SEA-BIRD BREEDING SEASONS ON CHRISTMAS ISLAND,PACIFIC OCEAN*

Christmas Island, at 2° N, 157° W in the Central Pacific Ocean, supports 18 breeding species of sea-birds. Data on the breeding seasons collected by the authors and other visitors to the island are analyzed in individual species accounts. Population estimates are given, the distribution of each species on the island is outlined, and for some species information on the sexual and moult cycles of marked individuals is presented. The Discussion concerns the ultimate and proximate factors controlling breeding seasons and the role of social factors in maintaining breeding synchrony in sea-birds, the diversity of the breeding regimes exhibited on Christmas Island (summary and analysis in Fig. 2 and Table 5), and comparison of these regimes with those found in the birds of Ascension Island and the Galapagos Archipelago.     

Breeding seasons of sea-birds in the Galapagos Islands

The sea-birds breeding in the Galapagos Islands show a diversity of breeding cycles. Some species have rigidly fixed annual breeding while others breed throughout the year but have peaks of breeding at less than annual intervals. The eight species which have non-annual breeding are probably breeding as often as possible with the interval between the end of a breeding attempt and the start of the next being the time needed to moult the wing and tail feathers. Only one species is definitely known to breed and moult at the same time.
Although there are well marked seasonal fluctuations in the sea temperature, regular sampling failed to demonstrate any regular fluctuations in the surface plankton. The available evidence suggests that food for some sea-birds is erratic and unpredictable. Some non-annual breeding species have their breeding synchronized by severe food shortages which delay breeding, presumably because females cannot find enough food to form eggs, until conditions improve.
Timing of the breeding season in annual breeders is less easily explained but some species may be feeding well away from the islands in areas where there is a regular fluctuation in the food supply. Most of the annual breeders have prolonged breeding seasons and in two species breeding is out of phase on different islands. Perhaps species are influenced by some weak annual variation in food supply which makes it disadvantageous to breed in a few months of the year.     

Regional biogeography of shallow reef fish and macro-invertebrate communities in the Galapagos archipelago

Aim To delineate biogeographical patterns in Galapagos shallow‐water reef fauna at regional scales. Location Galapagos Islands. Methods Fishes and macro‐invertebrates were quantitatively censused using underwater visual techniques along more than 500 transects at defined depth strata across the Galapagos archipelago. Data were analysed using multivariate techniques to define regional patterns and identify species typical of different regions. Results Subtidal communities of fishes and macro‐invertebrates on shallow reefs differed consistently in species composition across the Galapagos archipelago, with three major biogeographical groupings: (1) the ‘far‐northern area’ containing the islands of Darwin and Wolf, (2) the ‘central/south‐eastern area’, including the east coast of Isabela, and (3) the ‘western area’, encompassing Fernandina and western Isabela. In addition, the northern islands of Pinta, Marchena and Genovesa form a separate region in the central/south‐eastern area, and Bahia Elizabeth and Canal Bolivar separate from other parts of the western area. The far‐northern bioregion is characterized by high fish species richness overall, including a high proportion of species of Indo‐Pacific origin. However, very few endemic fishes or species with distributions extending south from Ecuador (‘Peruvian’ species) are present, and the bioregion also possesses relatively low species richness of mobile macro‐invertebrate taxa. By contrast, the ‘western’ bioregion possesses disproportionately high numbers of endemic fish taxa, high numbers of cool‐temperate Peruvian fish species, and high invertebrate species richness, but very few species of Indo‐Pacific origin. The Bahia Elizabeth/Canal Bolivar bioregion possesses more endemic species and fewer species with Peruvian affinities than coasts within the western bioregion. The northern bioregion of Pinta, Marchena and Genovesa represents an overlap zone with affinities to both the far‐northern and south‐eastern islands. The south‐eastern bioregion includes species from a variety of different sources, particularly ‘Panamic’ species with distributions extending north to Central America. Main conclusions On the basis of congruent divisions for reef fish and macro‐invertebrate communities, the Galapagos archipelago can be separated into three major biogeographical areas, two of which can be further subdivided into two regions. Each of these five bioregions possesses communities characterized by a distinctive mix of species derived from Indo‐Pacific, Panamic, Peruvian and endemic source areas. The conservation significance of different regions is not reflected in counts of total species richness. The regions with the lowest overall fish species richness possess a temperate rather than tropical climate and highest levels of endemism.     

Global phylogeography of the band-rumped storm-petrel (Oceanodroma castro; Procellariiformes: Hydrobatidae)

Factors shaping population differentiation in low latitude seabirds are not well-understood. In this study, we examined global patterns of DNA sequence variation in the mitochondrial control region of the band-rumped storm-petrel (Oceanodroma castro), a highly pelagic seabird distributed across the sub-tropical and tropical Atlantic and Pacific Oceans. Despite previous classification as a single, monotypic species, fixed haplotype differences occurred between Atlantic and Pacific populations, and among all Pacific populations. In addition, Cape Verde and Galapagos birds formed distinct clades, estimated to have diverged from all other populations at least 150,000years ago. Azores hot season populations were also genetically distinct, lending support to previous phenotypic evidence that they be recognized as a separate species. Seasonal populations in Madeira probably represent separate genetic management units. The phylogeography of the band-rumped storm-petrel appears to have been shaped by both nonphysical barriers to gene flow and Pleistocene oceanographic conditions. Ancestral populations likely expanded through contiguous range expansion and infrequent long-distance colonization into their current breeding range. These findings suggest several possible revisions to the taxonomy of the band-rumped storm-petrel.     

Peculiarities of island endemism in Lasiocampidae (Lepidoptera)

The distinctive features of island endemism in Lasiocampidae are extensive adaptive radiation and vicariance. These phenomena are especially typical of archipelagoes, where different taxa occur on closely located islands. The diverse ecological conditions of the islands determine the presence of a great number of subordinate taxa. Owing to the reduced flight activity, the species of Lasiocampidae are characterized by a high level of endemism on isolated islands. Islands of continental origin (Sumatra, Borneo) have a lower level of endemism, with centers on the mountain ranges. The endemism level is much higher in islands of biogenic origin (the Philippines). The Pacific islands have a higher index of specific endemism. At the same time, the islands of mixed and oceanic origin have low species diversity by a large fraction of endemic taxa. The boundaries of species distribution are determined not only by the landscape or climatic factors but also by biological ones.     

The evolution of canaliculate rudists in the light of a new canaliculate polyconitid rudist from the Albian of the Central Pacific

A new polyconitid rudist, Magallanesia canaliculata gen. et sp. nov., of probably late Albian age, is described from the Pulangbato area, central Cebu Island, the Philippines in the western Central Pacific and Takuyo‐Daini Seamount, now located in the Northwest Pacific. It is similar to Praecaprotina Yabe and Nagao, 1926, a Japanese–Central Pacific endemic genus of late Aptian – early Albian age, but differs in having canals that developed by partitioning of the large ectomyophoral cavity in the posterior part of the left valve. Its discovery strengthens the evidence for Pacific endemism in Albian times. Several other clades of canaliculate rudists flourished or evolved at the same time in different regions of the Tethyan Realm, suggesting the presence of common global biological and/or environmental factors stimulating the evolution of the canals despite such endemism. Furthermore, the finding of a canaliculate polyconitid provides evidence in favour of the evolutionary hypothesis of a polyconitid origin for the Late Cretaceous canaliculate rudist family Plagioptychidae Douvillé, 1888.     

Biogeography and evolution of the Galapagos: integration of the biological and geological evidence

Biogeographic tracks are mapped for Galapagos endemics representing 25 plant and animal taxa and including organisms with good and poor means of dispersal. These patterns confirm standard biogeographic tracks linking Galapagos with Central America, western North and South America, the Caribbean, Asia and Australasia. Discovery of the Galapagos Gore in the 1970s corroborates the biogeographic prediction for a major tectonic centre associated with the Galapagos. The biogeographic model developed by Croizat in 1958 of Galapagos colonization involving an ancestral biota inhabiting eastern Pacific geosynclinal forelands is congruent with plate tectonic models supporting a Pacific island arc origin for western American terranes. American relatives of Galapagos endemics may have originated within an eastern Pacific paleogeography rather than representing centres of origin for dispersal to the Galapagos. Galapagos colonization by an eastern Pacific biota between late Cretaceous and mid-Tertiary has significant implications for understanding the tempo and mode for both the origins of island biota and general models of evolutionary differentiation. Popular assertions that overwater dispersal represents the only viable origin for the entire Galapagos biota is no longer biogeographically or geologically tenable.     

Historical biogeographical patterns of the species of Bursera (Burseraceae) and their taxonomic implications

Aim The plant genus Bursera, with 104 species of trees and shrubs, has been used as a model for biogeographical analyses because of its high species richness and large number of endemic species. The biogeographical patterns of Bursera and their implications for its phylogenetic classification are reviewed in order that some hypotheses on the historical biogeography of tropical Mexico can be proposed. Location Bursera is found in the south‐western USA, most of Mexico, mainly below 1700 m elevation in tropical forests, with some species in xeric shrublands, diversifying along the Pacific slope, Central America, and north‐western South America. A few species occur on the Galapagos and Revillagigedo archipelagos, some of which are endemics, whereas in the Antilles species are distributed extensively, with several endemics in the Bahamas, Cuba, Jamaica, and Hispaniola. Methods Data from specimens in herbaria and the literature were used to construct a matrix of 104 species in 160 areas. Distributional patterns of the species of Bursera were inferred applying track analysis, parsimony analysis of endemicity (PAE), and Brooks parsimony analysis (BPA). Results Track analysis revealed four individual tracks: (1) a circum‐Caribbean track, comprising species of the Bursera simaruba species group; (2) an Antillean track, including species that have been transferred to Commiphora based on their pollen traits; (3) a Mexican Pacific track, including species of the B. fragilis, B. microphylla, and B. fagaroides species groups, called ‘cuajiotes’; and (4) a Neotropical Pacific track, including the two species groups assigned to section Bullockia, in which the individual track of the Bursera copallifera species group is nested within the track of the B. glabrifolia species group. The four tracks overlap in a node in the Mexican Pacific slope, where they are highly diversified. PAE allowed us to identify 22 areas of endemism: 12 in Mexico (11 along the Mexican Pacific slope), six in the Antilles, two in Central America, one in South America, and one in the Galapagos. The general area cladogram obtained by BPA has two main clades: one includes the greater Antilles; and the other, 12 Mexican areas of endemism. Main conclusions Bursera fragilis, B. microphylla, and B. fagaroides species groups can be treated together as a new section within Bursera, sect. Quaxiotea, because they are segregated from the other groups of sect. Bursera based on morphological, anatomical, molecular and geographical evidence.     

Diversity of migration strategies among great frigatebirds populations

Migratory behavior varies extensively between bird taxa, from long distance migration to purely sedentary behavior. Variability in migratory behavior also occurs within taxa, where individuals within some species, or even populations, show mixed strategies. The same variability occurs in seabird species. We examined the migratory behavior of distinct populations of great frigatebirds Fregata minor in three distant oceanographic basins. Great frigatebird populations showed extensive variation in post‐breeding migratory behavior. Birds from Europa Island (Mozambique Channel) made long‐distance migration to numerous distinct roosting sites in the Indian Ocean, New Caledonia birds made shorter distance migrations to roosting sites in the southwestern Pacific Ocean, and Galapagos birds were resident within the archipelago year round. Juvenile birds from Europa Is. and New Caledonia dispersed widely whereas Galapagos juveniles were resident year round. The migratory behavior of Europa Is. and New Caledonia resulted in complete separation of foraging grounds between breeding adults, non‐breeding adults, and juveniles, whereas in the Galapagos the overlap was complete. We suggest that population variability in migratory behavior may have arisen because of different environmental conditions at sea, and also depends on the availability of suitable roosting sites on oceanic islands. The results also highlight the capacity of frigatebirds to remain airborne most of the time even outside the breeding season when they have to molt.     

Long-term isolation of a highly mobile seabird on the Galapagos

The Galapagos Islands are renowned for their high degree of endemism. Marine taxa inhabiting the archipelago might be expected to be an exception, because of their utilization of pelagic habitats—the dispersal barrier for terrestrial taxa—as foraging grounds. Magnificent frigatebirds (Fregata magnificens) have a highly vagile lifestyle and wide geographical distribution around the South and Central American coasts. Given the potentially high levels of gene flow among populations, the species provides a good test of the effectiveness of the Galapagos ecosystem in isolating populations of highly dispersive marine species. We studied patterns of genetic (mitochondrial DNA, microsatellites and nuclear introns) and morphological variation across the distribution of magnificent frigatebirds. Concordant with predictions from life-history traits, we found signatures of extensive gene flow over most of the range, even across the Isthmus of Panama, which is a major barrier to gene flow in other tropical seabirds. In contrast, individuals from the Galapagos were strongly differentiated from all conspecifics, and have probably been isolated for several hundred thousand years. Our finding is a powerful testimony to the evolutionary uniqueness of the taxa inhabiting the Galapagos archipelago and its associated marine ecosystems.     

Late Cretaceous and Cainozoic bathyal Ostracoda from the Central Pacific (DSDP Site 463)

Cainozoic deep-sea ostracod assemblages from the summits of Mid-Pacific guyots point to high levels of endemism possibly as a result of their bathymetric separation from the surrounding sea floor. However, the interpretation of these fossil assemblages is hampered by the paucity of comparative material from surrounding non-guyot sites. Fifteen ostracod assemblages from DSDP Site 463 (Late Cretaceous-Pleistocene) were studied to compare with those from nearby guyots. Three distinct faunal assemblages are recognised at Site 463: Assemblage A (Maastrichtian-Eocene), Assemblage B (Oligocene-Upper Miocene) and Assemblage C (Upper Miocene-Pleistocene) although the palaeoenvironmental significance of these units is unclear. Sixty-two ostracod species are identified, the thirteen most abundant are discussed in the taxonomic section, five of which are described as new. Between 30 and 100% of the species encountered in each sample are considered as endemic to Site 463, while some of the remaining species were previously thought to be endemic to individual guyots. Similarly high levels of endemism on nearby guyots probably reflect an incomplete knowledge of deep-sea ostracod faunas rather than the establishment of geographically or bathymetrically restricted populations. The presence of globally pandemic and geographically widespread taxa on sites such as the Mid-Pacific Mountains, surrounded by abyssal depths which lie below the CCD, indicates that some faunal exchange or migration of ostracods does take place. This must be achieved within the intermediate waters and probably occurs passively.     

Evolution of Cyrtandra (Gesneriaceae) in the Pacific Ocean: the origin of a supertramp clade

Cyrtandra comprises at least 600 species distributed throughout Malesia, where it is known for many local endemics and in Polynesia and Micronesia, where it is present on most island groups, and is among the most successfully dispersing genera of the Pacific. To ascertain the origin of the oceanic Pacific island species of Cyrtandra, we sequenced the internal transcribed spacers of nuclear ribosomal DNA of samples from throughout its geographical range. Because all oceanic Pacific island species form a well-supported clade, these species apparently result from a single initial colonization into the Pacific, possibly by a species from the eastern rim of SE Asia via a NW-to-SE stepping stone migration. Hawaiian species form a monophyletic group, probably as a result of a single colonization. The Pacific island clade of Cyrtandra dispersed across huge distances, in contrast to the apparent localization of the SE Asian clades. Although highly vagile, the Pacific clade is restricted to oceanic islands. Individual species are often endemic to a single island, characteristic of the "supertramp" life form sensu Diamond (1974, Science 184: 803-806). The evolution of fleshy fruit within Cyrtandra provided an adaptation for colonization throughout the oceanic Pacific via bird dispersal from a single common ancestor.     

Seals of the Galapagos Islands

The Galapagos archipelago has been colonized by two species of otariid, the fur seal, Arctocephalus galapagoensis , and the sea lion, Zalophus californianus wollebaeki. The former probably arrived from South America and the latter from North America, both by way of periodic incursions of colder water forming the east Pacific corridor. The terrestrial behaviour of both these otariids is affected by the high ambient temperatures in the Galapagos Patterns of breeding behaviour of otariids which lead to intense polygyny and sexual dimorphism appear to be modified. The habit of prolonging lactation, widespread in otariids, is carried to an extreme in the Galapagos fur seal. The reason for this is unclear.     

THE SEA-BIRDS OF THE SOUTHEAST COAST OF ARABIA

The present study of an upwelling area off the southeast coast of Arabia, between 52° and 60° E. is based primarily on observations on board the R.R.S, `Discovery’ during the International Indian Ocean Expedition. During oceanographic surveys off the Arabian coast from June to August 1963 and in early March and late May 1964 I made 234 counts of birds of about an hour each, the results of which have been used as an index of bird density. In this area, the only offshore islands known to be important to sea-birds are the Kuria Muria Islands, which were apparently at the centre of an upwelling area. The upwelling of cold water along the Arabian coast during the southwest monsoon from May to September greatly increases organic production in the sea, and large populations of organisms at every level of the food chain develop there. Previous work in Arabia and the Arabian Sea is reviewed. Little is recorded about the ecology of sea-birds there, but the composition of the fauna is quite well-known. The distribution of every sea-bird species recorded from 52° E. to 60° E., and within 200 miles offshore, is described, with particular reference to my own observations. Details are given of the distribution of common species during the southwest monsoon of mid-June-mid-August 1963 and in March and May 1964. Specimens collected on the `Discovery’ are recorded together with their measurements. Of 12 sea-bird species seen commonly off Arabia during the southwest monsoon in 1963, 11 were seen in late May 1964, but only five in March. There is certain evidence that two species have bred on the Kuria Muria Islands and suggestive evidence for a further three. Information on breeding seasons in the Arabian Sea is based on short visits to breeding colonies, mostly outside the breeding season, and on the plumage condition of specimens. Nevertheless, the sum of the evidence suggests that breeding is regular at the same time every year, and in most species seems to be in the northern summer. The food of sea-birds in the Arabian Sea, determined from stomach contents and visual observation, only serves to stress the lack of knowledge on this subject. A brief summary of feeding methods recorded by me suggests that they may be important in avoiding interspecific competition, for there seems to be little overlap. The density of sea-birds during the southwest monsoon 1963, expressed as the number of each species seen per hour, was analysed in relation to: (i) the sea surface temperature, which was inversely correlated with the zooplankton density from 0–200 m. (ii) the distance from the Kuria Muria Islands, the only likely breeding station; (iii) the distance from the nearest land which may have been important to land-tied sea-birds. All the abundant species were commonest close to land in the cool-water area and, with the exception of migrants from the southern hemisphere, most were concentrated around the Kuria Muria Islands in the centre of upwelling. A multiple analysis suggested that the islands were of real importance to some species. A separate analysis also demonstrated the existence of a correlation between sea-bird numbers and the abundance of zooplankton from 0–200 m. depth, but not the abundance of zooplankton at the sea surface. During the southwest monsoon the southeast Arabian coast is inhabited by a distinctive cool-water fauna within the tropical zone of the Indian Ocean. The high degree of endemism, the high proportion of migrants, including some from the southern hemisphere, and the absence of most pantropical species, suggest that the marked changes in the environment off southeast Arabia demand considerable adaptation. A brief discussion of the possible origins of the Arabian coast sea-bird fauna shows that it is not typical of either a subtropical or a tropical community in other regions. The likelihood that sea-birds breed in the summer, the concentration of most species in the upwelling area at that time and their absence during the winter, clearly demonstrates the importance of the upwelling. However, the results of the analysis suggest that some species were concentrated around the Kuria Muria Islands in the centre of the upwelling because the islands had a real importance to them, possibly as a breeding station. The correlation between sea-bird density and zooplankton abundance in the top 200 m., but not at the surface, may be explained if sea-birds concentrate in areas of high productivity rather than in areas of abundant surface plankton, which is largely irrelevant as food.     

Endemism in the Flora of China—Studies on the Endemic Genera

China, under highly varied ecological conditions resulted from wide latitudinal and altitudinal ranges and from the adequate precipitation, has developed a very rich flora of great diversity. As far as flowering plants are concerned, there are 2980 genera, 214 of which, belonging to 64 families, are endemic. Among these endemic genera, there are 9 genera of taxads and conifers, 19 genera of monocots and others of dicots. Of the approximately 129 herbaceous endemic genera in the Chinese flora as a whole, about 22 (17%) are annual and 107 (83%) are biennial or perennial. In the present paper the ecological distribution, the nature of endemic genera and the centers of endemism are discussed. 1. Three types of endemic genera are distinguished, neoendemics, palaeoendemics and active epibiotics, The endemic genera in the flora of China are, for the most part, considered to be very old ones, and most of them are of temperate nature. 2. the degree of endemism in our 22 floristic regions is shown in Figure 1. The areas richest in endemic genera in the Chinese flora as a whole are the 13, 16 and 17 regions. The poorest are the 2, 4, 9 and 10 regions, and no one in the 1 and 3 regions These results on floristic richness are of general applicability. As shown in table 1, the difference in the degree of endemism among the seven Chinese floristic subkingdoms are most pronounced. 101 endemic genera are known to occur in one subkingdom, 72 to occur in two subkingdoms, and 3 to occur in four subkingdoms, only one genus widely distributed in five subkingdoms. However, there is no genus occurring in seven subkingdoms. The difference in the degree of endemism in each subkingdom reveals that the distribution of endemic genera is not well-distributed in the Chinese flora as a whole. Analysis of the vertical distribution of the 200 endemic genera of the Chinese flora bears out that there is no evident increase in endemism as a whole with altitude. 3. Three centers of endemism are found (Fig. 2). These are as follows: a). Eastern Sichuan-western Hubei center. b). Southeastern Yunnan-western Guangxi center. c). Western Sichuan-northwestern Yunnan center. The degree of endemism andcharacters of endemic genera in each center are discussed.     

Budding speciation and neotropical origin of the Azorean endemic liverwort, Leptoscyphus azoricus

The origin of plant species endemism in Macaronesia, one of the 25 world biodiversity hotspots, has traditionally been either interpreted as a result of the dramatic reduction of a broader tertiary distribution range during the Ice Age or neoendemism. This hypothesis is tested here in the context of a species-level phylogeny employing chloroplast trnL-trnF and atpB-rbcL sequences in the leafy liverwort genus Leptoscyphus (Lophocoleaceae). The data suggest that the Azorean endemic Leptoscyphus azoricus originated from parental populations of the Neotropical Leptoscyphus porphyrius by long-distance dispersal across the Atlantic and subsequent isolation. Possible reasons for the differences in the origin of endemism in angiosperms, wherein by far most endemic species have their close relatives on the European and North African continents, are discussed.     

THE BREEDING SEASONS OF AFRICAN BIRDS—2. SEA BIRDS.

1. All the available data, largely unpublished, are assembled for sea-birds breeding in African waters, about 36° N.-36° S.
2. An ill-defined breeding season by any species at any station is exceptional.
3. North of the Equator practically all sea-birds breed in spring or summer.
4. South of the Equator there is much more variation. Round the Cape there is a good deal of mid-winter breeding, mainly in stations affected by the warm Agulhas current.
5. On the east coast most of the breeding takes place in the period June–August from the Gulf of Suez (27° N.) to the mouth of the Zambesi (19° S.) and beyond, i.e. in the hottest months north of the Equator and the coolest months south of it.     

无量山种子植物区系的特有现象

地处滇中南的无量山地区迄今计有种子植物２０７科,１０２６属,２５４０种,其中东亚特有科１０个,中国特有属２７个,无量山特有种子６７个,这一地区不仅植物种类丰富,而且特有现象较为显著,在对科级持有现象进行较细致的研究后,本文认国无量山具有较多的分类系统上隔离的东亚特有科反映了该地作为东亚古老植物区系的一部分,其地质历史与整个东亚是一致的,且与东亚植物区系的发端密切相关,属的特有现象表明,地处中国特有     

Patterns of endemism in south-eastern Pacific benthic polychaetes of the Chilean coast

Aim In this study we evaluate patterns of endemism for benthic polychaete species along the southeastern Pacific coast of Chile. Our goals were (1) to describe latitudinal gradients of endemism and identify areas of high endemism, (2) to evaluate the effect of biogeographical limits on endemism patterns, and (3) to evaluate indirectly the role played by evolutionary dynamics on patterns of endemism. Location South‐eastern Pacific coast of Chile, ranging from Arica (18° S) to Cape Horn (56° S). Methods We used a list of 178 species of endemic, shallow benthic polychaetes to evaluate patterns of endemism. Parsimony analysis of endemicity (PAE) and the endemism index (EI) were used to evaluate hierarchical relationships of endemism between different latitudinal bands, and to identify areas with high degrees of endemism and differences in endemism. We evaluated the effect of biogeographical limits on endemic polychaete fauna by testing for the existence of geometric constraints (mid‐domain effect). The role of evolutionary dynamics on latitudinal patterns of endemism was evaluated with nestedness analysis (NA) using the temperature index. Results The PAE analysis indicated two large, separate areas of endemism: (1) the northern area between 18° S and 38° S, and (2) the southern area between 39° S and 56° S. The endemism index showed a maximum value (32 species) around 39°–41° S. Species‐richness curves of each 3° band of latitude showed a clear mid‐domain effect (69%), but the two maximum points of species richness at mid‐latitudes (36° S to 38° S and 39° S to 41° S) did not correspond to the mid‐domain peak in species richness, presenting a greater number of species than expected by the mid‐domain effect. The nestedness analysis showed that the number of genera reaches a maximum of 70 at mid‐latitudes (36°–41° S), decreasing towards both the northern and southern areas. The spatial distribution of the entire data set of endemic species showed a nested pattern (T° = 24.5°, P < 0.0001). Main conclusions Our results strongly support the existence of a latitudinal gradient of endemism for benthic polychaete species along the Chilean coast. The shape of this gradient is clearly non‐linear, with a marked peak of endemism occurring at mid‐latitudes (36°–41° S, endemism hotspot), which also corresponds to a peak in species richness. Furthermore, this hotspot is the midpoint separating two distinct areas of endemism to the north and south. We suggest that the observed pattern of endemism for benthic polychaete taxa of the Chilean coast can be explained by a combination of geometric constraints and historical mechanisms, such as the processes that affected the Chilean coast during the Neogene (e.g. ENSO, oxygen minimum zone, glaciations).     

Fine scale endemism on coral reefs: archipelagic differentiation in turbinid gastropods

The perceived wide geographic range of organisms in the sea, facilitated by ready dispersal of waterborne dispersal stages, is a challenge for hypotheses of marine speciation but a boon to efforts of marine conservation. Wide species ranges are especially striking in the reef-rich Indo-west Pacific, the largest and most diverse marine biogeographic region, extending across half the planet. The insular marine biota of the tropical Pacific is characterized by wide-ranging species and provides the most striking examples of long distance dispersal, with endemism largely confined to the most remote island groups. Here we show that the gastropod Astralium "rhodostomum" has developed endemic clades on almost every Pacific archipelago sampled, a pattern unprecedented in marine biogeography, and reminiscent of the terrestrial biota of oceanic islands. Mitochondrial DNA sequences indicate that this species-complex is comprised of at least 30 geographically isolated clades, separated by as little as 180 km. Evidence suggests that such fine scale endemism and high diversity is not exceptional, but likely characterizes a substantial fraction of the reef biota. These results imply that (1) marine speciation can regularly occur over much finer spatial scales than generally accepted, (2) the diversity of coral reefs is even higher than suggested by morphology-based estimates, and (3) conservation efforts need to focus at the archipelagic level in the sea as on land.