44–46 In the present study, the age

44–46 In the present study, the age SB203580 research buy difference between patients with BPU and uPUD, or symptomatic and asymptomatic PUD was only 10 years. Thus it is unlikely that age is a major determinant of differences in symptom status in our patients. Male gender may also be associated with asymptomatic PUD. In the present study, men formed the majority of asymptomatic patients and were significantly less common in the symptomatic group. Whilst ulcer size has been reported to be a determinant of symptoms,13,16 we did not detect an effect of either ulcer size or location on symptoms after a meal challenge in this study. The study also shows that patients with uncomplicated or

symptomatic ulcers reported significantly higher scores for anxiety but not depression than patients with BPU and HC. Psychological factors, especially anxiety, are associated with gastrointestinal symptoms in patients with functional gastrointestinal disorders47 and in the general population.48 It has also been shown that BI 2536 chemical structure self-reported PUD, presumably due to symptomatic ulcers, is associated with a generalized anxiety disorder.49 Gastric sensorimotor function can be altered by experimentally-induced anxiety in healthy subjects, which suggested that psychological factors may play a role in dyspeptic symptoms even though those subjects did not

have psychological disorders.50 Such observations may explain why patients with dyspeptic symptoms reported anxiety scores higher than asymptomatic peptic ulcer patients. However, the mechanism of the association between psychological factors and dyspeptic symptoms remains unclear. This

study has some unavoidable limitations. First, we were not able to assess visceral sensation in patients with asymptomatic uPUD as these patients do not seek any medical attention and the ulcers are found only serendipitously or when complications occur. Second it might be argued that the size of ulcers in the uPUD group was relatively small and, in some cases, were over-diagnosed erosions. However, we set criteria based on those previously published and accepted20,21 and all, in contrast to erosions, had depth. The small size of the ulcers in some patients can be explained by the use of 上海皓元医药股份有限公司 PPI therapy before the endoscopy. Third, the questionnaires were completed 8 weeks after the diagnosis. However, it appeared problematic to assess the dyspeptic symptoms immediately after the ulcer presentation with, in some cases, very life-threatening manifestations. Nevertheless, the BDQ addressed the patients’ symptoms over the previous 12 months, which included the period before PUD was diagnosed. The findings of this study have implications for our understanding and management of PUD. Normally, visceral pain is one of the reasons patients seek medical attention.

We have recently shown that, two years after H pylori eradicatio

We have recently shown that, two years after H. pylori eradication, 30% of children became reinfected [38] therefore the possibility to reduce this phenomenon

by the simple administration of a probiotic is fascinating. H. pylori is known to suppress MUCI and MUC5A gene expression in a human gastric cell line [39]. In vitro studies have shown that L. plantarum strain 299v and L. rhamnosus GG increase the expression of MUC2 and MUC3 genes [40] and the subsequent extracellular secretion of mucin by colon cell cultures [41]. This property can mediate the ability of these strains to restore the mucosal permeability of gastric mucosa or inhibit the adherence of pathogenic Veliparib solubility dmso bacteria, including H. pylori [28]. Pantoflikova et al. have shown a significant increase of mucus thickness after long-term probiotic intake (L. jonhsonii Lj1) both in antrum and corpus [42]. The inflammatory response to H. pylori cause an increase of IL8 leading to release of TNFα and IL1–6 that stimulate CD4+ cells to produce IFNγ and IL4, -5, -6 that leads to gastric inflammation [43]. Probiotics could modify the

immune response of the host [28]. L. salivarius WB 1004 has shown in vitro to reduce IL-8 secretion by gastric epithelial cells [27] and in animal studies certain lactic acid bacteria (L. casei, L. acidophilus, L. rhamnosus, L. delbrueckii subsp. bulgaricus, L. plantarum, Lactococcus lactis and Streptococcus thermophilus) were been able to increase the number medchemexpress of IgA producing cells associated Acalabrutinib datasheet to the lamina propria of small intestine [44]. However, the specific interaction of probiotics with the immune system and the mechanism by which they can exert a beneficial effect are still unclear; moreover, the immunoadjuvant capacity observed would be a property of the strain assayed and can not be generalized to genus or species. The reduction of inflammation has been demonstrated

directly on gastric biopsies by Pantoflikova et al. [42] and indirectly by the decrease of serum gastrin-17 in H. pylori infected patients after probiotic dietetic supplementation [45] (L. jonhsonii Lj1 and L. rhamnosus GG, L. rhamnosus LC705, Propionibacterium freudenreichii JS, Bifidobacterium lactis Bb12, respectively). Recent studies have defined potentially new probiotic strains of L. reuteri, a small minority of which showed strong anti-inflammatory combined with anti-pathogen effects. L. reuteri ATCC PTA 6475 produces and exports substances that can interfere with TNFα production in human macrophages [46] and suppresses NFKB activation affecting apoptosis [47] whilst still retaining its basic anti-pathogen activity during both planktonic and biofilm growth [48]. Initial human studies on this strain in our clinic show good safety and tolerance (personal data). Clinical studies on a combination of the anti-inflammatory effects of this strain with the earlier known anti-H. pylori effect of L.

We have recently shown that, two years after H pylori eradicatio

We have recently shown that, two years after H. pylori eradication, 30% of children became reinfected [38] therefore the possibility to reduce this phenomenon

by the simple administration of a probiotic is fascinating. H. pylori is known to suppress MUCI and MUC5A gene expression in a human gastric cell line [39]. In vitro studies have shown that L. plantarum strain 299v and L. rhamnosus GG increase the expression of MUC2 and MUC3 genes [40] and the subsequent extracellular secretion of mucin by colon cell cultures [41]. This property can mediate the ability of these strains to restore the mucosal permeability of gastric mucosa or inhibit the adherence of pathogenic Lumacaftor datasheet bacteria, including H. pylori [28]. Pantoflikova et al. have shown a significant increase of mucus thickness after long-term probiotic intake (L. jonhsonii Lj1) both in antrum and corpus [42]. The inflammatory response to H. pylori cause an increase of IL8 leading to release of TNFα and IL1–6 that stimulate CD4+ cells to produce IFNγ and IL4, -5, -6 that leads to gastric inflammation [43]. Probiotics could modify the

immune response of the host [28]. L. salivarius WB 1004 has shown in vitro to reduce IL-8 secretion by gastric epithelial cells [27] and in animal studies certain lactic acid bacteria (L. casei, L. acidophilus, L. rhamnosus, L. delbrueckii subsp. bulgaricus, L. plantarum, Lactococcus lactis and Streptococcus thermophilus) were been able to increase the number 上海皓元 of IgA producing cells associated Angiogenesis inhibitor to the lamina propria of small intestine [44]. However, the specific interaction of probiotics with the immune system and the mechanism by which they can exert a beneficial effect are still unclear; moreover, the immunoadjuvant capacity observed would be a property of the strain assayed and can not be generalized to genus or species. The reduction of inflammation has been demonstrated

directly on gastric biopsies by Pantoflikova et al. [42] and indirectly by the decrease of serum gastrin-17 in H. pylori infected patients after probiotic dietetic supplementation [45] (L. jonhsonii Lj1 and L. rhamnosus GG, L. rhamnosus LC705, Propionibacterium freudenreichii JS, Bifidobacterium lactis Bb12, respectively). Recent studies have defined potentially new probiotic strains of L. reuteri, a small minority of which showed strong anti-inflammatory combined with anti-pathogen effects. L. reuteri ATCC PTA 6475 produces and exports substances that can interfere with TNFα production in human macrophages [46] and suppresses NFKB activation affecting apoptosis [47] whilst still retaining its basic anti-pathogen activity during both planktonic and biofilm growth [48]. Initial human studies on this strain in our clinic show good safety and tolerance (personal data). Clinical studies on a combination of the anti-inflammatory effects of this strain with the earlier known anti-H. pylori effect of L.

It is well known that Child–Pugh class closely correlates with su

It is well known that Child–Pugh class closely correlates with survival of HCC patients. It takes a certain period to metastasize to other organs so that the HCC patients of Child–Pugh B or C may die before the emergence of EHM. As the result, Child–Pugh A arose as a risk factor for EHM. There are few reports examining the relationship between EHM of HCC and clinical parameters, including platelet counts. Kanda et al. reported that advanced intrahepatic Selleck CX5461 lesions, presence of vascular tumor invasion, elevated tumor markers and presence of viral hepatitis were risk factors for EHM.[8] However, platelet count was not

selected as the significant risk factor of EHM. The reason for this discrepancy with our results is not clear; however, the difference of timing in the enrollment of patients may be a possible factor. Our cohort study analyzed the parameters at the first non-curative treatment; whereas in most

existing reports in the published work, the clinical parameters of the patients at the time of the first treatment have been used. However, HCC usually recurs several times, and the clinical course is long. Therefore, the clinical parameters at the time of the first treatment may not directly reflect the characteristics of the patients at the time of EHM development. NVP-LDE225 cost There are some limitations in the current study. This experimental design is retrospective and was carried out as a single-center study. The number of patients was relatively small, and we did not observe statistically significant correlations between platelet counts and EHM 上海皓元 in the cohort study, although a clear tendency was observed (P = 0.055). In addition, the mechanism

by which platelets contribute to EHM of HCC has not been validated in vitro. From this study, which was carried out in two different experimental settings, we conclude that high platelet counts, large numbers of tumors, elevated DCP and a good Child–Pugh class are risk factors for EHM in patients with HCC. The results suggest that patients with high platelet counts should be followed up carefully as patients at great risk for EHM. THIS WORK WAS supported by a Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (KAKENHI 23590976). “
“Endoscopic diagnosis of gastroesophageal reflux disease (GERD) remains challenging. Autofluorescence imaging (AFI) can identify indistinct mucosal lesions; however, its ability to diagnose GERD has not been determined. This study aimed to compare the diagnostic capabilities of standard white light imaging (WLI) and AFI using pH/impedance testing as gold standard. In this prospective observational trial, 95 consecutive patients with classic reflux symptoms were screened in two tertiary care referral hospitals and 82 were included. GerdQ questionnaire was administered to each patient. Endoscopy with WLI and AFI, and ambulatory 24-h pH/impedance monitoring were performed.

Primary hepatocytes were plated in 100 mm collagen-coated plates

Primary hepatocytes were plated in 100 mm collagen-coated plates at 2.4 million cells/plate. Matrigel (Cat. no. 354234) was obtained from BD Biosciences. After the 2-hour attachment period hepatocytes

were treated as follows: (1) HGM medium with growth factors and 0.233 mg/mL Matrigel (+MTG+GF); (2) HGM without growth factors and 0.233 mg/mL Matrigel (+MTG−GF); (3) HGM with growth factors but no Matrigel (−MTG+GF); and (4) HGM without growth factors and without Matrigel (−MTG−GF). Plates were harvested on days 2, 6, and 10 for RNA. Standard PCR was performed using 50 ng cDNA and Amplitaq RAD001 ic50 DNA polymerase (Applied Biosystems). PCR products were resolved on 2% agarose gels and

visualized with ethidium bromide staining. The bands on gel were scanned for optical density using ImageJ software for quantitation purposes. Short hairpin RNA (shRNA) for REST: we used a commercially available kit from Invivogen (Cat. CHIR-99021 in vivo no. ksirn4-gz21) to generate the plasmid containing shRNA targeted against REST. The shRNA vector employed also encodes a red-shifted variant of the jellyfish GFP. This plasmid is specifically designed for the cloning of small synthetic oligonucleotides that encode two complementary sequence of 21 nt, homologous to a segment of REST. The insert is cloned downstream of a human 7SK promoter. It is transcribed into a short double-strand RNA (dsRNA) with a hairpin structure (shRNA) consisting of a 21 basepair double-stranded 上海皓元医药股份有限公司 region corresponding to REST and a small loop formed by the spacer region. Sequences for REST shRNA insert: Forward: 5′-ACC TCTTGGTGAAGAGAGACAGATTC AAGAGATCTGTCTCTCTTCACC AAT T-3′; Reverse: 5′-CAAAAATTGGTGAAGAGAGACAGATC TCTTGAATCTGTCTCTCTTCAC CAA G-3′. Primary hepatocytes were plated at a density of 1 × 106 cells per 100 mm dish or 0.25 × 106

cells per well (6-well plate) on day 1. After the 2-hour attachment period, plating media was replaced with HGM complete without growth factors. On the second day hepatocytes were either transfected with shRNA for luciferase (C), or shRNA for REST (R). The transfection media was replaced with fresh HGM without growth factors after 6 hours. On the next day (day 3) media was changed to HGM with growth factors and thereafter replaced every 48 hours throughout the time course. Cells were harvested at days 0, 1, 2, 3, 4, and 5 after transfections for RNA and protein. MTT assay was done on days 2, 3, 4, and 5 as a marker of live cells. Tritiated thymidine incorporation was measured on days 1-2 after transfections to assess proliferation of hepatocytes.

These provided the highest growth rates and the

largest r

These provided the highest growth rates and the

largest removal of ammonium. Growth increased with concentration of the supplement to an optimum at 0.12 M Na-acetate. This carbon source was consumed completely within 10 d of incubation. Higher concentrations inhibited the growth of C. vulgaris. The microalgal populations under heterotrophic growth conditions were one level of magnitude higher than that under autotrophic growth conditions that served as a comparison. No growth occurred in the dark in the absence of a carbon source. Na-acetate was superior to d-glucose. In municipal wastewater, when Na-acetate or d-glucose was added, C. vulgaris significantly enhanced ammonium removal under heterotrophic conditions, and its capacity was equal to ammonium removal under autotrophic growth conditions. This study ABT263 showed that sterilized wastewater can be treated by C. vulgaris under heterotrophic conditions if supplemented with the appropriate organic carbon source for the microalgae. “
“In the current post-genomics world, a relevant question on the minds of many phycologists might be: do we really need more algal genomes or, should we stop and LEE011 focus on the hard job of developing genetic tools and other resources for already sequenced taxa? This question has, in our opinion, a clear answer: we need to do both. Here we focus on the genome sequencing side and discuss the following

reasons why we think algal (and related heterotrophic protist) genome sequencing should remain a focus of phycological research: 1) transcriptomes that aim to create gene inventories or study gene expression differences (primarily Illumina RNAseq data), although cheap to produce and relatively easy to analyze, may not be sufficient for in-depth study of genomes, 2) much of natural biodiversity is still unstudied, necessitating MCE approaches such as single cell genomics (SCG) that, although

still challenging when applied to algae, can sample taxa isolated directly from the environment, 3) horizontal gene transfer (HGT) in algae is no longer controversial, but rather a major contributor to the evolution of photosynthetic lineages, and its study benefits greatly from completed (or draft) genomes, and 4) epigenetics and genome evolution among populations are best studied using assembled genome data. This article is protected by copyright. All rights reserved. “
“The formation of archeospores is characteristic of Porphyra yezoensis Ueda and is important for Porphyra aquaculture. Recently, it has been regarded as a valuable seed source for propagation of thalli in mariculture. Cell wall composition changes are associated with archeospore formation in P. yezoensis. Here, we report changes of cell walls of P. yezoensis during archeospore formation. The surfaces of vegetative cells that were originally smooth became rougher and more protuberant as archeosporangia were formed.

1-TOPO TA (Invitrogen, Carlsbad, CA) Colony formation assay

1-TOPO TA (Invitrogen, Carlsbad, CA). Colony formation assay selleck was performed using monolayer culture. Cells (4 × 105/well) were plated in a 6-well plate and transfected with expression plasmids pcDNA3.1-PAX5

or the empty vector pcDNA3.1 (4 μg each) using lipofectamine 2000 (Invitrogen). After 48 hours of transfection, cells were collected and seeded (1 × 104/well) in a fresh 6-well plate, and selected with G418 for 10 days. Colonies (≥50 cells/colony) were counted after staining with crystal violet solution. All the experiments were performed in triplicate wells three times. Cell viability was measured by the MTS assay (Promega). Briefly, the cells (2 × 103/well) were stably transfected with pcDNA3.1-PAX5 or the empty vector in a 96-well plate for 1, 3, 5, or 7 days. Twenty μL of reaction solution containing

333 μg/mL MTS and 25 μM phenazine ethosulfate was added to cells in 100 μL culture medium, incubated at 37°C for 1.5 hours, and measured at a wavelength of 490 nm. Cell cycle distribution was determined GPCR & G Protein inhibitor by flow cytometry. Briefly, after 12 hours of synchronization by serum starvation, the stably transfected HCC cells with pcDNA3.1-PAX5-expressing vector or pcDNA3.1 empty vector were restimulated with 10% fetal bovine serum (FBS) for 24 hours. Cells were fixed in 70% ethanol and stained with 50 μg/mL propidium iodide (BD Pharmingen, San Jose, CA). The cells were then sorted by FACSCalibur (BD Biosciences, Franklin Lakes, NJ) and cell-cycle profiles were analyzed by WinMDI v. 2.9 software (Scripps Research Institute, La Jolla, CA). Cells

undergoing MCE公司 apoptosis were detected as sub-G1 population because of loss of fragmented DNA. Hep3B cells (1 × 107 cells in 0.1 mL phosphate-buffered saline [PBS]) transfected with PAX5 or pcDNA3.1 were injected subcutaneously into the dorsal left flank of 4-week-old male Balb/c nude mice (5/group). Tumor diameter was measured every 2-3 days for 4 weeks. Tumor volume (mm3) was estimated by measuring the longest and shortest diameter of the tumor and calculated as described.14 An orthotopic HCC mouse model was also established to determine the intrahepatic tumorigenicity. Subcutaneous tumors were harvested 1 week after subcutaneous injection and cut into 1.0 mm3 pieces. One piece was then implanted into the left liver lobe of each mouse (6/group). The mice were sacrificed after 2 weeks and the tumor size and tumor weight were measured. All experimental procedures were approved by the Animal Ethics Committee of the Chinese University of Hong Kong. Terminal deoxynucleotidyl transferase-mediated dUTP-digoxigenin nick end labeling (TUNEL) assay was performed with the Dead End Colorimetric TUNEL System (Promega) following the manufacturer’s protocol. Nuclei with clear brown staining were regarded as TUNEL-positive apoptotic cells. The apoptosis index was calculated as the percentage of TUNEL-positive cell after counting at least 1,000 cells.

The size of SET ranged from 8 to 120 mm (mean diameter-28,5+15,4 

The size of SET ranged from 8 to 120 mm (mean diameter-28,5+15,4 mm). Primary haemostasis was perfomed during endoscopy in 13 (20,3%) patients. As far as the bleeding SET is the absolute indication for their removal 45 (70,3%) patients were operated: open surgery underwent 31 (68,8%), laparoscopic removal – 7 (15,6%), endoscopic removal – 7 (15,6%). Remaining 19 (29,7%) patients were treated conservatively: refuse of patients from operation-9, high operational risk–5, chemotherapy-5. The results of histology and immunohistochemistry: GIST-16; leiomyoma-16; leiomyosarcoma-3; hemangioma-3; lymphoma-2; neurinoma-2;

lipoma-1; mezenhimoma-1; retention cyst-1. Intraoperative complications weren’t observed. Postoperative complications (all after open surgery) were recorded in 4 (6,3%) patients: bleeding from acute ulcer of stomach-1, jugular vein thrombosis-1, acute adhesive intestinal obstruction-1, pulmonary thromboembolism-1. click here Postoperative mortality was 4,4% (2/45), overall mortality – 4,7% (3/64). Conclusion: The EGD+enteroscopy+EUS are valuable methods for diagnostics of bleeding SET and initial haemostasis. Endoscopic and laparoscopic procedures are the method of choice for minimally invasive treatment of patients with bleeding gastrointestinal SET. Key Word(s): 1. subepitelial tumour; 2. bleeding; 3. stomach; 4. enteroscopy; Presenting Author: MAXIM BAGLAENKO Additional Authors: VICTOR STUPIN, VLADIMIR KAHN, SERGEY

SILOUYANOV, VIOLETA BNEYAN, NINA LEVCHUK Corresponding Author: MAXIM BAGLAENKO Affiliations: Moscow Municipal Hospital #15 n. a. O. M. Filatov Objective: Development

of bleeding from stress-induced upper GI ulcers observed selleck inhibitor in 1.5–25% of critically ill patients, the objective is to reduce the risk of bleeding. Methods: In a retrospective study included 517 patients with symptoms of overt upper GI bleeding during the period from 2010 to 2012. 上海皓元医药股份有限公司 In Group 1 enrolled 86 (16.6%) patients with bleeding from stress-induced ulcers during hospital stay. In Group 2 included 431 patients initially hospitalized with signs of bleeding ulcer. Prevention of upper GI ulceration for Group 1 was performed with IV forms of proton pump inhibitors. Results: in Group 1 in 46 (53.5%) patients had ulcers attributed to the high-risk group, which corresponded to FIa, FIIa, FIIb, in Group 2 – in 184 (42.7%) (p = 0.085). HP infection by serological test was positive in 70% in Group 1 and – 73.6% in Group 2 (p = 0,58). NSAIDs registered in 50 (57.9%) patients in Group 1, in Group 2–76 (17.6%) (p = 0.001). The intake of anticoagulants confirmed in 41 (47.4%) patients in Group 1 and in Group 2–29 (6.8%) (p = 0.001). Most of the patients in Group 1–75 (82.7%) had the SAPS II score higher than 30. The rebleeding rate in Group 1 was observed in 13.2% patients in Group 2–7.9% (p = 0.169). In Group 1 8 (7.9%) patients were operated due to unstoppable bleeding, in Group 2–30 (6.9%) (p = 0.92). The mortality in Group 1 was 15.7%, in Group 2–6.25% (p = 0.

All four deaths occurred during or after treatment with intraveno

All four deaths occurred during or after treatment with intravenous steroids. In one of the patients with relapsed disease, Azathioprine was added. Conclusion: Interstitial pneumonitis is a rare, but life-threatening side effect that should be considered in the differential diagnosis of patients INK 128 nmr presenting with respiratory symptoms during or after Interferon-based therapy. There is lack of data to guide treatment and current practice is to cease the drug and commence high dose steroids, either in oral or intravenous form. Pre-treatment respiratory

function tests and CT scan with mid-treatment follow-up should be considered in all patients on treatment and the early withdrawal of treatment is advocated in patients with rapid clinical decline. A-J GREENUP,1 PK TAN,1 V NGUYEN,1 A GLASS,1 H LORD,1 U CHATTERJEE,2 S DAVISON,1 L SMITH,1 A AYRES,2 S HOLDAWAY,3 D SAMARASINGHE,3 S LOCARNINI,4 M LEVY1,2 1Gastroenterology, Liverpool Hospital, Sydney, 2University of New South Wales, Sydney, 3Gastroenterology, Westmead Hospital, Sydney, NSW, 4Victorian

Infectious Diseases Reference Laboratory, Melbourne, VIC, Australia Background and Aims: Oral antiviral use in pregnancy reduces perinatal transmission of Hepatitis B Virus(HBV) in mothers with high viral load. We have previously reported that lamivudine has lower potency and emergence of resistance even after buy BEZ235 short term therapy. Tenofovir may be more favourable, though data regarding use for HBV in pregnancy is limited. Concerns about tenofovir include impact on infant growth parameters

from animal studies. Aims of this study were to examine efficacy of tenofovir in reducing HBV maternal viral load compared to lamivudine, the effectiveness of tenofovir in reducing HBV perinatal transmission and maternal and fetal safety of tenofovir. medchemexpress Methods: In this multi-centre, prospective real life study, pregnant women with high viral load (>7 log IU/ml) were offered tenofovir, commencing at 32 weeks gestation. Virological responses, safety in pregnancy and neonatal data were collected. Perinatal transmission was assessed at 9 months of age. Data from 60 women commencing tenofovir was compared to an historical cohort of lamivudine treated (21 women) and untreated (9 women, including four in current study) mothers. Results: Median baseline viral load was 8.1 log IU/mL (+/− 0.23). 18 women had prior antiviral therapy (10 during prior pregnancies; 8 short duration therapy). Median baseline ALT was 27 U/L (range 6–517). Four developed marked gastrointestinal intolerance within one week and were switched to lamivudine. Median duration of treatment prior to birth was 57 days. Median birth viral load (tested in 54 women) was 4.56 log IU/mL (+/− 0.31), a 3.6 log IU/mL drop. This was a one log greater reduction than lamivudine. Viral load remained >7 log IU/mL at birth in two pregnancies, despite 3 log viral load reduction.

Isotope fractionation from mother to pup was validated using pair

Isotope fractionation from mother to pup was validated using paired whisker and blood serum samples with no significant difference between δ13C and δ15N enrichment of +1.27‰ (whiskers) and +1.92‰ (blood serum) from mothers to pups. Isotope ratios from whisker samples representing over 50% of pups born

at three colonies revealed significant intercolony differences in maternal foraging ecotype frequencies. These results are unique in that ecological partitioning over www.selleckchem.com/products/KU-60019.html such a small spatial scale has not been described in any other otariid species. “
“On 16 June 1979, a herd of 41 sperm whales stranded near the mouth of the Siuslaw River in Florence, Oregon. The stomach contents from 32 whales were collected, identified to the lowest taxonomic level possible, enumerated, and measured. A total of 20,247 cephalopod lower beaks that represented 24 species from 14 different families were recovered. The most numerous species were Histioteuthis hoylei (25.9%), Taonius borealis (12.9%), Galiteuthis phyllura (11.2%), Gonatopsis/Berryteuthis type (10.9%), and Moroteuthis robusta (10.7%). Reconstructed estimates of mass indicated that M. robusta contributed almost 50% of the total mass of cephalopods consumed, followed by H. hoylei (19.3%), Selumetinib mouse and T. borealis (7.0%). The most important species in the diet of stranded whales were M. robusta, H. hoylei, T. borealis, G. phyllura,

Octopoteuthis deletron, and Gonatopsis/Berryteuthis type. There were significant differences in the diet of males and females, but no differences between sperm whales of different age groups. Overall, sperm whales primarily consumed small cephalopods that were likely eaten south of 45ºN in or near the California Current System. This study medchemexpress provides new estimates of the food habits of sperm whales in the northeast Pacific from one of the largest strandings of this species. “
“Fission-fusion dynamics typical of many delphinid populations allow for a variety of social grouping patterns. Identifying these groupings is crucial before conducting a detailed social structure analysis. This study analyzed the structure of a population of Bahamian spotted dolphins, Stenella

frontalis. Through long-term observations and preliminary analysis, three clusters were defined: Northern, Central, and Southern. To quantitatively investigate these delineations, we conducted analysis on 12 yr of sighting data using SOCPROG 2.3. Coefficients of association (CoA) were calculated using the half-weight index, with individuals sighted six or more times per pooled period (3 yr each). Nonmetric multidimensional scaling (MD), hierarchical agglomerative cluster analysis and Mantel tests were conducted to determine if any divisions were present. Mantel tests and MD plots analysis supported the delineations into the three clusters. Cluster analysis showed cluster groupings, but with less clear distinctions between the clusters.