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On the breeding of the Grey Heron Ardea cinerea in Algeria

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On the breeding of the Grey Heron Ardea cinerea in


Algeria
a a a b
Riad Nedjah , Farrah Samraoui , Abdennour Boucheker , Ahmed H. Alfarhan &
ab
Boudjéma Samraoui
a
Laboratoire de Recherche et de Conservation des Zones Humides, University of
Guelma, Guelma 24000, Algeria
b
Department of Botany and Microbiology, Centre of Excellence for Research in
Biodiversity, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi
Arabia
Published online: 23 Apr 2014.

To cite this article: Riad Nedjah, Farrah Samraoui, Abdennour Boucheker, Ahmed H. Alfarhan & Boudjéma
Samraoui (2014): On the breeding of the Grey Heron Ardea cinerea in Algeria, Zoology and Ecology, DOI:
10.1080/21658005.2014.909155

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Zoology and Ecology, 2014
http://dx.doi.org/10.1080/21658005.2014.909155

On the breeding of the Grey Heron Ardea cinerea in Algeria


Riad Nedjaha, Farrah Samraouia, Abdennour Bouchekera, Ahmed H. Alfarhanb and Boudjéma Samraouia,b*
a
Laboratoire de Recherche et de Conservation des Zones Humides, University of Guelma, Guelma 24000, Algeria;
b
Department of Botany and Microbiology, Centre of Excellence for Research in Biodiversity, College of Science,
King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia
(Received 20 September 2013; accepted 14 March 2014)

During the period 2002–2012, we assessed the breeding status of the Grey Heron Ardea cinerea in Algeria by surveying
all the major wetlands in the region. We located two distinct breeding sites; one of them was recorded for the first time.
We also investigated nest site selection, measured breeding parameters and derived a growth curve for developing
chicks. Although wintering Grey Herons increased in numbers in the region, the number of breeding pairs did not
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change markedly over the past century. The reasons for the scarcity of Grey Heron breeding pairs in Algeria and in the
rest of North Africa are discussed.

2002–2012 metais atlikus stebėjimus didžiausiose regiono pelkėse buvo įvertintas pilkojo garnio Ardea cinerea perėjimas
Alžyre. Aptiktos dvi perimvietės, viena iš jų užregistruota pirmą kartą. Ištirtas lizdo vietos pasirinkimas, perėjimo para-
metrai, sudaryta jauniklių augimo kreivė. Nors per praėjusį šimtmetį žiemojančių pilkųjų garnių skaičius regione didėjo,
perinčių porų skaičius beveik nesikeitė. Straipsnyje aptariamos priežastys, susijusios su nedideliu perinčių pilkųjų garnių
porų skaičiumi Alžyre ir visoje šiaurės Afrikoje.
Keywords: wetlands; water birds; Ardeidae; breeding success; distribution; North Africa

Introduction century. Although the breeding biology of the Grey


The Grey Heron is the most widespread heron in Eurasia Heron is relatively well documented in Europe (Milstein,
(Kushlan and Hancock 2005). Common in winter and on Prestt, and Bell 1970; Marion 1979; Campos and
passage, the Grey Heron Ardea cinerea is the least abun- Fernández-Cruz 1991; Lekuona and Campos 1995), there
dant species of the colonial herons and egrets breeding is scant information on its breeding ecology in North
in North Africa (Thévenot, Vernon, and Bergier 2003; Africa. The present study assesses the reproductive status
Isenmann et al. 2005; Samraoui et al. 2011). In the nine- of the Grey Heron in Algeria and documents the breed-
teenth century, breeding in North Africa was only certain ing phenology and habitat characteristics of the species
for Lake Fetzara with probable but unconfirmed reports at the southern edge of its range. Information on egg
for Lake Ichkeul (Tunisia) and Northern Morocco (Heim dimensions and chick development is also provided and
de Balsac and Mayaud 1962). A century later, the situa- compared to that of other species of herons and ibis. The
tion in the region has barely changed with rare and spo- study of the reproduction of the Grey Heron in the
radic breeding being the rule in Tunisia (Isenmann et al. region may shed light on important selective forces that
2005), Algeria (Ledant et al. 1981; Isenmann and Moali regulate its populations across its distributional range.
2000; Samraoui et al. 2011) and Morocco (Thévenot,
Vernon, and Bergier 2003; El Hamoumi and Qninba
Materials and methods
2008). In sharp contrast, following the decline in human
persecution and the expansion of rice agriculture, the Between 2002 and 2012, we sampled all major wetlands
Grey Heron staged a remarkable recovery in Southern within Numidia, North-East Algeria (Figure 1), looking
Europe in the late part of the twentieth century (Marion for heron colonies (Samraoui and Samraoui 2008). We
1997; Schmid, Volet, and Thoma 2004; Campos and focus in this paper on the Grey Heron which was
Fernández-Cruz 2006; Fasola et al. 2010). In the recorded to breed at two sites (see Results): Lake
Camargue, the increase went from two pairs in 1964 Fetzara, a vast brackish marsh of 24,000 ha dominated
(Blondel 1965) to a peak of 877 pairs in 1989 (Hafner, by Phragmites australis and Scirpus maritimus, and
Johnson, and Walmsley 1984; Kayser et al. 1994). Dakhla, a freshwater marsh of 8 ha covered by Salix
Contrary to what happened on the northern shores of the atrocinerea, Cladium mariscus and Scirpus lacustris
Mediterranean Basin, there was no significant increase in (Figure 2). Each nest was labelled with a distinct code,
Numidia or other parts of North Africa over the past and nest height above water and nest diameters were

*Corresponding author. Email: bsamraoui@yahoo.fr

© 2014 Nature Research Centre


2 R. Nedjah et al.
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Figure 1. Study location in Numidia, North-Eastern Algeria.

measured. Eggs were weighted using a Pesola spring bal- Phragmites contained a loose colony of the Purple Heron
ance with an accuracy of 0.1 g, and their lengths (L) and Ardea purpurea. The same year, two nests of Grey Heron
breadths (B) were measured to the nearest 0.1 mm using were also discovered at Dakhla, a new breeding site, but
vernier calipers. Egg volume (V, in cm3) was calculated they proved to be inaccessible. They were located in the
using Hoyt’s formula (V = 0.509 L × B2) (Hoyt 1979). middle of a plurispecific heron and ibis colony which
Chicks were individually marked, and their mass, total included Purple Heron Ardea purpurea, Cattle Egret
tarsus, and head and bill length (tip of bill to back of Ardea ibis, Little Egret Egretta garzetta, Black-crowned
skull) were recorded at the age of 1–27 days (Figure 3). Night Heron Nycticorax nycticorax, Squacco Heron
Chicks were measured on 5–6 occasions before they Ardeola ralloides and Glossy Ibis Plegadis falcinellus.
became too mobile and no measurements could be made On 30 May 2007, another nest containing a brood of
after the age of one month. Hatching dates were used to four chicks was discovered at Dakhla. Once again, it
infer the sequence of egg-laying. Data analysis was car- was part of a mixed heron and ibis colony (Figure 2).
ried out using R (R Development Core Team 2009). The latest breeding event was also noted at Dakhla in
Mean values are given ±1 standard deviation (SD). 2012 when a preliminary visit on 26 April allowed the
records of two breeding pairs. A subsequent visit on 30
April led to the discovery of two nests with broods of
Results three and two chicks, respectively. These chicks were
Nesting sites and timing of breeding aged between two and three weeks, indicating a hatching
On 7 April 2006, two nests of Grey Heron, one of them date around 10 April. Based on an incubation period of
unoccupied and the other containing a clutch of three 25–26 days (Cramp and Simmons 1977), the onset of
eggs, were discovered at Lake Fetzara. Both nests were egg-laying must have occurred in the first half of March.
located in a stand of Phragmites australis, which occurred Grey Heron nests were located on Salix atrocinerea
in patches across the marsh. Other nearby stands of surrounded by dense stands of Cladium mariscus and
Zoology and Ecology 3
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Figure 2. General (top) and closer (bottom) view of the heron colony at Dakhla in 2007.

they were distinguishable from Purple Heron nests only


because of their larger sizes and nest height. A summary
of nest characteristics is presented in Table 1.

Egg measurements
The mean egg weight, length, breadth and volume
recorded in one single clutch (N = 3 eggs) at Lake
Fetzara were 57.0 ± 5.1 g, 60.9 ± 2.2 mm, 42.2 ± 1.1 mm
and 55.3 ± 4.7 cm3, respectively.

Breeding
In 2006, the fate of the clutch at Lake Fetzara and two
nests at Dakhla could not be monitored but observations
of provisioning by adults in the latter site strongly sug-
gest successful breeding. In 2007, the Grey Heron man-
aged to fledge three chicks out of a brood of four. One
Figure 3. A brood of three Grey Heron nestlings at Dakhla in chick, with a hatching rank C, died within a week. In
2007.
4 R. Nedjah et al.

Table 1. Characteristics of four Grey Heron nests at Lake Fetzara and Dakhla, North-East Algeria.

Sites Ext. diam. (cm) Nesting height (cm) Vegetation Veg. height (cm) Water depth (cm)
Fetzara 100 70 Phragmites australis 300 105
Dakhla 2006 70 160 Salix atrocinerea 310 92
Dakhla 2012 100 100 Salix atrocinerea 350 –
Dakhla 2012 70 240 Salix atrocinerea 350 –
Mean ± SD 85.0 ± 17.3 142.5 ± 75.0 327.5 ± 26.3 98.5 ± 9.2

2012, all five chicks survived up to the fledging time compared to that recorded in Europe (February and
when last monitored. March) (Owen 1955; Milstein, Prestt, and Bell 1970;
Campos and Fernández-Cruz 1991), suggesting late arri-
val of breeding pairs. A ringing scheme is, thus, needed to
Growth of nestlings map up the dispersion and/or migration of breeding Grey
No attempt was made to fit a more elaborate function as Herons in the region to resolve this pending issue.
for the age considered (1–27 days) the growth rates for Answering such questions is of conservation value as
all variables (mass, tarsus, head and bill) (Table 2) conditions at both breeding sites and wintering grounds
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were essentially linear, best described by the equation may influence population dynamics (Den Held 1981;
y = ax + b, calculated by the least squares regression of Cavé 1983; Deerenberg and Hafner 1999; Fasola et al.
body measurements against chick age (Figure 4). 2010).
The Grey Heron occupies larger nests at greater
heights than the Purple Heron does in similar habitats.
Discussion External nest diameters were 85.0 ± 17.3 cm (N = 4) and
This study documents for the first time a successful breed- 50.15 ± 7.21 cm (N = 190), and nest heights were 142.5
ing of the Grey Heron in Algeria suggesting that local ± 75.0 cm (N = 4) and 98.2 ± 36.55 cm for the Grey
habitats are adequate to cater for successful development Heron and Purple Heron, respectively. Data on mean egg
of Grey Heron broods. Ground surveys were used to find weight (57.0 g), length (60.9 mm) and breadth (42.2 mm)
heron nests, although in marshes like Lake Fetzara or the agree well with means and ranges cited in literature
Mekhada aerial surveys are more suited for covering such (Bauer and Glutz Von Blotzheim 1966): weight 60.8 g
huge and inaccessible wetlands. However, numerous visits (48.2–68.5 g), length 60.6 mm (55.4–68.4 mm) and
to all major wetlands in Numidia over 11 consecutive breadth 43.0 mm (39.4–46.4 mm). The recorded breeding
years (Samraoui and Samraoui 2008) make it unlikely that success, though based on a small sample, appears to be
colonies or even large numbers of solitary nests could high although the presence of unoccupied nests may
have escaped our notice. The species previously bred in indicate breeding failure.
Algeria at Lake Fetzara (Heim de Balsac and Mayaud Previous studies of the growth rates of the Grey
1962), Lake Tonga (Ledant et al. 1981) and in a few scat- Heron have shown that chicks at birth have a mass of
tered localities (Isenmann and Moali 2000). Dakhla is a approximately 30 g and that they reach an asymptote of
new breeding site for the Grey Heron in Algeria and is so around 1700 g prior to fledging (Marion 1979). Similar
far an unprotected marsh threatened by human encroach- asymptotes for tarsus and bill were 150 and 118 mm,
ment. Estimates of the present study indicate that the Grey respectively. Heinroth (in Voisin 1991) recorded a maxi-
Heron population in Numidia could not exceed a total of mum food intake of 330 g d−1 for chicks of 17 days of
12–15 breeding pairs. These results are in line with previ- age, which is a real challenge for adults provisioning
ous distribution and estimates of breeding pairs of Grey broods of three or four chicks. The chicks of the Grey
Heron in Algeria. Heron, due to a larger size of the species, exhibit the
It is unknown whether breeding pairs are residents. highest developmental rate among all colonial herons
They might be just aestivating birds like many other colo- and ibis breeding in the region (Table 3).
nial herons (Purple Heron, Squacco Heron, Black- The successful breeding of the Grey Heron in north-
crowned Night Heron). The onset of egg-laying (from east Algeria begs the question why the species does not
March to early April) in Numidia is relatively late breed more frequently in North Africa. Results indicate
that competition with the Purple Heron, suggested as a
possible factor (Fasola and Alieri 1992; Thomas and
Table 2. Growth rates of a brood of Grey Heron chicks from Hafner 2000), may not fully answer the question. Both
1 to 27 days of age at Dakhla in 2007. Grey Heron and Purple Heron favour the same micro-
habitats as nesting sites in Numidia and they were found
Mean Intercept r2 p N (chicks)
to coexist with each other and with other species of her-
−1
Mass gain (g d ) 49.6 67.3 0.97 0.0001 3 ons. Both species are known to occupy a wide range of
Tarsus growth (mm d−1) 4.8 18.3 0.96 0.0001 3 habitats from tall trees to reedbeds (van der Kooij 1991;
Head and bill (mm d−1) 5.2 49.8 0.96 0.0001 3 Voisin 1991; Nedjah et al. 2010), and the habitats, in no
Zoology and Ecology 5

Table 3. Comparative growth rates of heron and ibis chicks in


North-East Algeria (Samraoui, Menaï, and Samraoui 2007;
Boucheker et al. 2009; Nedjah et al. 2010; Samraoui, Nedjah
et al. 2012).

Mass Head and


Age gain Tarsus bill
Species (days) (g d−1) (mm d−1) (mm d−1) N
Ixobrychus 5–12 10.20 2.90 4.10 13
minutus
Ardea ibis 1–23 14.53 2.69 1.93 26
Plegadis 4–15 29.91 4.45 NA 37
falcinellus
Ardea 4–20 34.10 3.77 4.47 71
purpurea
Ardea cinerea 1–27 49.60 4.80 5.20 3

short supply, occupied by both species in Numidia (reed-


beds and bushes) are well within this range. Both species
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are mainly piscivorous, but Purple Herons mainly hunt


in freshwater wetlands with dense vegetation (Fasola
1986). This latter species also has a broader diet
(Barbraud et al. 2001; Montesinos, Santoul, and Green
2008). In contrast, Grey Herons forage in wetlands with
a wide range of salinity with a preference for open water
bodies (Voisin 1991). They take a great variety of prey
but rely heavily on fish: eels Anguilla anguilla, carps
Cyprinus carpio, barbells Barbus spp., etc. (Owen 1955;
Moser 1986). Grey Herons may also be opportunistic,
taking full advantage of introduced prey (Peris, Briz, and
Campos 1994; Adams and Mitchell 1995; Jakubas
2004). In Numidia, carps which have been introduced in
the past two decades have spread across many wetlands
only in recent years, and eels, as elsewhere, are in sharp
decline. A rather poor ichthyofauna, early drought and
fast emerging vegetation combine to make local wetlands
less attractive for breeding Grey Herons. In contrast, the
region hosts a rich and diverse insect fauna (Riservato
et al. 2009; Annani, Alfarhan, and Samraoui 2012) and
herpetofauna (Samraoui, Samraoui et al. 2012), which
may favour species with a broad diet (Nedjah et al.
2010; Samraoui, Nedjah et al. 2012). Thus, contrasting
abundance and prey availability at a critical stage of the
life cycle of each species (Van Vessem and Draulans
1986) may explain the divergent population dynamics
between the Purple Heron and the Grey Heron in North
Africa and southern Europe.
Local habitats are far from secure with many over-
hanging anthropogenic pressures threatening the sustain-
ability of heron colonies in Algeria. Unfortunately,
illegal shooting of herons and egg and chick harvesting
within protected and unprotected areas continue unabated
(Samraoui, Menaï, and Samraoui 2007). However, loss
of habitats and hydrological changes affecting wetlands
harbouring heron colonies are considered the major
threat in the area (Samraoui, de Belair, and Benyacoub
Figure 4. Growth of mean body mass (top), mean total tarsus 1992). Local conservation efforts have gained ground in
(middle), and mean head and bill (bottom) of three chicks from recent decades but are still insufficient to provide sanctu-
a single brood during early development. aries to breeding water birds.
6 R. Nedjah et al.

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