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U krainian Journal of Ecology
Ukrainian Journal ofEcology, 2022, 12(3), 1-10, doi: 10.15421/2022_348
ORIGINAL ARTICLE
Contribution to the knoweldge of earthworm fauna of Chrea
National Park (Algeria)
H. Zerrouki*, S. Hamil, M. Alili, W. Isserhane, M. Baha
Laboratory of Eco-biology Animals, École Normale Supérieure de Kouba Bachir El Ibrahimi, B.P. 92, 6050,
Algeria
Corresponding author E-mail: [email protected] Received: 12-Feb-2022, Manuscript No. UJE-22-54309; Accepted: 07-Mar-2022f Pre QC No. P-54309; Editor assigned: 18-Feb-2022, Pre QC No. P-54309; Reviewed: 25-Feb-2022, QC No. Q-54309; Revised: 02-Mar-2022, Manuscript No. R-54309; Published: 15-Mar-2022.
This preliminary study was conducted to identify the different species of earthworms that live in the region of Chréa in north Algeria. A total of 3196 earthworms were sampled and represented by three families: Acanthodrilidae, Megascolecidae, and Lumbricidae. Eleven genera represented by nineteen species are discovered. The individuals were identified to the following taxa: Aporrectodea caiiginosa, Allolobophora rosea, Allolobophora cholorotica, Allolobophora antipai, Allolobophora miniscuia, Aporrectodea trapezoides, Eisenieiia tetraedra, Amynthas sp., Amynthas caiffornica, Microscoiex phosphoreus, Criodriius lacuum, Octodriius compianatus, Octodriius maghrebinus triginta, Octodriius maghribinus maghribinus, Eisenia xyiophíia, Ocnerodriius sp, Eisenia andre, Heiodriius ocuiatus, Dendrobaena pantaieoni. D. pantaieoni is new record for Algeria. High abundance of earthworms have been recorded under the cork oak, where the soil is rich in organic matter, followed by cedar soils that are characterized by lower organic matter content. Both species A. caiiginosa and O. compianatus are absent in a soil poor of organic matter and under Quercus canariensis. Keywords: Earthworms fauna, Soil, Diversity, Chrea national park.
Introduction
For several decades, the study of soil's living world has become increasingly important. Among these organisms, earthworms have always aroused the most interest. Aristotle was one of the first people who draw attention to the role of earthworms in turning over the soil. In his last work, Charles Darwin (1881) drew the attention of the scientific world to earthworms. Several researchers then became interested in physiology, general biology, their participation in soil fertility, and their pedogenetic activities as (Hensen, 1877; Bornebusch, 1930; Laverack, 1963 and others to date.
For the taxonomic purpose, first works came from Cuvier and Lamarck whose recognized the class of Annelids (Lamarck, 1800). Important studies were subsequently published by: Savigny 1826; Rosa, 1893; Michaelsen,1906; Tetry, 1937; Zajonc, 1959; Graff, 1962; Bouché, 1972; and Omodeo, 1987. Earthworms in the Maghreb had been little studied and the knowledge of their diversity is limited and incomplete. The first collection of earthworms in Maghreb was carried out in Egypt. These studies started with Napoleon's expedition of 1798 and his attempts to record Egypt's natural history. The (few) worms collected were described by Savigny (1809), but do not fit any identifiable species.
Establishment of protected areas is a key strategy in biodiversity conservation (Vale, et al., 2018), but at the same time, it is primarily driven by available opportunities rather than scientific knowledge (Baldi, et al., 2017). In this regard, it is very important to study biodiversity on a local scale in order to provide the best possible management options.
Earthworms are essential service providers for terrestrial ecosystems (Lavelle, et al., 2006). Their activity, generating galleries and casts, contributes to formation and maintenance of soil structure (Lavelle, 1997; Capowiez, et al., 2012), increasing porosity, infiltration and water retention (Fiuza, et al., 2012), as well as re-distribution and breakdown of soil organic matter (Brown, et al., 2000). However, earthworms are sensitive to land use and management, and can be used as soil quality and management as well as environmental bioindicators (Brown and Domínguez, 2010; Bartz, et al., 2013; Bünemann, et al., 2018). Algeria is home to more than 31 described earthworm species (Zeriri, et al., 2013; Baha and Isserhane, 2017), but practically nothing is known of the species and populations inhabiting protected area in the country.
The earthworms of Algeria started receiving attention in the second half of the past century Beddard (1892), Rosa (1893). A few additional records were published in the first decades of this century Michaelsen (1903-1930); (Bouché, 1972). However, these older records were scanty and all came from occasional collections.
The first extensive survey was made by Omodeo and Martinucci (1987), who found 24 species, of which three were new to science and 14 were new for Algeria. BAHA (1997) presented a collection of 500 earthworms taken during (1990-1991) from various soils under orange cultivation in Mitidja, a coastal plain to the south of Algiers. Of the 11 species identified, Allolobophora chiorotica Savigny (1826) was new for North Africa, other three species had not yet been reported from Algeria, and a fifth Prosellodrilus doumandjii Baha and Berra 2001, was shortly to be described as new to science.
During that study a variety of habitats were prospected, but no sampling was made in cultivate areas. In this paper were stadied a collection of earthworms taken during (2015-2018) from different soils under different vegetation in Chrea National Park (Algeria). It emerges of all these studies more than 8000 species from about 800 genera in the world (Edward, 2004). In Algeria Twelve genera, represented by 31 species (Zeriri, et al., 2013; Baha and Isserhane, 2017), have been revealed. Earthworms are common all over the world in natural forests and grasslands as well as agrosystems and found in most regions of the world. However, almost no data on earthworms are available from the northern part of Algeria (Chrea National Park). The present study aimed to investigate earthworms' diversity and spatial distribution and abundance in the Chrea Biosphere Reserve and its vicinity, situated in the north center of Algeria, and give the first systematic data on earthworms from this region.
The main objective of the present research was to gain a piece of scientific information about kind of earthworms, their relative abundance, seasonal fluctuations of population and evaluate earthworm communities (abundance, biomass, species composition) associated with different forest habitats of Chrea Biosphere Reserve. Such information could be used to suggest measures for the improvement of soil to increase forest land production.
Materials and Methods Study area
This research was carried out in the Chrea National Park. It is located in central area of Algeria (36°19'-36°30'N and 2°38'-3°02'E), about 50 km south-west of Algiers (Fig. 1). It covers around 26 587 ha over a length of 40 km from E/W and a width of 7 to 14 km from N/S (Meddour, 1994); of higher mountains (900-1550 m) in the Mitidja area. The climate is fresh and humid, with a mean annual rainfall of 950-1200 mm, monthly mean of temperatures between 3-7°C in winter and 18-23°C in summer; snow is relatively frequent (50-100 cm annually) (Sbabdji, 2012).
0 1,5 3 6 9 12
Fig. 1. Geographical location of the study site within Chrea National Park (PNC). Earthworms sampling and laboratory analyses
Earthworms were sampled during the four seasons from September 2014 to June 2017. The six sampled sites are between 36°19'-36°30'N and 2°38'-3°02'E, their respective altitude, latitude, longitude, type of vegetation and the bioclimat are listed in Table 1. Sampling was made according to the criteria suggested by Lavelle (1988) and Anderson and Ingram (1993): at each site 10 samples of 25 x 25 x 30 cm were taken at regular 5 m intervals, along a line whose origin and direction had been randomly chosen. Each sample was given a code, and preserved worms were then transferred to labelled specimen bottles. They were preserved in 10% formalin and then transferred to 70% alcohol for permanent fixation. Only a minimum number of worms was preserved from each study site, and others were released back into the soil. Identification of the species was principally based on Bouche's descriptions, 1972; Omodeo, 1987; Sims, 1972; Tetry, 1937; Lee, 1985.
Diversity analysis: In order to exploit the results obtained from ecological indices such as the Specific richness SR
(SR=Spi+Sp2+.........+Spn) is the total number of species observed during N surveys, the Shannon-Weaver diversity (H'), H'=-I(ni/N)
log2 (ni/N), Shannon and Weaver (1963) corresponds to the calculation of the entropy applied to a community, Clarke and Warwick (2001) and Margalef index (Dmg) (MARGALEF, 1958), Dmg=(S-1)/ln N; where pi=ni/N, ni=the average density of species, N=the average density of individuals in the sample, and S=number of species. Here, the event categories will therefore be represented for the species and their probability of occurrence pi by the ratio of the number of units of each of them nor to the total number of individuals present in the community N the maximum diversity (H'max) diversity is maximum when all the species in the stand would be represented by the same number of individuals. and equity (E) are used. fairness E varies between 0 and 1, Shannon and Weaver (1963). It tends towards 0 when almost all the numbers correspond to a single species in the stand and tends towards 1 when each species is represented by a similar number of individuals. The value of the Shannon-Weaver diversity index usually
Ukrainian Journal of Ecology, 12(3), 2022
ranges from 1.5 to 3.5, only rarely exceeds 4.5, equity Equality Index (E) It expresses the degree of equality in species abundance in the sample, are used.
Table 1. Sampling sites and their characteristics in Chrea National Park (September 2014 to June 2017).
Sites Characteristics
Altitude Latitude UTM
Longitude UTM
Slope (%)
Stratum herbaceum
Vegetation
Shrub layer
Tree layer
Col des
Fougères
(CF)
1541
36°25'45.0"N 489725.6583 02°53'10.9"E 4031569.4260 10
Sedum
villosum
Senecio
vulgaris
Paranychia
argenea
Lamium
Erodium
cicani
Citrus villusus
Juniperus
oxycedrus
Cedrus atlantica
Forêt noire (FN)
1333
36°25'08"N
490097.8583
02°53'25"E
403429.0050
5
Satureja
vulgaris
Orchidée
Sedum
villosum
Juniperus oxycedrus
Cedrus atlantica
Bioclimatic stage
Sub humide à hiver frais Sub Wet in cool winter
Hakou Ferraoun (HF) Sidi Rabah (SR) Dhaia (DH) Hammam Melouane (ML)
750 500 1230 373
36°27'09.1"N 36°22'04.3"N 36°21'58.33"N 36°25'43.4"N
487685.0466 490662.0976 472312.3169 497307.6452
02°51'47.9"E 02°53'47.9"E 02°41'31.56"E 02°58'43.4"E
4034163.2530 4024768.5062 4024623.5744 4031514.5142
10 15 10 10
Galium Geranium
rotundffolium robertianum
Rubus Galium Origanum
ulmffolium rotundifolium glandulosum Galactites
Geranium Galactites Sinapis mentosa
robertianum tomentosa pubescens Andryala
Tamus Andryala Fedia integrffolia
communis integrifolia cornucopiae Campanula
Andryala Quercus Geranium ranunculus
integrffolia suber robertianum
Campanula Lodesma
ranunculus mauritanica
Cistus triflorus Rosa carina Rhamnus alternus Pistacia lentiscus Rosa carina Juniperus oxycedrus Cystus villosus Quercus ilex Rosa carina Cistus triflorus
Quercus canadensis Quercus Quercus faganae Clematis flammula Crataegus monogyna Prunus avium Humide a hiver froid Wet in cold winter Pinus
Cedrus suber alepensis
atlantica Quercus ilex Quercus ilex Quercus ilex Sub humide a hiver doux Sub wet in mild winter
Soil analysis
Soil was collected from each region and divided into subsets for analysis. Soil texture was determined using the rapid method (Kettler, et al., 2001). To determine soil moisture, the soil was dried at 105°C for 48h. CE (Electrical Conductivity) and pH were measured using a digital meter. Soil N was determined by Kjeldahl technique (Misra, 1968). Organic C was determined using air dried and sieved soils samples using the wet oxidation method.
Statistical analysis
Different statistical analysis were carried out to exploit our results and to study the effect of numerous factors on the ear thworms' repartition, we have chosen the Factorial Analysis of Correspondences (AFC) analysis, have been realized with the use of PAST v 1.9. mustache boxes and ecological index graphs are produced by R programme (R version 3.4.4; R Development Core Team 2018).
Results
Soil characteristics
The results of the physico-chemical properties are shown on Table 2. The texture range from silty clay to silty sand. The granulometric analyses of the soil samples showed that the highest percentage of sand (61.17%) recorded was in the Dhaia while the lowest percentage (25.20%) was registered in the Col des Fougeres. Soil pH was slightly neutral in the majority of soil samples.
The maximum and minimun soil moisture was 48.82% and 2.46% in Foret Noire, Dhaia respectively. The rate of organic matter is medium to high, it varies between 1.58 and 2.26%. The total nitrogen rate varies between 0.009 and 0.019%, with an increasing value in the Dhaia station. The CE is between 0.3 and 0.82 pS/cm; results indicate unsalted soils. For the other elements, the variation ranges for:P (141.75-160.16 ppm), K+ (0.43-0.5 mEq/100 g), Ca++ (8.8-9.96 mEq/100 g), C.E.C. (16.49-17.4 mEq/100 g), Na+ (3.15-4.2 mEq/100g) and Mg++ (1.38-2.63 mEq/100 g).
Table 2. Physico-chemical analysis of the soil collected from different study sites in National Park of Chrea.
Sites Chrea sector El Hamdania sector Hammam Melouane
sector
Characteristics CF FN HF SR DH ML
Texture Silty Clay Silty Silty sand Silty Clay Silty sand Silty Clay
Soil type Poorly evolved
A 34.93 23.9 26.1 29.7 12.25 31.2
LF 23 19.87 20.17 19.97 30.75 21.17
Granulometry LG 16.87 18.83 17.4 17.6 16.2 18.3
SF 3.93 3.27 5.27 5.27 4.17 7.27
SG 21.27 34.13 31.07 27.47 57 22.07
pH 7.08 6.88 7.44 6.25 7.4 6.58
CE 25° ms/cm 0.65 0.82 0.56 0.43 0.3 0.58
Humidity (%) 27 48.82 17.7 28.72 2.46 33.4
Organic carbon % 1.03 1.07 0.79 0.89 1.2 1.13
Organic matter % 2.06 2.14 1.58 1.78 2.06 2.26
Total Nitrogen % 0.011 0.019 0.01 0.009 0.002 0.015
Assimilable phosphorus P2O5 (ppm) Exchangeable K+ mEq/100g of soil 145.95 152.3 141.75 142.3 160.16 153.17
0.47 0.44 0.46 0.5 0.44 0.43
Exchangeable Ca++ mEq/100 g of soil 9.5 9.35 9.77 9.96 9.7 8.8
Exchangeable Na+ mEq/100 g of soil 3.57 3.75 3.15 4.2 4.1 3.9
Exchangeable Mg++ mEq/100 g of soil 2.05 1.65 2.63 1.38 2.2 2.56
Cation exchange capacity 16.89 16.49 17.35 17.4 17.2 17.08
Oligochaetes
Nineteen earthworm taxa have been recorded in Chrea National Park belonging to three families (Table 3). Acanthodrilidae had the lowest diversity of species, with only one species. In contrast, Lumbricidae had the greatest diversity with 16 identified taxa. Table 3. Species composition, frequency, and distribution of the Oligochaetes assemblage in National Park of Chrea.
S.No Code Species name Freq. (%) Dom. (%) Seasons distributi on Station.
Acanthodrilidae 2.19
1 Mph Microscolex phosphoreus (Duges, 25 2.19 A, Sp CF, SR, HF and FN
1837)
Megascolicidae 3.31
2 Ams Amynthas sp. 29.16 1.43 A, Sp, W SR, HF and DH
3 Amc Amynthas caiffornica (Kinberg, 25 1.87 all Seasons SR, HF and ML
1867)
Lumbricidae 94.3
4 Crl Criodrlus lacuum (Hoffmeister, 41.66 9 all Seasons SR, HF and ML
1845) 1.78
5 Eit Eiseniella tetraedra (Savigny, 1826) 29.16 1.68 all Seasons SR, HF and DH
6 Ocm OctcdrHus complanatus (Duges, 70.83 21.50 all Seasons CF, SR, HF, FN and ML
7
8
9
10 11
12
13
14
15
16
17
18
19
Omt
Omm
Apc
Apt
Eix
Alr Ala
Alm
Alc
Odr
Eia
Hlo
Del
1828)
Octodrlus maghribinus triginta, 66.66 (Omodeo and Martinucci, 1983) Octodrlus maghribinus maghribinus 58.33 (Omodeo and Martinucci, 1983) Aporrectodea caiiginosa (Savigny 83.33 1826)
Aporrectodea trapezoides (Savigny, 20.83 1826)
Eisenia xylophila Omodeo and 16.66 Martinucci 1987
Allolobophora rosea (Savigny 1826) 83.33 Allolobophora antipai (Michaelsen, 25 1891)
Allolobophora miniscula (Rosa, 29.16 1905)
Allolobophora chlorotica (Savigny, 37.50 1826)
Ocnerodrilus Sp Eisenia andrei(Bouché, 1972) Helodrílus oculatus (Hoffmeister, 8.33 1845)
Dendrobaena lusitana (Graff, 1957)
29.16 29.16
12.50
7.23 all Seasons CF, SR, HF, FN and DH 6.16 all Seasons CF, SR, HF and FN 11.61 all Seasons CF, SR, HF, FN and ML SR, HF, FN and ML DH
9.95 A, Sp 0.47 all Seasons
16.86 all Seasons CF, SR, HF, FN and ML
2.47 all Seasons ML and DH
1.94 all Seasons HF, FN and ML
5.63 all Seasons SR, HF and ML
2.69 A, Sp, W
1.03 A, Sp, W
2.69 A, Sp
0.78 A, Sp
CF, SR, HF and FN CF, SR and HF CF
CF, SR and FN
Note: Frequency (Freq. %) indicates percentage of species occurrence from samples (n=19), (Dom. %) Dominance of species in groups. Note that species codes are the same as those used in the Canonical Correspondence Analysis (AFC). The Seasons of years coded: A Autumn, Sp Spring, W Winter, Su Summer.
The analysis of the total collection at Chrea National Park indicated the dominates of, the Lumbricidae family with 94.39% of individuals and 16 taxa. O. complanatus and A. rosea appear by far the most common and widespread taxa. They represent 21.50% and 16.86% of the specimens collected, they are found from east to west throughout the entire region (respectively 71% and 83% of the localities). The two families Acanthodrilidae and Megascolicidae had minor contributions (2.19 to 3.31% of individuals, respectively), and are not recorded in one of the six stations (ML).
Fig. 2. Spatial variation in the abundance (ind/m2) of Oligochaetes in Chrea NP.
Fig. 2 shows that the study sites seems to play an important role in the abundance distribution of earthworm. We have noticed that CF and HF are characterized by variable abundances. In CF station A. rosea (362 ind/m2) represents the maximum abundance, but M. phosphoreus 19 ind/m2 constitutes the minimum abundance. The existence of existence of O. complanatus was observed in the HF sation with a max abundance (478 ind/m2) whereas the minimum one is represented by C. lacuum (11 ind/m2). However, in the DH site we notice only low abundances. For the other sites (ML, NF, SR) we remark an average interval.
The Fig. 3 shows that the season factor seems to play an important in the repartition of earthworm species. Autumn is characterized by variable abundances. In fact, we have observed existence of the species in big abundances, it is the case of O. complanatus (519 ind/m2) and A. rosea (509 ind/m2), but also low abundances concerning O. maghribinus maghribinus (117 ind/m2). All the species are low abundance in winter and summer. There are two atypical abundances for the spring group O. complanatus species with abundance 478, D. lusttana 19.
Autumn Winter Spring
Seasen
Fig. 3. Temporal variation of the abundance of Oligochaetes in CNP.
Fig. 4. Temporal variation in the diversity indices of Chrea National Park.
The results indicate a significant fluctuation in the Shannon-Weaver H Diversity Index and E Equality Index in function of the seasons and study sites. Referring to the Shannon-Weaver H and Equality Index values, the results show a great diversity of species in spring, fall and winter seasons compared to summer. In addition, the most important diversity is observed in two sites Sidi Rabeh and Hakou Ferraoun, compared to the other study sites. The Fig. 4 specific richness SR, margalef index (Wealth Index) Dmg hows that, the highest abundance values are reported in periods of spring and fall, while the lowest are recorded in summer and winter seasons. The comparison of abundances according to study sites shows that, the highest abundance is reported in Hakou Ferraoun and Col des Fougères by compared with other sites.
Analysis of Oligochaete species from different stations Chréa Natinal Park
Three groupes of olighochaete species were found when changing the station, the latter are clearly visible within the dendrogram of the ascending hierarchical classification on the basis of a similarity of -3.2 (Fig. 5).
So as to exploit the results through statistical analysis methods and explain distribution of earthworms according to several factors, we have chosen the Analysis of Factor Analysis of Correspondences (AFC)The AFC was followed by automatic classifications on the first factorial coordinates using the Ward's grouping criterion. by the software PAST v 1.9.
• The first group is represented by the species in the Dhaia and Sidi Rabah stations, this group is composed by E tetraedra and
• The second group is represented by the species in the Magtaa Lazrag station, this group is composed of C lacuumn, A.
caifornica, A. chlorotcca, A. antipai, A. miniscula. The third group is represented by two subgroups, the first subgroup is composed of the species in the Col des fougères and Foret noir stations, this group is composed by D. lusttana, Ocnerodrllus Sp, A. rosea, H. oculatus, A. caliginosa. The second subgroup is composed of the species in the Hakou Ferraoun station this subgroup is composed of O. maghribinus maghribinus, O. maghribinus triginta, O. complanatus, A. trapezoides, E. andrei, Amynthas sp., M. phosphoreus.
Fig. 5. Factorial Correspondence Analysis (FCA) of the inter-station variation of oligochaetes identified by automatic classification according to Ward's criterion.
Nineteen species belonging to Eleven genera and three families have been identified: Acanthodrilidae (Dom, 2.19%), Megascolecidae (Dom, 3.31%), and Lumbricidae (Dom, 94.39%). The individuals were identified to the following taxa: A. caiiginosa, A. rosea, A. cholorotica, A. antipai, A. miniscula, A. trapezoides, E. tetraedra, Amynthas sp, A. caifforncca, M phosphoreus, C lacuum, O. complanatus, O. maghrebinus triginta, O. maghribinus maghribinus, E. xylophla, Ocnerodrllus sp, E andre, H. oculatus, D. pantaleoni.
Earthworms are one of the most diversified groups of soil fauna; these species vary mainly according to the physical and chemical properties of the soil. Their numbers fluctuate randomly every year depending on environmental conditions and biological interactions with other organisms. Temperatures, humidity and soil factors are key regulators of the abundance and activity of earthworms in the wild. Earthworm populations respond relatively quickly to changes of these environmental factors (Sims and Gerard, 1999). According to Bachelier (1963), their number fluctuates randomly every year depending on environmental conditions. Humidity affects the spatial distribution of worms, it varies dynamics of populations (Edward and Bohlin, 1996) positively in high humidity, negatively in the case of low humidity. Resistance to drought as well as to water excess vary according to species and regions. We note that in four stations O. complanatus is the predominant species because humidity is high. But if we refer to the DH station, where humidity is low, its abundance is low (5 ind/m2). We note that in these five stations, the presence of endogeic earthworms is eminent according to (Johnston, et al., 2017), this group supports well large variations. In contrast to sensitive anecics whose presence is low.
When the soil dries up, earthworms, if they do not die, go deep in the soil, wrap as a ball and partially dry. They lose up to half of their water; their inactivity ceases with the return of water and their re-imbibition was diapause (Bouché, 1972). Analyzing our samples, we found that some species returned to Diapause, other types dug in depth, especially in dry seasons, while others were spread near the presence of water, this explains the difference in environmental groups. They prefer oak leaves, drop needles of conifers, and avoid herbs with thick and narrow roots (Bachelier, 1972). What we noticed in our work is that they dominate under oak in SR, ML and HF terminals, while in DH station with conifer dominance is minimal.
Omodeo, et al. (2003) believe that earthworm biodiversity is low over the whole Maghreb area (Morocco, Algeria and Tunisia). They identified 33 species, of which 24 taxa were collected in Algeria. Baha (1997) has identified 11 species in the Mitidja Algiers area. In our works, we have identified 19 studied species belonging to the Megascolecidae, Lumbricidae and Acanthodrilidae families. Earthworms are generally well-known in humid Europe and to a lesser extent in the Mediterranean countries of western Europe (Bouche, 1972). This fauna is probably similar to that of North Africa (Omodeo and Martinucci, 1987; Bouché, 2003). The three worm families have been observed in six stations of Chréa National Park; small and large tribal areas (Omodeo and Martinucci, 1987); in northern Algeria (Omodeo, et al., 2003); in eastern Algeria (Zeriri, et al., 2013).
Worms are distributed according to pH; according to Bouche's study (1972), the species are distributed with respect to soil pH and distinguishes between acidophils (pH<6), neutrophils (6<pH<7) and basophils (pH>7). In 1965, El-Duweini and Ghabbour reported little information about the distribution of earthworms according to the pH. Satchell's work (1955) distinguished the acid-tolerant
E. xylophila.
O 0.4 0.8 1.2 1.6 2 2,4 2.8 3.2 3.6 4
A ■cis 1:4». 55%
Discussion
animals, living in litter and those "acid-intolerant" digging the ground. Basic soils with a pH above 10 are unfavorable for worms (Lavelle and Spain, 1995). We note that most stations have a pH of 6.5 to 7.5. In general, most species are likely to be encountered in soils with a pH higher than 7. However, some species such as C. lacuum, E andrei and E tetraedra have been found in soils at pH 6.25-6.5; note that A. caiiginosa is present in soils with a pH ranging from 6.25 to 7.5.
Salinity increases in dry soils because they are poor in organic matter. Earthworms cannot survive in this type of soils that are characterized by high or medium salinity. Most of the studied stations are less salty except for the DH station. Logically, in DH station the numbers of worms are very low.
Abundance or not Organic matter also plys a key role in distribution of earthworm. Earthworm populations feed on more or less decomposed Organic matter, on the surface or in the soil. It is the main food resource, and thus, this has considerable effect on the populations of earthworms. In most ecosystems, insects of soils are a key factor in the fragmentation of organic matter (Lavelle and Spain, 1995). It is thus estimated that they are able to consume almost all of annual litter (Brown, et al., 2002). The obtained results in our work show that soils of the six selected stations of the PNC are considered to be rich in organic matter. These stations representing a high rate of organic matter reveal a low abundance of the earthworms. This is indeed due to the effect of anthropization that some species do not support (Lavelle and Spain, 2001). This highly degraded organic matter will continue its cycle by being ingested by the earthenware, it undergoes then a new process of degradation and dissolution. This joint activity of earthworms and thus, contributes to the entry of carbon into soils and will allow all physical, chemical and biological processes. Distribution according to the carbon/nitrogen ratio. The C/N ratio is one of the most explanatory elements in the distribution of Earthworms; it has a high biological significance (Bouché, 1972). The distribution study of the C/N distributions in which these species are found makes it possible to characterize three types of taxa. Eubiotics are major consumers favoring aerobic phenomena and soil structure; C/N=13. The forms living in at C/N>13, are qualified as mesobiotics. The extreme case, C/N>17, includes species from very specific environments. Note that the results obtained show a variable nitrogen content from one station to another. The DH station has a high nitrogen content; this can be explained by the presence of a category of earthworm (anecic) such as A. chlorotica which rejects the turricules on the soil surface. These biostructures are thus generally characterized by higher mineral content than in the surrounding soil. In particular, the contents of mineral nitrogen phosphorus are highly available in earth turricules (Blanchart and Brauman, 2010). The first two groups are distinguished in the PNC. The mesobiotics group includes: M. phosphoreus and C. lacuum. The species belonging to the eubiotics group are: M. phosphoreus, E tetraedra, O. complanatus, O. maghribinus triginta, O. maghribinus maghribinus, A.caiiginosa, A. rosea, A. chlorotica. This group is spread in CF, FN, SR and HF, but it is rare in DH and ML.
Distribution by Phosphorus; the obtained results showed that DH station is characterized by a high level of phosphorus, due to the presence of species like E tetrahedra and E xlylophila, terricules of earthworms and the abundance of endogeous species. These terricules are characterized by a higher P content (Kuczak, et al., 2006; Chapuis-Lardy, et al., 2011). However, the increase in P also concerns organic P and microbial P (Guggenberger, et al., 1996; Jimenez, et al., 2003). However, Zhang, et al. (2000) observed an increase in inorganic P in the soil in presence of earthworms.
Conclusion
A systematic survey of the Chrea National Park (Algeria) has made it possible to collect nineteen species of terrestrial Oligochaetes, which belong to the families of Lumbricidae, Megascolecidae and Acanthodrilidae. The Lumbricidae family dominates 94.39% and 16 species, the Species A. rosea, O. complanatus and A. caiiginosa was found at all sites except Station Dhaia, often with very large populations; O. complanatus and A. rosea.
Acknowledgement
We are grateful to Mr R. Dahel, Director of Chréa National Park. We also thank the head of the El Hamdania sector and all his team for their help with the fieldwork. We also thank all members of the animal ecobiology laboratory for all their assistance to us, and their head is Mrs. Lebili Namcha, head of the laboratory.
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Citation:
Zerrouki, H., Hamil, S., Alili, M., Isserhane, W., Baha, M. (2022). Contribution to the knoweldge of earthworm fauna of Chrea National Park (Algeria). Ukrainian Journal of Ecology. 12:1-10. I (et)Е^^^И This work is licensed under a Creative Commons Attribution 40 License
