Comparative genomics reveals the hybrid origin of a macaque group

Although species can arise through hybridization, compelling evidence for hybrid speciation has been reported only rarely in animals. Here, we present phylogenomic analyses on genomes from 12 macaque species and show that the fascicularis group originated from an ancient hybridization between the sinica and silenus groups ~3.45 to 3.56 million years ago. The X chromosomes and low-recombination regions exhibited equal contributions from each parental lineage, suggesting that they were less affected by subsequent backcrossing and hence could have played an important role in maintaining hybrid integrity. We identified many reproduction-associated genes that could have contributed to the development of the mixed sexual phenotypes characteristic of the fascicularis group. The phylogeny within the silenus group was also resolved, and functional experimentation confirmed that all extant Western silenus species are susceptible to HIV-1 infection. Our study provides novel insights into macaque evolution and reveals a hybrid speciation event that has occurred only very rarely in primates

Ion-Unquenchable and Thermally “On–Off” Reversible Room Temperature Phosphorescence of 3‑Bromoquinoline Induced by Supramolecular Gels

Ion-unquenchable and thermally on–off reversible room temperature phosphorescence (RTP) can be induced by entrapping 3-bromoquinoline (3-BrQ) into supramolecular gels formed by the self-assembly of a sorbitol derivative (DBS). In comparison with conventional substrates inducing RTP, the gel state 3-BrQ/DBS can produce strong RTP due to the efficient restriction of the vibration of 3-BrQ. Notably, the rather inconvenient deoxygenation is no longer necessary in the preparation of 3-BrQ/DBS gels. The produced RTP was found to be very fast to reach stable, not depending on the standing time. As a reference, in the liquid state of 3-BrQ/sodium deoxycholate (NaDC), stable RTP can be observed after standing for 5 h. The investigation of RTP quenching indicates that the mechanism of RTP induced by DBS gels mainly involves the microenvironment in which 3-BrQ is located. 3-BrQ was entrapped in the hydrophobic 3D network structure of DBS gels, thereby restricting the motion and collision of 3-BrQ and avoiding RTP quenching and additionally quenching by ions. Furthermore, the RTP of 3-BrQ/DBS gels show an excellent “on–off” effect at 10 or 80 °C. This indicates that the solid DBS gel is beneficial for the preparation of RTP sensor devices

Shape controllable microgel particles prepared by microfluidic combining external ionic crosslinking

Alginate microgels with varied shapes, such as mushroom-like, hemi-spherical, red blood cell-like, and others, were generated by combining microfluidic and external ionic crosslinking methods. This novel method allows a continuous fine tuning of the microgel particles shape by simply varying the gelation conditions, e.g., viscosity of the gelation bath, collecting height, interfacial tension. The release behavior of iopamidol-loaded alginate microgel particles with varied morphologies shows significant differences. Our technique can also be extended to microgels formation from different anionic biopolymers, providing new opportunities to produce microgels with various anisotropic dimensions for the applications in drug delivery, optical devices, and in advanced materials formation

Vorticity Deformation in Polymeric Emulsions Induced by Anisotropic Ellipsoids

We study the influence of particle shape on shear-induced droplet deformation in polymeric emulsions. During shearing, droplets become elongated and rotate periodically about their major axes while aligning along the vorticity direction in ellipsoid-filled emulsions, while similar behavior is not observed in the pristine, microsphere-filled or ellipsoid-filled inverse systems. Based on the Jeffery orbit theory, the formation of anisotropic droplets with extremely small Reynolds number due to arrested coalescence in Newtonian matrix and strong confinement effect are suggested to be responsible for the vorticity alignment of droplets during slow shearing

Controlling the Orientation of Droplets in Ellipsoid-Filled Polymeric Emulsions with Particle Parameters and Flow Conditions

The effect of particle parameters [aspect ratio (AR) and concentration] and flow conditions (gap spacing and shear rate) on droplet orientation deformation behavior in polystyrene (PS) particle-filled binary polymeric emulsions is investigated by using a rheo-optical technique and confocal microscopy. Interesting vorticity orientation behavior is achieved by tailoring experimental conditions to yield rigid anisotropic droplets during slow confined shear flow. PS ellipsoids with a high AR are found to reside both at the fluid interface in a monolayer side-on state and inside droplets, leading to the formation of rigid anisotropic droplets because of the interfacial/bulk jamming effect at appropriate particle concentrations. In unconfined bulk samples, droplets with a vorticity orientation can also be observed under the wall migration effect and confinement effect arising from nearby droplets. However, the overly strong wall confinement effect remarkably facilitates the coalescence of vorticity-aligned droplets during slow shear, eventually leading to the formation of a long stringlike phase aligning along the flow direction. High shear rates generate refined droplets with lower particle coverage and weak rigidity, which restrain the formation of anisotropic droplets and thus suppress the droplet vorticity orientation

Conducting Hydrogels of Tetraaniline-g-poly(vinyl alcohol) in Situ Reinforced by Supramolecular Nanofibers

Novel conducting hydrogels (PVA-TA) with dual network structures were synthesized by the grafting reaction of tetraaniline (TA) into the main chains of poly­(vinyl alcohol) and in situ reinforced by self-assembly of a sorbitol derivative as the gelator. The chemical structure of the PVA-TA hydrogels was characterized by using FT-IR and NMR. The mechanical strength of the PVA-TA hydrogels was strongly improved due to the presence of supramolecular nanofibers. For instance, the compressive and tensile strengths of supramolecular nanofiber-reinforced hydrogels were, respectively, 10 times and 5 times higher than those of PVA-TA hydrogels. Their storage modulus (G′) and loss modulus (G″) were 5 times and 21 times higher than those of PVA-TA hydrogels, respectively. Cyclic voltammetry and conductivity measurements indicated that the electroactivity of reinforced hydrogels is not influenced by the presence of supramolecular nanofibers