ABSTRACT The Laboratoire de Mesure du Carbone 14 (LMC14) has operated a radiocarbon dating laboratory for almost twenty years with ARTEMIS, the Accelerator Mass Spectrometer (AMS) based on a NEC 9SDH-2 Pelletron tandem accelerator. A first status report describing the chemical pretreatment methods was published in 2017 (Dumoulin et al. 2017). This article summarizes updates of the routine procedures and presents new protocols. The quality checks in place at the LMC14 and results obtained for the GIRI international inter-comparison are reported. New protocols developed by the laboratory over the last five years are described with the preparation of iron, lead white, cellulose, calcium oxalate, and mortar. This report also provides a summary of practical information for sample preparation and can help the laboratory users who provide samples and publish results to better understand all the work behind a 14 C dating.

ABSTRACT In 2001, five French public organizations (CNRS, CEA, IRD, IRSN, and the Ministère de la Culture) signed an agreement to purchase a new accelerator mass spectrometer to provide radiocarbon dating services at the national level. The Laboratoire de Mesure du Carbone 14 (LMC14) was set up in Saclay (France) around ARTEMIS, an AMS system based on a 3MV Pelletron from NEC and installed in early 2003. In 2015, the LMC14 joined the Laboratoire des Sciences du Climat et de l’Environnement, making it possible to develop research projects in addition to the service activity and since 2021, the LMC14 has been a member of the IAEA Collaborating Centre “Atoms for Heritage” at the Université Paris-Saclay. Since 2003, 70,000 samples have been measured. Two-thirds of the samples have been prepared on site and one-third in two associated laboratories in Paris and Lyon. Over the past years, the LMC14 has participated in several international inter-comparisons and has continuously improved its capabilities by developing new protocols for preparation and measurement. In this paper, the radiocarbon dating services of the last 20 years for research institutions, museums and environmental monitoring are reviewed and recent results from environmental and archaeological research programs are highlighted.

ABSTRACTEstuaries and deltas are crucial zones to better understand the interactions between continents and oceans, and to characterize the mineralization and burial of different sources of organic matter (OM) and their effect on the carbon cycle. In the present study, we focus on the continental shelf of the northwest Mediterranean Sea near the Rhône river delta. Sediment cores were collected and pore waters were sampled at different depths at one station (Station E) located on this shelf. For each layer, measurements of dissolved inorganic carbon concentration (DIC) and its isotopic composition (δ13C and Δ14C) were conducted and a mixing model was applied to target the original signature of the mineralized OM. The calculated δ13C signature of the mineralized organic matter is in accordance with previous results with a δ13COM of marine origin that is not significantly impacted by the terrestrial particulate inputs from the river. The evolution with depth of Δ14C shows two different trends indicating two different Δ14C signatures for the mineralised OM. In the first 15 cm, the mineralized OM is modern with a Δ14COM = 100 ± 17‰ and corresponds to the OM produced during the nuclear period of the last 50 years. Deeper in the sediment, the result is very different with a depleted value Δ14COM = –172 ± 60‰ which corresponds to the pre-nuclear period. In these two cases, the marine substrate was under the influence of the local marine reservoir effect with more extreme Δ14C results. These differences can be largely explained by the influence of the river plume on the local marine DIC during these two periods.

AbstractThe main objective of this report is to present the dating process routinely applied to different types of samples at the Laboratoire de Mesure du Carbone 14 (LMC14). All the results and protocols refer to our procedures over the last 5 years. A description of the sorting and chemical pretreatments of the samples as well as the extraction and graphitization of CO2 are reported. Our last study concerning the degradation of the blank level according to the storage time of the targets between graphitization and accelerator mass spectrometry (AMS) measurement is also presented. This article also provides information on how to submit a valid laboratory sample. We give details relating to sampling procedures on site as well as contamination issues relative to the 14C dating methodology.

The new facility Artemis was installed in 2003 in Saclay, France. This 3MV NEC Pelletron is dedicated to high-precision radiocarbon measurements for French 14C laboratories. We will present information on Artemis along with our sample preparation methods. Results from measurements on some intercalibration samples will be given along with the val- ues of measured blanks. Finally, we report on some problems we have encountered when measuring sputter cathodes with high CH- outputs.

The new facility Artemis was installed in 2003 in Saclay, France. This 3MV NEC Pelletron is dedicated to high-precision radiocarbon measurements for French 14C laboratories. We will present information on Artemis along with our sample preparation methods. Results from measurements on some intercalibration samples will be given along with the values of measured blanks. Finally, we report on some problems we have encountered when measuring sputter cathodes with high CH− outputs.

The objective of this study is to examine the growth status of children post-treatment with the ketogenic diet. The ketogenic diet is one of the most effective therapies for intractable seizures in the pediatric population. There are 5 simple-articles that reported ketogenic diet patients’ growth status, but there is no study that examines the children’s growth status post-ketogenic diet.

A short-term retrospective test trial was carried out using 90 open-pollinated families representing 30 provenances of black spruce (Picea mariana (Mill.) BSP) from Quebec. Seedlings were transplanted on three sites along a latitudinal gradient, and eleven growth and phenological traits were measured during the second and the third growing seasons. Analyses of variance indicated for most of the traits significant differences among provenances and families-within-provenances. Principal component analysis was used to summarize the variation observed among provenances into two principal components, which accounted for 79% of the total variation for all traits. Regression models developed to relate each trait and the principal component scores to geoclimatic variables explained between 55% and 86% of the variation observed among provenances. Variation in growth traits and phenological traits appeared to be related to geoclimatic factors. The models were validated using data from a range-wide provenance test, and relative risks associated with seed source transfer were estimated. The R-2 values between the transfer risk and the provenance heights ranged from 0.02 to 0.58, whereas they were slightly lower for diameters. On average, the relative risks varied from 36% to 67%. Individual provenance values ranged from 4% to 94%. A geographic information system tool was designed to assist the forest managers in making seed transfer decisions.

Profilin is an actin monomer-binding protein implicated in the polymerization of actin filaments. In the budding yeast Saccharomyces cerevisiae, the pfy1-111 rho2delta double mutant has severe growth and actin cytoskeletal defects. The GEA1 and GEA2 genes, which code for paralog guanosine exchange factors for Arf proteins, were identified as multicopy suppressors of the mutant phenotype. These two genes restored the polarized distribution of actin cortical patches and produced visible actin cables in both the pfy1-111 rho2delta and pfy1delta cells. Thus, overexpression of GEA1 or GEA2 bypassed the requirement for profilin in actin cable formation. In addition, gea1 gea2 double mutants showed defects in budding and in actin cytoskeleton organization, while overexpression of GEA1 or GEA2 led to the formation of supernumerary actin cable-like structures in a Bni1p/Bnr1p-dependent manner. The ADP-ribosylation factor Arf3p may be a target of Gea1p/Gea2p, since overexpression of ARF3 partially suppressed the profilin-deficient phenotype and a deletion of ARF3 exacerbated the phenotype of a pfy1-111 mutant. Gea1p, Gea2p, Arf1p, and Arf2p but not Arf3p are known to function in vesicular transport between the endoplasmic reticulum and the Golgi. In this work, we demonstrate a role for Gea1p, Gea2p, and Arf3p in the organization of the actin cytoskeleton.

Primers previously developed to amplify specific non-coding regions of the mitochondrial genome in Angiosperms, and new primers for additional non-coding mtDNA regions, were tested for their ability to direct DNA amplification in 12 conifer taxa and to detect sequence-tagged-site (STS) polymorphisms within and among eight species in Picea. Out of 12 primer pairs, nine were successful at amplifying mtDNA in most of the taxa surveyed. In conifers, indels and substitutions were observed for several loci, allowing them to distinguish between families, genera and, in some cases, between species within genera. In Picea, interspecific polymorphism was detected for four loci, while intraspecific variation was observed for three of the mtDNA regions studied. One of these (SSU rRNA V1 region) exhibited indel polymorphisms, and the two others ( nad1 intron b/c and nad5 intron1) revealed restriction differences after digestion with Sau3AI (PCR-RFLP). A fourth locus, the nad4L- orf25 intergenic region, showed a multibanding pattern for most of the spruce species, suggesting a possible gene duplication. Maternal inheritance, expected for mtDNA in conifers, was observed for all polymorphic markers except the intergenic region nad4L- orf25. Pooling of the variation observed with the remaining three markers resulted in two to six different mtDNA haplotypes within the different species of Picea. Evidence for intra-genomic recombination was observed in at least two taxa. Thus, these mitotypes are likely to be more informative than single-locus haplotypes. They should be particularly useful for the study of biogeography and the dynamics of hybrid zones.

Black spruce (Picea mariana [B.S.P.] Mill.) and red spruce (Picea rubens Sarg.) are two conifer species known to hybridize naturally in northeastern North America. We hypothesized that there is a progenitor-derivative relationship between these two taxa and conducted a genetic investigation by using sequence-tagged-site markers of expressed genes. Based on the 26 sequence-tagged-site loci assayed in this study, the unbiased genetic identity between the two taxa was quite high with a Value of 0.920. The mean number of polymorphic loci, the mean number of alleles per polymorphic locus, and the average observed heterozygosity were lower in red spruce (P = 35%. A(P) = 2.1. H-O = 0.069) than in black spruce (P = 54%, A(P) = 2.9, H-O = 0.103). No unique alleles were found in red spruce, and the observed patterns of allele distribution indicated that the genetic diversity of red spruce was essentially a subset of that found in black spruce. When considered in combination with ecological evidence and simulation results, these observations clearly support the existence of a progenitor-derivative relationship and suggest that the reduced level of genetic diversity in red spruce may result from allopatric speciation through glaciation-induced isolation of a preexisting black spruce population during the Pleistocene era. Our observations signal a need for a thorough reexamination of several conifer species complexes in which natural hybridization is known to occur.

Using species‐specific random amplified polymorphic DNA (RAPD) markers and morphological characters, natural hybridization between the closely related black spruce Picea mariana (Mill.) B.S.P. and red spruce P. rubens Sarg. was evaluated in natural populations from north‐eastern North America. Sampling included populations from both areas of allopatry and also 14 populations from part of the area of sympatry located in the province of Québec and covering several thousands of square kilometres. Classification results from RAPD species‐specific markers and from a discriminant function based on morphology were compared. Molecular analysis of the allopatric populations indicated a small amount of interspecific gene leakage with no asymmetric directionality to introgression. A high occurrence of hybrid/introgressant individuals was observed within sympatric populations, suggesting weak reproductive isolation. As expected, the detection of such individuals was more efficient using molecular markers than with morphological traits. The hybrid zone appeared extensive with variable species structure and, in some stands, the main component composed of hybrid/introgressant trees. Implications for the genecology and genetic management of these species are discussed.

Species-specific molecular markers were designed to assist in the identification of closely related black spruce (Picea mariana [B.S.P.] Mill.) and red spruce (P. rubens Sarg.) in northeastern North America. Trees from six provenances of black spruce and three provenances of red spruce were sampled from outside the sympatric zone. They were first classified using a composite index of five qualitative morphological traits. The species-specific genetic markers were developed using random amplified polymorphic DNAs (RAPD) and a combination of bulk sample and individual tree analyses. Each species bulk sample was constructed from DNAs obtained from 12 trees that were from outside the sympatric zone and showed a morphological composite index specific of each species. A total of 161 primers were screened with the bulk samples. From these, 52 primers showing segregating fingerprints were further screened with the individual trees. Most of the markers observed were shared by the two species, and there was less diversity in P. rubens. A small number of markers were found to be monomorphic or nearly monomorphic and specific to either P. mariana or P. rubens. These markers remained species-specific when F1 progenies derived from independent intraspecific crosses were screened, and they were subsequently found to co-segregate in hybrids derived from independent interspecific crosses here used as controls.