Untersuchungen über die Kreuzbarkeit innerhalb des Subtribus Triticinae

Ohne ZusammenfassungMit 2 Textabbildungen     

Pollination biology of Aristolochia bianorii Sennen & Pau: promoting cross-pollination but assuring reproductive success in island ecosystems

• Deceptive pollination has been reported in the genus Aristolochia, but the floral biology and pollination strategy of A. bianorii, an endemic of the Balearic Islands, have not yet been studied. Here, we investigated floral anthesis, mating system, pollinators and volatile organic compounds (VOCs) emitted by its flowers.
• Flower buds were marked and monitored daily to define floral stages and their duration. Experimental bagging and hand-pollination were performed to test for autonomous self-pollination, induced self-pollination and cross-pollination. Flowers were collected to analyse the presence of entrapped pollinators. VOCs emitted by flowers were evaluated by means of solid phase microextraction followed by immediate GC–MS.
• Anthesis lasted between 63 and 96 h, and the species exhibited autonomous self-pollination with moderate inbreeding depression. Pollinators were mainly females of Oscinomorpha longirostris (Diptera; Chloropidae). The number of pollinators inside flowers was affected by floral stage and time of flowering. The most common VOCs were alkanes, oximes, esters, alkenes, cyclic unsaturated hydrocarbons, isocyanates, amides and carboxylic acids.
• Aristolochia bianorii can set seed by autonomous self-pollination, in contrast to other Aristolochia species, in which both protogyny and herkogamy prevent autonomous self-pollination. However, the species may encourage cross-pollination by attracting female chloropid flies though emission of floral scents that may mimic an oviposition site and, possibly, freshly killed true bugs (i.e. Heteroptera). In conclusion, A. bianorii promotes cross-pollination, but delayed autonomous self-pollination assures reproductive success in the putative absence of pollinators.

     

Population genetic suggestions to offset the extinction ratchet in the endangered Canarian endemic Atractylis preauxiana (Asteraceae)

We examined the levels and apportionment of genetic variation of the 11 known subpopulations of Atractylis preauxiana at 95 RAPD loci to help streamline a conservation strategy for this Canarian endemic taxon, which is in a critical situation because of the constant exposure of plants to intensive, uncontrolled anthropic action in the last few decades. Our results revealed low genetic variation levels that match with the general picture of demographic and habitat degradation that this taxon is undergoing. Although geographic isolation between Tenerife and Gran Canaria is an effective barrier to gene flow, genetic heterogeneity within islands is also substantial, plausibly due to the negative impact of fragmentation on genetic variation. Our genetic results, together with declining population sizes, poor seedling survival, and recent population extinctions, compellingly indicate that A. preauxiana is undergoing an extinction ratchet, whereby every further local extinction will add up to the probability of total species’ extinction. Our genetic results suggest that mitigating the deleterious consequences of this effect entails urgent mixed reinforcements of all sub-populations with sub-populations from the same island and urgent translocation of the two sub-populations from Tenerife that are doomed to extinction to ecologically suitable areas, together with seed collection and preservation in a convenient ex situ banking facility.     

Ecological and Conservation Significance of Herpesvirus Infection in Neotropical Bats

EcoHealth - Bats are the second most diverse order of mammals and key species for ecosystem functioning, providing a wide range of ecosystem services, from pest control to seed dispersal....     

Molecular mechanism of the association and dissociation of Deltarasin from the heterodimeric KRas4B-PDEδ complex

The formation of the KRas4B-PDEδ complex activates different signaling pathways required for the development and maintenance of cancer. Previous experimental and theoretical studies have allowed researchers to design an inhibitor of the KRas4B-PDEδ complex, “Deltarasin.” This inhibitor binds to the prenyl-binding pocket of PDEδ and subsequently inhibits the proliferation of human pancreatic ductal adenocarcinoma cells that depend on oncogenic KRas4B. Nevertheless, structural and energetic information about the inhibitory effects of Deltarasin on the KRas4B-PDEδ complex are not available. In this study, we explore the properties of Deltarasin in inhibiting the formation of wild-type and mutant KRas4B-PDEδ complexes present in different cell lines expressing mutant RAS genes (G12D, G12C, G12V, G13D, Q61L, and Q61R) using 1.7 μs molecular dynamics (MD) simulations in combination with the MMGBSA approach. Our results revealed the energetic and structural mechanisms that suggest a higher affinity of Deltarasin for PDEδ than the farnesylated HVR. Moreover, Deltarasin exerts another dissociative effect by binding to the protein-protein dimeric interface of wild-type KRas4B-PDEδ, whereas associative and dissociative effects were observed for mutant KRas4B-PDEδ, providing a mechanistic explanation for the inhibitory effects of Deltarasin on different cancer cell lines.