Evapotranspiration from Spider and Jade Plants Can Improve Relative Humidity in an Interior Environment

Citation: Kerschen, E., Garten, C., Williams, K., & Derby, M. (2016). Evapotranspiration from Spider and Jade Plants Can Improve Relative Humidity in an Interior Environment. HortTechnology, 26(6), 803-810. doi: 10.21273/HORTTECH03473-16Plants in the interiorscape have many documented benefits, but their potential for use in conjunction with mechanical heating, ventilation, and air conditioning (HVAC) systems to humidify dry indoor environments requires more study. In this research, evaporation and evapotranspiration rates for a root medium control, variegated spider plants (Chlorophytum comosum), and green jade plants (Crassula argentea) were measured over 24 hours at 25% and 60% relative humidity (RH) and 20 °C to generate data for calculation of the leaf surface area and number of plants necessary to influence indoor humidity levels. Evaporation and evapotranspiration rates were higher for all cases at 25% RH compared with 60% RH. At 25% RH during lighted periods, evapotranspiration rates were ?15 g·h?1 for spider plants and 8 g·h?1 for jade plants. Spider plants transpired during lighted periods due to their C3 photosynthetic pathway, whereas jade plants had greater evapotranspiration rates during dark periods—about 11 g·h?1—due to their crassulacean acid metabolism (CAM) photosynthetic pathway. A combination of plants with different photosynthetic pathways (i.e., C3 and CAM combination) could contribute to greater consistency between evapotranspiration rates from day to night for humidification of interior spaces. Using the measured data, calculations indicated that 32,300 cm2 total spider plant leaf surface area, which is 25 spider plants in 4-inch-diameter pots or fewer, larger plants, could increase the humidity of an interior bedroom from 20% RH to a more comfortable 30% RH under bright interior light conditions

Genetic elimination of prothrombin in adult mice is not compatible with survival and results in spontaneous hemorrhagic events in both heart and brain

Mice carrying a conditional prothrombin knockout allele (fIIlox) were established to develop an experimental setting for exploring the importance of thrombin in the maintenance of vascular integrity, the inflammatory response, and disease processes in adult animals. In the absence of Cre-mediated recombination, homozygous fIIlox/lox mice or compound heterozygous mice carrying one fIIlox allele and one constitutive-null allele were viable. Young adults exhibited neither spontaneous bleeding events nor diminished reproductive success. However, the induction of Cre recombinase in fIIlox mice using the poly I:C-inducible Mx1-Cre system resulted in the rapid and near-complete recombination of the fIIlox allele within the liver, the loss of circulating prothrombin, and profound derangements in coagulation function. Consistent with the notion that thrombin regulates coagulation and inflammatory pathways, an additional early consequence of reducing prothrombin was impaired antimicrobial function in mice challenged with Staphylococcus aureus peritonitis. However, life expectancy in unchallenged adults genetically depleted of prothrombin was very short (∼5-7 days). The loss of viability was associated with the development of severe hemorrhagic events within multiple tissues, particularly in the heart and brain. Unlike the constitutive loss of either clotting or platelet function alone, the conditional loss of prothrombin is uniformly not compatible with maintenance of hemostasis or long-term survival