» Articles » PMID: 28438763

The Performing Animal: Causes and Consequences of Body Remodeling and Metabolic Adjustments in Red Knots Facing Contrasting Thermal Environments

Overview
Specialty Physiology
Date 2017 Apr 26
PMID 28438763
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Using red knots () as a model, we determined how changes in mass and metabolic activity of organs relate to temperature-induced variation in metabolic performance. In cold-acclimated birds, we expected large muscles and heart as well as improved oxidative capacity and lipid transport, and we predicted that this would explain variation in maximal thermogenic capacity (M). We also expected larger digestive and excretory organs in these same birds and predicted that this would explain most of the variation in basal metabolic rate (BMR). Knots kept at 5°C were 20% heavier and maintained 1.5 times more body fat than individuals kept in thermoneutral conditions (25°C). The birds in the cold also had a BMR up to 32% higher and a M 16% higher than birds at 25°C. Organs were larger in the cold, with muscles and heart being 9-20% heavier and digestive and excretory organs being 21-36% larger than at thermoneutrality. Rather than the predicted digestive and excretory organs, the cold-induced increase in BMR correlated with changes in mass of the heart, pectoralis, and carcass. M varied positively with the mass of the pectoralis, supracoracoideus, and heart, highlighting the importance of muscles and cardiac function in cold endurance. Cold-acclimated knots also expressed upregulated capacity for lipid transport across mitochondrial membranes [carnitine palmitoyl transferase (CPT)] in their pectoralis and leg muscles, higher lipid catabolism capacity in their pectoralis muscles [β-hydroxyacyl CoA-dehydrogenase (HOAD)], and elevated oxidative capacity in their liver and kidney (citrate synthase). These adjustments may have contributed to BMR through changes in metabolic intensity. Positive relationships among M, CPT, and HOAD in the heart also suggest indirect constraints on thermogenic capacity through limited cardiac capacity.

Citing Articles

A comparison of seasonal flexibility in pectoralis muscle fiber type and enzyme activity in migratory and resident sparrow species.

Lewicki L, Zhang M, Staples J, Guglielmo C, Ivy C J Exp Biol. 2025; 228(3).

PMID: 39902596 PMC: 11832126. DOI: 10.1242/jeb.249392.


How important is hidden phenotypic plasticity arising from alternative but converging developmental trajectories, and what limits it?.

Metcalfe N J Exp Biol. 2024; 227(Suppl_1).

PMID: 38449324 PMC: 10949067. DOI: 10.1242/jeb.246010.


Individual response in body mass and basal metabolism to the risks of predation and starvation in passerines.

Broggi J, Nilsson J J Exp Biol. 2023; 226(2).

PMID: 36628936 PMC: 10086538. DOI: 10.1242/jeb.244744.


Dancing drives evolution of sexual size dimorphism in manakins.

Shogren E, Anciaes M, Barske J, Cestari C, DuVal E, Gaiotti M Proc Biol Sci. 2022; 289(1974):20212540.

PMID: 35506220 PMC: 9065976. DOI: 10.1098/rspb.2021.2540.


Phenotypic flexibility in heat production and heat loss in response to thermal and hydric acclimation in the zebra finch, a small arid-zone passerine.

Wojciechowski M, Kowalczewska A, Colominas-Ciuro R, Jefimow M J Comp Physiol B. 2020; 191(1):225-239.

PMID: 33070274 PMC: 7819915. DOI: 10.1007/s00360-020-01322-0.