The nature and affinities of the “robust” Australopithecines: a review

The fossil evidence of the “robust” australopithecines is reviewed with an emphasis on the taxonomic divisions and evolutionary relationships among this group of hominids. The hypodigms of A. robustus, A. crassidens and A. boisei are described, and the significance of morphological variation within and between these species is assessed. Phylogenetic relationships among the “robust” australopithecines are examined using maximum parsimony analysis, and evolutionary scenarios are evaluated in the light of recent discoveries in East Africa.     

STABILIZATION MECHANISM IN SWIMMING ODONTOCETE CETACEANS BY PHASED MOVEMENTS

Propulsive movements of the caudal oscillating flukes produce large forces that could induce equally large recoil forces at the cranial end of the animal, and, thus, affect stability. To examine these vertical oscillations, video analysis was used to measure the motions of the rostrum, pectoral flipper, caudal peduncle, and fluke tip for seven odontocete cetaceans: Delphinapterus leucas, Globicephala melaena, Lagenorhynchus obliquidens, Orcinus orca, Pseudorca crassidens, Stenella plagiodon , and Tursiops truncatus. Animals swam over a range of speeds of 1.4–7.30 m/sec. For each species, oscillatory frequency of the fluke tip increased linearly with swimming speed. Peak-to-peak amplitude at each body position remained constant with respect to swimming speed for all species. Mean peak-to-peak amplitude ranged from 0.02 to 0.06 body length at the rostrum and from 0.17 to 0.25 body length at the fluke tip. The phase relationships between the various body components remain constant with respect to swimming speed. Oscillations of the rostrum were nearly in phase with the fluke tip with phase differences out of—9.4°-33.0° of a cycle period of 360°. Pectoral flipper oscillations trailed fluke oscillations by 60.9°-123.4°. The lower range in amplitude at the rostrum compared to the fluke tip reflects increased resistance to vertical oscillation at the cranial end, which enhances the animal's stability. This resistance is likely due to both active and passive increased body stiffness, resistance on the flippers, phased movements of body components, and use of a lift-based propulsion. Collectively, these mechanisms stabilize the body of cetaceans during active swimming, which can reduce locomotor energy expenditure and reduce excessive motions of the head affecting sensory capabilities.     

MAXIMUM SWIM SPEEDS OF CAPTIVE AND FREE-RANGING DELPHINIDS: CRITICAL ANALYSIS OF EXTRAORDINARY PERFORMANCE

Research into dolphin swimming historically was guided by false assumptions pertaining to maximum speed. Accurate measurements on swimming speed and duration of effort of free-ranging dolphins are rare. To examine the variance of maximum swimming speeds, nearly 2,000 speed measurements were obtained for both captive and free-ranging dolphins, including Tursiops truncatus, Pseudorca crassidens, Delphinus capensis , and Delphinus delpbis . Measurements were made from videotapes of dolphins trained to swim fast around a large pool or jumping to a maximum height, videotapes of captured wild dolphins immediately after release, and sequential aerial photographs of a school of free-ranging dolphins startled by a passing airplane. Maximum horizontal speeds for trained animals were 8.2 m/sec for T. truncatus , 8.0 m/sec for D. delphis , and 8.0 m/sec for P. crassidens . Maximum speeds for T. truncatus swimming upwards, prior to vertical leaps ranged from 8.2 to 11.2 m/sec. Wild T. truncatus demonstrated a maximum speed of 5.7 m/sec. Maximum swimming speed of free-ranging D. capensis responding to multiple passes by a low flying airplane was 6.7 m/sec. There was no evidence that the freeranging dolphins have superior swimming capabilities to captive animals. The results of this study imply that realistic maximum swimming speeds for dolphins are lower than previous reports which were based on sparse data and imprecise measurement techniques.     

False killer whales (Pseudorca crassidens) from Japan and South Africa: Differences in growth and reproduction

Age and reproductive information for 65 false killer whales stranded in South Africa in 1981 are compared with similar material from 156 animals examined from drive fisheries in Japan in 1979 and 1980. Sizes at birth, sexual maturation, and physical maturity all indicated that both sexes were 10%–20% larger in Japan than South Africa. Females reached sexual maturation at similar ages (8–10.5 yr) in both populations, and although sample sizes were too small to establish male ages at puberty precisely the ranges in Japan (10.5–18.5 yr) and South Africa (5.25–17.5 yr) were not inconsistent. The initial ovulation rate for females from South Africa was 65% lower (and the apparent pregnancy rate 82% lower) than those from Japan and there were fewer animals ≤2 yr old within the school, but the magnitude of these differences suggests that the stranded school's reproductive performance was probably impaired. Collectively these comparisons and the literature indicate substantive size differences between false killer whales in different populations, although the patterns of growth appear similar. Firm conclusions about any geographical differences in reproduction require additional data.     

ACOUSTIC IDENTIFICATION OF NINE DELPHINID SPECIES IN THE EASTERN TROPICAL PACIFIC OCEAN

Acoustic methods may improve the ability to identify cetacean species during shipboard surveys. Whistles were recorded from nine odontocete species in the eastern tropical Pacific to determine how reliably these vocalizations can be classified to species based on simple spectrographic measurements. Twelve variables were measured from each whistle ( n = 908). Parametric multivariate discriminant function analysis (DFA) correctly classified 41.1% of whistles to species. Non-parametric classification and regression tree (CART) analysis resulted in 51.4% correct classification. Striped dolphin whistles were most difficult to classify. Whistles of bottlenose dolphins, false killer whales, and pilot whales were most distinctive. Correct classification scores may be improved by adding prior probabilities that reflect species distribution to classification models, by measuring alternative whistle variables, using alternative classification techniques, and by localizing vocalizing dolphins when collecting data for classification models.     

一头罕见伪虎鲸的测量

2005 年10 月山东省荣成市远洋渔船的渔民偶然误捕了一头海豚,经鉴定,系伪虎鲸,且为畸形。主要鉴别特征:全身呈暗黑色,体细长,背鳍狭长而呈镰刀形,胸鳍前缘有一特有的隆起,即所谓的“肘部”,牙齿大,呈圆锥形,上颌齿数为14,下颌齿数为16。同时,还对其进行了较详细的观察和测量。畸形表现在:左右口角的形状不一;左鳍肢前缘有一明显的二分叉;雌性,乳沟内无乳头,但经解剖发现腹内却有一胎儿,系雄性,体长1.8 m,体重40 kg。
     

黄海伪虎鲸mtDNA 控制区序列的测定和初步分析

测定了黄海7 头伪虎鲸mtDNA 控制区5’端533 bp 的序列, 共发现54 个变异位点, 定义了4 种单元型。最大似然法和邻接法的系统树均把单元型聚为2 分支。两支之间没有共享单元型且无姊妹关系。分支间的核苷酸序列差异显著地超过了其它海豚类种间的序列差异水平, 提示传统意义上的伪虎鲸可能包括了具有显著遗传差别的不同物种, 迫切需要开展进一步的研究。     

False killer whales (Pseudorca crassidens) around the main Hawaiian Islands: Long-term site fidelity, inter-island movements, and association patterns

Despite their world-wide distribution throughout the tropics and subtropics, false killer whales ( Pseudorca crassidens ) are one of the lesser-known large odontocetes. Genetic evidence indicates a demographically isolated population around the main Hawaiian Islands. We examine site fidelity, movements and association patterns in this population using data from directed surveys and opportunistic photographs from 1986 to 2007. This species was only infrequently encountered, and while found in depths from 38 to 4,331 m, sighting rates were greatest in depths >3,000 m. We photo-identified 152 distinctive individuals. Resighting rates were high, with an average of 76.8% of distinctive individuals within groups documented on more than one occasion. Most (86.6%) were linked by association into a single social network; only one large group (16 distinctive individuals), documented the farthest offshore (42–70 km), did not link by association to that large network, and may be part of an offshore population. Individual movements of up to 283 km were documented, with a large proportion of individuals moving among islands. Individuals were resighted up to 20.1 yr after first being documented, showing long-term fidelity to the islands. Repeated associations among individuals were documented for up to 15 yr, and association analyses indicate preferred associations and strong bonds among individuals.     

How to tell them apart? Discriminating tropical blackfish species using fin and body measurements from photographs taken at sea

The misidentification of species and populations is a hindrance to effective cetacean management. We devised a method of species identification using 10 fin and body measurements obtainable from at‐sea photographs, and demonstrated its ability to distinguish four species of Hawaiian “blackfish”: pygmy killer, melon‐headed, short‐finned pilot, and false killer whales. Measurements from photos of 382 known individuals were converted into 14 ratios and reduced using nonmetric multidimensional scaling and principal component analysis. The first three components of the PCA explained 81% of variance among species. Ratios indicated by PCA and NMDS were tested using analysis of variance, and results identified three fin ratios that had distinct means across all four species: height/base, depth (from anterior insertion) at trailing edge apex/depth at topmost point, and width (from leading edge) at posterior point/base. Dual analysis of adults and all age classes showed near‐identical sources of variance, 90% similarity in interspecies ratio relationships, and overlapping ratio means and ranges. Results suggest similar ontogenetic growth across these four species, and confirm the efficacy of this discrimination technique for all age classes. This study established a reliable means of distinguishing these cetacean species, which will improve the efficacy of management in areas with sympatric distributions.     

Occurrence of false killer whales (Pseudorca crassidens) and their association with common bottlenose dolphins (Tursiops truncatus) off northeastern New Zealand

On a global scale, false killer whales (Pseudorca crassidens) remain one of the lesser‐known delphinids. The occurrence, site fidelity, association patterns, and presence/absence of foraging in waters off northeastern New Zealand are examined from records collected between 1995 and 2012. The species was rarely encountered; however, of the 61 distinctive, photo‐identified individuals, 88.5% were resighted, with resightings up to 7 yr after initial identification, and movements as far as 650 km documented. Group sizes ranged from 20 to ca. 150. Results indicate that all individuals are linked in a single social network. Most observations were recorded in shallow (<100 m) nearshore waters. Occurrence in these continental shelf waters is likely seasonal, coinciding with the shoreward flooding of a warm current. During 91.5% of encounters, close interspecific associations with common bottlenose dolphins (Tursiops truncatus) were observed. Photo‐identification reveals repeat inter‐ and intraspecific associations among individuals with 34.2% of common bottlenose dolphins resighted together with false killer whales over 1,832 d. While foraging was observed during 39.5% of mixed‐species encounters, results suggest that social and antipredatory factors may also play a role in the formation of these mixed‐species groups.