scholarly journals Stomach contents of sperm whales Physeter macrocephalus stranded in the North Sea 1990-1996

1999 ◽  
Vol 183 ◽  
pp. 281-294 ◽  
Author(s):  
MB Santos ◽  
GJ Pierce ◽  
PR Boyle ◽  
RJ Reid ◽  
HM Ross ◽  
...  
2016 ◽  
Vol 42 (1) ◽  
pp. 35-41 ◽  
Author(s):  
Mette S. Hansen ◽  
Aage K. O. Alstrup ◽  
Jørgen H. Hansen ◽  
Mohammad N. S. Al-Sabi ◽  
Bettina Nonnemann ◽  
...  

2018 ◽  
Vol 88 ◽  
pp. 156-160 ◽  
Author(s):  
Marijke Autenrieth ◽  
Anja Ernst ◽  
Rob Deaville ◽  
Fabien Demaret ◽  
Lonneke L. IJsseldijk ◽  
...  

Author(s):  
Apolline ALFSEN ◽  
Mark BOSSELAERS ◽  
Olivier LAMBERT

In spite of a continuously expanding physeteroid fossil record, our understanding of the origin and early radiation of the two modern sperm whale families Kogiidae Gill, 1871 (including the pygmy and dwarf sperm whales, Kogia spp.) and Physeteridae Gray, 1821 (including the great sperm whale, Physeter Linnaeus, 1758) remains limited, especially due to the poorly resolved phylogenetic relationships of a number of extinct species. Among those, based on fragmentary cranial material from the late early to middle Miocene of Antwerp (Belgium, North Sea basin), the small-sized Thalassocetus antwerpiensis Abel, 1905 has been recognized for some time as the earliest branching kogiid. The discovery of a new diminutive physeteroid cranium from the late Miocene (Tortonian) of Antwerp leads to the description and comparison of a close relative of T. antwerpiensis. Thanks to the relatively young ontogenetic stage of this new specimen, the highly modified plate-like bones making the floor of its supracranial basin could be individually removed, a fact that greatly helped deciphering their identity and geometry. Close morphological similarities with T. antwerpiensis allow for the reassessment of several facial structures in the latter; the most important reinterpretation is the one of a crest-like structure, previously identified as a sagittal facial crest, typical for kogiids, and here revised as the left posterolateral wall of the supracranial basin, comprised of the left nasal (lost in kogiids for which the postnarial region is known) and the left maxilla. Implemented in a phylogenetic analysis, the new anatomical interpretations result in the new Belgian specimen and T. antwerpiensis being recovered as sister-groups in the family Physeteridae. Consequently, the geologically oldest kogiids are now dated from the Tortonian, further extending the ghost lineage separating these early late Miocene kogiid records from the estimated latest Oligocene to earliest Miocene divergence of kogiids and physeterids.


PLoS ONE ◽  
2018 ◽  
Vol 13 (8) ◽  
pp. e0201221 ◽  
Author(s):  
Lonneke L. IJsseldijk ◽  
Abbo van Neer ◽  
Rob Deaville ◽  
Lineke Begeman ◽  
Marco van de Bildt ◽  
...  

2000 ◽  
Vol 57 (12) ◽  
pp. 2363-2367 ◽  
Author(s):  
Sara A Adlerstein ◽  
Henny C Welleman

Results show that the weight of cod (Gadus morhua) stomach contents sampled in the North Sea varies significantly within 24 h. To determine whether feeding varied with time, over 1100 cod stomachs were collected around the clock between 7 and 18 May 1984 in two areas in the central North Sea thought to be representative for feeding studies. Here we investigate temporal feeding patterns based on the analysis of stomach-content data, using generalized additive models (GAMs). Results show significant variation of content weight and indicate morning and evening peaks. The relative peak importance differed between and within areas. We propose that differences are due to diet composition, namely, prey size and diel availability. Cod fed primarily on molluscs, mainly ocean quahog (Cyprina islandica), crustaceans, sandeels (Ammodytes spp.), haddock (Melanogrammus aeglefinus), herring (Clupea harrengus), and several flatfish species. In one area, the diet was dominated by fish, relatively large prey that perform diel vertical migration, and in the other by invertebrates, smaller prey that are digested faster. The diel pattern was more pronounced where invertebrate prey were dominant. Generalisation of results and implications for predation-mortality estimates based on data from the North Sea Stomach Content Database, used to implement multispecies models in the region, are discussed.


2016 ◽  
Vol 112 (1-2) ◽  
pp. 134-141 ◽  
Author(s):  
Bianca Unger ◽  
Elisa L. Bravo Rebolledo ◽  
Rob Deaville ◽  
Andrea Gröne ◽  
Lonneke L. IJsseldijk ◽  
...  

Author(s):  
G.J. Pierce ◽  
M.B. Santos ◽  
R.J. Reid ◽  
I.A.P. Patterson ◽  
H.M. Ross

During 1992–2002 approximately 110 strandings of minke whales Balaenoptera acutorostrata were recorded in Scotland (UK). Most strandings were recorded between April and November, with a peak of strandings of males in July and August. There were two length modes at 4–6 m and 7–10 m. Stomach contents samples were obtained from ten animals. The diet comprised mainly sandeels (Ammodytidae, around two-thirds of the diet by number or weight) and clupeids (herring Clupea harengus and sprat Sprattus sprattus). Results on diet are consistent with results from whaling catches in the North Sea. The possibility that minke whales compete with fisheries is discussed.


Stomach contents from 17 sperm whales, 15 males and two females, caught during commercial activities in 1981-1984 in the Azores region were identified and measured. A total of 28 738 cephalopods and 16 fish were represented in the collections. In addition, there were tunicates in two whales and m an-m ade products in three whales. None of the stomachs were empty. Flesh was present in 94.1% and indigestible fragments alone, including mandibles (beaks) of cephalopods, were present in 5.9% of the stomachs. Twelve species of cephalopod were represented by flesh and 40 species were represented by lower beaks. The cephalopod families contributing food to the whales in this region are, in order of their contribution by estimated mass, the O ctopoteuthidae (39.8%), the Histioteuthidae (32.7%), the Architeuthidae (12.1%), the Lepidoteuthidae (4.5% ), the Ommastrephidae (3.4% ), the Pholidoteuthidae (2.1% ), the Cycloteuthidae (1.9% ), the Cranchiidae (1.7%) and eight other families each contributing less than 1 % by mass. Presence of Gonatus beaks in the stomachs show which whales have migrated southwards to the Azores just prior to capture and the presence of a large Megalocranchia species possibly shows which whales have m igrated from higher latitudes off Iceland. However, the presence of Teuthowenia maculata shows which whales came north from the West coast of Africa, just prior to capture. The modal mass of cephalopods consumed is 400-450 g which represents 0.00001 of the whales’ body mass. 77.5% of the species eaten have luminous organs and 82% of the species are neutrally buoyant. It seems likely that the sperm whale is obtaining 77% of its food by swimming through luminous shoals of slow-swimming, neutrally bouyant squids and only about 23% by chasing faster swimming, larger cephalopods. Cephalopods not previously recorded from the North Atlantic are Onychoteuthis boreali-japonicus , and Histioteuthis bonnellii corpuscula . Histioteuthis ?miranda may have been collected by the whales much further south than the Azores. Species not recorded previously in the diet of sperm whales in the North Atlantic are Ommastrephes bartrami , Gonatus steenstrupi , Histioteuthis ?miranda , H. bonnellii corpuscula , H. meleagroteuthis , Discoteuthis laciniosa , Mastigoteulhis species, Chiroteulhis species, ?Helicocranchia , Liocranchia reinhardti , and ?Liguriella .


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