Pablo Liedo

Dr. Pablo Liedo

El Colegio de la Frontera Sur (ECOSUR)
orcid

Research Focus & Metrics

Academic Career Length

40Years (1987-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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8 May 1998 in Science
Verified
Journal Article
Closed access
PDF file
JVJames W. Vaupel
James W. Vaupel
JCJames R. Carey
James R. Carey
KCKaare Christensen
Kaare Christensen
TJThomas E. Johnson
Thomas E. Johnson
AYAnatoli I. Yashin
Anatoli I. Yashin
JCJames W. Curtsinger
James W. Curtsinger
Old-age survival has increased substantially since 1950. Death rates decelerate with age for insects, worms, and yeast, as well as humans. This evidence of extended postreproductive survival is puzzling. Three biodemographic insights—concerning the correlation of death rates across age, individual differences in survival chances, and induced alterations in age patterns of fertility and mortality—offer clues and suggest research on the failure of complicated systems, on new demographic equations for evolutionary theory, and on fertility-longevity interactions. Nongenetic changes account for increases in human life-spans to date. Explication of these causes and the genetic license for extended survival, as well as discovery of genes and other survival attributes affecting longevity, will lead to even longer lives.

16 October 1992 in Science
Verified
Journal Article
Closed access
PDF file
JCJ R Carey
J R Carey
PLPablo Liedo
Pablo Liedo
DOD Orozco
D Orozco
JVJ W Vaupel
J W Vaupel
It is generally assumed for most species that mortality rates increase monotonically at advanced ages. Mortality rates were found to level off and decrease at older ages in a population of 1.2 million medflies maintained in cages of 7,200 and in a group of approximately 48,000 adults maintained in solitary confinement. Thus, life expectancy in older individuals increased rather than decreased with age. These results cast doubt on several central concepts in gerontology and the biology of aging: (i) that senescence can be characterized by an increase in age-specific mortality, (ii) that the basic pattern of mortality in nearly all species follows the same unitary pattern at older ages, and (iii) that species have absolute life-span limits.


1 June 2015 in Florida Entomologist
Verified
Journal Article
Open access
WEWalther Enkerlin
Walther Enkerlin
JGJosé Manuel Gutiérrez-Ruelas
José Manuel Gutiérrez-Ruelas
ACAntonio Villaseñor Cortes
Antonio Villaseñor Cortes
EREdgar Cotoc Roldan
Edgar Cotoc Roldan
DMDavid Midgarden
David Midgarden
FAFrancisco Javier Trujillo Arriaga
Francisco Javier Trujillo Arriaga

14 August 1998 in Science
Verified
Journal Article
Closed access
PDF file
JCJames R. Carey
James R. Carey
PLPablo Liedo
Pablo Liedo
HMHans-Georg MülLer
Hans-Georg MülLer
JWJane-Ling Wang
Jane-Ling Wang
JVJames W. Vaupel
James W. Vaupel
The life history of medflies is characterized by two physiological modes with different demographic schedules of fertility and survival: a waiting mode in which both mortality and reproduction are low and a reproductive mode in which mortality is very low at the onset of egg laying but accelerates as eggs are laid. Medflies stay in waiting mode when they are fed only sugar. When fed protein, a scarce resource in the wild, medflies switch to reproductive mode. Medflies that switch from waiting to reproductive mode survive longer than medflies kept in either mode exclusively. An understanding of the physiological shift that occurs between the waiting and reproductive modes may yield information about the fundamental processes that determine longevity.

10 July 2008 in Aging Cell
Verified
Journal Article
Open access
PDF file
JCJames R. Carey
James R. Carey
LHLawrence G. Harshman
Lawrence G. Harshman
PLPablo Liedo
Pablo Liedo
HMHans‐Georg Müller
Hans‐Georg Müller
JWJane‐Ling Wang
Jane‐Ling Wang
ZZZhen Zhang
Zhen Zhang
Summary: Although it is widely known that dietary restriction (DR) not only extends the longevity of a wide range of species but also reduces their reproductive output, the interrelationship of DR, longevity extension and reproduction is not well understood in any organism. Here we address the question: ‘Under what nutritional conditions do the longevity‐enhancing effects resulting from food restriction either counteract, complement or reinforce the mortality costs of reproduction? To answer this question we designed a fine‐grained DR study involving 4800 individuals of the tephritid fruit fly,Anastrepha ludens, in which we measured sex‐specific survival and daily reproduction in females in each of 20 different treatments (sugar : yeast ratios) plus 4 starvation controls. The database generated from this 3‐year study consisted of approximately 100 000 life‐days for each sex and 750 000 eggs distributed over the reproductive lives of 2400 females. The fertility and longevity‐extending responses were used to create contour maps (X‐Y grid) that show the demographic responses (Z‐axis) across dietary gradients that range from complete starvation to bothad libitumsugar‐only andad libitumstandard diet (3 : 1 sugar : yeast). The topographic perspectives reveal demographic equivalencies along nutritional gradients, differences in the graded responses of males and females, egg production costs that are sensitive to the interaction of food amounts and constituents, and orthogonal contours (equivalencies in longevity or reproduction) representing demographic thresholds related to both caloric content and sugar : yeast ratios. In general, the finding that lifespan and reproductive maxima occur at much different nutritional coordinates poses a major challenge for the use of food restriction (or a mimetic) in humans to improve health and extend longevity in humans.