Mike D. Picker
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Mike D. Picker has a total of 16 co-authors. Here are the top co-authors by number of shared publications:
- Klaus-Dieter Klass
Senckenberg Natural History Collections Dresden, Museum of Zoology, Königsbrücker Landstraße 159, 01109 Dresden, Germany
2 shared publications - Anna Maryańska-Nadachowska
Institute of Systematics and Evolution of Animals Polish Academy of Sciences Krakow Poland
1 shared publication Dane E. McDonald
Department of Botany and Zoology University of Stellenbosch Private Bag X1, Matieland Stellenbosch 7602 South Africa
1 shared publication- Dorota Lachowska-Cierlik
Department of Entomology, Institute of Zoology, Jagiellonian University, Kraków, Poland
1 shared publication Eugene Moll
Department of Biodiversity and Conservation Biology, University of the Western Cape, Cape Town, South Africa
1 shared publication- Horst Bohn
Zoologische Staatssammlung München, Münchhausenstrasse 21, 81247 München, Germany
1 shared publication
Latest Publications
- 2 January 2019
- Published by Taylor & Francis in Transactions of the Royal Society of South Africa
- Vol. 74 (1) , 104-105
The Dark Side of the Hive – the Evolution of the Imperfect Honey bee
(2019). Book Review. Transactions of the Royal Society of South Africa. Ahead of Print.
- 2 January 2019
- Published by Taylor & Francis in Transactions of the Royal Society of South Africa
- Vol. 74 (1) , 104-105
The Dark Side of the Hive – the Evolution of the Imperfect Honey bee
(2019). Book Review. Transactions of the Royal Society of South Africa. Ahead of Print.
- Open Access
- 21 November 2015
- Published by Biology Centre, AS CR in European Journal of Entomology
- Vol. 112 (4) , 599-605
First chromosomal study of Mantophasmatodea: Karyotype of Karoophasma biedouwense (Austrophasmatidae)
We have investigated for the first time the chromosomes of Karoophasma biedouwense, a species belonging to the Mantophasmatodea, a recently discovered order of carnivorous insects. Our study has revealed that males of this species display testes with numerous seminal tubes (follicles), as in other Polyneoptera, and short tubular seminal vesicles embedded in a utricular gland. The karyotype consists of 2n = 12A + X monocentric and biarmed, meta/submetacentric chromosomes (fundamental number of arms: FN = 26) with blocks of heterochromatin around centromeres. The autosomes are classified into two size groups, one represented by a single, very large pair of autosomes, the other by five smaller pairs which constitute a continuous series gradually decreasing in size. Among "monocentric" orders of Polyneoptera, K. biedouwense shares its low chromosome number, 2n = 13, as also found with some Orthoptera (Acridoidea, Grylloidea, Gryllacridoidea). Male meiosis is of the classical pre-reductional type and the X(0) sex determination system is probably an ancestral state. Use of FISH along with an 18S rDNA probe revealed multiple ribosomal clusters, which most likely represent an apomorphic condition. We identified the ancestral insect telomeric sequence (TTAGG)n in the terminal areas of the chromosomes. Currently available data on the polyneopteran orders putatively related to Mantophasmatodea showed a wide variability of cytogenetic characteristics within and between them. The only character allowing some tentative inference to be made on the ancestry of K. biedouwense is its low chromosome number, the karyotypic pattern so far unreported for the Polyneoptera except in certain Orthoptera.
- 21 November 2015
- Published by Biology Centre, AS CR in European Journal of Entomology
- Vol. 112 (4) , 599-605
Open AccessFirst chromosomal study of Mantophasmatodea: Karyotype of Karoophasma biedouwense (Austrophasmatidae)
We have investigated for the first time the chromosomes of Karoophasma biedouwense, a species belonging to the Mantophasmatodea, a recently discovered order of carnivorous insects. Our study has revealed that males of this species display testes with numerous seminal tubes (follicles), as in other Polyneoptera, and short tubular seminal vesicles embedded in a utricular gland. The karyotype consists of 2n = 12A + X monocentric and biarmed, meta/submetacentric chromosomes (fundamental number of arms: FN = 26) with blocks of heterochromatin around centromeres. The autosomes are classified into two size groups, one represented by a single, very large pair of autosomes, the other by five smaller pairs which constitute a continuous series gradually decreasing in size. Among "monocentric" orders of Polyneoptera, K. biedouwense shares its low chromosome number, 2n = 13, as also found with some Orthoptera (Acridoidea, Grylloidea, Gryllacridoidea). Male meiosis is of the classical pre-reductional type and the X(0) sex determination system is probably an ancestral state. Use of FISH along with an 18S rDNA probe revealed multiple ribosomal clusters, which most likely represent an apomorphic condition. We identified the ancestral insect telomeric sequence (TTAGG)n in the terminal areas of the chromosomes. Currently available data on the polyneopteran orders putatively related to Mantophasmatodea showed a wide variability of cytogenetic characteristics within and between them. The only character allowing some tentative inference to be made on the ancestry of K. biedouwense is its low chromosome number, the karyotypic pattern so far unreported for the Polyneoptera except in certain Orthoptera.
- 7 June 2013
- Published by Wiley in Zoologica Scripta
- Vol. 42 (6) , 656-674
Evolutionary insight into thePeripatopsis balfourisensu lato species complex (Onychophora:Peripatopsidae) reveals novel lineages and zoogeographic patterning
- 7 June 2013
- Published by Wiley in Zoologica Scripta
- Vol. 42 (6) , 656-674
Evolutionary insight into thePeripatopsis balfourisensu lato species complex (Onychophora:Peripatopsidae) reveals novel lineages and zoogeographic patterning
- 19 January 2012
- Published by Wiley in Ecological Entomology
- Vol. 37 (1) , 33-42
Ants and the enigmatic Namibian fairy circles – cause and effect?
1. Parts of the Namibian landscape show extensive surface perturbation in the form of long‐lived, yet dynamic ‘fairy circles'. While exerting profound ecological effects on 7.3% of the land surface, the origin and nature of these large bare discs embedded in an arid grassland matrix remains unresolved. 2. We found no evidence to support the current hypothesis of a termite origin for fairy circles but instead observed a strong spatial association between fairy circles and large nests of the ant Black pugnacious ant Anoplolepis steingroeveri Forel, with much higher ant abundances on the circles compared with the matrix. 3. Aggression trials showed that different colonies of A. steingroeveri were located on different circles, and that the species was polydomous. 4. Fairy circles and Pogonomyrmex ant nests both have a bare disc surrounding the nest, are overdispersed (evenly spaced), and are associated with elevated soil moisture. Fairy circle soils exhibited a five‐fold increase in soil moisture when compared with the matrix. 5. Senescent Stipagrostis obtusa (Delile) Nees seedlings were only observed on the circles and not in the matrix, and were found to have a reduction in both root length and number of roots. 6. Anoplolepis steingroeveri excavated the root system of both S. obtusa seedlings on the disc and Stipagrostis ciliata (Desf.) de Winter grasses on the perimeter of the circles, where they tended honeydew‐secreting Meenoplidae bugs that fed on grass roots and culms. The bugs occurred almost exclusively on grasses associated with the circles. This ant–bug interaction is a possible mechanism for the observed reduction in root length and number of senescent grass seedlings on the circles.
- 19 January 2012
- Published by Wiley in Ecological Entomology
- Vol. 37 (1) , 33-42
Ants and the enigmatic Namibian fairy circles – cause and effect?
1. Parts of the Namibian landscape show extensive surface perturbation in the form of long‐lived, yet dynamic ‘fairy circles'. While exerting profound ecological effects on 7.3% of the land surface, the origin and nature of these large bare discs embedded in an arid grassland matrix remains unresolved. 2. We found no evidence to support the current hypothesis of a termite origin for fairy circles but instead observed a strong spatial association between fairy circles and large nests of the ant Black pugnacious ant Anoplolepis steingroeveri Forel, with much higher ant abundances on the circles compared with the matrix. 3. Aggression trials showed that different colonies of A. steingroeveri were located on different circles, and that the species was polydomous. 4. Fairy circles and Pogonomyrmex ant nests both have a bare disc surrounding the nest, are overdispersed (evenly spaced), and are associated with elevated soil moisture. Fairy circle soils exhibited a five‐fold increase in soil moisture when compared with the matrix. 5. Senescent Stipagrostis obtusa (Delile) Nees seedlings were only observed on the circles and not in the matrix, and were found to have a reduction in both root length and number of roots. 6. Anoplolepis steingroeveri excavated the root system of both S. obtusa seedlings on the disc and Stipagrostis ciliata (Desf.) de Winter grasses on the perimeter of the circles, where they tended honeydew‐secreting Meenoplidae bugs that fed on grass roots and culms. The bugs occurred almost exclusively on grasses associated with the circles. This ant–bug interaction is a possible mechanism for the observed reduction in root length and number of senescent grass seedlings on the circles.
- 7 December 2011
- Published by The Royal Society in Biology Letters
- Vol. 8 (3) , 390-392
A cockroach that jumps
We report on a newly discovered cockroach (Saltoblattella montistabularis) from South Africa, which jumps and therefore differs from all other extant cockroaches that have a scuttling locomotion. In its natural shrubland habitat, jumping and hopping accounted for 71 per cent of locomotory activity. Jumps are powered by rapid and synchronous extension of the hind legs that are twice the length of the other legs and make up 10 per cent of the body weight. In high-speed images of the best jumps the body was accelerated in 10 ms to a take-off velocity of 2.1 m s−1so that the cockroach experienced the equivalent of 23 times gravity while leaping a forward distance of 48 times its body length. Such jumps required 38 µJ of energy, a power output of 3.4 mW and exerted a ground reaction force through both hind legs of 4 mN. The large hind legs have grooved femora into which the tibiae engage fully in advance of a jump, and have resilin, an elastic protein, at the femoro-tibial joint. The extensor tibiae muscles contracted for 224 ms before the hind legs moved, indicating that energy must be stored and then released suddenly in a catapult action to propel a jump. Overall, the jumping mechanisms and anatomical features show remarkable convergence with those of grasshoppers with whom they share their habitat and which they rival in jumping performance.
- 7 December 2011
- Published by The Royal Society in Biology Letters
- Vol. 8 (3) , 390-392
A cockroach that jumps
We report on a newly discovered cockroach (Saltoblattella montistabularis) from South Africa, which jumps and therefore differs from all other extant cockroaches that have a scuttling locomotion. In its natural shrubland habitat, jumping and hopping accounted for 71 per cent of locomotory activity. Jumps are powered by rapid and synchronous extension of the hind legs that are twice the length of the other legs and make up 10 per cent of the body weight. In high-speed images of the best jumps the body was accelerated in 10 ms to a take-off velocity of 2.1 m s−1so that the cockroach experienced the equivalent of 23 times gravity while leaping a forward distance of 48 times its body length. Such jumps required 38 µJ of energy, a power output of 3.4 mW and exerted a ground reaction force through both hind legs of 4 mN. The large hind legs have grooved femora into which the tibiae engage fully in advance of a jump, and have resilin, an elastic protein, at the femoro-tibial joint. The extensor tibiae muscles contracted for 224 ms before the hind legs moved, indicating that energy must be stored and then released suddenly in a catapult action to propel a jump. Overall, the jumping mechanisms and anatomical features show remarkable convergence with those of grasshoppers with whom they share their habitat and which they rival in jumping performance.
- 13 January 2011
- Published by Springer Nature in Organisms Diversity & Evolution
- Vol. 11 (1) , 43-59
Sympatry in Mantophasmatodea, with the description of a new species and phylogenetic considerations
- 13 January 2011
- Published by Springer Nature in Organisms Diversity & Evolution
- Vol. 11 (1) , 43-59
Sympatry in Mantophasmatodea, with the description of a new species and phylogenetic considerations
- Open Access
- 28 February 2010
- Published by Pensoft Publishers in Arthropod Systematics & Phylogeny
- Vol. 68 (1) , 53-69
A jumping cockroach from South Africa, Saltoblattella montistabularis, gen. nov., spec. nov. (Blattodea: Blattellidae)
A jumping cockroach (Saltoblattella montistabularis) from Table Mountain, Cape Town, South Africa, is described. The new genus is defined, the characteristics of the species are thoroughly described with particular emphasis on unusual morphological adaptations for jumping. These include dramatic elongation of hind femur and tibia and enlargement of hind femur. The femur ventrally has a longitudinal groove for reception of the tibia during extreme fl exure prior to a jump. The euplantulae have unusual surface papillae which may assist landing after a jump. Further modifi cations from the standard cockroach design probably related to jumping locomotion are hemispherically-protruding compound eyes and a second point of articulation for the fi rst antennal segment. The hook of the male phallomeres is on the left, and the female does not rotate the ootheca prior to deposition. The exact position of the genus within the family Blattellidae is not clear; it is preliminarily placed in Blattellinae. The species and its jumping adaptations are compared with another recently discovered, but extinct jumping ‘cockroach’.
- 28 February 2010
- Published by Pensoft Publishers in Arthropod Systematics & Phylogeny
- Vol. 68 (1) , 53-69
Open AccessA jumping cockroach from South Africa, Saltoblattella montistabularis, gen. nov., spec. nov. (Blattodea: Blattellidae)
A jumping cockroach (Saltoblattella montistabularis) from Table Mountain, Cape Town, South Africa, is described. The new genus is defined, the characteristics of the species are thoroughly described with particular emphasis on unusual morphological adaptations for jumping. These include dramatic elongation of hind femur and tibia and enlargement of hind femur. The femur ventrally has a longitudinal groove for reception of the tibia during extreme fl exure prior to a jump. The euplantulae have unusual surface papillae which may assist landing after a jump. Further modifi cations from the standard cockroach design probably related to jumping locomotion are hemispherically-protruding compound eyes and a second point of articulation for the fi rst antennal segment. The hook of the male phallomeres is on the left, and the female does not rotate the ootheca prior to deposition. The exact position of the genus within the family Blattellidae is not clear; it is preliminarily placed in Blattellinae. The species and its jumping adaptations are compared with another recently discovered, but extinct jumping ‘cockroach’.
- 31 May 2008
- Published by Elsevier in Molecular Phylogenetics and Evolution
- Vol. 47 (2) , 443-462
Phylogeny of the Heelwalkers (Insecta: Mantophasmatodea) based on mtDNA sequences, with evidence for additional taxa in South Africa
- 31 May 2008
- Published by Elsevier in Molecular Phylogenetics and Evolution
- Vol. 47 (2) , 443-462
Phylogeny of the Heelwalkers (Insecta: Mantophasmatodea) based on mtDNA sequences, with evidence for additional taxa in South Africa