Foraging strategies of southern Buller's albatrossesDiomedea b. bulleribreeding on The Snares, New Zealand

2000 ◽  
Vol 30 (3) ◽  
pp. 299-318 ◽  
Author(s):  
J. C. Stahl ◽  
P. M. Sagar
Diversity ◽  
2020 ◽  
Vol 12 (2) ◽  
pp. 46 ◽  
Author(s):  
Gerald Mayr ◽  
Vanesa L. De Pietri ◽  
Leigh Love ◽  
Al A. Mannering ◽  
Joseph J. Bevitt ◽  
...  

We describe a partial skeleton of a stem group penguin from the Waipara Greensand in New Zealand, which is tentatively assigned to Muriwaimanu tuatahi. The fossil includes the first complete wing of a Paleocene penguin and informs on previously unknown features of the mandible and tibiotarsus of small-sized Sphenisciformes from the Waipara Greensand. The wing is distinguished by important features from that of all geologically younger Sphenisciformes and documents an early stage in the evolution of wing-propelled diving in penguins. In particular, the wing of the new fossil exhibits a well-developed alular phalanx and the distal phalanges are not flattened. Because the wing phalanges resemble those of volant birds, we consider it likely that the wing feathers remained differentiated into functional categories and were not short and scale-like as they are in extant penguins. Even though the flippers of geologically younger penguins may favor survival in extremely cold climates, they are likely to have been shaped by hydrodynamic demands. Possible selective drivers include a diminished importance of the hindlimbs in subaquatic propulsion, new foraging strategies (the caudal end of the mandible of the new fossil distinctly differs from that of extant penguins), or increased predation by marine mammals.


PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e8906 ◽  
Author(s):  
Leigh G. Torres ◽  
Dawn R. Barlow ◽  
Todd E. Chandler ◽  
Jonathan D. Burnett

To understand how predators optimize foraging strategies, extensive knowledge of predator behavior and prey distribution is needed. Blue whales employ an energetically demanding lunge feeding method that requires the whales to selectively feed where energetic gain exceeds energetic loss, while also balancing oxygen consumption, breath holding capacity, and surface recuperation time. Hence, blue whale foraging behavior is primarily driven by krill patch density and depth, but many studies have not fully considered surface feeding as a significant foraging strategy in energetic models. We collected predator and prey data on a blue whale (Balaenoptera musculus brevicauda) foraging ground in New Zealand in February 2017 to assess the distributional and behavioral response of blue whales to the distribution and density of krill prey aggregations. Krill density across the study region was greater toward the surface (upper 20 m), and blue whales were encountered where prey was relatively shallow and more dense. This relationship was particularly evident where foraging and surface lunge feeding were observed. Furthermore, New Zealand blue whales also had relatively short dive times (2.83 ± 0.27 SE min) as compared to other blue whale populations, which became even shorter at foraging sightings and where surface lunge feeding was observed. Using an unmanned aerial system (UAS; drone) we also captured unique video of a New Zealand blue whale’s surface feeding behavior on well-illuminated krill patches. Video analysis illustrates the whale’s potential use of vision to target prey, make foraging decisions, and orient body mechanics relative to prey patch characteristics. Kinematic analysis of a surface lunge feeding event revealed biomechanical coordination through speed, acceleration, head inclination, roll, and distance from krill patch to maximize prey engulfment. We compared these lunge kinematics to data previously reported from tagged blue whale lunges at depth to demonstrate strong similarities, and provide rare measurements of gape size, and krill response distance and time. These findings elucidate the predator-prey relationship between blue whales and krill, and provide support for the hypothesis that surface feeding by New Zealand blue whales is an important component to their foraging ecology used to optimize their energetic efficiency. Understanding how blue whales make foraging decisions presents logistical challenges, which may cause incomplete sampling and biased ecological knowledge if portions of their foraging behavior are undocumented. We conclude that surface foraging could be an important strategy for blue whales, and integration of UAS with tag-based studies may expand our understanding of their foraging ecology by examining surface feeding events in conjunction with behaviors at depth.


2017 ◽  
Vol 95 (12) ◽  
pp. 955-963 ◽  
Author(s):  
B.L. Chilvers

Recognizing the individual variability of foraging behaviour of marine predators is important for understanding their role in the marine ecosystem and identifying how species may respond to environmental variability or human impacts. This research examines stable isotope signatures (δ13C and δ15N) of blood serum and whiskers from 22 female New Zealand sea lions (Phocarctos hookeri (Gray, 1844)) to determine if the isotopic composition of serum reflects foraging strategy, and whether serum and proximal whisker growth have similar signatures, therefore indicating the isotopic composition of whiskers also reflects the foraging strategy diet at the time of their growth. Female New Zealand sea lions are known to have two distinct foraging strategies (mesopelagic or benthic ecotypes), shown to be habitual within and between years. Females who are known to be mesopelagic foragers have higher overlap and are at greater risk of harmful interactions with fisheries. This research found that the two foraging strategies identified from telemetry are also associated with different δ13C and δ15N isotopic values from blood serum and whiskers. Therefore, stable isotope analysis could be used to determine the proportion of the female population that are likely to be exposed to the detrimental direct and indirect interactions with fisheries.


The Condor ◽  
2006 ◽  
Vol 108 (2) ◽  
pp. 348-365
Author(s):  
Jean-Claude Stahl ◽  
Paul M. Sagar

Abstract Foraging strategies of nonbreeding seabirds attending colonies remain virtually unknown. Here we report the results of a satellite telemetry study of nonbreeding Buller's Albatrosses (Thalassarche bulleri) from the Snares island group south of New Zealand in 2000–2001. Two 6- to 7-year-old prebreeding birds dispersed to Tasmania, Australia, from late May until at least late July. Six older birds (five prebreeding birds, one former breeding adult) all adopted a dual strategy of short trips (mean duration 1.3 days, mean foraging range 129 km) and long trips to southern New Zealand (9.6 days, 871 km) or Tasmania (22.0 days, 1918 km). Time allocation to short trips increased with age and experience (both sexes) and nest-site attendance (males), and decreased during the guard (when the chick is attended) and late postguard (chick left unattended) stages (females). Up to the guard stage, most birds present at their colony on consecutive days foraged overnight (mean foraging range 101 km). Nonbreeding birds used the same foraging areas as breeding adults, but allocated more foraging time to short trips during the corresponding incubation period and early postguard stage, and to long trips during the guard stage. Results suggest that prebreeding birds explore foraging areas sequentially, and increase their time ashore by progressing from making only long trips, to introducing short overnight trips, to modifying the duration of and allocation between long and short trips. Changes in body mass recorded on Solander Island (160 km north of the Snares) show that experienced nonbreeding birds initiate long foraging trips to regain mass lost during short trips, and suggest that less frequent short trips (and hence fewer returns ashore) among inexperienced birds are related to less efficient foraging during long trips.


2001 ◽  
Vol 254 (2) ◽  
pp. 267-277 ◽  
Author(s):  
D. E. Crocker ◽  
N. J. Gales ◽  
D. P. Costa

2009 ◽  
Vol 378 ◽  
pp. 299-308 ◽  
Author(s):  
BL Chilvers ◽  
IS Wilkinson

1999 ◽  
Vol 190 ◽  
pp. 563-566
Author(s):  
J. D. Pritchard ◽  
W. Tobin ◽  
J. V. Clausen ◽  
E. F. Guinan ◽  
E. L. Fitzpatrick ◽  
...  

Our collaboration involves groups in Denmark, the U.S.A. Spain and of course New Zealand. Combining ground-based and satellite (IUEandHST) observations we aim to determine accurate and precise stellar fundamental parameters for the components of Magellanic Cloud Eclipsing Binaries as well as the distances to these systems and hence the parent galaxies themselves. This poster presents our latest progress.


Author(s):  
Ronald S. Weinstein ◽  
N. Scott McNutt

The Type I simple cold block device was described by Bullivant and Ames in 1966 and represented the product of the first successful effort to simplify the equipment required to do sophisticated freeze-cleave techniques. Bullivant, Weinstein and Someda described the Type II device which is a modification of the Type I device and was developed as a collaborative effort at the Massachusetts General Hospital and the University of Auckland, New Zealand. The modifications reduced specimen contamination and provided controlled specimen warming for heat-etching of fracture faces. We have now tested the Mass. General Hospital version of the Type II device (called the “Type II-MGH device”) on a wide variety of biological specimens and have established temperature and pressure curves for routine heat-etching with the device.


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