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Ex situ genetic conservation of tree species at the São Paulo Forest Institute, Brazil[23] (A.M. Sebbenn et al)

by

Alexandre Magno Sebbenn
Antonio Carlos Scatena Zanatto
Lígia de Castro Ettori
Omar Jorge Di Dio Junior[24]

INTRODUCTION

The São Paulo Forest Institute, Brazil (SPIF) has since 1979 been conserving a number of Brazilian forest tree species which are endangered or subject to genetic depletion caused by the growing industrialization and unplanned agricultural and urban development. Vitor (1975) gives an idea of the worrying situation in the natural forests in São Paulo state, reporting that at the beginning of the nineteenth century, 70.5% of the area of the State was covered with natural forests but that in 1975 only 7% of these forests remained. The FAO Panel of Experts on Forest Gene Resources lists the following species of Brasil as being in need of attention: Aspidosperma polyneuron, Araucaria angustifolia, Balfourodendron riedelianum, Cariniana legalis, Dipterix alata, Hymenaea coubaryl, Myracrodruon urundeuva (FAO, 1998, 2000). An interesting historical reference is the one made in the middle of 1900 by the Swedish naturalist Albert Löfgren:“The devastation of the forests is destroying what took nature millions of years to create; the price of this destruction will be very high; in the name of life itself and our future, we need to halt this devastation “ (SPIF, 1994).

Today the lack of a forest policy to stimulate genetic conservation of the remaining forests, reforestation and recuperation of degraded areas and sustainable forest management is keenly felt. While in 1886, more than 70% of the Atlantic Forest remained, this area is now only 7%.

The ex situ genetic conservation program of native Brazilian species at SPIF aims to conserve the genetic variability existing among and within the populations of forest species, for present or future use, to meet economic social and environmental needs. Objectives of the program also include the study of the genetic structure, silvicultural behavior, heredity of traits of economic interest and improved seed production for reforestation of degraded and altered areas.

THE SÃO PAULO FOREST INSTITUTE

The SPIF is a branch of the Environmental Agency of the Government of the State of São Paulo, founded in 1888 by the Swedish naturalist Alberto Löfgren and was originally known as the Horto Botânico. In 1911 the Horto Botânico was transformed into the São Paulo State Forest Service and in 1970 it became the São Paulo Forest Institute (SPIF, 1994). The Institute has several ecological stations, parks, forests, experimental stations, nurseries and state forest reserves, distributed throughout the State of São Paulo, and occupying approximately 3.4% of the area[25]. Of the total area administered by the SPIF, 94% (0.8 million hectares) are used for conservation activities. The largest of the last remnants of Atlantic Forest in São Paulo State are found in these areas, providing in situ conservation and sources of seed and progagules for future rehabilitation of the natural forests of the State. The value of these areas is therefore incalculable. The SPIF also ensures ex situ conservation of Brazilian native and exotic forest species. Presently, the ex situ conservation programme includes 24 native forest tree species and 45 introduced tree species. The latter include 23 species of Eucalyptus, 14 species of Pinus and eight species of other genera: Liriodendron, Toona, Grevillea, Cupressus, Cryptomeria, Cordia and Araucaria (see Gurgel Garrido, 1997).

EX SITU CONSERVATION

The ex situ conservation activities were initiated by Dr. Ana Cristina Machado de Franco Siqueira, who was one of the first scientists to acknowledge the problems of accelerated loss of forest genetic resources in São Paulo State and Brazil and to take corresponding action.

Table 1 gives information on the native forest species included in ex situ conservation areas. These areas have been established since 1979. They include, however, also two provenance trials of Araucaria angustifolia established in 1973, which were subsequently incorporated into the ex situ conservation program. Presently, the program includes 24 species and 41 experimental areas. Some experiments are replicated in two sites. The ex situ areas include progeny and progeny/populations tests, initially established as pure plantations, following experimental designs such as randomized blocks, complete randomized blocks and compact family block design, always with six blocks and five plants per plot, totalling 30 plants per progeny/site. Since 1990, recognizing the importance of respecting the successional stages for better adaptation and growth of the majority of the native forest tree species in Brazil, the experiments have been established mixing several successional phase species in the blocks, including pioneers, secondary and climax species. The bracket with a number in table 1 indicates that this species is mixed with species with the same number in bracket.

Table 1: Ex situ genetic conservation experiments with native forest species in the SPIF, Brazil. Compiled by Gurgel Garrido (1997)[26]

Species

 

Experiment

Establishment

Number of provenances

 

Total number of plants

 

Type

Design

Year

Sites

Anadenathera falcata

pt

IC

1994

1

1

20

Araucaria angustifolia

pt

BC

1974

2

1

32

Araucaria angustifolia

Or

BC

1985

1

1

19

Araucaria angustifolia

p/p

BFC

1973

2

5

115

Araucaria angustifolia

pt

BC

1981

1

7

70

Araucaria angustifolia

p/p

BFC

1980

1

15

121

Aspidosperma polyneuron

pt

BC (1)

1992

1

1

23

Astronium graveolens

pt

BC

1990

1

1

23

Balfourodendron riedelianum

p/p

BFC

1984

1

3

48

Cariniana legalis

p/p

BFC

1992

2

3

50

Cordia trichotoma

pt

BC

1986

1

1

32

Cordia trichotoma

pt

BC

1986

1

1

25

Dipteryx alata

p/p

BFC

1980

1

2

38

Dipteryx alata

p/p

BFC

1986

1

2

42

Dipteryx alata

pt

IC

1981

1

1

25

Dipteryx alata

pt

BC

1986

1

1

25

Enterolobium contortisiliquum

pt

BC

1990

1

1

23

Esenbeckia leiocarpa

pt

BC (2)

1992

1

1

25

Gallesia gorarema

pt

BC

1985

1

1

25

Gallesia gorarema

p/p

CFB

1982

2

3

65

Genipa americana

pt

BC (3)

1997

1

1

21

Guazuma ulmifolia

pt

BC (3)

1997

1

1

20

Hymenaea courbaryl

p/p

IC

1985

1

3

68

Machaerium villosum

p/p

BC (1)

1992

1

1

13

Machaerium villosum

p/p

CFB

1981

1

4

26

Myracrodruon urundeuva

pt

BC (2)

1993

1

1

23

Myracrodruon urundeuva

p/p

BFC

1981

1

5

91

Myracrodruon urundeuva

pt

BC

1986

1

1

42

Myracrodruon urundeuva

pt

BC

1988

1

1

28

Myroxylon peruiferum

p/p

IC

1984

1

4

45

Parapiptadenia rigida

pt

BC (1)

1991

1

1

25

Peltophorum dubium

pt

BC (2)

1992

1

1

26

Peltophorum dubium

p/p

BFC

1985

2

2

28

Peltophorum dubium

pt

BC

1985

1

1

18

Persea condata

pt

BC (1)

1992

1

1

9

Prunus sellowii

pt

IC

1989

1

1

17

Pterogyne nitens

p/p

BFC

1989

1

4

36

Pterogyne nitens

p/p

BFC

1989

1

5

93

Tabebuia heptaphylla

pt

BC

1984

1

1

19

Tabebuia heptaphylla

pt

BC

1985

1

1

15

Tabebuia vellosoi

p/p

BFC

1986

1

1

18


It should be noted that 63% of the ex situ stands and experiments consist of genetic material from only one population, and only two include genetic material from more than five populations; both of these latter ones are of Araucaria angustifolia. Thus, in spite of the relatively large number of species included, the conservation areas presently do not address genetic variability among populations. Inclusion of a range of populations of each species is needed, preferably covering the full distribution area. A further problem is that the banks are established in only eight of the 21 SPIF experimental stations, and 70% of them are located in only two localities (E.E. Luiz Antonio and E. E. de Pederneiras). This constitutes a serious risk especially due to frequent fires during the dry season (winter) in São Paulo State. However, one of the advantages is that the design of the conservation areas is statistically valid, experimental designs, which allows periodic monitoring of the genetic variability of the populations, and the study of population structure, heritabilities and silvicultural behavior. Another advantage is the possibility of transforming the experimental areas into seed orchards to produce seed for reforesting degraded and deforested areas in the State. The low intensity of artificial selection used in the ex situ conservation stands and experiments will allow the production of seeds with high levels of genetic variability, with the added advantage that the orchards are easy to harvest. However, the great majority of the species tested are not yet in the reproductive phase. The genetic and silvicultural traits assessed to date are breast height diameter, total height, stem form and survival. Recently, isoenzymatic studies and studies of the reproductive systems of some of the species have been initiated e.g. in Cariniana legalis.

RESULTS OF GENETIC STUDIES

Table 2 gives results from the analysis of genetic structure of conserved populations, estimated using methodology outlined by Hamrick (1976). The greatest part of genetic variability for all species was found within populations, notably among individuals within progenies. This is in agreement with most of the population structure studies carried out based on quantitative traits in tropical and temperate forest species (Hamrick 1976; Khalil, 1985; Li et al., 1993; Moraes, 1993; Buliuckas et al. 1999, Rehfeldt, 1999; Sebbenn et al. 1999), as well as with isoenzyme data (Hamrick & Godt, 1990). It is believed that the low genetic variation found among populations is associated with the small number of the populations of each species included in the experiments, and points to the need to include a greater number of populations in ex situ conservation banks to conserve the variability among populations. The absence of observed molecular level genetic variability among the population seems to indicate that, for tree breeding purposes, advantage in the selection of one or other population may be limited. If this observation is confirmed, selection of materials to be included in seed orchards can be made based on the performance of progenies across populations.

Genetic variability within the populations was also assessed, estimating heritability, the genetic variation coefficient, and phenotypic variation among the progeny. The heritability in height and diameter was generally low. Inconsistencies found in estimates of genetic parameters are possibly associated with the use of a low number of progeny per population, and flawed basic assumptions in quantitative genetics for the estimation of genetic parameters (see e.g. Nogueira et al., 1986b, Siqueira et al., 1993, Sebbenn et al., 2000). In this regard, Moraes (1993) studying the reproductive systems in populations of Myracrodruon urundeuva based on isoenzymes, observed that the outcrossing rate of the species was 0.49. Later it was found that this species has mixed reproductive behaviour (outbreeding, inbreeding) underlining the need for basic information on reproductive systems, as suggested by Ritland (1989) or Surles et al. (1990). Sebbenn (2000), when comparing the estimate of genetic parameters in Cariniana legalis populations using (i) the classical model, and (ii) incorporating principles of Ritland, observed over-estimates in the heritability coefficients of up to 33% when using the classical models. There is strong evidence from the literature that the majority of the native Brazilian forest species have mixed reproductive behaviour (see e.g. Paiva, 1993; Lepsch-Cunha, 1996; Sebbenn et al., 1998; Souza, 1997; Moraes, 1997; Oliveira, 2000). Thus, it is clear that genetic parameters in native forest species cannot be uncritically estimated based on the classical quantitative genetic models.

Table 2. Proportion of phenotypic variation within progenies (), genetic variation among progenies within populations () and genetic variation among populations () for some tropical tree species under ex situ conservation at SPIF, Brazil.

Species

Trait

Pop.

(%)

(%)

(%)

Reference

Balfourodendron riedelianum

 

DAP

3

84.1

12.7

3.1

Siqueira et al. (2000)

 

ALT

3

81.5

11.8

6.7

Pterogyne nitens

DAP

4

91.9

7.7

0.4

Sebbenn et al. (2000)

ALT

4

84.7

8.7

6.7

Peltophorum dubium

DAP

2

80.9

17.8

1.2

Sebbenn et al. (2000)

ALT

2

74.4

24.2

1.5

Cariniana legalis

FF

3

91.6

2.4

6.0

Sebbenn (2000)

DAP

3

96.5

3.4

0.1

ALT

3

97.3

2.6

0.1

VC

3

85.7

1.5

12.8


FUTURE PERSPECTIVES

The Atlantic Forest of Brazil is one of the greatest pools of forest biological diversity on the planet, and many areas contain more than 400 tree species per hectare; 90% of the species are found at frequencies of only one individual per hectare (Kageyama et al, 1997). However, as reported above, the SPIF ex situ conservation areas include only 24 species, and less than five populations have been included for most species. All the ex situ areas and experiments were set up with resources from the SPIF but there has been a gradual reduction in the financial investments from the State Government in the institution and the inclusion of new species has been drastically reduced in recent years: 73% of the 41 experiments were established before 1990.

There is a need to increase the number of populations of the species already established in the ex situ stands to improve the coverage of genetic variation conserved. There is, further, a need to continue to assess, periodically, the material contained in the ex situ conservation banks, to gain better understanding of the genetic characteristics and silvicultural behavior of the species. Thirdly, there is a need to consider transforming the experiments into seed orchards, using low intensity selection to maintain large effective population sizes. Finally, there is a need to increase the number of species under ex situ conservation, and to include a range of populations of each new species included. A sample of 30 populations, each represented by 25 progenies and 30 plants per progeny established in at least three localities, would likely meet conservation objectives and to guarantee the conservation also of rare alleles (frequency < 5%).

New candidate species to be included have been identified based on two criteria: (i) occurrence in São Paulo State, and (ii) economic value. These species are listed in table 3 according to the successional groups they belong to.

Table 3: List of new candidate species to be included in the ex situ conservation program.

Species

Common name

Family

Pioneer species



Cecropia glaziovi Snethl.

Embaúbavermelha

Cacropiaceae

Cecropia hololeuca Miquel

Imbaúba prateada

Cacropiaceae

Clethra scabra Pers.

Carne de vaca

Clethraceae

Croton floribundus Spreng

Capixingui

Euphorbiaceae

Piptadenia paniculata Bentham

Angico

Mimosaceae

Secondary species



Cabraela canjerana

Canjarana

Meliaceae

Cariniana estrellensis

Jequitibá branco

Lecithidacea

Cedrela fissilis Vellozo

Cedro

Meliaceae

Centrolobium robustum (Vell.) Martius ex Bentham

Araribá rosa

Fabaceae

Centrolobium tomentosum Guillem ex Bentham

Arauva

Fabaceae

Chlorophora tinctoria (Linnaeus) Gaudichaud

Taiúva

Moraceae

Chorisia speciosa (A. S. Hil.) Dawson

Paineira

Bombacaceae

Cinnamomum glaziovii (Mez) Kosterm

Garuva

Lauraceae

Copaifera langsdorffii Desf.

Bálsamo

Caesalpinaceae

Copaifera trapezifolia Hayne

Copaíba

Caesalpinaceae

Cryptocarya moschata Nees & Martius ex Nees

Canela branca

Lauraceae

Dalbergia brasiliensis Vogel

Jacaranda

Fabaceae

Erytrina falcata Benth.

Corticeira

Fabaceae

Inga striata

Inga

Mimosoidae

Joannesia princeps Vell.

Boleira

Euphorbiaceae

Lafoensia pacari A. Saint-Hilaire

Dedaleiro

Lythraceae

Luehea divaricata Martius & Zuccarini

Açoito a cavalo

Tiliaceae

Machaerium scleroxylon Tulasne

Caviuna

Fabaceae

Nectandra lanceolata Nees et Matius ex Nees.

Canela-amarela

Lauraceae

Platypodium elegans Vog.

Amendoin do campo

Fabaceae

Podocarpus lambertii Klotzsch ex Endl.

Pinheiro bravo

Podocarpaceae

Talauma ovata A. Saint-Hilaire

Baguaçu

Magnoliaceae

Climax species



Calophyllum brasiliensis Combessedes

Guanandi

Clusiaceae

Casealpinia leiostachya Ducke

Pauferro

Caesalpiniaceae

Dalbergia nigra (Vell.) Freire Allemão ex Bantham

Jacaranda da Bahia

Fabaceae

Holocalyx balansae Micheli

Alecrim

Fabaceae

Laplacea fruticosa (Schrader) Kobuski

Santa Rira

Theaceae

Ocotea catharinensis Mez

Canela-preta

Lauraceae

Ocotea odorifera (Vell.) Rohwer

Canela-sassafrás

Lauraceae

Ocotea porosa (Nees ex Martius) Libarato Barroso

Imbuia

Lauraceae

Plathymenia reticulata Benth.

Amarelinho

Mimosaceae

Tabebuia impetiginosa

Ipê-rosa

Bignoniaceae


ACKNOWLEDGEMENTS

The authors thank the heads/directors of the SPIF Experimental Stations who have carried out the maintenance of the conservation banks; and the field assessment teams, who have ensured high quality and efficiency in data collection. We are also grateful to Girlei Costa da Cunha, Forest Engineer for reading the manuscript, and for valuable suggestions of new species to be included in the SPIF conservation bank.

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[23] Received May 2001. Original language: English.
[24] Instituto Florestal, C. Postal 1322, 01059-970, São Paulo, SP, E-mail: [email protected]
[25] See IFSP (1994) for details.
[26] Notes: pt: progeny test; p/p: progeny/populations test; orc: seed orchard; IC: entirely random; BC: random blocks; BFC: compact family block; Brackets: () indicate combined test with more than one species;

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