Sex and reproduction of the alfonsino Beryx splendens (Pisces, Berycidae) from the Macaronesian archipelagos

This paper provides comparative information on the reproductive biology of the alfonsino, Beryx splendens Lowe, 1834, species with commercial interest in the Azores, Madeira and the Canary Islands. A total of 846 individuals from Azores (14.0–42.0 cm fork length), 621 from Madeira (17.2–50.0 cm fork length) and 643 from the Canaries (18.2–38.9 cm fork length) were used for the study. The alfonsino is gonochoric with no evidence of sexual dimorphism. Females are more abundant than males; this dominance probably reflects certain differences in the spatial distribution and/or the catchability of males and females in the Macaronesian archipelagos. The spawning season was distinct for the three Macaronesian areas, with an observed North–South variation in the reproductive period: September–March in the Azores, March–June in Madeira and July–September in the Canary Islands. The size at sexual maturity estimated for Madeira and the Canary Islands is similar (32 and 30 cm fork length, respectively), while for the Azores it is reached at smaller length (23 cm fork length). The differences observed in the size at sexual maturity can be explained by the different exploitation levels in each archipelago. Life‐history parameters of the alfonsino suggest that this species has a specialistic life‐history strategy and fisheries based on this species are more susceptible to growth overfishing and population depletion.     

Colonization patterns and genetic structure of peripheral populations of the trumpeter finch (Bucanetes githagineus) from Northwest Africa, the Canary Islands and the Iberian Peninsula

Aim This paper has three aims: (1) to reconstruct the colonization history of two peripheral populations of the trumpeter finch (Bucanetes githagineus) presumably originating from the same source, one the result of an ancient expansion process and the other recently established and still expanding; (2) to estimate the importance of key events, such as past and current gene flow and bottlenecks, in both expansion processes and their contribution to the present population structure and genetic diversity; and (3) to find out whether two peripheral populations that established at widely differing times also differ in terms of genetic diversity. Location Northwest Africa (assumed source population), Canary Islands (long‐established peripheral) and south‐eastern Iberian Peninsula (recently established peripheral). Methods Bayesian analysis of population structure, individual assignment tests, F‐statistics, maximum likelihood migration estimates, genetic diversity indices and bottleneck tests were calculated with microsatellite data from 194 trumpeter finches from five breeding and two seasonal non‐breeding sites. Results Our data support the existence of two subpopulations (Canary Island and Ibero‐African) as the most likely population structure. Seasonal sites in the Iberian Peninsula had the highest percentage of birds assigned to other, mainly Iberian, sites. Pairwise F_ST values showed that the Canary Island localities were very similar to each other, but differed from the rest. Gene flow estimates within subpopulations were only slightly higher in the Canary Island population than in the Ibero‐African one. Gene diversity indices were similar at all localities. Canary Island sites show evidence of bottlenecks, whereas the Ibero‐African sites do not. Main conclusions Our data show that, at present, birds from the Canary Islands are genetically differentiated from those in North Africa and continental Spain. We could not unequivocally confirm the African origin of Canary populations because the contrary is also plausible. The Iberian Peninsula seems to have repeatedly received individuals from North Africa, which would have led to the relatively high genetic diversity found in these recently established localities and prevented bottlenecks. Movements of individuals towards sites outside their current range during the non‐breeding season are likely to precede the establishment of new breeding sites at the periphery of the distribution range.     

Age and growth of the Black Sea turbot, Psetta maxima (Linneaus, 1758) (Pisces: Scophthalmidae), estimated by reading otoliths and by back-calculation

Age and growth of the Black Sea turbot, Psetta maxima, were determined from a total of 1445 individuals collected along the eastern Black Sea coast between 1990 and 1996. Age was estimated by interpreting growth rings in whole and broken sagittal otoliths. The former method underestimated the age over 5 years, and a maximum age of 11 years was observed by the latter. Marginal increment analysis clearly showed that a single annulus is formed in early summer each year. Growth in length differed between sexes, and females attained a larger size than males at the same age. No significant difference was found between the mean observed total length (TL), the back‐calculated TL derived from radius measurements and the TL estimated from otolith size–fish size relationship. The von Bertalanffy growth parameters estimated by the length‐at‐age data were: L_∞ = 96.24 cm; K = 0.119 year^?1; t₀ = ?0.01 year for the entire population.     

PHYLOGEOGRAPHIC STUDIES IN THE TROPICAL SEAWEED CLADOPHOROPSIS MEMBRANACEA (CHLOROPHYTA,ULVOPHYCEAE) REVEAL A CRYPTIC SPECIES COMPLEX1

The seaweed Cladophoropsis membranacea (Hofman Bang ex. C. Agardh) Børgesen is a widely distributed species on coral reefs and along rocky coastlines throughout the tropics and subtropics. In a recent population‐level survey openface>1600 individuals with eight microsatellite loci, a number of isolates from biogeographically disjunct locations could not be amplified for any of the loci. Nonamplifiable and amplifiable isolates co‐occurred within the Canary Islands, Cape Verde Islands, and in the Caribbean. These unexpected results led to question whether or not C. membranacea is a single species. Phylogenetic relationships were evaluated using rDNA ITS1 and ITS2 sequence comparisons from 42 isolates sampled from a subset of 30 of the 66 locations. Four well‐supported clades were identified. Sequence divergence within clades was <1%, whereas between‐clade divergence was 2%–3%. Intraindividual variation was extremely low with no effects on the analysis. A strong, but imperfect, correspondence was found between ITS clades and amplifiable microsatellite loci. It is concluded that C. membranacea consists of three cryptic species. Using Pacific isolates as an outgroup, the most basal clade included the Central Canary Islands, Cape Verde, and Bonaire (Caribbean) isolates and thus spanned the widest latitude. Two derived sister clades consisted of a southern transtropical group stretching across the SE Caribbean to the Cape Verde Islands and African coast (but not the Canary Islands) and a NE‐Canary Island‐Mediterranean clade that also included the Red Sea. The detection of overlapping biogeographic distributions highlights the importance of ecotypic differentiation with respect to temperature and the importance of shifting sea surface isotherms that have driven periodic extinctions and recolonizations of the Canary Islands—a crossroads of marine floral exchange—since the last glacial maximum.     

Late Pliocene and Quaternary Eurasian locust infestations in the Canary Archipelago

Meco, J., Muhs, D.R., Fontugne, M., Ramos, A.J.G., Lomoschitz, A. & Patterson, D. 2010: Late Pliocene and Quaternary Eurasian locust infestations in the Canary Archipelago. Lethaia, Vol. 44, pp. 440–454. The Canary Archipelago has long been a sensitive location to record climate changes of the past. Interbedded with its basalt lavas are marine deposits from the principal Pleistocene interglacials, as well as aeolian sands with intercalated palaeosols. The palaeosols contain African dust and innumerable relict egg pods of a temperate‐region locust (cf. Dociostaurus maroccanus Thunberg 1815 ). New ecological and stratigraphical information reveals the geological history of locust plagues (or infestations) and their palaeoclimatic significance. Here, we show that the first arrival of the plagues to the Canary Islands from Africa took place near the end of the Pliocene, ca. 3 Ma, and reappeared with immense strength during the middle Late Pleistocene preceding MIS (marine isotope stage) 11 (ca. 420 ka), MIS 5.5 (ca. 125 ka) and probably during other warm interglacials of the late Middle Pleistocene and the Late Pleistocene. During the Early Holocene, locust plagues may have coincided with a brief cool period in the current interglacial. Climatically, locust plagues on the Canaries are a link in the chain of full‐glacial arid–cold climate (calcareous dunes), early interglacial arid–sub‐humid climate (African dust inputs and locust plagues), peak interglacial warm–humid climate (marine deposits with Senegalese fauna), transitional arid–temperate climate (pedogenic calcretes), and again full‐glacial arid–cold climate (calcareous dunes) oscillations. During the principal interglacials of the Pleistocene, the Canary Islands recorded the migrations of warm Senegalese marine faunas to the north, crossing latitudes in the Euro‐African Atlantic. However, this northward marine faunal migration was preceded in the terrestrial realm by interglacial infestations of locusts. □Locust plagues, Canary Islands, Late Pliocene, Pleistocene, Holocene, palaeoclimatology.     

Getting there and around: Host range oscillations during colonization of the Canary Islands by the parasitic nematode Spauligodon

Episodes of expansion and isolation in geographic range over space and time, during which parasites have the opportunity to expand their host range, are linked to the development of host–parasite mosaic assemblages and parasite diversification. In this study, we investigated whether island colonization events lead to host range oscillations in a taxon of host‐specific parasitic nematodes of the genus Spauligodon in the Canary Islands. We further investigated whether range oscillations also resulted in shifts in host breadth (i.e., specialization), as expected for parasites on islands. Parasite phylogeny and divergence time estimates were inferred from molecular data with Bayesian methods. Host divergence times were set as calibration priors after a priori evaluation with a global‐fit method of which individual host–parasite associations likely represent cospeciation links. Parasite colonization history was reconstructed, followed by an estimation of oscillation events and specificity level. The results indicate the presence of four Spauligodon clades in the Canary Islands, which originated from at least three different colonization events. We found evidence of host range oscillations to truly novel hosts, which in one case led to higher diversification. Contemporary host–parasite associations show strong host specificity, suggesting that changes in host breadth were limited to the shift period. Lineages with more frequent and wider taxonomic host range oscillations prior to the initial colonization event showed wider range oscillations during colonization and diversification within the archipelago. Our results suggest that a lineage's evolutionary past may be the best indicator of a parasite's potential for future range expansions.     

Age and Growth Patterns of Brazil Nut Trees (Bertholletia excelsa Bonpl.) in Amazonia,Brazil

Various techniques have been used to estimate the age of Brazil nut trees (Bertholletia excelsa Bonpl.), but these techniques produce large discrepancies. Here, we first verified that two individuals of known ages from a plantation in central Amazonia, Brazil, have a congruent number of growth rings. The indexed average tree‐ring curve was significantly correlated with total precipitation during the rainy season (November–June) over a 50‐yr period, confirming the annual nature of the tree rings. Second, we analyzed Brazil nut trees from two populations in the Trombetas (eastern Amazon) and Purus (central Amazon) regions, performing tree‐ring analysis to estimate tree age and diameter increment rates. We compared age–diameter relationships, mean passage time through 10‐cm diameter size classes, and growth trajectories of individual trees. The maximum age of Brazil nut trees analyzed was 361 yr in the Purus and 401 yr in the Trombetas. Trees at the Purus site had higher mean diameter increment rates and showed more variation compared to trees at the Trombetas site. Individual growth trajectories show that the majority of trees attained the canopy by direct growth, while a smaller number passed through one release or one suppression event before becoming established in the canopy. None of the trees passed through multiple release and suppression events. The age estimations presented here are comparable to previous tree‐ring analyses for the species, and the observed growth patterns support earlier work indicating B. excelsa as a gap‐dependent tree species.     

Assessing the utility of direct and indirect methods for estimating tropical tree age in the Western Ghats, India

The knowledge of tree age is important for understanding tree growth and forest dynamics. It may be estimated by ‘direct’ methods involving growth ring counts, or by ‘indirect’ methods involving field measurements of growth rates. Direct methods are considered more accurate, but it is not clear if they are appropriate for all species, notably from the humid tropics. In this paper we assess the occurrence of annual growth rings and their utility for age estimation in three tropical tree species, Acrocarpus fraxinifolius, Dalbergia latifolia (Fabaceae) and Syzygium cumini (Myrtaceae), growing in traditional shade coffee plantations of the southern Western Ghats, India. These species previously were described as having “indistinct or absent” growth rings. We used anatomical studies, field measurements and computational methods to characterise growth rings and assess similarities between directly and indirectly estimated tree ages. Our study revealed that annual growth rings were characterised by different sets of anatomical features per species and were most distinct in the fast-growing deciduous A. fraxinifolius. Growth rates measured in the field showed annual periodicity in all three species, and reflected annual rainfall-drought cycles in D. latifolia and S. cumini. Direct age estimates were most similar to indirect estimates in D. latifolia, and least so in S. cumini. The results of direct age estimation by counting rings are consistent with them being annual in nature in tropical species with distinct and reliable annual growth ring formation. However, for species with poorly defined growth rings, indirect age estimation methods might be more useful.     

Parallel evolution of insular Olea europaea subspecies based on geographical structuring of plastid DNA variation and phenotypic similarity in leaf traits

Strong geographical isolation within the distribution of a species may result in differentiated lineages exhibiting conspicuous phenotypic differences. In the present paper, we investigate whether plastid and phenotypic variation is geographically structured within the Olea europaea complex in Macaronesia, which comprises three subspecies separated by oceanic barriers: maroccana (south‐west Morocco), guanchica (Canary Islands) and cerasiformis (Madeira archipelago). Plastid variation showed a significant pattern of geographical structure (N_ST > G_ST = 0.56), because of the lack of shared haplotypes among subspecies and the presence of a single and private haplotype in the eastern Canary Islands. Such a clear molecular structure, however, was not reflected in a congruent pattern of phenotypic differentiation among taxa in leaf morpho‐functional traits. Despite the substantial genetic differentiation observed between the subspecies from Madeira and the Canary Islands, they displayed both higher leaf size (leaf area) and specific leaf area (leaf surface area‐to‐mass ratio) than their continental counterparts, probably as a result of oceanic conditions in subtropical environments. Unlike most of the plant groups previously studied in the Macaronesian region, the lineages of Olea illustrate how low phenotypic differentiation can be also related to a clear molecular differentiation in oceanic island enclaves. © 2010 The Linnean Society of London, Botanical Journal of the Linnean Society, 2010, 162 , 54–63.     

Population history,gene flow,and bottlenecks in island populations of a secondary seed disperser,the southern grey shrike (Lanius meridionalis koenigi)

Studying the population history and demography of organisms with important ecological roles can aid understanding of evolutionary processes at the community level and inform conservation. We screened genetic variation (mtDNA and microsatellite) across the populations of the southern grey shrike (Lanius meridionalis koenigi) in the Canary Islands, where it is an endemic subspecies and an important secondary seed disperser. We show that the Canarian subspecies is polyphyletic with L. meridionalis elegans from North Africa and that shrikes have colonized the Canary Islands from North Africa multiple times. Substantial differences in genetic diversity exist across islands, which are most likely the product of a combination of historical colonization events and recent bottlenecks. The Eastern Canary Islands had the highest overall levels of genetic diversity and have probably been most recently and/or frequently colonized from Africa. Recent or ongoing bottlenecks were detected in three of the islands and are consistent with anecdotal evidence of population declines due to human disturbance. These findings are troubling given the shrike's key ecological role in the Canary Islands, and further research is needed to understand the community‐level consequences of declines in shrike populations. Finally, we found moderate genetic differentiation among populations, which largely reflected the shrike's bottleneck history; however, a significant pattern of isolation‐by‐distance indicated that some gene flow occurs between islands. This study is a useful first step toward understanding how secondary seed dispersal operates over broad spatial scales.     

Refugia,colonization and diversification of an arid‐adapted bird: coincident patterns between genetic data and ecological niche modelling

Phylogeographical studies are common in boreal and temperate species from the Palaearctic, but scarce in arid‐adapted species. We used nuclear and mitochondrial markers to investigate phylogeography and to estimate chronology of colonization events of the trumpeter finch Bucanetes githagineus, an arid‐adapted bird. We used 271 samples from 16 populations, most of which were fresh samples but including some museum specimens. Microsatellite data showed no clear grouping according to the sampling locations. Microsatellite and mitochondrial data showed the clearest differentiation between Maghreb and Canary Islands and between Maghreb and Western Sahara. Mitochondrial data suggest differentiation between different Maghreb populations and among Maghreb and Near East populations, between Iberian Peninsula and Canary Islands, as well as between Western Sahara and Maghreb. Our coalescence analyses indicate that the trumpeter finch colonized North Africa during the humid Marine Isotope Stage 5 (MIS5) period of the Sahara region 125 000 years ago. We constructed an ecological niche model (ENM) to estimate the geographical distribution of climatically suitable habitats for the trumpeter finch. We tested whether changes in the species range in relation to glacial–interglacial cycles could be responsible for observed patterns of genetic diversity and structure. Modelling results matched with those from genetic data as the species' potential range increases in interglacial scenarios (in the present climatic scenario and during MIS5) and decreases in glacial climates (during the last glacial maximum, LGM, 21 000 years ago). Our results suggest that the trumpeter finch responded to Pleistocene climatic changes by expanding and contracting its range.     

Ascidiacyclamides containing oxazoline and thiazole motifs assume square conformations and show high cytotoxicity

Four cyclic octapeptides were designed from ascidiacyclamide [cyclo(–Ile–Oxz–D ‐Val– Thz–)₂] (ASC, 1 ) to investigate the effects of oxazoline (Oxz) and thiazole (Thz) rings on the structures and cytotoxicities of the peptides. cyclo(–Ile–Thz–D ‐Val–Oxz–)₂ ( 2 ) had the same number of Oxz and Thz rings as ASC, but the ring positions were switched. cyclo(–Ile–Oxz–D ‐Val–Thz–Ile–Thz–D ‐Val–Thz–) ( 3 ) and cyclo(–Ile–Thz–D ‐Val–Oxz–Ile–Thz–D ‐Val–Thz–) ( 4 ) contained one Oxz and three Thz rings within the molecule. All Oxz rings were substituted with Thz in cyclo(–Ile–Thz–D ‐Val–Thz–)₂ ( 5 ). These analogues had new Oxz and Thz blocks forming the 24‐membered ring. Based on CD spectra and X‐ray diffraction analyses, the structures of all four analogues were classified as square ASC forms. But the structures of 2 and 5 differed from the original square form of 1 , and they showed no cytotoxicity. The structure of 3 was very similar to that of 1 , and 3 showed 10 times greater cytotoxicity than 1 . Although no definite structure of 4 was obtained, it showed three times greater cytotoxicity than 1 . It appears that the position and number of Oxz residues are essential determinants in the structure‐cytotoxicity relationship of ASC analogues.     

Evolution of an invasive rodent on an archipelago as revealed by molar shape analysis: the house mouse in the Canary Islands

Aim The aim of this paper is to identify the patterns in the morphological differentiation in Canary Island mice, based on fossil and modern samples. In order to achieve this, the mouse species present on the archipelago were first compared with a set of continental mice. The differences between the continental and Canary Island samples, and among the Canary Island samples, provide insights into the processes of colonization and the subsequent insular evolution. Location Canary archipelago. Methods An outline analysis based on Fourier transformation was used to quantify shape differences between lower molars. Together with the fossil and modern Canary Island samples, a reference set of genotyped continental populations of the commensal Mus musculus and the wild Mus spretus was used for comparison. Results The morphometric analysis showed that all the mouse specimens from the Canary Islands and Cape Verde belonged to Mus musculus domesticus. Lower molars of extant mice from La Gomera, El Hierro, Gran Canaria, Tenerife, and to a lesser degree from Lanzarote, were similar to those of genotyped M. m. domesticus from the continent, while teeth of extant mice from Fuerteventura were more divergent. Fossil mice from Fuerteventura were very similar to the extant representatives on this island, and similar to the fossil mice on the nearby islands of Lobos and La Graciosa. Main conclusions The mouse present on the Canary archipelago has been identified as the house mouse M. m. domesticus. Based on the shape of the lower molar, the Canary Island mice are divergent from the continental ones, but the degree of divergence varies with the geography of the archipelago. Overall, populations from eastern islands are more divergent from the continental mice than populations from western ones. Fossil populations indicate that this situation was established several centuries ago. Two main factors may have contributed to this pattern: the appearance of different types of environment on the islands since the successful settlement of the mouse, and/or the number of subsequent introductions of continental individuals via shipping.     

Riccia boumanii Dirkse,Losada & M.Stech sp. nov. (Ricciaceae,Marchantiophyta) in the Canary Islands,the first species of Riccia subgenus Riccia section Pilifer Volk outside South Africa

A morpho-molecular study was undertaken to solve the taxonomic identity of Riccia plants from the Canary Islands. These plants were assumed to belong to the South African endemic Riccia section Pilifer, but could not be assigned to a particular species in that section. In the interim they were named R. lamellosa (section Riccia), since R. lamellosa is the only European species with conspicuous white ventral scales. Molecular phylogenetic reconstructions based on trnL-F and ITS2 sequences confirmed that the respective Riccia plants belong to section Pilifer. The respective clade is clearly separated from the clades of R. lamellosa and R. elongata, the latter being morphologically most similar within section Pilifer. Based on the combined molecular and morphological evidence the Riccia plants from Canary Islands are described as a new species, R. boumanii, which represents the first species of section Pilifer outside South Africa. Based on revised herbarium specimens, R. boumanii occurs on five islands of the Canary Islands archipelago, namely El Hierro, Gran Canaria, La Gomera, La Palma, and Tenerife.     

Reproductive biology of the blue jack mackerel,Trachurus picturatus (Bowdich, 1825), off the Canary Islands

The reproductive cycle of the blue jack mackerel, Trachurus picturatus, had not been described for the Canary Islands. Between March 2005 and March 2006 monthly samples of T. picturatus were collected randomly at the central fishery wharf from the commercial catches of purse‐seiners in Tenerife Island waters (Canary Islands). Some 2472 specimens were analysed, with total lengths from 10.4 to 31.9 cm. Although females outnumbered males in summer, males were more abundant in the sex ratio (1.36 : 1). Based on the monthly evolution of the gonado‐somatic index and the proportion of mature individuals, the spawning season occurred between January and April, peaking in February. Lengths at first maturity (LFM) were calculated from the maturity ogives by the Gompertz model for all specimens (22.79 cm), for males (21.20 cm) and for females (23.05 cm). In this area the minimum legal size for T. picturatus is actually smaller than the length at first maturity and should be revised to avoid depletion of the stock.     

Evolution of cave Axiokebuita and Speleobregma (Scalibregmatidae,Annelida)

The evolutionary history of Axiokebuita and Speleobregma, two poorly known lineages of annelids exclusive from deep‐sea or marine caves but always from crevicular habitats, is explored here. Speleobregma lanzaroteum Bertelsen, 1986, and Axiokebuita cavernicola sp. n. are described from anchialine and marine caves of the Canary Islands using light and electron microscopy. Speleobregma lanzaroteum is previously known only from a single specimen from the water column of an anchialine cave in Lanzarote. Emended diagnosis, details on the ciliary patterns and behavioural observations are provided based on newly collected material and in situ observations. Axiokebuita cavernicola sp. n. is found in Pleistocene gravel deposits in a shallow water marine cave in Tenerife (Canary Islands). The new species is characterized by the presence of dorsal ciliary bands and short knob‐like neuropodial cirri from segment two. The porosity and permeability of the gravelly environment of A. cavernicola sp. n. are shown to be equivalent to the water column or crevices of Speleobregma and other Axiokebuita spp. Phylogenetic analyses of five gene fragments and 44 terminals using maximum‐likelihood and Bayesian methods support a derived position of A. cavernicola sp. n. within Axiokebuita and confirm a sister‐group relationship of Axiokebuita with Speleobregma with high nodal support. The Axiokebuita–Speleobregma clade is morphologically characterized by a globular pygidium with adhesive glands and ventral ungrooved ciliated palps. Our results support two independent cave colonization events, favoured by the preadaptation of the members of Axiokebuita–Speleobregma lineage to crevicular habitats.     

Radiation of Atlantic goldcrests Regulus regulus spp.: evidence of a new taxon from the Canary Islands

Phylogenetic relationships between goldcrest populations from the Atlantic Islands (Azores and Canary Islands) were investigated by two molecular markers (mitochondrial control region and cytochrome b sequences), and partly by morphology and territorial song. The Azorean goldcrest populations are closely related to European nominate R. r. regulus. Most probably, the Azores were colonized by goldcrests in a single late‐pleistocene invasion, while colonization of the Canary Islands presumably occurred in two steps: An early invasion to Tenerife and La Gomera 1.9–2.3 million years (my) ago and a more recent one to El Hierro and La Palma 1.3–1.8 my ago. Distribution of haplotypes on the Azores suggests a division of R. r. azoricus on São Miguel into an eastern population with close affinities to R. r. sanctaemariae and a western population belonging to the lineage of R. r. inermis on the central and western island group. The Canarian populations are genetically substructured into a northeastern group embracing Tenerife and La Gomera and a second, southwestern group including El Hierro and La Palma. Genetic distances between members of the two Canarian clades range at 3.1–3.4% (TrN distance, control region and cytochrome b). Differentiation between the two groups is also supported by morphology and by territorial song. Substitution rate estimates for the both genes range at approximately the same values of 0.0031 and 0.0044 substitutions per site and lineage per my which roughly corresponds 0.61–0.83% divergence between Regulus lineages per my. Highest local rates occur in island clades of the Azorean and the Canarian population and in R. r. japonensis from the Russian Far East and Japan. However, a general acceleration of a molecular clock in island populations is not evident from the Regulus data set due to extremely low local rate estimates in the Canarian clade of Tenerife and La Gomera. As a taxonomic consequence of the marked differentiation of the two Canarian goldcrest clades the populations from El Hierro and La Palma are described as a taxon new to science and are named Regulus regulus ellenthalerae n. ssp.     

Tree age estimates in Fagus sylvatica and Quercus robur: testing previous and improved methods

The accuracy of direct (based on increment cores) and indirect (based on age-size relationships) methods of tree age estimation in Fagus sylvatica and Quercus robur was tested. This was done through increment cores and stem discs taken in an old-growth forest of Northern Spain. It was found that cross-dating was more precise than ring counting by up to 7 years per tree. Furthermore, cross-dating permitted the estimation of the age of trees with floating ring-width series, which were 7% of cored F. sylvatica and 40% of Q. robur ones. In partial cores with the arcs of the inner rings, the length of the missing radius was estimated with both a geometric method, based on the curvature of the arcs, and a new graphical method, based on the convergence of xylem rays at the pith. The graphical method was more accurate when the radial growth was eccentric, as happens in Q. robur, while both methods showed a similar accuracy for F. sylvatica, whose growth is relatively concentric. Empirical models of initial radial growth (IRG), built to estimate the number of missing rings, reduced the errors associated with other methods that assume constant growth rates. Age estimates obtained from the graphical method combined with the IRG models were within 4% of the actual age. This combination ensured age estimates with a mean accuracy of 8 years for 98% of the F. sylvatica trees, and 4 years for 89% of the Q. robur. In partial cores without the arcs of the inner rings, the length of the missing radius was estimated as the distance to the geometric centre of the tree. In that case, age estimates obtained by extrapolating the mean growth rate of the 20 innermost rings in the cores were from 10 to 20% of actual age, which coincided with results obtained in other tree species with this method. Finally, the age-diameter equations of the different cohorts produced better age estimates (from 8 to 14% of actual age) than equations of the population as a whole (from 20 to 40% of actual age). These results proved that the errors derived from doubtful assumptions, such as concentric radial growth, constant growth and recruitment rates, or the absence of anomalous rings, could be reduced by applying more realistic methods of tree age estimation.     

The potential use of scales for estimating age and growth of Mediterranean albacore (Thunnus alalunga)

The ability to accurately estimate the age of fishes is critical for conducting stock assessments and developing fishery management policies. Scales were collected from albacore, Thunnus alalunga, caught in the Mediterranean Sea during the years 1989–1995 to estimate their age and growth. Ages, which ranged from 1+ to 6+ years, were estimated from the interpretation of the concentric rings on the scales of 473 individuals that ranged in fork length from 55.5 to 89 cm. Males reached a greater size and age than females. The relatively close agreement in the mean lengths at ages estimated by scales and other techniques constituted a preliminary verification of the method. The von Bertalanffy growth model was fitted to mean lengths at estimated ages, resulting in the following growth parameters for the combined sexes: L_∞ = 86 cm, K = 0.4, t_o = ?0.8 years. Parameter estimates were in agreement with what is known about life history of the species in the Mediterranean. Moreover, the growth rates were consistent with length increment observations from five tag returns, which lend support to our working hypothesis that the scale‐rings are annual structures. When the Mediterranean albacore growth parameters were compared with those of Atlantic Ocean albacore using scale age estimates, there were significant differences between the two populations, and Mediterranean albacore remain significantly smaller than Atlantic Ocean albacore.     

Extreme longevity in freshwater mussels revisited: sources of bias in age estimates derived from mark–recapture experiments

1. There may be bias associated with mark–recapture experiments used to estimate age and growth of freshwater mussels. Using subsets of a mark–recapture dataset for Quadrula pustulosa, I examined how age and growth parameter estimates are affected by (i) the range and skew of the data and (ii) growth reduction due to handling. I compared predictions from von Bertalanffy growth models based on mark–recapture data with direct observation of mussel age and growth inferred from validated shell rings. 2. Growth models based on a dataset that included observations from a wide range of length classes (spanning ≥ the upper 50% of the population length range) produced only slightly biased age estimates for small and medium‐sized individuals (overestimated by 1–2 years relative to estimates from validated shell rings) but estimates became increasingly biased for larger individuals. Growth models using data that included only observations of larger animals (< the upper 50% of length range) overestimated age for all length classes, and estimated maximum age was two to six times greater than the maximum age observed in the population (47 years). Similarly, growth models using a left‐skewed dataset overestimated age. 3. Reductions of growth due to repeated handling also resulted in overestimates of age. The estimated age of mussels that were handled in two consecutive years was as much as twice that of mussels that were handled only once over the same period. Assuming a constant reduction in the annual rate of growth, handling an individual for five consecutive years could result in an estimated age that is five times too high. 4. These findings show that mark–recapture methods have serious limitations for estimating mussel age and growth. A previous paper (Freshwater Biology, 46, 2001, 1349) presented longevity estimates for three mussel species that were an order of magnitude higher than estimates inferred from shell rings. Because those estimates of extreme longevity were based on mark–recapture methods and subject to multiple, additive sources of bias, they cannot be considered accurate representations of life span and cannot be used to conclude that traditional methods of bivalve ageing by interpretation of shell rings are flawed.