THE TAPETUM FIBROSUM IN THE EYES OF TWO SMALL WHALES

The pygmy sperm whale ( Kogia breviceps ) and the bottlenose dolphin ( Tursiops truncatus ) are equipped with a tapetum fibrosum and, with other Cetacea, are the only carnivores known to possess this typically ungulate tapetal type. Tapeta from two regions of a retina, each with a different spectral reflectance (blue and green), were found to have significantly different fibrillar diameters and inter-fibrillar spacing. When the measured values are applied to a dielectric reflector model, the predicted wavelengths agree with the observed reflectance of the flat-mounted tapeta. The spatial properties of the fibrils change progressively from the tapetal origin in the fibroblast layer to the pigment epithelium, suggesting that different wavelengths may be reflected systematically with tapetal depth. The very large number of reflecting layers characterizing these tapeta, relative to those of other carnivores, may provide for increased spectral purity and efficiency.     

POLYPHYLY OF THE BLACKBIRD GENUS AGELAIUS AND THE IMPORTANCE OF ASSUMPTIONS OF MONOPHYLY IN COMPARATIVE STUDIES

A phylogeny for Agelaius blackbirds was constructed using sequence data from an 890 base-pair (bp) region of the mitochondrial cytochrome-b gene in nine species of Agelaius and a single species from all but 1 of the 28 described blackbird genera and subgenera. The genus was found to be polyphyletic with the South American members of Agelaius more closely related to other South American blackbird genera. Application of bootstrap and jackknife manipulations supports this conclusion. That this relatively well-known genus is polyphyletic represents a warning to those attempting to construct phylogenies without first demonstrating monophyly of the ingroup. The conclusion that Agelaius is polyphyletic necessitates (1) the reinterpretation of previous studies that assumed monophyly and (2) the initiation of a variety of new comparative behavioral and ecological studies suggested by this finding.     

THE ORIGIN OF THE SPINNING APPARATUS IN SPIDERS

• 1 Previous attempts to explain the evolution of spider silk have relied heavily on conjecture. The formulation of testable historical hypotheses to replace such speculation is discussed.
• 2 The importance of phylogenetic reconstructions and other historical hypotheses for use in generating and testing hypotheses concerning the evolution of specific adaptations is examined. Recent ideas on arachnid phylogeny are reviewed and their relevance to the problem of silk evolution in spiders is explored.
• 3 Evidence from the analysis of three historical problems (origin of spinnerets, origin of silk glands, original selective pressure favouring evolution of silk) is reviewed from three different frames of reference (in-group analysis, out-group analysis, convergence analysis). Several lines of evidence are found which suggest that silk use originated in spiders due to selective pressures associated with reproduction (specifically, the transfer of sperm or the protection of eggs).
• 4 The prevalence of segmental appendages retained for use in manipulating genital products in both arachnids and non-arachnid arthropods and the probable placement of spinnerets near the genital opening in ancestral spiders suggest that spinnerets represent modified gonopods.
• 5 The most primitive types of silk glands are retained in virtually all spiders, in part, for use in the construction of sperm webs and egg sacs. Similar silk glands are found near the genital opening in many male spiders and used in building a portion of the sperm web.
• 6 The silk of adult arthropods other than spiders is used largely in manipulating or protecting sex cells. If there are multiple functions, use in reproduction is typically one of them. Thus, there is evidence for strong selective pressure favouring the evolution of silk for use in reproduction.
• 7 Two hypotheses are proposed which are consistent with the conclusion that silk in spiders evolved for reproductive needs (the spermatophore-sperm web and egg sac hypotheses). Testable predictions of each hypothesis are proposed.

     

MOVEMENTS AND POPULATION STRUCTURE OF HUMPBACK WHALES IN THE NORTH PACIFIC

Despite the extensive use of photographic identification methods to investigate humpback whales in the North Pacific, few quantitative analyses have been conducted. We report on a comprehensive analysis of interchange in the North Pacific among three wintering regions (Mexico, Hawaii, and Japan) each with two to three subareas, and feeding areas that extended from southern California to the Aleutian Islands. Of the 6,413 identification photographs of humpback whales obtained by 16 independent research groups between 1990 and 1993 and examined for this study, 3,650 photographs were determined to be of suitable quality. A total of 1,241 matches was found by two independent matching teams, identifying 2,712 unique whales in the sample (seen one to five times). Site fidelity was greatest at feeding areas where there was a high rate of resightings in the same area in different years and a low rate of interchange among different areas. Migrations between winter regions and feeding areas did not follow a simple pattern, although highest match rates were found for whales that moved between Hawaii and southeastern Alaska, and between mainland and Baja Mexico and California. Interchange among subareas of the three primary wintering regions was extensive for Hawaii, variable (depending on subareas) for Mexico, and low for Japan and reflected the relative distances among subareas. Interchange among these primary wintering regions was rare. This study provides the first quantitative assessment of the migratory structure of humpback whales in the entire North Pacific basin.     

THE DISTRIBUTION OF BOWHEAD WHALES, BALAENA MYSTICETUS, IN THE CHUKCHI SEA

Under a U.S.-U.S.S.R. cooperative Marine Mammal Project, shipboard cruises were made in 1979, 1980 and 1982, primarily to determine whether there is a substock of western Arctic bowhead whales ( Balaena mysticetus ) that summers in the western Chukchi Sea instead of migrating to the Beaufort Sea. More than 100 bowheads were sighted along the north Chukotka coast of Siberia in October 1979, and more than 200 bowheads were sighted there in September 1980. None were seen anywhere in the Chukchi Sea in late July and August 1982. We conclude that the September and October sightings were of animals returning early from the Beaufort Sea and that, other than occurrences peripheral to the main migration, there are no large concentrations in the Chukchi in the summer and there is apparently no western Chukchi substock.