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Synopsis
With support from various public and
private institutions such as the National Institutes of Health and the Electric
Power Research Institute, Applied Biomathematics has been conducting
methodological research on various topics in human and ecological risk
analysis. The topics of current focus include
Contrary to what one might conclude
from review of the mathematical expressions currently used in risk analysis,
total exposure does not equal average daily exposure times days exposed.
Suppose we are interested in estimating the probability distribution among
exposed individuals of their total exposures over some time period. Using
simple convolution (i.e., what @Risk or Crystal Ball does) with the
distribution of toxicant concentrations and the distribution of
individuals bodyweights leads to an answer whose variance can be grossly
overestimated if exposures are iterated over the time period. The reason is
that this calculation assumes that the magnitude of every exposure event
through time is the same for an individual. In other words, if a person is
given a small exposure once, then he will always experience exposures of the
same size over the entire time period. This approach fails to appreciate that
the toxicant concentration encountered may be different for different exposure
events. When time periods are long, as they are for lifetime exposures needed
in cancer risk assessments, the resulting error can be substantial. Even if the
temporal autocorrelation among sequential exposures for an individual is
exceedingly high (e.g., 0.99), sufficiently many iterations will eventually
overwhelm the autocorrelation. The simplistic calculation is appropriate only
if exposure events are perfectly correlated (which seems unlikely in
most practical cases). Nevertheless, this approach has been almost universally
used since exposure assessments have been conducted within the probabilistic
framework. Several recent high-profile assessments have made this mistake. In
most cases, the effect of the error is to very strongly overestimate the chance
of large lifetime exposures. We need techniques that can be used to improve the
estimate for the distribution of total exposure that do not require a full
description of the autocorrelation function or an elaborate simulation of
event-to-event variation in exposures.
Time-dependent risk analysis
Throughout its development as a
science, human health risk analysis has consistently avoided facing the
temporal aspects of the processes it models. This has led to the use of
asymptotic or integrating models in many situations where time-dependent models
would clearly be better. As a result, the field has never really developed the
techniques necessary to make time-dependent risk analyses. The calculations of
lifetime body burdens for environmental contaminants are almost surely wrong,
and probably wrong by many orders of magnitude. We argue that intelligent
decision making about environmental protection and regulation requires much
better estimates that explicitly address the temporal processes involved. About
ten years ago, conservation biologists faced this same technical problem in
trying to estimate the risk of extinction with deterministic, asymptotic and
time-dependent models. The predictions from the models are very
different and, further, only the time-dependent model is correct. We need
techniques and software for use in human health risk assessments that can
explicitly handle the temporal dimension of risk.
Ecological risk analysis for food chains
Most of ecotoxicological risk
assessment is performed at the individual level, with endpoints such as LC-50
and LD-50. Recently, assessments at the population and species levels have
gained momentum as a result of accumulated information on the dynamics of
well-studied target (or indicator) species. Risk assessment at the ecosystem
level has always been a major topic of discussion and a long-term goal of
applied ecology in general, and ecotoxicology in particular. However,
quantitative assessments at the ecosystem level are hampered by a lack of
detailed data on the interactions among species, coupled with the complexity of
these interactions. We aim to bridge the gap between individual and ecosystem
level assessments by using the available data in models of trophic chains that
are simple enough to be parameterized with our current knowledge.
Our approach is to expand to the
ecosystem level of ecological risk analysis at a level of complexity that is
compatible with the current knowledge about the dynamics of food webs and with
the available data on interactions in marine and freshwater communities. While
it is relatively simple to construct food web models with hundreds, even
thousands of species, models with this level of detail are not reliable due to
the compounded uncertainty of the large number of species interactions
(competition, predation, mutualism) that are poorly understood, and are
difficult, if not impossible, to quantify. This complexity has hampered the
application of ecosystem-level models to practical problems of ecological risk
assessment. We propose that the first step towards building an ecosystem-level
risk assessment methodology for aquatic systems should involve models of
trophic chains composed of variables such as nutrients, toxicants,
phytoplankton, zooplankton and fish. Aggregating whole trophic levels into
single variables is undoubtedly a vast simplification, but it allows the
estimation of model parameters based on available data, because of the fewer
number of parameters necessary to model an aquatic system in sufficient detail.
Concentrations of toxicants are often
not uniform throughout an ecosystem. For example, the discharge of a toxicant
into a lake from a single point creates a distribution (sometimes called a
"plume") that depends on physical characteristics of the system, and the
chemical characteristics of the toxicant and the aquatic medium. Such
distributions are often predicted with physical models (e.g., of fluid
dynamics) with great spatial resolution, and can be incorporated into
geographic information systems ( GIS). We propose to integrate such spatial
data on the distribution of a toxicant into the ecological models. Different
trophic levels of the ecological model would require these data in different
resolutions. Whereas the spatial data may be used at a high resolution or the
phytoplankton level, they may need to be "averaged" for the whole lake and
marine ecosystem for the fish level. Thus, this step of the research will
require developing the ecological models at different spatial scales.
Multispecies approaches to habitat conservation
There are several situations in which
the suitability or ecological value of sites, parcels or regions from a
multispecies perspective might be used in decision making and natural resource
management. These include assessment of human impact, mitigation for impact,
and management for biodiversity. The Endangered Species Act (ESA) of 1973
prohibits actions which might jeopardize the continued existence of threatened
or endangered species. Commonly in response to this legislation, individuals or
private companies set aside some of the site in question as a protected reserve
while impacting the remaining area. Alternatively, a separate parcel may be
purchased for conservation ("mitigation banking"), so that the entire site may
be impacted. Therefore, methods to evaluate and rank the "value" of a
particular site in terms of its ecological components are needed by utility
companies, government agencies, private citizens, real-estate developers,
companies specializing in resource extraction and conservation organizations.
Due to limited funds for purchasing land conservationists are forced to choose
what to protect. Such decisions focus on a single threatened or endangered
species and its habitat requirements. While this approach works well for
single-species protection, it is driven by the specific requirements of the
focus or keystone species while ignoring those of other components of these
ecosystems.
The proposed approach is based on the
suitability of habitat for a list of species. For each species, the habitat
suitability will be expressed as a raster (grid) map with values ranging from 0
(unsuitable) to 1 (most suitable). Habitat suitabilities are calculated based
on the species habitat requirements such as a preference for a type of
vegetation, proximity to bodies of water, size of home range or territory, type
of soil required for optimal growth, etc. Estimating the habitat suitability
usually involves statistically procedures which relate the presence of the
species to various biological and geographical features or entities. Each of
these individual maps can then be combined into a single aggregate map that
expresses the worth, in conservation terms, of the site(s). The habitat
suitability maps would be combined mathematically by using a weighted average
of all of the maps.
This approach can be used in
management in two ways. One is the assessment of the "conservation value" of
predefined parcels for purposes of conservation planning or mitigation. These
might be based on ownership boundaries and may include lands that are
considered for purchase for protection, or lands that are subject to regulation
or mitigation. Such pre-determined parcels may be valued by the sum of the
multispecies habitat suitability values for all cells (points/pixels) within
that parcel. The sum of habitat values takes into account both the size of the
parcel (a larger parcel will have a higher sum, all other things being equal),
and the quality of the habitat (a parcel with higher average of multi-species
habitat quality will have a higher sum, all other things being equal).
Another use is in identifying patches
or locations with high "multispecies habitat suitability", for purposes of
reserve design. The combined map can be used to identify areas that are
suitable for the collection of the species included in the analysis, using an
algorithm to identify contiguous patches of high habitat suitability. Such
patch-recognition algorithms have been developed by Applied Biomathematics.
Quality assurance of Monte Carlo
methods
The straightforward application of
risk analysis via Monte Carlo methods to environmental problems often yields
underestimates of the chances of severe environmental consequences.
There are two reasons for this: Firstly, risk analysis using Monte Carlo
methods requires that the statistical distributions for the input variables be
precisely specified even when empirical evidence supporting the particular
choices is sparse. Secondly, analysts almost always simply assume variables are
in dependent of one another even when they are obviously not (e.g., body
mass and skin surface area in dermal exposure studies). Although methods to
simulate correlations among variables exist, they are not sufficient for use in
risk analysis and, in any case, are useless when the dependencies are not
empirically well known.
The critical issue is not so much how
wide the range of possible impacts might be, but rather whether the
estimates of the risks are conservative or optimistic. A simple-minded
application of Monte Carlo methods with default assumptions about input
distributions and their correlations can yield results that are overly
optimistic. They can underestimate the chances that a person will
receive a large dose of some environmental toxicant, or the chances that an
endangered species will go extinct.
Simple methods based on the notion of
interval probabilities have recently been developed that can effect the
calculations in a risk assessment without requiring the analyst to
specify precise distributions or assume anything about the dependence among
variables. This approach, called probability bounds analysis, can be used to
conduct what are, in essence, quality assurance reviews of probabilistic risk
assessments. Research is needed to demonstrate the workability of these methods
on the kinds of analytical problems encountered by environmental risk assessors
in both human health and (non-human) ecological risk analyses.
Assessing the validity of risk assessments
Increasingly, risk assessments are
being made as an integral part of the justification for public policy
decisions. These risk assessments are classic "gray literature" reports which
rarely receive the public attention they might deserve. They probably do not
get the professional scrutiny they deserve either. Part of the problem is that
the assessments are usually complex documents, often multidisciplinary in
scope. It is not unusual, for instance, for a single assessment to use methods
and arguments from chemistry, geology, hydrology, physiology, toxicology,
pharmacology, demography, ecology, statistics, and risk analysis. As a result,
such assessments are beyond the training of any single reader.
There is a strong need for software
tools that can be used to automatically review the calculations used in risk
assessments. The idea is to extend the notion of a spell checker which uses a
computer to make a preliminary review of a document and assess whether its
contents pass certain rudimentary checks for consistency and syntax.
Weve developed methods that will
automatically check that the units and equations used in a calculation run
stream balance dimensionally (the sine qua non of a valid assessment). In
applications of this software, a shocking number of serious (indeed,
fundamental) errors have been found in published and unpublished risk
assessments. Weve also described a battery of additional checks, many of
which can be deployed in software to automatically review the assumptions made
in ecological risk assessments. Given the growing complexity of risk
assessments, it is likely that such software tools will become ever more
indispensible.
Remediation planning in a probabilistic
framework
Estimating a remediation target under
a deterministic risk assessment is straightforward. For instance, if exposure
is computed as environmental concentration times intake, then a permitted
concentration can be computed as the permitted exposure divided by the intake.
When the assessment is probabilistic, however, the estimation of cleanup
targets that ensure subsequent risks will not exceed certain levels is much
more difficult. Ordinary division under a Monte Carlo or Latin hypercube
strategy yields a distribution that results in exposures being much
larger than permitted. Solving the remediation planning problem in a
probabilistic framework requires a special operation known as deconvolution.
Unfortunately, the available algorithms for deconvolution are notoriously
unstable numerically.
A new, potentially useful method based
on probability bounds allows the calculation of extreme distributions for
environmental concentration that are guaranteed to result in exposures no more
extreme than permitted. Using such a method, the bounds on the permitted
exposure need not be specified completely. Specifications may be simple
constraints on the distribution, e.g., 95% of realized exposures should be no
larger than X and the average realized exposure should be no larger than
Y.
Risk
communication
Risk analysts have been notoriously
poor at risk communication (explaining and justifying their analyses and
conclusions to stakeholders and the public). Their seeming insensitivity to the
interests, values and intuitions of nonprofessionals has led to several public
relations disasters, including very well publicized controversies at superfund
sites. While controversy can often be healthy in public policy debates, there
can be no question that misunderstanding, mistrust and miscommunication are to
be avoided.
Many policy analysts have suggested
that humans are irrational when it comes to risks and consequently make
self-defeating decisions both personally and in the public sphere.
Psychometricians have long documented the "faults" of human perception with
respect to probability, the most important of which are insensitivity to prior
probabilities, insensitivity to sample size, overestimation (overestimation) of
risks for conjunctive (disjunctive) events, and the fault of
availability by which recent news of an incidence can radically
alter the perceived risk for an event.
Part of the problem certainly lies
with the failure of risk analysts to understand how humans perceive and weigh
risks and benefits. It is clear, for instance, that human evolution did not
favor the development of an internal calculus suitable for evaluating joint
probabilities of independent events. Humans seem to employ a
possibilistic rather than strictly probabilistic calculus for
making decisions. Research is needed to delineate the features of the calculus
which humans comprehend and use in their perceptions of risk.
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