Oxidative stress as a mediator of life history trade-offs: mechanisms, measurements and interpretation.

By P. Monaghan, N. Metcalfe, Roxana Torres. Ecology Letters, 2009

1,329 citations recorded by the source corpus.

Subfields: Aging, Ecology, Ecology, Evolution, Behavior and Systematics

View Paper: https://www.semanticscholar.org/paper/1cf66b96ffa80f7e19368fb74871bf5dac3398da

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Aging

1. D. Nussey
2. J. Speakman
3. N. Marchetto
4. C. Isaksson
5. M. Donaldson
6. M. Haussmann
7. D. Costantini
8. S. Mitchell

In Ecology

1. S. Cooke
2. C. Suski
3. Denis Réale
4. M. Donaldson
5. D. Nussey
6. R. Kilner
7. S. Cotter
8. C. Isaksson

In Ecology, Evolution, Behavior and Systematics

1. Denis Réale
2. D. Nussey
3. S. Cotter
4. R. Kilner
5. M. Humphries
6. C. Isaksson
7. T. Uller
8. C. Suski

Citations in the corpus

• Age-specific reproductive investment in female burying beetles: independent effects of state and risk of death (2011, background): “Here the suggestion is that older 85 individuals are so worn out or damaged or lacking in resources (e.g. Cichon, 2001; Kirkwood 86 et al., 1991; Monaghan et al., 2009; Partridge, 2010; Partridge et al., 2006) that they are 87 simply incapable of investing very much in reproduction in late life.”
• Marine Ecosystem Assessment for the Southern Ocean: Birds and Marine Mammals in a Changing Climate (2020, background): “The importance of oxidative stress in influencing fitness components and the resolution of life history trade-offs is attracting increasing attention (Monaghan et al., 2009).”
• Increased brood size leads to persistent eroded telomeres (2014, background): “ORIGINAL RESEARCH ARTICLE published: 22 April 2014 doi: 10.3389/fevo.2014.00009 Increased brood size leads to persistent eroded telomeres”
• Telomeres: Linking stress and survival, ecology and evolution (2010, background): “If free radicals and antioxidants are in homeostatic balance oxidative stress is low, but if free radical generation exceeds antioxidant defense, oxidative stress is high resulting in oxidative damage (Monaghan et al., 2009).”
• Stress Indicators in Fish (2016, background): “STRESS INDICATORS IN FISH 427 organismal senescence, has become an emerging field of research (Ricklefs, 2008; Monaghan et al., 2009).”
• The energetic and oxidative costs of reproduction in a free‐ranging rodent (2011, background): “Yet, whether an antioxidant decline with reproductive effort translates into oxidative damage, especially under realistic environmental conditions, remains for the most part unknown (Costantini 2008; Monaghan, Metcalfe & Torres 2009; Costantini et al. 2010; Metcalfe & Alonso-Alvarez 2010).”
• Carotenoid-based signals in behavioural ecology : a review (2011, background): “Regrettably, few studies have investigated carotenoid limitation in the wild (Monaghan et al., 2009).”
• Essential Biomolecules in Food Webs (2019, background): “This suggests that, in contrast to other nutritional biomolecules, the response to oxidative stressmay be the trait here, and the costs are related to features mitigating the damaging effects of LC-PUFA peroxidation (Monaghan et al., 2009).”
• Physiological mechanisms mediating costs of immune responses: what can we learn from studies of birds? (2012, background): “Oxidative stress is another potential cost of immunity with the decisive negative effects acting over a prolonged time frame (Monaghan et al. 2009).”
• Life history correlates of oxidative damage in a free‐living mammal population (2009, background): “…lack of a correlation between oxidative damage and either age, reproductive effort or parasite burden serve to highlight the potential limitations of cross-sectional data and plasma samples for addressing these issues in both laboratory and natural settings (Costantini 2008; Monaghan et al. 2009).”
• Oxidative Stress, Prooxidants, and Antioxidants: The Interplay (2014, background): “Stress has a significant ecological and evolutionary role and may help in understanding the functional interactions among life history traits [77–79].”
• Biological carryover effects: linking common concepts and mechanisms in ecology and evolution (2014, positive): “There has also been recent interest in endocrine mechanisms (Zera and Harshman 2001, Ricklefs and Wikelski 2002) and oxidative stress (Monaghan et al. 2009) as mechanisms driving lifehistory trade-offs, and it is probable that these mechanisms are equally important in driving seasonal carryover…”