To save content items to your account,
please confirm that you agree to abide by our usage policies.
If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account.
Find out more about saving content to .
To save content items to your Kindle, first ensure no-reply@cambridge.org
is added to your Approved Personal Document E-mail List under your Personal Document Settings
on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part
of your Kindle email address below.
Find out more about saving to your Kindle.
Note you can select to save to either the @free.kindle.com or @kindle.com variations.
‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi.
‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
The Norway lobster, Nephrops norvegicus is a target fishery species in European waters. The stock assessment of N. norvegicus is complicated because it is caught in commercial gear only when it emerges from its burrow. Landings are lower in winter, and feeding limitations have been hypothesized as the cause. Wild large-sized male lobsters were sampled each season (winter, spring, summer and autumn), and two groups of animals were kept in captivity for 90 d (fed and food-deprived). The hepatopancreas and muscle were dissected, weighted, frozen for biochemical analyses (proximal analyses and DNA/RNA) and fixed in Bouin solution for microscopic observations. The oxygen consumption rates in the wild individuals caught in the spring and in the captive animals after the treatments were measured. Significant differences among the experimental groups were observed in the lipid concentration of the hepatopancreas and muscle, the water content in the hepatopancreas, and the numbers of vacuoles and pyknotic nuclei in the cells of the tubules of the hepatopancreas. The results showed that the wild Norway lobsters generally presented intermediate values between those observed in the food-deprived and the fed lobsters kept in captivity, but the values were closer to those obtained for the fed animals. This finding indicates that the wild animals exhibit a good nutritional condition throughout the year. Therefore, the wild males of N. norvegicus do not face food deprivation during winter as is suggested by the pattern of commercial catches, the flow of organic matter, and the moulting period/reproductive behaviour of the species.
Balanophyllia europaea is an endemic Mediterranean sublittoral zooxanthellate solitary coral. Given the broad distribution of the species throughout many areas of the Mediterranean surprisingly little is known of preferred habitat niches or susceptibility of the species to environmental change. In this study we investigated in the laboratory the net prey capture rates of the coral achievable under a range of flow velocities (2.5, 5, 7.5 and 15 cm s−1) and under exposure to different suspended particulate concentrations (0, 7.3 and 170 mg l−1). In recirculation flumes we simulated both commonly occurring and the occasionally high flow velocities and various suspended particulate concentrations reported from the Gulf of Lions (north-west Mediterranean). We then delivered ca 500 A. salina nauplii l−1 as food (Artemia salina nauplii) to the flumes and monitored net prey capture over time. We found net prey capture rates by the species to be highest under flow velocities of 5 cm s−1, with 230 µg C coral individual−1 h−1 achieved. The presence or absence of even environmentally high particulate concentrations (up to 170 mg l−1 resuspended seabed material) did not significantly affect the net prey capture rates achieved by the coral polyps. We found that net prey capture in Balanophyllia europaea is not inhibited during periods of heavy particle exposure, as has been observed in other temperate scleractinian corals. Also, flow velocities of ca ~5 s−1 appear to be optimal for maximum net prey capture by the species.
Benthic habitat and epibenthic megafauna are described from seabed photographs taken in or near three potential deep-water Marine Protected Areas on the Hebridean Slope, surveyed in 1988, 1995–96 and 1998. Broad bathymetric zones are defined by visible substratum characteristics, and by cluster analysis using presence/absence of identified fauna. The shelf edge and upper slope (to 350 m depth) showed current-swept coarse substrata with a very sparse fauna. A transition to finer sandy sediments was apparent at 350–470 m, with a greater abundance of mobile epifauna. The brittlestar Ophiocten gracilis occurred at high density below 600 m depth in all three areas. Southern stations indicated an abrupt lower boundary for this zone at ca 1000 m. In the north, rippled sands with xenophyophores occurred below the O. gracilis zone at 1000–1100 m. Xenophyophores were also seen in smaller numbers at this depth in the south. From ~1300–1600 m a seabed of burrowed fine mud was recorded in both northern and southern areas. Bioturbated sediments on the Rockall Trough floor at ~2060 m supported more visible epifauna, principally the brittlestar Ophiomusium lymani and the octocoral Acanella arbuscula. The bathymetric pattern differs from a scheme proposed in 2010 for the deep north-east Atlantic in the lack of any obvious zonal boundary at 750 m. No cold-water corals or sponge aggregations were observed. Trawl marks were observed in all three areas, particularly in the 1998 northern survey, with highest frequency at 1300–1400 m.
Pinna nobilis is an endemic Mediterranean species of high economic and cultural importance. Nowadays, it is under strict protection as a dramatic decline in its populations has been recognized, assigned to the combined effect of fisheries and habitat degradation. This study attempts to evaluate, by non-destructive sampling, the current status of P. nobilis populations in the south Aegean Sea (Dodecanese island complex), where they have been affected for centuries by practically uncontrolled harvesting. Population density and total length of individuals was estimated by diving along strip transects at six islands. Two stations were randomly selected per island, and two depth zones were surveyed per station. Additionally, temporal sampling was carried out at Astypalaia Island from March 2004 to June 2006, to assess relevant trends in density of individuals and size structure of the population. In total 1372 P. nobilis individuals were measured in situ to estimate maximum shell length. The studied populations showed increased density in the shallower depth zone and sheltered sites; small-scale environmental regimes are proposed as shaping factors of P. nobilis distribution. Increased density was also detected during the cold period of the year, probably related to recruitment success. In the lower depth zone the P. nobilis population consisted of larger individuals. A significant decrease in size was detected temporally as mean length was smaller in December 2004; in the same month the presence of small-sized juveniles was depicted in a left-shift in size–frequency distribution. These observations are probably related to the reproductive biology of the species.
With its iconic appearance and historic popular appeal, the giraffe is the world's tallest living terrestrial animal and the largest ruminant. Recent years have seen much-needed new research undertaken to improve our understanding of this unique animal. Drawing together the latest research into one resource, this is a detailed exploration of current knowledge on the biology, behaviour and conservation needs of the giraffe. Dagg highlights striking new data, covering topics such as species classification, the role of infrasound in communication, biological responses to external temperature changes and motherly behaviour and grief. The book discusses research into behaviour alongside practical information on captive giraffe, including diet, stereotypical behaviour, ailments and parasites, covering both problems and potential solutions associated with zoo giraffe. With giraffe becoming endangered species in Africa, the book ultimately focuses on efforts to halt population decline and the outlook for conservation measures.
We examined the benthic macroinfauna at three strata during two seasons (winter and summer) on two sandy beaches (dissipative and reflective) in south-eastern Brazil. The hypothesis raised is that effects of morphodynamics and zonation determine the structure of macroinfauna, with dissipative beaches having comparatively higher species richness and density than the reflective beaches. Flamengo beach (dissipative) had higher species richness but lower density compared to Grumari beach (reflective). A high dissimilarity in assemblage structure (91.75%) was detected between the two beaches. Zonation in the occurrence of macroinfauna was detected for the two beaches in the two examined seasons. At Grumari beach, Emerita brasiliensis occurred mainly in stratum 1 (intertidal swept zone) while Saccocirus sp. occurred in stratum 2 (infralittoral at 0.5 m depth), whereas at Flamengo beach E. brasiliensis and Enoploides sp. had the highest density in stratum 1 (intertidal swept zone) whereas Scolelepis goodbodyi and Donax uncinata dominated in stratum 3 (infralittoral at 1.0 m depth). Scolelepis goodbodyi, Dispio uncinata, Enoploides sp., Nematoda and Trileptium sp. were associated with higher a Dean parameter and content of organic matter at Flamengo beach. In contrast, Hastula sp., Donax sp., Pisionidens indica, Hemipodus californiensis, Saccocirus sp. and Phyllodocidae were associated with the higher wave period and grain size of Grumari beach. The hypothesis that macroinfauna structure differs between the beaches and strata was confirmed, with the dissipative beaches having comparatively higher richness but lower density than the reflective beaches.
Two new species of South African Syllidae of the genus Syllis Lamarck, 1818 are described. Syllis unzima sp. nov. is characterized by having unidentate compound chaetae with long spines on margin, a characteristic colour pattern and its reproduction by vivipary. Vivipary is not common among the polychaetes, but most representatives occur in the family Syllidae Grube, 1850 (in five other Syllis species, two species of Dentatisyllis Perkins, 1981 and two species of Parexogone Mesnil & Caullery, 1818). Syllis unzima sp. nov. differs from the other viviparous species in having large broods (>44 juveniles) which develop synchronously. Development of the juveniles is similar to that of free-spawning Syllis species, but the appearance of the first pair of eyespots and the differentiation of the pharynx and proventricle occur later in S. unzima. Syllis amicarmillaris sp. nov., is characterized by having an elongated body with relatively short, fusiform dorsal cirri and the presence of one or two pseudosimple chaeta on midbody parapodia by loss of blade and enlargement of shaft. Syllis unzima sp. nov. was found in high densities on cultured Holothuria scabra Jaeger, 1833 with single specimens found on a cultured Crassostrea gigas Thunberg, 1793 and on coralline algae, respectively, while S. amicarmillaris was found mainly in sediment outside an abalone farm and less frequently on cultured Haliotis midae Linnaeus, 1758. We discuss the possible benefits of the association with H. scabra to S. unzima sp. nov.
Through application of carbon (C) and nitrogen (N) stable isotope analyses, we investigated the benthic trophic structure of the upper-slope off southern Chile (~45°S) including a recent methane seep area discovered as part of this study. The observed fauna comprised 53 invertebrates and seven fish taxa, including remains of chemosymbiotic fauna (e.g. chemosymbiotic bivalves and siboglinid polychaetes), which are typical of methane seep environments. While in close-proximity to a seep, the heterotrophic fauna had a nutrition derived predominantly from photosynthetic sources (δ13C > –21‰). The absence of chemosynthesis-based nutrition in the consumers was likely a result of using an Agassiz trawl to sample the benthos, a method that is likely to collect a mix of fauna including individuals from adjacent non-seep bathyal environments. While four trophic levels were estimated for invertebrates, the fish assemblage was positioned within the third trophic level of the food web. Differences in corrected standard ellipse area (SEAC), which is a proxy of the isotopic niche width, yielded differences for the demersal fish Notophycis marginata (SEAC = 5.1‰) and Coelorinchus fasciatus (SEAC = 1.1‰), suggesting distinct trophic behaviours. No ontogenic changes were detected in C. fasciatus regarding food sources and trophic position. The present study contributes the first basic trophic data for the bathyal area off southern Chile, including the identification of a new methane seep area, among the furthest south ever discovered. Such information provides the basis for the proper sustainable management of the benthic environments present along the vast Chilean continental margin.
Renibacterium sp. QD1, a bacteria strain capable of hydrolysing chitosan, was isolated from the homogenate of small crabs. An extracellular chitosanase, Csn-A, was purified from the QD1 fermentation broth. The enzyme was purified to homogeneity, with a yield of eight-fold, 67% recovery and a specific activity of 1575 U/mg proteins. The molecular weight of Csn-A was estimated to be 26.1 kDa by SDS-PAGE. Unlike other chitosanases, the purified Csn-A displayed maximal activity at a pH range of 5.3–6.5, and it was stable in a broad pH range of 5.0–10.0. The optimum temperature for chitosanlytic activity was 55°C. The enzyme activity was strongly stimulated by Mn2+ but inhibited by Fe3+, Cu2+, Al3+, Zn2+ and SDS. TLC analysis demonstrated that Csn-A hydrolysed N-deacetylated polymeric glucosamines into chito-biose and -triose in an endo-type manner. The amino acid seuquence of Csn-A showed close identity with an uncharacterized chitosanase of strain ATCC33209.
All animals detect and react to molecules in the external environment, including pheromones, signature mixtures of other individuals, and the chemical cues that indicate food, shelter, pathogens or predators. Despite the great external diversity in appearance of antennae and noses, animals of all kinds perceive these chemical stimuli in the same way (Hildebrand & Shepherd 1997; Su et al. 2009; Touhara & Vosshall 2009). Chemosensory receptor proteins are exposed to the outside world in the membrane of chemosensory nerve cells, often through a “window” in an otherwise impermeable skin or cuticle (Figure 9.1). The arrival of an odor molecule (odorant) is converted into a signal to the brain by first binding to a chemosensory receptor protein. Odorants can be any kind of molecule, as large as a protein or as small as formic acid.
Whether in air or water, olfaction is the key sense used to detect most chemical cues, rather than taste (gustation) (see Box 9.1 for the differences between these senses). All signature mixtures (the molecules learned highly varied individual or colony odors; Chapters 1 and 6; Sections 9.8 and 9.9), and probably most pheromones, whatever the size of molecules, are detected by olfaction. However, some pheromones in invertebrates are detected by gustation, including some in Drosophila (Section 9.5.2). Some pheromones in both vertebrates and invertebrates may act directly on the brain or other organs (Sections 9.5.2 and 9.7.3.2).
Progress in science depends on new techniques, new discoveries and new ideas, probably in that order.
Sydney Brenner (2002)
Since Butenandt’s landmark identification in 1959 of the silk moth sex pheromone bombykol, there have been spectacular developments in our ability to identify semiochemicals (Meinwald 2009). In their work over some two decades, Butenandt’s team needed more than 10 metric tonnes of female moths, providing 500,000 pheromone glands from which they extracted ~12 mg of the pheromone to identify (Billen 2006; Butenandt et al. 1959). The identification of the first ant trail pheromone in 1971 still required 3.7 kg of Atta texana ants (Tumlinson et al. 1971).
Today, it is possible to work with far, far less than a single moth’s pheromone gland. The revolution has come from chromatographic techniques in particular and the direct coupling of these with mass spectrometers, and other detection devices including animals’ own sensors. The ever-increasing power of nuclear magnetic resonance (NMR) spectroscopy has made complete structure determination (though perhaps not complete stereochemistry) possible on a microgram scale (Meinwald 2009). Insect pheromone identifications can be made from picogram to femtogram quantities, using gas chromatography–electroantennogram detector (GC-EAD, with the insect’s antenna) to get retention indices, and microchemical reactions to determine presence/absence of functional groups (e.g., with a gall midge sex pheromone, Gries et al. 2002).
Aggregation pheromones lead to the formation of animal groups near the pheromone source, either by attracting animals from a distance or stopping (“arresting”) passing conspecifics (Chapter 10) (Wertheim et al. 2005). In contrast to sex pheromones (which attract only the opposite sex), aggregation pheromones by definition attract both sexes (and/or, possibly, larvae). However, the benefits of aggregation to individuals may be complex and two rather different mechanisms may apply. First, individuals may be aggregating for the benefits of living in a group. Second, what we call aggregation pheromones may be the response of eavesdropping conspecifics, for example males responding to sex pheromones released by other males to attract females, in order to mate with those females (Chapters 3 and 11).
By contrast, host-marking pheromones deposited on hosts by insects parasitizing fruits or caterpillars, for example, lead to dispersion as host-marking pheromones deter other females from laying eggs in that host. How host-marking pheromones evolved is discussed in Section 4.2.
For species across the animal kingdom, pheromones and chemical cues play essential roles in successful mate location and mate choice. Given the ubiquity of chemical communication among animals, chemical cues are likely to emerge among the key criteria animals use for mate choice (Johansson & Jones 2007; Smadja & Butlin 2009; Thomas 2011; Wyatt 2010). These include a wide variety of species-specific sex pheromones but also non-pheromone chemical cues such as those associated with genetic compatibility, with the immune system, and with health or disease, which are also important in mate choice.
Darwin proposed sexual selection to explain why the males of so many species have conspicuous bright colors or long tail feathers even though such extravagant features or behavior might reduce survival by natural selection (Darwin 1871). He included chemical signals alongside visual and sound signals as outcomes of sexual selection, describing the distinctive odors of breeding male insects, reptiles, birds, and many mammals. Darwin concluded that the development of elaborate odor glands in male mammals is “intelligible through sexual selection, if the most odoriferous males are the most successful in winning the females, and in leaving offspring to inherit their gradually perfected glands and odors” (Darwin 1871, Vol. 2, p. 281). I have called this “success of the smelliest” (Wyatt 2009).
This book is designed to bring together people already working on chemical communication and to encourage others, especially chemists (who have a vital role in this research), to take up the challenge. My aim has been to make an evolutionary understanding of chemical communication, including pheromones, accessible to a broad scientific and lay audience.
Pheromone research brings together scientists with many different areas of expertise, from a rich diversity of chemists to biologists of many kinds. Each area of expertise has its own jargon and concepts – a behavioral ecologist speaks a different language from a neuroscientist. The book recognizes that every scientist is a novice outside their own subject, even science close to their own, so I try to explain ideas in terms understandable by non-specialists while at the same time aiming to be up to date and detailed enough for the specialist. I also wanted to write a book that could be enjoyed by the majority of the world’s scientists whose first language is not English and thus also clearer for everyone.
Ancestors of the giraffe came into Africa from Asia through what is now Ethiopia, then spread out over the continent. When members of Giraffa camelopardalis evolved, probably in the Pliocene (Churcher, 1978), they spread throughout Africa wherever there were savannahs and open woodlands; their range was restricted only by a lack of trees and bushes from which to forage (although they did not inhabit dense forests) and by too cold weather in the south. Populations of giraffe became isolated in different areas, and over as much as a million or more years developed along different genetic paths leading to distinct subspecies/races. Nine of these have been commonly accepted for giraffe (Lydekker, 1904; Dagg, 1962a, c; Brown et al., 2007), but as we shall see, there are still grey areas.
As men with guns advanced into the interior of Africa in the 1800s, they shot many of these giraffe and gradually took over the best land to farm and build towns and cities which precluded the presence of large wildlife. The races were all undermined to some extent, and some are now on the verge of extinction. Today, the distribution of giraffe is patchy and discontinuous. Some giraffe have been reintroduced to new areas (notably G. c. rothschildi) where it is hoped they will thrive, although occasionally these extralimital areas had never before been inhabited by giraffe, as at the southern edge of the continent.