Case Law[2023] ZAGPPHC 520South Africa
African Centre for Biodiversity NPC v Minister of Agriculture, Forestry and Fisheries and Others [2023] ZAGPPHC 520; 27524/2017 (27 June 2023)
High Court of South Africa (Gauteng Division, Pretoria)
27 June 2023
Headnotes
the Appeal Board’s decision.
Judgment
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## African Centre for Biodiversity NPC v Minister of Agriculture, Forestry and Fisheries and Others [2023] ZAGPPHC 520; 27524/2017 (27 June 2023)
African Centre for Biodiversity NPC v Minister of Agriculture, Forestry and Fisheries and Others [2023] ZAGPPHC 520; 27524/2017 (27 June 2023)
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sino date 27 June 2023
IN THE HIGH COURT OF
SOUTH AFRICA
GAUTENG DIVISION,
PRETORIA
CASE NO: 27524/2017
In
the matter between:
AFRICAN
CENTRE FOR BIODIVERSITY NPC
(NPO
Registration no: 2004/025137/08)
Applicant
And
MINISTER
OF AGRICULTURE, FORESTY AND FISHERIES
First
Respondent
DIRECTOR-GENERAL:
DEPARTMENT OF
AGRICULTURE,
FORESTRY AND FISHERIES
Second
Respondent
APPEAL
BOARD: GENETICALLY MODIFIED ORGANISMS
Third
Respondent
EXECUTIVE
COUNCIL FOR GENETICALLY MODIFIED ORGANISMS
Fourth
Respondent
MONSANTO
SOUTH AFRICA (PTY) LTD
(Registration
no: 1968/001485/08)
Fifth
Respondent
JUDGMENT
# Tolmay J
Tolmay J
Introduction
1.
This is an application to review and set aside the approval of
the general release of MON 87460, a genetically modified variety of
maize. The applicant (ACB) brings this application for the review and
setting aside of three decisions (the impugned decisions),
namely the approval by the fourth respondent (EC) given during June
2015 for the general release of MON 87460 (the EC decision)
, the
dismissal of the third respondent (the Appeal Board) on 1 September
2016 of ACB’s appeal against the EC decision
(the Appeal
Board decision) and the first respondent’s (The Minister)
confirmation of the Appeal Board decision dated 2 December
2016 (The
Minster’s decision).
2.
ACB seeks an order referring the fifth respondent’s
(Monsanto) application for approval for the general release of MON
87460
back to the EC for reconsideration. After the launch of this
application, Bayer (Pty) Ltd (Bayer) acquired full ownership of
Monsanto
and was joined as a party to the proceedings. The crux of
ACB’s case is that the respective decision makers accepted the
data included in Monsanto’s application at face value and
without ensuring that the necessary health and safety risks
associated
with MON 87460 had been properly and independently
assessed.
3.
ACB did not launch the application under rule 53 and did not
call for a record. Monsanto however called for such a record and ACB
failed to file a supplementary founding affidavit after the filing of
the record.
Background
4.
The permit for the
general release of MON 87460 was issued in terms of the Genetically
Modified Organisms Act 15 of 1997 (GMO Act)
by the EC, which is a
body created by the GMO Act to determine whether such permits should
be granted.
[1]
The decision was
taken in consultation with the Advisory Committee (AC) which is a
specialist body comprised of experts
[2]
.
Both the EC and the AC found MON 87460 to be safe for animals,
humans, and the environment. ACB brought the review application
under
the Promotion of Administrative Justice Act 3 of 2000 (PAJA).
5.
On the 14
th
of July 2014, Monsanto applied for a
permit for the general release of MON 87460, a genetically modified
maize variety. On the
15
th
of June 2015, the EC granted
the permit. ACB made no submissions to the EC, as it was unaware of
the application. ACB had been
engaging the respondents in various
applications relating to MON 87460 since 2007. ACB, due to a lack of
resources did not see
the notices that were published in three
newspapers as is required by the GMO regulations, and only became
aware of the EC decision
by way of an email dated 18 June 2015. ACB
requested reasons and this was provided. On 7 August 2015 it lodged
and appeal, de novo.
On 1 September 2016 ACB was informed that the
appeal was dismissed and on 2 December 2016 it was informed that the
Minister had
upheld the Appeal Board’s decision.
6.
Monsanto claims that MON 87460 suffers less yield loss in
water limited conditions, than conventional maize, it is referred to
as
a drought tolerant variety of maize. It has been approved for use
in food, animal feed and environmental release in 17 countries,
including the United States, the European Union, Korea, and Japan.
Certain field trials were also concluded in South Africa, although
the results of these trials were confidential, ACB’s legal
representatives and experts were granted access to this information
by way of a court order.
Issues to be decided
7.
The court has to decide whether the impugned decisions should
be reviewed and set aside in terms of PAJA and in particular whether;
a) the EC decision
complied with section 5(1)(a) of the GMO Act.
b) the EC decision
was procedurally fair.
c) the EC provided
adequate reasons for its decision.
d) the EC failed to
apply its mind to the information provided.
e) the EC’s
decision was supported by the evidence before it.
f) the Appeal
Board adequately addressed the appeal grounds raised by the
applicant.
g) the Minister failed to
give reasons for her decision or failed to engage with the issues
before the EC and Appeal Board.
h) the application for
the general release of MON87460 ought to be referred to the EC for
reconsideration.
Review proceedings
8.
It is trite that
in review proceedings that the question is not whether the relevant
decision is correct, it is whether the decision
maker exercised its
powers properly. The focus thus is on the process and the way in
which the decision maker came to the decision.
[3]
It is common cause that the decisions made in this matter are
administrative actions and that ACB must establish grounds of review
under PAJA as the decisions were taken “by an organ of State in
the performance of a public function”
[4]
.
In review applications, the doctrine of separation of powers requires
a court, when reviewing administrative actions, to treat
administrative decisions with appropriate deference and respect and
is required to “give due weight to findings of fact and
policy
decisions made by those with special expertise and experience in the
field.”
[5]
9.
In this case, the
court is confronted with disputes of fact as the experts of ACB have
conflicting views with the experts of the
Advisory Committee (AC),
who advised the EC, and those experts consulted by Monsanto. ACB
accepted that there are disputes between
the relevant experts relied
on by the parties, ACB however invited the court to follow the
approach set out in Michael v Linksfield
Park Clinic (Pty) Ltd
[6]
,
in that instance however, the claim was for damages and the
hearing was conducted by way of a trial. It follows that disputes
of
fact were resolved by, inter alia, assessing the credibility and
inherent probabilities of the evidence led. The witnesses were
subjected to cross-examination and the court had the opportunity to
properly consider and evaluate the evidence led. This matter
is to be
distinguished from the Linksfield matter, as no evidence was led, and
the Court was confronted with conflicting opinions
of experts. The
evidence is of a highly technical and scientific nature.
10.
There was no
attempt to refer this matter to oral evidence. In motion proceedings
the principle established in Plascon-Evans Paints
Ltd V Van Riebeek
Paints (Pty) Ltd
[7]
, must be
applied. This well-known principle holds that in motion proceedings
an applicant can only succeed if its case can be established
based on
the facts alleged by the respondent, read together with the facts
alleged by the applicant, and admitted by the respondent.
With the
exception that if the respondent’s denial is far-fetched or
untenable the court may reject it on the papers, or
if the
respondent’s denial does not raise a bona fide dispute of fact.
The rule in Plascon-Evans was confirmed by the Constitutional
Court.
[8]
11.
In this instance, the expert’s opinions are highly
technical and based on scientific analysis. To test the veracity of
the
different viewpoints evidential scrutiny is required. The Court
is ill-suited to, without evidence, determine the disputes between
different expert opinions and is therefore obliged to follow the
so-called Plascon-Evans rule. To deviate from the Plascon-Evans
rule
would, as counsel for Monsanto argued, amount to a substantial
intrusion on the separation of powers. The starting point in
considering this review, must therefore be to apply the Plascon-Evans
rule and the Court must therefore accept the expert evidence
provided
by the State Respondents and Monsanto.
Compliance with
section 5(1)(a) of the GMO Act and application of the precautionary
principle
12.
Section 5 (1)(a) provides that the Council shall, when an
applicant applies for a permit, determine whether the applicant must
in
addition, submit an assessment in accordance with the provisions
of the National Environmental Management Act 107 of 1998 (NEMA),
of
the impact on the environment and an assessment of the socio-economic
consideration of such activities. ACB is of the view that
the
decision not to call for an independent assessment was procedurally
unfair, and that the precautionary principle was not applied.
13.
ACB,
in the founding affidavit, stated that the EC ought to have called on
Monsanto to submit risk assessment and environmental
impact studies.
The record shows that Monsanto provided a risk assessment, but ACB
insists that an independent risk assessment
should have been
provided. Monsanto’s argument is that the EC did not fail to
take a decision as envisaged in section 5(1)(a)
but took a decision
not to request an independent assessment based on the evidence before
it.
14.
The State Respondents pointed out, in their answering
affidavit that Monsanto was not required to submit an environmental
impact
assessment (EIA) in accordance with NEMA, because section 24
of NEMA only requires EIA’s to be conducted for listed
activities,
as published in section 24 (d) of NEMA. Monsanto was not
required to submit an environmental assessment, because the South
African
trials did not show that the GMO may pose a threat to any
indigenous species, or the environment.
15.
The failure to
call for an EIA is linked to the precautionary principle. ACB argued
that the precautionary principle should be applied.
This principle is
included in chapter 2 of NEMA. Section 2(4)(a)(vii) of NEMA provides
that a risk adverse and cautionary approach
should be followed. This
implies that the limits of current knowledge about the consequences
of decisions and actions should be
considered when decisions are
taken. The precautionary rule has been incorporated in the GMO
Regulations.Regulation4(6) reads:”
lack of scientific knowledge
or scientific consensus shall not be interpreted as indicating a
particular level of risk, an acceptable
risk, or an absence of risk.”
In Fuel Retailers
[9]
it was
confirmed that the principle will apply, where due to unavailable
scientific knowledge “there is uncertainty as to
the future
impact of the proposed development” and emphasised that NEMA
requires a “risk averse and cautious”
approach. In WWF
South Africa v Minister of Agriculture, Forestry and Fisheries
[10]
the court referred with approval to the Australian decision of
Telstra Corporation v Hornsby Shire Council
[11]
two conclusions were made, firstly that there must be a threat of
serious or irreversible environmental damage and secondly that
there
must be scientific uncertainty as regards the environmental damage,
for the precautionary principle to find application.
It was held that
the risk must be adequately sustained by scientific evidence and
should not be based on unsupported speculation.
[12]
The second criterium requires considerable scientific uncertainty ,
which will be established when “empirical data(as opposed
to
simply hypothesis, speculation or intuition) make it reasonable to
envisage a scenario, even if it does not enjoy unanimous
support”
[13]
.It was also pointed out
that the precautionary principle does not seek to avoid all risk.
16.
Once the two
conditions referred to above are met, the precautionary principle is
activated and the evidentiary burden shifts
[14]
.In this case, as was argued on behalf of Monsanto, it means that
once the threat is established the evidentiary burden will shift
to
Monsanto to demonstrate that the release of MON 87460 does not pose a
risk, or the risk is negligible.
17.
The precautionary principle is, as was argued on behalf of
Monsanto, not directly applicable in review proceedings. Review
proceedings
are not concerned with the merits, but rather with
whether a decision was taken in a lawful, reasonable, and
procedurally fair
manner. The application of the precautionary
principle will require of this court to venture into the merits,
which is not appropriate
in review proceedings. The applicant, in
this case, ACB, bears the onus to establish the grounds of review
relied on. Based on
the Plascon-Evans principle, the court is obliged
to rely on the respondents’ experts’ evidence, unless it
is clearly
untenable. In the absence of oral evidence, the Court is
not able to evaluate the experts’ conflicting views and must
accept
the respondents’ expert evidence and their evidence
proclaims the safety of MON87460.
18.
ACB referred to
Sustaining the Wild Coast NPC and Others v. Minister of Mineral
Resources and Energy and others
[15]
to support the argument that the precautionary principle should be
applied. The facts were different as it dealt with an exploration
right to use seismic survey to seek out oil and gas reserves off the
Eastern Cape coast. The decision related to a listed activity
and as
a result an EIA was prescribed by NEMA. It was common cause that no
environmental authorisation was secured to undertake
the impugned
survey and exploration. The court also found that there was no proper
notification and consultation with affected
parties and the process
was accordingly procedurally unfair. In this instance there was
compliance with the statutory framework
regarding notification as is
explained later on, and apart from that an appeal process had been
followed, where ACB had the full
opportunity to partake in the
proceedings and to place submissions and evidence before the Appeal
Board.
19.
The EC and later the Appeal Board relied on the expert
opinions of the AC and the expert evidence provided by Monsanto to
determine
the environmental risks. It can accordingly not be said
that the impugned decisions were unlawful, unreasonable, or
procedurally
unfair. Furthermore, an EIA was not called for under the
circumstances of this application. The result is that there was
compliance
with section 5(1)(a) of the GMO Act and this point must
fail.
Procedural Fairness
with reference to public participation
20.
ACB argued that there was no proper public participation as it
did not have the opportunity to place its submissions before the EC.
Section 3(5) of PAJA provides that when an administrator is empowered
by any empowering provision to follow a provision which is
fair, but
different from the provisions of section 3 (2) of PAJA, the
administrator may act in accordance with that different procedure.
In
this instance Regulation 9 of the GMO regulations prescribes the
process for public participation of the proposed release of
a GMO and
for interested parties to make submissions. It follows that the
procedure set out in the regulation could have been followed.
21.
ACB’s complaint with the process is, that it was not
given direct notice of the application. It had been engaging with the
respondents since 2007 about MON8746 and says that, because of this,
it should have been notified specifically. Regulation 9 of
the GMO
Regulations prescribes the process for public participation for the
general release of a GMO. The process is the following:
21.1
The proposed release must
be advertised in three national newspapers;
[16]
21.2
Certain particulars must
be included in the notice;
[17]
21.3
The notice must indicate
that any interested party may submit comments or objections within a
period of not less than 30 days;
[18]
21.4
Any comments or
objections received must be referred to the EC.
[19]
22.
It was alleged that it has not been established that the
application was advertised in three national newspapers. However
public
notices were published in the Beeld on the 25
th
of
March 2014, Business Day on the 26
th
of Match 2014 and
Rapport of 3 April 2014. In the replying affidavit, ACB explained
that it did not become aware of the notices
due to the constraints it
operates under. There was no attempt, during argument, to deny that
the publications referred to, are
national publications, or that the
notification itself suffered from any defects. Even if one is of the
view, that in the light
of the longstanding opposition of ACB to the
release of MON87460, direct notice should ideally have been given to
it, ACB failed
to establish that Regulation 9 is unfair, nor did it
establish any statutory basis on which it was entitled to direct
notice of
the application.
23.
In any event,
despite not having had the opportunity to submit submissions to the
EC, this was eventually done when ACB submitted
their opposition and
submissions to the Appeal Board. The appeal is an appeal in the
wide sense, which entails a full rehearing
of the objection.
[20]
ACB, accordingly had the opportunity to fully ventilate its
opposition to the granting of the permit during the appeal. This then
raises the question whether the relief claimed, which is a referral
back to the EC, is at all appropriate. The opportunity of being
heard
was fully granted during the appeal process and a referral back to
the EC would be pointless, due to the very nature of a
wide appeal.
Adequacy of the
reasons
24.
ACB argues that the reasons provided by the EC were
insufficient as it did not indicate whether the EC was properly
constituted
and did not record whether Monsanto submitted all the
necessary information, including the risk assessment and risk
management
measures. ACB also complained that the EC’s reasons
did not suggest that the information provided by Monsanto was
evaluated
critically and were nothing but an overview of Monsanto’s
application. It was also alleged that the reasons did not contain
any
explanation as to what, if any, other evidence, apart from those
provided by Monsanto, were considered, and did not explain
why
Monsanto’s claims were accepted.
25.
The EC’s decision records that MON 87460 is
substantially equivalent to conventional maize and has a low
environmental
risk. The decision makes it clear that the EC was
satisfied that there was adequate scientific support to indicate that
MON87460
is safe and nutritionally adequate for human and animal
consumption, and is expected to be beneficial to the environment due
to
the protection of yield loss under drought conditions. The reasons
record that the conclusions referred to above were drawn from
certain
findings of fact. The facts on which the conclusions were based were
set out.
26.
The EC’s decision furthermore sets out the conclusion
based on its factual findings and concluded that MON 87460 is
equivalent
to conventional maize, does not pose a threat to the
environment and does not pose a threat to human or animal safety. It
explains
the factual findings which underlie the conclusion.
27.
To determine
whether there is merit in ACB’s criticism of the reasons
provided, one should consider what the requirements
for adequate
reasons are. In Koyabe v Minister of Home Affairs
[21]
it was held that, although the reasons must be sufficient, they need
not be set out in minute detail and ordinarily, reasons will
be
adequate if a complainant can make out a reasonable substantial
case.
[22]
28.
In Phambili
Fisheries
[23]
the following
was said:
What constitutes
adequate reasons has been aptly described by Woodward J, sitting in
the Federal Court of Australia, in the case
of Ansett Transport
Industries (Operations) Pty Ltd and another v Wraith and others
[1983] FCA 179
;
(1983) 48 ALR 500
at 507 (23–41), as follows:
“
The passages
from judgments which are conveniently brought together in Re Palmer
and Minister for the Capital Territory
(1978) 23 ALR 196
at 206–7;
1 ALD 183
at 193–4, serve to confirm my view that s 13(1) of
the Judicial Review Act requires the decision-maker to explain his
decision
in a way which will enable a person aggrieved to say, in
effect: ‘Even though I may not agree with it, I now understand
why
the decision went against me. I am now in a position to decide
whether that decision has involved an unwarranted finding of fact,
or
an error of law, which is worth challenging.’
This requires that the
decision-maker should set out his understanding of the relevant law,
any findings of fact on which his conclusions
depend (especially if
those facts have been in dispute), and the reasoning processes which
led him
to those conclusions.
He should do so in clear and unambiguous language, not in vague
generalities or the formal language of legislation.
The appropriate
length of the statement covering such matters will depend upon
considerations such as the nature and importance
of the decision, its
complexity and the time available to formulate the statement. Often
those factors may suggest a brief statement
of one or two pages
only.”
To the same effect,
but more brief, is Hoexter The New Constitutional and Administrative
Law Vol 2 244:
“
[I]t is
apparent that reasons are not really reasons unless they are properly
informative. They must explain why action was taken
or not taken;
otherwise they are better described as findings or other
information.”
[24]
29.
For the reasons to
be adequate the decision maker, as was argued on behalf of Monsanto,
must set out his understanding of the law,
the findings of fact and
the reasons that led to the conclusions arrived at. In this
instance no finding of law was required
The EC decision sets out the
findings of fact and the conclusions arrived at. As a result, the EC
decision met the requirements
set out in Phambili and the other
authorities referred to. ACB was placed in a position to decide
whether the decision involved
“an unwarranted finding”,
which should be appealed or reviewed. The complainant was provided
with the decision maker’s
actual reasons to enable it to
formulate its objections thereto, the adequacy of reasons does not
include a consideration of the
cogency or rationality of the
reasons.
[25]
As a result, the
conclusion is that the reasons provided were adequate and this
objection must fail.
Did the EC apply its
mind to the information provided to it by Monsanto and was the
decision supported by the evidence before it
30.
The record shows that no submissions by third parties were
placed before the EC. However, it was assisted by the AC in coming to
the decision. The EC consisted of five members, who represented the
Department of Agriculture, Forestry and Fisheries, the Department
of
Environmental Affairs, the Department of Science and Technology, the
Department of Trade and Industry and Professor Bouwer,
the
Chairperson of the AC. Two meetings were held on 21 January 2015 and
26 June 2015 where Monsanto’s application was considered.
The
minutes were kept and form part of the record.
31.
ACB argues that the EC did not attend to a rigorous scientific
assessment in relation to the safety and efficacy of MON 87460 and
uncritically accepted the evidence contained in Monsanto’s
application. ACB argued that the EC should have called for an
independent risk assessment. This aspect was already dealt with
earlier in the judgment. It is also clear from the record that
there
was a proper consideration of all the aspects relevant to the
application. ACB failed to file a supplementary affidavit,
after the
filing of the record and forfeited an opportunity to address any
aspects pertaining to the recommendations and the minutes
of the
meetings held when the application was considered.
32.
A golden thread
throughout the application is ACB’s failure to specifically
identify the grounds of review relied on in terms
of PAJA clearly.
This resulted in the Court attempting to establish the exact grounds
relied on. There was also not always coherence
between the founding
affidavit and heads of argument in this regard. It seems that ACB
inter alia relied on section 6 (2)(a) (ii)
and(iii), section
(2(e)(vi) and section 6 (2)(h) of PAJA, which provides that a
decision is subject to review where the decision
maker acted
under an unauthorised delegation of power, was biased or
reasonably suspected of bias, where the decision
maker acted
arbitrarily or capriciously, and where a decision maker exercises its
power in such a manner that no reasonable person
could have exercised
the power in such a manner. This inference is drawn because ACB
relied inter alia on Minister of Environmental
Affairs and Tourism v
Scenematic Fourteen (Pty) Ltd
[26]
,
where it was held that a functionary must exercise her power herself
in the absence of a delegation and should not rubber stamp
the
application before her. However, considering the opinion of the AC
and the meetings held, there is no indication of either
an unlawful
delegation of power or a mere rubber stamp of the application of
Monsanto.
33.
Reliance was
also placed by ACB on Tantoush v Refugee Appeal Board
[27]
,
in support of the argument of bias in that instance however, there
was evidence of probable external influence. There is no evidence
of
external influence in this instance. ACB’s argument that where
a decision is influenced by pressure from an external source,
that
decision will be reviewable is correct, but the evidence does not
support its application in this case. There is no evidence
that the
EC did not exercise its own decision-making power. The record shows
that the views of the AC was provided and there are
minutes of the
meetings held when the application was considered. The highwater mark
in this instance of ACB’s criticism
is that Monsanto’s
application was uncritically accepted, but the record indicates
otherwise.
34.
The record and the EC’s decision make it clear
that the EC did consider the risk assessment provided by Monsanto, in
the absence of submissions by third parties, and concluded that MON
87460 was safe for humans, animals and the environment. It
was
already pointed out that neither NEMA, nor the GMO Act and
Regulations requires an EIA in the circumstances that prevailed
in
this matter. The fact of the matter is that procedures required
by legislation were followed. In any event any procedural
unfairness
was cured by the appeal that followed. I must therefore conclude that
the EC did apply its mind and considered the evidence
before it.
Did the Appeal Board
adequately address the appeal grounds raised by the Respondents.
35.
ACB did not indicate in either the founding affidavit, or the
heads of argument on which provisions of PAJA it based its review
against the Appeal decision. ACB alleges in its heads of argument
that the Appeal Board decision did not engage with the appeal
grounds, because it did not address the lack of adequate notice,
Professor Heinemann’s evidence, the absence of a determination
in terms of Section 5 (1) (a) of the GMO Act, the inadequacy of
Monsanto’s risk assessment; the claim of drought resistance
and
the South African field trials and the withholding of relevant
information which made it impossible to evaluate experimental
conditions and methods.
36.
The founding
affidavit, however, only deals with procedural irregularities. It
was pointed out that the Appeal Board decision
was not dated or
signed and did not identify its members. This point was not persisted
with in the heads of argument. The failure
to address the expert
opinions of Dr Hillbeck and Professor Heinemann in the Appeal Board
decision was raised. The point relating
to Dr Hillbeck’s
evidence was not persisted with in the heads of argument and
correctly so, as Dr Hillbeck assisted ACB in
the preparation of ACB’s
appeal and cannot be regarded as an independent expert.
[28]
37.
The other concerns were that certain of the Appeal
Board’s findings were set out in vague and generalised terms.
ACB
concluded that the Appeal Board failed in taking a rational
decision, failed to apply its mind to ACB’s grounds of appeal,
acted unreasonably, failed to take an independent and an unbiased
decision and did not provide reasons for its decision.
38.
The issue of notice was already dealt with, as notice was
given as required by legislation. As far as compliance with section
5(1)
(a) of the GMO Act is concerned, this was dealt with above.
Procedurally, there was no failure in this regard for the reasons set
out above.
39.
As far as the alleged inadequacy of the reasons provided
are concerned, the test for adequacy of reasons was already dealt
with above and the Appeal Board’s reasons must be tested with
reference to those requirements and for the same reasons as
set out
with reference to the EC decision there is no merit in this argument.
40.
ACB is especially concerned with the safety of MON 87460 and
dealt with the various arguments pertaining to its safety. Yet again,
it is not for this Court to determine the safety of MON 87460 and all
this Court can legally do is to examine the procedure followed.
The
Appeal Decision dealt with the safety of MON 87460 and concluded that
“all required scientific rigour has been applied,
including
review process from the Advisory Committee members, with relevant
scientific expertise to determine the safety of the
GM event in
respect of human, animal and environmental safety,” after being
presented with the opinions of all the stakeholders.
The Appeal
Decision deals with MON 87460 ‘s traits and draws comparisons
with conventional maize. It deals with unintended
gene flow and
concludes that the risk is minimal and in the rare event that it
occurs, it concludes that it does not necessarily
present a risk. The
Appeal Decision refers to the history of safe use and concludes that
the extent of the proposed yield loss
reduction is low, but
statistically significant.
41.
The Appeal Decision sets out its conclusions, the facts, and
the underlying reasoning for the conclusion. ACB, when considering
the Appeal Board’s decision should at least have been appraised
of the Appeal Decision, as to understand why the appeal was
rejected.
There is accordingly no merit in the assertion that the reasons were
inadequate.
42.
ACB raised concern that Dr Heinemann’s opinion was not
addressed by the Appeal Decision. Dr Heinemann’s opinion
related
to the safety of MON 87460. In concluding that MON 87460 is
safe, the Appeal Board did consider the safety and in concluding that
it was safe for use, rejected by implication Dr Heinemann’s
opinion. Dr Barthotomaeus, a toxicologist provided evidence that
Dr
Heinemann’s risk assessment had no basis. Dr Peters addressed
the issue of yield loss. Contradictory expert opinions flow
through
this application and ultimately as already stated, it is not for this
court to decide on either the merits or the safety
of MON87460, but
to determine whether the requirements for a review have been met.
43.
The Appeal Board relied on the evidence before it and
concluded, right or wrong, that MON87460 is safe. On the evidence
before
this court, it cannot be concluded that the decision was
either irrational or unreasonable. As far as the question of the
alleged
drought resistance is concerned, the Appeal Board considered
this issue and that should suffice for purposes of a review.
44.
ACB also relied on Section 68 of the Promotion to Access
to Information Act 2 of 2000 (PAIA), namely the refusal of access
to
information. This relates to the confidential information relating to
the field trials by Monsanto in South Africa. However,
once the
review was launched, redacted information was made available to ACB’s
legal representatives and experts. The conclusion
therefore that ACB
failed in proving its grounds of review relating to the Appeal Board
decision.
The Minister’s
failure to give reasons or to engage with the issues before the EC
and Appeal Board
45.
The Minster accepted the Appeal Board’s findings and
recommendations.
46.
The power to adjudicate an appeal lies with the Appeal Board.
Section 19 (4) of the GMO Act gives the power to the Appeal Board to
confirm, set aside or substitute the decision of the EC. Section 19
(6) of the GMO Act then provides that “the full decision
of the
Appeal Board must be put in writing and furnished to the Minster, the
registrar and all the parties directly involved”.
The Section
goes further to state that the Minister “may take such further
action as he or she may consider necessary”.
No obligation is
put on the Minister to provide reasons or take any further steps. As
a result, there is no merit in this ground
for review.
Conclusion
47.
There is no
indication that either the EC or the Appeal Board failed to comply
with the rationality test envisaged in Section 6
(2)(f)(ii) of PAJA.
Although one might not agree with the decisions, the test is
ultimately whether there is a rational objective
basis between the
material made available and the conclusion arrived at.
[29]
As far as reasonableness, as envisaged in Section 6(2)(h) of PAJA is
concerned, the EC relied on the AC, who consisted of experts
who
considered Monsanto’s application and who recommended that the
application be approved. A recommendation report was prepared
and
formed part of the record. The EC took its decision in consultation
with the AC. The information before the EC included a report
from a
statutory body whose specific function is to consider applications
for GMO permits. As a result, the EC’s decision
can neither be
irrational nor unreasonable.
48.
The Appeal Board considered everything that was before the EC
and had available the submissions of ACB, including the reports of
their experts. The Appeal Board considered all of this and concluded
that the permit could be granted. There is no evidence that
the
decision was either irrational or unreasonable. Nor was there any
credible evidence that either the EC or the Appeal Board
did not
apply their minds to the information before them. Despite the
allegations of bias and/or influence by third parties, no
objective
evidence was provided to prove that, or any unlawful delegation of
power.
.
49.
A perusal of the papers reveals that ACB’s real concern
is the safety of the release of MON 87460, which maybe a legitimate
concern, but it is something this Court is not able to determine
within the confines of a PAJA review and in the light of the
conflicting expert opinions, without the benefit of oral evidence. As
a result, the application stands to be dismissed.
Costs
50.
Considering the
nature of the litigation, it is appropriate that no order as to costs
is made following the Biowatch principle.
[30]
The following order is
made:
1. The application is
dismissed.
R.G Tolmay
Judge of the High
Court of South Africa
Gauteng Division,
Pretoria
Appearances:
Counsel
for Applicant
: Adv K Pillay SC; Adv
N Steyn
Attorney
for Applicant
: Legal-Aid South
Africa
Counsel for First to
Fourth Respondents
:
Adv M Jozana
Attorney for First to
Fourth Respondents
:
State Attorney Pretoria
Counsel for Fifth
Respondent
:
Adv P Lazarus SC; Adv I Learmonth
Attorney for Fifth
Respondent
:
Webber Wentzel
Date
of Hearing
: 8 February 2023
Date of Judgment
: 27 June 2023
[1]
GMO
Act section 5(1) (c).
[2]
GMO
Regulations 9 (1), 9 (5)(c) and (9)(6).
[3]
Rustenburg
Platinum Mines (Ltd) (Rustenburg Section) v CCMA
2007 (1) SA 576
(SCA) at para 31-32; South Durban Community Environmental Alliance v
MEC for Economic Development Tourism and Environmental Affairs,
Kwazulu-Natal Provincial Government
2020 (4) SA 453
(SCA) at para
12.
[4]
Fuel Retailers Association of Southern Africa v Director General
Environmental Management, Department of Agriculture, Conservation
and Environment, Mpumalanga Province
2007 (6) SA 4
at para 38 (Fuel
Retailers).
[5]
Bato
Star Fishing (Pty) Ltd v Minster of Environment Affairs and Tourism
[2004] ZACC 15
;
2004 (4) SA 490
(CC) at para 48; Somali Association of South Africa
v The Refugee Appeal Board 2021 JDR 2182 (SCA) at para 93.
[6]
2001
(3) SA 1188 (SCA).
[7]
[1984] ZASCA 51
;
1984
(3) SA 623
(A) 634 D-I, see also Mbethe v United Maganese of
Kalahari (Pty) Ltd
2017 (6) SA 409
(SCA) at para 23.
[8]
Walele
v City of Cape Town
[2008] ZACC 11
;
2008 (6) SA 129
CC at paras 17 & 33, Pilane
v Pilane
2013 (4) BCLR 431
(CC) at paras 47 & 48.
[9]
Fuel
Retailers at para 98.
[10]
2019(2) SA 403 (WCC) at para 104.
[11]
[2006] NSWLEC 199.
[12]
Telstra at para 134-135.
[13]
Telstra at para 147-148.
[14]
Telstra at para 150.
[15]
2022(6) SA 589 ECM.
[16]
GMO
Regulation 9 (2).
[17]
GMO
Regulation 9 (5).
[18]
GMO
Regulation 9 (5)(1).
[19]
GMO
Regulation 9 (6).
[20]
GMO
Regulation 11, Wings Park Port Elizabeth (Pty) Ltd v MEC for
Environmental Affairs, Eastern
2019 (2) SA 606
(ECG) at para 29.
[21]
2010
(4) SA 327
at para 63.
[22]
Minister
of Environmental Affairs and Tourism and Others v Phambili Fisheries
(Pty) Ltd; Minster of Environmental Affairs and
Tourism and Others v
Bato Star Fishing (Pty) Ltd 2003 (6) 407 (SCA). (Phambili Fisheries)
[23]
Ibid
a para 40, See also Commissioner of Revenue Services v Sprigg
Investment 117 CC t/a Global Investment 2011 (4) SA (SCA) at
para
11-14(Sprigg Investments)
[24]
GMO
Regulation 9 (5)(1).
[25]
Sprigg Investments at para 14.
[26]
[2005] ZASCA 11
;
2005
(6) SA 182
(Scenematic) at para 20.
[27]
2008
(1) SA 232 (T).
[28]
Price Waterhouse Coopers Inc. v National Potato
Co-Operative.Ltd.2015 JDR 0371 (SCA) at para 113.
[29]
Trinity
Broadcasting (Ciskei) v Independent Communications Authority of
South Africa
2004 (3) SA 346
at paras 20-21.
[30]
Biowatch Trust v Registrar, Genetic Resources
2009 (6) SA 232
(CC).
sino noindex
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