Depth and Seasonal Variations for the Soil Radon-Gas ... · This work aims to evaluate the soil...

11
Arab Journal of Nuclear Science and Applications, 46(5), (124-134) 2013 421 Depth and Seasonal Variations for the Soil Radon-Gas Concentration Levels at Wadi Naseib Area, Southwestern Sinai, Egypt 1 M.S.El Nagdy, * A.E.Shata, * S.F.Hassan,and *,1 K.A.korany 1 Department of Physics, Faculty of Science, Helwan University, Cairo, Egypt. * Nuclear Material Authority (NMA), P. O. Box: 530 El Maadi, Cairo, Egypt. Received: 1/3/2013 Accepted: 20/4/2013 ABSTRACT This work aims to evaluate the soil radon gas concentration levels at different depths in Wadi Nasieb area. The area under investigation is located about 40 km east of Abu Zeneima town in the southwestern part of Sinai Peninsula. It is bounded by Long. 33°22'/ and 33°25'/ E and Lat. 29°10' 30"and 29° 05'/ N, The radon gas concentration were measured using CR-39 etch track detectors in both summer and winter times at different depths (25, 50, 75 and 100 cm) covering several geological formation. Twenty one stations were chosen to cover several geological formations in the studied area. According to the obtained data , these stations were classified to three main sets of stations (low, medium and high level stations ).the obtained results were as follows : i) For low level zone the soil radon concentration ranges from 1.035±0.098 to 1.857±0.160 (KBq/m3) in summer and from 0.628±0.116 to 1.421±0.180 (K Bq/m3) in winter, ii) For the medium level zone, it ranges from 1.742±0.168 to 4.347±0.359 (KBq/m3) in summer and from 1.108±0.153 to 2.996±0.202 (K Bq/m3) in winter, iii) For high level zone, it range from 10.370±0.402 to 21.361±0.410 (K Bq/m3) in summer and 7.224±0.228 to 13.088±0.369 (K Bq/m3) in winter . The highest values of soil radon concentration obtained are found in station (9) in both seasons at all depths. This may be related to the high uranium content for this geological formation. As expected, the data show that the values of radon gas and its progeny concentrations increases as depth increases. The concentration of radon at a depth of 100 cm is about twice higher than the value of radon concentration at a depth of 25 cm. INTRODUCTION There are three separate decay chains in the earth. These series start with three different isotopes (Uranium 238 U, Actinium 235 U and Thorium 232 Th) and ends with three stable end products (Lead 206 Pb, Lead 207 Pb, Lead 208 Pb) respectively, during three different half-life times (4.47x10 9 , 7.04x10 8 , 1.41x10 10 ) years respectively. Naturally Radon (Rn) is found as a product of these three radioactive decay series (Uranium series Thorium series Actinium series) (1) . During the decay of Uranium series it produces Radium 226 Ra isotope which decays to radon 222 Rn with a half-life of (3.82 days). Also Thoron 220 Rn is the result of the decay of Thorium in the Thorium series, it has a half-life time of (54.4) seconds. Finally Actinon 219 Ra is the result of the decay of Actinium in the Actinium series, it has a half-life time of (3.92) seconds. All these isotopes decay by alpha emission unless actinon is also a gamma emitter. The abundance of actinon ( 219 Rn, t1/2 = 3.92 s) in gases from geological sources is limited due to its short half-life, which means that most of it will decay during the slow exhalation processes from rocks and soils, and also due to the fact that the precursor, 235 U, constitutes only 0.7% of natural uranium. The abundance of 232 Th in the Earth’s crust is around three times higher than that of 238 U, but since the half-life of 232 Th is longer by nearly the same factor, the average rate of

Transcript of Depth and Seasonal Variations for the Soil Radon-Gas ... · This work aims to evaluate the soil...

Arab Journal of Nuclear Science and Applications, 46(5), (124-134) 2013

421

Depth and Seasonal Variations for the Soil Radon-Gas Concentration

Levels at Wadi Naseib Area, Southwestern Sinai, Egypt

1M.S.El Nagdy,*A.E.Shata,*S.F.Hassan,and*,1 K.A.korany 1Department of Physics, Faculty of Science, Helwan University, Cairo, Egypt. *Nuclear Material Authority (NMA), P. O. Box: 530 El Maadi, Cairo, Egypt.

Received: 1/3/2013 Accepted: 20/4/2013

ABSTRACT

This work aims to evaluate the soil radon gas concentration levels at different

depths in Wadi Nasieb area. The area under investigation is located about 40 km

east of Abu Zeneima town in the southwestern part of Sinai Peninsula. It is bounded

by Long. 33°22'/ and 33°25'/ E and Lat. 29°10' 30"and 29° 05'/ N, The radon gas

concentration were measured using CR-39 etch track detectors in both summer and

winter times at different depths (25, 50, 75 and 100 cm) covering several geological

formation.

Twenty one stations were chosen to cover several geological formations in the

studied area. According to the obtained data , these stations were classified to three

main sets of stations (low, medium and high level stations ).the obtained results

were as follows : i) For low level zone the soil radon concentration ranges from

1.035±0.098 to 1.857±0.160 (KBq/m3) in summer and from 0.628±0.116 to

1.421±0.180 (K Bq/m3) in winter, ii) For the medium level zone, it ranges from

1.742±0.168 to 4.347±0.359 (KBq/m3) in summer and from 1.108±0.153 to

2.996±0.202 (K Bq/m3) in winter, iii) For high level zone, it range from 10.370±0.402

to 21.361±0.410 (K Bq/m3) in summer and 7.224±0.228 to 13.088±0.369 (K Bq/m3)

in winter .

The highest values of soil radon concentration obtained are found in station

(9) in both seasons at all depths. This may be related to the high uranium content for

this geological formation. As expected, the data show that the values of radon gas

and its progeny concentrations increases as depth increases. The concentration of

radon at a depth of 100 cm is about twice higher than the value of radon

concentration at a depth of 25 cm.

INTRODUCTION

There are three separate decay chains in the earth. These series start with three different isotopes

(Uranium 238U, Actinium 235U and Thorium 232Th) and ends with three stable end products (Lead 206Pb,

Lead 207Pb, Lead 208Pb) respectively, during three different half-life times (4.47x109, 7.04x108,

1.41x1010) years respectively. Naturally Radon (Rn) is found as a product of these three radioactive

decay series (Uranium series – Thorium series – Actinium series) (1). During the decay of Uranium

series it produces Radium 226Ra isotope which decays to radon 222Rn with a half-life of (3.82 days).

Also Thoron 220Rn is the result of the decay of Thorium in the Thorium series, it has a half-life time of

(54.4) seconds. Finally Actinon 219Ra is the result of the decay of Actinium in the Actinium series, it

has a half-life time of (3.92) seconds. All these isotopes decay by alpha emission unless actinon is also

a gamma emitter. The abundance of actinon (219Rn, t1/2 = 3.92 s) in gases from geological sources is

limited due to its short half-life, which means that most of it will decay during the slow exhalation

processes from rocks and soils, and also due to the fact that the precursor, 235U, constitutes only 0.7%

of natural uranium. The abundance of 232Th in the Earth’s crust is around three times higher than that

of 238U, but since the half-life of 232Th is longer by nearly the same factor, the average rate of

Arab Journal of Nuclear Science and Applications, 46(5), (124-134) 2013

421

production of 220Rn (t1/2 = 54.4 s) and 222Rn (t1/2 = 3.82 d) is about the same. However, the shorter half-

life of thoron results in a greater proportion of it decaying before it can be from the ground (2). Thus,

radon alone is usually considered as being important in studies of household radon levels. Soil gas

measurements made below the soil surface will normally register the presence of thoron, depending on

the soil composition. At least 80% of the radon emitted into the atmosphere comes from the top few

meters of the ground (3). The radon emanation rate varies from one place to another due to differences

in radium concentration and soil parameters such as moisture content, porosity, permeability, and

grain size (4, 5). The exhalation of radon from soil involves two mechanisms: emanation and transport

(diffusion and convection). These two mechanisms are affected by many factors including the

properties of the soil (6).Radon gas concentration. Radiation Hazards indices factor, Radon Emanation

and migration in the Earth and the atmosphere have been the subject of numerous studies, in Egypt (7-

9) and all over the world (10, 11).

The Paleozoic rocks of southern Sinai, including the area under investigation, were studied by

many authors especially from the geological, mineralogical geochemical and radioactivity points of

view (12-19). Some of the Paleozoic sediments in the southwestern part of Sinai, including the study

area, are of great importance especially from the mineralogical and radioactivity points of view. They

host several types of mineral deposits such as manganese-iron deposits (20, 21), copper deposits (21, 22),

silver deposits (18, 23), uranium deposits (13, 14, 16, 24, 25). The rock units occupied the Wadi Naseib area

consist mainly of different types of carbonates rocks; dolostones and marl interbedded within two

series of sandstones. The gas radon measured stations in the present study cover the whole area of

Wadi Naseib and inserted in the different rock units (Fig. 1).

The aim of the present work is to Study the relation between radon gas concentration and

Uranium concentration(ppm) at different depths and find relationship between the radon gas

concentration with depth and also the Uranium concentration (ppm),as well as soil parameters such as

moisture content, porosity, permeability, and grain size .

GEOLOGICAL SETTING:

The Wadi Nasieb area is a part of southwestern Sinai, Egypt (Fig. 1) and is occupied by

basement rocks of Late Proterozoic age, which unconformably overlain by Paleozoic rocks. Wadi

Naseib area is located about 40 km east of Abu Zeneima town in the southwestern part of Sinai

Peninsula. It is bounded by Lat. 29°10' 30" and 29° 05'/ N and Long. 33°22' and 33°25' E (Fig. 1).It

exists in the NE peripheries of the famous Gabal Um Bogma area. This area is considered the drainage

base of the important radioactive mineralized area which known as Gabal Allouga. Wadi Naseib area

is covered by different rocks of Precambrian and Paleozoic ages. The exposed Paleozoic rocks in

Wadi Naseib area are classified into two types: mineralized and non-mineralized sediments. The

important radioactive mineralized area in Gabal Allouga attributed to the presence of some secondary

uranium minerals.

The exposed rock units at Wadi Naseib include El Adedia Formation (mostly exposed at the

upstream floor of Wadi Naseib). It is highly ferruginated and composed of sandstones with few

intercalations of siltstones. Um Bogma Formation represented by dolomite - marl succession and Abu

Thora Formation is essentially composed of sandstones cemented by iron oxides and intercalated with

varicolored siltstone and carbonaceous shale. It is well exposed at Gabal Allouga and Gabal Lehian

(Fig.1). The basaltic sheets or silts of Jurassic age represent the Mesozoic rocks (26). It is directly

overlying Abu Thora Formation at Gabal Allouga.

Arab Journal of Nuclear Science and Applications, 46(5), (124-134) 2013

421

(Fig. 1)Geological map of wadi Nasib area, Ahmed El said Shata, 2013.

Measurement Technique:

Measurements were carried out by employing twenty one tubes of length 100 cm. Each one was

fitted with a four pieces of CR-39 plastic foil 500 µm thick and (1cm × 1cm) in cross section. These

detectors are sensitive to α-particles and are widely used for radon and its progeny measurements (27).

The detectors were fixed inside the pipe at different depths 25, 50, 75 and 100 cm from its top side and

covered from the top with metallic cover and from the bottom with filter paper. This configuration was

used in order to maintain the same calibration conditions and to stop the thoron (220Rn) from entering

Arab Journal of Nuclear Science and Applications, 46(5), (124-134) 2013

421

the tube, while allowing the radon gas to pass through the tube, For the selected measuring tube,

Fig.(2).

Twenty one holes of 10 cm in diameter and 100 cm in depth

were dug in each chosen point of measurement (Station). Every

station was filled with a tube fixed with CR-39 detectors at

different depths (25, 50, 75 and 100 cm). The detectors were

mounted in such a way that the sensitive surfaces facing the air

coming from the underground , taking due care that there was

nothing to obstruct the detectors. Then each hole was refilled

with soil. The α-particles originating from radon and its progeny

were registered as tracks in the detectors, if α-particles from

radon and its progeny have their energies in the range of about

1.7- 4.1 MeV(28).

Thus, the radon progeny, which plate out on the surface of the

detectors will not be detected because their α-particles are too

energetic (29). The detectors were left in each station for

approximately four weeks — long enough for the 222Rn to reach

equilibrium with its long-lived parent, radium and for a

significant number of tracks resulting from its alpha decay to be

registered on the CR-39 detector.

Fig, (2) Schematic diagram

showing the tube under the

soil surface and the CR-39 at

different depths

After exposure, the detectors were retrieved and etched for 8 hours in 6.25 N NaOH solutions at

70±10C in the laboratory. Subsequently the detectors were thoroughly scanned using an optical

microscope at a magnification of 400X to count the number of alpha tracks per cm2 registered on the

plastic detectors. The radon gas concentration (pCi/l) was determined using the relation.

Eq (1)

Where (P) is the corrected track density (number of tracks per cm2), (K) is the calibration factor

((tracks. Cm2.d-1). (pCi/l)-1) and (t) is the total time of exposure. The radon concentrations in KBq.m-3

were calculated by using the relation:

)(

3)/(037.0)/( CONCP LPCiCMKBqC Eq(2).

RESULTS AND DISCUSSIONS

The allover number of the measured stations were classified into three main zones according to the

measured Rn- Gas concentration, table(1) shows the station numbers that belongs to each zone, while

table (2) shows the lithology of each station.

Table (1) Classification of the station.

Zone Type Station number

Low level zone 1,6,7,8,10,11,13,14,19,20

Medium level zone 2,3,4,5,12,21

High level zone 9,15,16,17,18

tK

PCP

Arab Journal of Nuclear Science and Applications, 46(5), (124-134) 2013

421

Table (2) Lithology of the measured stations in W. Naseib, include locations.

Station

number Latitude Longitude Lithology

U

(ppm)

1 29° 03' 56" N 33° 23' 08"E Channel fill-Quaternary deposits 2

2 29° 03' 53" N 33° 23' 20"E Channel fill-Quaternary deposits 3

3 29° 03' 47" N 33° 23' 24"E Channel fill-Quaternary deposits 3

4 29° 03' 42" N 33° 23' 28"E Channel fill-Quaternary deposits 1

5 29° 03' 34" N 33° 23' 24"E Channel fill-Quaternary deposits 1

6 29° 03' 33" N 33° 23' 23"E Channel fill-Quaternary deposits 12

7 29° 03' 37" N 33° 23' 32"E Sandstones of Abu Thora in down-thown

of W. Naseib major fault 1

8 29° 03' 33" N 33° 23' 33"E Sandstones of Abu Thora in down-thown

of W. Naseib major fault 3

9 29° 03' 34" N 33° 23' 54"E Kaolinite and gibbsite bearing shale 89

10 29° 02' 21" N 33° 23' 57"E Kaolinite and gibbsite bearing shale 2

11 29° 02' 13" N 33° 23' 53"E Kaolinite and gibbsite bearing shale 9

12 29° 02' 06" N 33° 23' 42"E Middle marl of Um Bogma Fm. 10

13 29° 01' 57" N 33° 23' 33"E Aeolian sand over Abu Thora Fm. 1

14 29° 01' 57" N 33° 23' 28"E Aeolian sand over Abu Thora Fm. 1

15 29° 02' 03" N 33° 02' 27"E Gibbsite bearing shale 13

16 29° 02' 06" N 33° 02' 33"E Gibbsite bearing shale 14

17 29° 01' 44" N 33° 24' 08"E Gibbsite bearing marl 15

18 29° 01' 24" N 33° 24' 12"E Marly dolostone of Um Bogma Fm. 2

19 29° 01' 19" N 33° 24' 12"E Fractured Marly dolostone in G. El

Allouga 11

20 29° 01' 20" N 33° 24' 08"E Black and varicoloured shale 39

21 29° 01' 30" N 33° 24' 11"E Kaolinite and gibbsite in base of Abu

Thora Fm. 3

First for the low level zone:-

Table (3):- Average of the measured radon concentration in summer and winter and the ratio

between them at different depths in the low level zone.

Average Radon

concentration

(K Bq/m3) at

different depths

Average of the

measured radon

concentration

In summer(S)

Average of the

measured radon

concentration

In winter(W)

Ratio

S/W

At 25 cm 1.035±0.098 0.628±0.116 1.64

At 50 cm 1.318±0.126 0.784±0.121 1.68

At 75 cm 1.451±0.129 0.972±0.163 1.49

At 100 cm 1.857±0.160 1.421±0.180 1.30

It is shown that, the obtained ratios are nearly the same for the upper two depths (25 and 50 cm)

with slightly higher measurements in summer than winter time reflecting the effects of the

meteorological condition such as pressure and air temperature. Also the same behavior can be noted

for the lower two depths (75 and 100 cm) but with decreasing the ratio indicating a close readings

Arab Journal of Nuclear Science and Applications, 46(5), (124-134) 2013

421

between the two seasons which may reflect the effect of uranium content and the porosity and

permeability of the hosting rocks in these depths .

Summer(August, 2011)

Winter(Februry, 2012)

Second for medium level zone:-

Table (8):- Ratio between average radon concentration in summer and winter at different

depths in the medium level zone.

Average Radon

concentration

(K Bq/m3) at

different depths

Average of the

measured radon

concentration

In summer

(S)

Average of the

measured radon

concentration

In winter

(W)

Ratio

S/W

At 25 cm 1.742±0.168 1.108±0.153 1.572

At 50 cm 2.546±0.254 1.957±0.477 1.300

At 75 cm 3.053±0.265 2.503±0.263 1.219

At 100 cm 4.347±0.359 2.996±0.202 1.450

It is shown that, the obtained ratios are ranged from 1.219 to 1.572. the slightly great ratio at

100 depth ( slight difference between summer and winter readings )may be due to water movements

Arab Journal of Nuclear Science and Applications, 46(5), (124-134) 2013

431

in the deep layers , again the ratio decrease while depth decreases reflects the effect of U-content ,

while the great ratio near the surface reflects the effect of aeration ore porosity near the surface.

Summer(August, 2011)

Winter(Februry, 2012)

Third for high level zone:-

Table (11):- Ratio between average radon concentration in summer and winter at different

depths in the high level zone.

Average Radon

concentration

(K Bq/m3) at

different depths

Average of the

measured radon

concentration

In summer

(S)

Average of the

measured radon

concentration

In winter

(W)

Ratio

S/W

At 25 cm 10.370±0.402 7.224±0.228 1.435

At 50 cm 14.228±0.348 8.570±0.151 1.660

At 75 cm 16.590±0.297 10.378±0.202 1.598

At 100 cm 21.361±0.410 13.088±0.369 1.632

Arab Journal of Nuclear Science and Applications, 46(5), (124-134) 2013

434

From the table we can show that: the ratio is high and nearly constant while depths increases,

and it is smaller in less depth, whish may be indicates to the effect of porosity and permeability as will

as uranium content in the depth sits, while another factor such as aeration must be introduced as an

effective factor on the upper stations near the ground surfaces.

Summer(August, 2011)

Winter(Februry, 2012)

A systematic increase of soil radon concentration levels with depth is observed for all three

zones (low – medium – high) and for both seasons.

The observed variations with depth, for all three zone (low – medium – high), follow a similar

pattern. Figs. 3, 5, 7, 9, 11 and 13 show the data points for the low level zone, the medium level zone

and high level zone in both the summer and winter, respectively. They indicate that the variations of

soil radon concentrations exhibit, at a first sight, a linear pattern.

At a depth of 100 cm, the highest values for soil radon concentration in summer and winter are

observed in station (9) (32.831±0.410 and 27.156±0.389 (K Bq/m3), respectively) At the same depth

the corresponding lowest values are measured in station (14) (1.104±0.086 (K Bq/m3) in summer) and

station (7)( 0.676±0.081 (K Bq/m3) in winter). Intermediate values are observed for the other all

station. According to radiometric measurements station (9) ( Kaolinite and gibbsite bearing shale) in

Arab Journal of Nuclear Science and Applications, 46(5), (124-134) 2013

432

the studied region contains the highest content of uranium (89 ppm) and has the highest porosity

which allows radon gas to migrate and diffuse easily This would explain the higher radon

concentration levels obtained for station(9) compared to the others.

It is to be noticed that the radon concentration at the depth 100 cm is almost twice the radon

concentration at the depth 25 cm. This is due to the fact that moisture in these geological formations

concentrates in the 20–30 cm below the surface, in addition to the effect of the atmospheric pressure

which suppresses the diffusion of radon upward.

The measured soil radon concentration levels in winter were systematically lower than in

summer and this is true for all the studied formations. This result reflects the changes in porosity,

permeability and moisture content of the soil covering the geological formation between the two

seasons. It shows, in particular, that moisture, which is more important in winter, dissolves radon gas

and thus inhibits radon diffusion.

If we assume that the contribution of soil radon to indoor radon is of the order 100:1 (30-32)

taken at a depth of 50 cm, then the corresponding expected indoor radon concentration levels for the

low, medium and high level zone in Bq/m3 , 13, 25 and 142, in summer, respectively. In winter these

figures become 8, 20 and 86, respectively.

CONCLUSION

From the above obtained results we can conclude that:

1-Great dependency of soil radon concentration levels on depth in all three level zones (low, medium

and high level zone), this dependency may be referred to many factors such as:

i) Characteristics of the soil that covering the studied formations

ii) The values of U-content for the host rock.

iii) Properties of each of the rock formation.

2- Significant seasonal variations of soil radon concentration levels were found between summer and

winter seasons especially at low depths which indicate the effect of air movement on the ground

surface.

3- The largest values of soil radon concentration obtained in the case station (9) seem to be due to the

higher content in uranium in this formation.

4- Using the obtained results for summer and winter we can determine the radon exhalation rates and

the radon concentration at the surface of the soil covering each geological formation, which is very

important because it contributes to a greater extent to the indoor radon concentration levels which is

considered to be a health hazard. The obtained values of indoor radon concentration levels derived

from our results, for both seasons, are below the standard action level (4 pCi/L = 148 Bqm−3) (4).

REFERENCES

(1) M.N.Tawfik, 2012 "Radon Evaluation Studies Using Various Monitoring Devices, Pilot Plant

Case Study"master,Thesis, Biophysics, Physics Department, Ain Shams University,Egypt,25pp.

(2) S.A. Al-Shereideha, B.A. Bataina" Seasonal variations and depth dependence of soil radon

concentration levels in different geological formations in DeirAbu-Said District, Irbid—Jordan"

Radiation Measurements 41 (2006) 703 – 707.

(3) NCRP, 1984. Report No. 78. Evaluation of occupational and environmental exposures to radon

and radon daughters in the United States.

Arab Journal of Nuclear Science and Applications, 46(5), (124-134) 2013

433

(4) Shweikani, R., Giaddui, T.G., Durrani, S.A., 1995. The effect of soil parameters on the radon

concentration values in the environment. Radiat. Meas. 25, 581–584.

(5) Khayrat, A.H., Oliver, M.A., Durrani, S.A., 2001. The effect of soil particle size on soil radon

concentration. Radiat. Meas. 34, 365–371.

(6) Tauner, A.B., 1964. Radon Migration in the Ground. A Review. The Natural Radiation

Environment, University of Chicago, pp. 161–190.

(7) Sayed F.Hassn and Ashraf F. Moharem, 2009 "Geochmical,Radioactive and Enviromental stadies

on behavior of radio-elements in some Younger Granites of central Eastern Desert,Egypt"J,of the

faculty of education,Benha University,V. 4/1, p.111-123,

(8) A.A.El-Abnody, 2010"Active technique for Radon gas concentrations and working level

measurments in Abu Hamata and El-Ramsa tunnels,South western Sinai,Egypt" J,of the faculty of

education,Benha University,V. 5/1, p.105-119,

(9) S. F. Hassan, 2011"Radon emanation and radiation hazards indices for sedimentry rocks of Wadi

Abu-Mogherat area,Sinai,Egypt"Journal of the Faculty of education, Ain Shams University.

(10) Holkko, J., Liukkonen, S., 1992. Radon diffusion in Finnish glacial Till soil. Radiat. Prot. Dosim.

45, 231–233.

(11) Sun, K., Guo, Q., Zhuo, W., 2004. Feasibility for mapping radon exhalation rate from soil in

China. J. Nucl. Sci. Technol. 41 (1), 86–90.

(12) Kora, M., 1984. The Palaeozoic outcrops of Um Bogma area, Sinai. Ph.D. Thesis, Mansoura

University, Egypt, 280pp.

(13) El Aassy, I.E., Botros, N.H., Abdel Raziq, A., Sherif, H., Al Moafy, A., Atia, K., EL Terb, R., Al

Shami, A., 1986. Report on the prospection and proving of some radioactive occurrences in West

Central Sinai, Egypt. Internal Report, Nuclear Materials Authority (NMA),Cairo.

(14) Dabbour, G.M., Mahdy, M.A., 1988. Mineralogical studies on the lower uraniferous sediments of

Wadi Naseib, Sinai, Egypt. In: C.N.S.A. Conference, Cairo.

(15) El Rakaiby, M.I., El Aassy, I.E., 1990. Structural interpretation of Paleozoice Mesozoic rocks,

southwestern Sinai, Egypt. Ann. Geol. Surv. Egypt XVI.

(16) Afifi, S.Y., 1991. Geochemical investigation of some radioactive Lower Carboniferous

sedimentary rocks of Wadi Nasieb area, west central Sinai, Egypt. M. Sc. Thesis, Suez Canal

University, Egypt. 253 pp.

(17) Kora, A., El-Shata, A., Abu Shabana, M., 1994. Lithostratigraphy of the manganese bearing Um

Bogma Formation, southwest Sinai, Egypt. J. Afr. Earth Sci. 18, 151 to162.

(18) El Agami, N. L. 1996. Geology and radioactivity studies on the Paleozoic rock units in the Sinai

Peninsula, Egypt. Ph.D. Thesis, Mansoura University, Egypt, 302.

(19) Shata, A. E. 2002. Geological and geochemical studies on uranium and thorium of the selected

exposures of basal sandstone in southern Sinai, Egypt. Ph. D. Thesis, Mansoura University, 186

pp.

(20) Mart, J. and Sass, E. (1972): Geology and origin of the manganese ore of Um Bogma, Sinai,

Reprint from Economic Geology, vol. 67: No.2, p. 145-155.

(21) El Sharkawi, M.A., El Aref, M.M. and Abd El Motelib, A. (1990): Manganese deposite in a

Carboniferous Paleokarst profile, Um Bogma region, West Central Sinai,. Egypt. Mineral

Deposita, V.25, pp.34-43.

(22) Hilmy, M.E., Mohsen, I. A., 1965. Secondary copper minerals from west central Sinai, Egypt.

Egypt. J. Geol. 9, 1 12.

(23) Amer, E.A., 1993. Physical and Chemical Studies on the Uranium-Copper Mineralization of

Uraniferous Paleozoic Sediments, West Central Sinai, Egypt. M. Sc. thesis, Cairo University.

(24) Hussein, A.H., Abdel Monem, A.A., Mahdy, M.A., El-Aassy, I.E., Dabbour, G.M., 1992. On the

genesis of surficial uranium occurrences in west central Sinai, Egypt. Ore Geol. Rev. 7.

(25) Abdel Monem, A.A., El Aassy, I.E., Hegab, O.A., El-Fayoumy, I.F., El-Agami, N.L., 1997.

Gibbsite, uranium and copper mineralization, Um Bogma area, southwestern Sinai, Egypt. J.

Sedimentol. Egypt 5, 117 132.

Arab Journal of Nuclear Science and Applications, 46(5), (124-134) 2013

431

(26) Weissbrod, T., 1969. The Paleozoic of Israel and adjacent countries, part II: the Paleozoic

outcrop of southwestern Sinai and their correlation with those of southern Israel. Isr. Geol. Surv.

Bull. 48, 32.

(27) Durrani, S. A. and Bull, R. K. (1987) “Solid State Nuclear Track Detection” Principle, Methods

and Application International Series in Natural Philosophy. III. Oxford: Pergamon Press.

(28) S. A. Durrani, Y.M. Amin and J.M. Alves, Nucl. Tracks, 8, 79-(1984).

(29) D. E. Cherouati, S. Djeffal and S.A. Durrani, Nucl. Tracks Radiat. Meas., 13, 583 (1988).

(30) Michel, J., 1987. In: Cither, C.R., Smith Jr.,J.E. (Eds.), Sources in Environmental Radon. Plenum

Press, New York. (Cg. 4).

(31) Varley, N. R., Flowers, A .G., 1998. Indoor radon prediction from soil gas measurements. Health

Phys. 74 (6), 714–718.

(32) Al-Bataina, B., Abu-Kharma, H., 2004. Study of radon concentration in soil of Samma Town

Jordan. Abhath Al-Yarmouk. Basic Sci. Eng. 13 (2), 177–190.