According to the current paradigm, galaxies initially form as disc galaxies at the centres of their own dark matter haloes. During their subsequent evolution, they may undergo a transformation to a red, early‐type galaxy, thus giving rise to the build‐up of the red sequence. Two important, outstanding questions are (i) which transformation mechanisms are most important and (ii) in what environment do they occur. In this paper, we study the impact of transformation mechanisms that operate only on satellite galaxies, such as strangulation, ram‐pressure stripping and galaxy harassment. Using a large galaxy group catalogue constructed from the Sloan Digital Sky Survey, we compare the colours and concentrations of satellites galaxies to those of central galaxies of the same stellar mass, adopting the hypothesis that the latter are the progenitors of the former. On average, satellite galaxies are redder and more concentrated than central galaxies of the same stellar mass, indicating that satellite‐specific transformation processes do indeed operate. Central‐satellite pairs that are matched in both stellar mass and colour, however, show no average concentration difference, indicating that the transformation mechanisms operating on satellites affect colour more than morphology. We also find that the colour and concentration differences of matched central‐satellite pairs are completely independent of the mass of the host halo (not to be confused with the subhalo) of the satellite galaxy, indicating that satellite‐specific transformation mechanisms are equally efficient in host haloes of all masses. This strongly rules against mechanisms that are thought to operate only in very massive haloes, such as ram‐pressure stripping or harassment. Instead, we argue that strangulation is the main transformation mechanism for satellite galaxies. Finally, we determine the relative importance of satellite quenching for the build‐up of the red sequence. We find that roughly 70 per cent of red‐sequence satellite galaxies with M*∼ 109 h−2 M⊙ had their star formation quenched as satellites. This drops rapidly with increasing stellar mass, reaching virtually zero at M*∼ 1011 h−2 M⊙. Therefore, a very significant fraction of red satellite galaxies were already quenched before they became a satellite.
We demonstrate three-dimensional (3D) super-resolution imaging of stochastically switched fluorophores distributed across whole cells. By evaluating the higher moments of the diffraction spot provided by a 4Pi detection scheme, single markers can be simultaneously localized with <10 nm precision in three dimensions in a layer of 650 nm thickness at an arbitrarily selected depth in the sample. By splitting the fluorescence light into orthogonal polarization states, our 4Pi setup also facilitates the 3D nanoscopy of multiple fluorophores. Offering a combination of multicolor recording, nanoscale resolution and extended axial depth, our method substantially advances the noninvasive 3D imaging of cells and of other transparent materials.
We conducted a review of published information on Tuta absoluta parasitoids for the Neotropical region to (1) corroborate species records, (2) analyze associations including the T. absoluta, other insect and plant hosts and (3) identify research directions for enhancing their use as biological control agents. The literature review shows more than 50 species or morphospecies of Hymenoptera associated with T. absoluta, but less than a half (23) could be confirmed as parasitizing T. absoluta. Erroneous reports or invalid names of species, two new species records were found. Over a 100 pests and non-economically important insect and cultivated and non-cultivated plants directly or indirectly interact with T. absoluta in the region. Four T. absoluta parasitoid species include in their host range predatory insects or act as hyperparasitoids, a negative feature considered for a biological control agent. Five larval parasitoids have a narrow host range and could be considered for classical biological control programs in the areas of new invasion. Six Trichogrammatidae species are commercially used in various countries; of those, T. minutum and T. pretiosum are considered to be moderately generalist, being able to exploit several insect hosts. Apart from Apanteles gelechiidivoris and Pseudapanteles dignus, other native species have been the subject of field studies as biological control agents. The review presented here provides useful insights for identifying species that deserve further evaluation as T. absoluta biological control agents through augmentative or conservation strategies in South America, as well as for potential classical biological control programs in other continents. Keywords Taxonomy • Parasitoid ecology • South American tomato pinworm • Host range • Food webs Key message• We provide a review of published records on Tuta absoluta parasitoids of the Neotropics. • From more than 50 parasitoid species or morphospecies reported, only 23 hymenopteran species were confirmed as T. absoluta natural enemies. • Other insect hosts, their host plants and the current knowledge on their potential as biological control agents were tracked. • The low number of available parasitoids and those thathave not yet been identified suggest that much work remains for optimizing the existing biological control services provided by T. absoluta parasitoids.Communicated by M. Traugott.SPECIAL ISSUE 2019: The South American tomato pinworm Tuta absoluta: recent advances in management methods against the background of an ongoing worldwide invasion.
The described Neotropical species of the common and speciose fairyfly genus Gonatocerus Nees ab Esenbeck (Hymenoptera: Mymaridae) are reviewed and re-diagnosed. Eighty-four valid species are recognized including 11 newly described ones. Illustrated identification keys are provided to identify the 5 subgenera recognized in Gonatocerus and to females of each subgenus. The keys include 79 of the treated species, the other five species are known from males only. The known distribution ranges of the species, including new records of extralimital specimens examined, are given. Host associations of the treated species are also given, with emphasis on those species that parasitize eggs of proconiine sharpshooters (Hemiptera: Cicadellidae: Cicadellinae: Proconiini), all of which belong to the ater and morrilli subgroups of the ater species group of G. (Cosmocomoidea Howard), stat. rev. The other four recognized subgenera within Gonatocerus are the nominate subgenus, G. (Gonatocerus) (= sulphuripes species group of authors), G. (Lymaenon Walker), stat. rev. (= litoralis and straeleni species groups of authors), G. (Gastrogonatocerus Ogloblin), stat. rev. (= membraciphagus species group of authors), and G. (Gahanopsis Ogloblin), syn. n. & stat. n. (= deficiens species group of authors). Newly treated as synonyms of G. (Lymaenon) are Rachistus Foerster, Oophilus Enock, Agonatocerus Girault, Gonatoceroides Girault, and Decarthrius Debauche, all syn. n. Two species groups are recognized within G. (Cosmocomoidea) in the New World: the ater group, to which most Neotropical species belong (with the ater, bucculentus, morrilli, and the newly defined chusqueicolus subgroups) and the masneri group, with two described species from the Dominican Republic. The 11 new species described are G. (Gahanopsis) arkadak Triapitsyn sp. n. (Colombia), G. (Cosmocomoidea) barbos Triapitsyn sp. n. (Costa Rica and Mexico), G. (Cosmocomoidea) blefuscu Triapitsyn sp. n. (Costa Rica), G. (Cosmocomoidea) cuscus Triapitsyn sp. n. (Peru), G. (Cosmocomoidea) garchamp Triapitsyn sp. n. (Argentina), G. (Cos- mocomoidea) gerasim Triapitsyn sp. n. (Mexico), G. (Cosmocomoidea) hispaniolus Triapitsyn & Huber sp. n. (Dominican Republic), G. (Cosmocomoidea) kiskis Triapitsyn sp. n. (Argentina), G. (Cosmocomoidea) logarzoi Triapitsyn sp. n. (Argentina), G. (Cosmocomoidea) mumu Triapitsyn sp. n. (Argentina), and G. (Cosmocomoidea) rakitovi Triapitsyn sp. n. (Costa Rica). Seven new synonymies are proposed: Gonatocerus h-luteum (Ogloblin) syn. n. under G. (Cosmoco- moidea) nigriflagellum (Girault); G. enicmophilus Huber syn. n. and G. necator (Ogloblin) syn. n. under G. (Cosmoco- moidea) bonariensis (Brèthes); G. dimorphus (Ogloblin) syn. n. and G. monrosi (Ogloblin) syn. n. under G. (Gastrogonatocerus) margiscutum Girault; and G. setulosus (Ogloblin) syn. n. and G. dorsiniger (Ogloblin) syn. n. under G. (Gastrogonatocerus) membraciphagus Ogloblin. Litus maculipennis Ashmead, Gahanopsis deficiens (Ogloblin), and Gahanopsis straeleni (Debauche) are transferred to Gonatocerus as, respectively, G. (Cosmocomoidea) maculipennis (Ashmead) comb. n., G. (Gahanopsis) deficiens (Ogloblin) comb. n., and G. (Lymaenon) straeleni (Debauche) comb. n. Lectotypes are designated for the following 23 species: G. (Gahanopsis) acanophorae (Ogloblin), G. (Gahanopsis) aethalionis (Ogloblin), G. (Cosmocomoidea) annulicornis (Ogloblin), G. (Gastrogonatocerus) anomocerus Crawford, G. (Gonatocerus) appendiculatus (Ogloblin), G. (Gonatocerus) bonaerensis (Ogloblin), G. (Cosmocomoidea) caudatus (Ogloblin), G. (Cosmocomoidea) concinnus (Ogloblin), Lymaenon (Gastrogonatocerus) dimorphus Ogloblin, G. (Gona- tocerus) excisus (Ogloblin), G. (Cosmocomoidea) gracilicornis (Ogloblin), G. (Cosmocomoidea) grandis (Ogloblin), Lymaenon h-luteum Ogloblin, G. (Cosmocomoidea) inauditus (Ogloblin), G. (Gastrogonatocerus) juvator Perkins, G. (Gastrogonatocerus) margiscutum Girault, G. (Cosmocomoidea) metanotalis (Ogloblin), G. (Cosmocomoidea) nasutus (Ogloblin), Lymaenon necator Ogloblin, G. (Cosmocomoidea) nigrithorax (Ogloblin), G. (Lymaenon) pratensis (Ogloblin), G. (Gonatocerus) stenopterus (Ogloblin), and G. (Gonatocerus) urocerus (Ogloblin).
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