Phylogeography of Eastern Polynesian sandalwood (Santalum insulare), an endangered tree species from the Pacific: a study based on chloroplast microsatellites

Aim Patterns of genetic variation within forest species are poorly documented in island ecosystems. The distribution of molecular variation for Santalum insulare, an endangered tree species endemic to the islands of eastern Polynesia, was analysed using chloroplast microsatellite markers. The aims were to quantify the genetic diversity; to assess the genetic structure; and to analyse the geographical distribution of the diversity within and between archipelagoes. The ultimate goal was to pre‐define evolutionary significant units (ESUs) for conservation and restoration programmes of this species, which constitutes a natural resource on small, isolated islands. Location Eleven populations, each representative of one island, covering most of the natural occurrence of S. insulare were sampled: five populations from the Marquesas Archipelago; three from the Society Archipelago; and three from the Cook–Austral Archipelago. These South Pacific islands are known for their high degree of plant endemism, and for their human occupation by Polynesian migrations. The extensive exploitation of sandalwood by Europeans nearly 200 years ago for its fragrant heartwood, used overseas in incense, carving and essential oil production for perfume, has dramatically reduced the population size of this species. Methods We used chloroplast microsatellites, which provide useful information in phylogeographical forest tree analyses. They are maternally inherited in most angiosperms and present high polymorphism. Among the 499 individuals sampled, 345 were genotyped successfully. Classical models of population genetics were used to assess diversity parameters and phylogenetic relationships between populations. Results Four microsatellite primers showed 16 alleles and their combinations provided 17 chlorotypes, of which four exhibited a frequency > 10% in the total population. The gene diversity index was high for the total population (H_e = 0.82) and varied among archipelagoes from H_e = 0.40 to 0.67. Genetic structure is characterized by high levels of differentiation between archipelagoes (36% of total variation) and between islands, but differentiation between islands varied according to archipelago. The relationship between genetic and geographical distance confirms the low gene flow between archipelagoes. The minimum spanning tree of chlorotypes exhibits three clusters corresponding to the geographical distribution in the three main archipelagoes. Main conclusions The high level of diversity within the species was explained by an ancient presence on and around the hotspot traces currently occupied by young islands. Diversity in the species has enabled survival in a range of habitats. Relationships between islands show that the Cook–Austral chlorotype cluster constitutes a link between the Marquesas and the Society Islands. This can be explained by the evolution of the island systems over millions of years, and extinction of intermediary populations on the Tuamotu Islands following subsidence there. Based on the unrooted neighbour‐joining tree and on the genetic structure, we propose four ESUs to guide the conservation and population restoration of Polynesian Sandalwood: the Society Archipelago; the Marquesas Archipelago; Raivavae Island; and Rapa Island.     

The phytogeographical affinities of the Pitcairn Islands – a model for south‐eastern Polynesia?

Aim To identify how the Pitcairn group relates biogeographically to the south‐eastern Polynesian region and if, as a subset of the regions flora, it can then be used as a model for biogeographical analyses. Location The Pitcairn group (25°4′ S, 130°06′ W) comprises four islands: Pitcairn, a relatively young, high volcanic Island; Henderson, an uplifted atoll, the uplift caused by the eruption of Pitcairn; and two atolls, Ducie and Oeno. The remote location, young age and range of island types found in the Pitcairn Island group makes the group ideal for the study of island biogeography and evolution. Methods A detailed literature survey was carried out and several data sets were compiled. Dispersal method, propagule number and range data were collected for each of the 114 species that occurs in the Pitcairn group, and environmental data was also gathered for islands in Polynesia. Analyses were carried out using non‐metric multidimensional scaling and clustering techniques. Results The flora of the Pitcairn Islands is derived from the flora of other island groups in the south‐eastern Polynesian region, notably those of the Austral, Society and Cook Islands. Species with a Pacific‐wide distribution dominate the overall Pitcairn group flora. However, each of the islands show different patterns; Pitcairn is dominated by species with Pacific, Polynesian and endemic distributions, with anemochory as the dominant dispersal method (39.5%); Henderson is also dominated by species with Pacific, Polynesian and endemic distributions, but zoochory is the dominant dispersal method (59.4); Oeno and Ducie are dominated by Pantropic species with hydrochory as the most common dispersal method (52.9% and 100%, respectively). Main conclusions ? Habitat availability is the most significant factor determining the composition and size of the flora. ? South‐east Polynesia is a valid biogeographical unit, and should include the Cook, Austral, Society, Marquesas, Gambier, Tuamotu and Pitcairn Islands with Rapa, but should exclude Easter Island, Tonga and Samoa. ? Regionalization schemes should take island type into consideration. ? The Pitcairn Island group can serve as a useful model for Pacific biogeographical analyses.     

Genetic differentiation associated with commercial traffic in the Polynesian mosquito, Aedes polynesiensis Marks 1951

The population structure of the Polynesian mosquito Aedes polynesiensis was investigated using electrophoretic data from two polymorphic protein loci. Considerable differentiation was observed both within and between islands in different archipelagos (Society, Tuamotu, Austral). Gene flow evaluated by F_st estimates was independent of geographic distance between islands but related to commercial traffic intensity. The results are discussed in view of recent findings on the variability of susceptibility to insecticides and of suitability as a vector for the nematode Wuchereria bancrofti.     

Spatial and Temporal Variability in the Abundance and Size Structure of Larvae of the White Sea Herring (<Emphasis Type="Italic">Clupea pallasii marisalbi</Emphasis>) in Onega and Kandalaksha Bays of the White Sea

According to the data of ichthyological surveys conducted in Onega and Kandalaksha bays of the White Sea in June 2015, the abundance and pattern of spatial distribution of larvae of the White Sea herring Clupea pallasii marisalbi are comparable with those of 2012. Aggregations of herring larvae detected at a distance of 12?14 km from the coast in the apex part of Kandalaksha Bay are probably the result of their mass drift caused by fresh floodwater discharge. In coastal waters of the bays adjacent to the littoral part, the abundance of herring larvae above the depths less than 5 m varies considerably due to their drift under effect of alongshore and/or tidal currents. The White Sea herring larvae reach high abundance only in the inlets (Chupa, Knyazhaya, Belaya, and Maikova inlets) with the river runoff; their length increases with the distance from spawning grounds. In different years, the main bulk of herring larvae in Knyazhaya Inlet is concentrated at depths about 12–15 m at 6?8°C, or moved to the upper 5-m quasi-homogeneous layer when the water temperature at the depth was 0?1°C.     

Uniform phenotype conceals double colonization by reed-warblers of a remote Pacific archipelago

Aim Remote oceanic islands often provide good illustrations of adaptive radiations, but phylogenetic studies have also demonstrated unexpected multiple colonization events for a given archipelago. In this study we investigate the relationships among endemic populations of the Marquesas reed‐warbler, Acrocephalus mendanae Tristram, 1883, which have colonized nearly all islands of this remote Polynesian archipelago, and which exhibit a very uniform plumage pattern. We study the phylogeny and morphology of all subspecies in the Marquesas, providing an examination of the position of the Marquesas lineages in relation to reed‐warblers distributed across multiple Polynesian archipelagos. Location This study focused on all the main islands of the Marquesas archipelago, along with samples from other Polynesian archipelagos (Society, Tuamotu, Austral, Cook, Kiribati) and Australia. Methods We used mitochondrial DNA markers (cytochrome b and ND2 genes) to develop a phylogeny of the main eastern Polynesian taxa. All subspecies for the Marquesas were investigated, including multiple individuals per island. Phylogenetic analyses using maximum‐likelihood and Bayesian approaches were employed to infer relationships among A. mendanae populations and between the main Polynesian archipelagos. Morphometric analyses based on 110 specimens from museum collections were performed on external characters to investigate the differences between islands, and these results were compared to the phylogeny. Results Our data indicate that the Marquesas reed‐warbler is in fact a polyphyletic taxon including two independent lineages: the northern Marquesas reed‐warbler, closely related to the Tuamotu reed‐warbler, and the southern Marquesas reed‐warbler, sister taxon to that endemic to the Kiribati. Analyses of morphological characters show that the size and shape features of the Marquesas reed‐warblers exhibit high plasticity linked to adaptation to ecological factors, particularly habitat richness (the diversity of vegetation structure that provides suitable resources and habitat for reed‐warblers, simplified here as the number of indigenous plant species). Main conclusions Our results suggest that reed‐warblers have successfully colonized the Marquesas archipelago, one of the most remote groups of islands in the Pacific Ocean, at least twice. Both events occurred more or less simultaneously at ca. 0.6 Ma, and are more recent than the islands' formation. We outline the taxonomic consequences of our phylogeny and discuss the supertramp strategy of reed‐warblers in the Pacific.     

Significance of new records of Tridacna squamosa Lamarck, 1819, in the Tuamotu and Gambier Archipelagos (French Polynesia)

The giant clam subfamily Tridacninae (family Cardiidae) is an important group of bivalve molluscs found throughout the Red Sea and Indo-Pacific, from East Africa to the Eastern Pacific biogeographic region. The Tridacna genus is currently revised with numerous cryptic species identified with molecular markers. New Tridacna records from the fringe of the known distribution areas are extremely useful to identify genetically unique species, geographic ranges, and to examine processes associated with species differentiation. While Tridacna maxima is abundant in French Polynesia (Central South Pacific Ocean) the larger fluted giant clam Tridacna squamosa was formerly reported only in the Austral Islands in the south. Following a recent survey that spanned 23 islands and atolls of the Society, Tuamotu and Gambier Archipelagos, the presence of T. squamosa between the Cook Islands and Pitcairn Islands is confirmed using both morphological and molecular information, suggesting a relic distribution across the Central Pacific Ocean. Tridacna squamosa is rare, but present throughout Tuamotu and Gambier. However, it remained undetected from the Society Islands, probably due to historical over-fishing. This species is valued by local inhabitants, and is sought after mainly as gifts and also for a limited local shell trade. The rarity of T. squamosa may call for conservation measures in the near future.     

Island hopping across the central Pacific: mitochondrial DNA detects sequential colonization of the Austral Islands by crab spiders (Araneae: Thomisidae)

Aim Phylogenetic studies concerning island biogeography have been concentrated in a fraction of the numerous hot‐spot archipelagos contained within the Pacific Ocean. In this study we investigate relationships among island populations of the thomisid spider Misumenops rapaensis Berland, 1934 across the Austral Islands, a remote and rarely examined southern Pacific hot‐spot archipelago. We also assess the phylogenetic position of M. rapaensis in relation to thomisids distributed across multiple Polynesian archipelagos in order to evaluate the proposed hypothesis that thomisid spiders colonized Polynesia from multiple and opposing directions. The data allow an examination of genetic divergence and species accumulation in closely related lineages distributed across four Polynesian archipelagos. Location The study focused on four Polynesian hot‐spot archipelagos: the Austral, Hawaiian, Marquesan and Society islands. Methods Mitochondrial DNA sequences comprising c. 1400 bp (portions of cytochrome oxidase subunit I, ribosomal 16S and NADH dehydrogenase subunit I) were obtained from thomisid spiders (64 specimens, representing 33 species) collected in the Australs, the Hawaiian Islands, the Society Islands, the Marquesas, Tonga, Fiji, New Zealand, New Caledonia and North and South America. Phylogenetic analyses using parsimony, maximum‐likelihood and Bayesian approaches were employed to resolve relationships of M. rapaensis to other Polynesian Misumenops and across the Austral Islands. Results Rather than grouping with other Misumenops spp. from the archipelagos of the Society Islands, Marquesas and Hawaiian Islands, M. rapaensis appears more closely related to Diaea spp. from Tonga, Fiji, New Zealand and New Caledonia. Phylogenetic analyses strongly support M. rapaensis as monophyletic across the Austral Islands. Misumenops rapaensis sampled from the two older islands (Rurutu and Tubuai) form reciprocally monophyletic groups, while individuals from the younger islands (Raivavae and Rapa) are paraphyletic. Across the Austral Islands, M. rapaensis exhibits a surprising level of genetic divergence (maximally 11.3%), an amount nearly equivalent to that found across the 16 examined Hawaiian species (14.0%). Main conclusions Although described as a single morphologically recognized species, our results suggest that M. rapaensis comprises multiple genetically distinct lineages restricted to different Austral Islands. Phylogenetic relationships among the island populations are consistent with sequential colonization of this lineage down the Austral archipelago toward younger islands. Analyses support the hypothesis that thomisid spiders colonized the central Pacific multiple times and suggest that M. rapaensis arrived in the Austral Islands from a westward direction, while Misumenops found in neighbouring archipelagos appear to be more closely related to New World congeners to the east. Finally, our data detect asymmetrical rates of morphological evolution and species diversification following colonization of four different Polynesian archipelagos.     

Optimization of environmental parameters for <Emphasis Type="Italic">Nannochloropsis salina</Emphasis> growth and lipid content using the response surface method and invading organisms

Algae biofuel has the potential to replace fossil fuels. However, cultivation and productivity of target algae need improvement, while controlling undesired organisms that can lower the efficiency of production systems. A central composite design and response surface model were utilized to predict cultivation optima of marine microalga, Nannochloropsis salina, under a suite of environmental parameters. The effects of salinity, pH, and temperature and their interactions were studied on maximum sustainable yield (MSY, a measure for biomass productivity), lipid content of N. salina, and invading organisms. Five different levels of each environmental predictor variable were tested. The environmental factors were kept within ranges that had previously been determined to allow positive N. salina growth (14.5–45.5 PSU; pH 6.3–9.7; 11–29 °C). The models created for this experiment showed that N. salina’s MSY and lipid content are not strongly affected over the broad range of salinity and temperature values. Calculated optima levels were 28 PSU/20 °C for MSY and 14.5 PSU/20 °C for lipid accumulation, but neither value significantly influenced the model. However, pH was the most important factor to influence algae productivity, and pH optimum was estimated around 8. Both MSY and lipid content were strongly reduced when pH deviated from the optimum. Occurrence of invading organisms seemed stochastic, and none of the environmental factors studied significantly influenced abundance. In conclusion, pH should be kept around 8 for maximum productivity of N. salina. Temperature and salinity should be kept around 20 °C and 28 PSU; however, moderate variations are not too much of a concern and might enhance lipid content of N. salina.     

TEMPERATURE-GROWTH RESPONSES OF ALGAL ISOLATES FROM ANTARCTIC OASES1

Thirty-five taxa (128 clonal cultures) of Antarctic algae isolated from various habitats were assayed for growth over a range of 2–34°C. Isolates, all unialgal and two axenic, varied markedly in their temperature-growth responses. Only four taxa belonging to either the Chlamydomonadaceae or Ulotrichaceae were obligately cold-adapted and incapable of growth at ≥20°C. All isolates grew at temperatures ranging from 7.5 to 18°C, and a few were incapable of growth at ≤5°C. Over one-third of the isolates grew at 30°C, but none grew at 34°C. Percentages of cold-adapted clones correlated well with the more stable low temperature habitats. Four chlamydomonad isolates displayed optimum temperatures for growth near their maximum temperatures for growth, both temperatures being well above those of the native habitats. This temperature-growth response suggests a closer relationship to algae from more moderate thermal regions than one might have supposed. However, the ability to grow at low temperatures and the inability to grow at 34°C suggest that these Antarctic algae are cold temperature adapted. Growth capability at low in situ temperatures is considered more useful ecologically than physiologically-defined categories for algae based on their maximum temperature for growth.     

Environmental adaptation and genetic variations in geographically isolated Emma field crickets Teleogryllus emma (Orthoptera: Gryllidae)

The Emma field cricket, Teleogryllus emma (Ohmachi & Matsuura), distributed between 43°N and 30°N in the Japanese archipelago, is univoltine and overwinters in the egg stage. Its eggs hatch on the slope of the Oishi Dam (38.03°N, 139.57°E, 160–170 m a.s.l.) in late June, adults begin emerging from late August, and oviposition lasts until early October. Oviposition is limited to the period when the water level of the Oishi Dam is low. The period from egg hatching to adult emergence is approximately 1 month shorter than that of the T. emma population on the Arakawa riverside (38.09°N, 139.57°E, 29 m a.s.l.), which is approximately only 7 km from the Oishi Dam. The egg and body sizes of T. emma on the slope of the Oishi Dam were smaller than those of T. emma on the Arakawa riverside, and the egg and nymphal periods were shorter; these variations were inherited by the next generation of T. emma. The egg period, nymphal period and head width of T. emma on the dam slope correspond to those of the populations near 40°N. Several traits of the T. emma population on the dam slope were naturally selected by adapting to the isolated environment, resulting in the genetic variations. However, their variations were small and the period after isolation is short, suggesting that it is in the early stages of speciation.     

Cationic oligopeptides with the repeating sequence L‐lysyl‐L‐alanyl‐L‐alanine: conformational and thermal stability study using optical spectroscopic methods

The infrared (IR), vibrational circular dichroism (VCD), and electronic circular dichroism (ECD) spectra of short cationic sequential peptides (L ‐Lys‐L ‐Ala‐L ‐Ala)_n (n = 1, 2, and 3) were measured over a range of temperatures (20–90 °C) in aqueous solution at near‐neutral pH values in order to investigate their solution conformations and thermally induced conformational changes. VCD spectra of all three oligopeptides measured in the amide I′ region indicate the presence of extended helical polyproline II (PPII)‐like conformation at room temperature. UV‐ECD spectra confirmed this conclusion. Thus, the oligopeptides adopt a PPII‐like conformation, independent of the length of the peptide chain. However, the optimized dihedral angles ? and ψ are within the range ?82 to ?107° and 143–154°, respectively, and differ from the canonical PPII values. At elevated temperatures, the observed intensity and bandshape variations in the VCD and ECD spectra show that the PPII‐like conformation of the Lys‐Ala‐Ala sequence is still preferred, being in equilibrium with an unordered conformer at near‐neutral pH values within the range of temperatures from 20 to 90 °C. This finding was obtained from analysis of the temperature‐dependent spectra using the singular value decomposition method. The study presents KAA‐containing oligopeptides as conformationally stable models of biologically important cationic peptides and proteins. Copyright © 2009 European Peptide Society and John Wiley & Sons, Ltd.     

Latitudinal patterns and regionalization of plant diversity along a 4270‐km gradient in continental Chile

According to the global latitudinal diversity gradient, a decrease in animal and plant species richness exists from the tropics towards higher latitudes. The aim of this study was to describe the latitudinal distribution patterns of Chilean continental flora and delineate biogeographic regions along a 4270‐km north–south gradient. We reviewed plant lists for each of the 39 parallels of continental Chile to build a database of the geographical distribution of vascular plant species comprising 184 families, 957 genera and 3787 species, which corresponded to 100%, 94.9% and 74.2% of the richness previously defined for Chile, respectively. Using this latitudinal presence–absence species matrix, we identified areas with high plant richness and endemism and performed a Cluster analysis using Jaccard index to delineate biogeographic regions. This study found that richness at family, genus and species levels follow a unimodal 4270‐km latitudinal distribution curve, with a concentration of richness in central Chile (31–42°S). The 37th parallel south (central Chile) presented the highest richness for all taxonomic levels and in specific zones the endemism (22–37°S) was especially high. This unimodal pattern contrasts the global latitudinal diversity gradient shown by other studies in the Northern hemisphere. Seven floristic regions were identified in this latitudinal gradient: tropical (18–22°S), north Mediterranean (23–28°S), central Mediterranean (29–32°S), south Mediterranean (33–37°S), north temperate (38–42°S), south temperate (43–52°S) and Austral (53–56°S). This regionalization coincides with previous bioclimatic classifications and illustrates the high heterogeneity of the biodiversity in Chile and the need for a reconsideration of governmental conservation strategies to protect this diversity throughout Chile.     

Sea level,topography and island diversity: phylogeography of the Puerto Rican Red‐eyed Coquí, Eleutherodactylus antillensis

Quaternary climatic oscillations caused changes in sea level that altered the size, number and degree of isolation of islands, particularly in land‐bridge archipelagoes. Elucidating the demographic effects of these oscillations increases our understanding of the role of climate change in shaping evolutionary processes in archipelagoes. The Puerto Rican Bank (PRB) (Puerto Rico and the Eastern Islands, which comprise Vieques, Culebra, the Virgin Islands and associated islets) in the eastern Caribbean Sea periodically coalesced during glaciations and fragmented during interglacial periods of the quaternary. To explore population‐level consequences of sea level changes, we studied the phylogeography of the frog Eleutherodactylus antillensis across the archipelago. We tested hypotheses encompassing vicariance and dispersal narratives by sequencing mtDNA (c. 552 bp) of 285 individuals from 58 localities, and four nuDNA introns (totalling c. 1633 bp) from 173 of these individuals. We found low support for a hypothesis of divergence of the Eastern Islands populations prior to the start of the penultimate interglacial c. 250 kya, and higher support for a hypothesis of colonization of the Eastern Islands from sources in eastern Puerto Rico during the penultimate and last glacial period, when a land bridge united the PRB. The Río Grande de Loíza Basin in eastern Puerto Rico delineates a phylogeographic break. Haplotypes shared between the PRB and St. Croix (an island c. 105 km south‐east of this archipelago) likely represent human‐mediated introductions. Our findings illustrate how varying degrees of connectivity and isolation influence the evolution of tropical island organisms.     

Dynamic disequilibrium: a long-term, large-scale perspective on the equilibrium model of island biogeography

• 1 The equilibrium model of island biogeography developed in the 1960s by MacArthur and Wilson has provided an excellent framework in which to investigate the dynamics of species richness in island and island‐like systems. It is comparable in many respects to the Hardy–Weinberg equilibrium model used in genetics as the basis for defining a point of reference, thus allowing one to discover the factors that prevent equilibrium from being achieved. Hundreds of studies have used the model effectively, especially those dealing with brief spans of time and limited geographical areas. In spite of this utility, however, there are important limitations to the MacArthur–Wilson model, especially when we consider long‐term and large‐scale circumstances.
• 2 Although their general theory is more complex, the MacArthur–Wilson equilibrium model treats colonization and extinction as the only two processes that are relevant to determining species richness. However, it is likely that phylogenetic diversification (phylogenesis) often takes place on the same time‐scale as colonization and extinction; for example, colonization, extinction, and phylogenesis among mammals on oceanic and/or old land‐bridge islands in South‐east Asia are all measured in units of time in the range of 10 000–1 million years, most often in units of 100 000 years.
• 3 Phylogenesis is not a process that can be treated simply as ‘another form of colonization’, as it behaves differently than colonization. It interacts in a complex manner with both colonization and extinction, and can generate patterns of species richness almost independently of the other two processes. In addition, contrary to the implication of the MacArthur–Wilson model, extinction does not drive species richness in highly isolated archipelagoes (those that receive very few colonists) to progressively lower values; rather, phylogenesis is a common outcome in such archipelagoes, and species richness rises over time. In some specific instances, phylogenesis may have produced an average of 14 times as many species as direct colonization, and perhaps 36 species from one such colonization event. Old, stable, large archipelagoes should typically support not just endemic species but endemic clades, and the total number of species and the size of the endemic clades should increase with age of the archipelago.
• 4 The existence of long‐term equilibrium in actual island archipelagoes is unlikely. The land masses that make up island archipelagoes are intrinsically unstable because the geological processes that cause their formation are dynamic, and substantial changes can occur (under some circumstances) on a time‐scale comparable to the processes of colonization, phylogenesis, and extinction. Large‐scale island‐like archipelagoes on continents also are unstable, in the medium term because of global climatic fluctuations, and in the long term because of the geologically ephemeral existence of, for example, individual mountain ranges.
• 5 Examples of these phenomena using the mammals of South‐east Asia, especially the Philippines, make it clear that the best conceptual model of the long‐term dynamics of species richness in island archipelagoes would be one in which colonization, extinction, and phylogenesis are recognized to be of equivalent conceptual importance. Furthermore, we should expect species richness to be always in a dynamic state of disequilibrium due to the constantly changing geological/geographical circumstances in which that diversity exists, always a step or two out of phase with the constantly changing equilibrium point for species richness.

     

Genetic variation and population genetic structure of Rhizophora apiculata (Rhizophoraceae) in the greater Sunda Islands,Indonesia using microsatellite markers

Genetic variations within and among Rhizophora apiculata populations in the Greater Sunda Islands of Indonesia were studied using microsatellite markers. The study found 38 alleles on five loci in 15 populations. The observed (H _o) and expected (H _e) heterozygosity values are 0.338 and 0.378, respectively. Inbreeding effect from self-pollination might explain its heterozygote deficiency. Population genetic differentiation (F _ST = 0.381) was similar to other mangrove species. The genetic diversity of R. apiculata populations along the coastline inside the archipelago (e.g., Buleleng, Donggala, Mamuju, and Takalar) was higher than those of population along the coastline outside the archipelago, especially northern Sumatra populations (i.e., Langkat, Tapanuli Tengah, Dumai, and Padang). The isolation by distances and sea currents directions as well as their connectivity might affect the gene flow and genetic exchange. The more isolated with fewer connections by sea currents, the smaller gene flow and genetic exchange observed between populations. The higher genetic exchange, on the contrary, occurred when population location was closer to the meeting point of the sea currents. The study also showed that the patterns of sea current movement seemed to have influence genetic clustering of populations which fell into three main groups (Sunda Shelf Mangroves) and one isolated population (New Guinea Mangroves).     

Evolutionary biogeography of the terrestrial biota of the Marquesas Islands,one of the world's remotest archipelagos

Aim

Here I review phylogenetic studies concerning the biogeography of the Marquesas Islands, an oceanic hotspot archipelago in the Pacific Ocean formed <5.5 Ma, and compare patterns (particularly pertaining to colonization and diversification) within the archipelago to those reported from the Hawaiian and Society Islands.

Location

Marquesas Islands, French Polynesia (Pacific Ocean).

Methods

I reviewed 37 phylogenetic studies incorporating Marquesas‐endemic taxa. I asked the following questions: (a) where are the sister‐groups of Marquesas lineages distributed? (b) are Marquesas‐endemic “radiations” monophyletic or polyphyletic? (c) what major between‐island phylogeographic barriers are seen in the Marquesas? (d) what evidence exists for diversification within islands? (e) how old is the Marquesas biota compared to the archipelago's age? Finally, these patterns are compared with those seen in the Society Islands and Hawaii.

Results

Most Marquesan lineages have their closest known relatives on other Pacific plate archipelagos (particularly the Society, Hawaiian, and Austral islands). Most Marquesas‐endemic radiations are found to be monophyletic, and among‐island diversification appears to be common. There is limited evidence for within‐island diversification. Some radiations may be consistent with a weak progression rule in which younger lineages are on younger islands. Crown ages of no Marquesas radiations appear to be older than the age of the archipelago (with one exception).

Main conclusions

Diversification of the Marquesas biota resembles that of the Hawaiian Islands more than that of the Society Islands. Many radiations are monophyletic and some appear to diversify in parallel with the formation of the archipelago.

     

Length‐weight and length–length relationships of three algae‐scraping cyprinid species from Iran

The study presents length–weight relationships (LWRs) and length–length relationships (LLRs) for three algae‐scraper species; Capoeta coadi from the Kouhrang River (Iran; 32°23′N, 50°08′E) a part of the Tigris drainage basin, Capoeta pyragyi from Cheshmeh Langan River (32°55′N, 50°10′E) a part of Zayanderud River basin and Capoeta umbla from Chooman River (35°57′N, 45°47′E). Fish were sampled by electro fishing (Samus1000; Power Out: 200 watts) in August, September and October 2017. Sampling was carried out each months in sites covering an area of about 100 m² including runs, riffles and pools at a water depth of 10–60 cm. The obtained LWRs and LLRs showed a high level of correlation (r² > 0.99).     

Non-permanent radiotelemetry leg harness for small birds

I developed a modified leg harness for mounting radiotelemetry transmitters to small birds, which includes a weak link that allows telemetry equipment to be shed. Over 4 years, I mounted 62 transmitters on 49 Tuamotu kingfishers (Todiramphus gambieri) using weak-link harnesses. Kingfishers retained 86% of transmitters for the duration of monitoring periods (23–66 days) whereas 22 of 23 transmitters were shed from birds resighted after 6–15 months. Apparent mortality was no higher for radio-marked birds than for birds without transmitters. The weak-link harness is an improvement to existing transmitter attachment techniques and provides a useful, effective, and ethical means of studying bird movements. © 2011 The Wildlife Society.     

The biogeochemical background and trace metal accumulation by brown algae of the genus <Emphasis Type="Italic">Fucus</Emphasis> in coastal waters of the Sea of Japan,the Sea of Okhotsk,and the White Sea

The ranges of background concentrations of Fe, Mn, Zn, Cu, and Cd in Fucus algae from the Sea of Japan, the Sea of Okhotsk, and the White Sea were determined. The lower background threshold of element concentration was calculated as Me₁₅–2MAD₁₅, the upper background threshold was determined as Me+2MAD. The upper background threshold of the metal contents in Fucus algae can be used as the maximum permissible regional concentration in assessing pollution levels of marine habitats. Comparison of the Me₁₅–2MAD₁₅ values showed that Fucus algae of the White Sea had increased Mn and decreased Cd concentrations compared to those in Pacific algae. The concentrations of Zn were higher in Fucus algae of the Sea of Japan than in macrophytes from the White Sea and the Sea of Okhotsk. The background concentration range of Fe in Fucus algae of the Sea of Japan was much narrower compared to that in their counterparts from the White Sea and the Sea of Okhotsk. The background metal concentrations in Fucus algae are specific to a sea region; their variations are connected not only with the trace element contents in abiotic components of the environment, but also with the functioning of coastal ecosystems.     

Influence of the Thin Drift Algal Mats on the Distribution of Macrozoobenthos in Kõiguste Bay, NE Baltic Sea

Macrozoobenthic communities within and outside of the drift algal mats were compared in Kõiguste Bay, NE Baltic Sea. The patches of the drift algae were on average 0.5–1 km wide in diameter covering about 25% of the total bottom area of the bay. Thickness of the mat did not exceed 6 cm. The biomass of the mat varied between 35 and 1391 g dw m^?2. The drift algal mats had no clear negative effect on macrozoobenthos except for a few infaunal species. The drift algae favoured several detrivorous, herbivorous and carnivorous species. Among the studied variables, the thickness of algal mat and oxygen concentration at near-bottom layer explained the best the structure of macrozoobenthos. Total number of invertebrate species increased curvilinearly with the thickness of algal mat having the peak value at 3–5 cm thick algal mat. To conclude, moderate drift algal mats increased habitat complexity and, thus, the diversity of benthic faunal assemblages in otherwise poorly vegetated coastal areas.