The domestic hypercarnivores cat and mink have a higher protein requirement than other domestic mammals. This has been attributed to adaptation to a hypercarnivorous diet and subsequent loss of the ability to downregulate amino acid catabolism. A quantitative analysis of brain glucose requirements reveals that in cats on their natural diet, a significant proportion of protein must be diverted into gluconeogenesis to supply the brain. According to the model presented here, the high protein requirement of the domestic cat is the result of routing of amino acids into gluconeogenesis to supply the needs of the brain and other glucose-requiring tissues, resulting in oxidation of amino acid in excess of the rate predicted for a non-hypercarnivorous mammal of the same size. Thus, cats and other small hypercarnivores do not have a high protein requirement per se, but a high endogenous glucose demand that is met by obligatory amino acid-based gluconeogenesis. It is predicted that for hypercarnivorous mammals with the same degree of encephalisation, endogenous nitrogen losses increase with decreasing metabolic mass as a result of the allometric relationships of brain mass and brain metabolic rate with body mass, possibly imposing a lower limit for body mass in hypercarnivorous mammals.

A dramatic reduction in catch rates of Antarctic toothfish in McMurdo Sound, Antarctica, has led to conclusions that the commercial bottom longline fishery for toothfish in the Ross Sea has drastically altered the toothfish population with cascading effects on the McMurdo Sound ecosystem. However, results from a new monitoring programme for Antarctic toothfish and other top predators carried out in McMurdo Sound in 2014 have shown toothfish catch rate, fish size and fish age similar to those observed prior to 2002. These results suggest that either large and old fish have returned to McMurdo Sound following a temporary environmentally driven absence or that they remained locally present but were not detected in the areas sampled. These findings highlight the importance of continued standardized monitoring for detecting the potential effects of fishing on the Ross Sea ecosystem.

We report a novel method of investigating foraging in marine mammals based on detecting biomarkers of strictly dietary origin in blood. Arsenobetaine (AsB), the arsenic analogue of the osmolyte glycine betaine, and trimethylamine N-oxide (TMAO), an osmolyte used by marine fish and invertebrates, were measured in plasma of lactating Weddell seals Leptonychotes weddellii during the postpartum fast and at different stages of lactation. Plasma dietary biomarker concentrations were low in early lactation ( ). In lactating females (n = 6) monitored longitudinally, plasma TMAO remained low for the first 3 wk p.p. Increases in AsB concentrations observed in late lactation were closely correlated (Pearson correlation r = 0.96, p < 0.01, n = 6) with increases in plasma insulin-like growth factor 1 (IGF1), a growth factor known to reflect nutritional status in other mammals. Two seals outfitted with time-depth recorders began regular deep diving at different times p.p. and showed corresponding differences in biomarker concentrations. Our results indicate that (1) most lactating Weddell seals at the study site (70% of 20 seals studied) feed after 3 to 4 wk p.p., (2) individual lactating Weddell seals may forage as early as 9 d p.p., and (3) some Weddell seals may consume little or no food throughout lactation. Dietary biomarkers provide a simple method for distinguishing feeding and fasting in freeliving marine mammals.

The microscopic anatomy of the eye of the Weddell seal was studied with various light and electron microscopic methods with a view to correlating morphological findings with the biology of this seal which is adapted to the extremes of the Antarctic environment and to extreme diving excursions into the lightless depths of the sea. In the retina an area centralis was found but no fovea centralis. The densely packed photoreceptors consist exclusively of highly differentiated rods, which in primates detect light at low intensity but have rather poor image discrimination. The ganglion cells are relatively scarce, suggesting a high degree of convergence of the light-sensitive cells on the ganglion cells. The pigment epithelium is almost devoid of pigment granules. The extensive tapetum lucidum is about 400-500 microm thick and is composed of about 30 layers of specialized cells. The cornea is 650 (center) to 800-900 (periphery) microm thick. Its structure and glycosaminoglycan histochemistry correspond to that of other mammals. The iridocorneal angle is unusually deep and pervaded by an elaborate trabecular meshwork, which together with a complex canal of Schlemm can be correlated with the ability to absorb large amounts of fluid. The ciliary muscle and its antagonist, the membrane of Bruch, are poorly developed, suggesting relatively poor abilities of accommodation. The combination of a well-developed tapetum lucidum, an unpigmented pigment epithelium, well-developed rods, and a high number of rods converging on only few ganglion cells is obviously an adaptation to an extreme light sensitivity, enabling the animals to make use of the little light available in the deep sea.

Nototheniid and myctophid Wsh are primary prey for marine piscivores, yet little is known about their nutritional value. In this study, we characterized the proximate composition [PC: water, fat (neutral lipids), crude protein (CP) and ash] and energy density (ED; kJ g ¡1 ) of Wfteen Wsh species from McMurdo Sound and the Ross Sea, Antarctica. We assayed the entire Wsh for all species except for the large Antarctic toothWsh, Dissostichus mawsoni (muscle tissue only). On a wet mass basis (WM), Wsh were variable in composition: moisture content ranged from 64.9 to 87.3% WM, fat from 0.5 to 17.4% WM, CP from 7.7 to 16.7% WM, ash from 11.2 to 21.0% FFDM (fat-free dry mass), and ED from 2.9 to 10.3 kJ g ¡1 . Myctophids and pelagic nototheniids such as Pleuragramma antarcticum and D. mawsoni were high in fat content (7-17% WM), while a bathylagid and benthic nototheniids including most Trematomus spp. and Lepidonotothen squamifrons were low in fat (0.5-4% WM). The epibenthic Trematomus species (T. eulepidotus and T. lepidorhinus) were intermediate. Energy density tracked fat content, with highest values in myctophids and pelagic nototheniids. The variation in nutrient and energy density conWrms that prey composition must be taken into account when modelling energy and nutrient Xuxes within the Antarctic ecosystem. Further analyses of prey collected over a number of diVerent locations and seasons are needed in order to determine how the nutritional value of certain species might aVect annual or decadal variation in reproductive success or population size of top predators.

We propose that secretion of milk sugar has important consequences for the metabolic economies of lactating phocid seals and their pups. Milk was collected from 21 Weddell seals Leptonychotes weddellii in McMurdo Sound, Antarctica, and assayed by standard methods. Milk composition changed over the course of lactation, but at mid- to late lactation (16-40 d postpartum), Weddell seal milk composition was relatively constant at 33.8% +/- 0.82% water, 54.0% +/- 0.80% fat, 10.1% +/- 0.16% crude protein, 0.84% +/- 0.03% sugar, 0.75% +/- 0.02% ash, and 23.3 +/- 0.3 kJ g−1 whole milk (WM). At this stage, milk composition varied among individual seals in all assayed constituents except ash. The concentration of sugar in the aqueous phase of Weddell seal milk ( 24.9 +/- 0.6g sugar L−1 water) was ca. 44%-77% of levels found in terrestrial carnivores, indicating that the low sugar concentration of WM is primarily due to its high fat content, not alteration of the aqueous phase. In early lactation, fasting Weddell seals were estimated to devote 39 g d(-1) glucose to milk sugar synthesis, an amount similar to the estimated demand of the maternal brain. This additional glucose demand must be covered by gluconeogenesis in fasting animals and represents a considerable additional drain on maternal resources. However, provision of sugar to offspring at rates sufficient to meet neonatal substrate requirements appears to be essential for efficient fat and protein deposition and thus may be an important component of the phocid reproductive strategy of rapid growth and early weaning.

Mammalian milks may differ greatly in composition from cow milk, and these differences may affect the performance of analytical methods. High-fat, high-protein milks with a preponderance of oligosaccharides, such as those produced by many marine mammals, present a particular challenge. We compared the performance of several methods against reference procedures using Weddell seal (Leptonychotes weddellii) milk of highly varied composition (by reference methods: 27-63% water, 24-62% fat, 8-12% crude protein, 0.5-1.8% sugar). A microdrying step preparatory to carbon-hydrogen-nitrogen (CHN) gas analysis slightly underestimated water content and had a higher repeatability relative standard deviation (RSDr) than did reference oven drying at 100°C. Compared with a reference macro-Kjeldahl protein procedure, the CHN (or Dumas) combustion method had a somewhat higher RSDr (1.56 vs. 0.60%) but correlation between methods was high (0.992), means were not different (CHN: 17.2±0.46% dry matter basis; Kjeldahl 17.3±0.49% dry matter basis), there were no significant proportional or constant errors, and predictive performance was high. A carbon stoichiometric procedure based on CHN analysis failed to adequately predict fat (reference: Röse-Gottlieb method) or total sugar (reference: phenol-sulfuric acid method). Gross energy content, calculated from energetic factors and results from reference methods for fat, protein, and total sugar, accurately predicted gross energy as measured by bomb calorimetry. We conclude that the CHN (Dumas) combustion method and calculation of gross energy are acceptable analytical approaches for marine mammal milk, but fat and sugar require separate analysis by appropriate analytic methods and cannot be adequately estimated by carbon stoichiometry. Some other alternative methods-low-temperature drying for water determination; Bradford, Lowry, and biuret methods for protein; the Folch and the Bligh and Dyer methods for fat; and enzymatic and reducing sugar methods for total sugar-appear likely to produce substantial error in marine mammal milks. It is important that alternative analytical methods be properly validated against a reference method before being used, especially for mammalian milks that differ greatly from cow milk in analyte characteristics and concentrations.

The structures of milk oligosaccharides were characterized for four strepsirrhine primates to examine the extent to which they resemble milk oligosaccharides in other primates. Neutral and acidic oligosaccharides were isolated from milk of the greater galago (Galagidae: Otolemur crassicaudatus), aye-aye (Daubentoniidae: Daubentonia madagascariensis), Coquerel's sifaka (Indriidae: Propithecus coquereli) and mongoose lemur (Lemuridae: Eulemur mongoz), and their chemical structures were characterized by (1)H-NMR spectroscopy. The oligosaccharide patterns observed among strepsirrhines did not appear to correlate to phylogeny, sociality or pattern of infant care. Both type I and type II neutral oligosaccharides were found in the milk of the aye-aye, but type II predominate over type I. Only type II oligosaccharides were identified in other strepsirrhine milks. α3'-GL (isoglobotriose, Gal(α1-3)Gal(β1-4)Glc) was found in the milks of Coquerel's sifaka and mongoose lemur, which is the first report of this oligosaccharide in the milk of any primate species. 2'-FL (Fuc(α1-2)Gal(β1-4)Glc) was found in the milk of an aye-aye with an ill infant. Oligosaccharides containing the Lewis x epitope were found in aye-aye and mongoose lemur milk. Among acidic oligosaccharides, 3'-N-acetylneuraminyllactose (3'-SL-NAc, Neu5Ac(α2-3)Gal(β1-4)Glc) was found in all studied species, whereas 6'-N-acetylneuraminyllactose (6'-SL-NAc, Neu5Ac(α2-6)Gal(β1-4)Glc) was found in all species except greater galago. Greater galago milk also contained 3'-N-glycolylneuraminyllactose (3'-SL-NGc, Neu5Gc(α2-3)Gal(β1-4)Glc). The finding of a variety of neutral and acidic oligosaccharides in the milks of strepsirrhines, as previously reported for haplorhines, suggests that such constituents are ancient rather than derived features, and are as characteristic of primate lactation is the classic disaccharide, lactose.