Color patterns of the shrimps Heptacarpus pictus and H. paludicola (Caridea: Hippolytidae)

Color patterns of the shallow-water shrimps Heptacarpus pictus and H. paludicola are formed by chromatosomes (usually termed chromatophores) located beneath the translucent exoskeleton. Development of color patterns is related to size (age) and sex. The color expressed is determined by the chromatosome pigment dispersion, arrangement, and density. In populations with well-developed coloration (H. pictus from Cayucos, California, 1976–1978, H. paludicola from Argyle Channel, San Juan Island, Washington, June–July, 1978), prominent coloration was a characteristic of maturing females, breeding females, and some of the larger males. In the Morro Bay, California, population of H. paludicola (sampled 1976–1978), color patterns were poorly developed except in a few large females. In both species, most shrimp lose color at night because of pigment retraction in certain chromatosomes. In both species, there are 5 basic morphs: 1 transparent and 4 colored morphs. In the colored morphs, the color patterns are composed of bands, stripes, and spots which appear to disrupt the body outline. Each color morph also has a common environmental color in its color pattern, e.g the green of green algae, the whites and pinks of dead and living coralline algae, and various shades of tidepool litter. These shrimps are apparently under heavy predation pressure by fish, and it is suggested that the color patterns are camouflage against such visually-hunting predators.     

Mechanisms of changes in population numbers of Caucasian red deer (<Emphasis Type="Italic">Cervus elaphus maral</Emphasis>) in the northwestern Caucasus

Mechanisms of changes in the numbers of red deer in the Caucasian State Biosphere Reserve (the northwestern Caucasus) were studied from 1958 to 2004 using simulation models developed on the basis of concepts concerning the combined effect of density-dependent and density-independent factors. The results show that changes in population numbers are accounted for by larger (more numerous) local subunits, with small groups remaining relatively stable. In the periods of depression, such a mechanism provides for the maintenance of the spatial population structure.     

The Use of Natural Taraxacum officinale Wigg. Populations for Assessing the State of Technogenically Disturbed Areas

Russian Journal of Ecology -     

Interaction webs in arctic ecosystems: Determinants of arctic change?

How species interact modulate their dynamics, their response to environmental change, and ultimately the functioning and stability of entire communities. Work conducted at Zackenberg, Northeast Greenland, has changed our view on how networks of arctic biotic interactions are structured, how they vary in time, and how they are changing with current environmental change: firstly, the high arctic interaction webs are much more complex than previously envisaged, and with a structure mainly dictated by its arthropod component. Secondly, the dynamics of species within these webs reflect changes in environmental conditions. Thirdly, biotic interactions within a trophic level may affect other trophic levels, in some cases ultimately affecting land–atmosphere feedbacks. Finally, differential responses to environmental change may decouple interacting species. These insights form Zackenberg emphasize that the combination of long-term, ecosystem-based monitoring, and targeted research projects offers the most fruitful basis for understanding and predicting the future of arctic ecosystems.     

Acoustically detected year-round presence of right whales in an urbanized migration corridor

Species' conservation relies on understanding their seasonal habitats and migration routes. North Atlantic right whales (Eubalaena glacialis), listed as endangered under the U.S. Endangered Species Act, migrate from the southeastern U.S. coast to Cape Cod Bay, Massachusetts, a federally designated critical habitat, from February through May to feed. The whales then continue north across the Gulf of Maine to northern waters (e.g., Bay of Fundy). To enter Cape Cod Bay, right whales must traverse an area of dense shipping and fishing activity in Massachusetts Bay, where there are no mandatory regulations for the protection of right whales or management of their habitat. We used passive acoustic recordings of right whales collected in Massachusetts Bay from May 2007 through October 2010 to determine the annual spatial and temporal distribution of the whales and their calling activity. We detected right whales in the bay throughout the year, in contrast to results from visual surveys. Right whales were detected on at least 24% of days in each month, with the exception of June 2007, in which there were no detections. Averaged over all years, right whale calls were most abundant from February through May. During this period, calls were most frequent between 17:00 and 20:00 local time; no diel pattern was apparent in other months. The spatial distribution of the approximate locations of calling whales suggests they may use Massachusetts Bay as a conduit to Cape Cod Bay in the spring and as they move between the Gulf of Maine and waters to the south in September through December. Although it is unclear how dependent right whales are on the bay, the discovery of their widespread presence in Massachusetts Bay throughout the year suggests this region may need to be managed to reduce the probability of collisions with ships and entanglement in fishing gear.     

Polygyny and male parental care in Savannah sparrows: effects on female fitness

Summary To determine the effects of male mating status on female fitness, we compared the reproductive success, survival, and future fecundity of female Savannah sparrows (Passerculus sandwichensis) mated to monogamous vs. polygynous males in a 5-year study on Kent Island, New Brunswick, Canada. The proportion of males with more than one mate varied from 15 to 43% between years and sites. Polygynous and monogamous males fledged young of equal size in every year of the study. Females who shared paternal care with other females laid as many eggs per clutch and clutches per season as monogamously mated females. In most years polygynously mated females showed no delay in laying a second clutch, and they suffered no reduction in fecundity the following year. Recruitment of a female's offspring into the breeding population was generally independent of her mating status. Fitness costs of being mated to a polygynous male were only apparent in one year of the study, during which females mated to polygynous males had higher over-winter mortality than those mated to monogamous males. That same year, young raised by polygynous males were only one-third as likely to survive to reproductive maturity (as inferred by returns) as those raised by monogamous males. A male's mating status had no effect on his own survivorship. A male's mating status did not necessarily reflect his contributions to raising nestlings, which may partially explain why monogamously and polygynously mated females had equal fitness. At 35 nests the proportion of food deliveries brought by individual males varied from 0 to 75%; on average, males brought fewer than 30% of all food deliveries. Yet parental care by polygynous males was no less than that of monogamous males, at least at the nests of their primary females. Secondary females tended to receive less male assistance during the nestling stage, but their reproductive success was indistinguishable from that of primary females. Females feeding young without male assistance made as many food deliveries/h as did pairs in which males brought at least 30% of all food deliveries. Unassisted females did not suffer diminished fledging success or produce smaller fledglings. The benefits of polygyny for male Savannah sparrows are clear: polygynous males recruit more surviving offspring into the breeding population than monogamous males. The fitness of females, on the other hand, appears to be unaffected by whether their mate was monogamous or polygynous except in occasional years. Polygyny may be maintained in this population by the constraints of a female-biased sex ratio, the inability of females to predict a male's paternal care based on his morphology or behavior, the poor correlation between a male's mating status and his assistance at the nest, and inconsistent natural selection against mating with a polygynous male. Correspondence to: N.T. Wheelwright     

Relative size of Aristotle's lantern in Echinometra mathaei occuring at different densities

Like species of sea urchins in Zanzibar and Oregon (USA), Echinometra mathaei (de Blainville) at Rottnest Island, Western Australia, displays variation in the size of Aristotle's lantern relative to the maximum diameter of the test. This variation was associated with local variations in density of urchins at each of two sites in each of two years (1980 and 1981); this association with density was consistent with the proposal that relatively larger lanterns are a response to decreased food availability. Furthermore, variation of relative lantern size associated with local density was similar in magnitude to the variation displayed between sites and between years. This temporal variation demonstrated the plasticity of the relative lantern size over periods as short as 12 mo. Further experimental studies are required before relative length of lanterns can be used as estimates of food availability.     

Exuviaella cordata red tide in Bulgarian coastal waters (May to June 1986)

The structure and some functional characteristics of the plankton community at the time of aExuviaella cordata red tide were investigated in Burgas Bay, Bulgaria, in May and June 1986. Characteristics of main plankton components (phyto-, bacterio-, nanoheterotrophic plankton, ciliates and mesoplankton) in the bloom area are presented. Development of theE. cordata bloom was determined by abiotic conditions among which eutrophication and salinity decrease caused the patchy character of its rapid development. Attainment of maximum red tide (ca. 1x10⁹ cells l^-1; 1x10³ g m^-3) from background (500 to 800x10³ cells l^-1; 600 mg m^-3) took 3 to 7d. Growth rate () during that period was 1.2 to 2.2 doublings per day. A sharp bloom decline (3 to 4d) was caused by parasitic flagellates destroying the alga's chloroplast. Diel biomass losses due to grazing remained below 5%. Metabolites and degradation products ofE. cordata revealed no pronounced toxic effects on the other components of the planktonic community. The rapid bloom degradation due to the effects of parasitic flagellates indicates the high potential of ecosystem self-regulation.     

Molecular phylogeny and population structure of tideland snails in the genus Cerithidea around Japan

Phylogenetic relationships and genetic population structures were analyzed for tideland gastropods in the genus Cerithidea around Japan on the basis of partial sequence of the mitochondrial COI gene. Large genetic divergence was shown between individuals of Cerithidea cingulata in the southern Ryukyus and those in the central Ryukyus and the Japanese Islands. Haplotypes of C. cingulata from the Japanese Islands were paraphyletic with the exclusion of a monophyletic group from the central Ryukyus. Genetic differentiation of C. cingulata was also detected between Amami-Oshima Island and Okinawajima Island. No genetic divergence was found between Cerithidea rhizophorarum in the Japanese Islands and its subspecies C. rhizophorarum morchii in the Ryukyu Islands. The lack of genetic divergence of Cerithidea largillierti between continental China and Japan suggests relatively recent migration between the Japanese Islands and the Asian continent. For all three Cerithidea species distributed in both the Japanese Islands and the Ryukyu Islands, the Tokara Gap and the Kerama Gap were shown to have acted as barriers to the dispersal.