Orographically, the deposit is located within the limits of the Hodna mountain range on the northeastern flank of the Jebel Hadjar Labiod chain, culminating at 1371m. East of the deposit, there is a vast inter-mountainous depression, with gentle slopes towards Ain Azel (Figure 1).

The polymetallic deposit of Kherzet Youcef recognized since the beginning of the century by the exploitation of the ore of Zn and Pb. This deposit is associated with a Barremian age carbonate layer. Since the beginning of operation, several water flows, at different amplities, have been recorded [10].

Based on available data at the mine level, recorded outflows as a function of operating depth are recorded in Table 1.

Between The reserves between levels 835 and 775 (800,000 tons) were extracted from 1979 to 1987 by the chamber and pillar method.

The year 1982 and 1990 the water flows evolved as shown in the graph of Figure 2.

The arrivals observed at the bottom of the Kherzet Youcef mine during the period from 1982 to 1990, gradually evolved from 298 m³/h to almost 1000 m³/h

before the accident of June 2^nd 1990.

We have old chemical analysis data on wastewater from 1974 to 1990, as well as groundwater analyses on wells carried out by ENOF.

As part of our hydrogeological study, we monitored the change in trace element (ETM) levels during a period from June 2015 to November 2016.

These samples are manual and are carried out at the head of the borehole. Samples are taken in plastic vials of 1 l capacity. Before the actual sampling, the vial is thoroughly rinsed with the collected water.

The location of samples is presented in Figure 3.

The water samples were previously filtered using a 0.45 µm Wattman GFC filter, then analyzed by emission spectroscopy whose source is a plasma generated by inductive coupling (ICPAES).

The role of plasma is to break molecular bonds to produce ions, free atoms so that they are excited.

Principal component analysis (PCA) was used to explain the origin at the bottom of the mine. The PCA is a multi-variegated analysis method allowing the simultaneous study of a large number of variables whose total information cannot be visualized because of a space with more than three dimensions [11]. This method would make it possible to clarify the relationships between the variables and the phenomena at the origin of these relationships. The objective is to have information concentrated on a minimum of axis [12]. This method is widely used to interpret hydrochemical data [13].

The statistical analysis of the physico-chemical data was carried out on a data matrix consisting of ten (10) variables and ten (10) samples distributed around the Kherzet Youcef deposit. The statistical software Statistica version 10 was used for data processing.

The correlation matrix gives a first idea of the existing associations between the different variables such as bicarbonate, chlorine, sulphates and pH. These parameters are relatively well correlated with each other (Table 2).

The eigenvalues of the correlation matrix make it possible to measure the percentage of the variance explained by each factorial (Figure 4). The eigenvalue graph shows that the first factorial plane, consisting of the axes F1 and F2, represents 66.42% of the total inertia. It proves to be sufficient to reflect the essence of this inertia. Because if we observe the distribution of the eigenvalues, we find that the main offset occurs just after the first two values, which means that the first two axes are sufficient to represent the information in its entirety.

The graphs resulting from factor analysis, highlight groupings, oppositions and directional trends. The F1 axis expresses 46.37% of the variance and represents most of the variables in the same direction in a negative way, these are bicarbonate, alkaline earth, sulphates and pH (Figure 5), which expresses the same origin of these variables. For two variables, depth and calcium are related and evolve in the same direction and differ on the F2 axis which expresses 20.05% of the variance.

Principal component analysis (Figure 6) makes it possible to determine the waters according to their origin, the waters belonging to the surface table and the waters coming from the Barremian table, these waters are of bicarbonated character. For water from the bottom of the mine (Pit II) are individualized and do not belong to any group. This can be explained by the change in the chemical quality of the waters after the rock is crushed and the time it takes to store the water at the bottom of the mine before discharging it to the outside.

In the vicinity of the Kherzet Youcef deposit lies a vast expanse. This area is agricultural land used for potato and cereal crop production.

A decision has been made to use the drainage water of the Kherzet Youcef deposit for irrigation of a perimeter on an area of about 350 ha.

To characterize the irrigability of exhaust water, we use the values of electrical conductivity at 25˚C and those of the sodium adsorption ratio (SAR).

S .A .R . = [ Na + ] [ Ca 2 + ] + [ Mg 2 + ] 2

The SAR is less than 5 (Figure 7) and waters do not cause the risk of alkalinization of soils [13] [14]. The transfer of the samples placed on the irrigation water classification diagram shows that the waters are between the good class (S1) and the middle class (S2) where the danger of alkalinization of the soil is appreciable in soils with fine texture and high exchange capacity.

The exchangeable Na+ ions can replace the alkaline earth ions (Ca²⁺ and Mg²⁺) of the clays, thus causing the blocking of the soil pores and thus its waterproofing.

The results of analysis of the trace metal elements are shown in Figures 8-10. These values are compared to the limit values set by the Algerian regulations [15] and the limit values set by WHO [16]. Note that the WHO has no indication regarding the maximum allowable value of iron [16].

For Zn (Figure 8), the analysis values on all waters sampled do not exceed 1 mg/l. this result remains admissible by the WHO standard set at 3 mg/l and the

Algerian standard, less demanding, set at 5 mg/l.

For Pb (Figure 9), the majority of assay values are not permissible under the WHO standard (0.01 mg/l). For the Algerian standard, only one sample, on borehole 3 dated July 2016, we note that this value is higher than the Algerian standard.

As regards the Fe element, the majority of the values of the results obtained are higher than the maximum value fixed by the Algerian regulations.