我国沿海拟虎鲸骨骼研究

本文对我国沿海所捕获的拟虎鲸骨骼系统,进行了较全面的研究和测量,并对其骨骼特点及形态、功能方面也做了些探讨。     

KILLER WHALE PREDATION ON BELUGAS IN COOK INLET, ALASKA: IMPLICATIONS FOR A DEPLETED POPULATION

Killer whale predation on belugas in Cook Inlet, Alaska, has become a concern since the decline of these belugas was documented during the 1990s. Accordingly, killer whale sightings were compiled from systematic surveys, observer databases, and anecdotal accounts. Killer whales have been relatively common in lower Cook Inlet (at least 100 sightings from 1975 to 2002), but in the upper Inlet, north of Kalgin Island, sightings were infrequent (18 in 27 yr), especially prior to the 1990s. Beach cast beluga carcasses with teeth marks and missing flesh also provided evidence of killer whale predation. Most observed killer whale/beluga interactions were in the upper Inlet. During 11 of 15 observed interactions, belugas were obviously injured or killed, either through direct attacks or indirectly as a result of stranding. Assuming at least one beluga mortality occurred during the other four encounters, we can account for 21 belugas killed between 1985 and 2002. This would suggest a minimum estimate of roughly 1/yr and does not include at least three instances where beluga calves accompanied an adult that was attacked.     

SPECIES SPECIFIC PATTERN OF CILIOGENESIS IN DEVELOPING SEA URCHIN EMBRYOS

The events of cell division and ciliogenesis in individual blastomeres of developing embryos of the sea urchins Temnopleurus toreumaticus and Hemicentrotus pulcherrimus were followed with a Nomarski differential interference microscope. The number of cell divisions before initiation of ciliogenesis was determined with respect to species. In T. toreumaticus , ciliogenesis began about 4 hr after fertilization at 25°C. The sequence of ciliogenesis was as follows: cilia appeared first on smaller micromeres, followed in order by blastomeres derived from larger micromeres, those from mesomeres and finally those derived from macromeres. Blastomeres originating from mesomeres, macromeres, larger micromeres and smaller micromeres had completed the 8th, 9th, 7th and 5th divisions respectively, before they generated cilia.
In H. pulcherrimus , embryos started to form cilia about 9 hr after fertilization at 18°C. Cilia appeared first on blastomeres of mesomere origin and, then on those of macromere origin. Before initiation of ciliogenesis, descendants of mesomeres and macromeres completed 9 and 10 rounds of cell division. Descendants of larger micromeres and the majority of cells derived from smaller micromeres did not acquired cilia even when the embryo began to rotate within the fertilization membrane. At this stage, the former had completed the 6th division and the latter the 8th division. Cell counts of blastomeres per embryo at the blastula stage also supported this observation.     

HETEROCHRONIC DEVELOPMENTAL PLASTICITY IN LARVAL SEA URCHINS AND ITS IMPLICATIONS FOR EVOLUTION OF NONFEEDING LARVAE

Preexisting developmental plasticity in feeding larvae may contribute to the evolutionary transition from development with a feeding larva to nonfeeding larval development. Differences in timing of development of larval and juvenile structures (heterochronic shifts) and differences in the size of the larval body (shifts in allocation) were produced in sea urchin larvae exposed to different amounts of food in the laboratory and in the field. The changes in larval form in response to food appear to be adaptive, with increased allocation of growth to the larval apparatus for catching food when food is scarce and earlier allocation to juvenile structures when food is abundant. This phenotypic plasticity among full siblings is similar in direction to the heterochronic evolutionary changes in species that have greater nutrient reserves within the ova and do not depend on particulate planktonic food. This similarity suggests that developmental plasticity that is adaptive for feeding larvae also contributes to correlated and adaptive evolutionary changes in the transition to nonfeeding larval development. If endogenous food supplies have the same effect on morphogenesis as exogenous food supplies, then changes in genes that act during oogenesis to affect nutrient stores may be sufficient to produce correlated adaptive changes in larval development.     

RISK OF EXTIRPATION OF STELLER SEA LIONS IN THE GULF OF ALASKA AND ALEUTIAN ISLANDS: A POPULATION VIABILITY ANALYSIS BASED ON ALTERNATIVE HYPOTHESES FOR WHY SEA LIONS DECLINED IN WESTERN ALASKA

We estimated the risk that the Steller sea lion will be extirpated in western Alaska using a population viability analysis (PVA) that combined simulations with statistically fitted models of historical population dynamics. Our analysis considered the roles that density‐dependent and density‐independent factors may have played in the past, and how they might influence future population dynamics. It also established functional relationships between population size, population growth rate and the risk of extinction under alternative hypotheses about population regulation and environmental variability. These functional relationships can be used to develop recovery criteria and guide research and management decisions. Life table parameters (e.g., birth and survival rates) operating during the population decline (1978–2002) were estimated by fitting simple age‐structured models to time‐series of pup and non‐pup counts from 33 rookeries (subpopulations). The PVA was carried out by projecting all 33 subpopulations into the future using these estimated site‐specific life tables (with associated uncertainties) and different assumptions about carrying capacities and the presence or absence of density‐dependent population regulation. Results suggest that the overall predicted risk of extirpation of Steller sea lions as a species in western Alaska was low in the next 100 yr under all scenarios explored. However, most subpopulations of Steller sea lions had high probabilities of going extinct within the next 100 yr if trends observed during the 1990s were to continue. Two clusters of contiguous subpopulations occurring in the Unimak Pass area in the western Gulf of Alaska/eastern Aleutian Islands and the Seguam–Adak region in the central Aleutian Islands had relatively lower risks of extinction. Risks of extinction for a number of subpopulations in the Gulf of Alaska were reduced if the increases observed since the late 1990s continue into the future. The risks of subpopulations going extinct were small when density‐dependent compensation in birth and survival rates was assumed, even when random stochasticity in these vital rates was introduced.     

GROWTH LAYER GROUPS (GLGs) IN THE TEETH OF AN ADULT BELUKHA WHALE (DELPHINAPTERUS LEUCAS) OF KNOWN AGE: EVIDENCE FOR TWO ANNUAL LAYERS

Growth layer groups (GLGs) were counted in teeth from an adult male belukha whale ( Delphinapterus leucas ) that had lived for 23 yr in captivity and was estimated to have been 14 mo at capture. As defined here, GLGs are repeating areas of alternating opaque (denser) and translucent (less dense) dentin or cementurn, or nodes at the dentin-cementum interface. A GLG involves at least one change from opaque to translucent, dense to less dense or ridge to groove, but may be further subdivided by incremental growth layers or laminations. Teeth were prepared by two techniques. Thick sections (longitudinal half sections) were examined with a dissecting microscope under reflected light. Thinner cross and longitudinal sections were x-rayed and the plates scanned with a microdensitometer. Scanning electron photomicrographs were prepared from thick sections, but SEM proved to be the least useful technique. Counts of GLGs were variable because the laminations were numerous and some surface layers had been lost from wear. Thick- and thinner-section techniques gave comparable results, and approximately 40 GLGs were counted consistently. Although captive environments are less variable than natural ones, our findings are further evidence that belukhas in the wild deposit more than one—and probably two—GLGs per year.     

GENERAL PATTERN, 35SO4-INCORPORATION AND INTRACELLULAR LOCALIZATION OF GLYCANS IN DEVELOPING SEA URCHIN (ANTHOCIDARIS) EMBRYOS

Glycosaminoglycan (GAG) prepared from sea urchin embryos ( Anthocidaris crassispina ) at various stages with or without pulse ³⁵SO₄-labelling was separated into various fractions by chromatography on DEAE-cellulose with a linear NaCl concentration gradient: fraction P (nonacidic) and fractions A through F (of increasing acidities). The ³⁵SO₄-radioactivity was negligible in P and A, largest in B and C, and decreased in the other fractions three alphabetical order. During development (hatched blastulae to gastrulae) the glycans in fractions P and A decreased in amount, whereas those in E and F increased. E contained heparin-like (AMPS-1) and dermatanpolysulfate-like (AMPS-2) GAG in addition to a sulfated fucogalactan-like (E₁) glycan. Another sulfated fucogalactan-like (F₁) glycan was found in F. A sulfated polysialic acid-like (S₁) glycan was found in C. An EDTA-extract of gastrulae gave AMPS-2, E₁ and F₁. The mitochondria-rich fraction gave AMPS-1, whereas the yolk granule-rich fraction gave S₁. Most of the other still unidentified components in B, C, and D appeared to be derived from glycoproteins and were mainly located in the crude yolk-mitochondrial and cytosol fractions.     

颗石藻自动鉴定系统及其古海洋学应用——以南海MD05-2901柱状样研究为例

颗石藻自动鉴定系统SYRACO(Système de Reconnaissance Automatique de Coccolithes)是一种通过人工智能神经网络自动识别颗石藻种类并统计数量的工具软件。该软件能够快速可靠识别观察视域中的所有颗石个体,大幅度提高工作效率并弥补了在颗石藻属种鉴定过程中的人为误差。经过训练的SYRACO系统可以鉴定第四纪以来14个主要颗石藻属种,适用于第四纪以来的古环境研究。作者使用SYRACO自动鉴定系统对南海MD05-2901柱状样进行颗石藻属种鉴定,同时获得了Florisphaera profunda,Emiliania huxleyi,Gephyrocapsa oceani-ca等主要属种含量信息。将结果与先前人工统计数据对比表明二者具有很好的一致性,证明其在古海洋学研究中的应用价值。     

LOCAL ATTITUDES, MORAL OBLIGATION, CUSTOMARY OBEDIENCE AND OTHER CULTURAL PRACTICES: THEIR INFLUENCE ON THE PROCESS OF GAINING INFORMED CONSENT FOR SURGERY IN A TERTIARY INSTITUTION IN A DEVELOPING COUNTRY

The process of obtaining informed consent in a teaching hospital in a developing country (e.g. Nigeria) is shaped by factors which, to the Western world, may be seen to be anti-autonomomous: autonomy being one of the pillars of an ideal informed consent. However, the mix of cultural bioethics and local moral obligation in the face of communal tradition ensures a mutually acceptable informed consent process. Paternalism is indeed encouraged by the patients who prefer to see the doctor as all-powerful and all-knowing, and this is buttressed by the cultural practice of customary obedience to those 'above you': either in age or social rank. The local moral obligation reassures the patients that those in authority will always look after others placed in their care without recourse to lengthy discussions or signed documentation, while the communal traditions ensure that the designated head of a family unit has the honor and sole responsibility of assenting and consenting to an operation to be carried out on a younger, or female, member of the family. Indeed it is to only a few educated patients that the informed consent process is deemed a shield against litigation by the doctors. This paper later addresses the need for physicians to update their knowledge on the process of informed consent through the attendance of biomedical ethics courses, which should highlight socio-cultural practices that may make this process different from the Western concept, but perfectly acceptable in this setting.