Search for: All records

Abstract Community science programs enable the collection of large amounts of important data and enhance the appreciation of science among members of the public. However, there are challenges in the establishment of successful community science programs.We report the challenges associated with the recent establishment of a community science program to monitor rare plants in the geographically diverse southern Illinois, USA region.Over the first 3 years, our program has been successful in the collection of over 250 monitoring records for rare species through the recruitment of a group of passionate volunteers. However, our volunteers are predominantly middle‐income, college educated, white females who are not representative of the population at large of the region. We propose a recruitment strategy to broaden the diversity of our volunteers by better engaging community members who are not typically involved with plant monitoring but are interested in hiking, walking in natural areas, gardening, and restoration activities, and others who would like the opportunity to collaborate with scientists and researchers in addressing an environmental issue.Practical implication: Community science plant monitoring programs face challenges in recruitment, retention, remoteness of field sites and data quality. Addressing these challenges through targeted recruitment strategies aimed at reducing structural and cultural barriers to participation, along with frequent program assessment, is necessary to enhance the success of these programs. 

Although the evolution of spores was critical to the diversification of plants on land, sporogenesis is incompletely characterized for model plants such as Physcomitrium patens . In this study, the complete process of P. patens sporogenesis is detailed from capsule expansion to mature spore formation, with emphasis on the construction of the complex spore wall and proximal aperture. Both diploid (sporophytic) and haploid (spores) cells contribute to the development and maturation of spores. During capsule expansion, the diploid cells of the capsule, including spore mother cells (SMCs), inner capsule wall layer (spore sac), and columella, contribute a locular fibrillar matrix that contains the machinery and nutrients for spore ontogeny. Nascent spores are enclosed in a second matrix that is surrounded by a thin SMC wall and suspended in the locular material. As they expand and separate, a band of exine is produced external to a thin foundation layer of tripartite lamellae. Dense globules assemble evenly throughout the locule, and these are incorporated progressively onto the spore surface to form the perine external to the exine. On the distal spore surface, the intine forms internally, while the spiny perine ornamentation is assembled. The exine is at least partially extrasporal in origin, while the perine is derived exclusively from outside the spore. Across the proximal surface of the polar spores, an aperture begins formation at the onset of spore development and consists of an expanded intine, an annulus, and a central pad with radiating fibers. This complex aperture is elastic and enables the proximal spore surface to cycle between being compressed (concave) and expanded (rounded). In addition to providing a site for water intake and germination, the elastic aperture is likely involved in desiccation tolerance. Based on the current phylogenies, the ancestral plant spore contained an aperture, exine, intine, and perine. The reductive evolution of liverwort and hornwort spores entailed the loss of perine in both groups and the aperture in liverworts. This research serves as the foundation for comparisons with other plant groups and for future studies of the developmental genetics and evolution of spores across plants. 

Weed community structure, including composition, taxonomic and functional diversity, may explain variability in crop quality, adding to the variability accounted by management, climatic and genetic factors. Focusing on Mediterranean rainfed wheat crops, we sampled weed communities from 26 fields in Spain that were either organically or conventionally managed. Weed communities were characterized by their abundance and taxonomic, compositional and trait-based measures. Grain protein concentration and the glutenin to gliadin ratio were used as indicators of wheat grain quality. Linear mixed effects models were used to analyze the relationship between crop quality and weed community variables, while accounting for environmental factors. Nitrogen fertilization, previous crop and precipitation explained a large portion of the variation in wheat grain protein concentration (R2marginal = 0.39) and composition (R2marginal = 0.26). Weed community measures had limited effects on grain quality (increasing R2marginal of models by 1% on average). The weed effects were related to the composition and the functional structure of their communities, but not to their abundance. Environmental conditions promoting higher protein concentration were also selecting for weed species with competitive attributes, whereas the role of weed functional diversity depended on the functional trait and on the resource limiting crop grain quality. Understanding the mechanisms of weed effects on crop quality could aid on designing sustainable weed management practices. 

Urban green space, comprising parks, fields, woodlands, and other semi-natural areas, is a fundamental component of urban ecosystems. The determination of the relationship between urban green space and urban sprawl is necessary to understand urbanization and the provision of urban ecosystem services. It has been hypothesized that the center of urban (i.e., population and economic) areas in fast-growing cities would migrate toward urban green space over time. To test this hypothesis, urban expansion and urban green space expansion were examined in five cities in China and five cities in the U.S. that were experiencing high rates of growth. Landsat images of those cities from 2000 to 2017 were combined with annual population and economic data and used to quantify the extent and migration of the urban green space. These data were analyzed using the center of gravity method by Grether and Mathys and circular statistics were used to determine the relationship between urban green space and urban expansion. Eight out of the ten cities showed a divergent pattern, i.e., the population and economic centers moved in a different direction to that of the urban green space. The movement of the mean centers of the urban green spaces in the U.S. cities was more consistent than that of the Chinese cities. Over 18 years, the movement of urban green space and urban expansion in the 10 cities showed a synchronous growth trend; however, the proportion of urban green space in the cities decreased. The urban expansion rate exceeded the population growth rate, which led to problems with an unreasonable urban sprawl that is likely to deplete the provision of ecosystem services in the future. In conclusion, the centrifugal forces of urban green space that lead to the movement of population and economic centers away from green spaces play a larger role in urban change than the centripetal forces that pull these centers toward urban green space. 

The placenta of hornworts is unique among bryophytes in the restriction of transfer cells that are characterized by elaborate wall labyrinths to the gametophyte generation. During development, cells around the periphery of the sporophyte foot elongate, forming smooth-walled haustorial cells that interdigitate with gametophyte cells. Using immunogold labeling with 22 antibodies to diverse cell wall polymers, we examined compositional differences in the developmentally and morphologically distinct cell walls of gametophyte transfer cells and sporophyte haustorial cells in the placenta of Phaeoceros. As detected by Calcofluor White fluorescence, cellulose forms the cell wall scaffolding in cells on both sides of the placenta. Homogalacturonan (HG) and rhamnogalacturonan I (RG-I) pectins are abundant in both cell types, and haustorial cells are further enriched in methyl-esterified HGs. The abundance of pectins in placental cell walls is consistent with the postulated roles of these polymers in cell wall porosity and in maintaining an acidic apoplastic pH favorable to solute transport. Xyloglucan hemicellulose, but not mannans or glucuronoxylans, are present in cell walls at the interface between the two generations with a lower density in gametophytic wall ingrowths. Arabinogalactan proteins (AGPs) are diverse along the plasmalemma of placental cells and are absent in surrounding cells in both generations. AGPs in placental cell walls may play a role in calcium binding and release associated with signal transduction as has been speculated for these glycoproteins in other plants. Callose is restricted to thin areas in cell walls of gametophyte transfer cells. In contrast to studies of transfer cells in other systems, no reaction to the JIM12 antibody against extensin was observed in Phaeoceros. 

A robust spore wall was a key requirement for terrestrialization by early plants. Sporopollenin in spore and pollen grain walls is thought to be polymerized and cross-linked to other macromolecular components, partly through oxidative processes involving H 2 O 2 . Therefore, we investigated effects of scavengers of reactive oxygen species (ROS) on the formation of spore walls in the moss Physcomitrella patens (Hedw.) Bruch, Schimp & W. Gümbel. Exposure of sporophytes, containing spores in the process of forming walls, to ascorbate, dimethylthiourea, or 4-hydroxy-TEMPO prevented normal wall development in a dose, chemical, and stage-dependent manner. Mature spores, exposed while developing to a ROS scavenger, burst when mounted in water on a flat slide under a coverslip (a phenomenon we named “augmented osmolysis” because they did not burst in phosphate-buffered saline or in water on a depression slide). Additionally, the walls of exposed spores were more susceptible to alkaline hydrolysis than those of the control spores, and some were characterized by discontinuities in the exine, anomalies in perine spine structure, abnormal intine and aperture, and occasionally, wall shedding. Our data support the involvement of oxidative cross-linking in spore-wall development, including sporopollenin polymerization or deposition, as well as a role for ROS in intine/aperture development.