Biology subjects

Schmahl, W. W.

Publications and source records attributed to Schmahl, W. W..

3 recordsLinked to original sources

bioRxiv2022

Molecular and mineral responses of corals grown under artificial Calcite Sea conditions

The formation of skeletal structures composed of different calcium carbonate polymorphs (aragonite and calcite) appears to be regulated both biologically and environmentally. Among environmental factors influencing aragonite and calcite precipitation, changes in seawater conditions - primarily in the molar ratio of magnesium and calcium during so-called "Calcite" (mMg:mCa below 2) or "Aragonite" seas (mMg:mCa above 2) - have had profound impacts on the distribution and performance of marine calcifiers throughout the Earths history. Nonetheless, the fossil record shows that some species appear to have counteracted such changes and kept their skeleton polymorph unaltered. Here, the aragonitic octocoral Heliopora coerulea and the aragonitic scleractinian Montipora digitata were exposed to Calcite Sea-like mMg:mCa with various levels of changes in magnesium and calcium concentration, and both mineralogical (i.e., CaCO3 polymorph) and gene expression changes were monitored. Both species maintained aragonite deposition at lower mMg:mCa ratios, while concurrent calcite presence was only detected in M. digitata. Despite a strong variability between independent experimental replicates for both species, the expression for a set of putative calcification-related genes, including known components of scleractinian skeleton organic matrix, was found to consistently change at lower mMg:mCa. These results support previously proposed involvements of the skeleton organic matrix in counteracting decreases in seawater mMg:mCa. Although no consistent changes in expression for calcium and magnesium transporters were observed, down-regulation calcium channels in H. coerulea in one experimental replicate and at an mMg:mCa of 2.5 might indicate the possibility of active calcium uptake regulation by the corals under altered mMg:mCa.

paleontology↗

bioRxiv2020

Sponges as bioindicators for microparticulate pollutants

Amongst other threats, the worlds oceans are faced with man-made pollution, including an increasing number of microparticulate pollutants. Sponges, aquatic filter-feeding animals, are able to incorporate fine foreign particles, and thus may be a potential bioindicator for microparticulate pollutants. To address this question, 15 coral reef demosponges sampled around Bangka Island (North Sulawesi, Indonesia) were analyzed for the nature of their foreign particle content using traditional histological methods, advanced light microscopy, and Raman spectroscopy. Sampled sponges accumulated and embedded the very fine sediment fraction (< 200 {micro}m), absent in the surrounding sand, in the ectosome (outer epithelia) and spongin fibers (skeletal elements), which was confirmed by two-photon microscopy. A total of 34 different particle types were identified, of which degraded man-made products, i.e., polystyrene, cotton, titanium dioxide and blue-pigmented particles, were incorporated by eight specimens at concentrations between 91 to 612 particle/g dry sponge tissue. As sponges can weigh several hundreds of grams, we conservatively extrapolate that sponges can incorporate on average 10,000 microparticulate pollutants in their tissue. The uptake of particles, however, appears independent of the material, which suggests that the fluctuation in material ratios is due to the spatial variation of surrounding microparticles. Therefore, sponges have a strong potential to biomonitor microparticulate pollutants, such as microplastics and other degraded industrial products.

ecology↗

bioRxiv2020

Textile waste and microplastic induce activity and development of unique hydrocarbon-degrading marine bacterial communities

Biofilm-forming microbial communities on plastics and textile fibers are of growing interest since they have potential to contribute to disease outbreaks and material biodegradability in the environment. Knowledge on microbial colonization of pollutants in the marine realm is expanding, but metabolic responses during substrate colonization remains poorly understood. Here, we assess the metabolic response in marine microbial communities to three different micropollutants, virgin high-density polyethylene (HDPE) microbeads, polysorbate-20 (Tween), and textile fibers. Intertidal textile fibers, mainly cotton, virgin HDPE, and Tween induced variable levels of microbial growth, respiration, and community assembly in controlled microcosm experiments. RAMAN characterization of the chemical composition of the textile waste fibers and high-throughput DNA sequencing data shows how the increased metabolic stimulation and biodegradation is translated into selection processes ultimately manifested in different communities colonizing the different micropollutant substrates. The composition of the bacterial communities colonizing the substrates were significantly altered by micropollutant substrate type and light conditions. Bacterial taxa, closely related to the well-known hydrocarbonoclastic bacteria Kordiimonas spp. and Alcanivorax spp., were enriched in the presence of textile-waste. The findings demonstrate an increased metabolic response by marine hydrocarbon-degrading bacterial taxa in the presence of microplastics and textile waste, highlighting their biodegradation potential. The metabolic stimulation by the micropollutants was increased in the presence of light, possibly due to photochemical dissolution of the plastic into smaller bioavailable compounds. Our results suggest that the development and increased activity of these unique microbial communities likely play a role in the bioremediation of the relatively long lived textile and microplastic pollutants in marine habitats. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=104 SRC="FIGDIR/small/939876v1_ufig1.gif" ALT="Figure 1"> View larger version (40K): org.highwire.dtl.DTLVardef@19322f3org.highwire.dtl.DTLVardef@dbae7dorg.highwire.dtl.DTLVardef@9c9d4aorg.highwire.dtl.DTLVardef@1aa636_HPS_FORMAT_FIGEXP M_FIG C_FIG

microbiology↗