The Summary Notification Information Format for genetically modified higher plant releases, has been established for the purposes and according to the procedures envisaged by Article 9 of Directive 90/220/EEC.

It is recognized that the Summary Notification Information Format for genetically modified higher plant releases is not designed to contain all the information required for carrying out an environmental risk assessment. The space provided after each question is not indicative of the depth of the information required for the purposes of the Summary Notification Information Format.

1. Details of notification

Notification number: ......................................

Date of acknowledgment of notification: ........................................

Title of the project: .......................................

Proposed period of release: .............................................

2. Notifier

Name of institute or company: ........................................

3. Is the same GMPt release planned elsewhere in the Community (in conformity with Article 5 (1))?

Yes No Not known

If yes, insert the country code(s) ......................................

4. Has the same GMPt been notified for release elsewhere in the Community by the same notifier?

Yes No

If yes, notification number: ...........................................

1. Complete name of the recipient or parental plant
(a) family name
(b) genus
(c) species
(d) subspecies
(e) cultivar/breeding line
(f) common name

2. Description of the traits and characteristics which have been introduced or modified, including marker genes and previous modifications
......................................................................................................................

3. Type of the genetic modification:
(a) Insertion of genetic material
(b) Deletion of genetic material
(c) Base substitution
(d) Cell fusion
(e) Other, please specify

4. In the case of insertion of genetic material, give the source and intended function of each constituent fragment of the region to be inserted
......................................................................................................................

5. In the case of deletion of genetic material, give information on the function of the deleted sequences
......................................................................................................................

6. Brief description of the method used for the genetic modification
......................................................................................................................

1. Purpose of the release
......................................................................................................................

2. Geographical location of the release site
......................................................................................................................

3. Size of the site (m²)
......................................................................................................................

D. Summary of the potential environmental impact from the release of the GMPts
......................................................................................................................

E. Brief description of any measures taken for the management of risks
......................................................................................................................

The Summary Notification Information Format has been established for the purposes and according to the procedures envisaged by Article 9 of Directive 90/220/EEC.

It is recognized that the Summary Notification Information Format is not designed to contain all the information required for carrying out an environmental risk assessment in the detail necessary for such an assessment. The information entered should, however, adequately reflect (in a condensed form) the information submitted to the competent authority according to Articles 5 and 6 of Directive 90/220/EEC under the conditions specified in the preface to Annex II. The space provided after each question is not indicative of the depth of the information required for the purposes of the Summary Notification Information Format.

1. Details of notification

Member State of notification: ................................................

Notification number: ....................................................

Date of acknowledgment of notification: .........................................................

Title of the project: .....................................................

Proposed period of release: ........................................................

2. Notifier

Name of institution or company: ................................................

3. GMO characterization

(a) Indicate whether the GMO is a:
viroid
RNA virus
DNA virus
bacterium
fungus
animal
other, please specify ..............................................

(b) Identity of the GMO: ..................................................

4. Is the same GMO release planned elsewhere in the Community (in conformity with Article 5 (1))?

Yes No Not known

If yes, insert the country code(s) ............................................

5. Has the same GMO been notified for release elsewhere in the Community by the same notifier?

Yes No

If yes:
- Member State of notification: ............................................................
- Notification number: .............................................................

A. Information relating to the recipient or parental organisms from which the GMO is derived

1. Indicate whether the recipient or parental organism is a:
viroid
RNA virus
DNA virus
bacterium
fungus
animal
other, please specify .............................................................

2. Complete name
(i) order and/or higher taxon (for animals)
(ii) genus
(iii) species
(iv) subspecies
(v) strain
(vi) pathovar (biotype, ecotype, race, etc.)
(vii) common name

3. Geographical distribution of the organism

(a) Indigenous to the country where the notification is made:
Yes No Not known

(b) Indigenous to other EC countries:
(i) Yes
If yes, indicate the type of ecosystem in which it is found:
Atlantic Mediterranean
Arctic Continental

(ii) No Not known

(c) Is it regularly used in the country where the notification is made?
Yes No

(d) Is is regularly kept in the country where the notification is made?
Yes No

4. Natural habitat of the organism

M (a) If the organism is a microorganism
water
soil, free-living
soil in association with plant-root systems
in association with plant leaf/stem systems
in association with animals
other (specify)

A (b) If the organism is an animal:
natural habitat or usual agroecosystem:
......................................................................................................................................

5. (a) Detection techniques
......................................................................................................................................

(b) Identification techniques
......................................................................................................................................

6. Is the recipient organism classified under existing Community rules relating to the protection of human health and/or the environment?

Yes No
If yes, specify:
......................................................................................................................................

7. Is the recipient organism pathogenic or harmful in any other way (including its extracellular products), either living or dead?

Yes No

If yes:
(a) to which of the following organisms:
humans
animals
plants

(b) give the relevant information specified under Annex II, point II. (A).(11).(d)
......................................................................................................................................

8. Information concerning reproduction:

(a) Generation time in natural ecosystems: ..........................................

(b) Generation time in the ecosystem where the release will take place: ..................................................................

(c) Way of reproduction:
Sexual Asexual

(d) Factors affecting reproduction:
......................................................................................................................................

9. Survivability

(a) Ability to form structures enhancing survival or dormancy:
(i) endospores
(ii) cysts
(iii) sclerotia
(iv) asexual spores (fungi)
(v) sexual spores (fungi)
(vi) eggs
(vii) pupae
(viii) larvae
(ix) other, please specify

(b) Relevant factors affecting survivability:
......................................................................................................................................

10. (a) Ways of dissemination
......................................................................................................................................

(b) Factors affecting dissemination
......................................................................................................................................

11. Previous genetic modifications of the recipient or parental organism already notified for release in the country where the notification is made (give notification numbers)
......................................................................................................................................

1. Type of the genetic modification
(i) Insertion of genetic material
(ii) Deletion of genetic material
(iii) Base substitution
(iv) Cell fusion
(v) Other, please specify

2. Intended result of the genetic modification
......................................................................................................................................

3. (a) Has a vector been used in the process of modification?
Yes No
If no, go straight to question 5.

(b) If yes, is the vector wholly or partially present in the modified organism?
Yes No
If no, go straight to question 5.

4. If the answer to 3 (b) is yes, supply the following information:

(a) Type of vector
plasmid
bacteriophage
virus
cosmid
phasmid
transposable element
other, please specify
......................................................................................................................................

(b) Identity of the vector
......................................................................................................................................

(c) Host range of the vector
......................................................................................................................................

(d) Presence in the vector of sequences giving a selectable or identifiable phenotype

                             Yes     No

(e) Constituent fragments of the vector
......................................................................................................................................

(f) Method for introducing the vector into the recipient organism
(i) transformation
(ii) electroporation
(iii) macroinjection
(iv) microinjection
(v) infection
(vi) other, please specify
......................................................................................................................................

5. If the answer to question B.3 (a) and (b) is no, what was the method used to introduce the insert into the recipient/parental cell?
(i) transformation
(ii) microinjection
(iii) microencapsulation
(iv) macroinjection
(v) other, please specify
......................................................................................................................................

6. Information on the insert

(a) Composition of the insert
......................................................................................................................................

(b) Source of each constituent part of the insert
......................................................................................................................................

(c) Intended function of each constituent part of the insert in the GMO
......................................................................................................................................

(d) Location of the insert in the host organism
- on a free plasmid
- integrated in the chromosome
- other, please specify ..................................................................

(e) Does the insert contain parts whose product or function are not known?
Yes No
If yes, please specify: ....................................................................

1. Indicate whether it is a:
viroid
RNA virus
DNA virus
bacterium
fungus
plant
animal
other, please specify .............................................

2. Complete name
(i) order and/or higher taxon (for animals)
(ii) family name (for plants)
(iii) genus
(iv) species
(v) subspecies
(vi) strain
(vii) cultivar/breeding line
(viii) pathovar
(ix) common name

3. Is the organism pathogenic or harmful in any other way (including its extracellular products), either living or dead?

Yes No Not known

If, yes, specify the following:

(a) to which of the following organisms?
humans
animals
plants

(b) are the donated sequences involved in any way to the pathogenic or harmful properties of the organism?

Yes No Not known

If yes, give the relevant information under Annex II, II A, 11 d:
...............................................................................................................................

4. Is the donor organism classified under existing Community rules relating to the protection of human health and the environment?

Yes No

If yes, please specify:
...............................................................................................................................

5. Do the donor and recipient organism exchange genetic material naturally?

Yes No Not known

1. Genetic traits and phenotypic characteristics of the recipient or parental organism which have been changed as a result of the genetic modification.

(a) Is the GMO different from the recipient as far as survivability is concerned?

Yes No Not known
If yes, please specify
...............................................................................................................................

(b) Is the GMO in any way different from the recipient as far as mode and/or rate of reproduction is concerned?

Yes No Not known
If yes, please specify:
...............................................................................................................................

(c) Is the GMO in any way different from the recipient as far as dissemination is concerned?

Yes No Not known
If yes, please specify:
...............................................................................................................................

2. Genetic stability of the genetically modified organism
...............................................................................................................................

3. Is the GMO pathogenic or harmful in any other way (including its extracellular products), either living or dead?

Yes No Not known

If yes,

(a) to which of the following organisms?:
humans
animals
plants

(b) give the relevant information specified under Annex II, point II (A) (11) (d) and II (C) (2) (i)
...............................................................................................................................

4. Description of identification and detection methods

(a) Techniques used to detect the GMO in the environment
...............................................................................................................................

(b) Techniques used to identify the GMO
...............................................................................................................................

1. Purpose of the release
...............................................................................................................................

2. Is the site of the release different from the natural habitat or from the ecosystem in which the recipient organism is regularly used, kept or found?

Yes No
If yes, please specify: .........................................................................

3. Information concerning the release and the surrounding area

(a) Geographical location (administrative region and where appropriate grid reference):
...............................................................................................................................

(b) Size of the site (m²):
(i) actual release site (m²):
...............................................................................................................................
(ii) wider release area (m²):
...............................................................................................................................

(c) Proximity to internationally recognized biotopes or protected areas (including drinking water reservoirs), which could be affected:
...............................................................................................................................

(d) Flora and fauna including crops, livestock and migratory species which may potentially interact with the GMO:
...............................................................................................................................

4. Method and amount of release

(a) Quantities of GMOs to be released:
...............................................................................................................................

(b) Duration of the operation:
...............................................................................................................................

(c) Methods and procedures to avoid and/or minimize the spread of the GMOs beyond the site of the release:
...............................................................................................................................

1. Complete name of target organisms
(i) order and/or higher taxon (for animals)
(ii) family name (for plants)
(iii) genus
(iv) species
(v) subspecies
(vi) strain
(vii) cultivar
(viii) pathovar
(ix) common name

2. Anticipated mechanism and result of interaction between the released GMOs and the target organism
...............................................................................................................................

3. Other potentially significant interactions with other organisms in the environment
...............................................................................................................................

4. Is post-release selection for the GMO likely to occur?

Yes No Not known
If yes, give details:
...............................................................................................................................

5. Types of ecosystems to which the GMO could be disseminated from the site of release and in which it could become established
...............................................................................................................................

6. Complete name of non-target organisms which may be effected unwittingly
(i) order and/or higher taxon (for animals)
(ii) family name (for plants)
(iii) genus
(iv) species
(v) subspecies
(vi) strain
(vii) cultivar
(viii) pathovar
(ix) common name

7. Likelihood of genetic exchange in vivo
(a) from the GMO to other organisms in the release ecosystem:
...............................................................................................................................

(b) from other organisms to the GMO:
...............................................................................................................................

8. Give references to relevant results from studies of the behaviour and characteristic of the GMO and its ecological impact carried out in simulated natural environments (e.g. microcosms, etc.):
...............................................................................................................................

1. Methods for monitoring the GMOs
...............................................................................................................................

2. Methods for monitoring ecosystem effects
...............................................................................................................................

3. Methods for detecting transfer of the donated genetic material from the GMO to other organisms
...............................................................................................................................

4. Spatial extent of the monitoring area (m²)
...............................................................................................................................

5 Duration of the monitoring
...............................................................................................................................

6. Frequency of the monitoring
...............................................................................................................................

1. Post-release treatment of the site
...............................................................................................................................

2. Post-release treatment of the GMOs
...............................................................................................................................

3. (a) Type and amount of waste generated
...............................................................................................................................

(b) Treatment of waste
...............................................................................................................................

1. Methods and procedures for controlling GMOs in case of unexpected spread
...............................................................................................................................

2. Methods for decontamination of the areas affected
...............................................................................................................................

3. Methods for disposal or sanitation of plants, animals, soils etc. that were exposed during or after the spread
...............................................................................................................................

4. Plans for protecting human health and the environment in case of the occurence of an undesirable effect
...............................................................................................................................