scholarly journals Comparative survival analyses among captive chimpanzees (Pan troglodytes) in America and Japan

PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e11913
Author(s):  
Judy Che-Castaldo ◽  
Kristin Havercamp ◽  
Koshiro Watanuki ◽  
Tetsuro Matsuzawa ◽  
Satoshi Hirata ◽  
...  
Keyword(s):  
Life History ◽  
Pan Troglodytes ◽  
Life Histories ◽  
Ex Situ ◽  
First Year ◽  
Record Keeping ◽  
Species Comparisons ◽  
Survival Patterns ◽  
Birth Type

Detailed, long-term datasets on the life histories of long-lived species such as great apes are necessary to understand their survival patterns but are relatively rare. Such information requires prolonged and consistent record-keeping over many generations, so for chimpanzees (Pan troglodytes), this equates to many decades of input. As life history variables can be altered by differences in environmental influences (whether natural or artificial), there is substantial value to being able to compare across populations. Here, we present the first comparative analysis of life history data for two ex situ chimpanzee populations residing in North America (1975–2020; n = 730) and Japan (1980–2020; n = 660). Overall, survival patterns were similar between regions, and the median life expectancy from birth is estimated at 35.7 (95% CI = [32.4–40.0]) years for females and 30.1 (27.3–34.3) years for males across both populations. Females who survive to their first birthday are estimated to survive 42.4 (40.0–46.3) years and males 35.5 (32.6–38.0) years. We found that birth type (wild-born or captive-born) did not influence survival patterns in either population, but there were differential effects of sex on longevity. In the America population, males had higher mortality rates than females, whereas in the Japan population we found no differences between the sexes. First year mortality did not differ between populations for males (18–20%), but for females it was lower in America (15%) compared to Japan (25%). Survival patterns of chimpanzees in the present study will be useful for future investigation into potential causes of regional differences and cross-species comparisons.

Benthic Life Histories: Summary and Future Needs

1979 ◽  
Vol 36 (3) ◽  
pp. 342-345 ◽  
Author(s):  
T. F. Waters
Keyword(s):  
Life History ◽  
Physical Environment ◽  
Life Histories ◽  
Future Research ◽  
Life History Stages ◽  
History Information ◽  
History Of ◽  
Taxonomic Methods ◽  
Key Words Life History

The symposium indicated many ways in which greater knowledge of benthic life histories can be used to develop and improve techniques such as sampling, taxonomic methods, and bioassays. Benthic organisms' diet and physical environment, factors variable in nature, were shown to be capable of modifying certain life history features such as growth rate and voltinism. The lack of accumulated life history data and the need to tailor sampling schedules to life history events were commonly identified elements in the symposium. Future research needs included (1) basic data on benthic life history, (2) improved taxonomy of immature benthic invertebrates, and (3) understanding the entire life history of an organism in relation to the seasonal progression of its environment. Management implications of benthic life history information included more applicable data from long-term bioassays on all life history stages, and improved management of stream fisheries through habitat alteration to manipulate benthic production. Key words: life history, benthos, symposium

Constraints in the evolution of life histories

1991 ◽  
Vol 332 (1262) ◽  
pp. 3-13 ◽  
Keyword(s):  
Life History ◽  
Life Histories ◽  
Ecological Impact ◽  
Genetic Studies ◽  
Local Optima ◽  
Trade Offs ◽  
Evolution Of Life ◽  
Diversity Of Life ◽  
Irreversible Evolution

The life history favoured by natural selection maximizes fitness, and this implies maximization of fecundity and survival at all ages. The observed diversity in life histories suggests that there are constraints on what can be achieved in practice. Functional constraints occur if only certain combinations of age-specific fertility and survival are possible, either because of the physiology of the organism or because of the ecological impact of its environment. The resulting constrained optimization means that the organism is involved in making trade-offs between life-history characters. A major task for the future is the measurement of trade-off functions in the environment in which the life-history evolved. Natural variation between individuals and populations, genetic studies and experimental manipulations have all been used to detect trade-offs. The last two methods are the most satisfactory, and can be complementary. Experimental manipulations are at their best when based on sound physiological understanding of the traits under manipulation. Constraints can also operate on the long-term. Local optima, evolutionary lags and irreversible evolution may all have contributed to the diversity of life histories.

scholarly journals A complex interplay between balancing selection and introgression maintains a genus-wide alternative life-history strategy.

2021 ◽  
Author(s):  
kalle tunström ◽  
Alyssa Woronik ◽  
Joseph J Hanly ◽  
Pasi Rastas ◽  
Anton Chichvarkhin ◽  
...  
Keyword(s):  
Life History ◽  
Life Histories ◽  
Balancing Selection ◽  
Genetic Locus ◽  
Regulatory Region ◽  
Life History Strategy ◽  
Life History Strategies ◽  
Pigment Synthesis ◽  
Evolutionary Forces

Alternative life-history strategies (ALHS) are genetic polymorphisms generating phenotypes differing in life histories that generally arise due to metabolic resource allocation tradeoffs. Althouigh ALHS are often be limited to a single sex or populations of a species, they can, in rare cases, be found among several species across a genus. In the butterfly genus Colias, at least a third of the species have a female limited ALHS called Alba. While many females develop brightly pigmented wings, Alba females reallocate nitrogen resources used in pigment synthesis to reproductive development, producing white-winged, more fecund females. Whether this ALHS evolved once or many times, and whether it has moved among species via introgression or been maintained via long-term balancing selection, has not been established. Answering these questions presents an opportunity to investigate the genetic basis and evolutionary forces acting upon ALHS, which have rarely been studied at a genus level. Here we identify the genetic locus of Alba in a second Colias species, allowing us to compare this with previous results in a larger phylogenetic context. Our findings suggest Alba has a singular origin and has been maintained in Colias through a combination of balancing selection and introgression for nearly one million years and at least as many generations. Finally, using CRISPR/Cas9 deletions in the cis-regulatory region of the Alba allele, we demonstrate that the Alba allele is a modular enhancer for the BarH1 gene and is necessary for the induction of the ALHS, which potentially facilitates its long-term persistence in the genus.

CARDIOLOGICAL PROBLEMS IN THE LONG-TERM PERIOD IN CHILDREN AFTER AORTIC COARCTATION SURGERY TREATMENT IN THE FIRST YEAR OF LIFE

2018 ◽  
Vol 97 (3) ◽  
pp. 24-28
Author(s):  
M.R. Tumanyan ◽  
◽  
A.A. Svobodov ◽  
E.G. Levchenko ◽  
A.G. Anderson ◽  
...  
Keyword(s):  
Aortic Coarctation ◽  
First Year ◽  
First Year Of Life

Muenke syndrome: long-term outcome of a syndrome-specific treatment protocol

2019 ◽  
Vol 24 (4) ◽  
pp. 415-422 ◽  
Author(s):  
Bianca K. den Ottelander ◽  
Robbin de Goederen ◽  
Marie-Lise C. van Veelen ◽  
Stephanie D. C. van de Beeten ◽  
Maarten H. Lequin ◽  
...  
Keyword(s):  
Treatment Protocol ◽  
First Year ◽  
Ventricular Size ◽  
Term Outcome ◽  
Long Term Outcome ◽  
Skull Growth ◽  
Muenke Syndrome ◽  
First Year Of Life

OBJECTIVEThe authors evaluated the long-term outcome of their treatment protocol for Muenke syndrome, which includes a single craniofacial procedure.METHODSThis was a prospective observational cohort study of Muenke syndrome patients who underwent surgery for craniosynostosis within the first year of life. Symptoms and determinants of intracranial hypertension were evaluated by longitudinal monitoring of the presence of papilledema (fundoscopy), obstructive sleep apnea (OSA; with polysomnography), cerebellar tonsillar herniation (MRI studies), ventricular size (MRI and CT studies), and skull growth (occipital frontal head circumference [OFC]). Other evaluated factors included hearing, speech, and ophthalmological outcomes.RESULTSThe study included 38 patients; 36 patients underwent fronto-supraorbital advancement. The median age at last follow-up was 13.2 years (range 1.3–24.4 years). Three patients had papilledema, which was related to ophthalmological disorders in 2 patients. Three patients had mild OSA. Three patients had a Chiari I malformation, and tonsillar descent < 5 mm was present in 6 patients. Tonsillar position was unrelated to papilledema, ventricular size, or restricted skull growth. Ten patients had ventriculomegaly, and the OFC growth curve deflected in 3 patients. Twenty-two patients had hearing loss. Refraction anomalies were diagnosed in 14/15 patients measured at ≥ 8 years of age.CONCLUSIONSPatients with Muenke syndrome treated with a single fronto-supraorbital advancement in their first year of life rarely develop signs of intracranial hypertension, in accordance with the very low prevalence of its causative factors (OSA, hydrocephalus, and restricted skull growth). This illustrates that there is no need for a routine second craniofacial procedure. Patient follow-up should focus on visual assessment and speech and hearing outcomes.

Engineering for good: A case of community driven engineering innovation

2018 ◽  
Vol 6 (1) ◽  
Author(s):  
Chinweike Eseonu ◽  
Martin A Cortes
Keyword(s):  
Engineering Students ◽  
Technology Innovation ◽  
Local Communities ◽  
First Year ◽  
Engineering Curriculum ◽  
Engineering Design Process ◽  
The World ◽  
The University ◽  
Social Consideration

There is a culture of disengagement from social consideration in engineering disciplines. This means that first year engineering students, who arrive planning to change the world through engineering, lose this passion as they progress through the engineering curriculum. The community driven technology innovation and investment program described in this paper is an attempt to reverse this trend by fusing community engagement with the normal engineering design process. This approach differs from existing project or trip based approaches – outreach – because the focus is on local communities with which the university team forms a long-term partnership through weekly in-person meetings and community driven problem statements – engagement.

Hormones and Behavior

2019 ◽  
pp. 11-26
Author(s):  
Maren N. Vitousek ◽  
Laura A. Schoenle
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Traits ◽  
Developmental Plasticity ◽  
Endocrine System ◽  
Phenotypic Traits ◽  
Social Environments ◽  
Trade Offs ◽  
And Behavior

Hormones mediate the expression of life history traits—phenotypic traits that contribute to lifetime fitness (i.e., reproductive timing, growth rate, number and size of offspring). The endocrine system shapes phenotype by organizing tissues during developmental periods and by activating changes in behavior, physiology, and morphology in response to varying physical and social environments. Because hormones can simultaneously regulate many traits (hormonal pleiotropy), they are important mediators of life history trade-offs among growth, reproduction, and survival. This chapter reviews the role of hormones in shaping life histories with an emphasis on developmental plasticity and reversible flexibility in endocrine and life history traits. It also discusses the advantages of studying hormone–behavior interactions from an evolutionary perspective. Recent research in evolutionary endocrinology has provided insight into the heritability of endocrine traits, how selection on hormone systems may influence the evolution of life histories, and the role of hormonal pleiotropy in driving or constraining evolution.

The ontogeny of long-term memory over the first year-and-a-half of life

1998 ◽  
Vol 32 (2) ◽  
pp. 69-89 ◽  
Author(s):  
Kristin Hartshorn ◽  
Carolyn Rovee-Collier ◽  
Peter Gerhardstein ◽  
Ramesh S. Bhatt ◽  
Teresa L. Wondoloski ◽  
...  
Keyword(s):  
Long Term Memory ◽  
First Year ◽  
Term Memory

scholarly journals Contributions to Management Strategies in the NE Atlantic Regarding the Life History and Population Structure of a Key Deep-Sea Fish (Mora moro)

Biology ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 522
Author(s):  
Régis Santos ◽  
Wendell Medeiros-Leal ◽  
Osman Crespo ◽  
Ana Novoa-Pabon ◽  
Mário Pinho
Keyword(s):  
Population Structure ◽  
Life History ◽  
Deep Sea ◽  
Management Strategies ◽  
Size Composition ◽  
Large Size ◽  
The Common ◽  
Fishing Impacts ◽  
Sea Fish

With the commercial fishery expansion to deeper waters, some vulnerable deep-sea species have been increasingly captured. To reduce the fishing impacts on these species, exploitation and management must be based on detailed and precise information about their biology. The common mora Mora moro has become the main deep-sea species caught by longliners in the Northeast Atlantic at depths between 600 and 1200 m. In the Azores, landings have more than doubled from the early 2000s to recent years. Despite its growing importance, its life history and population structure are poorly understood, and the current stock status has not been assessed. To better determine its distribution, biology, and long-term changes in abundance and size composition, this study analyzed a fishery-dependent and survey time series from the Azores. M. moro was found on mud and rock bottoms at depths below 300 m. A larger–deeper trend was observed, and females were larger and more abundant than males. The reproductive season took place from August to February. Abundance indices and mean sizes in the catch were marked by changes in fishing fleet operational behavior. M. moro is considered vulnerable to overfishing because it exhibits a long life span, a large size, slow growth, and a low natural mortality.

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