosystem progression and retrogression to quantify the importance of host plant identity as a factor driving fungal community composition during ecosystem development. We identified arbuscular mycorrhizal fungi and plant species from 50 individual roots from each of 10 sites spanning 5–120 000 yr of ecosystem age using terminal restriction fragment length polymorphism (T‐RFLP), Sanger sequencing and pyrosequencing. Arbuscular mycorrhizal fungal communities were highly structured by ecosystem age. There was strong niche differentiation, with different groups of operational taxonomic units (OTUs) being characteristic of early succession, ecosystem progression and ecosystem retrogression. Fungal alpha diversity decreased with ecosystem age, whereas beta diversity was high at early stages and lower in subsequent stages. A total of 39% of the variance in fungal communities was explained by host plant and site age, 29% of which was attributed to host and the interaction between host and site (24% and 5%, respectively). The strong response of arbuscular mycorrhizal fungi to ecosystem development appears to be largely driven by plant host identity, supporting the concept that plant and fungal communities are tightly coupled rather than independently responding to habitat.

Two genetic variants in strong linkage disequilibrium (rs9536314 and rs9527025) in the Klotho ( KL ) gene, encoding a transmembrane protein, implicated in longevity and associated with brain resilience during normal aging, were recently shown to be associated with Alzheimer disease (AD) risk in cognitively normal participants who are APOE ε4 carriers. Specifically, the participants heterozygous for this variant (KL-SV HET+ ) showed lower risk of developing AD. Furthermore, a neuroprotective effect of KL-VS HET+ has been suggested against amyloid burden for cognitively normal participants, potentially mediated via the regulation of redox pathways. However, inconsistent associations and a smaller sample size of existing studies pose significant hurdles in drawing definitive conclusions. Here, we performed a well-powered association analysis between KL-VS HET+ and five different AD endophenotypes; brain amyloidosis measured by positron emission tomography (PET) scans (n = 5,541) or cerebrospinal fluid Aβ42 levels (CSF; n = 5,093), as well as biomarkers associated with tau pathology: the CSF Tau (n = 5,127), phosphorylated Tau (pTau181; n = 4,778) and inflammation: CSF soluble triggering receptor expressed on myeloid cells 2 (sTREM2; n = 2,123) levels. Our results found nominally significant associations of KL-VS HET+ status with biomarkers for brain amyloidosis (e.g., CSF Aβ positivity; odds ratio [OR] = 0.67 [95% CI, 0.55–0.78], β = 0.72, p = 0.007) and tau pathology (e.g., biomarker positivity for CSF Tau; OR = 0.39 [95% CI, 0.19–0.77], β = -0.94, p = 0.007, and pTau; OR = 0.50 [95% CI, 0.27–0.96], β = -0.68, p = 0.04) in cognitively normal participants, 60–80 years old, who are APOE e4-carriers. Our work supports previous findings, suggesting that the KL-VS HET+ on an APOE ε4 genotype background may modulate Aβ and tau pathology, thereby lowering the intensity of neurodegeneration and incidence of cognitive decline in older controls susceptible to AD.

We aimed to determine the effects of long-term collagen peptide (CP) supplementation and resistance exercise training (RET) on body composition, strength, and muscle fiber cross-sectional area (fCSA) in recreationally active men. Fifty-seven young men were randomly and double-blinded divided into a group receiving either collagen peptides (COL, 15 g/day) or a placebo (PLA). Strength testing, bioimpedance analysis, and muscle biopsies were used prior to and after an RET intervention. Food record protocols were performed during the RET intervention. The groups trained three times a week for 12 weeks. Baseline parameters showed no differences between groups, and the external training load and dietary food intake were also similar. COL showed a significant increase in fat-free mass (FFM) compared with the placebo group (p < 0.05). Body fat mass (BFM) was unchanged in COL, whereas a significant increase in BFM was observed in PLA. Both groups showed significant increases in all strength tests, with a trend for a slightly more pronounced effect in COL. The fCSA of type II muscle fibers increased significantly in both groups without differences between the two groups. We firstly demonstrated improved body composition in healthy, recreationally active men subsequent to prolonged CP supplementation in combination with RET. As the observed increase in FFM was not reflected in differences in fCSA hypertrophy between groups, we assume enhanced passive connective tissue adaptations in COL due to CP intake.

Environmental DNA (eDNA) analysis has advanced conservation biology and biodiversity management. However, accurate estimation of age and origin of eDNA is complicated by particle transport and the presence of legacy genetic material, which can obscure accurate interpretation of eDNA detection and quantification. To understand the state of genomic material within the environment, we investigated the degradation relationships between (a) size of fragments (long vs short), (b) genomic origins (mitochondrial vs nuclear), (c) nucleic acids (eDNA vs eRNA), and (d) RNA types (messenger (m)RNA vs ribosomal (r)RNA) from non-indigenous Dreissena mussels. Initial concentrations of eRNA followed expected transcriptional trends, with rRNAs found at > 1000 × that of eDNA, and a mitosis-associated mRNA falling below detection limits within 24 h. Furthermore, the ratio of eRNA:eDNA significantly decreased throughout degradation, potentially providing an estimate for the age of genomic material. Thus, eRNA quantification can increase detection due to the high concentrations of rRNAs. Furthermore, it may improve interpretation of positive detections through the eRNA:eDNA ratio and/or by detecting low abundant mitosis-associated mRNAs that degrade within ~ 24 h.