Many aquatic species have restricted dispersal capabilities, making them the most vulnerable organisms to climate change and land use change patterns. These factors deplete Nymphaea species’ suitable habitats, threatening their populations and survival. In addition, the species are poorly documented, which may indicate how scarce they are or will become. Members of Nymphaea are ecologically important as well as having cultural and economic value, making them of conservation interest. Therefore, using the maximum entropy (MaxEnt) approach, climatic variables, land use, and presence points were modeled for seven Nymphaea species in South America, using three general circulation models (CCSM4, HADGEM2-AO, and MIROC5) and in two representative concentration pathways (RCPs 4.5 and 8.5) and two scenarios (2050 and 2070). Our results indicated that mean diurnal range (bio2), precipitation of the wettest month (bio13), temperature seasonality (bio15), and land use (dom_lu) were the main influencing factors. For all species, suitable areas were concentrated east of Brazil, and they were variable in northern parts of the continent. Besides, inconsistent expansion and contraction of suitable habitats were noticed among the species. For example, N. amazonum, N. rudgeana, and N. lasiophylla future habitat expansions declined and habitat contraction increased, while for N. ampla and N. jamesoniana, both future habitat expansion and contraction increased, and for N. pulchella and N. rudgeana it varied in the RCPs. Moreover, the largest projected suitable habitats were projected outside protected areas, characterized by high human impacts, despite our analysis indicating no significant change between protected and unprotected areas in suitable habitat change. Finally, understanding how climate change and land use affect species distribution is critical to developing conservation measures for aquatic species.

Lupeol, a natural lupane-type pentacyclic triterpene, possesses various pharmacological properties, and its production attracts attention. Significant quantities of lupeol are deposited on the castor aerial organ surface and are easily extractable as a predominant wax constituent. Thus, castor might be considered as a potential bioreactor for the production of lupeol. The lupeol biosynthesis pathway is well known, but how it is regulated remains largely unknown. Among large numbers of castor cultivars, we targeted one accession line (337) with high levels of lupeol on its stem surface and low levels thereof on its hypocotyl surface, implicating that lupeol synthesis is differentially regulated in the two organs. To explore the underlying mechanisms, we did comparative transcriptome analysis of the first internode of 337 stem and the upper hypocotyl. Our results show that large amounts of auxin-related genes are differentially expressed in both parts, implying some possible interactions between auxin and lupeol production. We also found that several auxin-responsive cis-elements are present in promoter regions of HMGR and LUS genes encoding two key enzymes involved in lupeol production. Furthermore, auxin treatments apparently induced the expression levels of RcHMGR and RcLUS. Furthermore, we observed that auxin treatment significantly increased lupeol contents, whereas inhibiting auxin transport led to an opposite phenotype. Our study reveals some relationships between hormone activity and lupeol synthesis and might provide a promising way for improving lupeol yields in castor.

Protea kilimandscharica is endemic to the heath zone of Mt Kenya, restricted to the rocky slopes of the mountain. The complete chloroplast genome of P. kilimandscharica was determined by next-generation sequencing technology, with a total length of 158,657 bp. The cp genome encodes 115 unique genes, with four rRNA genes, 81 protein-coding genes (PCGs), and 30 tRNA genes. A 3.1 kb inversion was noted in the LSC. Phylogenetic analysis, based on 75 common protein-coding genes revealed P. kilimandscharica as sister to Macadamia integrifolia and Macadamia ternifolia.