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Author(s): Thomas R. Watters (corresponding author) [1]; Carl J. Leuschen [2]; Jeffrey J. Plaut [3]; Giovanni Picardi [4]; Ali Safaeinili [3]; Stephen M. Clifford [5]; William M. Farrell [6]; Anton [...]

Currently, the absolute chronology of Martian rocks, deposits and events is based mainly on crater counting and remains highly imprecise with epoch boundary uncertainties in excess of 2 billion years. Answers to key questions concerning the comparative origin and evolution of Mars and Earth will not be forthcoming without a rigid Martian chronology, enabling the construction of a time scale comparable to Earth's. Priorities for exploration include calibration of the cratering rate, dating major volcanic and fluvial events and establishing chronology of the polar layered deposits. If extinct and/or extant life is discovered, the chronology of the biosphere will be of paramount importance. Many radiometric and cosmogenic techniques applicable on Earth and the Moon will apply to Mars after certain baselines (e.g. composition of the atmosphere, trace species, chemical and physical characteristics of Martian dust) are established. The high radiation regime may pose a problem for dosimetry-based techniques (e.g. luminescence). The unique isotopic composition of nitrogen in the Martian atmosphere may permit a Mars-specific chronometer for tracing the time-evolution of the atmosphere and of lithic phases with trapped atmospheric gases. Other Mars-specific chronometers include measurement of gas fluxes and accumulation of platinuqa group elements (PGE) in the regolith. Putting collected samples into geologic context is deemed essential, as is using-multiple techniques on multiple samples. If in situ measurements are restricted to a single technique it must be shown to give consistent results on multiple samples, but in all cases, using two or more techniques (e.g. on the same lander) will reduce error. While there is no question that returned samples will yield the best ages, in situ techniques have the potential to be flown on multiple missions providing a larger data set and broader context in which to place the more accurate dates. Keywords: Mars; Chronology: Surficial processes; Dating

In this paper we consider the hydraulic and thermal conditions that gave rise to the elevated source regions of the Late Hesperian outflow channels and explore their implications for the evolution of the Martian hydrosphere. We find that if the outflow channel floodwaters were derived from a subpermafrost aquifer, then it implies that, throughout the planet's first billion years of evolution, as much as one third of its surface was covered by standing bodies of water and ice. Following the development of the global dichotomy, the bulk of this water would have existed as an ice-covered ocean in the northern plains. We demonstrate that the progressive crustal assimilation of this early surface reservoir of [H.sub.2]O (punctuated by possible episodes of less extensive flooding) was a natural consequence of the planet's subsequent climatic and geothermal evolution--potentially cycling the equivalent of a km-deep global ocean of water through the atmosphere and subsurface every ~[10.sup.9] years. In response to the long-term decline in planetary heat flow, the progressive cold-trapping of [H.sub.2]O into the growing cryosphere is expected to have significantly depleted the original inventory of groundwater--a development that could well explain the apparent decline in outflow channel activity observed during the Amazonian. Although primarily a theoretical analysis, our findings appear remarkably consistent with the geomorphic and topographic evidence that Mars once possessed a primordial ocean and that a substantial relic of that body continues to survive as massive ice deposits within the northern plains. Confirmation of the presence of such deposits, combined with the potential detection of a global-scale groundwater system, would provide persuasive support for the validity of this analysis. Key Words: Mars, surface; Mars, atmosphere; Mars, climate; ices; exobiology.

Abstract Background Previous phylogenetic analyses of African elephants have included limited numbers of forest elephant samples. A large-scale assessment of mitochondrial DNA diversity in forest elephant populations here reveals a more complex evolutionary history in African elephants as a whole than two-taxon models assume. Results We analysed hypervariable region 1 of the mitochondrial control region for 71 new central African forest elephants and the mitochondrial cytochrome b gene from 28 new samples and compare these sequences to other African elephant data. We find that central African forest elephant populations fall into at least two lineages and that west African elephants (both forest and savannah) share their mitochondrial history almost exclusively with central African forest elephants. We also find that central African forest populations show lower genetic diversity than those in savannahs, and infer a recent population expansion. Conclusion Our data do not support the separation of African elephants into two evolutionary lineages. The demographic history of African elephants seems more complex, with a combination of multiple refugial mitochondrial lineages and recurrent hybridization among them rendering a simple forest/savannah elephant split inapplicable to modern African elephant populations.

Objectives: Curing light sources propel the photopolymerization process. The effect of 3 curing units on polymerization shrinkage and depth of cure was investigated. Method and Materials: The curing lights were a conventional and a soft-start quartz-tungstenhalogen (QTH) light source and a light-emitting diode (LED) source. The soft-start QTH and LED intensity outputs were 9% and 17% less than the conventional QTH source, respectively. For a 40-second light cure, the light energy was 32% and 14% lower, respectively. The light sources were applied to 4 restorative composites (microfilled, 2 hybrids, and nanofilled). For each light unit-composite combination, the development of postgel shrinkage during polymerization was measured with strain gauges (n = 15), and the Knoop hardness was tested at 0.5-mm-depth increments to assess degree of cure 15 minutes after polymerization (n = 5). The results were statistically analyzed with 2-way ANOVA at .05 significance level, followed by pairwise comparisons. Results: Both factors, light source and composite, significantly affected postgel shrinkage and hardness (P < .05). The conventional QTH unit generally produced the highest shrinkage and hardness (at composite surface and 2-mm depth). The soft-start QTH unit generated the least shrinkage but achieved the lowest depth of cure. The resulting values for the LED unit were mostly in between the results of the other 2 units. Conclusion: Curing lights should provide sufficient light energy to thoroughly cure composite restorations, which might be achieved without compromising shrinkage stresses if initial intensity is reduced. [ABSTRACT FROM AUTHOR]

The search for evidence of past or present life on Mars is the principal objective of the 2020 ESA-Roscosmos ExoMars Rover mission. If such evidence is to be found anywhere, it will most likely be in the subsurface, where organic molecules are shielded from the destructive effects of ionizing radiation and atmospheric oxidants. For this reason, the ExoMars Rover mission has been optimized to investigate the subsurface to identify, understand, and sample those locations where conditions for the preservation of evidence of past life are most likely to be found. The Water Ice Subsurface Deposit Observation on Mars (WISDOM) ground-penetrating radar has been designed to provide information about the nature of the shallow subsurface over depth ranging from 3 to 10 m (with a vertical resolution of up to 3 cm), depending on the dielectric properties of the regolith. This depth range is critical to understanding the geologic evolution stratigraphy and distribution and state of subsurface H2O, which provide important clues in the search for life and the identification of optimal drilling sites for investigation and sampling by the Rover's 2-m drill. WISDOM will help ensure the safety and success of drilling operations by identification of potential hazards that might interfere with retrieval of subsurface samples. Key Words: Ground penetrating radar-Martian shallow subsurface-ExoMars. Astrobiology 17, 565-584. [ABSTRACT FROM AUTHOR]

Identifying microbial pathogens with zoonotic potential in wild-living primates can be important to human health, as evidenced by human immunodeficiency viruses types 1 and 2 (HIV-1 and HIV-2) and Ebola virus. Simian foamy viruses (SFVs) are ancient retroviruses that infect Old and New World monkeys and apes. Although not known to cause disease, these viruses are of public health interest because they have the potential to infect humans and thus provide a more general indication of zoonotic exposure risks. Surprisingly, no information exists concerning the prevalence, geographic distribution, and genetic diversity of SFVs in wild-living monkeys and apes. Here, we report the first comprehensive survey of SFVcpz infection in free-ranging chimpanzees (Pan troglodytes) using newly developed, fecal-based assays. Chimpanzee fecal samples (n = 724) were collected at 25 field sites throughout equatorial Africa and tested for SFVcpzspecific antibodies (n = 706) or viral nucleic acids (n = 392). SFVcpz infection was documented at all field sites, with prevalence rates ranging from 44% to 100%. In two habituated communities, adult chimpanzees had significantly higher SFVcpz infection rates than infants and juveniles, indicating predominantly horizontal rather than vertical transmission routes. Some chimpanzees were co-infected with simian immunodeficiency virus (SIVcpz); however, there was no evidence that SFVcpz and SIVcpz were epidemiologically linked. SFVcpz nucleic acids were recovered from 177 fecal samples, all of which contained SFVcpz RNA and not DNA. Phylogenetic analysis of partial gag (616 bp), pol-RT (717 bp), and pol-IN (425 bp) sequences identified a diverse group of viruses, which could be subdivided into four distinct SFVcpz lineages according to their chimpanzee subspecies of origin. Within these lineages, there was evidence of frequent superinfection and viral recombination. One chimpanzee was infected by a foamy virus from a Cercopithecus monkey species, indicating cross-species transmission of SFVs in the wild. These data indicate that SFVcpz (i) is widely distributed among all chimpanzee subspecies; (ii) is shed in fecal samples as viral RNA; (iii) is transmitted predominantly by horizontal routes; (iv) is prone to superinfection and recombination; (v) has co-evolved with its natural host; and (vi) represents a sensitive marker of population structure that may be useful for chimpanzee taxonomy and conservation strategies. [ABSTRACT FROM AUTHOR]

Abstract: Nuclear integrations of mitochondrial DNA (Numts) are widespread in many taxa and if left undetected can confound phylogeny interpretation and bias estimates of mitochondrial DNA (mtDNA) diversity. This is particularly true in gorillas, where recent studies suggest multiple integrations of the first hypervariable (HV1) domain of the mitochondrial control region. Problems can also arise through the inadvertent incorporation of artifacts produced by in vitro recombination between sequence types during polymerase chain reaction amplification. This issue has attracted little attention yet could potentially exacerbate errors in databases already contaminated by Numts. Using a set of existing diagnostic tools, this study set out to systematically inventory Numts and PCR recombinants in a gorilla HV1 sequence database and address the degree to which existing public databases are contaminated. Phylogenetic analysis revealed three distinct gorilla HV1 Numt groups (I, II, and III) that could be readily differentiated from mtDNA sequences by Numt-specific diagnostic sites and sequence-based motifs. Several instances of genuine recombination were also identified by a suite of detection methods. The location of putative breakpoints was identified by eye and by likelihood analysis. Findings from this study reveal widespread nuclear contamination of gorilla HV1 GenBank databases and underline the importance of recognizing not only Numts but also PCR recombinant artifacts as potential sources of data contamination. Guidelines for the routine identification of Numts and in vitro recombinants are presented and should prove useful in the detection of similar artifacts in other species mtDNA databases. [Copyright &y& Elsevier]

Background: Previous phylogenetic analyses of African elephants have included limited numbers of forest elephant samples. A large-scale assessment of mitochondrial DNA diversity in forest elephant populations here reveals a more complex evolutionary history in African elephants as a whole than two-taxon models assume. Results: We analysed hypervariable region 1 of the mitochondrial control region for 71 new central African forest elephants and the mitochondrial cytochrome b gene from 28 new samples and compare these sequences to other African elephant data. We find that central African forest elephant populations fall into at least two lineages and that west African elephants (both forest and savannah) share their mitochondrial history almost exclusively with central African forest elephants. We also find that central African forest populations show lower genetic diversity than those in savannahs, and infer a recent population expansion. Conclusion: Our data do not support the separation of African elephants into two evolutionary lineages. The demographic history of African elephants seems more complex, with a combination of multiple refugial mitochondrial lineages and recurrent hybridization among them rendering a simple forest/savannah elephant split inapplicable to modern African elephant populations. [ABSTRACT FROM AUTHOR]

The geographical distribution of genetic variation within western lowland gorillas (Gorilla gorilla gorilla) was examined to clarify the population genetic structure and recent evolutionary history of this group. DNA was amplified from shed hair collected from sites across the range of the three traditionally recognized gorilla subspecies: western lowland (G. g. gorilla), eastern lowland (G. g. graueri) and mountain (G. g. beringei) gorillas. Nucleotide sequence variation was examined in the first hypervariable domain of the mitochondrial control region and was much higher in western lowland gorillas than in either of the other two subspecies. In addition to recapitulating the major evolutionary split between eastern and western lowland gorillas, phylogenetic analysis indicates a phylogeographical division within western lowland gorillas, one haplogroup comprising gorilla populations from eastern Nigeria through to southeast Cameroon and a second comprising all other western lowland gorillas. Within this second haplogroup, haplotypes appear to be partitioned geographically into three subgroups: (i) Equatorial Guinea, (ii) Central African Republic, and (iii) Gabon and adjacent Congo. There is also evidence of limited haplotype admixture in northeastern Gabon and southeast Cameroon. The phylogeographical patterns are broadly consistent with those predicted by current Pleistocene refuge hypotheses for the region and suggest that historical events have played an important role in shaping the population structure of this subspecies. [ABSTRACT FROM AUTHOR]

Discusses books claiming for the reconsideration of Ernest Hemingway's place in the American literary canon. Includes `Reading Hemingway,' by Miriam B. Mandel; `Hemingway's Genders,' by Nancy R. Comley; `Critical Essays on Ernest Hemingway's A Farewell to Arms,' by George Monteiro.

A personal narrative is presented which explores the author's experience of dealing with the difficulties of having a son with fetal alcohol spectrum disorder (FASD).