Different species visit or exploit cavities for survival or reproduction, including human-made boxes. Ants and Paridae from mainland southern France share artificial boxes at different life-history stages. Colonies of the ant Crematogaster scutellaris occasionally prevent Paridae from roosting or breeding in boxes and therefore might influence nest-site selection in avian cavity-nesters. Factors that influence coexistence or avoidance in bird-ant interactions in the Mediterranean region are discussed.
The ants of the genus Protalaridris are revised based upon their morphology. Seven species are recognized; the type species (P. armata Brown, 1980) and six species described as new: P. aculeata Lattke & Alpert, sp. n., P. arhuaca Guerrero, Lattke & Alpert, sp. n., P. bordoni Lattke, sp. n., P. leponcei Delsinne & Lattke, sp. n., P. loxanensis Lattke, sp. n., and P. punctata Lattke, sp. n. The genus is patchily distributed in mesic forested areas from western Panama to northern Venezuela and along the Andes to the Amazon watershed of southwestern Peru. The generic description is modified to accommodate a short-mandibulate species. Sporadic biological observations of one long-mandibulate species suggest they are sit-and-wait ambush predators that open their jaws to approximately 180° when stalking. All species are described and imaged, an identification key and a distribution map is provided. Comparing the mandibular morphology of long-mandibulate Protalaridris with other extant and extinct ants bearing elongate, dorsoanterior arching mandibles suggests the supposed mandibular apex in these taxa is actually a hypertrophied, preapical tooth and their supposed basal mandibular tooth is the main mandibular shaft., John E. Lattke, Thibaut Delsinne, Gary D. Alpert, Roberto J. Guerrero., and Obsahuje bibliografii
A new species of caligid copepod (Siphonostomatoida), Anuretes grandis sp. п., parasitic on the painted sweetlips [Diagrammapictum (Thunberg)] in Taiwan is described. The new species is distinguished from its congeners by having: (1) free margin of céphalothorax not covering fourth pediger, (2) large genital complex longer than 2/3 of the cephalic shield, (3) no maxillary whip, (4) leg 3 with 9 setae on the terminal segment of exopod and 8 plumose setae on the terminal segment of endopod, and (5) armature of I,III on leg 4 exopod. Genus Anuretes Heller, 1865 is reviewed and redefined. Based on the new diagnosis three species (A. chelatus Prahha et Pillai, A. fedderni Price and A. parvulus Wilson) were transferred to Pseudanureles, and two species (A.furcatus Capart and A. renalis Ileegaard) were transferred to Lepeophtheirus. In addition, the following three species of caligids were transferred to Anuretes: Lepeophtheirus fallolunulus Lewis, Heniochophilus indicus Pillai, and Lepeophtheirus rotundigenitalis Prabha et Pillai. The latter is renamed Anuretes occullus nom. n. due to the homonym encountered through this transfer. “Anuretes plectorhynchi Yamaguti” reported by Prabha and Pillai (1986) is renamed Anuretes similis sp. n. and Anuretes yamagutii Prabha et Pillai is relegated to the synonym of Anuretes anomalus Pillai. A key to the 18 species of Anuretes is provided.
Despite the fact that vessels have sparse cholinergic innervation, acetylcholine (ACh), the primary neurotransmitter of parasympathetic nervous system, has been commonly used in physiological experiments to assess vascular function. ACh is hydrolyzed by two cholinesterases (ChE), namely acetylcholinesterase and butyrylcholinesterase (BChE). However, little is known about these enzymes in blood vessels. The aim of the project was to characterize the expression and activity of ChE in rat aorta. As the effect of ACh on vascular tone depends on the presence of endothelium, Wistar rats were used as a model with intact endothelium and spontaneously hypertensive rats as a model of impaired endothelial function. Relative expressions of both ChE in different parts of the aorta were determined using RT-qPCR. Enzyme activities were assessed in tissue homogenates by Ellman's assay. Here we showed that both ChE are present in each part of rat aorta, while mRNA is more abundant for BChE than for AChE, irrespective of aortic compartment or genotype. Normotensive Wistar rats possess higher aortic mRNA expression and activity of BChE compared to SHR. We concluded that BChE is the dominant type of ChE in rat aorta and it might play an important role in the regulation of vascular tone., Kristína Szmicseková, Lenka Bies Piváčková, Zuzana Kiliánová, Ľubica Slobodová, Peter Křenek, Anna Hrabovská., and Obsahuje bibliografii
Human post-edited test sentences for the WMT 2017 Automatic post-editing task. This consists in 2,000 English sentences belonging to the IT domain and already tokenized. Source and target segments can be downloaded from: https://lindat.mff.cuni.cz/repository/xmlui/handle/11372/LRT-2132. All data is provided by the EU project QT21 (http://www.qt21.eu/).
Atrial fibrillation is associated with atrial remodeling, in which connexin 43 (Cx43) and cell hypertrophy play important roles. In this study, apelin-13, an aliphatic peptide, was used to explore the protective effects of the adenosine monophosphate-activated protein kinase (AMPK)/mTOR signaling pathway on Cx43 expression and autophagy, using murine atrial HL-1 cells. The expression of Cx43, AMPK, B-type natriuretic peptide (BNP) and pathway-related proteins was detected by Western blot analysis. Cellular fluorescence imaging was used to visualize Cx43 distribution and the cytoskeleton. Our results showed that the Cx43 expression was significantly decreased in HL-1 cells treated with angiotensin II but increased in cells additionally treated with apelin-13. Meanwhile, apelin-13 decreased BNP expression and increased AMPK expression. However, the expression of Cx43 and LC3 increased by apelin-13 was inhibited by treatment with compound C, an AMPK inhibitor. In addition, rapamycin, an mTOR inhibitor, promoted the development of autophagy, further inhibited the protective effect on Cx43 expression and increased cell hypertrophy. Thus, apelin-13 enhances Cx43 expression and autophagy via the AMPK/mTOR signaling pathway, and serving as a potential therapeutic target for atrial fibrillation., Yifan Chen, Xi Qiao, Lijun Zhang, Xuewen Li, Qinghua Liu., and Obsahuje bibliografii