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Key words: Ecological restoration, Endangered species, Endemic species, Gypsophytes, Gypsum
outcrops
Abstract. The southeast of the Iberian Peninsula, more precisely, the province of Almerı́a, has the most
important gypsum quarries in Spain. Despite the severe environmental impact of these quarries, so far
little attention has been paid to either the effect on the flora, especially on the more restricted endemic
taxa, or to the restoration of the habitats after the end of exploitation. It is our view that restoration of
gypsum quarries should not only aim at correcting the visual impact of mining on the landscape, but
should also attend to the biological impact of the quarrying. Although the ‘cicatrising’ potential of
gypsophytes is already well known, not all the species are able to recolonise worked-out quarries. Using
species abundances, all analyses clearly show that artificial rehabilitation results in very altered com-
munities. The preservation of the gypsum flora merits prioritary protective strategies which, at least to
some extent, would make gypsum mining and nature conservation compatible.
Introduction
The close relationship between plants and a particular geological substrate has long
been recognised (Rivas Goday 1969; Kruckeberg 1984). In recent times, a number of
botanists and plant ecologists have dealt extensively with this topic (e.g., Kruckeberg
1991; Roberts and Proctor 1992; Mota et al. 1993). Gypsum substrates, for example,
when occurring in dry areas, have significant geobotanical effects (Johnston 1941;
Parsons 1976; Turner and Powell 1979; Meyer 1986). Although among gypsophytes,
that is, plants inhabiting only gypsum soils, the adaptive features are not remarkable,
many of them show foliage succulence, salt excretion (Duvigneaud and Denaeyer de
Smet 1966, 1968), or deeply penetrating roots (Guerrero 1998).
Plant gypsophily has been explained in two ways. While some researchers
postulate physical constraints to account for gypsophily, others stress chemical or
nutritional requirements as causative factors (Parsons 1976; Merlo et al. 1998). On
the one hand, crusts either of biogeneous (mostly lichens) or other origin (rocky
edaphic horizons) and the hydric performance of the superficial soil layer (Meyer
and Garcı́a Moya 1989; Meyer et al. 1992) have been quoted as physical factors
inducing gypsophily. On the other hand, some of the chemical hypotheses aiming at
explaining gypsophily are deficiency of macronutrients (N, K and P), excess of
others (Ca, Mg and S), ionic antagonisms (Ca/Mg) and toxicity caused by micro-
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nutrients. These restrictive factors can affect plant development in different stages
of their life cycle, for example, during germination (Merlo et al. 1997) or during
establishment (Escudero et al. 1999, 2000).
The Iberian flora has about 30 endemic gypsophytes (Merlo et al. 1998). This
enormous amount of endemic taxa is mostly due to the impressive gypsum deposits in
Spain, with over 30,000 km2 some of the largest in Europe (Riba and Macau 1962;
Ayala et al. 1986) and an antiquity which ranges from the Triassic to the Quaternary
period. Many of the vascular plants inhabiting these deposits are protected either by
international, national or regional laws (Pintos and Rodrı́guez-Hiraldo 1994). Gómez-
Campo’s catalogue (1987) lists up to 12 gypsophytes which are also mentioned in
Appendix II of the EU Habitats Directive (Anonymous 1992). Although some of these
species are also protected by the Bern Convention (Anonymous 1979), their extent of
occurrence and the area of occupancy have diminished. As a matter of fact, Blanca et al.
(1999) report a reduction of almost 15%, which continues and will presumably do so
until the expiration of the exploitation licences. This is probably the main reason why
the endemic taxa of Almerı́a, Teucrium turredanum and Helianthemum alypoides, are
also mentioned in the recently published ‘Lista Roja Española’ (VV.AA. 2000) to-
gether with Teucrium balthazaris Sennen, another endemic gypsophyte of the south-
east of the Iberian Peninsula.
The richness and rarity of the vascular flora colonising these gypsum deposits
strongly justify the official conservation of these habitats (indeed, the EU Habitats
Directive gives priority to their conservation). The future Nature 2000 Network
provides a good opportunity to promote the preservation of these gypsum outcrops
which, due to their geographically punctuated distribution, present such an extra-
ordinarily varied flora. The gypsum deposits are also the habitat of other plant
communities of great interest, such as the therophyte grasslands (e.g., Izco 1976)
and the crusts of bryolichens (Casares-Porcel and Gutiérrez 1995).
The rich variety of vascular plants and cryptogams is most remarkable in the
south of the Iberian Peninsula, particularly in the province of Almerı́a (Guerra et al.
1995; Mota et al. 1998). This province also includes one of the most valuable
karstic systems on gypseous soil in the Mediterranean area (Calaforra and Pulido-
Bosch 1997). Since these areas concentrate 25% of the gypsum extraction in Spain
(Junta de Andalucı́a 1999), the conflict between conservation and exploitation is
inevitable. The industrial use of gypsum, either as a raw material for building or as
an ingredient of stucco and cement, seriously endangers the conservation of these
plant communities and ignores their biological and evolutive value (Parsons 1976;
Meyer 1986). Gypsum quarries do indeed provide a vital and multirole material in
any industrialised society, but at the same time the environment is seriously affected
(Davis 1982). Gypsum quarrying has a tremendous visual impact on karstic land-
scapes, altering them as dramatically as limestone quarrying has done in other
places (e.g., Gagen et al. 1993; Gunn 1993; Gunn and Bailey 1993). Modern
exploitation techniques, with sophisticated machinery and more powerful
explosives, produce long-lasting alterations in the landscape. In addition, in gypsum
quarrying these effects are not only visual (pollution occurs only to a minor extent),
but they also affect the karstic system and the flora too.
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This work deals with the gypsum outcrops of the province of Almerı́a (Iberian SE)
distributed in three large geographical units: the depression of Rı́o de Aguas, the
corridor of Tabernas and the basin of Rı́o Almanzora. Figure 1 shows the UTM quadrats
in which both the gypsum outcrops colonised by gypsicolous flora and the location of
the quarries under study are shown. Table 1 presents some basic data of the spots.
Data analysis
Impact on flora
There is no doubt about the serious impact of mining on gypsicolous flora, parti-
cularly on strict gypsophytes of a comparatively restricted geographical distribution
(narrow endemism). However, some studies have revealed that Gypsophila
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Figure 1. Location of the areas under study. The map shows the UTM 10 km 10 km grid encom-
passing the 1 km 1 km grid mentioned in the text.
Table 1. Basic data of the spots: UTM quadrats, abbreviations of the quarries sampled in each area and
gypsophytes of the non-disturbed scrubland.
Study area UTM Abbreviation Gypsophytes of the nearest
non-disturbed scrubland
struthium L. cannot only recolonise worked-out quarries, but also prosper and form
populations larger than those of unaltered areas (Merlo et al. 1997, 1998). In order
to assess the impact of mining on the whole gypsicolous flora, we recorded the
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taken in order to compare the abundance of the gypsophytes with the corresponding
records of both the autogeneous primary succession and of the bushes of the
neighbouring, unaltered outcrop.
Impact on flora
Most gypsophytes show significant differences in their cover rates, both inside and
outside the quarry (Table 2). The abundance rates of the main species can be seen in
the histograms of Figures 2 and 3, and the result of the comparative analysis of
medians for each two pairs of phases in Table 2.
G. struthium is the only gypsophyte whose cover rate in quarries is always higher
than in unaltered areas. This pattern can be seen in all the quarries and is even more
noticeable in the initial phases of the colonising process (Figure 2). There is
probably no easy explanation for this. Presumably, biological features both in
connection with the colonising potential and the endurance of G. struthium on
crystalline gypsum substrates are in some way accountable (Mota et al. 2003). The
quarry squares are extremely adverse environments and are almost nothing but
crystalline and very hard gypsum rock, that is, solid rock.
Leaving aside G. struthium, the rest of the gypsophytes show a completely
different pattern: many of them hardly occur in recently abandoned quarries or
are entirely absent. In the quarries of Rı́o de Aguas, almost all species are absent
in the first stage of succession (Figure 3a and Table 2); this also goes for the
local endemic species T. turredanum and H. alypoides. Only the pattern of L.
subulatum in the earlier stages of succession is similar to that of G. struthium
(Figure 3b).
Although in the quarries of Cuevas del Almanzora, during the earlier stages of
succession, the pattern is very similar to the one observed in Rı́o de Aguas and
Venta de los Yesos, there are some noteworthy differences, particularly if we take
into account the abundance of G. struthium (Figure 2). Firstly, the local endemic
species T. balthazaris is relatively abundant from the very beginning (Figure 3c).
Secondly, S. viscosa, an endemic plant of the Iberian southeast occurring in all
the areas under study, thrives more rapidly in the quarries of the river Almanzora
than elsewhere (Figure 3b and c). Why should this be? The physical profile of
gypsum, mostly hard and macrocrystalline in the outcrops of Rı́o de Aguas and
Venta de los Yesos, whereas it is soft and saccharoidal in the Almanzora river
valley (Calaforra and Pulido-Bosch 1999), has probably much to do with this
performance. These differences are so remarkable that gypsum karstic landscapes
with singular surface formations, such as tumuli and dolines or underground
caves, can be found only in the first gypsum type (Calaforra and Pulido Bosch
1997).
As far as the late stages of succession are concerned, most of the gypsophytes
tend to increase their coverage, although the records are well below the
values measured in the scrub (Figure 3a–c). Nevertheless, when the records of
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Table 2. Results of a Mann–Whitney test to compare the cover medians of each species in the four
environments studied (M, QII, QI and Re). The sign ** indicates different medians with p < 0.01, and *
with p < 0.05. A sign indicates that the species is absent in either of the two environments being
compared.
QI-QII QI-M QII-M QI-Re QII-Re M-Re
So
Gyp_str n.s. ** ** ** ** **
Hel_aly – – ** – n.s. **
Teu_tur – – ** – n.s. **
San_vis – – * – ** **
Cor_his n.s. ** ** n.s. n.s. **
Hel_squ n.s. ** ** – – –
Lau_fra – – ** – n.s. **
VY
Gyp_str ** ** n.s.
San_vis ** ** **
Cor_his n.s. ** **
Lep_sub ** n.s. **
Fra_thy – – **
Hel_squ ** ** **
Lau_fra ** ** **
CA
Gyp_str * n.s. n.s.
Teu_bal * ** *
San_vis n.s. n.s. *
Cor_his – – –
Hel_squ * ** **
Lau_fra – – n.s.
Figure 2. Cover (%) of G. struthium in the abandoned quarries and in the non-altered scrubland in each
studied area. The cover in the restoration made in Sorbas is also shown.
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Figure 3. Cover (%) of the main gypsophytes in each successional stage: (a) Sorbas; (b) Venta de los
Yesos-Tabernas; and (c) Almanzora valley.
recently abandoned quarries (QI) are compared with those of quarries abandoned
long ago (QII), all the species, even those with low colonising potential, such as
F. thymifolia, H. squamatum or C. hispanica, clearly tend to recuperate as the
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Figure 4. Average cover (of the studied areas) of all gypsophytes (GIPSO-T), G. struthium (GS), all
gypsophytes except G. struthium (GIPSO-P), the non-gypsophytes (NGIPSO), and the ruderal species.
The cover in the restoration exclusively accounts for Sorbas.
Conclusions
To sum up, the rehabilitation of gypsum quarries should not only aim at correcting
the visual impact of mining on the landscape, but should also concern itself with the
biological impact of the quarrying. The ever-growing quarrying area seriously
reduces the sites suitable for the endemic flora which colonises them. As gypso-
phytes inhabit edaphic archipelagos, we face the risks and eventually fatal con-
sequences of destroying and fragmenting natural habitats.
Acknowledgement
This research was financially supported by a grant from the DGES (PB98-1385).
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