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<strong>Deliverable</strong> <strong>28</strong>:<br />

<strong>Specification</strong> <strong>of</strong> <strong>low</strong> <strong>risk</strong> <strong>products</strong><br />

<strong>REBECA</strong><br />

Regulation <strong>of</strong> Biological Control Agents<br />

Specific Support Action<br />

Project no. SSPE-CT-2005-022709<br />

Contract Start Date: 01-06-2006<br />

Duration: 24 months<br />

Project Coordinator: Ralf-Udo Ehlers, Christian-Albrechts-University <strong>of</strong> Kiel.


Document Classification<br />

Title<br />

<strong>Specification</strong> <strong>of</strong> <strong>low</strong> <strong>risk</strong> <strong>products</strong><br />

<strong>Deliverable</strong> <strong>28</strong><br />

Reporting Period 2<br />

Contractual Date <strong>of</strong> Delivery Project Month 12, February 2007<br />

Actual Date <strong>of</strong> Delivery December 2007<br />

Authors<br />

Work package<br />

Dissemination<br />

Nature<br />

Version<br />

Keywords<br />

Anita Fjelsted, Rüdiger Hauschild, Hermann Strasser<br />

WP7<br />

Public<br />

Report<br />

01.00, Final<br />

Low <strong>risk</strong><br />

Document History<br />

The document is based (i) on the recommendation expressed in a questionnaire<br />

sent to participants prior to the Salzau workshop in September 2006, (ii) on<br />

recommendations expressed during discussions at the Salzau workshop in<br />

September 2006 and (iii) on recommendations expressed at the regulators meeting<br />

in September 2006 (iv) the QPS work carried out within an EFSA working group and<br />

the final opinion <strong>of</strong> the Scientific Committee (v) a <strong>risk</strong> index model proposed by<br />

Tobias Längle and Hermann Strasser.<br />

Document Abstract<br />

At present no definition or criteria <strong>of</strong> <strong>low</strong> <strong>risk</strong> plant protection <strong>products</strong> or active<br />

substances exists in the EU regulation. However, it is being introduced in the new<br />

proposal for an EU regulation <strong>of</strong> plant protection <strong>products</strong>, whish is still being<br />

negotiated.<br />

During the <strong>REBECA</strong> project period various stakeholders have given their opinion on<br />

which BCAs should be regarded as <strong>low</strong> <strong>risk</strong> active substances/<strong>products</strong> and why.<br />

Also the work initiated within EFSA on Qualified Presumption <strong>of</strong> Safety (QPS) which<br />

relates to this subject is discussed within this document. The micro-organisms<br />

suggested to be given a QPS status is included in Annex 1 and in Annex 2 a<br />

publication by Längle and Strasser introduce a newly developed <strong>risk</strong> index system,<br />

which can be <strong>of</strong> significance in the definition <strong>of</strong> “<strong>low</strong> <strong>risk</strong>” <strong>products</strong>. The suitability <strong>of</strong><br />

the model was demonstrated by calculating the <strong>risk</strong> scores for 17 selected wellstudied<br />

biological control agents and chemical <strong>products</strong> used for similar purposes.<br />

The authors conclude that the score <strong>of</strong> “<strong>low</strong> <strong>risk</strong>” <strong>products</strong> should not exceed 100,<br />

whereas a threshold <strong>of</strong> 500 seems justified for the term "reduced <strong>risk</strong>".<br />

1


Table <strong>of</strong> contents<br />

Introduction................................................................................................................. 3<br />

Questionnaire on <strong>low</strong> <strong>risk</strong> ........................................................................................... 5<br />

Regulator’s experiences in defining <strong>low</strong> <strong>risk</strong> <strong>products</strong> ................................................ 6<br />

QPS – Qualified Presumption <strong>of</strong> Safety...................................................................... 6<br />

USA: Minimal Risk Pesticides (25b list)...................................................................... 8<br />

Low <strong>risk</strong> semiochemicals and botanicals.................................................................... 9<br />

Low <strong>risk</strong> microbials ..................................................................................................... 9<br />

Annex I: List <strong>of</strong> taxonomic units proposed for QPS status........................................ 10<br />

Annex 2: Developing a <strong>risk</strong> indicator to comparatively assess environmental <strong>risk</strong>s<br />

posed by microbial and conventional pest control agents ........................................ 12<br />

Abstract .................................................................................................................... 13<br />

Introduction............................................................................................................... 13<br />

Overview <strong>of</strong> current <strong>risk</strong> indices................................................................................ 15<br />

Environmental Impact Quotient (EIQ)....................................................................... 15<br />

Norwegian Indicator (NARI)...................................................................................... 16<br />

Québec Pesticide Risk Indicator (IRPeQ)................................................................. 17<br />

Canadian Agri-Environmental Standards (NAESI) ................................................... 17<br />

ERBIC Risk Indicator................................................................................................ 18<br />

Defining a Risk Indicator suitable to compare biological and convential pesticides.. 18<br />

Proposed <strong>risk</strong> indicator and rationale ....................................................................... 19<br />

Basic components and their integration.................................................................... 19<br />

Scoring and rationales.............................................................................................. 20<br />

Conclusions and envisaged applications.................................................................. 25<br />

Acknowledgements .................................................................................................. <strong>28</strong><br />

References ............................................................................................................... 29<br />

2


Introduction<br />

The main purpose <strong>of</strong> the <strong>REBECA</strong> project is to speed up the registration process <strong>of</strong><br />

BCAs in order to speed up the market introduction <strong>of</strong> such <strong>products</strong>. One way <strong>of</strong><br />

doing this would be to differentiate between <strong>low</strong> <strong>risk</strong> and high <strong>risk</strong> active substances<br />

in the EU and national evaluation processes and in this way make a fast track<br />

regulatory system for the <strong>low</strong> <strong>risk</strong> substances (which, among others, would be<br />

expected to be a number <strong>of</strong> BCAs). In order to do that, it is necessary to establish a<br />

definition or criteria <strong>of</strong> <strong>low</strong> <strong>risk</strong> substances that can be used to place the active<br />

substances into one <strong>of</strong> these two categories even prior to a <strong>risk</strong> assessment process.<br />

However, this is quite difficult. This document describes activities carried out within<br />

<strong>REBECA</strong> in order to investigate whether it would be possible to make such a<br />

differentiation at an early stage <strong>of</strong> the evaluation and registration process, with the<br />

view <strong>of</strong> obtaining a faster introduction <strong>of</strong> new <strong>low</strong> <strong>risk</strong> <strong>products</strong> on the market.<br />

Legal framework<br />

Plant protection <strong>products</strong><br />

In the present EU regulation on pesticides (Directive 91/414/EEC) there is no<br />

differentiation between <strong>low</strong> <strong>risk</strong> and higher <strong>risk</strong> active substances.<br />

However, the Commission’s proposal for a new pesticide Regulation 2006/0136<br />

(COD) which is still being negotiated among EU member states contains separate<br />

paragraphs relating to “<strong>low</strong>-<strong>risk</strong> substances”, “basic substances” and “substances <strong>of</strong><br />

concern”. Article 22 extends the period <strong>of</strong> approval from the normal 10 years to 15<br />

years for <strong>low</strong> <strong>risk</strong> active substances.<br />

Based on the still ongoing negotiations the Commission has published a revised<br />

proposal in order to seek agreement between the member states. In the most recent<br />

amended proposal <strong>of</strong> Regulation 2006/0136, which is dated 11 March 2008, the<br />

fol<strong>low</strong>ing definition <strong>of</strong> <strong>low</strong> <strong>risk</strong> is included:<br />

Low <strong>risk</strong>: <strong>of</strong> a nature considered inherently unlikely to cause an adverse effect on<br />

humans, animals or the environment.<br />

Further more a number <strong>of</strong> criteria are listed in Article 22 for <strong>low</strong> <strong>risk</strong> substances. The<br />

active substances can not be regarded as <strong>low</strong> <strong>risk</strong> if they are classified as one <strong>of</strong> the<br />

fol<strong>low</strong>ing:<br />

• carcinogenic<br />

• mutagenic<br />

• toxic to reproduction<br />

• very toxic<br />

• toxic<br />

• sensitising<br />

• explosive<br />

3


Further more the substances which are qualified as the fol<strong>low</strong>ing can not be regarded<br />

as <strong>low</strong> <strong>risk</strong> either:<br />

• persistent (half life <strong>of</strong> less than 60 days)<br />

• endocrine disrupter<br />

• bioaccumulative and non readily-degradable.<br />

Article 46 sets timelines for the authorization <strong>of</strong> plant protection <strong>products</strong> based on<br />

<strong>low</strong> <strong>risk</strong> substances. The member state shall within 90 days decide whether to<br />

approve an application for authorisation <strong>of</strong> a <strong>low</strong>-<strong>risk</strong> plant protection product. This<br />

period should only be 60 days in case an authorisation has already been granted for<br />

the same <strong>low</strong>-<strong>risk</strong> plant protection product by another Member State located in the<br />

same zone. However, in case the Member State will need additional information, it<br />

shall set a time limit not exceeding 6 months for the applicant to supply it.<br />

These timeframes are shorter than those suggested for active substances that are<br />

not regarded as <strong>of</strong> <strong>low</strong> <strong>risk</strong> (article 36). For those the timeframe is 12 months with the<br />

possibility <strong>of</strong> asking for additional information within a period <strong>of</strong> further 6 months.<br />

Article 23 provides criteria for basic substances and extends the period <strong>of</strong> their<br />

approval to an unlimited time. The basic substances will have to be applied included<br />

into a separate list. Article <strong>28</strong> states that plant protection <strong>products</strong> only containing<br />

basic substances (from this list) do not need to go through a national authorization in<br />

order to be placed on the market.<br />

The criteria for <strong>low</strong> <strong>risk</strong> substances are clearly made with chemical active substances<br />

in mind. First <strong>of</strong> all, there is a general <strong>risk</strong> <strong>of</strong> micro-organisms being sensitizers,<br />

which would thus right away disqualify them as <strong>low</strong> <strong>risk</strong> substances. However, so far<br />

no proper guidelines are available that can be used to carry out studies in order to<br />

investigate the sensitising properties <strong>of</strong> micro-organisms. In the data requirements for<br />

micro-organisms (Annex IIB to Directive 91/414/EEC) which are listed in Dir.<br />

2001/36/EC, it is mentioned that it is not necessary to present data on sensitisation,<br />

due to this lack <strong>of</strong> guidelines, but in this case the micro-organism is considered to be<br />

sensitising.<br />

.<br />

Secondly, the three terms: persistence, bioaccumulative and non readily-degradable<br />

and endocrine disrupters are all terms originating from the classification <strong>of</strong> chemical<br />

active substances. These criteria do not take into account that e.g. micro-organisms<br />

are naturally occurring substances.<br />

Biocides<br />

In the Biocide directive 98/8/EC the active substances regarded as being <strong>of</strong> <strong>low</strong> <strong>risk</strong><br />

are included into a specific list: 1A. The criteria for substances to be included into this<br />

list are quite similar to the criteria which are now suggested included in the new<br />

regulation on plant protection product. However, the biocide criteria does not include:<br />

toxic, very toxic, explosive and endocrine disrupters.<br />

4


Questionnaire on <strong>low</strong> <strong>risk</strong><br />

Prior to the <strong>REBECA</strong> workshop held in Salzau 18-22 September 2006 a<br />

questionnaire was sent to all participants in which they were asked to list active<br />

substances (BCAs consisting <strong>of</strong> micro-organisms, botanicals, semiochemicals or<br />

macrobials) which they would regard as being <strong>of</strong> <strong>low</strong> <strong>risk</strong> and to give their reasoning<br />

for such proposals for <strong>low</strong> <strong>risk</strong> substances. Further more the participants were asked<br />

to give a definition and/or criteria for <strong>low</strong> <strong>risk</strong> substances.<br />

46 persons replied to the questionnaire (9 regulators, 12 persons representing the<br />

industry, 22 from the scientific community and 3 from consultancies).<br />

The participants representing the industry and the scientific community all gave lists<br />

<strong>of</strong> active substances which they regarded as <strong>of</strong> <strong>low</strong> <strong>risk</strong>. In particular the participants<br />

gave a long list <strong>of</strong> macrobials. However, also the semiochemicals, in particular the<br />

SCLP were mentioned by representatives from both the industry and regulatory<br />

authorities as a category <strong>of</strong> <strong>low</strong> <strong>risk</strong>. It was mentioned by several participants that if<br />

SCLP were applied in concentrations similar to the background concentration<br />

occurring in areas with high densities <strong>of</strong> the pest insect, they should definitely be<br />

regarded as <strong>of</strong> <strong>low</strong> <strong>risk</strong>. Baculoviruses was another group <strong>of</strong> active substances that<br />

was mentioned by many participants as being <strong>of</strong> <strong>low</strong> <strong>risk</strong>.<br />

A number <strong>of</strong> botanicals were listed as well. These were <strong>products</strong> which are also used<br />

for human consumption.<br />

Arguments for listing these as <strong>low</strong> <strong>risk</strong> were:<br />

Long history <strong>of</strong> safe use<br />

Micro-organisms that frequently cause natural epizootics in presence <strong>of</strong> the host pest<br />

Micro-organisms which are ubiquitous in soils around the world<br />

Micro-organisms that do not grow at 37 °C<br />

Narrow host range/very specific<br />

Low persistence<br />

Substances used for human consumption (e.g. rapeseed oil, garlic oil, olive oil)<br />

Substances used as household <strong>products</strong> (e.g. for cleaning)<br />

During the discussion <strong>of</strong> the questionnaire at the <strong>REBECA</strong> workshop in Salzau the<br />

general opinion expressed by regulators and the European Commission (DG Sanco)<br />

was, that it would not be possible to establish a list <strong>of</strong> substances <strong>of</strong> <strong>low</strong> <strong>risk</strong> prior to a<br />

<strong>risk</strong> assessment, i.e. a list <strong>of</strong> substances that would not need a <strong>risk</strong> assessment.<br />

However, all regulators seemed to agree, that there was a need for a<br />

definition/criteria <strong>of</strong> <strong>low</strong> <strong>risk</strong> substances for the new EU regulation <strong>of</strong> pesticides, but,<br />

such criteria will be applied only after the <strong>risk</strong> assessment has been carried out and<br />

will rather determine which substances will get an Annex I inclusion <strong>of</strong> a longer<br />

period (15 years) and an easier/faster process for national registration. As mentioned<br />

already, the text <strong>of</strong> the Commission proposal for a new EU regulation <strong>of</strong> pesticides is<br />

still being discussed and negotiated among EU member states.<br />

5


Regulator’s experiences in defining <strong>low</strong> <strong>risk</strong> <strong>products</strong><br />

At the <strong>REBECA</strong> stakeholder meeting for regulators which took place in Salzau,<br />

Germany on 18 September 2006 (a meeting attended by 27 regulators from Europe,<br />

Australia and USA) the participants discussed the possibility <strong>of</strong> the national<br />

authorities to give priority to <strong>low</strong> <strong>risk</strong> <strong>products</strong> during the evaluation and authorisation<br />

process.<br />

This issue had been discussed in Sweden, the Netherlands and in the UK. The<br />

purpose in all three countries was to increase the number <strong>of</strong> such <strong>products</strong> at their<br />

market e.g. by reducing the fee requested for <strong>low</strong> <strong>risk</strong> <strong>products</strong> and in the<br />

Netherlands and the UK also to provide further guidance to applicants in order to<br />

speed up the preparation <strong>of</strong> dossiers and the subsequent evaluation <strong>of</strong> those dossier.<br />

However, none <strong>of</strong> the regulatory authorities in the three countries found the term “<strong>low</strong><br />

<strong>risk</strong>” very helpful, simply due to the difficulties in defining such a category. In the UK<br />

the Pesticide Safety Directorate (PSD) has not used the term <strong>low</strong> <strong>risk</strong> <strong>products</strong> in<br />

their BioPesticide Scheme but instead the term alternative <strong>products</strong> (however, also<br />

without a specific definition). For this product group they have <strong>low</strong>ered the fees, are<br />

arranging pre-submission meetings, they have increased the web-site information <strong>of</strong><br />

the regulatory process, established a specific contact point in PSD for these product<br />

types (a champion) and the applicants can be guided throughout the process <strong>of</strong><br />

putting together an application.<br />

A somewhat similar project is taking place in the Netherlands, where the project is<br />

called GENOEG. It is also aiming at getting further <strong>low</strong> <strong>risk</strong> <strong>products</strong> on the market.<br />

In the Netherlands they have used the term natural pesticides rather than <strong>low</strong> <strong>risk</strong><br />

<strong>products</strong>. Via this project the applicants can get up to 100,000 € co-finance for<br />

registration fees and extra studies needed for the <strong>risk</strong> assessment, and the<br />

regulatory authority here also help applicants put together good dossiers and invite<br />

applicants for pre-submission meetings.<br />

QPS – Qualified Presumption <strong>of</strong> Safety<br />

At several <strong>REBECA</strong> workshops the EFSA initiative on developing a QPS concept<br />

(Qualified Presumption <strong>of</strong> Safety) was discussed. The reason being that it was<br />

anticipated, that if the microbial plant protection <strong>products</strong> were included in the<br />

development <strong>of</strong> this new concept, it would be a way <strong>of</strong> defining groups <strong>of</strong> <strong>low</strong> <strong>risk</strong><br />

micro-organisms, and a way <strong>of</strong> obtaining a faster evaluation and market introduction<br />

<strong>of</strong> microbial plant protection <strong>products</strong>.<br />

The development <strong>of</strong> a QPS concept was initiated in 2003 by a working group<br />

consisting <strong>of</strong> members <strong>of</strong> several former (EC) scientific committees. The work was<br />

continued within an EFSA working group. The aim was to develop a scheme that<br />

would harmonize the <strong>risk</strong> assessment <strong>of</strong> micro-organisms throughout the various<br />

EFSA panels and a scheme developed as a tool for setting priorities within the <strong>risk</strong><br />

assessment <strong>of</strong> micro-organisms used in food/feed. By using this tool <strong>risk</strong> assessors<br />

will for some micro-organisms be able to take a generic approach in the <strong>risk</strong><br />

assessment instead <strong>of</strong> a full case-by-case assessment, and in this way make better<br />

use <strong>of</strong> assessment resources by focussing on those organisms that present greatest<br />

<strong>risk</strong> or uncertainties, and which would need a case-by-case <strong>risk</strong> assessment.<br />

6


It is proposed, that a safety assessment <strong>of</strong> a defined taxonomic group should be<br />

made based on four pillars (establishing identity, body <strong>of</strong> knowledge, possible<br />

pathogenicity and end use). If the taxonomic group did not raise safety concerns or, if<br />

safety concerns existed, but could be defined and excluded the grouping could be<br />

granted QPS status. Thereafter, any strain <strong>of</strong> the micro-organisms given QPS status<br />

would be freed for further safety assessments other than satisfying any qualifications<br />

specified.<br />

The final opinion <strong>of</strong> the Scientific Committee (including 4 appendices) was adopted<br />

on 19 November 2007. Table 1 contains the 4 groups <strong>of</strong> micro-organisms included in<br />

the concept. The committee explains in this document that the group consisting <strong>of</strong><br />

filamentous fungi could not be recommended QPS status. Further more they explain<br />

that all strains belonging to the Bacillus cereus sensu lato group (e.g. Bacillus<br />

thuringiensis) should not be given a QPS status either, since it is known that the vast<br />

majority <strong>of</strong> strains within this group are toxin producers and thus can not meet the<br />

required qualifications.<br />

Table 1. The four groups <strong>of</strong> micro-organisms which are so far considered in the QPS<br />

concept and the number <strong>of</strong> species proposed for QPS status so far<br />

Group <strong>of</strong> micro-organism<br />

Number <strong>of</strong> species proposed for QPS<br />

status so far<br />

non-spore forming gram positive bacteria<br />

Bacillus spp.<br />

yeasts<br />

commonly encountered filamentous fungi<br />

48 species<br />

13 species<br />

11 species<br />

None<br />

The Scientific Committee writes as fol<strong>low</strong>s in their opinion <strong>of</strong> 19 November 2007:<br />

“The Scientific Committee is <strong>of</strong> the opinion that the use <strong>of</strong> strains from the B. cereus<br />

group should be avoided whenever there is a possibility <strong>of</strong> human exposure whether<br />

intended or incidental. The B. cereus group is therefore excluded from consideration<br />

for QPS status.<br />

There is an artificial distinction held between B. cereus and B. thuringiensis (used for<br />

plant protection) which has little scientific basis. The plasmid encoding the<br />

insecticidal enterotoxin, which provides the phenotypic distinction for B. thuringiensis,<br />

is readily lost, particularly when grown at 37 ºC, leaving an organism<br />

indistinguishable from B. cereus. Consequently it is likely that B. thuringiensis has<br />

been the causative organism <strong>of</strong> some instances <strong>of</strong> food poisoning but identified as B.<br />

cereus because clinical investigations would have failed to recognise the<br />

distinguishing features characteristic <strong>of</strong> B. thuringiensis.<br />

However, the Scientific Committee recognises that B. thuringiensis has value to the<br />

industry as a means <strong>of</strong> biological pest control and that its widespread use for this<br />

purpose may not lead to significant human exposure.”<br />

7


Bacteria directly consumed by humans only qualify for QPS status, if they are free <strong>of</strong><br />

acquired resistance to antibiotics <strong>of</strong> importance in clinical and veterinary medicine.<br />

Furthermore, all bacteria capable <strong>of</strong> toxin production should be demonstrated to be<br />

free <strong>of</strong> any toxigenic potential.<br />

It is important to stress that QPS does not carry any legal status.<br />

Since neither B. thuringiensis nor any <strong>of</strong> the filamentous fungi are included on the list<br />

<strong>of</strong> species proposed for QPS status, the QPS in its present form does not <strong>of</strong>fer a<br />

generic approach to the safety assessment <strong>of</strong> most micro-organisms used as<br />

biological control agents. Never the less, the EFSA Scientific Committee considers<br />

that it may be possible to devise robust use qualifications which would al<strong>low</strong> a QPS<br />

approach for further groups <strong>of</strong> micro-organisms relevant for biological control in the<br />

future. The system is developed in order to provide a generic assessment system for<br />

use within EFSA that can be applied to all requests for the safety assessment <strong>of</strong><br />

micro-organisms deliberately introduced into the food chain or used as producer<br />

strains for food/feed additives. This implies, that when industry applies for Annex I<br />

inclusion <strong>of</strong> micro-organisms belonging to microbial taxonomic units, which are now<br />

included in the list <strong>of</strong> organisms for which a QPS status is proposed (e.g. Bacillus<br />

subtilis and B. pumilus) with the intention to market these in plant protection<br />

<strong>products</strong>, the industry can in their dossier argue that the species are given QPS<br />

status, and that the <strong>risk</strong> for consumer health (due to exposure from residues on<br />

crops) is likely to be <strong>low</strong> when these strains are applied as plant protection <strong>products</strong>.<br />

This information can be used as a waiver for residue data for micro-organisms given<br />

QPS status. The list <strong>of</strong> taxonomic units for which QPS status has been proposed can<br />

be found in Annex 1.<br />

The applicability <strong>of</strong> the QPS approach for broad use <strong>of</strong> micro-organisms as plant<br />

protection <strong>products</strong> needs to be discussed further.<br />

USA: Minimal Risk Pesticides (25b list)<br />

In the USA, there is a list <strong>of</strong> substances that can be used as pesticides without any<br />

registration, however, they still need a residue limit, or exemption, for food or feed<br />

uses. These substances are called Minimal Risk Pesticides, as described in the US<br />

Code <strong>of</strong> Federal Regulation, 40CFR 152.25(f). The list contains many essential oils 1 .<br />

All inerts must be on EPA’s 4A inert list, all ingredients must be identified on the<br />

label, and the label may not contain false or misleading claims. This regulation was<br />

developed by an EPA workgroup in 1994 and revised in accordance with public<br />

comments for a final Federal Register publication in 1996. The EPA has experienced<br />

a problem since it has been difficult identifying exactly which chemical substances<br />

are included under the names listed. Currently, CAS numbers are used to describe<br />

the substances on the EPA inert substance classification lists.<br />

1 Currently, the list includes the fol<strong>low</strong>ing substances: castor oil, cedar oil, cinnamon and cinnamon oil,<br />

citric acid, citronella and citronella oil, cloves and clove oil, corn gluten meal, corn oil, cottonseed oil,<br />

dried blood, eugenol, garlic and garlic oil, geraniol, gernanium oil, lauryl sulfate, lemongrass oil,<br />

linseed oil, malic acid, mint and mint oil, peppermint and peppermint oil, 2-phenethyl propionate (2-<br />

phenylethyl propionate), potassium sorbate, putrescent whole egg solids, rosemary and rosemary oil,<br />

sesame (includes ground sesame, plant) and sesame oil, sodium chloride (common salt), sodium<br />

lauryl sulfate, soybean oil, thyme and thyme oil, white pepper and zinc metal strips.<br />

8


Low <strong>risk</strong> semiochemicals and botanicals<br />

In <strong>REBECA</strong> <strong>Deliverable</strong> 18 (Positive list <strong>of</strong> <strong>low</strong> <strong>risk</strong> candidate botanicals and<br />

semiochemicals), gives a discussion on <strong>low</strong> <strong>risk</strong> semiochemicals and botanicals and<br />

provide lists <strong>of</strong> such substances which <strong>REBECA</strong> propose should be given <strong>low</strong> <strong>risk</strong><br />

status.<br />

Low <strong>risk</strong> microbials<br />

Baculoviruses<br />

Baculoviruses in general have <strong>low</strong> <strong>risk</strong> for all organisms except their specific hosts.<br />

As stated in the “OECD Consensus document No 20 on information used in the<br />

assessment <strong>of</strong> environmental applications involving baculoviruses” from January<br />

2002, «Baculoviruses are naturally occurring pathogens <strong>of</strong> arthropods. Their host<br />

range is exclusively restricted to arthropods. No member <strong>of</strong> this virus family is<br />

infective to plants or vertebrates». Likewise, no sensitisation was observed for<br />

baculoviruses so far. The OECD Consensus Document concludes that «No adverse<br />

effect on human health has been observed in any <strong>of</strong> these investigations indicating<br />

that the use <strong>of</strong> baculovirus is safe and does not cause any health hazards.»<br />

The majoritiy <strong>of</strong> baculoviruses has a very restricted host range, which mainly<br />

comprises one or a few species <strong>of</strong> the same genus, rarely different genera <strong>of</strong> the<br />

same family. Baculoviruses with a broader host range are the exception. Therefore,<br />

<strong>risk</strong>s for non-target species can be excluded as well.<br />

Low <strong>risk</strong> bacterial and fungal <strong>products</strong><br />

In <strong>REBECA</strong> <strong>Deliverable</strong> 12 (Positive list <strong>of</strong> <strong>low</strong> <strong>risk</strong> candidate microbials), gives a<br />

discussion on <strong>low</strong> <strong>risk</strong> microbials and provide lists <strong>of</strong> such substances which<br />

<strong>REBECA</strong> propose should be given <strong>low</strong> <strong>risk</strong> status.<br />

This recommendation is based (i) on a case by case evaluation <strong>of</strong> microbial<br />

biocontrol agents, assessed by international experts, recognised by <strong>REBECA</strong><br />

consortium, (ii) the safety data fact sheet published by the US Environment<br />

Protection Agency (EPS) and (iii) publication <strong>of</strong> the European Council regulations,<br />

reporting the opinion <strong>of</strong> the safe use <strong>of</strong> Annex I listed micro-organisms.<br />

Annexes<br />

1. List <strong>of</strong> taxonomic units proposed for QPS status<br />

2. Publication: Developing a <strong>risk</strong> indicator to comparatively assess environmental<br />

<strong>risk</strong>s posed by microbial and conventional pest control agents.<br />

9


Annex I.<br />

List <strong>of</strong> taxonomic units proposed for QPS status<br />

Gram-Positive Non-Sporulating Bacteria 2<br />

Species<br />

Bifidobacterium adolescentis Bifidobacterium bifidum<br />

Bifidobacterium animalis Bifidobacterium breve<br />

Corynebacterium glutamicum<br />

Lactobacillus acidophilus<br />

Lactobacillus amylolyticus<br />

Lactobacillus amylovorus<br />

Lactobacillus alimentarius<br />

Lactobacillus aviaries<br />

Lactobacillus brevis<br />

Lactobacillus buchneri<br />

Lactobacillus casei<br />

Lactobacillus crispatus<br />

Lactobacillus curvatus<br />

Lactobacillus delbrueckii<br />

Lactococcus lactis<br />

Lactobacillus farciminis<br />

Lactobacillus fermentum<br />

Lactobacillus gallinarum<br />

Lactobacillus gasseri<br />

Lactobacillus helveticus<br />

Lactobacillus hilgardii<br />

Lactobacillus johnsonii<br />

Lactobacillus<br />

kefiran<strong>of</strong>aciens<br />

Lactobacillus kefiri<br />

Lactobacillus mucosae<br />

Lactobacillus panis<br />

Bifidobacterium longum<br />

Lactobacillus paracasei<br />

Lactobacillus paraplantarum<br />

Lactobacillus pentosus<br />

Lactobacillus plantarum<br />

Lactobacillus pontis<br />

Lactobacillus reuteri<br />

Lactobacillus rhamnosus<br />

Lactobacillus sakei<br />

Lactobacillus salivarius<br />

Lactobacillus<br />

sanfranciscensis<br />

Lactobacillus zeae<br />

Leuconostoc citreum Leuconostoc lactis Leuconostoc mesenteroides<br />

Pediococcus acidilactici Pediococcus dextrinicus Pediococcus pentosaceus<br />

Propionibacterium.<br />

freudenreichii<br />

Streptococcus thermophilus<br />

Qualifications<br />

QPS status applies only<br />

when the species is<br />

used for production<br />

purposes.<br />

Bacillus 6<br />

Species<br />

Bacillus amyloliquefaciens<br />

Bacillus atrophaeus<br />

Bacillus clausii<br />

Bacillus coagulans<br />

Bacillus fusiformis<br />

Bacillus lentus<br />

Bacillus licheniformis<br />

Bacillus megaterium<br />

Bacillus mojavensis<br />

Bacillus pumilus<br />

Bacillus subtilis<br />

Bacillus vallismortis<br />

Geobacillus<br />

stearothermophillus<br />

Qualifications<br />

Absence <strong>of</strong> emetic food<br />

poisoning toxins with<br />

surfactant activity.*<br />

Absence <strong>of</strong> enterotoxic<br />

activity.*<br />

* When strains <strong>of</strong> these QPS units are to be used as seed coating agents, testing for toxic<br />

activity is not necessary, provided that the <strong>risk</strong> <strong>of</strong> transfer to the edible part <strong>of</strong> the crop at<br />

harvest is very <strong>low</strong> (section 4.3 <strong>of</strong> Appendix C).<br />

2<br />

Absence <strong>of</strong> acquired antibiotic resistance should be systematically demonstrated unless cells are<br />

not present in the final product.<br />

10


Yeasts<br />

Species<br />

Debaryomyces hansenii<br />

Hanseniaspora uvarum<br />

Kluyveromyces lactis<br />

Pichia angusta<br />

Kluyveromyces<br />

marxianus<br />

Pichia anomala<br />

Qualifications<br />

Saccharomyces bayanus<br />

Schizosaccharomyces<br />

pombe<br />

Xanthophyllomyces<br />

dendrorhous<br />

Saccharomyces<br />

cerevisiae<br />

Saccharomyces pastorianus<br />

(synonym <strong>of</strong> Saccharomyces<br />

carlsbergensis)<br />

S. cerevisiae, subtype<br />

S. boulardii is<br />

contraindicated for<br />

patients <strong>of</strong> fragile<br />

health, as well as for<br />

patients with a central<br />

venous catheter in<br />

place. A specific<br />

protocol concerning<br />

the use <strong>of</strong> probiotics<br />

should be formulated<br />

11


Annex 2<br />

Developing a <strong>risk</strong> indicator to comparatively assess environmental <strong>risk</strong>s posed<br />

by microbial and conventional pest control agents<br />

Tobias Laengle 1,2 , and Hermann Strasser 1*<br />

1 Institute <strong>of</strong> Microbiology, University Innsbruck, Technikerstrasse 25,<br />

A 6020 Innsbruck, Austria<br />

2 Pest Management Centre, Agriculture and Agri-Food Canada, Central Experimental Farm,<br />

Building #57, 960 Carling Ave, Ottawa, Ontario K1N 8L4, Canada<br />

* Corresponding author: Email: hermann.strasser@uibk.ac.at;<br />

phone: +43-512-507-6008; fax: +43-512-507-2938;<br />

Keywords:<br />

plant protection; microbial biocontrol agents; <strong>risk</strong> assessment; <strong>risk</strong> indicator;<br />

registration; comparative <strong>risk</strong> assessment<br />

12


Abstract<br />

Selected biological control agents and conventional pesticides were used to critically<br />

review the applicability <strong>of</strong> a newly developed <strong>risk</strong> indicator (RI) system. Five basic<br />

components are proposed for the calculation <strong>of</strong> the overall environmental <strong>risk</strong> score:<br />

persistence <strong>of</strong> the active ingredient, dispersal potential, range <strong>of</strong> non-target<br />

organisms that are affected, and direct and indirect effects on the ecosystem.<br />

Several <strong>risk</strong> measurement systems were reviewed, <strong>risk</strong> categories in the proposed<br />

system were modified from a widely-accepted model (i.e. ERBIC model).<br />

Additionally, one new category was implemented to assess the <strong>risk</strong>s to vertebrate<br />

non-target species.<br />

Besides a detailed discussion <strong>of</strong> the new <strong>risk</strong> indicator model, the suitability <strong>of</strong> the<br />

model was demonstrated by calculating the <strong>risk</strong> scores for seventeen selected<br />

<strong>products</strong>. It became obvious, that the environmental <strong>risk</strong> score greatly varied within<br />

the assessed chemical <strong>products</strong>, and also, yet at a much <strong>low</strong>er level, within the group<br />

<strong>of</strong> biological <strong>products</strong>. The use pattern greatly influenced the estimated<br />

environmental <strong>risk</strong> posed by any given product. The overall environmental <strong>risk</strong> score<br />

varied between 24 (Coniothyrium minitans, soil application) and 4.275 (DDT, foliar<br />

spray).<br />

The proposed model can be used to communicate environmental <strong>risk</strong> and to design<br />

<strong>low</strong>er <strong>risk</strong> integrated pest management strategies. It is recommended, that the<br />

proposed <strong>risk</strong> indicator system may serve to define <strong>low</strong> <strong>risk</strong> (i.e., RI ≤ 100) and<br />

reduced <strong>risk</strong> (i.e., 500 ≥RI > 100) pesticides. Yet, it remains debatable whether RI will<br />

be useful in determining acceptability <strong>of</strong> data waivers. Use pattern, application<br />

method, persistence, growth temperature range and taxonomic relatedness to<br />

known/suspected pathogens should all be considered when justifying data waivers.<br />

Introduction<br />

In recent years, significant progress has been made in the development <strong>of</strong> fungal<br />

biocontrol agents (BCAs) for the suppression <strong>of</strong> pests (insects, nematodes), weeds<br />

and diseases <strong>of</strong> a wide range <strong>of</strong> forest, horticultural and agricultural crops.<br />

Nevertheless, relatively few <strong>of</strong> these <strong>products</strong> have reached the market: For<br />

instance, at the time <strong>of</strong> writing this manuscript no mycoinsecticide has been<br />

registered in the European Union under the harmonized registration procedure <strong>of</strong><br />

Council Directive 91/414/EEC. Likewise, no fungal insecticides have been approved<br />

under the Pest Control Act in Canada. Today, only 17 fungal insecticides comprising<br />

five fungal species are registered in all 30 OECD countries (Kabaluk & Gazdik,<br />

2007).<br />

The biocontrol industry and regulators agree that relatively few microbials have been<br />

registered in recent years in part due to insufficient experience with such <strong>products</strong><br />

and the fact that methods and tools used for <strong>risk</strong> assessment are still not applicable<br />

to biological systems (Scientific Committee on Plants, 2002; International Biocontrol<br />

Manufacturers Association, 2003; Strasser & Kirchmair, 2006). An additional problem<br />

for microbial pesticides, however, lies in the structure <strong>of</strong> the biopesticide industry:<br />

most biopesticide companies are small and medium sized enterprises with limited<br />

financial resources and experience in the registration <strong>of</strong> plant protection <strong>products</strong>,<br />

respectively. This fact is important to point out because these enterprises <strong>of</strong>ten<br />

13


cannot afford the high costs for a successful registration <strong>of</strong> their biological control<br />

agents (BCAs), which are in most cases niche <strong>products</strong>.<br />

Microbial pesticides are generally regarded as posing <strong>low</strong>er <strong>risk</strong>s to human health<br />

and the environment than chemical pesticides (OECD, 2007). Many governments<br />

have responded to growing public demands for safer means <strong>of</strong> plant protection and<br />

have recognized that the obstacles for safer biological pesticides need to be<br />

addressed. In the European Union, the multidisciplinary <strong>REBECA</strong> (acronym;<br />

Regulation <strong>of</strong> Biological Control Agents) consortium sought to find more appropriate<br />

protocols to address data requirements for biological pesticides and thereby facilitate<br />

access to <strong>low</strong>er <strong>risk</strong> biological controls (<strong>REBECA</strong>, 2007).<br />

In Canada, the pesticide regulatory authority, Health Canada’s Pest Management<br />

Regulatory Agency (PMRA) has waived all registration review fees for microbial<br />

pesticides. To complement this measure, the federal department <strong>of</strong> Agriculture and<br />

Agri-food Canada has set up a regulatory support program for biopesticides needed<br />

by the grower community. The new Canadian pesticide legislation explicitly requires<br />

that the registration to <strong>low</strong>er <strong>risk</strong> <strong>products</strong> will be facilitated by the regulator<br />

(Government <strong>of</strong> Canada, 2002). Both in Canada and in the United States the<br />

respective regulatory agencies have established data requirements that reflect the<br />

current scientific knowledge about the <strong>risk</strong>s posed by microbial pest control agents<br />

(Pest Management Regulatory Agency, 2001; Environmental Protection Agency,<br />

2006).<br />

Unlike chemical pesticides, microbial agents may infect other living organisms<br />

causing diseases. Potential adverse effects <strong>of</strong> microbial pesticides include the<br />

displacement <strong>of</strong> non-target micro-organisms and allergenic, toxic, and pathogenic<br />

effects on humans or other non-target organisms (Cook et al., 1996; OECD, 2003).<br />

The key challenge in <strong>risk</strong> assessment method development is to establish protocols<br />

and guidelines that enable an efficient yet responsible <strong>risk</strong> assessment.<br />

In the area <strong>of</strong> exotic natural enemies van Lenteren et al. (2003) proposed the use <strong>of</strong><br />

a <strong>risk</strong> indicator developed in the ERBIC project (Hokkanen et al., 2003) as an<br />

objective approach to a comparative <strong>risk</strong> assessment <strong>of</strong> “classical biocontrol agents”<br />

(definition as in Eilenberg et al., 2001). This approach has been implemented in a<br />

guideline for the <strong>risk</strong> assessment <strong>of</strong> arthropods as part <strong>of</strong> the OECD Plant Protection<br />

Programme (OECD, 2004a).<br />

Legislators in Canada (Government <strong>of</strong> Canada, 2002) and US EPA (US EPA, 2000)<br />

have recognized the value <strong>of</strong> objectively comparing the <strong>risk</strong>s <strong>of</strong> different pesticides<br />

for the same pattern <strong>of</strong> use and al<strong>low</strong>ing regulators to consider the <strong>risk</strong>s <strong>of</strong> other<br />

pesticides when registering a new product. A similar approach has been suggested<br />

by the European Parliament (European Parliament, 2003).<br />

Several authors have suggested concepts to compare the health or environmental<br />

<strong>risk</strong>s or hazards <strong>of</strong> conventional pesticides, but, unfortunately, the applicability <strong>of</strong><br />

these tools to biological control agents is limited. The availability <strong>of</strong> a tool to<br />

objectively compare the environmental impact <strong>of</strong> biological and conventional<br />

pesticides is desirable in light for the promotion <strong>of</strong> safe biological control options and<br />

the measurement <strong>of</strong> resulting <strong>risk</strong> reduction in agricultural use.<br />

In this paper we propose such a tool for microbial BCAs by using data gathered in<br />

the EU funded BIPESCO (FAIR6-CT-98-4105) and RAFBCA (QLK1-CT-2001-01391)<br />

research projects, as well as data from public regulatory documents and scientific<br />

literature. Selected microbial pest control agents were used to critically review the<br />

14


applicability <strong>of</strong> the proposed environmental <strong>risk</strong> indicator. Furthermore, advantages <strong>of</strong><br />

the suggested <strong>risk</strong> indicator are compared to existing <strong>risk</strong> indicators used for<br />

conventional pesticides.<br />

Overview <strong>of</strong> current <strong>risk</strong> indices<br />

Numerous attempts have been made to compare the <strong>risk</strong>s associated with different<br />

pesticides to one another. The complexity <strong>of</strong> these systems varies widely and ranges<br />

from a simple grouping <strong>of</strong> pesticides into toxicity classes, to more sophisticated<br />

measures, which use numerical data such as toxicity endpoints used for regulatory<br />

purposes. A thorough review <strong>of</strong> <strong>risk</strong> comparison systems currently used in different<br />

countries has been conducted elsewhere (Reus et al., 1999; Reus et al., 2002;<br />

OECD, 2004b; Mineau & Whiteside, 2005). Selected models are introduced here<br />

fol<strong>low</strong>ed by a discussion <strong>of</strong> their merits and shortcomings in comparing the <strong>risk</strong>s <strong>of</strong><br />

microbials to those <strong>of</strong> conventional pesticides.<br />

Environmental Impact Quotient (EIQ)<br />

Among first <strong>risk</strong> indices developed for pesticides was the Environmental Impact<br />

Quotient (EIQ), which was published in 1992 (Kovach et al., 1992). The EIQ is used<br />

predominantly in North America, and classifications for new pesticides are regularly<br />

updated on Cornell University’s website (http://www.nysipm.cornell.<br />

edu/publications/eiq/).<br />

Essentially, the base EIQ for an active ingredient is the average <strong>risk</strong> calculated for<br />

the three sub-indices which describe the <strong>risk</strong> to (i) producers, (ii) consumers, and (iii)<br />

the environment. These sub-indices are calculated by using regulatory data such as<br />

dermal, oral and chronic toxicity to mammals (for consumer and producer <strong>risk</strong>), and<br />

toxicity to fish, birds, bees, other arthropods (for environmental <strong>risk</strong>). Various<br />

weighting coefficients, as well as soil and plant half life <strong>of</strong> the substance are also<br />

used as factors in the calculation. The "field EIQ" is derived by multiplying the base<br />

EIQ with the application rate and number <strong>of</strong> applications per year.<br />

While a good estimate to roughly assess the impact <strong>of</strong> pesticides, there are some<br />

major points <strong>of</strong> criticism that limit the usefulness <strong>of</strong> the EIQ.<br />

Firstly, the EIQ solely relies on the data established for the active ingredient. The<br />

type <strong>of</strong> application (e.g. soil incorporation, foliar spray), and formulation type are not<br />

taken into account. These are significant factors that will affect exposure to the<br />

pesticide and as such have a major influence on the <strong>risk</strong>, and hence the potential<br />

impact, resulting from a pesticide application. The EIQ should therefore be better<br />

described as a hazard quotient rather than a <strong>risk</strong> quotient.<br />

Secondly, the EIQ averages producer, consumer and environmental <strong>risk</strong>s, which may<br />

result in a significant <strong>risk</strong> to one component being averaged out and overseen by a<br />

<strong>low</strong>er <strong>risk</strong> to others. For instance, a relatively high toxicity to fish or birds would not<br />

be appropriately accounted for if the <strong>risk</strong> to humans and mammals is <strong>low</strong>.<br />

Thirdly, weighting factors used on the EIQ are not explained or justified in the<br />

original publication and seem to be assigned arbitrarily. For instance, Mineau et al.<br />

(2005) noted that the environmental section <strong>of</strong> the EIQ is biased towards arthropods.<br />

With respect to the EIQ's application to microbials, there is <strong>of</strong>ten insufficient data<br />

available to feed into the EIQ equation, because <strong>of</strong> a higher likelihood <strong>of</strong> studies<br />

being waived in the registration process. Furthermore, the factors affecting the <strong>risk</strong>s<br />

15


esulting from microbial pest control <strong>products</strong> are not necessarily determined by the<br />

same variables as those for conventional chemical pesticides.<br />

Norwegian Indicator (NARI)<br />

The Norwegian Agricultural Inspection service has established separate pesticide<br />

<strong>risk</strong> indicators to assess human health and environmental <strong>risk</strong> with the purpose <strong>of</strong><br />

tracking <strong>risk</strong> reduction over time. This was aimed to assist a government initiative,<br />

which had a declared goal <strong>of</strong> reducing pesticide <strong>risk</strong> by 25 % between 1998 and<br />

2002, and also encompassed the introduction <strong>of</strong> <strong>risk</strong> based taxes on pest control<br />

<strong>products</strong> (Norwegian Agricultural Inspection Service, 2002). Compared to <strong>risk</strong> indices<br />

implemented in other OECD countries (OECD, 2004b), the Norwegian model is a<br />

step towards a more integrated model that attempts to include both exposure and<br />

toxicity. For the calculation <strong>of</strong> the Norwegian environmental <strong>risk</strong> indicator, scores are<br />

assigned for (i) terrestrial adverse effects, (ii) aquatic adverse effects, (iii) leaching<br />

potential, (iv) persistence, and (v) bioaccumulation. Scores in the terrestrial and<br />

aquatic categories are calculated using both toxicity <strong>of</strong> and exposure to a substance;<br />

values are assigned in two different groups <strong>of</strong> organisms (bees/earthworms/birds and<br />

fish/aquatic invertebrates/plants, respectively), the highest value in each category is<br />

used for the calculation. Values for persistence, mobility and bioaccumulation are<br />

also assigned according to set intervals. The environmental <strong>risk</strong> indicator is then<br />

calculated as the squared sum <strong>of</strong> all components. Modifications <strong>of</strong> the indicator are<br />

possible, defined for specific scenarios such as seed treatments or greenhouse<br />

applications. Microbial pest control agents are routinely assigned a value <strong>of</strong> one<br />

(<strong>low</strong>est <strong>risk</strong>).<br />

The inclusion <strong>of</strong> exposure considerations, as well as the breakdown into separate<br />

environmental and health indices in the Norwegian model marks a significant<br />

advantage over the EIQ. Certainly, this al<strong>low</strong>s for a more differentiated assessment<br />

<strong>of</strong> pesticide <strong>risk</strong>s to humans and the environment. The advantage <strong>of</strong> the Norwegian<br />

system is that it is entirely based on data commonly requested by registration<br />

authorities, and as such data to calculate the <strong>risk</strong> score should be readily available,<br />

at least within governments.<br />

However, the Norwegian system also has some significant weaknesses. Most<br />

importantly, the indicator is simply a sum <strong>of</strong> its subcomponents, which is not<br />

reflective <strong>of</strong> interactions between the different components. For instance a high level<br />

<strong>of</strong> persistence, mobility or toxicity will each increase the <strong>risk</strong> posed to aquatic and<br />

terrestrial organisms. However, a very short half-life will significantly mitigate a high<br />

level <strong>of</strong> toxicity, whereas a highly persistent substance <strong>of</strong> the same toxicity will<br />

expose and possibly kill multiple times more non-target organisms.<br />

Another shortcoming <strong>of</strong> the Norwegian approach is the treatment <strong>of</strong> microbial pest<br />

control <strong>products</strong>. The simple flat-rate assignment <strong>of</strong> the minimal <strong>risk</strong> score to all<br />

microbial active ingredients may be a pragmatic approach useful in the context in<br />

which the Norwegian indicator is used but does not al<strong>low</strong> for a differentiated<br />

comparison between conventional chemicals and biological pesticides. For a<br />

regulatory comparative <strong>risk</strong> assessment or a farm level decision tool, a more<br />

sophisticated assessment <strong>of</strong> microbial pest control <strong>products</strong> is required.<br />

16


Québec Pesticide Risk Indicator (IRPeQ)<br />

The Indicateur de risque des pesticides du Québec (IRPeQ, Onil et al., 2007), is<br />

largely based on the Norwegian approach, but was fine-tuned to be applicable to<br />

agricultural practices and conditions in Québec, Canada. The tool is novel ins<strong>of</strong>ar as<br />

it is accompanied by a website that al<strong>low</strong>s farmers to enter individualised information<br />

and assists informed decision-making on a field level.<br />

Modifications <strong>of</strong> the Norwegian model include a different weighting assigned to<br />

persistence, aquatic and terrestrial effects, and the addition <strong>of</strong> separate sub-indices<br />

for birds and bees. None <strong>of</strong> the major shortcomings <strong>of</strong> the Norwegian model outlined<br />

above were improved in the system adapted for Québec.<br />

Canadian Agri-Environmental Standards (NAESI)<br />

An entirely new approach to assess comparative <strong>risk</strong>s <strong>of</strong> pesticides was presented<br />

by the Canadian Wildlife Service <strong>of</strong> Environment Canada (Mineau, 2002; Mineau &<br />

Whiteside, 2005; Mineau et al., 2008). The starting point <strong>of</strong> this study was the<br />

analysis <strong>of</strong> comprehensive sets <strong>of</strong> actual field data, which included field studies and<br />

reported incidents resulting in losses <strong>of</strong> non-target organisms due to pesticide<br />

applications. The initial study focused on birds, and the author attempted to correlate<br />

field mortality data to known chemical and toxicological properties recorded during<br />

the registration <strong>of</strong> these compounds through the application <strong>of</strong> different mathematical<br />

models. These approaches used factors such as oral toxicity, half-life, and other<br />

factors, and the deducted model al<strong>low</strong>ed the correct prediction <strong>of</strong> bird mortality in 85<br />

% <strong>of</strong> tested cases (Mineau & Whiteside, 2005).<br />

These techniques were further developed and refined under the Canadian National<br />

Agri-Environmental Standards Initiative (NAESI), where, among others, acceptable<br />

standards were set for pesticide effects on all environmental compartments. The<br />

NAESI approach al<strong>low</strong>s a statistically calibrated prediction <strong>of</strong> pesticide-caused losses<br />

suffered by birds, mammals, non-target arthropods, edaphic invertebrates<br />

(particularly earthworms) and aquatic organisms (Mineau et al., 2008).<br />

As such, this model is the only available system that al<strong>low</strong>s for the direct prediction <strong>of</strong><br />

field mortality on the basis <strong>of</strong> laboratory parameters. Hence, this approach breaks<br />

new ground by providing a calibrated prediction <strong>of</strong> adverse effects as opposed to a<br />

theoretical <strong>risk</strong> score.<br />

Regarding the application <strong>of</strong> this approach to microbial pesticides, there is, in theory,<br />

no compelling reason why it could not be used for microbial active ingredients.<br />

However, as indicated by the authors, the method relies on the ability to link field<br />

mortality directly to the pesticide application. The longer the time between exposure<br />

and measurement <strong>of</strong> damage, the more difficult it is to establish such a correlation in<br />

the field. This can certainly cause problems for microbial pest control agents<br />

particularly those that have an infective rather than toxic mode <strong>of</strong> action. For example<br />

entomopathogenic fungi can <strong>of</strong>ten have a considerable latent period <strong>of</strong> several days<br />

or longer. Further the availablity <strong>of</strong> the required data is <strong>of</strong>ten limited for microbials.<br />

Nevertheless, the NAESI approach has great potential, and its implementation in <strong>risk</strong><br />

assessment models is highly recommended.<br />

17


ERBIC Risk Indicator<br />

To our knowledge, the only attempt to numerically describe the environmental <strong>risk</strong>s<br />

<strong>of</strong> biological organisms was developed by the New Zealand Environmental Risk<br />

Management Authority (ERMA). First developed by Hickson et al. (2000) to assess<br />

the <strong>risk</strong>s related to the introduction <strong>of</strong> genetically modified organisms into New<br />

Zealand, this approach was further developed in the European Union research<br />

project ERBIC (Evaluating Environmental Risks <strong>of</strong> Biological Control Introductions<br />

into Europe; Hokkanen et al., 2003; van Lenteren et al., 2003). In part, this approach<br />

has also been adopted by the OECD for the review <strong>of</strong> inundative releases <strong>of</strong><br />

beneficial insects (OECD, 2004a).<br />

The underlying principle for the ERBIC/ERMA system is the definition <strong>of</strong> <strong>risk</strong> as the<br />

product <strong>of</strong> the probability <strong>of</strong> an effect, and the magnitude <strong>of</strong> its impact. The <strong>risk</strong> <strong>of</strong><br />

adverse effects <strong>of</strong> a certain organism is scored and calculated on the basis <strong>of</strong> this<br />

principle in five separate <strong>risk</strong> categories, which are then added up to form the overall<br />

<strong>risk</strong> indicator. The categories used are (i) the <strong>risk</strong> <strong>of</strong> establishment in non-target<br />

habitat, (ii) dispersal potential, (iii) host range, (iv) direct and (v) indirect effects.<br />

One advantage <strong>of</strong> this system is the very simple calculation and ease with which to<br />

interpret the <strong>risk</strong> score, hence al<strong>low</strong>ing a direct and meaningful comparison between<br />

different agents.<br />

The authors <strong>of</strong> the ERBIC report have attempted to compare the obtained <strong>risk</strong> scores<br />

to values obtained for some conventional chemicals and microbial control agents for<br />

illustrative purposes. While this may be useful for a rough comparison, it is necessary<br />

to exercise caution when applying the system beyond its original scope without<br />

modification, because the <strong>risk</strong> categories were clearly defined with the goal <strong>of</strong><br />

assessing insect biocontrol agents.<br />

In the context <strong>of</strong> this paper, a key weakness <strong>of</strong> the ERBIC/ERMA approach is that<br />

the applied <strong>risk</strong> categories are treated as independent <strong>of</strong> each other. As was<br />

discussed for the Norwegian Indicator, the simple addition <strong>of</strong> sub-indices does not<br />

reflect the complexity <strong>of</strong> the interaction between all defined categories.<br />

Despite this weakness, the basic principles in calculating sub-indices are valid and<br />

merit considerations when constructing a <strong>risk</strong> indicator for a related purpose.<br />

Defining a Risk Indicator suitable to compare biological and convential<br />

pesticides<br />

When building a <strong>risk</strong> indicator for pesticides, a number <strong>of</strong> factors need to be taken<br />

into account.<br />

Upfront, it is important to differentiate between ‘<strong>risk</strong> indicator’ systems, which are<br />

intended to summarize the environmental <strong>risk</strong>s for the purpose <strong>of</strong> making<br />

environmental policy decisions and communicating <strong>risk</strong>, and ‘impact assessment<br />

systems’, which can be used to accurately predict impacts on a particular<br />

environmental component (Levitan, 2000; Mineau et al., 2008). With the exception <strong>of</strong><br />

the NAESI approach, all the systems presented above fall under the ‘<strong>risk</strong> indicator’<br />

category.<br />

Upon review <strong>of</strong> several reports on this topic (Reus et al., 2002; Mineau & Whiteside,<br />

2005) we deemed the fol<strong>low</strong>ing factors to be most important for successfully deriving<br />

a <strong>risk</strong> indicator model to al<strong>low</strong> for a adequate comparison between conventional and<br />

microbial control agents:<br />

18


Firstly, it is necessary to have a specific purpose in mind for which the <strong>risk</strong><br />

assessment is to be used. Further, the system should be relatively simple to use and<br />

understand to al<strong>low</strong> for broad acceptance (this should, however, not be achieved at<br />

the expense <strong>of</strong> accuracy). To be useful in judging environmental <strong>risk</strong> it is critical for<br />

an indicator system to score <strong>risk</strong>, not hazard.<br />

Moreover, a <strong>risk</strong> indicator should discriminate between higher and <strong>low</strong>er <strong>risk</strong><br />

substances, should avoid a bias resulting from different mechanisms <strong>of</strong> action, and<br />

should take into account both acute and chronic effects where possible. In this<br />

context it should be noted, that the actual numerical differences are less significant<br />

than the trends that they show.<br />

It is critical that the pesticide application method and formulation type are factored<br />

into the environmental <strong>risk</strong> assessment. This is necessary because the use pattern <strong>of</strong><br />

a substance dictates how different groups <strong>of</strong> organisms are exposed.<br />

Finally, a system should be adaptable to accommodate new scientific information<br />

without major revision and should al<strong>low</strong> for input <strong>of</strong> expert judgement where data<br />

gaps are identified.<br />

We consider these factors essential for such a system to yield valid and valuable<br />

results for the comparative assessment <strong>of</strong> environmental pesticide <strong>risk</strong>s.<br />

Proposed <strong>risk</strong> indicator and rationale<br />

Based on the above arguments we propose a <strong>risk</strong> indicator for balanced comparative<br />

assessment <strong>of</strong> both conventional and biological pesticides. The main emphasis <strong>of</strong><br />

our system is to focus on microbial pesticides, but the proposed structure should also<br />

enable the assessment <strong>of</strong> substances with other modes <strong>of</strong> action such as<br />

semiochemicals or growth regulators.<br />

Basic components and their integration<br />

Five basic components are proposed for the calculation <strong>of</strong> the <strong>risk</strong> indicator (RI).<br />

These are the persistence <strong>of</strong> the substance (P), the dispersal potential (D), the range<br />

<strong>of</strong> non-target organisms that are affected (N), direct effects (E D ) and indirect effects<br />

(E I ) on the ecosystem.<br />

Each <strong>of</strong> the component values consists <strong>of</strong> a ‘likelihood’ and a ‘magnitude’ factor. Both<br />

values score on a scale between 1 and 5, resulting in a component range from 1 to<br />

25, where 25 marks the highest <strong>risk</strong>. The direct effects score (E D ) is multiplied by a<br />

weighting factor (W) if vertebrates or other groups <strong>of</strong> specific importance are<br />

affected.<br />

These components are modified from the ERBIC model to accommodate microbial<br />

and conventional chemical pesticides. The category <strong>of</strong> vertebrate toxicity was added<br />

to give special consideration to this group.<br />

Because both persistence and dispersal potential increase the potential for negative<br />

effects in the other categories, we propose the fol<strong>low</strong>ing integration <strong>of</strong> the variables<br />

to calculate the overall environmental <strong>risk</strong> score as fol<strong>low</strong>s:<br />

RI = (P+D)*[N+(E D *W)+E I ]<br />

19


The multiplication <strong>of</strong> non-target <strong>risk</strong>s with persistence and dispersal factors is in our<br />

opinion the only appropriate way to account for the elevated <strong>risk</strong> resulting from<br />

increased exposure <strong>of</strong> non-targets.<br />

There are three factors at play which affect environmental pesticide <strong>risk</strong>: these are<br />

label rates, formulation type, and application method. We consider it necessary to<br />

calculate the <strong>risk</strong> indicator on an application basis for the end-use product, as label<br />

rates, application method and formulation will strongly affect environmental exposure.<br />

Scoring and rationales<br />

Persistence. Persistence <strong>of</strong> an active ingredient in the environment is an important<br />

factor in determining its <strong>risk</strong> because it strongly influences the likelihood for nontarget<br />

organism exposure. However, it is a difficult task to define a scoring system<br />

where conventional chemicals and microbials can be fairly compared. Clearly, living<br />

organisms can have an entirely different behaviour in the environment than<br />

chemicals in that they can proliferate in the environment. On the other hand microorganisms<br />

<strong>of</strong>ten have a narrow host range and may, in the absence <strong>of</strong> a suitable host<br />

for proliferation, degrade in the environment similarly to chemical substances.<br />

Further, it is important to note that, from a <strong>risk</strong> assessment perspective, an organism<br />

or substance naturally present in the environment must be regarded differently than a<br />

new species or substance introduced into an ecosystem.<br />

We postulate that a naturally occurring substance or organism will pose no additional<br />

<strong>risk</strong> to the environment if introduced into a comparable system at similar<br />

concentrations. For instance, the concentrations <strong>of</strong> entomopathogenic fungi <strong>of</strong>ten<br />

heavily fluctuate depending on host densities and micro-climatic conditions, and<br />

concentrations found during naturally occurring epizootics are <strong>of</strong>ten as high as those<br />

found after artificial inoculations (Kessler, 2004; Laengle, 2005).<br />

Therefore, a relatively high and persistent concentration <strong>of</strong> an indigenous organism in<br />

the environment, even if a result <strong>of</strong> artificial inoculation, does not necessarily add an<br />

environmental <strong>risk</strong>. Contrarily, persistence <strong>of</strong> non-indigenous micro-organism in the<br />

environment also means prolonged exposure <strong>of</strong> potential non target organisms that<br />

may never have been previously exposed to the micro-organism. Likewise, persistent<br />

or increasing concentrations <strong>of</strong> a micro-organism in the absence <strong>of</strong> its natural host<br />

could be an indicator <strong>of</strong> vegetative growth or even multiplication in non-target hosts.<br />

To account for these considerations in a systematic manner, we propose to score the<br />

persistence component in our <strong>risk</strong> indicator as laid out in Table 1. The persistence<br />

score for both chemicals and microbials is dependent on its half-life in the absence <strong>of</strong><br />

the target host, where the half-life is the highest value from all environmental<br />

compartments. The reduced <strong>risk</strong> for indigenous micro-organisms and naturally<br />

occurring substances is taken into account by assigning a <strong>low</strong> persistence score if<br />

concentrations return to levels comparable to natural concentrations within one or<br />

two years <strong>of</strong> application.<br />

Table 1 Scores assigned for persistence <strong>of</strong> the assessed active ingredient. Values<br />

are assigned based on its half-life in the environmental compartment where the agent<br />

is most stable, or based on the percentage <strong>of</strong> CFUs (colony forming units) <strong>of</strong> BCA<br />

found one or two years post application (in target absence).<br />

20


Persistence factor<br />

Score<br />

Persistence in target absence (use column 2 or 3, depending on available<br />

information)<br />

1 2 ( = 1)<br />

No BCA detectable in soil 1 yr after application<br />

(or at levels found naturally for indigenous T 0.5 < 30 d<br />

species)<br />

2 2 ( = 2)<br />

> 0 % - 16 % <strong>of</strong> original CFUs 1 yr after application<br />

T<br />

(for indigenous species: at natural levels after 2 0.5 = 0.1 a - 0.25 a (36 d - 91<br />

d)<br />

yrs)<br />

3 2 (= 9) 16 % - 40 % <strong>of</strong> original CFUs 1 yr after application T 0.5 = 0.25 a - 0.75 a (91 d -274<br />

d)<br />

4 2<br />

40 % -62 % <strong>of</strong> original CFUs 1 yr after application T<br />

(= 16)<br />

0.5 = 0.75 a – 1.5 a<br />

5 2 No significant reduction <strong>of</strong> CFUs 1 yr after<br />

T<br />

(= 25) application<br />

0.5 > 1.5 a<br />

T 0.5 stands for half life in the absence <strong>of</strong> the target.<br />

For the purpose <strong>of</strong> the proposed <strong>risk</strong> indicator system, the persistence <strong>of</strong> biological<br />

and conventional pesticides scores as described in Table 1. Where there is variation<br />

<strong>of</strong> persistence in different environmental compartments, the highest value is applied<br />

to determine the persistence score.<br />

Dispersal. As with persistence, the dispersal potential <strong>of</strong> a substance or organism<br />

greatly influences the likelihood <strong>of</strong> non-target exposure. The <strong>risk</strong> level resulting from<br />

this component is dependent on the distance <strong>of</strong> dispersal and the quantity <strong>of</strong><br />

dispersed material.<br />

Many factors affect the dispersal potential <strong>of</strong> pest control <strong>products</strong>. These include<br />

spray drift, bioaccumulation, leaching and run-<strong>of</strong>f. Specific to microbials is the<br />

dispersal by infected organisms. We propose to calculate the dispersal <strong>risk</strong> factor as<br />

detailed in Table 2 by multiplying the score for the maximum dispersed distance with<br />

the score given for dispersed quantity. The dispersal factor is calculated on an<br />

application basis, and will therefore vary significantly between, for instance, a spray<br />

application and a seed treatment with the same active ingredient.<br />

Table 2 Scoring <strong>of</strong> dispersal factor on the basis <strong>of</strong> dispersal distance and quantity.<br />

Dispersal factor<br />

Score Distance Quantity<br />

1 < 10 m < 1 %<br />

2 < 100 m < 5 %<br />

3 < 1 000 m < 10 %<br />

4 < 10 000 m < 25 %<br />

5 > 10 000 m > 25 %<br />

21


For a given chemical pesticide, the dispersal factor would be calculated by<br />

determining the maximum dispersal distance and quantity, taking into account spray<br />

drift, run-<strong>of</strong>f and leaching, dispersal via bioaccumulation, and through evaporation.<br />

Similarly, when scoring for micro-organisms spray drift, leaching and run-<strong>of</strong>f will be<br />

considered. Additionally, the dispersal through infected organisms must be<br />

accounted for, as this can involve the transport <strong>of</strong> significant quantities <strong>of</strong> infectious<br />

material over long distances.<br />

In the absence <strong>of</strong> more detailed knowledge the fol<strong>low</strong>ing generalized worst case<br />

assumptions are applied: for spray applications, drift is assumed to disperse 10 % <strong>of</strong><br />

the applied active ingredient up to 100 m (Pest Management Regulatory Agency,<br />

2007); for microbials pathogenic to insects, unless other information is available, a<br />

dispersal distance <strong>of</strong> up to 1000 m is assumed due to the possibility <strong>of</strong> infected<br />

insects spreading the inoculum.<br />

Range <strong>of</strong> non target effects. Most bacteria and fungi have, under certain<br />

conditions, the potential to act as opportunistic pathogens and infect species<br />

normally not susceptible to the organism. These conditions include high inoculum<br />

concentrations, climatic conditions suitable for the micro-organism, and/or<br />

circumstances under which the immune response <strong>of</strong> the potential host is weakened.<br />

It is, therefore, important to differentiate between the physiological and the ecological<br />

host range (Onstad & McManus, 1996; Jaronski et al., 1998; Jaronski et al., 2003;<br />

Meyling et al., 2005). For an environmental <strong>risk</strong> assessment only the ecological host<br />

range <strong>of</strong> a biological control agent is <strong>of</strong> interest. As a consequence, laboratory<br />

studies on non-target organisms should be designed to reflect natural conditions.<br />

Likewise for chemicals, the target range assessment should be done at<br />

concentrations realistic for a typical application scenario. Where available NOEL<br />

levels, dose-response curves or <strong>risk</strong> quotients (estimated environmental<br />

concentration over toxicity) should be used for this assessment.<br />

Table 3 Assignment <strong>of</strong> scores for non-target effects. Modified from Hickson et al.<br />

(2000) and Hokkanen et al. (2003) to better suit the inclusion <strong>of</strong> chemical pesticides<br />

in the proposed system.<br />

Range <strong>of</strong> non-target effects<br />

Score Likelihood Magnitude<br />

1 1 species Genus<br />

2 2-3 species Family<br />

3 4-10 species Order<br />

4 11-30 species Class<br />

5 > 30 species >= Phylum<br />

Once the range <strong>of</strong> possible affected non-targets is determined, the score in this<br />

category can be calculated as described in Table 3. Should significant indirect effects<br />

occur, the number <strong>of</strong> affected species (irrespective <strong>of</strong> the taxonomic level) must be<br />

included when scoring for the range <strong>of</strong> non-target species.<br />

While the scoring guidance for non-targets described above is relatively<br />

straightforward, the antagonistic suppression <strong>of</strong> microbial growth to control plant<br />

22


diseases is difficult to capture in this section. Effects described above focus on nontarget<br />

mortality - an approach not suited to describe the dynamics <strong>of</strong> a microbial<br />

community. Therefore, in the absence <strong>of</strong> more detailed knowledge, the likelihood and<br />

magnitude values in this category are set to three for antagonistic micro-organisms.<br />

As in the previous category, the <strong>risk</strong> score results from the multiplication <strong>of</strong> likelihood<br />

and magnitude <strong>of</strong> the effect.<br />

Direct Effects. Whereas the host/target range describes the spectrum <strong>of</strong> organisms<br />

affected by the pest control product, the direct and indirect effects characterise the<br />

impact on the most sensitive non-target organism or group. This portion <strong>of</strong> the <strong>risk</strong><br />

indicator is calculated by multiplication <strong>of</strong> the likelihood <strong>of</strong> an adverse effect<br />

(mortality) with its magnitude. The likelihood <strong>of</strong> non target mortality can, for instance,<br />

be deduced from dose/response data or an ‘impact assessment system’ such as the<br />

NAESI approach presented above (compare Mineau et al., 2008).<br />

Somewhat more challenging is the assessment <strong>of</strong> the non-target effects for<br />

antagonistic organisms used for disease suppression. These organisms do not kill<br />

their targets, but rather suppress the growth <strong>of</strong> disease-causing micro-organisms by<br />

establishing in their ecological niche. Capturing the suppression <strong>of</strong> non target microorganisms<br />

by an antagonist in the proposed indicator will only be considered if a<br />

substantial long-term suppression and/or consequential indirect effects are expected.<br />

For instance, suppression <strong>of</strong> a saprotrophic basidiomycete fungus in the soil after<br />

application <strong>of</strong> an antagonist to wild blueberry would be considered as a non-target<br />

effect, whereas transient changes in the soil or phylloshpere microbiota would not.<br />

The scoring regime for direct effects, described in Table 4, al<strong>low</strong>s for an assessment<br />

based on likelihood and magnitude <strong>of</strong> the effect (derived from ERBIC system), or<br />

alternatively on the basis <strong>of</strong> the highest <strong>risk</strong> quotient as determined from a<br />

deterministic <strong>risk</strong> assessment approach as described by PMRA (Pest Management<br />

Regulatory Agency, 2007).<br />

Table 4. Risk <strong>of</strong> direct effects. The overall score is either the product <strong>of</strong> scores<br />

assigned for likelihood and magnitude, or the square <strong>of</strong> the score assigned for the<br />

highest <strong>risk</strong> quotient as described by the PMRA.<br />

Direct Effects<br />

Score Likelihood Magnitude Score<br />

Highest<br />

Quotient<br />

1<br />

Very unlikely (<<br />

< 5 % mortality<br />

1 %)<br />

1 2 ( = 1) < 0.1<br />

2 Unlikely (1 %-10 %) < 50 % mortality 2 2 ( = 4) < 1<br />

3<br />

Possible (10 %- > 50 % mortality or > 10 %<br />

3 2 ( = 9)<br />

50 %)<br />

short term suppression<br />

< 10<br />

4 Likely (50 %-80 %)<br />

> 50 % mortality ore > 10 %<br />

4 2 (= 16)<br />

permanent suppression<br />

< 100<br />

> 10 % long term<br />

5 Very likely (> 80 %) suppression or local 5 2 (= 25) > 100<br />

extinction<br />

Risk<br />

23


Indirect Effects. Indirect effects in this context are defined as changes in the<br />

ecosystem that are a consequence <strong>of</strong> a direct effect caused by the use <strong>of</strong> a pesticide.<br />

For instance, the reduction <strong>of</strong> pollinators will reduce the reproduction <strong>of</strong> plants that<br />

rely on these pollinators. Likewise, pesticide effects on earthworms, aquatic plants, or<br />

microbial activity will temporarily or permanently alter the ecosystem the product is<br />

applied to. Because <strong>of</strong> their indirect nature, the level <strong>of</strong> uncertainty in assessing<br />

these effects is greater than for the other components <strong>of</strong> the <strong>risk</strong> indicator system,<br />

and the assessment must mainly rely on expert judgement. However, the estimation<br />

<strong>of</strong> how severe the occurrence <strong>of</strong> a non-target effect is on an ecosystem level is<br />

considered significant for the appropriate assessment <strong>of</strong> pesticide <strong>risk</strong> to the<br />

ecosystem.<br />

Table 5. Score for indirect effects on the ecosystem. Assignments are generally<br />

based on expert judgement as indicated by the ecosystematic position <strong>of</strong> organisms<br />

affected by direct effects, and the severity <strong>of</strong> anticipated effects.<br />

Indirect Effects<br />

Score Likelihood Magnitude<br />

1 Very unlikely no significant impact on whole ecosystem<br />

2 Unlikely<br />

minor and short-term impact on parts <strong>of</strong><br />

ecosystem<br />

3 Possible<br />

significant short-term impact on parts <strong>of</strong><br />

4 Likely<br />

ecosystem<br />

significant long-term impact on parts <strong>of</strong><br />

ecosystem<br />

5 Very likely significant long-term impact on whole ecosystem<br />

Table 5 describes the scoring mechanism for indirect effects. As a general guidance,<br />

substances that score high in the host range and direct effects sections will in most<br />

cases have a higher likelihood for indirect effects.<br />

Vertebrate toxicity. We propose to apply a weighting factor to direct effects (E D ) to<br />

increase the value for non-target losses if vertebrates are affected. The weighting<br />

scheme is described in Table 6.<br />

Table 6 Factors assigned whether or not direct effects concern vertebrates.<br />

Vertebrate toxicity<br />

Factor Magnitude<br />

1 No vertebrates are affected<br />

1.5 Poikilothermic vertebrates are affected by non-target effects<br />

2 Homeothermic vertebrates are affected<br />

24


Demonstration <strong>of</strong> Risk Indicator using selected pest control agents<br />

In order to demonstrate the validity <strong>of</strong> the proposed <strong>risk</strong> indicator we applied this<br />

system to a number <strong>of</strong> well-studied biological control agents and selected chemical<br />

<strong>products</strong> used for similar purposes. Organisms scored were Bacillus thuringiensis,<br />

Beauveria brongniartii, Beauveria bassiana, Coniothyrium minitans, Metarhizium<br />

anisopliae, Pantoea agglomerans, Pseudomonas fluorescens, Trichoderma<br />

harzianum; conventional pesticides assessed were atrazine, chlorpyrifos, benomyl,<br />

DDT, methyl bromide, phorate and streptomycin. Indices were calculated using open<br />

literature and published regulatory documents. The results are displayed in Table 7.<br />

The organisms with the <strong>low</strong>est <strong>risk</strong> indicator were soil applied fungi with very narrow<br />

host ranges when used in environments to which they are native. These organisms<br />

consistently scored <strong>low</strong> in all categories. Biocontrol agents with broader host ranges<br />

delivered by spray application typically had a higher dispersal potential and also<br />

scored higher under direct and indirect effects, but remained about one magnitude or<br />

more be<strong>low</strong> conventional chemical alternatives.<br />

The highest scoring substances were DDT, methyl bromide, and chlorpyriphos.<br />

These scores were largely a consequence <strong>of</strong> high persistence and dispersal<br />

potential, combined with wide target ranges and high values assigned for direct and<br />

indirect effects.<br />

On average, biopesticides had an approximately 40 times (range 9-200) <strong>low</strong>er <strong>risk</strong><br />

indicator than conventional <strong>products</strong> used for the same purpose.<br />

Conclusions and envisaged applications<br />

The proposed <strong>risk</strong> indicator is, to our knowledge, the first indicator to al<strong>low</strong> a direct<br />

numerical comparison <strong>of</strong> relative environmental <strong>risk</strong>s posed by microbials and<br />

conventional chemical pesticides.<br />

While microbials are <strong>of</strong>ten reported to pose <strong>low</strong> <strong>risk</strong>s to the environment (OECD,<br />

2007), it is <strong>of</strong> critical importance for the credibility <strong>of</strong> the promoters <strong>of</strong> microbial pest<br />

control <strong>products</strong> to be able to underline such generic statements with solid data.<br />

The presented framework permits the unbiased generation <strong>of</strong> an environmental <strong>risk</strong><br />

score for biological and chemical <strong>products</strong> on the basis <strong>of</strong> scientific and regulatory<br />

data.<br />

Key advantages <strong>of</strong> the proposed system compared to previously available <strong>risk</strong><br />

indicator systems are (i) the applicability to biological and conventional pesticides to<br />

al<strong>low</strong> a direct comparison between <strong>products</strong>, (ii) the ability to score the <strong>risk</strong> on an<br />

application basis rather than on an active ingredient basis, (iii) the flexibility <strong>of</strong> the<br />

system that permits the use <strong>of</strong> regulatory data or published literature, and (iv) a<br />

readily understandable output. The latter al<strong>low</strong>s for a broader discussion beyond the<br />

highly specialised expert community <strong>of</strong> the environmental advantages certain<br />

<strong>products</strong> may <strong>of</strong>fer from an environmental <strong>risk</strong> perspective.<br />

In our analysis <strong>of</strong> selected <strong>products</strong> we found that the environmental <strong>risk</strong> score<br />

greatly varied within the assessed chemical <strong>products</strong>, and also, yet at a much <strong>low</strong>er<br />

level, within the group <strong>of</strong> microbial <strong>products</strong>. Further to this, it was demonstrated, that<br />

the use pattern <strong>of</strong> a product has a great influence on the estimated environmental<br />

<strong>risk</strong> posed by a specific product.<br />

25


Table 7 Risk scores and calculated <strong>risk</strong> indicator for selected microbial and conventional pest control <strong>products</strong>.<br />

Active Ingredient<br />

Persistence factor<br />

Dispersal<br />

factor<br />

Distance<br />

Quantity<br />

Host Range Direct<br />

Effect<br />

Species<br />

Taxonomic<br />

level<br />

Likelihood<br />

Magnitude<br />

Indirect<br />

Effects<br />

Likelihood<br />

Magnitude<br />

Vertebrate effects<br />

Risk Score<br />

Sources<br />

Bacillus thuringiensis (foliar spray) 4 2 3 4 4 3 2 2 3 1 <strong>28</strong>0<br />

Beauveria brongniartii (soil) 1 3 1 2 1 1 1 1 1 1 16<br />

Beauveria bassiana (foliar spray) 1 3 3 4 4 3 2 2 2 1 260<br />

Beauveria bassiana (soil) 1 3 1 4 4 3 2 1 2 1 96<br />

Joung & Coté (2000); Pest Management<br />

Regulatory Agency (2006c)<br />

Kessler et al. (2004); Kessler (2004);<br />

Laengle et al. (2005); Laengle (2005);<br />

Traugott et al. (2005)<br />

Vänninen et al. (2000); BIPESCO (2001);<br />

Hokkanen et al. (2003); Butt (2004);<br />

Laengle (2006); US EPA, (2006a)<br />

Vänninen et al. (2000); BIPESCO (2001);<br />

Hokkanen et al. (2003); Butt (2004);<br />

Laengle (2006); US EPA, (2006a)<br />

Coniothyrium minitans (soil) 1 1 3 1 1 1 1 2 2 1 24 US EPA (2002b)<br />

Metarhizium anisopliae (soil) 1 3 1 4 4 3 2 1 2 1 96<br />

Metarhizium anisopliae (foliar<br />

spray)<br />

Pantoea. agglomerans (foliar<br />

spray)<br />

1 3 3 4 4 3 2 1 2 1 240<br />

1 3 2 3 3 2 1 1 1 2 98<br />

Vänninen et al. (2000); BIPESCO (2001);<br />

Hokkanen et al. (2003); Butt (2004);<br />

Meyling et al. (2005)<br />

Vänninen et al. (2000); BIPESCO (2001);<br />

Hokkanen et al. (2003); Butt (2004);<br />

Meyling et al. (2005)<br />

Pest Management Regulatory Agency<br />

(2006a)<br />

26


Pseudomonas fluorescens (foliar<br />

spray)<br />

1 2 3 3 3 2 1 1 1 1.5 91<br />

Trichoderma harzianum (soil) 4 1 1 3 3 3 2 2 2 1 95<br />

Chlorpyrifos (foliar spray) 9 5 4 5 5 5 5 5 3 2 2610<br />

Lindemann et al., (1982); Beattie & Lindow<br />

(1995); Beattie & Lindow (1999); Lindow &<br />

Brandl (2003); Lindow & Sus<strong>low</strong> (2003);<br />

Moore et al. (2004); US EPA (2006b)<br />

Pest Management Regulatory Agency<br />

(2006b)<br />

US EPA (2002a); Pest Management<br />

Regulatory Agency (2003a)<br />

Benomyl (foliar spray) 16 2 3 5 5 5 4 5 3 2 1760 Extension Toxicology Network (1996a)<br />

Methyl bromide (fumigation) 25 5 5 5 5 5 3 3 3 2 3200 Extension Toxicology Network (1996b)<br />

Streptomycin (foliar spray) 9 3 3 5 5 3 3 5 3 1 882 US EPA (2006)<br />

Atrazine (foliar spray) 25 5 4 5 5 5 5 3 3 1.5 3218<br />

Pest Management Regulatory Agency<br />

(2007); Mineau et al. (2008)<br />

DDT (foliar spray) 25 5 4 5 5 5 5 5 4 2 4275 Extension Toxicology Network (1996c)<br />

Phorate (granular) 9 5 3 5 5 5 5 3 3 2 2016<br />

Pest Management Regulatory Agency<br />

(2003b)<br />

27


These results demonstrate that the proposed system enables a clear differentiation<br />

between <strong>products</strong> and use patterns.<br />

We acknowledge that no <strong>risk</strong> indicator scoring system can replace the <strong>risk</strong><br />

assessment frameworks used by regulatory bodies to reach a decision on the<br />

acceptability <strong>of</strong> <strong>risk</strong>s posed by a certain product. However, we can certainly envisage<br />

the proposed <strong>risk</strong> indicator helping in regulatory decisions:<br />

The system could help in defining <strong>low</strong> <strong>risk</strong> <strong>products</strong>. We consider a <strong>risk</strong> score <strong>of</strong> 100<br />

to be a reasonable cut-<strong>of</strong>f value for "<strong>low</strong> <strong>risk</strong>" <strong>products</strong>, whereas a threshold <strong>of</strong> 500<br />

seems justified for the term "reduced <strong>risk</strong>". Regulatory implications should reduce<br />

data requirements or acceptance data waivers upon the submission <strong>of</strong> a well<br />

documented <strong>risk</strong> score, and a significant reduction <strong>of</strong> registration/submission fees for<br />

"<strong>low</strong> <strong>risk</strong>" and "reduced <strong>risk</strong>" <strong>products</strong>. An example for such reduced fees is the<br />

Canadian PMRA, which has waived review fees for certain reduced-<strong>risk</strong> <strong>products</strong><br />

such as microbial and semiochemical pesticides. Further, the <strong>risk</strong> score enables a<br />

measurement <strong>of</strong> <strong>risk</strong> reduction strategies and the impact <strong>risk</strong>-mitigation restrictions.<br />

A ranking <strong>of</strong> <strong>risk</strong>s posed by various pest control <strong>products</strong> would al<strong>low</strong> for more<br />

targeted efforts to reduce pesticide <strong>risk</strong>s in agriculture, and could thus be highly<br />

beneficial for the environment.<br />

For industry representatives, the calculation <strong>of</strong> the environmental <strong>risk</strong> score for both<br />

conventional chemicals and microbial agents could assist in the decision on which<br />

product to pursue at a relatively early stage <strong>of</strong> development. As indicated above, a<br />

<strong>risk</strong> score that is well documented with data and/or scientific literature could be used<br />

to support the request to waive certain environmental data requirements in support <strong>of</strong><br />

registration.<br />

Finally, the <strong>risk</strong> indicator data al<strong>low</strong>s the activation <strong>of</strong> clauses in pesticide legislation<br />

that al<strong>low</strong> regulators to consider relative <strong>risk</strong> in comparison with other <strong>products</strong><br />

available for the same uses (such as those in Canada’s updated Pest Control<br />

Products Act).<br />

We believe that the proposed system can help stakeholder groups (i.e. <strong>risk</strong><br />

assessors, academia, and industry) to facilitate discussions regarding the regulatory<br />

approaches to microbial and other biological pest control organisms. Maximum<br />

benefit from this system could be achieved through establishing a web-based<br />

database that could serve as a reference for experts, growers, and the interested<br />

public and al<strong>low</strong> informed decisions in areas ranging from product development and<br />

registration to product choice on the farm level.<br />

Acknowledgements<br />

This work was supported by the European Commission, Quality <strong>of</strong> Life and<br />

Management <strong>of</strong> Living Resources Programme (QoL), Key Action 1 on Food, Nutrition<br />

and Health, QLK1-2001-01391 and Specific Support Action, SSPE-022709. We also<br />

wish to thank Brian Belliveau (Pest Management Regulatory Agency <strong>of</strong> Canada),<br />

Anita Fjelsted (Danish Ministry <strong>of</strong> the Environment), Stefan Jaronski (USDA ARS<br />

Northern Plains Agricultural Research Laboratory), Olaf Strauch (University <strong>of</strong> Kiel),<br />

and Stefan Hutwimmer (University Innsbruck), for their helpful discussion and kindly<br />

reviewing the manuscript.<br />

<strong>28</strong>


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33

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