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Environ Geochem Health (2007) 29:197–207

DOI 10.1007/s10653-006-9065-x

ORIGINAL PAPER

The investigation of metal concentrations in street dust


samples in Aqaba city, Jordan
Omar Ali Al-Khashman

Received: 5 February 2006 / Accepted: 12 October 2006 / Published online: 8 February 2007
 Springer Science+Business Media B.V. 2007

Abstract The concentrations of metals (Fe, Zn, Keywords Street dust  Metals  Statistical
Cu, Cr, Pb, Cd, Ni, Mn and Co) in 140 street dust analysis  Pollution  Traffic  Jordan
samples were collected from Aqaba city, Jordan.
These samples were determined using flame
atomic absorption spectrophotometry after diges- Introduction
tion with aqua regia. The highest levels of metal
concentrations were found in the samples from Human activity increases the levels of metals
heavy traffic. While the lowest levels of metal ions contamination in the environment. Metals pol-
were noted in the street dust samples from lution accumulates in the street dust, soil, and
hospital and health centers and school gardens. surface water samples and influences the eco-
The results of this study were compared with system in the world (Al-Radady, Davis, &
several cities around the world. The levels of the French, 1994; Tüzen, 2003). The determination
metal concentrations found were generally below of metal in environmental samples including
the mean world-wide values of street dust sam- dusts, plants, soils and surface water is very
ples. Metal values in urban street dust samples necessary for monitoring environmental pollu-
were several times higher than the control levels. tion (Tüzen, 2003; Zhou, Wong, Koh, & Wee,
The statistical analyses were applied to the data 1997). Metals are released into the biosphere by
matrix to determine the analytical results and to natural processes and by anthropogenic activi-
identify the possible source of pollution in the ties. They are predominantly transferred as
studied area. Correlations between the metal molecules or particulate matter via the atmo-
concentrations of the street dust samples were sphere, mostly on large scales. The amount of
obtained. Factor analysis showed that the area anthropogenically derived metals has increased
was mainly influenced by three sources, namely continuously since the beginning of the indus-
lithogenic, traffic, and industrial. trial revolution, and the awareness and concern
about associated environmental and health risks
has risen sharply over the last few decades
(Gunter & Komarnicki, 2005). In urban areas,
O. A. Al-Khashman (&) metals may come from many different sources,
Prince Faisal Center for Dead Sea, Environmental
including vehicle emission, industrial discharges
and Energy Research, Mutah University, Al-Karak
61710, Jordan and weathered materials (Al-Khashman, 2004;
e-mail: omarkhashman@yahoo.com Al-Khashman & Shawabakh, 2006; Gibson &

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198 Environ Geochem Health (2007) 29:197–207

Farmer, 1986; Harrison, Laxen, & Wilson, 1981; of trace metals in dust have been reported to be
Li, Poon, & Pui, 2001; Thornton, 1991). Vehicle traffic and industrial activities. The monitoring
emission is one of the sources of emission of of the metals contents of dust samples is an
metals, and street dust metal pollution in urban efficient way of obtaining information on the
areas arises from a multitude of sources via current environmental state of large areas
water transported material from surrounding (Divrikli et al., 2003). The main purpose of
soils and slopes, dry and wet atmospheric the present work was to determine the
deposition, biological inputs, road surface wear, concentrations of metals in street dust samples
road paint degradation, vehicle wear and lubri- collected from various stations in Aqaba city
cating oil, and particulate emissions (Banerjee, and to identify their natural or anthropogenic
2003; Sutherland & Tolosa, 2000). Particulate sources.
matter can be attributed to different sources
according to its particle size; on the other hand, The study area
fine particles are derived from the combustion
process and are mainly attributed to anthropo- The study area is located at the north shore of the
genic sources (Gunter & Komarnicki, 2005). Gulf of Aqaba, in the southwestern part of
Street dust is environmental material for mon- Jordan. It is about 51 m above the sea level, and
itoring the levels of metal ions (Divrikli, Soylak, bounded by latitude 2933¢ N and longitude
Elic, & Dogan, 2003; Ramlan & Badri, 1989). 350¢ E (Fig. 1). Aqaba is a coastal city with a
Two main factors known to influence the levels population of 120,000 at time of this study

Fig. 1 Location map of the study area

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Environ Geochem Health (2007) 29:197–207 199

(Department of Statistics, 2004). The main indus- part of the Arabian plate, whereas most of Jordan
trial activities in Aqaba city are (Jordan Phosphate is located within the stable part of the plate.
C., 1985), cement, petroleum industry, Jordan Upper cretaceous carbonaceous facies dominated
Fertilizer industries plant, 1982), and some shells. the central part of the country, whereas ancient
The Red Sea port of Aqaba is an important basement (pre-Cambrian) and Cambrian Nubian
commercial shipping center. Aqaba has a modern sandstone dominated in the southern part of the
airport and port facilities sitting alongside the country. Basalt desert in the northeast and the rift
remains of the ancient city of Eyla. The mean valley form Jordan’s western borders (Fig. 2).
traffic density in the streets with heavy, medium, Furthermore, the sandy facies within the carbon-
light and low traffic were >500, 300, 150 and <100 ate rock increases southward through the country
vehicles/h respectively. (Banat, Howari, & Al-Hamad, 2005; Bender,
The climate of Jordan is predominantly 1974). Two geological formations occur predom-
Mediterranean; it is marked by sharp seasonal inantly in and around the study area. Jordan’s
variations in both temperature and precipitation. oldest rocks (pre-Cambrian age, 570 million years
Aqaba city climate is very hot in the summer and old) are the main component of the mountains
warm in the winter and is characterized by an behind Aqaba. They mainly consist of granite,
extremely small amount of precipitation, that is, which is crisscrossed with sheets of intruded
around (17.0 mm/year). Minimum temperature igneous rock, known as dykes. At the time of
in the study area is 9.7C in January and 26.3C dyke formation, the granitic rocks were deep
in July (Department of Meteorology, 2004). below the surface. In this area, sandstones are
The investigated area is located in the northwest present and composed primarily of fine and

Fig. 2 Geology of the


study area and
surrounding areas
(according to Banat et al.,
2005)

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200 Environ Geochem Health (2007) 29:197–207

medium-sized quartz grain, small amounts of Briefly, the samples were collected from both
kaolinite and illite (Bender, 1974). The sandstone sides of the road on a dry day and a composite
consists of yellow-brown and red-brown medium sample out of the two collected was obtained
to coarse grained arkosic and subarkosic sand- after coning and quartering (Table 1). The sam-
stone. The Gulf of Aqaba represents the southern ples were transferred to an air-tight polyethylene
portion of the Dead Sea fault system (Jordan rift), bag for transport to the laboratory. The samples
which connects the spreading of the Red Sea were left to dry at room temperature for 5 days
seafloor with continental rift propagation and were sieved through a 2-mm plastic sieve to
(Al-Zoubi, Abu-Hamatteh, & Abdelalkaderer, remove extraneous matter such as small pieces of
2006). brick, paving stone, and other debris. Care was
taken to reduce the disturbance of the fine
particles, which are readily lost by resuspension
Materials and methods (Baptista and De Miguel, 2005; Li et al., 2001;
Madrid, Barrientos, & Madrid, 2002; Manta,
Sample collection Angelone, Bellanca, Neri, & Sprovieri, 2002).
Control samples (n = 13), were collected from the
A total of 140 street dust samples were collected remote areas outside of Aqaba that were not
from various locations in Aqaba during the period affected by traffic and any source of contamina-
of June 2004 to August 2004 (Table 1). The tion (background sites). The samples were
sampling was chosen at the end of the dry collected from this area for comparison purposes.
summer months following at least four rainless
months. Rain has no effect on the trace metals, Preparation for the analysis
which accumulated in these months. A sampling
point within each unit was selected at random, Two grams of the sieved sample were weighed
and approximately 250 g of the dust particles that and transferred to a Pyrex tube. Then 10 ml of
had accumulated on impervious surfaces (gutter, aqua regia (1HNO3 and 3 HCL) was added. The
road pavement) within a 5-m radius circle around sample was transferred to a heating block for 8 h
the selected sampling point were collected to complete digestion, then centrifuged and
(Baptista and De Miguel, 2005). The dust sam- transferred to a volumetric flask and made up to
pling was carried out from pavement edges using 25 ml with 1 M HNO3 (Divrikli et al., 2003).
a plastic dustpan and brushes. Dust samples were Metals in the final solutions were determined
not collected adjacent to site specific pollution using a Shimadzu atomic absorption spectropho-
sources e.g. industrial sites and gasoline stations. tometer (model AA-6200). The pH was measured

Table 1 Description of sampling locations


Location/sampling point Number of Description
vehicles/h

School gardens (A), S1–S15 (n = 15) 125 Residential area, low traffic
Health and hospital centers (B), HS1–HS15 150 Low traffic, beside the parks
(n = 15)
Residential sites (C), R1–R18 (n = 18) 275 Residential areas, medium traffic
Industrial sites (D), IN1–IN16 (n = 16) 300 Major industries: phosphate, cement, and
petrochemicals
Parks (E), P1–P18 (n = 18) – Urban parks, highway type road, grass, and some old
trees
Heavy traffic (F), HT1–HT15 (n = 15) >500 Heavy traffic areas
Moderate traffic (G), MT1–MT15 (n = 15) 350 Medium traffic areas
Light traffic (H), LT1–LT15 (n = 15) <250 Low traffic areas
Background sites (I), BG1–BG13 (n = 13) 0 Rural area

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Environ Geochem Health (2007) 29:197–207 201

in 1 (sample, w):2.5 (distilled water, v) mixtures vary greatly according to the strength and direc-
(Banerjee, 2003; Okalebo, Gathua, & Woomer, tion of wind, composition of dust and pH values.
1993). The percentage of the organic matter of The pH values show relatively equal distribution
selective samples was determined by the chromic in the area, with their higher values in the street
acid digestion method (Jackson, 1973). Standard dust samples collected in the residential area. The
stock solutions for all the elements were procured pH values were relatively similar across the area,
from Merck as well as prepared in the laboratory with higher values in street dust samples collected
following the procedures as described in APHA closer to a workplace with construction materials.
(1989). To minimize the sources of error, blanks The relatively high average pH values measured
were run simultaneously for analysis of all the in this area is due to the neutralization of acidity
elements (Banerjee, 2003). Reagent blanks and in the dust by carbonate. The higher pH > 7,
duplicate samples were used in the analytical removal metals from aqueous phase to solid
programs to assess contamination, precision and phase. The organic matter in dust samples ranged
bias. The precision and bias in the analysis were from 1.23 to 1.96%. The highest value of organic
generally <7%. The glassware used was Pyrex, matter was found in the northeast of the inves-
which was washed several times with soap, tigated area; however, the distribution pattern of
distilled water and diluted nitric acid to remove organic matter reflects the variable dust of veg-
any impurities. All procedures of sampling and etation and plant cover in the investigated area.
handling were carried out without contact with
the metals, to avoid potential contamination of Concentration of metals
the samples.
The concentrations of metals in street dust
Statistical analysis samples are given in Table 2. The street dust
samples in the investigated area were classified
Statistical analyses were performed with SPSS for into nine groups, i.e., schools and gardens, health
Windows 10.0.5. Data were log-transformed prior and hospital centers, residential, industrial, parks,
to principle component analysis (PCA) to reduce streets with heavy traffic, streets with moderate
the influence of high data (Moller, Muller, traffic, streets with light traffic and control sam-
Abdullah, Abdelgawad, & Utermann, 2005). ples out of Aqaba city. The pH value varied from
Principle Component Analysis was conducted 7.6 in moderate traffic stations (MT10) to 8.20 in
using factor extraction with an eigenvalue larger light traffic stations (LT4) beside the construction
than 1 after varimax rotation. Pearson’s correla- material site (Table 2), which suggests neutral to
tion coefficient was used to measure the degree of sub-alkaline conditions for all the dust samples.
correlation between logarithms of the metal data The mean values of the metals are shows in Fig 2.
(Garcia & Millan, 1998). The highest levels of metal ions were found in the
samples from street dust of the heavy traffic area,
except for manganese and cobalt, the highest
Results and discussion level of which were found in the samples from the
industrial areas. As shown in Table 2, the mean
Physico-chemical parameters metal concentration values are arranged in the
following order: CFe > CZn > CPb > CNi > CMn >
Street dust is also potentially a source of metals CCu > CCr > CCo > CCd where C stands for
for people living in urban communities. The concentration. The lowest mean values of metals
values of metals in street dust samples collected were observed at school gardens compared with
from Aqaba city were determined using a the other sites in the investigated area. Lead
Shimadzu atomic absorption spectrophotometer pollution in the environmental samples including
after digestion with aqua regia (one part concen- soil, dust, sediment and natural water comes from
trated HNO3 and three parts concentrated HCL). combustion of gasoline that contains tetraethyl
The values of different metals in the street dust lead as an anti-knock agent (Tüzen, 2003). The

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202 Environ Geochem Health (2007) 29:197–207

Table 2 Mean and standard deviation for the descriptive parameters of street dust samples (lg g–1), n = 140 samples
Site pH OM% Fe Zn Cu Cr Pb Cd Ni Mn Co

A 8.1 ± 0.1 1.4 ± 0.1 4,540 ± 9.2 103 ± 2.1 21 ± 1.2 11 ± 0.1 93 ± 7.1 2.5 ± 0.4 53 ± 3.1 51 ± 2.1 15 ± 2.1
B 7.9 ± 0.2 1.8 ± 0.3 4,999 ± 8.7 106 ± 4.7 24 ± 8.2 16 ± 0.4 109 ± 5.2 2.2 ± 0.3 60 ± 4.3 54 ± 3.2 10 ± 0.1
C 8.1 ± 0.3 1.7 ± 0.2 5,125 ± 6.4 114 ± 4.1 26 ± 4.5 20 ± 2.4 138 ± 6.2 2.0 ± 0.1 51 ± 5.5 59 ± 1.5 11 ± 0.8
D 7.8 ± 0.1 1.9 ± 0.2 5,343 ± 9.1 118 ± 3.2 29 ± 1.9 22 ± 6.5 145 ± 5.1 2.1 ± 0.2 65 ± 2.6 90 ± 1.6 18 ± 0.8
E 7.9 ± 0.1 1.7 ± 0.1 5,477 ± 6.1 127 ± 3.5 24 ± 4.3 36 ± 7.5 164 ± 6.2 2.6 ± 0.1 70 ± 4.5 76 ± 1.9 19 ± 0.1
F 7.7 ± 0.2 1.6 ± 0.2 6,865 ± 0.1 160 ± 3.2 56 ± 2.1 41 ± 7.1 212 ± 6.8 2.9 ± 0.1 115 ± 4.5 107 ± 3.5 21.4 ± 0.6
G 7.6 ± 0.1 1.3 ± 0.1 5,678 ± 5.7 146 ± 4.1 50 ± 4.9 32 ± 4.5 194 ± 1.5 2.1 ± 0.2 66 ± 4.1 65 ± 2.6 16 ± 0.2
H 8.2 ± 0.6 1.2 ± 0.1 5,126 ± 5.5 126 ± 2.5 32 ± 4.5 21 ± 2.7 103 ± 4.5 1.9 ± 0.1 55 ± 1.5 48 ± 1.4 18 ± 0.7
I 7.9 ± 0.2 1.7 ± 0.3 3,340 ± 7.5 48 ± 1.5 1.4 ± 0.1 2.1 ± 0.1 19 ± 0.5 1.2 ± 0.2 10.2 ± 1.1 32 ± 1.8 5.3 ± 0.1
A: School gardens
B: Health and hospital centers
C: Residential areas
D: Industrial areas
E: Parks
F: Heavy traffic
G: Moderate traffic
H: Light traffic
I: Background sites

highest lead values have been detected in dust school gardens, the highest mean copper value
collected from streets carrying heavy traffic was found in the samples from heavy traffic areas
(Divrikli et al., 2003; Fergusson, 1991). As shown (Fig. 3). The source of copper in the street dust
in Table 2, the minimum mean lead concentration was indicated by research as being due to corro-
found in street dust samples from school gardens sion of metallic parts of cars derived from engine
was 93 lg g–1 (Fig. 3). The concentrations of lead wear, thrust bearing, brushing, and bearing metals
in the dust samples was highest in dust from (Al-Khashman, 2004; Al-Khashman & Shaw-
streets with heavy traffic (mean = 372.9 lg g–1). abkeh, 2006; Divrikli et al., 2003; Jaradat &
The high value of lead in the dust samples from Momani, 1999; Thornton, 1991). The levels of
heavy traffic sites comes from traffic, because all copper in the samples from Aqaba city were
the samples were in the street dust with high generally lower than the world-wide values (100–
traffic levels (>500 v/h). 300 lg g–1; Fergusson, 1991). The present study
However, the mean concentration of lead for found that copper levels were low compared with
street dust samples was lower than for dust several cities in the world (Table 3). The level of
samples reported by other literature, such as chromium in the dust samples was found to be
697.2 lg g–1 for Bahrain, 230.5 lg g–1 for Xian, within the range of 11 lg g–1 in school gardens to
China, 514 lg g–1 for Aviles, Spain, 1,030 lg g–1 41 lg g–1 in heavy traffic sites (Fig. 2). The
for London, UK, 265 lg g–1 for Manchester, UK, chromium in dust was associated with the chrome
and 236 lg g–1 for Amman, Jordan. On the other plating of some motor vehicle parts (Al-Shayep &
hand, the mean concentration of lead in street Seaward, 2001). Chromium highest concentra-
dust from Aqaba city was higher than reported by tions were observed in the samples from streets
other literature, such as 48 lg g–1 for Bursa, with heavy traffic (51 lg g–1). On the other hand,
Turkey, 69.2 lg g–1 for Yozgat, Turkey and the lowest value for chromium was observed in
47.1 lg g–1 for Coventry, UK. The mean contents school gardens (Fig. 3). The level of chromium in
of copper in the dust samples was within the the investigated area was generally lower than
range of 21–56 lg g–1. While the lowest mean those determined in other cities in developed
value of copper was found in the samples from countries, except Luanda in Angola (Table 3).

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Environ Geochem Health (2007) 29:197–207 203

0.12
0.1 Mn

0.08
0.06

ppm
0.05 0.06
0.04 Cu
ppm

0.03 0.04
0.02
0.02
0.01
0 0
A B C D E F G H I A B C D E F G H I
Sites Sites

0.05
Cr 7000 Fe
0.04 6000
ppm

0.03 5000

ppm
4000
0.02 3000
0.01 2000
1000
0 0
A B C D E F G H I A B C D E F G H I
Sites Sites

0.025
Co
0.25 0.02
Pb
ppm

0.2 0.015
ppm

0.15
0.01
0.1
0.05 0.005

0 0
A B C D E F G H I A B C D E F G H I
Sites Sites

0.003 0.16 Zn
Cd
0.14
0.0025
0.12
0.002 0.1
ppm
ppm

0.0015 0.08
0.001
0.06
0.04
0.0005 0.02
0 0
A B C D E F G H I A B C D E F G H I
Sites Sites

0.15
Ni

0.1
ppm

0.05

0
A B C D E F G H I
Sites

Fig. 3 Mean concentrations of the metals in the street dust samples. A school gardens, B health and hospital centers,
C residential areas, D industrial areas, E parks, F heavy traffic, G moderate traffic, H light traffic, I background sites

Higher concentrations of zinc and cadmium in 2003). The highest mean cadmium content was
heavy traffic zones indicates that fragmentation of found in the streets with heavy traffic (2.9 lg g–1).
car tires is a likely source of these metals (Elik, The cadmium is released as a combustion product

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204 Environ Geochem Health (2007) 29:197–207

Table 3 Mean concentration of metals (lg g–1) in street dust in several cities
City Fe Cu Cd Pb Zn Cr Co Mn Ni Digestion

Ammana 7,132 177 1.7 236 358 – – – 88 HCL+HNO3


Avilesb 42,200 183 22.3 514 4,829 41.6 – – – HCL+HNO3
Bahrainc – – 72 697.2 151.8 144.4 – – – HCL+HNO3
Birminghamd – 466.9 1.6 48 534 – – – – HCLO4+HNO3+H2SO4
Coventrye – 226.4 .9 47.1 385 – – – – HCLO4+HNO3+H2SO4
Kayserif – 66.7 10.1 165.5 – 72.8 26.1 274 57 HNO3
Londong 26,000 155 3.5 1,030 680 – – – – HCL+HNO3
Manchesterh 8,767 113 – 265 653 – – – – HNO3
LuandaI 11,572 42 1.1 315 317 26 2.9 258 10 HCL+HNO3
Tokatj – 38 5.4 266 98 41 22 415 128 HCL+HNO3
Xiank – 94.9 – 230.5 421.4 167.3 – 687 – HCLO4+HNO3+H2SO4
Yozgatl – 37.7 2.97 69.2 – 32.7 24.3 852 77 HNO3
a
Al-Khashman (2006); b Ordonez, Loredo, De Miguel, & Charlesworth (2003); c Akhter and Madany (1993); d Charlesworth
et al., (2003); e Charlesworth et al., (2003); f Divrikli et al., (2003); g Schwar, Moorcroft, Laxen, Thompson, & Armorgie
(1988); h Robertson, Taylor, & Hoon (2003); I Baptista and De Miguel (2005); j Tüzen (2003); k Yongming et al., (2006); l
Divrikli et al., (2003)

in the accumulators of motor vehicles or in source of manganese in dust samples was from the
carburetors (Charlesworth, Everett, McCarthy, geological material in Aqaba city (lithogenic
Ordonez, & de Miguel, 2003; Divrikli et al., 2003). source), from traffic, and from tire wear (Divrikli
The value of cadmium in street dust samples from et al., 2003). The mean manganese concentration
Amman, Jordan was reported to be within the in street dust samples was 300–800 lg g–1
range of 1.01–2.9 lg g–1 (Al-Khashman, 2006). (Fergusson, 1991). The concentration of cobalt
Many researchers have reported the mean con- in dust samples was within the range of 17.8–
centration of cadmium in several cities (Table 3). 22.3 lg g–1. The major source of manganese is
The range of the median value of cadmium in considered to be natural, sandstone and basement
street dust samples world-wide has been exam- rock being the main source of manganese in dust
ined as being 0.5–4.0 lg g–1 (Fergusson & Kim, samples. The highest mean level of cobalt was
1991). In general, the high values of Cr, Cd, Ni, found in heavy traffic sites (21.4 lg g–1). The level
and Cu were found in Aqaba city, which might be of cobalt in dust samples was found to be higher
due to the phosphate handling activities of the than mean values around the world, and the level
port of Aqaba, which emits phosphate aerosol of cobalt in the present study does not vary much
through the atmosphere. The zinc concentration from the investigated area in other localities.
was found in the range of 103–160 lg g–1. The Also, the source of cobalt in the dust samples
zinc levels found in the present study were lower from heavy traffic comes from the corrosion of
than those determined in other cities in develop- metallic parts of vehicles.
ing countries (Table 3). Iron was the most abun- Nickel values in dust samples were found to be
dant metal content in street dust. The possible within the range of 51–114.6 lg g–1.The highest
source of iron particles were brake lining material mean value of nickel was found in the street dust
(brake dust; Adachi & Tainosho, 2004; Garg samples and the lowest mean value of nickel was
et al., 2000; Hildemann, Markowski, & Cass, found in the control site. The range of mean
1991). The highest mean iron level was found in nickel concentration in world-wide street dust
the streets with heavy traffic (6,865 lg g–1). samples was 50–100 lg g–1 (Fergusson & Kim,
However, the mean concentration of iron in 1991). Nickel pollution on a local scale is caused
street dust samples was lower than determined by emissions from vehicle engines that use nickel
in several cities in developing countries (Table 3). gasolene and by the abrasion and corrosion of
Manganese content in the dust samples was found nickel from vehicle parts (Al-Shayeb & Seaward,
to be within the range of 48–107 lg g–1. The main 2001).

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Environ Geochem Health (2007) 29:197–207 205

Statistical analyses and data treatment identify the source of pollutants more accurately
using factor extraction with an eigenvalue larger
Correlation coefficient analysis than 1 after varimax rotation. The results of
statistical analysis are tabulated in Table 5.
Pearson’s correlation coefficient can be used to Table 5 displays the factor loadings with a
measure the degree of correlation between loga- varimax rotation, as well as the eigenvalues. The
rithms of the metal data (Garcia & Millan, 1998). results show that two eigenvalues are greater than
The correlations of metals in street dust samples 1 and the total variance for the two factors is
of Aqaba city are depicted in Table 4. Highly about 74%. The third eigenvalue, which is 1.11,
significant correlation data (>0.65) were found explains about 10% of the total variance, which is
between Cu and Cr, Cu and Pb, Cr and Ni, Pb and a significant contribution toward the explanation
Co, and Cd and Mn (Table 4). These high of cumulative variance. Factor 1 was dominated
correlations show that the origin of the metals by Cu, Cr, Cd, Ni, Co, and Zn, and accounts for
in the investigated area is highly related to the 41.12% of the total variance, in this case. Zn and
heavy traffic, industrial activities, structure of the Cd loadings (0.625 and 0.676 respectively) are not
soils, and street dust emissions. Lead values as high as the loadings of the other elements in
showed very weak positive correlations with the group; such a domination may be caused by
Mn, Zn, Ni, and Cd varying from 0.194 to 0.402. the behavior of the metals within the group. This
A meaningful correlation has not been found factor represents pollution caused by industrial
between Mn and Pb. The source of Pb in the activities and emissions from traffic (Banerjee,
street dust samples may be from heavy traffic 2003; Chen, Wong, Zhou, & Wong, 1997). The
activities in the studied area. The Mn–Co (0.113) second factor is highly dominated by pH, OM and
and Mn–Cr (0.224) pairs were weakly correlated Fe and Mn and accounts for 23.24% of the total
at 95% confidence level. variance. This factor was composed of the char-
acteristics of street dust pH and organic matter
Principle component analysis and metals (Fe and Mn), and represents the
contribution of metals from lithogenic and
Statistical analyses were performed with SPSS for anthropogenic sources. This factor’s high loadings
Windows 10.0.5. Data were log-transformed prior of the elements Fe and Mn suggest the influence
to PCA to reduce the influence of high data of natural sources and some anthropogenic input.
(Moller et al., 2005). PCA was used to help Relatively, the high loadings of Fe and Mn in the

Table 4 Correlation matrix between metals in urban samples; cells show the Pearson correlation coefficient and the
corresponding P value, n = 140 samples
Cu Cr Pb Cd Ni Mn Co Fe

Cr 0.851
0.000
Pb 0.722 0.762
0.000 0.000
Cd 0.51 0.313 0.201
0.000 0.000 0.000
Ni 0.552 0.692 0.402 0.384
0.003 0.000 0.001 0.001
Mn 0.410 0.224 0.194 0.692 0.564
0.000 0.002 0.000 0.000 0.000
Co 0.144 0.232 0.764 0.522 0.070 0.113
0.002 0.000 0.000 0.000 0.001 0.000
Fe 0.521 0.434 0.681 0.404 0.184 0.007
0.000 0.000 0.000 0.000 0.000 0.002
Zn 0.281 0.223 0.344 0.481 0.390 0.310 0.401 0.321
0.000 0.000 0.000 0.000 0.000 0.002 0.000 0.001

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206 Environ Geochem Health (2007) 29:197–207

Table 5 Factor loadings for varimax rotated PCA of in school gardens and hospital and health
metal data in street dust samples (loadings in bold type are centers. The mean concentrations of the studied
statistically significant)
metals were as follows: CFe > CZn > CPb > CNi >
Parameters Factor Factor Factor Communities CMn > CCu > CCr > CCo > CCd where C stands
1 2 3 for concentration. Results showed that dust
pH –1.370 0.908 –2.264 0.825 samples contained significant levels of the metals
OM –0.803 0.775 –0.335 0.765 studied with the control values. The statistical
Cu 0.823 0.222 –0.232 0.780 analysis, metal value analysis, and correlation
Cr 0.805 –0.164 0.323 0.781 analysis were applied as an effective tool to
Pb –9.652 –1.619 0.973 0.876
Cd 0.676 0.414 –0.152 0.633 identify the source of metals in street dust
Ni 0.881 0.129 –0.250 0.855 samples. The examined elements were classified
Mn –0.126 0.908 0.245 0.901 into three main groups according to their
Co 0.745 0.338 –0.162 0.696 sources: natural, traffic, and industrial. PCA
Fe 0.290 0.672 0.537
Zn 0.625 0.332 0.199 0.540 analysis coupled with correlation analysis was
Eigenvalues 4.523 2.556 1.109 used to gain additional insight into the origin of
% Variance 41.122 23.238 10.082 these metals in street dust samples from Aqaba
% 41.122 64.359 74.441 city. The trend of increasing industrial and traffic
Cumulative
activities in the city indicates the need for
pollution control in the city environment.
dusts are interpreted here to be the result of
natural enrichment by weathering and pedogen-
esis (Al-Khashman, 2006). The third factor was
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