Effects of some rare elements on nicotine content of the tobacco plant

Fifty-four rare elements were tested for their effects on the nicotine level of tobacco (Nicotiana tabacum L.) plants grown in solution culture. Be, Cu, Pd, Pt, and Sm definitely increased nicotine yield (over 25%), whereas Bi, Co, Ho, Pb, Ni, Rb, Ag, Tl, Sn, U. V. and Zr definitely decreased nicotine yield. Cs, Er, Li, Rh, Ru, Se, Sr, Ti, and Yb possibly increased (less than 25%) nicotine yield, whereas As, Ce, Cr, Dy, Gd, I, Mo, Nd, Re, Ta, and Th possibly decreased nicotine yield. Other elements including Al, Ge, Au, Hf, In, Ir, La, Lu, Hg, Os, Pr, Sc, Te, Tb, Tm, W, and Zn showed no significant effects.     

The Effect of Age and Gender on 59 Trace-Element Contents in Human Rib Bone Investigated by Inductively Coupled Plasma Mass Spectrometry

The effect of age and gender on 59 trace-element contents in rib bone of 80 apparently healthy 15–55-year-old women (n?=?38) and men (n?=?42) was investigated by inductively coupled plasma mass spectrometry. Mean values (M?±?SΕΜ) for the mass fraction (milligrams per kilogram, on dry-weight basis) of Ba, Bi, Cd, Ce, Cu, Dy, Er, Gd, La, Li, Mn, Mo, Nd, Pb, Pr, Rb, Sm, Sr, Tb, Tl, U, Yb, and Zn for both female and male taken together were: Ba 2.5?±?0.2, Bi 0.015?±?0.002, Cd 0.044?±?0.005, Ce 0.029?±?0.002, Cu 1.05?±?0.06, Dy 0.0020?±?0.0003, Er 0.0011?±?0.0002, Gd 0.0015?±?0.0001, La 0.020?±?0.002, Li 0.040?±?0.002, Mn 0.354?±?0.004, Mo 0.052?±?0.006, Nd 0.011?±?0.001, Pb 2.24?±?0.14, Pr 0.0032?±?0.0004, Rb 1.51?±?0.06, Sm 0.0014?±?0.0001, Sr 291?±?20, Tb 0.00041?±?0.00005, Tl 0.00050?±?0.00003, U 0.0013?±?0.0001, Yb 0.00072?±?0.00007, and Zn 92.8?±?1.5, respectively. The upper limit of mean contents of Ag, Al, B, Be, Br, Cr, Cs, Hg, Ho, Lu, Ni, Sb, Te, Th, Ti, Tm, and Y were: Ag?≤?0.011, Al?≤?7.2, B?≤?0.65, Be?≤?0.0032, Br?≤?3.9, Cr?≤?0.25, Cs?≤?0.0077, Hg?≤?0.018, Ho?≤?0.00053, Lu?≤?0.00024, Ni?≤?1.05, Sb?≤?0.0096, Te?≤?0.0057, Th?≤?0.0030, Ti?≤?2.8, Tm?≤?0.00006, and Y?≤?0.0047, respectively. In all bone samples, the contents of As, Au, Co, Eu, Ga, Hf, Ir, Nb, Pd, Pt, Re, Rh, Sc, Se, Sn, Ta, V, W, and Zr were under detection limits. The Ce, Dy, Er, Gd, La, Nd, Pr, Sm, Tb, and Yb contents increase with age. Higher Sr mass fraction is typical of female rib as compared to those in male bone.     

The chemical composition of bananas market basket values, 1968–1980

Forty-six elements have been detected in fresh banana pulp purchased weekly in Pittsburgh, PA for the past twelve years (1968–1980). Samples were prepared by lyophilization or low temperature ashing. Analyses were performed using X-ray fluorescence spectrometry, optical emission spectrometry, atomic absorption spectrometry, and wet chemistry. Whenever possible, comparative data from the literature are included. No comparative data were found for Rb, Cs, Li, Ag, Be, Ga, La, Ce, Ge, Sn, Ti, Zr, Sb, Bi, and Te. Bananas accumulate K, Mg, and B in comparison to their Na, Ca, and Al content. The K content has been rising steadily since 1968. Lead and Hg quantities have not materially changed during the pat three decades. Arsenic concentrations in bananas declined in the late 1960s and early 1970s, but have been rising since 1978, possibly owing to the increased use of As-bearing pesticides. Other toxic elements such as Be and Te are present in very small quantities and are detected infrequently. An appendix is attached that presents the chemical composition of orchard leaves NBS 1571 obtained by the methods utilized in this study.     

混合样品代表地衣元素积累的平均水平——来自元素含量不同的两种地衣的证据

地衣是大气元素沉降的良好监测生物,其元素积累能力具有物种间和个体间差异。地衣原位监测法常使用混合样品代表每个样点的地衣元素积累水平,但混合样品的代表性及其在不同地衣之间的差异尚需进一步研究。以电感耦合等离子体质谱法（inductively coupled plasma mass spectrometry,ICP-MS）测定了内蒙古多伦县的丽石黄衣Xanthoria elegans和皮果衣Dermatocarpon miniatum 52种元素的含量并比较了样点内变异和物种间差异。结果显示,丽石黄衣与相似生境中的地衣元素含量大致相似,证实了研究区域以沙尘沉降为主的大气沉降特点。两种地衣的元素排序基本一致,表明其元素来源相同。7种营养元素（Ca、K、Mo、P、Rb、S和Se）的含量在物种间差异不显著,与地衣的生理调节有关。Hg含量的物种间差异不显著,可能与Hg的挥发性有关。皮果衣中44种元素（Al、As、B、Ba、Be、Bi、Cd、Ce、Co、Cr、Cs、Cu、Dy、Er、Eu、Fe、Gd、Ge、Ho、La、Li、Lu、Mg、Mn、Na、Nb、Nd、Ni、Pb、Pr、Sb、Sc、Sm、Sr、Tb、Th、Ti、Tl、Tm、U、V、Y、Yb和Zn）的含量是丽石黄衣的1.32-2.05倍,表明皮果衣具有较高的、元素特异性的元素积累能力。样点内除Ca含量变异较大（CV>31%）之外,其他51种元素的含量样点内变异在皮果衣和丽石黄衣中均<27.5%,表明混合样品在两种地衣中均可较好地代表地衣元素积累的平均水平。     

Plant uptake of major and minor mineral elements as influenced by soil acidity and liming

This study reports effects on soil solution chemistry and plant uptake of 55 elements (Ag, Al, As, B, Ba, Be, Bi, Br, Ca, Cd, Ce, Co, Cr, Cs, Cu, Dy, Er, Eu, Fe, Gd, Ge, Hf, Hg, Ho, K, La, Li, Lu, Mg, Mn, Mo, Na, Nb, Nd, Ni, P, Pb, Pr, Rb, S, Sb, Sc, Se, Si, Sm, Sr, Tb, Th, Tl, U, V, W, Y, Yb, Zn, Zr) by raising the pH using addition of fine-grained precipitated calcium carbonate at 20 rates (yielding a soil solution pH range of 5.2 – 7.8) to A horizon samples of an acid Cambisol, cultivating a common grass (Agrostis capillaris L.) and determining the soil solution, root and shoot concentrations of these elements at the end of the experiment. For many of these elements, there is little or no previous information about concentrations in soil solutions, or in plant biomass, as related to soil pH/acidity or addition of calcium carbonate. Soil solutions were obtained by high speed centrifugation and ultrafiltration (0.2 m) of samples at 60% water-holding capacity. Concentrations of elements were determined by ICP-ES or (in most elements) ICP-MS, using isotopes specified. Soil solution pH, HCO₃ and organic C were also determined.Concentrations of elements in the biomass of A. capillaris were usually inversely related to soil solution pH. The most apparent (p<0.001) inverse, though often curvilinear, relationships between pH and concentrations in shoot biomass were measured for Ag, As, B, Ba, Eu, Ge, Li, Mn, Ni, P and Sr. Positive relationships (p<0.05) were only measured in Ca, Hg, Mg, Mo and S. For concentrations in root biomass, relationships were mostly, but not always, of the same sign and of a similar strength. Though soil solution pH and concentrations of elements were usually quite closely correlated, pH and/or HCO^– ₃ concentration more often accounted for a higher share of the variability in biomass concentration of elements than did soil solution concentration of the same element.     

Significance of Trace Element Profile of Blood of Persons with Multiple Caries versus Sound Teeth

In order to determine any possible relation between chemical composition of a person’s blood to formation of dental caries, whole blood was analyzed for 35 inorganic elements (Si, Al, Fe, Ca, Mg, K, Mn, Ti, P, Li, Be, B, V, Cr, Co, Ni, Cu, Zn, As, Sr, Y, Nb, Mo, Ag, Cd, Sn, Sb, Ba, La, Ce, W, Pb, Bi, Zr, and F) in the 15 people having sound teeth as well as an equal number of those having multiple caries. The results showed the absence of 13 elements (Si, Al, Mn, Ti, Be, Co, As, Y, Cd, Ba, La, Ce, and Zr) in the blood of both groups. Of the remaining 22 elements, the results of only seven elements (Fe, P, B, V, Sr, Sn, and F) were significantly different between the two groups. The most remarkable finding of this study was significantly decreased amount of phosphorus, strontium, and fluorine and perhaps increased boron in the blood of persons with caries.     

Mass Fractions of 52 Trace Elements and Zinc/Trace Element Content Ratios in Intact Human Prostates Investigated by Inductively Coupled Plasma Mass Spectrometry

Contents of 52 trace elements in intact prostate of 64 apparently healthy 13?C60-year-old men (mean age 36.5?years) were investigated by inductively coupled plasma mass spectrometry. Mean values (M ± S????) for mass fraction (in milligrams per kilogram, on dry-weight basis) of trace elements were as follows: Ag 0.041?±?0.005, Al 36?±?4, Au 0.0039?±?0.0007, B 0.97?±?0.13, Be 0.00099?±?0.00006, Bi 0.021?±?0.008, Br 29?±?3, Cd 0.78?±?0.09, Ce 0.028?±?0.004, Co 0.035?±?0.003, Cs 0.034?±?0.003, Dy 0.0031?±?0.0005, Er 0.0018?±?0.0004, Gd 0.0030?±?0.0005, Hg 0.046?±?0.006, Ho 0.00056?±?0.00008, La 0.074?±?0.015, Li 0.040?±?0.004, Mn 1.53?±?0.09, Mo 0.30?±?0.03, Nb 0.0051?±?0.0009, Nd 0.013?±?0.002, Ni 4.3?±?0.7, Pb 1.8?±?0.4, Pr 0.0033?±?0.0004, Rb 15.9?±?0.6, Sb 0.040?±?0.005, Se 0.73?±?0.03, Sm 0.0027?±?0.0004, Sn 0.25?±?0.05, Tb 0.00043?±?0.00009, Th 0.0024?±?0.0005, Tl 0.0014?±?0.0001, Tm 0.00030?±?0.00006, U 0.0049?±?0.0014, Y 0.019?±?0.003, Yb 0.0015?±?0.0002, Zn 782?±?97, and Zr 0.044?±?0.009, respectively. The upper limit of mean contents of As, Cr, Eu, Ga, Hf, Ir, Lu, Pd, Pt, Re, Ta, and Ti were the following: As ??0.018, Cr ??0.64, Eu ??0.0006, Ga ??0.08, Hf ??0.02, Ir ??0.0004, Lu ??0.00028, Pd ??0.007, Pt ??0.0009, Re ??0.0015, Ta ??0.005, and Ti ??2.6. In all prostate samples, the content of Te was under detection limit (<0.003). Additionally, ratios of the Zn content to other trace element contents as well as correlations between Zn and trace elements were calculated. Our data indicate that the human prostate accumulates such trace elements as Al, Au, B, Br, Cd, Cr, Ga, Li, Mn, Ni, Pb, U, and Zn. No special relationship between Zn and other trace elements was found.     

Quantification of 26 metals in human urine samples using ICP-MSMS in a random sample collective of an occupational and environmental health care center in Aachen,Germany

Despite several studies on metal exposure in the general population, the knowledge on the background burden of distinct metals is still sparse (e.g. Cu, In, Mn, Pb, Sn, Sr, Ta, Te). While up to date reference values exist for 16 distinct metals as Biological Reference Value (BAR) or the 95th percentile for Al, As, Ba, Be, Cd, Co, Cr, Hg, Li, Mo, Ni, Pt, Sb, Se, Tl and U respectively, the background burden of the general population for the remaining elements is unknown or yet no matter of scientific counselling. We established and validated an inductively coupled plasma triple quadrupole mass spectrometry (ICP-MSMS) human biomonitoring method (HBM), that enabled us to determine 26 metals in urine. Al, As, Ba, Be, Cd, Co, Cu, Ga, Gd, Hg, In, Li, Mo, Ni, Pb, Sb, Se, Sn, Sr, Ta, Te, Tl, V and Zn were analyzed. The method was applied to 88 urine samples collected in the ambulance of the Institute for Occupational, Social and Environmental Medicine (IASU) Aachen, Germany. Patients from two major metal processing companies (steel and copper) and a more heterogenous group of occupational exposed and non-exposed persons were defined and distinguished. HBM data from about 88, in general occupationally unexposed persons against certain metals served as a collective representing the general population in first approximation. For these the 95th percentiles are reported. Significant differences of urinary metal concentrations of the employees of the two metal processing companies compared to the third group were observed among others for Cu, Cr, Ni, Mn and are discussed, thus demonstrating the usefulness of the method for both environmental and occupational purposes.     

Assessment the Exposure Level of Rare Earth Elements in Workers Producing Cerium,Lanthanum Oxide Ultrafine and Nanoparticles

In order to assess occupational exposure level of 15 rare earth elements (REEs) and identify the associated influence, we used inductively coupled plasma mass spectrometry (ICP-MS) based on closed-vessel microwave-assisted wet digestion procedure to determinate the concentration of Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu in urinary samples obtained from workers producing ultrafine and nanoparticles containing cerium and lanthanum oxide. The results suggest that La and Ce were the primary component, together accounting for 97 % of total REEs in workers. The urinary levels of La, and Ce among the workers (6.36, 15.32 μg.g^?1 creatinine, respectively) were significantly enriched compared to those levels measured in the control subjects (1.52, 4.04 μg.g^?1 creatinine, respectively) (p < 0.05). This study simultaneously identified the associated individual factors, the results indicate that the concentrations in over 5 years group (11.64 ± 10.93 for La, 27.83 ± 24.38 for Ce) were significantly elevated compared to 1–5 years group (2.58 ± 1.51 for La, 6.87 ± 3.90 for Ce) (p < 0.05). Compared the urinary levels of La and Ce at the separation and packaging locations (9.10 ± 9.51 for La, 22.29 ± 21.01 for Ce) with the other locations (2.85 ± 0.98 for La, 6.37 ± 2.12 for Ce), the results show urinary concentrations were significantly higher in workers at separation and packaging locations (p < 0.01). Inter-individual variation in levels of La and Ce in urine is the result of multi-factorial comprehensive action. Further researches should focus on the multiple factors contributing to the REEs levels of the occupationally exposed workers.     

感耦等离子体发射光谱法研究土壤—铁芒萁系统中稀土元素的分布、累积和迁移特征

用感耦等离子体发射光谱法（ICP－AES）测定了东西赣南地区非稀土矿区和4处不同稀土矿区内,土壤－铁芒萁系统中La、Ce、Pr、Nd、Sm、Gd、Dy、Yb和Y的含量,并对其在土壤剖面层及铁芒萁植物体内的分布、迁移特征进行了研究,结果表明,土训层的底土层含量最高,但表土层铈相对富集、稀土元素总量（∑REE）在铁芒萁植物体内的分布规律是叶＞根＞茎＞叶柄,单一稀土的分布规律各异,La、Ce、Pr、Nd的分布规律表现为：叶＞根＞茎＞叶柄;Sm和Gd在不同采样点表现为叶＞根＞茎＞叶柄或根＞叶＞茎＞叶柄;Dy、Yb和Y均有3种不同的分布模式：叶＞根＞茎＞叶柄、根＞叶＞茎＞叶柄及根＞茎＞叶＞叶柄,稀土元素在铁芒萁体内的迁移过程中,发生了明显的分馏作用,茎、叶柄、叶中的重稀土相对贫乏。     

Trace and mineral elements in royal jelly and homeostatic effects

Royal jelly from Apis mellifera is a highly active natural biological substance and is probably one of the most interesting raw substances in natural product chemistry. Trace elements play a key role in the biomedical activities associated with royal jelly, as these elements have a multitude of known and unknown biological functions. For this reason concentrations of 28 trace (Al, Ba, Sr, Bi, Cd, Hg, Pb, Sn, Te, Tl, W, Sb, Cr, Ni, Ti, V, Co, Mo) and mineral (P, S, Ca, Mg, K, Na, Zn, Fe, Cu, Mn) elements were systematically investigated in botanically and geologically defined royal jelly samples. In addition, concentrations of 14 trace elements were measured in the associated honey samples--honey being the precursor of royal jelly. Concentrations of K, Na, Mg, Ca, P, S, Cu, Fe, Zn, Al, Ba and Sr in royal jelly were determined by inductively coupled plasma optical emission spectroscopy (ICP-OES), while concentrations of Bi, Cd, Hg, Pb, Sn, Te, Tl, W, Sb, Cr, Mn, Ni, Ti, V, Co and Mo in royal jelly were determined by double focusing magnetic sector field inductively coupled plasma mass spectrometry (SF-ICP-MS). In the honey samples, trace and mineral element concentrations strongly depended on botanical and geological origin, and substantial variation was found. In contrast, the concentrations of trace and mineral elements were highly constant in the associated royal jelly samples. The most important results were the homeostatic adjustments of trace and mineral element concentrations in royal jelly. This effect was evidently produced in the endocrine glands of nurse bees, which are adapted for needs of bee larvae. In conclusion, this research yielded a surprising and completely new finding--that royal jelly, as a form of lactation on the insect level, shows the same homeostatic adjustment as mammalian and human breast milk.     

New complexes of La(III), Ce(III), Pr(III), Nd(III), Sm(III), Eu(III) and Gd(III) ions with morin

New solid complex compounds of La(III), Ce(III), Pr(III), Nd(III), Sm(III), Eu(III) and Gd(III) ions with morin were synthesized. The molecular formula of the complexes is Ln(C₁₅H₉O₇)₃ · nH₂O, where Ln is the cation of lanthanide and n = 6 for La(III), Sm(III), Gd(III) or n = 8 for Ce(III), Pr(III), Nd(III) and Eu(III). Thermogravimetric studies and the values of dehydration enthalpy indicate that water occurring in the compounds is not present in the inner coordination sphere of the complex. The structure of the complexes was determined on the basis of UV-visible, IR, MS, ¹H NMR and ¹³C NMR analyses. It was found that in binding the lanthanide ions the following groups of morin take part: 3OH and 4CO in the case of complexes of La, Pr, Nd, Sm and Eu, or 5OH and 4CO in the case of complexes of Ce and Gd. The complexes are five- and six-membered chelate compounds.     

Rare earth elements (REEs) in PM10 and associated health risk from the polymetallic mining region of Nandan County,China

A total of 26 samples were collected from Dachang, Chehe and Liuzhai in Nandan County, China, in order to investigate the concentrations of rare earth elements (REEs) and associated health risk in particulate matter. The concentrations of REEs in Dachang (23.54 ng/m³), Chehe (20.29 ng/m³) were significantly higher than those in Liuzhai (8.1 ng/m³). The light rare earth elements (LREEs) account for 87.08%, 87.09%, and 86.17% of the total REE burden in PM10 at Dachang, Chehe, and Liuzhai, respectively, indicating that the distribution pattern of REEs in PM10 was characterized by the obvious fractionation of LREEs. Enrichment factor calculation indicated that EFs for La, Ce, Nd, Pr, and Nd in PM10 from Dachang and Chehe were greater than 2, indicating moderate enrichment. Source identification indicated that REEs in PM10 from Dacheng and Chehe originated from anthropogenic activities such as mining and smelting activities, while REEs in PM10 from Liuzhai were associated with natural sources, like soil erosion. Noncarcinogenic and carcinogenic risks associated with the exposure of REEs in PM10 were negligible based on the health risk assessment models. However, greater noncarcinogenic risk for children was found in studied areas compared with the adults.     

Concentrations of trace elements in osteoarthritic knee-joint effusions

Concentrations of the 18 elements, barium (Ba), beryllium (Be), bismuth (Bi), calcium (Ca), cadmium (Cd), cesium (Cs), copper (Cu), lanthanum (La), lithium (Li), magnesium (Mg), molybdenum (Mo), lead (Pb), rubidium (Rb), antimony (Sb), tin (Sn), strontium (Sr), thallium (Tl), and zinc (Zn), were determined in the synovial fluids of osteoarthritic knee joints and in the corresponding sera of 16 patients by inductively coupled plasma-mass spectrometry. Knee-joint effusions have lower elemental concentrations than their corresponding sera. For the essential elements Ca, Cu, Mg, and Zn and for the nonessential and toxic elements Ba, Be, Bi, La, and Sb, this difference was highly significant. Strong positive correlations between concentrations in effusions and sera for the essential elements Cu and Mg and for the nonessential elements Cs, Li, Rb, and Sr could be established. The grade of localized hyperperfusion of the knee region in the blood pool phase of ^99mTc HDP bone scan indicating inflammation did not correlate with any elemental concentration determined. Deceased.     

感耦等离子体发射光谱法研究土壤-铁芒萁系统中稀土元素的分布、累积和迁移特征

用感耦等离子体发射光谱法(ICP-AES)测定了江西赣南地区非稀土矿区和处不同稀土矿区内,土壤-铁芒萁系统中La、Ce、Pr、Nd、Sm、Gy、Db、Yb和Y的含量,并对其在土壤剖面层及铁芒萁植物体内的分布、迁移特征进行了研究.结果表明,土壤剖面层的底土层含量最高,但表土层铈相对富集.稀土元素总量(∑REE)在铁芒萁植物体内的分布规律是叶＞根＞茎＞叶柄,单一稀土元素的分布规律各异,La、Ce、Pr、Nd的分布规律表现为:叶＞根＞茎＞叶柄;Sm和Gd在不同采样点表现为叶＞根＞茎＞叶柄或根＞叶＞茎＞叶柄;Dy、Yb和Y均有3种不同的分布模式:叶＞根＞茎＞叶柄、根＞叶＞茎＞叶柄及根＞茎＞叶＞叶柄.稀土元素在铁芒萁体内的迁移过程中,发生了明显的分馏作用,茎、叶柄、叶中的重稀土相对贫乏.     

Effects of rare earth elements on the growth of Cistanche deserticola cells and the production of phenylethanoid glycosides

The rare earth elements Nd, La, Ce at proper concentrations had positive effects on the cell growth of Cistanche deserticola and production of phenylethanoid glycosides (PeG). A mixture of rare earth elements (MRE, La(2)O(3):CeO(2):Pr(6)O(11):Sm(2)O(3)=255:175:3:1, mol/mol) showed the most remarkable effects. After 30 day's culture, 0.02 mmoll(-1) MRE gave the highest content (20.8%) and production (1.6 gl(-1)) of PeG, which were 104 and 167% higher than those obtained in control (without rare earth elements).     

Radiocarbon dating and metal analyses of `fossil' and living tubes of Protula (Annelida: Polychaeta)

Since the initiation of benthic and trawling studies in southern California over 50 years ago, empty calcareous tubes, measuring up to 36 cm in length and 2.1 cm in diameter, have been collected and presumed to belong to the serpulid genus Protula. ¹⁴C dating of these `fossil' tubes, ranged from 631 ±34 to 3987 ±42 yrs. In connection with monitoring programs, living specimens of Protula superba Moore, 1909 were collected from the benthos off southern California. A comparison of the elemental profile of the ancient and extant tubes was conducted to ascertain the effects of time and the recent increase in various anthropogenically mobilized metals on the incorporation of Al, As, Ba, Cd, Ce, Co, Cr, Fe, Mo, Ni, Pb, U, V and Zn in the calcareous tube. Surprisingly, inductively coupled plasma mass spectroscopy (ICP-MS) analysis of the digested tubes showed the concentrations of the elements were generally higher in `fossil' tubes than those obtained from living animals. However, the concentration of elements was higher in `fossil' tubes collected from the vicinity of municipal outfall discharges compared to `fossil' tubes collected from near an offshore island. Laser ablation ICP-MS analyses across transverse sections of `fossil' and living tubes showed spatial heterogeneity of elements in the structure. Elevated signals for Pb, Gd, Ce, La, Pr, Sm, Eu and Nd were observed on both internal and external surfaces on all tubes. Elevated responses for Fe, Zn, Sr, Mn, Tb, Dy, Ho, Er and Bi were primarily noted on the outer surfaces. It is hypothesized that the higher concentrations of metals in the `fossil' tubes may be the result of surface contamination facilitating elemental adsorption or substitution over the years. It is concluded that the use of biomineralized structures as biomonitors of water quality should involve rigorous chelating procedures to remove contaminating metals from lattice bound elements locked in the mineral matrix.     

Effects of rare earth elements on telomerase activity and apoptosis of human peripheral blood mononuclear cells

To study the effects of rare earth exposure on human telomerase and apoptosis of mononuclear cells from human peripheral blood (PBMNCs). The blood contents of 15 rare earth elements, including La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, and Y, were measured by inductively coupled plasma-mass spectrometry. Telomeric repeat amplification protocol assay and flow cytometer analysis were carried out to analyze the telomerase activity and apoptosis of PBMNCs, respectively. The total content of rare earth elements in the blood showed significant differences between the exposed group and the control group. The rare earth exposure increased the telomerase activity and the percentages of cells in the S-phase and the G₂/M phase in PBMNCs, but it had no effect on the apoptotic rate of PBMNCs. Under the exposure to lower concentrations of rare earth elements, the telomerase activity of PBMNCs in the exposed group was higher than that of the control group, and there was no effect on the apoptotic rate of PBMNCs, but promoted the diploid DNA replication and increased the percentages of G₂/M- and S-phase cells.     

Rare earth elements in forest-floor herbs as related to soil conditions and mineral nutrition

Mixtures of rare earth elements (REEs) in fertilizers are widely used in Chinese agriculture to improve crop nutrition. REE concentrations in wild-growing plants, especially herbs, are little known. This study describes differences in the concentrations and proportions of REEs in eight forest-floor herbaceous plants and relates these differences to soil and mineral nutrient conditions. REEs studied were yttrium (Y), lanthanum (La), cerium (Ce), praseodymium (Pr), neodymium (Nd), samarium (Sm), europium (Eu), gadolinium (Gd), terbium (Tb), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), ytterbium (Yb), and lutetium (Lu). Leaf concentrations of sum REEs differed more than one order of magnitude between species, being highest in Anemone nemorosa (10.1 nmol/g dry mass) and lowest in Convallaria majalis (0.66 nmol/g) from the same site. Leaf concentrations of all REEs correlated positively (p<0.001), as did sum REE with calcium (Ca) and strontium (Sr) concentrations (p<0.001). A negative relationship (r=−0.83, (p<0.001) was measured between phosphorus (P) concentrations and sum REE concentrations in leaves. However, the proportions of the single REEs in the REE sum differed among species. In A. nemorosa, 57% of the molar REE sum was taken by Y+La, and only 21% by Ce. The other extreme was Maianthemum bifolium, with 37% La+Y and 41% Ce. These two species had 2.7–3.0% of the REE sum as heavier lanthanides, compared to 4.1–5.2% in the six other species. No clear relationship between soil properties or REE contents and leaf REE concentrations was detected. For La, however, an overrepresentation in leaves prevailed throughout all species compared to soils, whereas particularly Nd, Sm, and Tb had a lower proportion in the leaves of all species than in their soils. Possible uptake mechanisms of REEs in plants are discussed.     

Human biomonitoring of 73 elements in blood,serum, erythrocytes and urine

BackgroundHuman biomonitoring studies of trace elements in biological fluids are mostly limited to a certain number of elements or biological materials. In this study, we describe the significant extension of a biomonitoring to 73 elements being present in concentration ranges from ng/L to g/L in clinically relevant specimens such as blood, serum, erythrocytes and urine.MethodsThe samples were collected from 102 occupationally non-exposed inhabitants of northern Germany. The elements were determined either by inductively coupled plasma tandem mass spectrometry (ICP-MS/MS) in the low concentration range or by inductively coupled plasma optical emission spectrometry (ICP-OES) for essential trace elements and electrolytes.ResultsMean values and selected percentiles of element concentrations are presented for all sample materials. From the results, we calculated the distribution of elements between plasma and blood cells. Application of ICP-MS/MS improves selectivity and accuracy in the determination of elements that are strongly spectrally interfered, such as Cr, Ge, Pd or Ti in blood samples.ConclusionsThis publication provides very valuable information for occupational or environmental hygienists, toxicologists and clinical chemists due to the particularly high number of determined elements and presented concentration ranges.