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Abstracts (PDF file, 1.8MB) - Society for Risk Analysis

Abstracts (PDF file, 1.8MB) - Society for Risk Analysis

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SRA 2013 Annual Meeting <strong>Abstracts</strong><br />

T4-K.1 Stern, PC; National Research Council; pstern@nas.edu<br />

Design principles <strong>for</strong> governing risks from emerging<br />

technologies<br />

Technological innovations are developed and promoted <strong>for</strong> the<br />

benefits they are expected to bring. The benefits tend to be<br />

readily apparent, with data that are ostensible and repeatable;<br />

the costs, particularly those that are delayed or borne by<br />

non-adopters, are usually less so, at least at first. Consequently,<br />

initial judgments about the relative benefits and costs of<br />

innovations must often be revised in light of experience, in<br />

processes that can be contentious. This paper reports on a<br />

project that began in the National Research Council’s<br />

Committee on the Human Dimensions of Global Change (now<br />

the Board on Environmental Change and <strong>Society</strong>), which sought<br />

to distill general lessons on the governance of emerging<br />

technologies. It relied on two sources: (1) induction from<br />

experience with emerging technologies, mainly technologies<br />

now in place (nuclear power, radioactive waste management,<br />

and DNA manipulation) but also at some that were emerging at<br />

the time the project began in 2008 (nanotechnology,<br />

biotechnology, and in<strong>for</strong>mation science and technology); and<br />

(2) inference from the results of social scientific research on<br />

potentially relevant social processes, such as risk perception<br />

and management, management of common-pool resources, the<br />

workings of international institutions and networks, and science<br />

communication and utilization. The paper reports on this<br />

project and then proposes a set of design principles <strong>for</strong> the<br />

governance of emerging technological risks, and then briefly<br />

discuss how those principles might be applied to consider the<br />

risks associated with the extraction of natural gas and oil from<br />

shale <strong>for</strong>mations by horizontal drilling and hydraulic fracturing.<br />

T2-E.1 Stewart, RN*; Bright, EA; Rose, AN; McGinn, CW;<br />

Bhaduri, BL; Oak Ridge National Laboratory;<br />

stewartrn@ornl.gov<br />

Enriching Environmental <strong>Risk</strong> Based Decision Support<br />

Models with Large Scale, High Resolution Population<br />

Data<br />

For nearly two decades, the Spatial <strong>Analysis</strong> and Decision<br />

Assistance freeware package (SADA) has enabled<br />

environmental risk assessors to situate risk analytics within a<br />

spatial context. By integrating risk models articulated by EPA<br />

Superfund with advanced geospatial methods, methods have<br />

been developed <strong>for</strong> directly inferring risk in<strong>for</strong>med sample<br />

designs, remedial designs, cost analysis, and uncertainty<br />

analysis within a free and open modeling environment.<br />

Currently, these models focus on a hypothetical receptor<br />

engaging in contamination under current or future landuse<br />

scenarios and do not consider the existing population<br />

distribution or sociocultural processes near these impacted<br />

areas. In the next expansion of SADA, we integrate Oak Ridge<br />

National Laboratory’s LandScan population dataset with the<br />

current collection of existing analytics and significantly extend<br />

the ability to assess exposure and risks to impacted populations<br />

and demographic sub-populations. Explicitly modeling and<br />

visualizing the spatial context within which contamination,<br />

population dynamics, and exposure occur can substantially<br />

in<strong>for</strong>m policy <strong>for</strong>mulation and evaluation. This paper discusses<br />

integration of LandScan with SADA, adjustment and expansion<br />

of existing analytics, and presents a case study.<br />

P.52 Stewart, D*; Glass-Mattie, D; Dorman, D; McConnell, E;<br />

Adeshina, F; University of Tennessee and Oak Ridge National<br />

Laboratory; dstewart@utk.edu<br />

Provisional Advisory Level (PAL) Development <strong>for</strong><br />

Superwarfarins (Brodifacoum and Bromidalone)<br />

PAL values developed <strong>for</strong> hazardous materials by the US EPA<br />

represent general public emergency exposure limits <strong>for</strong> oral<br />

and inhalation exposures corresponding to three different<br />

severity levels (1, 2, and 3) <strong>for</strong> 24-hr, 30-d, 90-d, and 2-yr<br />

durations. PAL 1 represents the threshold <strong>for</strong> mild effects; PAL<br />

2 represents the threshold <strong>for</strong> serious, irreversible or<br />

escape-impairing effects; PAL 3 represents the threshold <strong>for</strong><br />

lethal effects. PALs have not been promulgated nor have they<br />

been <strong>for</strong>mally issued as regulatory guidance. They are intended<br />

to be used at the discretion of risk managers in emergency<br />

situations when site-specific risk assessments are not available.<br />

The mention of trade names does not imply EPA endorsement.<br />

PAL values were developed based on the SOP and QAPP<br />

requirements. Brodifacoum (CAS No. 56073-10-0) and<br />

Bromadiolone (CAS No. 28772-56-7) are both members of the<br />

newer generations of anticoagulant rodenticides collectively<br />

named superwarfarins. Anticoagulant rodenticides have been<br />

used historically as effective means to control populations of<br />

mice, rats and other rodents in urban and agricultural settings.<br />

All anticoagulants act by preventing the coagulation cascade,<br />

which can cause free bleeding that can be fatal. Superwarfarins<br />

work by inhibiting vitamin K1 epoxide reductase, which leads to<br />

a depletion of vitamin K1 and impairment of blood clotting<br />

ability. In humans and animals, Vitamin K1 can be administered<br />

after ingestion to act as an antidote to prevent free bleeding.<br />

Brodifacoum and bromadiolone are absorbed quickly,<br />

distributed primarily to the liver and excreted in the feces,<br />

mostly unchanged. Oral PAL values were developed by using<br />

human case reports and animal data. Oral PAL 1, 2, and 3<br />

values are 0.017, 0.16, and 1.8 mg/L <strong>for</strong> 24-hours and NR (not<br />

recommended), 0.0025, and 0.0075 mg/L <strong>for</strong> 30-days. Values<br />

are not recommended <strong>for</strong> 90-day and 2-year oral exposure and<br />

all inhalation durations due to insufficient data.<br />

M2-F.5 Stillman, M; Consultant; mstillman@kleinfelder.com<br />

<strong>Risk</strong>-based Need Assessments to Enhance Enterprise<br />

Program Management Offices<br />

In many industries team leaders and organizations are under<br />

constant pressure to deliver a portfolio of projects on time and<br />

within budget. Project Management Offices (PMO) are set up to<br />

address this challenge through the development of standard<br />

Project Management processes, and act as a central repository<br />

<strong>for</strong> Project Management knowledge, best practices and lessons<br />

learned. The best return on the PMO investment is realized by<br />

per<strong>for</strong>ming Need Assessments which result in the development<br />

of Project Management plans that decrease work flow<br />

complexity and increase project savings. Need Assessments are<br />

customarily conducted with key functional groups within an<br />

organization <strong>for</strong> the purpose of improving processes by<br />

identifying gaps between existing and desired conditions. The<br />

fundamental value is derived by gaining deeper insights into<br />

project risks from multiple perspectives that lead to improved<br />

clarity on the priority and sequence <strong>for</strong> task implementation.<br />

Key stages of the Need Assessment process to be described are:<br />

(1) goal setting with PMO Director, (2) data gathering to<br />

document existing conditions, (3) open-ended interviews that<br />

identify gaps and encourage “out of the box” brainstorming of<br />

solutions, (4) risk ranking of issues, (5) initial de-brief with<br />

organizational leaders, and (6) findings report to document risk<br />

findings and recommendations. Consistency of this process with<br />

the risk management framework in ISO 31000 will be<br />

highlighted. The collaborative risk assessment stage will be<br />

described in detail as it provides the core technical basis <strong>for</strong><br />

sequencing of response strategies.<br />

December 8-11, 2013 - Baltimore, MD

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