JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact support@jstor.org. . Wiley and Nordic Society Oikos are collaborating with JSTOR to digitize, preserve and extend access to Ornis Scandinavica. . 1992. Energy and nutrient use during moult by White-crowned Sparrows Zonotrichia leucophrys gambelii. -Ornis Scand. 23: 304-313.The apparent nutrient and energy costs of moult in Gambel's Sparrows estimated from the materials deposited in the integument are relatively mild compared with the maintenance requirements (5.3% of BMR, and 45% of the minimum maintenance requirement for protein (MMRP)) and with those of reproduction (34% BMR and 165% MMRP), except perhaps for cystine. Measures of the actual costs of moult indicate that processes in addition to plumage synthesis combine to create daily energy costs for peak moult equaling 58% BMR. These processes include (1) recrudescence of the integument, (2) a cyclic osteoporosis, and (3) a large diel cycling in body protein content (as much as 8%). The main adjustments in nutritional requirements during moult are greater needs for protein to supply substrate and for energy. Also, the needs for iron for erythrocyte production (item 1 above) and for calcium for bone formation (item 2 above) presumably increase. Analyses of several food groups reveal that the energy and essential amino acid (EAA) needs for moult can likely be met by a wide variety of food types. When the total daily EAA needs of moulting birds are taken together the profile of the EAA demands is realigned so that the disproportionately high demand for cystine for keratin synthesis is obscured. Consequently, dietary protein can be used more efficiently for whole-body protein synthesis.
It has often been alleged that avian molt can be interrupted or delayed by food deprivation or malnutrition. We examined this experimentally in captive White-crowned Sparrows (Zonotrichia leucophrys gambelii). Beginning either at the natural onset of postnuptial molt or 1 month before its onset, groups of birds were fed either inadequate amounts of a balanced diet (60 or 80% of the ad libitum intake of a control group) or unlimited amounts of a diet deficient only in cyst(e)ine and methionine. Except in the 60% premolt group, the malnourished birds did not postpone or interrupt molt in spite of losses ranging from 20 to 38% of initial body mass. Molt was significantly protracted in all except the 60% premolt group as a result of both increased shedding interval and decreased feather growth rates. Their new plumage weighed less than that of control birds, and their remiges were slightly shorter and often deformed or achromatic. The occurrence of fault bars corresponded to the times when the birds were handled, but was not correlated with other plumage defects. Surviving birds of the 60% premolt group did not molt until allowed to feed ad libitum, but then produced a normal plumage in about two-thirds of the time required by the controls. To summarize, molt is a very conservative aspect of self maintenance that is distorted only by planes of malnutrition that free-living sparrows either do not encounter during the summer or do not survive.
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