Pathways to quiescence: SHARDS view on the star formation histories of massive quiescent galaxies at 1.0 < z < 1.5

We present star formation histories (SFHs) for a sample of 104 massive (stellar mass M > 10^10 M_⊙) quiescent galaxies (MQGs) at z = 1.0–1.5 from the analysis of spectrophotometric data from the Survey for High-z Absorption Red and Dead Sources (SHARDS) and HST/WFC3 G102 and G141 surveys of the GOODS-North field, jointly with broad-band observations from ultraviolet (UV) to far-infrared (far-IR). The sample is constructed on the basis of rest-frame UVJ colours and specific star formation rates (sSFRs = SFR/Mass). The spectral energy distributions (SEDs) of each galaxy are compared to models assuming a delayed exponentially declining SFH. A Monte Carlo algorithm characterizes the degeneracies, which we are able to break taking advantage of the SHARDS data resolution, by measuring indices such as MgUV and D4000. The population of MQGs shows a duality in their properties. The sample is dominated (85 per cent) by galaxies with young mass-weighted ages, t_M t_M < 2 Gyr, short star formation time-scales, 〈τ〉 ∼ 60–200 Myr, and masses log(M/M_⊙) ∼ 10.5. There is an older population (15 per cent) with t_M t_M = 2–4 Gyr, longer star formation time-scales, 〈τ〉∼ 400 Myr, and larger masses, log(M/M_⊙) ∼ 10.7. The SFHs of our MQGs are consistent with the slope and the location of the main sequence of star-forming galaxies at z > 1.0, when our galaxies were 0.5–1.0 Gyr old. According to these SFHs, all the MQGs experienced a luminous infrared galaxy phase that lasts for ∼500 Myr, and half of them an ultraluminous infrared galaxy phase for ∼100 Myr. We find that the MQG population is almost assembled at z ∼ 1, and continues evolving passively with few additions to the population.

Aperture effects on the oxygen abundance determinations from Califa data

This paper aims to provide aperture corrections for emission lines in a sample of spiral galaxies from the Calar Alto Legacy Integral Field Area Survey (CALIFA) database. In particular, we explore the behavior of the log([O III] λ5007/Hβ)/([N II] λ6583/Hα) (O3N2) and log[N II] lambda 6583/Hα (N2) flux ratios since they are closely connected to different empirical calibrations of the oxygen abundances in star-forming galaxies. We compute the median growth curves of Hα, Hα/Hβ, O3N2, and N-2 up to 2.5R(50) and 1.5 disk R-eff. These distances cover most of the optical spatial extent of the CALIFA galaxies. The growth curves simulate the effect of observing galaxies through apertures of varying radii. We split these growth curves by morphological types and stellar masses to check if there is any dependence on these properties. The median growth curve of the Hα flux shows a monotonous increase with radius with no strong dependence on galaxy inclination, morphological type, and stellar mass. The median growth curve of the Hα/HβH ratio monotonically decreases from the center toward larger radii, showing for small apertures a maximum value of ≈10% larger than the integrated one. It does not show any dependence on inclination, morphological type, and stellar mass. The median growth curve of N-2 shows a similar behavior, decreasing from the center toward larger radii. No strong dependence is seen on the inclination, morphological type, and stellar mass. Finally, the median growth curve of O3N2 increases monotonically with radius, and it does not show dependence on the inclination. However, at small radii it shows systematically higher values for galaxies of earlier morphological types and for high stellar mass galaxies. Applying our aperture corrections to a sample of galaxies from the SDSS survey at 0.02 ≤ z ≤ 0.3 shows that the average difference between fiber-based and aperture-corrected oxygen abundances, for different galaxy stellar mass and redshift ranges, reaches typically to ≈11%, depending on the abundance calibration used. This average difference is found to be systematically biased, though still within the typical uncertainties of oxygen abundances derived from empirical calibrations. Caution must be exercised when using observations of galaxies for small radii (e.g., below 0.5 R_eff) given the high dispersion shown around the median growth curves. Thus, the application of these median aperture corrections to derive abundances for individual galaxies is not recommended when their fluxes come from radii much smaller than either R_50 or R_eff.

Role of the Tryptophan Residues in the Specific interaction of the Sea Anemone Stichodacty la helianthus’s Actinoporin Sticholysin II with Biological Membranes

Actinoporins are pore-forming toxins from sea anemones. Upon interaction with sphingomyelin-containing bilayers, they become integral oligomeric membrane structures that form a pore. Sticholysin II from Stichodactyla helianthus contains five tryptophans located at strategic positions; its role has now been studied using different mutants. Results show that W43 and W115 play a eterminant role in maintaining the high thermostability of the protein, while W146 provides specific interactions for protomer−protomer assembly. W110 and W114 sustain the hydrophobic effect, which is one of the major driving forces for membrane binding in the presence of Chol. However, in its absence, additional interactions with sphingomyelin are required. These conclusions were confirmed with two sphingomyelin analogues, one of which had impaired hydrogen bonding properties. The results obtained support actinoporins’ Trp residues playing a major role in membrane recognition and binding, but their residues have an only minor influence on the diffusion and oligomerization steps needed to assemble a functional pore.