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73 results for “albatross”
FIGURE 16 in Cranial osteology and taxonomy of albatrosses of genus Dimedea linneaus, 1758 and Thalassarche reichenbach, 1853 (procellariformes: Diomeidae)
FIGURE 16: Thalassarche melanophris (MZUSP 3): ventral view. BT – basal tubercles; LvPrP – lateral‑ventral process of the palatine; MPrP – maxillary process of the palatine; RoP – rostral end of the palatine; VFM – ventral fissures of the maxilla.
FIGURE 15 in Cranial osteology and taxonomy of albatrosses of genus Dimedea linneaus, 1758 and Thalassarche reichenbach, 1853 (procellariformes: Diomeidae)
FIGURE 15: Thalassarche melanophris (MZUSP 3): ventral view. BT – basal tubercles; LvPrP – lateral‑ventral process of the palatine; MPrP – maxillary process of the palatine; RoP – rostral end of the palatine; VFM – ventral fissures of the maxilla.
FIGURE 11 in Cranial osteology and taxonomy of albatrosses of genus Dimedea linneaus, 1758 and Thalassarche reichenbach, 1853 (procellariformes: Diomeidae)
FIGURE 11: Thalassarche cauta (MOVI33262): lateral view. FOc – fonticulus orbitocranialis; ONF – olfactory nerve foramen.
FIGURE 31 in Cranial osteology and taxonomy of albatrosses of genus Dimedea linneaus, 1758 and Thalassarche reichenbach, 1853 (procellariformes: Diomeidae)
FIGURE 31: Thalassarche chlororhynchos (MZUSP 95): lateral view. Note coloration pattern of the ramphotheca.
FIGURE 9 in Cranial osteology and taxonomy of albatrosses of genus Dimedea linneaus, 1758 and Thalassarche reichenbach, 1853 (procellariformes: Diomeidae)
FIGURE 9: Thalassarche chlororhynchos (AZ742): lateral view. FOc – fonticulus orbitocranialis; SMPr – suprameatic process.
FIGURE 8 in Cranial osteology and taxonomy of albatrosses of genus Dimedea linneaus, 1758 and Thalassarche reichenbach, 1853 (procellariformes: Diomeidae)
FIGURE 8: Thalassarche melanophris (MZUSP 3): lateral‑caudal view. CBM – curved blades of the maxilla; CPrM – caudal process of the maxilar; E – ectethmoid; LaCho – lateral‑dorsal expansion of the palatine.
FIGURE 7 in Cranial osteology and taxonomy of albatrosses of genus Dimedea linneaus, 1758 and Thalassarche reichenbach, 1853 (procellariformes: Diomeidae)
FIGURE 7: Thalassarche melanophris (MZUSP 3): lateral view. CBM – curved blades of the maxilla; E – ectethmoid; LaCho – lateraldorsal expansion of the palatine.
FIGURE 3 in Cranial osteology and taxonomy of albatrosses of genus Dimedea linneaus, 1758 and Thalassarche reichenbach, 1853 (procellariformes: Diomeidae)
FIGURE 3: Thalassarche cauta (MOVI33262): dorsal view of caudal region. FGN – fossae glandularis nasalis; RG – rectangular gap of frontal‑nasal articulation; VCP – vertical crest of the parietals.
FIGURE 12 in Cranial osteology and taxonomy of albatrosses of genus Dimedea linneaus, 1758 and Thalassarche reichenbach, 1853 (procellariformes: Diomeidae)
FIGURE 12: Thalassarche cauta (MOVI33262): lateral view. FOc – fonticulus orbitocranialis; ONF – olfactory nerve foramen.
FIGURE 5 in Cranial osteology and taxonomy of albatrosses of genus Dimedea linneaus, 1758 and Thalassarche reichenbach, 1853 (procellariformes: Diomeidae)
FIGURE 5: Thalassarche melanophris (MZUSP 3): lateral view of caudal region. CPrM – caudal process of the maxilar; E – ectethmoid; LaCho – lateral‑dorsal expansion of the palatine; SMPr – suprameatic process.
FIGURE 4 in Cranial osteology and taxonomy of albatrosses of genus Dimedea linneaus, 1758 and Thalassarche reichenbach, 1853 (procellariformes: Diomeidae)
FIGURE 4: Thalassarche melanophris (MZUSP 3): lateral view. E – ectethmoid; SMPr – suprameatic process.
FIGURE 2 in Cranial osteology and taxonomy of albatrosses of genus Dimedea linneaus, 1758 and Thalassarche reichenbach, 1853 (procellariformes: Diomeidae)
FIGURE 2: Thalassarche melanophris (MZUSP 3): dorsal view of caudal region. FGN – fossae glandularis nasalis; RG – rectangular gap of frontal‑nasal articulation.
FIGURE 6 in Cranial osteology and taxonomy of albatrosses of genus Dimedea linneaus, 1758 and Thalassarche reichenbach, 1853 (procellariformes: Diomeidae)
FIGURE 6: Thalassarche melanophris (MZUSP 1119): lateral view. OPr – orbital process of the lacrimal; SMPr – suprameatic process.
FIGURE 1 in Cranial osteology and taxonomy of albatrosses of genus Dimedea linneaus, 1758 and Thalassarche reichenbach, 1853 (procellariformes: Diomeidae)
FIGURE 1: Thalassarche melanophris (MZUSP 3): dorsal view. FGN – fossae glandularis nasalis; RG – rectangular gap of frontal‑nasal articulation.
Foraging in a dynamic environment: response of four sympatric sub-Antarctic albatross species to interannual environmental variability
Seasonal and annual climate variations are linked to fluctuations in the abundance and distribution of resources, posing a significant challenge to animals that need to adjust their foraging behaviour accordingly. Particularly during adverse conditions, and while energetically constrained when breeding, animals ideally need to be flexible in their foraging behaviour. Such behavioural plasticity may separate 'winners' from 'losers' in light of rapid environmental changes due to climate change. Here, the foraging behaviour of four sub-Antarctic albatross species was investigated from 2015/16 to 2017/18, a period characterized by pronounced environmental variability. Over three breeding seasons on Marion Island, Prince Edward Archipelago, incubating wandering (WA, Diomedea exulans; n=45), grey-headed (GHA, Thalassarche chrysostoma; n=26), sooty (SA, Phoebetria fusca; n=23) and light-mantled (LMSA, P. palpebrata; n=22) albatrosses were tracked with GPS loggers. The response of birds to environmental variability was investigated by quantifying inter-annual changes in their foraging behaviour along two axes: spatial distribution, using kernel density analysis, and foraging habitat preference, using generalized additive mixed models and Bayesian mixed models. All four species were shown to respond behaviourally to environmental variability, but with substantial differences in their foraging strategies. WA was most general in its habitat use defined by sea surface height, eddy kinetic energy, wind speed, ocean floor slope and sea level anomaly, with individuals foraging in a range of habitats. In contrast, the three smaller albatrosses exploited two main foraging habitats, with habitat use varying between years. Generalist habitat use by WA and inter-annually variable use of habitats by GHA, SA and LMSA would likely offer these species some resilience to predicted changes in climate such as warming seas and strengthening of westerly winds. However, future investigations need to consider other life history stages coupled with demographic studies, to better understand the link between behavioural plasticity and population responses.
Wandering Albatross observed and simulated GPS tracks from Crozet and Marion islands (2016-2019)
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Data from: Influence of device accuracy and choice of algorithm for species distribution modelling of seabirds: a case study using black-browed albatrosses
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Data from: Morphological and genomic comparisons of Hawaiian and Japanese Black-footed Albatrosses (Phoebastria nigripes) using double digest RADseq: implications for conservation
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Data from: Projected distributions of Southern Ocean albatrosses, petrels and fisheries as a consequence of climatic change
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Data from: Contrasting drivers of reproductive ageing in albatrosses
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