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ABSTRACT
Avian diversity is used to assess the functionality of diverse types of habitats around Salt Lake Djendli, Northeast Algeria. The landscape is stratified into five habitat types in a gradient from wetland to forested mountains.
Bird species found in these habitats can be classified into four ecological groups with decreasing degrees of
aquatic specialisation and increasing forest specialisation. For each surveyed species, five ecological status were
assigned. Overall, there was lower species richness in urban areas compared to other natural habitats. Birds
have a biogeographical affinity to the western Palaearctic according to the dominant faunal types. Interactions of
ecological status with phenological traits reveal that water birds are different from non-aquatic species because
most of them are migrants. Moreover, overall, there is no worrying conservation status for surveyed birds. Bird
diet is dependent on the ecological status that differentiate bird groups from each other due to differences in the
food resources of the habitats they frequent. Phenological categories tend to link together birds of urban and
open-lands. These two groups are affected by seasonal human activities. Our findings emphasise the importance
of using combinations within the birds ecological status, which would give information on the actual state of
avifauna. This approach is relevant for future programmes and conservation actions.
Keywords: Salt Lake Djendli, birds, biodiversity, ecological status, landscape
1. INTRODUCTION
Knowledge of species diversity is particularly useful in
monitoring biodiversity because it depends on a set of
characteristic habitats that are adequately anastomosed
(Breininger et al., 2002). As a biological model, we chose
ecological groups of birds to assess the level of biodiversity
in wetland ecosystems and the surrounding areas. Birds
are particularly useful because they are mobile and,
depending on species, require a wide variety of habitats
on different spatial scales (Angelstam et al., 2004).
Since birds are relatively easy to study, several
avifaunal surveys were performed in Algerian wetlands
especially in the East of the country. Several bird species/
populations were used: (i) to investigate the conditions
of the bird populations and (ii) to give an indication
of the health of the habitats (Ledant and Van Dijk,
1977; Ledant et al., 1981; Van Dijk and Ledant, 1983;
Isenmann and Moali, 2000; Saheb et al., 2006; Samraoui
et al., 2006; Samraoui and Samraoui, 2008; Samraoui
www.avianbiologyresearch.co.uk
doi: 10.3184/175815513X13577344603957
68
2. METHODS
This study was carried out in the Salt Lake Djendli, which
is a temporary saline wetland located in northeastern
Algeria, 46 km northeast of Batna city (Figure 1). The lake
covers 3700 ha of area at an average altitude of 833m
(a.s.l.). It is fed mostly by rainwater collected from the subwatershed of Oued Chemora that belongs to the Hauts
Plateaux Constantinois watershed.
The climate of the region is not uniform, great interannual fluctuations are observed. Long-term data (1974
2006) show that the coldest month was January with
average temperatures of 5.3C and the warmest month
was July with average temperatures of 25C. Rainfall was
also irregular with an annual average of 350.876.3mm.
The bioclimate is semiarid Mediterranean-type with cool
winters. Furthermore, the main economical activities
of Salt Lake Djendli are cereal crops, fruit growing and
sheep-farming (Chenchouni, 2007).
The lake covers a large area with low water depth, rarely
exceeding 0.5 m, even in wet years. The low water level
of the lake is due to low rainfalls and to the low slope of
the ground that disperses water over a large surface. Water
is alkaline (pH = 8.4 0.2) and salt (salinity at 25C =
58.4 4.0 g L-1) with a turbidity ranging between 41.1
and 53.3 Nephelometric Turbidity Unit (Chenchouni,
2007). The flooded area includes bare lands on which the
water level settles. The soil is impervious and salty due to
repeated evaporation of salt water. When drought occurs
in summer, the waterbody disappears completely.
Halophytic rangelands
The immediate vicinity of flooded areas is occupied by
belts of vegetation dominated by halophytic plants such
Figure1 Study area with the sampled ecological units (i.e. coarse landscape types) of Djendli Salt Lake (Batna, Northeastern Algeria).
69
70
3. RESULTS
3.1 Inventory and ecological status of birds
The study area included an avian community composed
of 108 bird species including 42 passerines, 66 nonpasserine birds with 46 waterbirds. This avifauna can be
classified into 13 orders, 35 families and 72 genera. The
Passeriformes order was the best represented with 42
species and 13 families, followed by Charadriiformes with
20 species and five families, then came Anseriformes with
12 species (Table1).
The surveyed avifauna belonged to 15 faunal types
following the classification of Voous (1960). The
Palaearctic faunal type dominated with more than a
EG
W
W
U
W
W
W
W
W
W
W
W
W
W
W
W
W
F
F
O
W
F
F
F
W
O
O
O
O
W
W
O
W
W
W
W
W
W
W
W
W
W
W
W
W
W
W
W
W
W
W
W
W
W
W
FT
IA
OW
P
S
PX
P
H
P
H
H
H
[S]
P
P
TM
OW
IA
IA
P
H
PX
IA
C
OW
ETH
M
OW
P
P
P
C
[TM]
[TM]
IA
P
ARC
C
P
ARC
ARC
SB
P
H
P
P
SB
P
SB
P
P
[S]
PHC
RB
WM
WMB
WMB
WMB
WMB
WM
WM
WM
WM
WMB
WM
WM
WM
WM
WM
SM[B]
SM
SM
WM
SM
RB
RB
WM
RB
RB
RB
RB
WM
RB
WM
RB
WMB
WM[B]
WM
WM
WM
WMB
WM
WM
WM
WM
WM
WM
WM
WM
WM
WM
WM
WM
WM
WM
SMB
WM
Ecological status
TC
PRC
[Inv]
LC,T,E,A
[Inv]
LC,T,E,A
[Inv]
LC,N,D,E,A
Pp
LC,T,N,L,D,E,A
Pp
LC,N,D,E,A
Pp
LC,N,D,E,A
Pp
LC,T,N,E,A
Pp
LC,N,E,A
Pp
LC,T,N,E,A
G
LC,T,N,E,A
Pp
LC,N,E,A
Pp
LC,T,N,E,A
Pp
VU,N,D,E,A
Pp
LC,N,E,A
Pp
LC,N,E,A
Pp
NT,T,N,E,A
Cr
LC,T,N,D,E
Cr
EN,T,N,D,E
Cv
LC,T,N,D,E
Cv
LC,T,N,D,E
Cv
LC,T,N,D,E
Cv
LC,T,N,D,E
Cv
LC,T,N,D,E
Cv
LC,T,N,L,D,E
Cv
LC,T,N,D,E
Cv
LC,T,N,D,E
G
LC,E
G
LC,E
Inv
LC,E,A
Pp
LC,E,A
Pp
LC,T,N,D,E,A
Inv
LC,N,D,E,A
Inv
LC,N,D,E,A
Inv
LC,N,E
Inv
LC,N,E,A
[Inv]
LC,N,E,A
[Inv]
LC,N,E,A
[Inv]
LC,N,E,A
[Inv]
LC,N,E,A
Inv
LC,N,E,A
Inv
LC,N,E,A
Inv
LC,N,E,A
Inv
LC,N,E,A
Inv
LC,N,E,A
Inv
NT,N,E,A
Pp
NT,N,E,A
Inv
LC,N,E,A
Pp
LC,N,E,A
Inv
LC,N,E,A
Inv
LC,N,E,A
Pp
LC,N,E,A
Pp
LC,E,A
Pp
LC,N,E,A
Pp
LC,E,A
FO
V
II
V
V
V
II
IV
IV
IV
IV
V
V
I
II
II
III
III
II
I
I
I
I
II
I
III
III
I
III
I
II
V
V
V
III
II
III
II
V
I
IV
III
II
I
I
I
II
IV
III
II
II
II
IV
I
I
71
72
Table 1. Contd.
Scientific name
Chlidonias niger
Chlidonias leucopterus
Sterna nilotica
Pterocles orientalis
Pterocles alchata
Columba livia
Streptopelia decaocto
Streptopelia turtur
Streptopelia senegalensis
Apus apus
Merops apiaster
Upupa epops
Melanocorypha calandra
Calandrella brachydactyla
Calandrella rufescens
Galerida cristata
Alauda arvensis
Ptyonoprogne rupestris
Hirundo rustica
Delichon urbica
Anthus pratensis
Motacilla flava
Motacilla alba
Erithacus rubecula
Phoenicurus moussieri
Phoenicurus ochruros
Saxicola torquata
Oenanthe oenanthe
Oenanthe leucopyga
Oenanthe leucura
Turdus merula
Cisticola juncidis
Hippolais polyglotta
Sylvia melanocephala
Sylvia atricapilla
Phylloscopus collybita
Ficedula hypoleuca
Parus caeruleus
Lanius excubitor
Lanius meridionalis
Lanius senator
Corvus corax
Sturnus vulgaris
Passer domesticus
Passer hispaniolensis
Passer montanus
Fringilla coelebs
Serinus serinus
Carduelis chloris
Carduelis carduelis
Carduelis cannabina
Emberiza cirlus
Emberiza cia
Miliaria calandra
a
EG
W
W
W
O
O
U
U
F
F
U
O
F
O
O
O
O
O
O
U
U
O
O
O
O
O
F
O
F
O
O
F
O
O
F
F
O
F
F
O
O
O
O
O
U
O
U
F
U
F
O
F
F
F
O
FT
H
P
C
PX
PX
[TM]
IA
ET
ET
P
TM
OW
M
TM
TM
P
P
PXM
H
P
E
P
P
E
PXM
P
P
M
M
P
IA
M
TM
E
P
E
E
H
H
M
H
ET
P
TM
P
E
M
ET
ET
ET
M
P
ET
PHC
WM
WM
SMB
RB
RB
RB
RB
SM
RB
SM
RB
RB
RB
RB
RB
RB
RB
SM
SMB
SMB
WM
WM
WM
R[B]
RB
RB
WM[B]
WM[B]
R[B]
RB
RB
RB
SM
SM
SM
SM
SM
RB
RB
RB
RB
RB
WM
RB
RB
RB
RB
RB
RB
RB
RB
RB
RB
RB
Ecological status
TC
PRC
Pp
LC,E,A
Pp
LC,N,E,A
Pp
LC,E
G
LC,E
G
LC,E
G
LC,T,E
G
LC,E
G
LC,E
G
LC,T,E
Inv
LC,E
Inv
LC,N,D,E
Inv
LC,D,E
Inv
LC,E
Inv
LC,E
Inv
LC,E
G
LC,E
Pp
LC,E
Inv
LC,E
Inv
LC,E
Inv
LC,E
Inv
LC,E
Inv
LC,E
Inv
LC,E
Pp
LC,E
Inv
LC,E
Inv
LC,E
Inv
LC,E
Inv
LC,E
Inv
LC,E
Inv
LC,E
Pp
LC,E
Inv
LC,E
Inv
LC,N,E
Inv
LC,N,E
Inv
LC,N,E
Inv
LC,N,E
Inv
LC,N,E
Pp
LC,E
[Inv]
LC,E
Inv
LC,E
Inv
LC,E
Pp
LC,E
Inv
LC
Pp
LC
G
LC,E
Pp
LC,E
G
LC,E
G
LC,D,E
G
LC,E
G
LC,E
G
LC,E
G
LC,E
G
LC,E
G
LC,E
FO
I
I
I
I
I
IV
IV
III
II
I
III
IV
III
III
I
IV
V
I
IV
III
I
III
IV
IV
III
III
II
I
II
IV
II
IV
I
II
I
IV
III
I
V
II
III
IV
III
V
III
II
III
IV
II
III
I
II
I
IV
NonPasserines Total
passerines
3
0
3
7
4
11
3
0
3
19
12
31
0
6
6
%
2.8
10.2
2.8
28.7
5.6
6.5
8.3
1
3
4
7
0
0
8
3
4
7.4
2.8
3.7
1.9
1
5
6
4
3
66
0
0
1
0
1
42
1
5
7
4
4
108
0.9
4.6
6.5
3.7
3.7
100
100
(A)
(B)
100
(C)
100
75
75
75
50
50
50
25
73
25
(E)
(F)
25
0
0
Cv Cr G Inv Pp WM SM R B [B] Inv Pp G Cv Cr I II III IV V Cv Cr G Inv Pp F U O W
(8) (2) (19) (49) (30) (48) (16) (44) (53) (6) (49) (30) (19) (8) (2) (29) (23) (23) (20) (13) (8) (2) (19) (49) (30) (20) (9) (34) (45)
Trophic categories
W (45)
O (34)
Phenological traits
U (9)
F (20)
WM (48)
RB (44)
Trophic categories
V (13)
IV (20)
III (23)
Bird groups
II (23)
I (29)
Figure2 Distribution of species richness number of bird species in % according to their ecological status combined in pairs. (A):
EG versus TC, (B): EG versus PHC, (C): PHC versus TC, (D): PHC versus FO, (E): FO versus TC, (F): FO versus EG. See Appendix 1 for
abbreviations; numbers in parentheses are the total number of bird species of each ecological status.
74
Table3 Distribution of the number of species by ecological bird groups following their protection state nationally and internationally
Treat and convention on bird protection
Code
Least Concern
Near Threatened
Vulnerable
Endangered
Appendix 1
Appendix 2
Appendix 1
Appendix 2
Appendix 2
Appendix 2
Appendix 3
AEWA Agreement
Algerian law
LC
NT
VU
EN
T
T
N
N
L
E
E
A
D
Forest
birds
19
0
0
1
5
1
0
8
0
16
4
0
6
Urban
birds
9
0
0
0
0
1
0
1
0
4
4
1
2
Open-habitat
birds
41
3
1
0
4
0
0
7
2
24
9
41
8
Water
birds
34
0
0
0
3
7
2
35
0
22
23
1
5
Total
103
3
1
1
12
9
2
51
2
66
40
43
21
95.4
2.8
0.9
0.9
11
8.3
1.9
47.0
1.9
61
37
40
19
75
76
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