Lung Cancer and Air Quality in a Large Urban County in the United States.

Lung cancer is the leading cancer-related killer in the United States. The incidence varies geographically and may be affected by environmental pollutants. Our goal was to determine associations within time series for specific air pollutants and lung cancer cases over a 33-year period in Wayne County, Michigan, controlling for population change. Lung cancer data for Wayne County were queried from the Michigan Cancer Registry from 1985 to 2018. Air pollutant data were obtained from the United States Environmental Protection Agency from 1980 to 2018. Autoregressive distributed lag (ARDL) models were estimated to investigate time lags in years between specific air pollution levels and lung cancer development. A total of 58,866 cases of lung cancer were identified. The mean age was 67.8 years. Females accounted for 53 percent of all cases in 2018 compared to 44 percent in 1985. Three major clusters of lung cancer incidence were detected with the most intense clusters in downtown Detroit and the heavily industrialized downriver area. Sulfur dioxide (SO2) had the strongest statistically significant relationship with lung cancer, showing both short- and long-term effects (lag range, 1-15 years). Particulate matter (PM2.5) (lag range, 1-3 years) and nitrogen dioxide (NO2) (lag range, 2-4 years) had more immediate effects on lung cancer development compared to carbon monoxide (CO) (lag range, 5-6 years), hazardous air pollutants (HAPs) (lag range, 9 years) and lead (Pb) (lag range, 10-12 years), which had more long-term effects on lung cancer development. Areas with poor air quality may benefit from targeted interventions for lung cancer screening and reductions in environmental pollution.

Ocean warming undermines the recovery resilience of New England kelp forests following a fishery-induced trophic cascade.

Ecological theory predicts that kelp forests structured by trophic cascades should experience recovery and persistence of their foundation species when herbivores become rare. Yet, climate change may be altering the outcomes of top-down forcing in kelp forests, especially those located in regions that have rapidly warmed in recent decades, such as the Gulf of Maine. Here, using data collected annually from 30+ sites spanning >350 km of coastline, we explored the dynamics of Maine's kelp forests in the ~20 years after a fishery-induced elimination of sea urchin herbivores. Although forests (Saccharina latissima and Laminaria digitata) had broadly returned to Maine in the late 20th century, we found that forests in northeast Maine have since experienced slow but significant declines in kelp, and forest persistence in the northeast was juxtaposed by a rapid, widespread collapse in the southwest. Forests collapsed in the southwest apparently because ocean warming has-directly and indirectly-made this area inhospitable to kelp. Indeed, when modeling drivers of change using causal techniques from econometrics, we discovered that unusually high summer seawater temperatures the year prior, unusually high spring seawater temperatures, and high sea urchin densities each negatively impacted kelp abundance. Furthermore, the relative power and absolute impact of these drivers varied geographically. Our findings reveal that ocean warming is redefining the outcomes of top-down forcing in this system, whereby herbivore removal no longer predictably leads to a sustained dominance of foundational kelps but instead has led to a waning dominance (northeast) or the rise of a novel phase state defined by "turf" algae (southwest). Such findings indicate that limiting climate change and managing for low herbivore abundances will be essential for preventing further loss of the vast forests that still exist in northeast Maine. They also more broadly highlight that climate change is "rewriting the rules" of nature, and thus that ecological theory and practice must be revised to account for shifting species and processes.

Inflammatory endotype of odontogenic sinusitis.

BACKGROUND: Odontogenic sinusitis (ODS) is distinct from non-odontogenic rhinosinusitis with regard to clinical features as well as diagnostic and therapeutic approaches. While numerous studies have explored immune profiles of chronic rhinosinusitis, very few studies have explored the inflammatory endotype of ODS. METHODS: Odontogenic sinusitis was diagnosed by confirming infectious sinusitis adjacent to infectious maxillary odontogenic pathology. Maxillary sinus cultures and mucosal biopsies were obtained during endoscopic endonasal surgery in ODS and control patients. Controls were patients undergoing endoscopic skull base surgery with no sinus disease. Specimens were snap frozen in liquid nitrogen and stored at -80°C. Analysis was performed using a multiplex assay to measure Th-1 (TNFα, IFNγ, IL-2,12,18), Th-2 (IL-4,5,9,13), Th-17 (IL-17A,17F,22), and innate (CCL5,CXCL9,CXCL10, IL-6,8,10,12,23,27) immune pathways. Groups were compared via independent sample t-tests; if assumptions were violated, nonparametric Wilcoxon ranked sum tests were performed. RESULTS: Specimens from 22 ODS patients were compared to nine controls. ODS mucosal tissue was sampled in the setting of the following dental pathologies: post-dental extraction (n = 15), untreated apical periodontitis (n = 2), apical periodontitis after root canal therapy (n = 2), and maxillary sinus bone grafting with or without dental implantation (n = 3). The following cytokines were significantly elevated in ODS compared to controls: IFNγ, TNFα, IL-6, 8, 10, 27, and CXCL9. IL-17 levels were similar in both ODS and controls. Therefore, ODS demonstrated heightened innate and Th1 immune activity. CONCLUSION: ODS demonstrated both innate immune and Th1 inflammatory endotypes. Further studies are needed to explore ODS immunopathobiology and its potential impact on ODS management.

The precursors of governance in the Maine lobster fishery.

Collective action is more likely to occur and to be effective when it is consistent with the self-interest of the affected individuals. The Maine lobster fishery is an instructive example of biological and technological circumstances combining with individual self-interest to create conditions favorable to collective action. The model describes the way social structure emerges from the adaptive behavior of competing fishers. Fishers compete in two ways: in a scramble to find the lobsters first and by directly interfering in other fishers' ability to compete, i.e., by cutting their traps. Both forms of competition lead fishers to interact frequently and to self-organize into relatively small groups. They learn to restrain their competitive behavior toward their neighbors but do not extend that same restraint to nonneighbors. Groups work within well defined boundaries, contact one another frequently, actively exchange information about the resource, and, most importantly, depend on continuing mutual restraint for their economic well-being. These self-organizing, competitive processes lay the foundation for successful collective action, i.e., mutual agreements that create the additional restraint required for conservation. The modeling approach we use is a combined multiagent and classifier systems simulation. The model allows us to simulate the dynamic adaptation (learning) of multiple individuals interacting in a complex, changing environment and, consequently, provides a way to analyze the fine-scale processes that emerge as the broad social-ecological patterns of the fishery. Patterns generated by the model are compared with patterns observed in a large dataset collected by 44 Maine fishers.

FLORAL STRUCTURE AND ORGANOGENESIS IN PODOPHYLLUM PELTATUM (BERBERIDACEAE).

The life cycle of Podophyllum can be divided into two phases, a subterranean phase during which a conspicuous winter mixed terminal bud forms at the end of a rhizome, and an aerial phase, during which the primordia of the structures within the winter bud give rise the next spring to an aerial shoot composed of a stem, 2 leaves, and a single flower. The transition from a vegetative to a floral apex occurs at the end of July, when the apical meristem becomes a globoid structure. During the first and second weeks of August, the floral organs are laid down along the sides of an elongated floral apex. The order of initiation of the floral organs is sepals, petals, stamens, gynoecium, and stamens. Petal primordia are initiated in early August, but growth ceases after they attain a height of about 2 mm. This inhibition persists until the middle of May in the next growing season, when the petals grow to 12 mm within 2 weeks. At anthesis the petals have enlarged to a length of 2 cm or more. The gynoecium is usually composed of a single terminal carpel. The ovules are chiefly supplied by branches from a ventral bundle complex, but that is supplemented by medullary bundles that are formed in the base of the gynoecium, below the loculus. It could be argued that these medullary bundles are surviving remnants of the vascular supply to a second carpel, no longer extant. A transmitting tract extends from the stigma about half the distance to the loculus. The tract is lined with unicellular glandular cells and is open from the stigma to the loculus.