ELECTRON SPIN RESONANCE STUDIES OF Mn2+ IN FRESHWATER SNAIL SHELLS: S. INGALLSIANA, P. AMPULLACEA, P. CANALICULATA LAMARCK AND FOSSILIZED SNAIL SHELL

2004 ◽  
Vol 18 (26) ◽  
pp. 3419-3428
Author(s):  
S. MEEJOO ◽  
N. UDOMKAN ◽  
P. WINOTAI ◽  
Y. CHAIMANEE

We have studied paramagnetic Mn 2+ ions present in the shells of today's univalve freshwater snails, Sinotaia ingallsiana (FS), Pila ampullaceal (PA), Pomacea canaliculata lamarck (PCL) and the fossilized freshwater snail (FFS), Viviparus which are abundant in Thailand. The FS, PA and AG shells in our study were ground into fine powder. A set of seven samples was each then separately annealed for 2 hours in air atmosphere at 300°C, 400°C, 450°C, 500°C, 550°C, 600°C and 900°C, respectively, while the FFS powder was characterized as received. The FS, PA and PCL shells mainly consist of aragonite and a fraction of calcite. The heat treatments higher than 450°C of the FS, PA and PCL powder samples resulted in an irreversible phase transformation from aragonite to calcite. However, it is found that the FFS shell is mainly made of calcite, with a minor fraction of aragonite. The crystal structure of high temperature annealed FS, PA and PCL samples are quite similar to that of FFS, which indicates that the metamorphosis (aragonite → calcite) in the FFS shell had occurred but not yet completed, although they remained under the pressure and temperature of the Earth's crust over millions of years. Our detailed ESR spectral analyses of FS, PA, PCL and FFS show that Mn 2+ ions enter Ca 2+ sites during a biomineralization process. Typical simulated ESR parameters of FS-500 of Mn 2+ at a uniaxial site of calcite are gx=gy=2.078±0.001, gz=2.002±0.001, Ax=Ay=87.50±1.00 G , Az=89.00±1.00 G and D=115±1 G , respectively. It is surprising to find that the ratio of Mn 2+ concentration present in FFS to those in FS, PA and PCL shells evaluated from ESR spectra is as much as 10:1. It is thus possible to gain some insight of manganese incorporation into the freshwater shells during the biomineralization process.

2006 ◽  
Vol 20 (09) ◽  
pp. 1097-1106 ◽  
Author(s):  
N. UDOMKAN ◽  
P. LIMSUWAN ◽  
Y. CHAIMANEE

Electron spin resonance spectroscopy (ESR) was used to study the Mn 2+ ions in snails of P. canaliculata lamarck (PCL). All these shells are abundant in Thailand. Fractions of aragonite and calcite phase in the shells have been approximately determined by ESR. The PCL shell was ground into fine powders and then four samples were separately annealed for 2 h in air at 400°C, 450°C, 500°C and 600°C, respectively. The phase transition from aragonite to calcite was monitored by X-ray diffractometer (XRD) and electron spin resonance spectrometer (ESR). Our results show that unheated PCL sample is mainly made of aragonite with only a small fraction of calcite. Annealing of the PCL powder sample at the temperature more than 450°C has resulted in the irreversible phase transformation from aragonite to calcite. The analysis of their ESR spectra has shown that Mn 2+ ions partially substituted Ca 2+ in the lattices. Finally, the spin Hamiltonian parameters for Mn 2+ distributed in both aragonite and calcite were evaluated. Our detailed ESR spectral analyses of PCL show that Mn 2+ ions enter Ca 2+ sites during a biomineralization process. Typical simulated ESR parameters of PCL-500 of Mn 2+ at a uniaxial site of calcite are gx=gy=2.078(1), gz=1.999(1), Ax=Ay=87.0 G, Az=89.00 G and D=115 G, respectively. It is thus possible to gain some insight of manganese incorporation into the fresh water shells during the biomineralization process.


2009 ◽  
Vol 23 (09) ◽  
pp. 1243-1247
Author(s):  
NITINAI UDOMKAN ◽  
PICHET LIMSUWAN

We have studied paramagnetic Mn 2+ ions present in the freshwater snail, Sinotaia ingallsiana (FS), Viviparus which are abundant in Thailand. The FS shells in our study were ground into fine powder. A set of seven samples was each then separately annealed for 2 hours in air atmosphere at 300°C, 400°C, 500°C, 600°C, 700°C, 800°C and 900°C, respectively. Our detailed ESR spectral analyses of FS show that Mn 2+ ions enter Ca 2+ sites during a biomineralization process. The hyperfine coupling constant (A) and zero-field splitting (D) in the ESR spectrum of Mn 2+ in calcite and aragonite were determined. The spreading of the non-central allowed transitions was analyzed and the experimental transitions were attributed. For calculating the hyperfine coupling constant, five methods for calculating the zero-field splitting, based on the analysis of the allowed and forbidden transitions, were provided. The values of the hyperfine coupling constant range from 87.50 to 89.00 G and those of the zero-field splitting range from 110.00 to 116.00 G.


Water ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1149
Author(s):  
Mi-Jung Bae ◽  
Eui-Jin Kim ◽  
Young-Seuk Park

Pomacea canaliculata (known as invasive apple snail) is a freshwater snail native to South America that was introduced into many countries (including Asia and North America) as a food source or for organic farming systems. However, it has invaded freshwater ecosystems and become a serious agricultural pest in paddy fields. Water temperature is an important factor determining behavior and successful establishment in new areas. We examined the behavioral responses of P. canaliculata with water temperature changes from 25 °C to 30 °C, 20 °C, and 15 °C by quantifying changes in nine behaviors. At the acclimated temperature (25 °C), the mobility of P. canaliculata was low during the day, but high at night. Clinging behavior increased as the water temperature decreased from 25 °C to 20 °C or 15 °C. Conversely, ventilation and food consumption increased when the water temperature increased from 25 °C to 30 °C. A self-organizing map (an unsupervised artificial neural network) was used to classify the behavioral patterns into seven clusters at different water temperatures. These results suggest that the activity levels or certain behaviors of P. canaliculata vary with the water temperature conditions. Understanding the thermal biology of P. canaliculata may be crucial for managing this invasive snail.


2021 ◽  
Author(s):  
Rob Cowie ◽  
Romi L. Burks ◽  
Amy E. Miller ◽  
Alexandria L. Hill

Abstract P. maculata is a freshwater snail native to a wide geographical area in South America from the Rio de la Plata in Argentina and Uruguay to the Amazon in Brazil. It is commonly confused with any number of similar large apple snails, including the well-known invasive golden apple snail Pomacea canaliculata (listed among '100 of the world's worst invasive species'). Both species have been introduced to South-East and East Asia, although for many years they were not distinguished and the Asian introductions were widely identified as "golden apple snails" and the name P. canaliculata was applied to them. Due to the confusion in species identification, the history of introduction of P. maculata remains somewhat uncertain as does its invasiveness and pest potential. Much of the literature is confounded, for example, the snails illustrated by Cowie (2002) as P. canaliculata are in fact P. maculata. The majority of invasive populations in Asia appear to be P. canaliculata, often not mixed with P. maculata (Hayes et al., 2008; Tran et al., 2008) and the pest potential of P. canaliculata in such cases is clear. However, much less has been written about the invasiveness and pest potential of 'P. maculata'.


1967 ◽  
Vol 45 (12) ◽  
pp. 1831-1839 ◽  
Author(s):  
W. F. Forbes ◽  
P. D. Sullivan

Polycrystalline amino acids, when irradiated with 2537 Å light, afford a variety of electron spin resonance signals. These signals are generally stable at room temperature for relatively long periods of time. For a number of the spectra obtained, there is evidence that more than one radical species contributes to the observed spectra. The signals obtained frequently differ from those obtained on exposure to ionizing radiation. The postulated species formed can often be visualized as being formed by effective hydrogen abstraction from the alkyl-substituted tertiary carbon atom or from the —OH, —SH or —NH group contained in the side chain. For L-phenylalanine a secondary radical is obtained, which is ascribed to a cyclohexadienyl radical.


1979 ◽  
Vol 57 (5) ◽  
pp. 600-602 ◽  
Author(s):  
K. S. Chen ◽  
T. Foster ◽  
J. K. S. Wan

Contact radical ion-pairs of ammonium and fluoro-substituted ketones were generated in photochemical systems and their here-to-fore elusive esr spectra were characterized.


MRS Advances ◽  
2018 ◽  
Vol 3 (32) ◽  
pp. 1831-1836
Author(s):  
C. L. Saiz ◽  
E. Castro ◽  
L. M. Martinez ◽  
S. R. J. Hennadige ◽  
L. Echegoyen ◽  
...  

ABSRTACTIn this article, we report low-temperature electron spin resonance (ESR) investigations carried out on solution processed three-layer inverted solar cell structures: PC61BM/CH3NH3PbI3/PEDOT:PSS/Glass, where PC61BM and PEDOT:PSS act as electron and hole transport layers, respectively. ESR measurements were conducted on ex-situ light (1 Sun) illuminated samples. We find two distinct ESR spectra. First ESR spectra resembles a typical powder pattern, associated with gx = gy = 4.2; gz = 9.2, found to be originated from Fe3+ extrinsic impurity located in the glass substrate. Second ESR spectra contains a broad (peak-to-peak line width ∼ 10 G) and intense ESR signal appearing at g = 2.008; and a weak, partly overlapped, but much narrower (peak-to-peak line width ∼ 4 G) ESR signal at g = 2.0022. Both sets of ESR spectra degrade in intensity upon light illumination. The latter two signals were found to stem from light-induced silicon dangling bonds and oxygen vacancies, respectively. Our controlled measurements confirm that these centers were generated during UV-ozone treatment of the glass substrate –a necessary step to be performed before PEDOT:PSS is spin coated. This work forms a significant step in understanding the light-induced- as well as extrinsic defects in perovskite solar cell materials.


1980 ◽  
Vol 3 ◽  
Author(s):  
E. L. Venturini

ABSTRACTElectron spin resonance (ESR) of dilute paramagnetic ions in nonmagnetic metallic hydrides provides microscopic information about the hydrogen ions in the immediate vicinity of the impurity. By comparing ESR spectra for different host metals and several hydrogen/metal ratios, one can determine material properties including host lattice symmetry, phase boundaries and occupation of available sites by hydrogen. Examples are presented of ESR of dilute Er in group IIIB and IVB metal hydrides, demonstrating the sensitivity and versatility of ESR as a spectroscopic technique.


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