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As part of an ongoing survey of scorpion diversity in Colima, Mexico, the isolated mountain Cerro Grande, part of the Biosphere Reserve Sierra de Manantlán, was investigated. Centruroides possanii sp. nov., the fifth species of the genus from the state, was discovered during fieldwork in the massif and is described in the present paper. Physiographical and climatic features of Cerro Grande may restrict the range of this new species; thus, we hypothesized that it may be a microendemic species that requires priority conservation. The new species is not assigned to any Centruroides species group recognized because some of its morphological features do not fit the current diagnosis of any of these groups, and these different groups are non-monophyletic and consequently ill-diagnosed. The new species is profusely illustrated, particularly the hemispermatophore. A distribution map is presented along with the other two more common species distributed in Colima. Because only indirect data on the potency of its venom is available, the medical importance of this new species described here is yet to be known.

Metamorphosis was a key innovation in insect evolution, wherein the individual acquires characteristic adult features and stops molting during postembryonic development. The ancestral metamorphosis mode was hemimetaboly, in which the embryogenesis gives rise to a first instar nymph with the essential adult body structure. The nymphs grow gradually and the final molt to the adult stage completes the formation of functional genitalia and wings. The metamorphosis mode known as holometaboly emerged from hemimetaboly, which is characterized by embryogenesis that produces a larva with a body form that may be substantially different from that of the adult. The larva grows through various stages until molting to the pupal stage, which bridges the gap between the morphologically divergent larva and that of the winged and reproductively competent adult. In the hemimetabolan and holometabolan modes, metamorphosis is regulated by two hormones: the juvenile hormone (JH) and the ecdysone, plus its biologically active derivative, 20-hydroxyecdysone (20E). 20E is a steroid, and its main role is to promote the successive molts, including the metamorphic one, whereas JH is a terpenoid, whose function is to repress metamorphosis [1] . The action of these hormones is underpinned by the mechanisms that transduce the hormonal signal through a pathway of gene activation. The 20E signaling pathway was first described in the 1990s [2] , whereas the most important details of the JH pathway were unveiled recently. Important components of the JH signaling pathway are the JH receptor, which is the basic helix–loop–helix-Per-ARNT-Sim (bHLH-PAS) protein known as methoprene tolerant (Met), to which JH binds, as unveiled by Jindra's group in the 2010 decade. Another important component is Taiman, also a bHLH-PAS protein that plays the role of co-receptor. Finally, the transcription factor Kruppel homolog 1 (Kr-h1) is the main transducer of the antimetamorphic signal of JH [1] . Kruppel homolog 1 Kr-h1 was discovered in Drosophila melanogaster as a gene with structural similarity to the segmentation gene Kruppel, with which it shares the zinc-finger motifs and amino acid spacers connecting them. The first evidence that connected Kr-h1 and JH was also obtained in D. melanogaster. In this fly, the adult abdominal epidermis derives from larval histoblasts, which start proliferating after puparium formation. The experiments of Ashburner in 1970 showed that administration of JH prior to the prepupal stage prevents the normal differentiation of the abdominal epidermis, and the bristles that should be formed in the adult are shorter or lacking. In 2008, the experiments of Minakuchi and coworkers indicated that Kr-h1 expressed ectopically in the abdominal epidermis during metamorphosis of D. melanogaster also resulted in missing or short bristles, thereby suggesting that Kr-h1 mediates the antimetamorphic action of JH. New experiments of Minakuchi and coworkers carried out in the beetle Tribolium castaneum in 2009 showed that RNAi depletion of Kr-h1 in young larvae caused a precocious larval–pupal transformation, providing clear evidence that Kr-h1 represses metamorphosis and works downstream from Met in the JH signaling pathway. The antimetamorphic action of Kr-h1 was generalized to hemimetabolans in two parallel papers published in 2011 and conducted, respectively, in the cockroach Blattella germanica by Lozano and Belles, and the bugs Pyrrhocoris apterus and Rhodnius prolixus by Konopova and coworkers. In these two studies, RNAi experiments showed that Kr-h1 depletion in nymphs in the penultimate or antepenultimate nymphal stage triggers precocious metamorphosis [1] ( Fig. 1 A). E93 E93 is an early gene in the ecdysone signaling cascade that is specifically expressed in late prepupae of D. melanogaster. As shown by the groups of Thummel and Baehrecke in the 1990 decade, the gene encodes for a protein with RHF domains significantly similar to pipsqueak motifs, which was found to be a key player in the degeneration process of the salivary glands during D. melanogaster metamorphosis. However, the action of E93 in metamorphosis is not restricted to the regulation of degeneration processes, given that it also plays morphogenetic roles. In 2012 Mou and coworkers observed that E93 is widely expressed in adult cells of the pupa of D. melanogaster, where it is required for patterning processes. Studying the induction of the Distal-less (Dll) gene within bract cells of the pupal leg using epidermal growth factor (EGF) receptor signaling, Mou and coworkers found that E93 causes Dll to become responsive to EGF receptor signaling, thus indicating that E93 is both necessary and sufficient for determining this switch. These results suggested that E93 controls the responsiveness of many other target genes and that it is generally required for patterning during metamorphosis. Subsequent RNAi experiments reported by Urena and coworkers in 2014 showed that E93-depleted D. melanogaster larvae are able to pupate but die at the end of the pupal stage. In T. castaneum, E93 depletion by RNAi prevented the pupal–adult transition, resulting in the formation of a supernumerary second pupa. Similar results were obtained in the cockroach B. germanica, where E93 depletion in nymphs prevented the nymphal–adult transition, giving rise to repeated supernumerary nymphal instars ( Fig. 1 B). The same year, Belles and Santos showed that the expression of E93 in juvenile nymphs of B. germanica is inhibited by the transcription factor Kr-h1, thus uncovering the essential mechanism by which JH represses metamorphosis, which was named MEKRE93 pathway [3] . The MEKRE93 pathway in hemimetabolan species The observation that Kr-h1 represses E93 expression led to propose the MEKRE93 pathway as the essential axis regulating insect metamorphosis. Accordingly, in nymph–nymph transitions, JH acts through its receptor Met-Taiman to induce the expression of Kr-h1, while Kr-h1 represses the expression of E93. In contrast, the decline of JH production in the final juvenile stage interrupts Kr-h1 expression, E93 becomes de-repressed, thus triggering adult morphogenesis ( Fig. 2 A) (Belles and Santos, 2014). RNAi experiments in B. germanica by the same authors also revealed that E93 depletion increases Kr-h1 expression, thus indicating that Kr-h1 and E93 are reciprocally repressed. The inhibitory action of Kr-h1 upon E93 expression was corroborated two years later in the holometabolan T. castaneum by Urena and coworkers, which extended the MEKRE93 pathway framework to holometabolan metamorphosis. The MEKRE93 pathway in holometabolan species The main difference between the hemimetabolan and holometabolan metamorphoses is the regulation and function of the Broad complex (BR-C) zinc-finger transcription factors. In hemimetabolan species, BR-C is mainly involved in promoting the growth of wing primordia. For example, this was shown in B. germanica by Huang and coworkers in 2013, who additionally reported that BR-C expression is induced by JH and Kr-h1 during juvenile stages. One year later, Urena and coworkers found that BR-C is repressed by E93 in the metamorphic transition. Furthermore, RNAi studies made in 2019 by the group of Mito and Noji in the cricket Gryllus bimaculatus, a hemimetabolan species, confirmed the mentioned interactions, and additionally discovered that BR-C and Kr-h1 are reciprocally activated. In sharp contrast, and as shown mainly by the group of Riddiford in the decade of 1990, BR-C triggers the formation of the pupal stage in holometabolan species, where JH inhibits the expression of BR-C during larval stages and stimulates BR-C expression after pupal commitment ( Fig. 2 B). In 2019, Chafino and co-workers showed that E93 is involved in triggering the pupal stage, as it promotes BR-C expression in T. castaneum. The whole data indicates that the MEKRE93 pathway is conserved in the holometabolan species, which added the E93/BR-C interaction loop to the ancestral (hemimetabolan) pathway during the evolutionary transition from hemimetaboly to holometaboly ( Fig. 2 C).

Exploiting the annotation of the western clawed frog Silurana tropicalis genome, we identified a new metallothionein (MT) gene, exhibiting all the features to be considered an active gene, but with an atypical coding region, showing only 17 cysteine residues instead of the canonical 20 cysteines of vertebrate metallothioneins and two anomalous cysteine triplets. However, the presence of a gene in the genome does not ensure its effective expression. By using conventional and Real-Time PCR analyses, we demonstrated that this atypical MT is constitutively expressed throughout the life cycle of the African clawed frog Xenopus laevis; moreover, this gene is highly expressed in the adult liver, the major site of MT expression and synthesis in vertebrates. To our knowledge, the X. laevis MT described in this paper is the first sequence of a vertebrate MT showing only 17 cysteine residues, arranged in two Cys–Cys–Cys motifs. Phylogenetic analyses also demonstrated that the atypical X. laevis MT merges in the anuran clade, but is the most derived sequence among tetrapods MTs. Finally, Tajima's Relative Rate Test suggested a different evolutionary rate between the canonical X. laevis MT and this novel isoform.

The aims of this paper were (i) to define how contrasting land uses affected plant biodiversity in Mediterranean agro-silvo-pastoral-systems across a gradient of disturbance regimes: cork oak forests, secondary grasslands, hay crops, grass covered vineyards, tilled vineyards; (ii) to determine whether these patterns mirrored those of below-ground microorganisms and whether the components of γ-diversity followed a similar model. The disturbance regimes affected plant assemblage composition. Species richness decreased with increasing land use intensity, the Shannon index showed the highest values in grasslands and hay crops. Plant assemblage composition patterns mirrored those of Basidiomycota and Ascomycota. Richness in Basidiomycota, denitrifying bacteria and microbial biomass showed the same trend as that observed for vascular plant richness. The Shannon index pattern of below-ground microorganisms was different from that of plants. The plant γ-diversity component model weakly mirrored those of Ascomycota. Patchy diversity patterns suggest that the maintenance of contrasting land uses associated with different productions typical of agro-silvo-pastoral-systems can guarantee the conservation of biodiversity.

Discocyrtanus canjinjim sp. n., belonging to the family Gonyleptidae Sundevall, 1833 is described based on nineteen specimens, eleven adult males and eight adult females, collected in the Vila Bela da Santissima Trindade, in the State of Mato Grosso, Brazil. This new species represents an endemic component for the harvestmen fauna of Chiquitano Dry Forests terrestrial eco-region, being the most occidental point of distribution of the genus, notably found in the Cerrado and the Atlantic Forest. The new species is characterized by femur IV swollen with the same length of dorsal scutum, trochanter IV with prodorsal distal apophysis as a stout hook not bifurcated, and a unique form of genitalia in the genus. This paper also includes the first identification key to the species of the genus after its revalidation.

Three plant oils (Cymbopogon citratus, Cymbopogon martini, and Pelargonium graveolens) were developed as EC formulations and tested for their physical stabilities. EC formulations (10EC, 20EC and 30EC) of C. citratus, C. martini and P. graveolens had emulsion stability, spontaneity property, heat and cold stability. EC formulated plant oils were screened against the major seed borne fungi of rice such as Curvularia lunata, Fusarium moniliforme, Bipolaris oryzae, and Sarocladium oryzae. The level of inhibition varied among the concentrations of EC formulations. Among the three EC formulations, that of C. citratus oil 30EC recorded 100% inhibition on the mycelial growth of test pathogens. In the blotter paper method, rice seeds treated with a formulation of C. citratus oil 30EC controlled the infection of C. lunata, F. moniliforme, B. oryzae and S. oryzae in rice seed to the tune of 66.0%, 60.4%, 66.0% and 69.1%, respectively. Seed soaking with formulation of C. citratus oil 30EC showed the highest percentage of normal seedlings, the lowest number of abnormal seedling and fresh ungerminated seeds when tested with the roll-towel method. Seed soaking with 30EC formulation of C. citratus oil increased seed germination, shoot length, root length and vigour of rice seedlings when tested with the plastic tray method. Transmission of pathogens from seed to seedling was reduced significantly by the 30EC formulation of C. citratus oil when tested with the plastic pot method. The effect of the storage life of the 30EC formulation of C. citratus oil showed that it had retained their antifungal effect till the end of the incubation period (120 days), and is able to inhibit the mycelial growth of all test pathogens to the 100% level.

The molecular techniques are the standard tool for the study of the taxonomic position and phylogenetic affinities of the lymnaeid genus Radix Montfort, 1810, and the majority of the European representatives of this taxon have been studied in this respect. However, a plethora of nominal species of Radix described from Northern Asia (Siberia and the Russian Far East) are still characterized only morphologically, raising some doubts concerning their validity. In this paper, we present the triple (morphological, molecular, and zoogeographical) evidence that there is at least one endemic species of Radix, Radix dolgini (Gundrizer and Starobogatov, 1979), widely distributed in Siberia and Western Mongolia. Phylogenetically, it is a sister species to the European R. labiata (Rossmaessler, 1835) [=R. peregra auct.], and their common ancestor most probably lived in the Pliocene, nearly 3.25Myr ago. Our results assume the existence of an extended dispersal barrier for freshwater hydrobionts between Europe and Siberia in the Late Pliocene that may be important for biogeographical explanations. Three other nominal Siberian species of Radix: R. kurejkae (Gundrizer and Starobogatov, 1979), R. gundrizeri (Kruglov and Starobogatov, 1983), and R. ulaganica (Kruglov and Starobogatov, 1983) proved to be the junior synonyms of R. dolgini.

The recently erected cestode order Diphyllobothriidea is unique among all tapeworm orders in that its species infect all major groups of tetrapods, including man. In the present paper, the vitellogenesis of representatives of all three currently recognized families of this order was evaluated, based on ultrastructural (transmission electron microscopy) and cytochemical (detection of glycogen) observations. Vitelline follicles of all taxa studied, i.e. Cephalochlamys namaquensis from clawed frogs (Xenopus), Duthiersia expansa from monitors (Varanus) and Schistocephalus solidus that matures in fish-eating birds, contain vitelline cells at various stages of development and interstitial cells. Developing vitellocytes are characterized by the presence of mitochondria, granular endoplasmic reticulum and Golgi complexes involved in the synthesis of shell globules and formation of shell globule clusters. Mature vitellocytes contain lipids and glycogen in different proportions. The most significant differences among the three diphyllobothriidean families were found in the presence or absence of lamellar bodies. Variations of vitelline clusters morphology and types of lipid droplets are described and discussed in relation to the presumed evolutionary history of diphyllobothriideans, which belong to the most basal cestode groups.