Thomas Aspray

Thomas Aspray

orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 June 2015 in Environmental Pollution
Verified
Journal Article
Open access
VEVirginia Echavarri-Bravo
Virginia Echavarri-Bravo
LPLynn Paterson
Lynn Paterson
TAThomas Aspray
Thomas Aspray
JPJoanne S. Porter
Joanne S. Porter
MWMichael K. Winson
Michael K. Winson
MHMark Hartl
Mark Hartl
The increasing use of silver nanoparticles (AgNPs) as a biocidal agent and their potential accumulation in sediments may threaten non-target natural environmental bacterial communities. In this study a microcosm approach was established to investigate the effects of well characterized OECD AgNPs (NM-300) on the function of the bacterial community inhabiting marine estuarine sediments (salinity 31‰). The results showed that a single pulse of NM-300 AgNPs (1 mg L(-1)) that led to sediment concentrations below 6 mg Ag kg(-1) dry weight inhibited the bacterial utilization of environmentally relevant carbon substrates. As a result, the functional diversity changed, but recovered after 120 h under the experimental conditions. This microcosm study suggests that AgNPs under environmentally relevant experimental conditions can negatively affect bacterial function and provides an insight into the understanding of the bacterial community response and resilience to AgNPs exposure, important for informing relevant regulatory measures.

1 December 2014 in Environmental Pollution
Verified
Journal Article
Closed access
FMFlorian Mallevre
Florian Mallevre
Teresa FernandesTeresa Fernandes
Teresa Fernandes
TAThomas Aspray
Thomas Aspray

16 September 2006 in Mycorrhiza
Verified
Journal Article
Closed access
PDF file
TAThomas Aspray
Thomas Aspray
PFPascale Frey-Klett
Pascale Frey-Klett
JJJulie E. Jones
Julie E. Jones
JWJohn M. Whipps
John M. Whipps
JGJean Garbaye
Jean Garbaye
GBGary Bending
Gary Bending

9 February 2013 in Mycorrhiza
Verified
Journal Article
Closed access
PDF file
TAThomas Aspray
Thomas Aspray
EJEirian Jones
Eirian Jones
MDM. W. Davies
M. W. Davies
MSM. Shipman
M. Shipman
GBGary Bending
Gary Bending

1 April 2006 in FEMS Microbiology Ecology
Verified
Journal Article
Open access
PDF file
TAThomas Aspray
Thomas Aspray
EJEirian Jones
Eirian Jones
JWJohn M. Whipps
John M. Whipps
GBGary Bending
Gary Bending
Mycorrhization helper bacteria, Paenibacillus sp. EJP73 and Burkholderia sp. EJP67, were used to study the importance of bacterial inoculum dose and bacterial derived soluble and volatile metabolites localization for enhancing mycorrhiza formation in the Pinus sylvestris-Lactarius rufus symbiosis, using a laboratory based microcosm. EJP73 and EJP67 produced different responses in relation to the inoculum dose; EJP73 significantly enhanced mycorrhiza formation to the same degree at all doses tested (105, 107, 109 and 1010 CFU mL−1), whereas, EJP67 only stimulated mycorrhiza formation within a narrow range of inoculum densities (107 and 109 CFU mL−1). The importance of soluble bacterial metabolites was assessed by applying spent broth derived from exponential and stationary phase bacterial cultures to microcosms. No spent broth enhanced mycorrhiza formation over the control. As EJP73 produced the helper effect over a wide range of inoculum doses, this bacterium was chosen for further study. Physical separation of EJP73 from the fungal and plant symbiosis partners was carried out, in order to determine the contribution of constitutively produced bacterial volatile metabolites to the mycorrhization helper bacteria effect. When EJP73 was physically separated from the symbiosis, it had a significant negative effect on mycorrhiza formation. These results suggest that close proximity, or indeed cell contact, is required for the helper effect. Therefore, fluorescent in situ hybridization in conjunction with cryosectioning was used to determine the localization of EJP73 in mycorrhizal tissue. The cells were found to occur as rows or clusters (∼10 cells) within the mycorrhizal mantle, both at the root tip and along the length of the mycorrhizal short roots.

10 February 2021 in Indoor Air
Verified
Journal Article
Open access
PDF file
Michael GormleyMichael Gormley
Michael Gormley
TAThomas Aspray
Thomas Aspray
DKDavid Kelly
David Kelly
Aerosols are readily transported on airstreams through building sanitary plumbing and sewer systems, and those containing microbial pathogens (known as bioaerosols) are recognized as contributors to infection spread within buildings. When a defect occurs in the sanitary plumbing system that affects the system integrity, a cross‐transmission route is created that can enable the emission of bioaerosols from the system into the building. These emission occurrences are characterized as short‐burst events (typically 99.5%) were 11 μm anywhere in the system. Particle count was influenced by toilet flush volume, but it was not possible to determine if there was any direct influence from airflow rate since both particle and biological data showed no correlation with upward airflow rates and velocities. Typical emissions resulting from a 6 L toilet flush were in the range of 280–400 particles per second at a concentration of typically 9–12 number per cm3 and a total particle count in the region of 3000 to 4000 particles, whereas the peak emissions from a 1.2 L toilet flush were 60–80 particles per second at a concentration of 2.4–3 number per cm3 and a total particle count in the region of 886 to 1045 particles. The reduction in particles is in direct proportion to the reduction in toilet flush volume. The slit‐to‐agar sampler was able to provide viable time course CFU data and confirmed the origin of the particles to be the tracer microorganism flushed into the system. The time course data also have characteristics consistent with the unsteady nature of a toilet flush.