This paper elucidates the phytoremediation potential of water hyacinth (Eichhornia crassipes [Mart.] Solms) for TN and TP rich industrial wastewaters determined for 15 weeks under different set-ups of 2-fold (56 TN mg/l and 15.4 TP mg/l), 1-fold, 1/2-fold, 1/4-fold and 1/8-fold and a control with no nutrients in duplicate. A mass balance was conducted to evaluate the phytoremediation efficiencies and to identify the key mechanisms of nutrient removal from the wastewaters. Our results manifested that water hyacinth is a promising candidate for a batch removal of TN and TP from wastewaters. 100% removal of both TN and TP was observed at the end of the 9th week in all the set-ups mainly due to assimilation and the period between 6Ð9 weeks became the optimum period after which complete harvesting is recommended. Plants having an age of 6 weeks are ideal to commence the free-floating wetland and 21 days hydraulic retention time (HRT) is recommended for optimum removal of TN and TP. Assimilation and denitrification were the key mechanisms of TN removal while assimilation and sorption became the prominent mechanisms in the removal of TP from wastewaters.

Significance: The fundamental processes of life are organized and based on common basic principles. Molecular organizers, often interacting with the membrane, capitalize on cellular polarity to precisely orientate essential processes. The study of organisms lacking apparent polarity or known cellular organizers (e.g., the bacterium Staphylococcus aureus ) may enable the elucidation of the primal organizational drive in biology. How does a cell choose from infinite locations in its membrane? We have discovered a structure in the S. aureus membrane that organizes processes indispensable for life and can arise spontaneously from the geometric constraints of protein complexes on membranes. Building on this finding, the most basic cellular positioning system to optimize biological processes, known molecular coordinators could introduce further levels of complexity.

Innate lymphoid cells are central to the regulation of immunity at mucosal barrier sites, with group 2 innate lymphoid cells (ILC2s) being particularly important in type 2 immunity. In this study, we demonstrate that microRNA(miR)-142 plays a critical, cell-intrinsic role in the homeostasis and function of ILC2s. Mice deficient for miR-142 expression demonstrate an ILC2 progenitor–biased development in the bone marrow, and along with peripheral ILC2s at mucosal sites, these cells display a greatly altered phenotype based on surface marker expression. ILC2 proliferative and effector functions are severely dysfunctional following Nippostrongylus brasiliensis infection, revealing a critical role for miR-142 isoforms in ILC2-mediated immune responses. Mechanistically, Socs1 and Gfi1 expression are regulated by miR-142 isoforms in ILC2s, impacting ILC2 phenotypes as well as the proliferative and effector capacity of these cells. The identification of these novel pathways opens potential new avenues to modulate ILC2-dependent immune functions. Key Points MicroRNA-142 isoforms critically regulate ILC2 homeostasis and effector functions. MicroRNA-142 isoforms regulate the ILC2 lineage cell intrinsically. Socs1 and Gfi1 are miR-142 isoform regulated targets in ILC2s. Visual Abstract