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Dive into the research topics where Ian J. Kitching is active.

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Featured researches published by Ian J. Kitching.


Molecular Ecology Resources | 2009

Integration of DNA barcoding into an ongoing inventory of complex tropical biodiversity

Daniel H. Janzen; Winnie Hallwachs; Patrick Blandin; John M. Burns; Jean Marie Cadiou; Isidro A. Chacón; Tanya Dapkey; Andrew R. Deans; Marc E. Epstein; Bernardo Espinoza; John G. Franclemont; William A. Haber; Mehrdad Hajibabaei; Jason P. W. Hall; Paul D. N. Hebert; Ian D. Gauld; Donald J. Harvey; Axel Hausmann; Ian J. Kitching; Don Lafontaine; Jean Fran Çois Landry; Claude Lemaire; Jacqueline Y. Miller; James S. Miller; Lee D. Miller; Scott E. Miller; Jose Montero; Eugene Munroe; Suzanne Rab Green; Sujeevan Ratnasingham

Inventory of the caterpillars, their food plants and parasitoids began in 1978 for todays Area de Conservacion Guanacaste (ACG), in northwestern Costa Rica. This complex mosaic of 120 000 ha of conserved and regenerating dry, cloud and rain forest over 0–2000 m elevation contains at least 10 000 species of non‐leaf‐mining caterpillars used by more than 5000 species of parasitoids. Several hundred thousand specimens of ACG‐reared adult Lepidoptera and parasitoids have been intensively and extensively studied morphologically by many taxonomists, including most of the co‐authors. DNA barcoding — the use of a standardized short mitochondrial DNA sequence to identify specimens and flush out undisclosed species — was added to the taxonomic identification process in 2003. Barcoding has been found to be extremely accurate during the identification of about 100 000 specimens of about 3500 morphologically defined species of adult moths, butterflies, tachinid flies, and parasitoid wasps. Less than 1% of the species have such similar barcodes that a molecularly based taxonomic identification is impossible. No specimen with a full barcode was misidentified when its barcode was compared with the barcode library. Also as expected from early trials, barcoding a series from all morphologically defined species, and correlating the morphological, ecological and barcode traits, has revealed many hundreds of overlooked presumptive species. Many but not all of these cryptic species can now be distinguished by subtle morphological and/or ecological traits previously ascribed to ‘variation’ or thought to be insignificant for species‐level recognition. Adding DNA barcoding to the inventory has substantially improved the quality and depth of the inventory, and greatly multiplied the number of situations requiring further taxonomic work for resolution.


Systematic Entomology | 1998

Phylogeny and classification of the Culicidae (Diptera)

Ralph E. Harbach; Ian J. Kitching

The generic relationships and higher classification of the family Culicidae are examined on the basis of a phylogenetic analysis. New and traditional morphological characters studied and compared throughout the Culicidae resulted in the acquisition of character data relative to the majority of species within each genus. Polymorphisms and morphological observations are discussed and additional information and illustrations are provided for the majority of characters and their character states. The analysis of seventy‐three adult, pupal and fourth‐instar larval characters coded for the thirty‐eight currently recognized genera of mosquitoes resulted in relationships and groupings which differ significantly from traditional hypotheses. The analysis supports the monophyly of the subfamily Anophelinae and the tribes Culicini and Sabethini. The Anophelinae form the most basal clade of the family. The results indicate that Aedini is a paraphyletic assemblage with respect to the Mansoniini, each of which is monophyletic in itself. The Aedini + Mansoniini form a sister group to the Culicini + Sabethini, with the Aedini and the Culicini placed in ancestral relationships to the Mansoniini and the Sabethini, respectively. Based on the topography of generic relationships among more ‘generalized’ mosquitoes, the boundaries and relationships of the tribes Aedeomyiini, Uranotaeniini, Ficalbiini, Hodgesiini, Orthopodomyiini and Culisetini appear to be problematic. Relationships between genera of the tribe Aedini are generally poorly resolved due to a significant amount of polymorphism, especially within the genus Aedes as currently defined. There is no support for separate subfamily recognition for the genus Toxorhynchites, which is downgraded to tribal status as a result of the analysis. The results are discussed in relation to previous hypotheses based on subjective inference and cladistic analyses.


Zoologica Scripta | 2010

A new molecular phylogeny offers hope for a stable family level classification of the Noctuoidea (Lepidoptera)

Reza Zahiri; Ian J. Kitching; J. Donald Lafontaine; Marko Mutanen; Lauri Kaila; Jeremy D. Holloway; Niklas Wahlberg

Zahiri, R., Kitching, I. J., Lafontaine, J. D., Mutanen, M., Kaila, L., Holloway, J. D. & Wahlberg, N. (2010). A new molecular phylogeny offers hope for a stable family level classification of the Noctuoidea (Lepidoptera). —Zoologica Scripta, 40, 158–173.


Ecology | 2007

A GLOBAL EVALUATION OF METABOLIC THEORY AS AN EXPLANATION FOR TERRESTRIAL SPECIES RICHNESS GRADIENTS

Bradford A. Hawkins; Fábio Suzart de Albuquerque; Miguel B. Araújo; Jan Beck; Luis Mauricio Bini; Francisco J. Cabrero-Sañudo; Isabel Castro‐Parga; José Alexandre Felizola Diniz-Filho; Dolores Ferrer-Castán; Richard Field; José F. Gómez; Joaquín Hortal; Jeremy T. Kerr; Ian J. Kitching; Jorge L. León‐Cortés; Jorge M. Lobo; Daniel Montoya; Juan Carlos Moreno; Miguel Á. Olalla-Tárraga; Juli G. Pausas; Hong Qian; Carsten Rahbek; Miguel Á. Rodríguez; Nathan J. Sanders; Paul H. Williams

We compiled 46 broadscale data sets of species richness for a wide range of terrestrial plant, invertebrate, and ectothermic vertebrate groups in all parts of the world to test the ability of metabolic theory to account for observed diversity gradients. The theory makes two related predictions: (1) In-transformed richness is linearly associated with a linear, inverse transformation of annual temperature, and (2) the slope of the relationship is near -0.65. Of the 46 data sets, 14 had no significant relationship; of the remaining 32, nine were linear, meeting prediction 1. Model I (ordinary least squares, OLS) and model II (reduced major axis, RMA) regressions then tested the linear slopes against prediction 2. In the 23 data sets having nonlinear relationships between richness and temperature, split-line regression divided the data into linear components, and regressions were done on each component to test prediction 2 for subsets of the data. Of the 46 data sets analyzed in their entirety using OLS regression, one was consistent with metabolic theory (meeting both predictions), and one was possibly consistent. Using RMA regression, no data sets were consistent. Of 67 analyses of prediction 2 using OLS regression on all linear data sets and subsets, two were consistent with the prediction, and four were possibly consistent. Using RMA regression, one was consistent (albeit weakly), and four were possibly consistent. We also found that the relationship between richness and temperature is both taxonomically and geographically conditional, and there is no evidence for a universal response of diversity to temperature. Meta-analyses confirmed significant heterogeneity in slopes among data sets, and the combined slopes across studies were significantly lower than the range of slopes predicted by metabolic theory based on both OLS and RMA regressions. We conclude that metabolic theory, as currently formulated, is a poor predictor of observed diversity gradients in most terrestrial systems.


Systematic Entomology | 2012

Molecular phylogenetics of Erebidae (Lepidoptera, Noctuoidea)

Reza Zahiri; Jeremy D. Holloway; Ian J. Kitching; J. Donald Lafontaine; Marko Mutanen; Niklas Wahlberg

As a step towards understanding the higher‐level phylogeny and evolutionary affinities of quadrifid noctuoid moths, we have undertaken the first large‐scale molecular phylogenetic analysis of the moth family Erebidae, including almost all subfamilies, as well as most tribes and subtribes. DNA sequence data for one mitochondrial gene (COI) and seven nuclear genes (EF‐1α, wingless, RpS5, IDH, MDH, GAPDH and CAD) were analysed for a total of 237 taxa, principally type genera of higher taxa. Data matrices (6407 bp in total) were analysed by parsimony with equal weighting and model‐based evolutionary methods (maximum likelihood), which revealed a well‐resolved skeleton phylogenetic hypothesis with 18 major lineages, which we treat here as subfamilies of Erebidae. We thus present a new phylogeny for Erebidae consisting of 18 moderate to strongly supported subfamilies: Scoliopteryginae, Rivulinae, Anobinae, Hypeninae, Lymantriinae, Pangraptinae, Herminiinae, Aganainae, Arctiinae, Calpinae, Hypocalinae, Eulepidotinae, Toxocampinae, Tinoliinae, Scolecocampinae, Hypenodinae, Boletobiinae and Erebinae. Where possible, each monophyletic lineage is diagnosed by autapomorphic morphological character states, and within each subfamily, monophyletic tribes and subtribes can be circumscribed, most of which can also be diagnosed by morphological apomorphies. All additional taxa sampled fell within one of the four previously recognized quadrifid families (mostly into Erebidae), which are now found to include two unusual monobasic taxa from New Guinea: Cocytiinae (now in Erebidae: Erebinae) and Eucocytiinae (now in Noctuidae: Pantheinae).


PLOS ONE | 2009

Phylogeny and Biogeography of Hawkmoths (Lepidoptera: Sphingidae): Evidence from Five Nuclear Genes

Akito Y. Kawahara; Andre A. Mignault; Jerome C. Regier; Ian J. Kitching; Charles Mitter

Background The 1400 species of hawkmoths (Lepidoptera: Sphingidae) comprise one of most conspicuous and well-studied groups of insects, and provide model systems for diverse biological disciplines. However, a robust phylogenetic framework for the family is currently lacking. Morphology is unable to confidently determine relationships among most groups. As a major step toward understanding relationships of this model group, we have undertaken the first large-scale molecular phylogenetic analysis of hawkmoths representing all subfamilies, tribes and subtribes. Methodology/Principal Findings The data set consisted of 131 sphingid species and 6793 bp of sequence from five protein-coding nuclear genes. Maximum likelihood and parsimony analyses provided strong support for more than two-thirds of all nodes, including strong signal for or against nearly all of the fifteen current subfamily, tribal and sub-tribal groupings. Monophyly was strongly supported for some of these, including Macroglossinae, Sphinginae, Acherontiini, Ambulycini, Philampelini, Choerocampina, and Hemarina. Other groupings proved para- or polyphyletic, and will need significant redefinition; these include Smerinthinae, Smerinthini, Sphingini, Sphingulini, Dilophonotini, Dilophonotina, Macroglossini, and Macroglossina. The basal divergence, strongly supported, is between Macroglossinae and Smerinthinae+Sphinginae. All genes contribute significantly to the signal from the combined data set, and there is little conflict between genes. Ancestral state reconstruction reveals multiple separate origins of New World and Old World radiations. Conclusions/Significance Our study provides the first comprehensive phylogeny of one of the most conspicuous and well-studied insects. The molecular phylogeny challenges current concepts of Sphingidae based on morphology, and provides a foundation for a new classification. While there are multiple independent origins of New World and Old World radiations, we conclude that broad-scale geographic distribution in hawkmoths is more phylogenetically conserved than previously postulated.


Systematics and Biodiversity | 2004

Automated identification of live moths (Macrolepidoptera) using digital automated identification System (DAISY)

Anna T. Watson; Mark A. O'Neill; Ian J. Kitching

Abstract Two hundred and thirty‐seven species of Macrolepidoptera were light trapped at Treborth Botanical Garden, Gwynedd, UK. Live adults were digitally imaged using a simple, inexpensive method suitable for field use, then released. Inconsistent lighting, variation in resting posture and inclusion of worn individuals produced image sets high in intraspecific variation. Thirty‐five common species were selected to provide training images for the Digital Automated Identification SYstem (DAISY). Twenty individuals per species were pre‐processed to standardize size and posture and to enhance features. The right forewing of each was highlighted manually and the pattern rendered polar and greyscale for DAISY analysis. Despite poor quality of some images, 83% of unknown species were identified correctly. The best species had 100% correct identification and the worst 35%. The most poorly identified images were those of moths that had lost scales or been unevenly illuminated. The precision with which the forewing was highlighted affected performance. When highlighted carefully, Laothoe populi was identified correctly twice as successfully as when the same image was highlighted poorly. Size of the training set was also important. Sets of 5, 10, 15 and 20 training images, plotted against performance produced a curve of diminishing returns. Colourimages and inclusion of size should improve accuracy.


BMC Ecology | 2011

When species matches are unavailable are DNA barcodes correctly assigned to higher taxa? An assessment using sphingid moths

John James Wilson; Rodolphe Rougerie; Justin Schonfeld; Daniel H. Janzen; Winnie Hallwachs; Mehrdad Hajibabaei; Ian J. Kitching; Jean Haxaire; Paul D. N. Hebert

BackgroundWhen a specimen belongs to a species not yet represented in DNA barcode reference libraries there is disagreement over the effectiveness of using sequence comparisons to assign the query accurately to a higher taxon. Library completeness and the assignment criteria used have been proposed as critical factors affecting the accuracy of such assignments but have not been thoroughly investigated. We explored the accuracy of assignments to genus, tribe and subfamily in the Sphingidae, using the almost complete global DNA barcode reference library (1095 species) available for this family. Costa Rican sphingids (118 species), a well-documented, diverse subset of the family, with each of the tribes and subfamilies represented were used as queries. We simulated libraries with different levels of completeness (10-100% of the available species), and recorded assignments (positive or ambiguous) and their accuracy (true or false) under six criteria.ResultsA liberal tree-based criterion assigned 83% of queries accurately to genus, 74% to tribe and 90% to subfamily, compared to a strict tree-based criterion, which assigned 75% of queries accurately to genus, 66% to tribe and 84% to subfamily, with a library containing 100% of available species (but excluding the species of the query). The greater number of true positives delivered by more relaxed criteria was negatively balanced by the occurrence of more false positives. This effect was most sharply observed with libraries of the lowest completeness where, for example at the genus level, 32% of assignments were false positives with the liberal criterion versus < 1% when using the strict. We observed little difference (< 8% using the liberal criterion) however, in the overall accuracy of the assignments between the lowest and highest levels of library completeness at the tribe and subfamily level.ConclusionsOur results suggest that when using a strict tree-based criterion for higher taxon assignment with DNA barcodes, the likelihood of assigning a query a genus name incorrectly is very low, if a genus name is provided it has a high likelihood of being accurate, and if no genus match is available the query can nevertheless be assigned to a subfamily with high accuracy regardless of library completeness. DNA barcoding often correctly assigned sphingid moths to higher taxa when species matches were unavailable, suggesting that barcode reference libraries can be useful for higher taxon assignments long before they achieve complete species coverage.


Systematic Entomology | 1985

The systematic position of Antirrhea and Caerois, with comments on the classification of the Nymphalidae (Lepidoptera)

Philip J. DeVries; Ian J. Kitching; R. I. Vane-Wright

Based on a Wagner tree analysis of ninety‐two characters (eighty‐five larval, one egg, six adult), the nymphalid butterfly genera Antirrhea and Caerois are demonstrated to be the closest relatives of the genus Morpho. Accordingly, Antirrhea and Caerois are formally transferred from the Satyrinae to the Morphinae. Without these two genera, the Morphinae (sensu Ehrlich) is at best a paraphyletic group. During the study, fourteen nymphalid genera were treated as potential outgroups. The analysis suggests that many currently accepted higher taxa within the Nymphalidae are probably untenable: the Satyrinae and Nymphalinae (sensu Ehrlich) are both probably polyphyletic; the Biinae (sensu Miller) must be abandoned, being polyphyletic; the Charaxidae (sensu Rydon), although probably monophyletic, appear to form a group subordinate to part of the ‘Satyrinae’; and Apatura does not cluster with the ‘Nymphalinae’, but appears to form the sister‐group of the ‘Satyrinae’ (less Antirrhea and Caerois) plus the Charaxinae. Re‐analyses of reduced data sets, in which potentially homoplasious larval head‐horn and adult wing venational characters were eliminated, leaves these conclusions essentially unaltered. The authors suggest that a solution to the seemingly intractable problem posed by nymphalid higher classification can be sought by the application of cladistic analysis to a large data set gathered from all developmental stages, with special emphasis on detailed comparative larval morphology.


ZooKeys | 2012

No specimen left behind: industrial scale digitization of natural history collections

Vladimir Blagoderov; Ian J. Kitching; Laurence Livermore; Thomas J. Simonsen; Vincent S. Smith

Abstract Traditional approaches for digitizing natural history collections, which include both imaging and metadata capture, are both labour- and time-intensive. Mass-digitization can only be completed if the resource-intensive steps, such as specimen selection and databasing of associated information, are minimized. Digitization of larger collections should employ an “industrial” approach, using the principles of automation and crowd sourcing, with minimal initial metadata collection including a mandatory persistent identifier. A new workflow for the mass-digitization of natural history museum collections based on these principles, and using SatScan® tray scanning system, is described.

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Jan Beck

American Museum of Natural History

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Akito Y. Kawahara

Florida Museum of Natural History

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