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Hazardous Effects of Cyprus Mining Corporation (CMC) and Consumption Risks of Cress, Lettuce, Radish and Spinach Irrigated with the Water of CMC Tailing Ponds

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Hazardous Effects of Cyprus Mining Corporation (CMC) and

Consumption Risks of Cress, Lettuce, Radish and Spinach Irrigated with the Water of

CMC Tailing Ponds

Şerife GÜNDÜZ, PhD

Near East University, Faculty of Education,

Northern Cyprus, Lefkoşa (via Mersin – Türkiye)

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1. INTRODUCTION

Mining in Cyprus started in Copper Age (3000 B.C.) and was an important phenomenon during:

 Phoenicians,

 Greeks and

 Romans.

“Copper” Cyprus

(Kurusakız and Uğur, 1999).

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- Cyprus covers 9251 km

2

- 32°17´ - 34°35´ east longitudes

- 34°33´ - 35°41´ north latitudes

(4)
(5)

CMC

1566 da

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Cyprus Mining Corporation (CMC) was established in 1916 in Gemikonağı and processed the mine till 1974.

Produced major metals:

 Copper (Cu),

 Gold (Au),

 Silver (Ag) and

Iron Pyrites (FeS 2 )

(Cohen, 2002).

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In 1974, CMC closed the corporation and left all buildings, tailing ponds and other wastes face to face with the environment (Kurusakız and Uğur, 1999).

During the operations of CMC, wastes were

flowed into the sea and caused a big pollution in

the area (Cohen, 2002).

(8)

Additionally to the sea and soil pollutions, there are 12 tailing ponds and mine wastes which are flowing on the soil surface (Cohen, 2002).

These ponds are surrounded with

~9 m hills.

hills

(9)

Heavy metals which aren’t problem naturally for thousands of years are started to be problem

because of the negative effects of human beings.

They are threating cities, agricultural areas and the natural environment (Robinson, 1997).

Heavy metals, such as; Arsenic, Lead, Copper,

Cadmium and Nickel, are extremely toxic in very

small amounts and are found in CMC area.

(10)

To determine the heavy metal accumulations of:

 Lepidum sativum L. spp. sativum (cress),

 Spinacia oleraceae L. (spinach),

 Raphanus sativus L. var. niger (radish) and

 Lactuca sativa L. convar. sativa (lettuce).

which are being planted around and inside the CMC area.

AIM

(11)

Selected test plants are belonging to the plant families which includes at least one hyper

accumulator plant species (Robinson, 1997; Baker et al ., 2000).

2. MATERIALS AND METHODS

20 seeds from each of

selected plant species

were firstly sowed into

violas filled with sandy-

soils (Pinto et al. , 1998)

in March 2003.

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These plants were irrigated by the

water obtained from the tailing ponds

(#12, 14, and 17) of the CMC.

Waters from tailing ponds were applied to the plants with 1/1, 1/10, 1/100 and 1/1000

concentrations and the plants were also irrigated with normal water for control (Hinchman and

Negri, 1994).

(13)

The Complatelly Randomized Design were used

with 3 replications for each plant species with 13 treatments (different irrigation waters).

3 weeks later;

4 healthy plants were selected for each plant

species and treatments, then were transplanted

into plastic pots filled with 5 kg (Vysloužilová et

al. , 2003) sandy soils (Küpper et al ., 1999).

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60 days later (Pinto et al. , 1998);

All plants were uprooted from the plastic pots

and were devided as below-ground and above-

ground. Thus, washed with pure water, placed

into nylon bags (Küpper et al. , 1999).

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 Plant samples were decomposed by Method 7300 (NIOSH, 2003) by using Nitric Acid (HNO 3 ) and Perchloric Acid (HClO 4 ).

 Soil samples were decomposed by the Method

SW-846, 3050B (USEPA, 1996).

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 Concentrations of ten elements (As, Cd, Co, Cr, Cu, Fe, Mn, Mo, Pb, Zn) in the digests of plants and soils were determined by Inductively

Coupled Plasma (ICP) (Fassel ve Kniseley, 1974;

NIOSH, 2003).

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Table 1. Heavy Metal Concentrations (ppm) of Irrigation Waters

Irrigation

Water Arsenic Cadmium Cobalt Crom Copper

Control-H2O 0.001 0.001 0.001±0.0008 0.115±0.0334 0.002±0.0004 17-1/1 0.010 0.010 3.246±0.0667 0.882±0.2180 26.97±0.348 14-1/1 0.010 0.010 38.16±0.215 21.81±0.613 676.50±3.200 12-1/1 0.010 0.010 31.48±0.208 56.18±10.61 299.60±1.450

Irrigation

Water Iron Manganese Molybdeniu

m Lead Zinc

Control-H2O 0.076±0.0326 1.000 0.001 0.011±0.0046 1.000

17-1/1 780.50±3.705 5.26±0.139 0.010 0.606±0.0371 6.89±0.0730 14-1/1 13280±149.2 84.13±1.188 0.010 3.603±0.5633 102.0±0.612 12-1/1 22530±313.0 41.00±0.300 0.010 5.995±0.2850 72.57±0.387

±stdev

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Results showed a linear relationship between the accumulation of heavy metals in plant tissues and the concentration of heavy metals in soils.

These results are similar with the findings of Wang et al., (1999) where they have reported that increase in soil acid concentration also

increases the heavy metal uptake of the plants.

3. RESULTS AND DISCUSSIONS

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Out of the ten elements studied;

 Arsenic,

 Cadmium,

 Iron and

 Lead

had been accumulated more than that of found in

plants under normal conditions.

(20)

Figure 1. Total Arsenic concentration in soil, water and removal by plants (above- and

below-ground).

(21)

Figure 2. Total Cadmium concentration in soil, water and removal by plants (above- and

below-ground).

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Figure 3. Total Iron concentration in soil, water and removal by plants (above- and

below-ground).

(23)

Figure 4. Total Lead concentration in soil, water and removal by plants (above- and

below-ground).

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One of the most important results of this study is that application of waste waters to the plants in concentration of 1/1, 1/10, 1/100 and 1/1000 had no significant effect on the metal accumulation of the plants and both were accumulated elements in high concentrations.

This is because of:

1) Waste waters were thinned out (1/10, 1/100, 1/1000)

and applied, however, application continued throughout

the growing period and it caused metals to accumulate

in soils. Therefore, concentration of the elements in

plants were found to have a linear relationship with

soils not waters.

(25)

2) Some plants excrete special extracts with small

molecular weight. These stabilite and mobilize some metals such as: Copper, Lead and Cadmium and this increase the uptake of heavy metals by plants

(Marschner, 1988).

3) The last mechanism to explain this situation is

antagonism. Increse in the concentration of one heavy metal in soil decrese the uptake of another heavy

metal, vice versa , and this phenomen is known as antagonism. Such as increase in the sulfate

concentration decrease Selenium uptake by the plants

(Marschner, 1988).

(26)

Determination of Consumption Risks of Test Plants:

Where, application of waste waters to the plant species in different concentration had no significant effect on the metal accumulation in plants, means of these

treatments (1/1, 1/10, 1/100 and 1/1000) were taken for each plant species and tailing ponds.

For L. sativum , L. sativa and S. oleraceae above-ground plant parts and

For R. sativus below-ground plant parts were taken into

account.

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Table 2. Comparison of the Cadmium Concentration of the Test Plants with the Maximum Limits (ML) Determined by the World Health Organization (WHO-Codex)

Cadmium (Cd)

Plant WHO ML # 12 # 14 # 17

L. sativum 0.1 0.3 0.2 0.2

S.

oleraceae 0.1 0.2 0.2 0.1

L. sativa 0.1 0.2 0.2 0.2

R. sativus 0.1 0.06* 0.09* 0.08*

*Cadmium concentration in the R. Sativus determined less than the Maximum Limits,

however Lead concentration of these plants were more than the Maximum Limits

(28)

Table 3. Comparison of the Lead Concentration of the Test

Plants with the Maximum Limits (ML) Determined by the World Health Organization (WHO-Codex)

Lead (Pb)

Plant WHO ML # 12 # 14 # 17

L. sativum 0.1 10.6 4.6 4.9

S.

oleraceae 0.1 1.7 1.3 2.0

L. sativa 0.1 2.0 1.3 1.8

R. sativus 0.3 0.8 1.6 1.2

(29)

1) These results indicate that # 12, 14 and 17 tailing ponds of CMC can not be thinned out to be used as

fetrilizer for L. sativum , S. oleraceae , R. sativus and L.

sativa .

2) Physiology of other plants may differ from the test plants, however, it seems that these tailing ponds are also not suitable to be used as fertilizer for other plants.

4. CONCLUSIVE RESULTS AND

SUGGESSIONS

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3) Additionally, results reveal that, plants being

produced closelly around and inside the Cyprus Mining Corporation area may be unhealthy and they have to be analyzed before consuming.

4) According to the results, it is therefore of paramount

importance to rehabilite CMC area for the health of

local people and for environment. Finally, rehabilitation

processess must be social, economic and environmental

to reach sustainability in the area.

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THANK YOU

FOR YOUR

ATTENTION

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