20 research outputs found
Intestinal parasites from public and private latrines and the harbour canal in Roman Period Ephesus, Turkey (1st c. BCE to 6th c. CE)
To improve our knowledge of the parasite species affecting the inhabitants of Roman period Asia Minor, we analysed faecal material from Ephesus, Turkey. Mineralised material from the drain from a private house latrine (3rd c. CE), sediment samples from the sewer drain of a public communal latrine (6th c. CE), and sediment from the harbour canal (ca. 1st c. BCE to ca. 6th c. CE) were studied for the presence of intestinal parasites. Samples were viewed by light microscopy for helminth eggs, and commercial enzyme-linked immunosorbent assay (ELISA) kits were used to test for protozoal parasites that cause dysentery. Eggs of roundworm were found in the public latrine, whipworm in the house latrine, and both whipworm and roundworm in the harbour canal. Sequential sampling of the harbour core suggests that whipworm was by far the most common parasite throughout the Roman period, and there was no clear evidence for change in parasite species over the centuries. Whipworm and roundworm are both spread by the contamination of food and drink by human faeces. Despite the large number of travellers to Ephesus, as the capital of its province and a major port city in the Roman Empire, there was a surprising lack of diversity in parasite species found. This is especially apparent when we consider that ten species of intestinal parasite have been found across the Roman Empire. This is the first Roman site to be directly assessed for differences between infection in individuals using private latrines, public latrines, and mixed town effluent (in the harbour) at the same site.This research was supported by a doctoral award from the Social Sciences and Humanities Research Council of Canada [752-2016-2085] and a Tidmarsh Cambridge Scholarship from the Cambridge Commonwealth, European and International Trust and Trinity Hall Colleg
Tropospheric column amount of ozone retrieved from SCIAMACHY limb–nadir-matching observations
Tropospheric ozone (O<sub>3</sub>), has two main sources: transport from the
stratosphere and photochemical production in the troposphere. It plays
important roles in atmospheric chemistry and climate change. Its amount and
destruction are being modified by anthropogenic activity. Global measurements
are needed to test our understanding of its sources and sinks. In this
paper, we describe the retrieval of tropospheric O<sub>3</sub> columns (TOCs)
from the combined limb and nadir observations (hereinafter referred to as
limb–nadir-matching (LNM)) of the SCanning Imaging Absorption spectroMeter
for Atmospheric CHartographY (SCIAMACHY) instrument, which flew as part of
the payload onboard the European Space Agency (ESA) satellite Envisat
(2002–2012). The LNM technique used in this study is a residual approach
that subtracts stratospheric O<sub>3</sub> columns (SOCs), retrieved from the limb
observations, from the total O<sub>3</sub> columns (TOZs), derived from the nadir
observations. The technique requires accurate knowledge of the SOCs, TOZs,
tropopause height, and their associated errors. The SOCs were determined from
the stratospheric O<sub>3</sub> profiles retrieved in the Hartley and Chappuis bands
from SCIAMACHY limb scattering measurements. The TOZs were also derived from
SCIAMACHY measurements, but in this case from the nadir viewing mode using
the Weighting Function Differential Optical Absorption Spectroscopy (WFDOAS)
technique in the Huggins band. Comparisons of the TOCs from SCIAMACHY and
collocated measurements from ozonesondes in both hemispheres between
January 2003 and December 2011 show agreement to within 2–5 DU
(1 DU = 2.69 × 10<sup>16</sup> molecules cm<sup>−2</sup>). TOC values
from SCIAMACHY have also been compared to the results from the Tropospheric
Emission Spectrometer (TES) and from the LNM technique exploiting Ozone
Monitoring Instrument (OMI) and Microwave Limb Sounder (MLS) data
(hereinafter referred to as OMI/MLS). All compared data sets agree
within the given data product error range and exhibit similar seasonal
variations, which, however, differ in amplitude. The spatial distributions of
tropospheric O<sub>3</sub> in the SCIAMACHY LNM TOC product show characteristic
variations related to stratosphere–troposphere exchange (STE) processes,
anthropogenic activities and biospheric emissions
Numerical simulations examining the possible role of anthropogenic and volcanic emissions during the 1997 Indonesian fires
�ber Vorkommen, Pathogenese und M�glichkeiten zur Prophylaxe der durch Nitrit verursachten Meth�moglobin�mie
Intercomparison of oxygenated volatile organic compound measurements at the SAPHIR atmosphere simulation chamber
This paper presents results from the first large-scale in situ intercomparison of oxygenated volatile organic compound (OVOC) measurements. The intercomparison was conducted blind at the large (270 m(3)) simulation chamber, Simulation of Atmospheric Photochemistry in a Large Reaction Chamber (SAPHIR), in Julich, Germany. Fifteen analytical instruments, representing a wide range of techniques, were challenged with measuring atmospherically relevant OVOC species and toluene (14 species, C-1 to C-7) in the approximate range of 0.5-10 ppbv under three different conditions: (1) OVOCs with no humidity or ozone, (2) OVOCs with humidity added (r.h. approximate to 50%), and (3) OVOCs with ozone (approximate to 60 ppbv) and humidity (r.h. approximate to 50%). The SAPHIR chamber proved to be an excellent facility for conducting this experiment. Measurements from individual instruments were compared to mixing ratios calculated from the chamber volume and the known amount of OVOC injected into the chamber. Benzaldehyde and 1-butanol, compounds with the lowest vapor pressure of those studied, presented the most overall difficulty because of a less than quantitative transfer through some of the participants' analytical systems. The performance of each individual instrument is evaluated with respect to reference values in terms of time series and correlation plots for each compound under the three measurement conditions. A few of the instruments performed very well, closely matching the reference values, and all techniques demonstrated the potential for quantitative OVOC measurements. However, this study showed that nonzero offsets are present for specific compounds in a number of instruments and overall improvements are necessary for the majority of the techniques evaluated here