Sound transmission in the nose of the sperm whale Physeter catodon. A post mortem study

During a sperm whale stranding at R?m?, the Wadden Sea, Denmark, on 4 December 1997, we were notified in time to start acoustic transmission measurements in the spermaceti complex 1 h after the specimen was seen alive. Frequency-modulated sound pulses, sweeping from 30 kHz to 10 kHz in 25 ms, were injected at the frontal surface at two positions: at the distal sac, and at the center of the junk (a compartmentalized structure below the spermaceti organ). A hydrophone next to the projector served as receiver. The analyses of the recordings show a repetitive, decaying reflection pattern at both projection sites, reminiscent of the multi-pulse click peculiar to sperm whales, although with minor differences in the duration of the intra-click intervals. This experimental evidence supports the Norris and Harvey (1972) theory of click generation in the spermaceti organ. Accordingly, the click is composed of a primary event, followed by a train of reflected pulses, spaced by the time required for the event to travel back and forth between air sacs (reflectors) at each end of the organ. The results also show that the junk readily transmits sound and probably is in acoustic contact with the spermaceti organ.     

Size Distribution of Sperm Whales Acoustically Identified during Long Term Deep-Sea Monitoring in the Ionian Sea

The sperm whale (Physeter macrocephalus) emits a typical short acoustic signal, defined as a “click”, almost continuously while diving. It is produced in different time patterns to acoustically explore the environment and communicate with conspecifics. Each emitted click has a multi-pulse structure, resulting from the production of the sound within the sperm whale’s head. A Stable Inter Pulse Interval (Stable IPI) can be identified among the pulses that compose a single click. Applying specific algorithms, the measurement of this interval provides useful information to assess the total length of the animal recorded. In January 2005, a cabled hydrophone array was deployed at a depth of 2,100 m in the Central Mediterranean Sea, 25 km offshore Catania (Ionian Sea). The acoustic antenna, named OνDE (Ocean noise Detection Experiment), was in operation until November 2006. OνDE provided real time acoustic data used to perform Passive Acoustic Monitoring (PAM) of cetacean sound emissions. In this work, an innovative approach was applied to automatically measure the Stable IPI of the clicks, performing a cepstrum analysis to the energy (square amplitude) of the signals. About 2,100 five-minute recordings were processed to study the size distribution of the sperm whales detected during the OνDE long term deep-sea acoustic monitoring. Stable IPIs were measured in the range between 2.1 ms and 6.4 ms. The equations of Gordon (1991) and of Growcott (2011) were used to convert the IPIs into measures of size. The results revealed that the sperm whales recorded were distributed in length from about 7.5 m to 14 m. The size category most represented was from 9 m to 12 m (adult females or juvenile males) and specimens longer than 14 m (old males) seemed to be absent.     

THE SPERM WHALE'S NOSE: SEXUAL SELECTION ON A GRAND SCALE?1

The world's largest nose belongs to the sperm whale, yet its functional significance remains equivocal. In order to help shed light on its function, the head of a postmortem neonate sperm whale was subjected to CT scanning. Geometric comparisons between homologous cephalic structures in sperm whales and dolphins (normalized for body size) show extreme hypertrophy and size sexual dimorphism in the sperm whale's lipid spermaceti organ. Anatomic geometry, energetics, and behavior suggest that this immense nasal apparatus is a bioacoustical machine. Sexual selection via an acoustic display is suggested as an explanation for the size and continuous (physiologically isolated) energy investment in the construction and maintenance of the male's spermaceti organ.     

An acoustic valve within the nose of sperm whales Physeter macrocephalus

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WEIGHTS AND ANATOMICAL MEASUREMENTS OF NORTHEASTERN ATLANTIC FIN (BALAENOPTERA PHYSALUS, LINNAEUS) AND SEI (B. BOREALIS, LESSON) WHALES

Piecemeal body weights of eleven fin and four sei whales and intact weights of three foetuses, obtained from Iceland, are compared with published weight data. The Icelandic fin are similar to other northern hemisphere animals but are significantly leaner than their Antarctic counterparts. The Icelandic sei appear heavier than the North Pacific sei whales. Their weights cannot be predicted from a North Pacific sei whale weight/length formula. Length, girth and blubber thickness measurements indicate changes in relative body dimensions in the early fin whale foetus compared with juveniles and adults; however, the midterm sei whale foetus is similar to the adult and juvenile sei whales. The blubber appears to form a major component even in the foetal body. The integration of a standard series of lengths, girths and blubber thicknesses in juveniles and adults can provide an estimate of the blubber component. Both girth and length are significant parameters in estimating body weight, a simple weight/length formula being found to be inadequate to allow for variability in body fatness. Evaluation of such a multiple parameter formula for calculating weight appears satisfactory for both fin and sei whales. Apparent weight/length differences between species and stocks may thus be partly due to variations in body fatness.     

Cetacean mitochondrial DNA control region: sequences of all extant baleen whales and two sperm whale species

The sequence of the mitochondrial control region was determined in all 10 extant species commonly assigned to the suborder Mysticeti (baleen or whalebone whales) and to two odontocete (toothed whale) species (the sperm and the pygmy sperm whale). In the mysticetes, both the length and the sequence of the control region were very similar, with differences occurring primarily in the first approximately 160 bp of the 5' end of the L-strand of the region. There were marked differences between the mysticete and sperm whale sequences and also between the two sperm whales. The control region, less its variable portion, was used in a comparison including the 10 mysticete sequences plus the same region of an Antarctic minke whale specimen and the two sperm whales. The difference between the minke whales from the North Atlantic and the Antarctic was greater than that between any acknowledged species belonging to the same genus (Balaenoptera). The difference was similar to that between the families Balaenopteridae (rorquals) and Eschrichtiidae (gray whales). The findings suggest that the Antarctic minke whale should have a full species status, B. bonaerensis. Parsimony analysis separated the bowhead and the right whale (family Balaenidae) from all remaining mysticetes, including the pygmy right whale. The pygmy right whale is usually included in family Balaenidae. The analysis revealed a close relationship between the gray whale (family Eschrichtiidae) sequence and those of the rorquals (family Balaenopteridae). The gray whale was included in a clade together with the sei, Bryde's, fin, blue, and humpback whales. This clade was separated from the two minke whale types, which branched together.      

Pilot Whales Attracted to Killer Whale Sounds: Acoustically-Mediated Interspecific Interactions in Cetaceans

In cetaceans’ communities, interactions between individuals of different species are often observed in the wild. Yet, due to methodological and technical challenges very little is known about the mediation of these interactions and their effect on cetaceans’ behavior. Killer whales (Orcinus orca) are a highly vocal species and can be both food competitors and potential predators of many other cetaceans. Thus, the interception of their vocalizations by unintended cetacean receivers may be particularly important in mediating interspecific interactions. To address this hypothesis, we conducted playbacks of killer whale vocalizations recorded during herring-feeding activity to free-ranging long-finned pilot whales (Globicephala melas). Using a multi-sensor tag, we were able to track the whales and to monitor changes of their movements and social behavior in response to the playbacks. We demonstrated that the playback of killer whale sounds to pilot whales induced a clear increase in group size and a strong attraction of the animals towards the sound source. These findings provide the first experimental evidence that the interception of heterospecific vocalizations can mediate interactions between different cetacean species in previously unrecognized ways.     

Building time-budgets from bioacoustic signals to measure population-level changes in behavior: a case study with sperm whales in the Gulf of Mexico

Evaluating changes in the collective behavior of a population can be an indirect method for inferring organismal responses to changing environmental conditions. Apex predators, such as the sperm whale (Physeter macrocephalus), can provide valuable insights into the ecosystem processes of the deep sea, where little direct observation can be made. Sperm whales are often difficult to observe at sea, as they inhabit deep, offshore waters and spend most of their lives beneath the surface. However, sperm whales are extremely amenable to passive acoustic monitoring, as their vocalizations are well-studied, highly distinguishable, produced regularly, and can be detected at relatively long ranges (>10 km). Sperm whales produce distinct clicks in two behavioral contexts (social interaction or foraging/prey capture); thus, we can use acoustic detection of these vocalizations to infer patterns of large-scale, collective behavior, which is similar to studying calling frogs or insects indicating their reproductive phenology. We recorded behaviorally-specific sperm whale vocalizations at three sites in the Northern Gulf of Mexico in July 2010 and 2011. We used these recordings to construct population-level time budgets, an empirical collective metric of behavior, based on the ratio of hours in a day with social clicks to the hours in a day with foraging clicks, and represented this as an “acoustic activity index.” Our index showed significant differences in the proportions of social and foraging behavior across the range of sperm whales in the Northern Gulf of Mexico, and the proportion of social activity increased by more than a factor of two from 2010 to 2011. These differences support previous evidence of differential habitat use by sperm whales in the Gulf of Mexico, and suggest possible changes in environmental conditions between years. Thus, the acoustic activity index may provide a powerful way to evaluate changes in behavior and link them to changing ecological conditions. This novel application of bioacoustics to constructing time budgets and creating a behaviorally-based index at the population scale can serve as an indicator of ecological change, and greatly enhance our ability to understand the behavior and ecology of many acoustically active species.     

Evolutionary Patterns among Living and Fossil Kogiid Sperm Whales: Evidence from the Neogene of Central America

Kogiids are known by two living species, the pygmy and dwarf sperm whale (Kogia breviceps and K. sima). Both are relatively rare, and as their names suggest, they are closely related to the sperm whale, all being characterized by the presence of a spermaceti organ. However, this organ is much reduced in kogiids and may have become functionally different. Here we describe a fossil kogiid from the late Miocene of Panama and we explore the evolutionary history of the group with special attention to this evolutionary reduction. The fossil consists of cranial material from the late Tortonian (~7.5 Ma) Piña facies of the Chagres Formation in Panama. Detailed comparison with other fossil and extant kogiids and the results of a phylogenetic analysis place the Panamanian kogiid, herein named Nanokogia isthmia gen. et sp. nov., as a taxon most closely related to Praekogia cedrosensis from the Messinian (~6 Ma) of Baja California and to Kogia spp. Furthermore our results show that reduction of the spermaceti organ has occurred iteratively in kogiids, once in Thalassocetus antwerpiensis in the early-middle Miocene, and more recently in Kogia spp. Additionally, we estimate the divergence between extant species of Kogia at around the late Pliocene, later than previously predicted by molecular estimates. Finally, comparison of Nanokogia with the coeval Scaphokogia cochlearis from Peru shows that these two species display a greater morphological disparity between them than that observed between the extant members of the group. We hypothesize that this reflects differences in feeding ecologies of the two species, with Nanokogia being more similar to extant Kogia. Nanokogia shows that kogiids have been part of the Neotropical marine mammal communities at least since the late Miocene, and gives us insight into the evolutionary history and origins of one of the rarest groups of living whales.     

Morphometric analysis of Chilean blue whales and implications for their taxonomy

In the Southern Hemisphere, blue whales are currently divided into two subspecies, Antarctic blue whales (Balaenoptera musculus intermedia) and pygmy blue whales (B. m. brevicauda), but there is some debate about whether Chilean blue whales should also be considered as a separate subspecies. Here, we provide novel morphometric data to directly address this taxonomic question from a biological survey of 60 blue whales taken during the 1965/1966 Chilean whaling season. The data show that maximum body length and mean body length of both sexually mature females and males for Chilean blue whales are intermediate between pygmy and Antarctic blue whales; and that fluke-anus lengths of Chilean blue whales are significantly different from pygmy blue whales, but not necessarily from Antarctic blue whales. There is also some support from the data that snout-eye measurements are different among all three groups. These data provide further confirmation that Chilean blue whales are a distinct population requiring separate management from other blue whale populations, and are also consistent with suggestions that Chilean blue whales are not the same subspecies as pygmy blue whales.     

A SIMPLE PHOTOGRAMMETRIC TECHNIQUE TO MEASURE SPERM WHALES AT SEA

Knowledge of whale length is important to ecological studies. However, photographic techniques to measure sperm whales traditionally require high vantage points or a complicated stereo system. Furthermore, these traditional techniques require an alongside approach that often prevents individual identification. For simple and fast size measurements at sea, I used a laser range finder alongside a digital camera to obtain distance to the fluke at the same time as photo-identification. The camera/lens and laser range finder were calibrated on objects of known lengths. The coefficient of variation (CV) for test objects was low (CV = 0.21%). Forty-seven individually identified sperm whales were measured repetitively on up to 12 different occasions, and the CV was lower (CV = 1.3%) than for other photogrammetric techniques (CV = 4.4%–5.1%). A regression of log fluke span to log total length from whaling and stranding data yielded an r  ² of 0.87 (CV of residuals = 6.7%). Thirty-eight female/immature sperm whales were measured in the Gulf of Mexico (median = 9.3 m, range = 7.1–12.3 m), 167 in the Gulf of California (median = 10.7 m, range = 8.4–13.1 m) and 13 bachelor males off Kaikoura, New Zealand (median = 14.2, range = 11.7–15.8 m). The results were within known sperm whale size and suggested that the population in the Gulf of Mexico was made up of smaller animals than that of the Gulf of California. This technique is easy to implement and allows the measurement of identified individuals.     

Automatic Realistic Real Time Stimulation/Recording in Weakly Electric Fish: Long Time Behavior Characterization in Freely Swimming Fish and Stimuli Discrimination

Weakly electric fish are unique model systems in neuroethology, that allow experimentalists to non-invasively, access, central nervous system generated spatio-temporal electric patterns of pulses with roles in at least 2 complex and incompletely understood abilities: electrocommunication and electrolocation. Pulse-type electric fish alter their inter pulse intervals (IPIs) according to different behavioral contexts as aggression, hiding and mating. Nevertheless, only a few behavioral studies comparing the influence of different stimuli IPIs in the fish electric response have been conducted. We developed an apparatus that allows real time automatic realistic stimulation and simultaneous recording of electric pulses in freely moving Gymnotus carapo for several days. We detected and recorded pulse timestamps independently of the fish’s position for days. A stimulus fish was mimicked by a dipole electrode that reproduced the voltage time series of real conspecific according to previously recorded timestamp sequences. We characterized fish behavior and the eletrocommunication in 2 conditions: stimulated by IPIs pre-recorded from other fish and random IPI ones. All stimuli pulses had the exact Gymontus carapo waveform. All fish presented a surprisingly long transient exploratory behavior (more than 8 h) when exposed to a new environment in the absence of electrical stimuli. Further, we also show that fish are able to discriminate between real and random stimuli distributions by changing several characteristics of their IPI distribution.     

SEASONAL OCCURRENCE OF SPERM WHALE (PHYSETER MACROCEPHALUS) SOUNDS IN THE GULF OF ALASKA, 1999–2001

An acoustic survey for sperm whales was conducted in the Gulf of Alaska. Six autonomous hydrophones continuously recorded sound signals below 500 Hz from October 1999 to May 2001. After recovery, recordings were processed using an automatic process to detect usual clicks of sperm whales. The detection algorithm equalized background noise, summed the data in a frequency band, and then used autocorrelation to detect the whales' highly regular clicks. Detections were checked manually, revealing that 98% of detections did contain clicks. Results indicate that sperm whales are present in the Gulf of Alaska year-round; this result extends what is known from whaling data, which were gathered principally in summer. Sperm whales were more common in summer than winter by a factor of roughly two, and occurred less often at the westernmost site surveyed (52°N, 157°W) than elsewhere in the Gulf. This is the first study of sperm whales based exclusively on remote acoustic sensing. This methodology is feasible because sperm whale clicks extend to frequencies (∼100 Hz) low enough to be recorded by low-sample-rate instruments that operate continuously, and because the detection algorithm has a low false-detection rate. The methodology may be replicated to facilitate comparisons between different time periods and geographic regions.     

KILLER WHALE PREDATION ON SPERM WHALES: OBSERVATIONS AND IMPLICATIONS

In October 1997 we observed a herd of approximately 35 killer whales ( Orcinus orca ) attack a pod of nine sperm whales ( Physeter macrocephalus ) 130 km off the coast of central California. During the four hours we watched, adult female killer whales, including some with calves, attacked in waves of four to five animals in what was apparently a "wound and withdraw" strategy. Adult male killer whales stood by until the very end when one charged in and quickly killed a seriously wounded sperm whale that had been separated from the group. The sperm whales appeared largely helpless: their main defensive behavior was the formation of a rosette ("marguerite"-heads together, tails out). When the killer whales were successful in pulling an individual out of the rosette, one or two sperm whales exposed themselves to increased attack by leaving the rosette, flanking the isolated individual, and leading it back into the formation. Despite these efforts, one sperm whale was killed and eaten and the rest were seriously, perhaps mortally, wounded. We also present details of two other encounters between sperm whales and killer whales that we observed. Although sperm whales, because of various behavioral and morphological adaptations, were previously thought to be immune to predation, our observations clearly establish their vulnerability to killer whales. We suggest that killer whale predation has potentially been an important, and underrated, selective factor in the evolution of sperm whale ecology, influencing perhaps the development of their complex social behavior and at-sea distribution patterns.     

Hydrodynamic performance of the flippers of large‐bodied cetaceans in relation to locomotor ecology

Cetaceans evolved flippers that are unique in both size and shape probably due to selection pressures associated with foraging and body size. Flippers function as control surfaces for maneuverability and stability. Flippers of cetaceans and engineered hydrofoils are similar with streamlined cross‐sections and wing‐like planforms, which affect lift, drag and hydrodynamic efficiency. Scale models of the flippers from large‐bodied (body length > 6 m) cetaceans (fin whale, killer whale, sperm whale) were constructed from computed tomography (CT) scans of flippers. Flipper planforms were highly tapered for the fin whale, a rounded, paddle‐like design for the killer whale, and a square geometry for the sperm whale. Hydrodynamic properties of the models at varying angles of attack (?40º to 40^o) were determined in a water tunnel with a multi‐axis load cell. The flippers were found to have hydrodynamic characteristics similar to engineered wings. Differences in flipper morphology of large‐bodied cetaceans and their hydrodynamic performance are associated with the requirements of aquatic locomotion involved with ecology of the whales. The flippers of the killer whale provided the greatest maneuverability, whereas the flippers of the fin whale had low drag for lunging and the flippers of the sperm whale provided lift for diving.     

Killer sperm whale: a new basal physeteroid (Mammalia, Cetacea) from the Late Miocene of Italy

Zygophyseter varolai , a new genus and species of Physeteroidea (Cetacea, Odontoceti), is based on an almost complete skeleton from the Late Miocene (Tortonian) in southern Italy. The extreme elongation of the zygomatic process of the squamosal and the circular supracranial basin (probably for housing the spermaceti organ) delimited by a peculiar anterior projection of the supraorbital process of the right maxilla are the most distinctive features of this bizarre sperm whale. Large body size, large teeth present in both lower and upper jaw, and anteroposteriorly elongated temporal fossa and zygomatic process of the squamosal indicate that this cetacean (for which we suggest the English common name killer sperm whale) was an active predator adapted to feeding on large prey, similarly to the extant killer whale ( Orcinus orca ). A phylogenetic analysis reveals that Zygophyseter belongs to a Middle–Late Miocene clade of basal physeteroids, together with Naganocetus (new genus for the type of ' Scaldicetus ' shigensis ). Moreover, the phylogenetic analysis shows evidence of a wide physeteroid radiation during the Miocene and that the extant Physeter and Kogia belong to two distinct families that form a clade representing the crown-group Physeteroidea.  © 2006 The Linnean Society of London, Zoological Journal of the Linnean Society , 2006, 148 , 103–131.     

MAJOR HISTOCOMPATIBILITY COMPLEX I POLYMORPHISM IN A CETACEAN: THE GRAY WHALE (ESCHRICHTIUS ROBUSTUS)

Vertebrate Major Histocompatibility Complex-I ( Mbc -I) proteins bind and display self and foreign peptides on the cell surface. Mbc -I polymorphism is considered critical for eliciting immune responses to a diversity of antigens, and thus, for the health and conservation of a species. Based on restriction fragment length polymorphism it was concluded that whales generally have low Mbc -I polymorphism. This was attributed to the weak pathogenic pressure in aquatic habitats. Since gray whales' habits might favor their encounter with diverse pathogens, resulting in selection pressures for Mbc variability, we searched for functional polymorphism of gray whale's Mbc -I exon 2 sequences that encode the α-1 protein domain of the antigen-binding region. We sequenced twelve Mbc -I exon 2 clones from each of seven gray whales. Most obtained sequences were similar to functional artiodactyl sequences, and their reconstructed phylogeny consistently showed three whale Mbc -I exon 2 sequence clusters (A, B, and C). Sequences within a given cluster and from distinct clusters, showed a greater number of non-synonymous than synonymous substitutions, that commonly shifted the physiochemical properties of the involved residue, suggesting the existence of a diverse repertoire of Mbc -I antigen recognition sites in gray whales, and that selection maintains gray whale's Mbc-I allelic diversity.     

Interspecific relationships in density among the whale community in the Antarctic

Interspecific relationships in density among a whale community in Antarctic feeding grounds were examined using the sightings data derived from the systematic surveys conducted between 1978/1979 and 1987/1988. A clear difference in densities against the physiographic variables (the sea floor-slope type) was identified between baleen whales and toothed whales. Densities of sperm whales and ziphiids were low in the waters over the continental shelf where minke whales' densities were highest. This led to an apparent negative correlation in the density between minke and sperm whales, and minke whale and ziphiids. A significant positive correlation in density between minke and blue whales was identified. No association in density between minke and humpback whales was observed. Distribution of killer whales shows strong positive correlation with that of minke whales. The positive correlation existed between minke and blue whales, and minke and killer whales even when the effect of environmental variables was excluded. Analysis also revealed that the environmental variables, including physiographic variables, are major factors affecting the distributions and density of whales, especially between baleen whales and toothed whales. Accepted: 8 December 1999     

SPERM WHALES IN THE GULF OF CALIFORNIA: RESIDENCY, MOVEMENTS, BEHAVIOR, AND THE POSSIBLE INFLUENCE OF VARIATION IN FOOD SUPPLY

Sperm whale movements, residency, population structure, and behavior were investigated in the Gulf of California in 1998 and 1999. Variations in sperm whale movement patterns and behavior were related to changes in prey abundance (jumbo squid, Dosidicus gigas ) determined by fishery statistics. Photo-identification data revealed that seven female sperm whales moved into the Gulf of California from the Galapagos Islands, traveling up to 3,803 km. These are among the longest documented movements for female sperm whales. There were significant differences in speed and distance traveled during a dive cycle between 1998 and 1999 (low and high squid abundance). In 1999 there were also significant differences in small-scale movements and behavior between the northern and the southern part of the study area (high and low prey abundance). These results suggest that when food resources are low, sperm whales travel in straighter lines, dive for longer periods, travel larger distances during dive cycles, and at higher speed. In 1999 there were significant differences in time spent socializing in areas of high prey abundance versus areas of low abundance. All of these changes in behavior were consistent with increased foraging effort when squid abundance was low. A high proportion of mature males and first-year calves were observed in the Gulf of California, suggesting that it is an important sperm whale breeding ground.