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At least 19 recordsLinked to original sources
PubMed2002

The role of sub-maximal force production in the enslaving phenomenon.

When individuals perform a force task involving only one finger, they involuntarily move other fingers as well. This phenomenon is referred to as the enslaving force or the interdependency of fingers. Given that previous literature on the enslaving force has focused on maximal isometric force production, the present research was designed to study the role of sub-maximal force production in the enslaving phenomenon. To this end, we examined behaviorally three levels of force production with a constant rate of force development. We also examined the temporal organization of enslaving separating the achievement of the desired force (ramp phase) and its maintenance (static phase). During the static phase we found: (i) the amount of enslaving increased with the increment of nominal force level whether the index, middle, ring or little fingers were used as the master finger; (ii) enslaving is strongest in the finger directly adjacent to the master finger; and (iii) in terms of enslaving, the index finger was more 'independent' than the other three fingers, regardless of nominal force produced, followed by the little, middle, and ring fingers. In terms of temporal organization, we found that the time-lag of activation of 'slave fingers' during the ramp phase was reduced as the amount of force level increased. Overall, our data suggest that enslaving effect is a task specific phenomenon and depends on the amount of force produced by the master finger.

Adult↗
PubMed2004

Motion enslaving among multiple fingers of the human hand.

The purpose of the current study was to examine motion enslaving characteristics of multiple fingers during isolated flexion of the distal interphalangeal joints. Because the distal interphalangeal joints are flexed by multiple tendons of the single flexor digitorum profundus, the current experimental design provided a unique advantage to understand inter-finger enslaving effects due to the flexor digitorum profundus. Eight subjects were instructed to flex the distal interphalangeal joint of each individual finger from the fully extended position to the fully flexed position as quickly as possible. Maximal angular displacements, velocities, or accelerations of individual fingers were used to calculate the enslaving effects. An independence index, defined as the ratio of the maximal displacement of a master finger to the sum of the maximal displacements of the master and slave fingers, was used to quantify relative independence of each finger. The angular displacements of the index, middle, ring, and little fingers were 68.6(degrees) (+/-7.7), 68.1(degrees) (+/-10.1), 68.1(degrees) (+/-9.7), and 74.7(degrees) (+/-13.3), respectively. The motion of a master finger was invariably accompanied by motion of 1 or 2 slave fingers. Angular displacements of master and slave fingers increased to maximum values with time monotonically. Velocity curves demonstrated bell-shaped profile, and the acceleration curves were sinusoidal. Enslaving effects were generated mainly on the neighboring fingers. The amount of enslaving on the middle and ring fingers exceeded more than 60% of their own maximum angular displacements when a single adjacent finger moved. The index finger had the highest level of independence as indicated by the lowest enslaving effects on other fingers or by other fingers. The independence indices of the index, middle, ring, and little fingers were 0.812 (+/-0.070), 0.530 (+/-0.051), 0.479 (+/-0.099), and 0.606 (+/-0.148), respectively. In all tasks, motion of slave fingers always lagged with respect to the master finger. Time delays, on average, ranged from 7.8 (+/-5.0) to 35.9 (+/-22.1) ms. Our results suggest that there exist relatively large enslaving effects among the compartments of the flexor digitorum profundus, and functional independence of fingers in daily activities is likely enhanced through synergistic activities of multiple muscles, including flexors and extensor.

Adult↗
PubMed2003

Enslaved Africans and doctors in South Carolina.

This interpretation of the relationship between enslavement and American medicine in 19th century South Carolina reveals the intimacy that existed between Africans enslaved in that state and the doctors who practiced and taught there. Enslaved Africans were resourceful and reliable medical figures in the slave community. Their knowledge of medical botany permeated the slave quarters and plantation hospitals and was appropriated into southern medical knowledge. The trajectories of the careers of three South Carolina physicians are tied to their practice around and on the enslaved. The beginnings of gynecological surgery are linked to 1840s experimentation on enslaved African women performed by one of them.

Black or African American↗
PubMed2006

The effect of enslaving on perception of finger forces.

The primary purpose was to examine the effect of enslaving on finger force perception during isometric finger force production using an ipsilateral force-matching paradigm. Fourteen subjects were instructed to produce varying levels of reference forces [10, 20, 30, and 40% maximal voluntary contraction (MVC)] force using one finger (index, I or little, L) and to reproduce these forces using the same finger (homo-finger tasks, I/I and L/L) or a different finger (hetero-finger tasks, I/L and L/I). Forces of all fingers were recorded. During homo-finger tasks, no differences were found in force magnitude or relative level of force (expressed as a proportion of MVC). The index finger matching force magnitudes were greater than the little finger reference force magnitudes, with significantly lower levels of relative force during L/I tasks; while the little finger matching forces underestimated the index finger reference forces with significantly higher levels of relative force during I/L tasks. The difference in the matching and reference forces by the instructed finger(s), i.e., matching error, was larger in hetero-finger tasks than in homo-finger tasks, particularly at high reference force levels (30, 40% MVC). When forces of all fingers were considered, enslaving (uninstructed finger forces) significantly minimized matching errors of the total force during both I/L and L/I hetero-finger tasks, especially at high reference force levels. Our results show that there is a tendency to match the absolute magnitude of the total force during ipsilateral finger force-matching tasks. This tendency is likely related to enslaving effects. Our results provide evidence that all (instructed and uninstructed) finger forces are sensed, thus resulting in perception of the absolute magnitude of total finger force.

Adult↗
PubMed2000

Enslaving effects in multi-finger force production.

When a person produces isometric force with one, two, or three fingers, the other fingers of the hand also produce a certain force. Enslaving is the involuntary force production by fingers not explicitly involved in a force-production task. This study explored the enslaving effects (EE) in multi-finger tasks in which the contributions of the flexor digitorum profundus (FDP), flexor digitorum superficialis (FDS), and intrinsic muscles (INT) were manipulated. A new experimental technique was developed that allows the redistribution of the muscle activity between the FDP, FDS, and INT muscles. In the experiment, ten subjects were instructed to perform maximal voluntary contractions with all possible one-, two-, three-, and four-finger combinations. The point of force application was changed in parallel for the index, middle, ring, and little fingers from the middle of the distal phalanx, to the distal interphalangeal joint, and then to the proximal interphalangeal joint. It was found that: (1) the EE of similar amplitude were present in various experimental conditions that involved different muscle groups for force production; (2) the EE were large on average--the slave fingers could produce forces reaching 67.5% of the maximal forces produced by themselves in a single-finger task; (3) the EE were larger for neighboring fingers; and (4) the EE were non-additive--in most cases, the EE from two or three fingers were smaller than the EE from at least one finger. EE among different muscles suggest a widespread neural interaction among the structures controlling flexor muscles in the hand as the main mechanism of finger enslaving.

Adult↗
PubMed2004

Practice-related modulations of force enslaving and cortical activity as revealed by EEG.

OBJECTIVE: To examine the role of practice in the modification of force enslaving and motor-related cortical potentials using finger force production tasks. This study follows-up previous studies in our laboratory using experienced piano players. METHODS: Two experiments were performed. In Expt. 1, 6 subjects participated in a pre and post EEG session separated by 12 practice sessions which were conducted 3 days a week for 4 weeks. With visual feedback regarding the accuracy of force output, subjects produced one of two force levels with either their ring or index finger. Experiment 2 followed a similar procedure to that of Expt. 1 with additional visual feedback to the degree of finger independency. Both behavioral (isometric force output) and EEG data preceding and accompanying force responses were measured. RESULTS: In Expt. 1 we found that forced enslaving increased along with improved accuracy following 4 weeks of practice. We found a reduction of motor potential (MP) amplitude for the index but not the ring finger following practice. Experiment 2 showed an increase in accuracy and reduction in force enslaving after practice with adequate feedback. The amplitude of MP for the index finger also decreased after practice as in Expt. 1. In contrast, the amplitude of MP for the ring finger increased after practice. CONCLUSIONS: The present study extends our earlier work with piano players and shows the role of practice in modifying behavioral and cortical measures. The concluding theme emergent from our studies is that individuated finger control is not hard-wired, but rather plastic and greatly influenced by deliberate practice. SIGNIFICANCE: This research supports the idea that experience and practice are associated with changes in behavioral and EEG correlates of task performance and have clinical implications in disorders such as stroke or dystonia. Practice-related procedures offer useful approaches to rehabilitation strategies.

Adult↗
PubMed2002

Motor-related cortical potentials accompanying enslaving effect in single versus combination of fingers force production tasks.

OBJECTIVES: This study examined behavioral indices and motor-related cortical potentials (MRCP) of the enslaving phenomenon (i.e. interdependency of finger movement) during isometric force production tasks using each of the four fingers separately and in combination. We examined MRCP preceding force production and those during the achievement of the desired force (ramp phase) and its maintenance (static phase). METHODS: Our experimental design systematically controlled the isometric force output, including both ramp and static phases of force production. We applied time-domain averaging of electroencephalographic single trials in order to extract 3 components of MRCP (Bereitshaftspotential, motor potentials, and motor monitoring potentials) preceding and accompanying force responses. RESULTS: We report two major findings. First, we found the index finger to be more independent, accurate, and to display the larger MRCP amplitude whereas the ring finger was more dependent, less accurate, and displayed smaller MRCP amplitude. Second, adding the neighboring finger when the ring finger produced the task significantly reduced its dependency on uninvolved fingers and increased the accuracy of both ramp and static phases which was not the case with the index finger. The amplitude of MRCP was increased when the ring finger produced the task in combination as compared to when the ring finger performed the task in isolation. In contrast, the amplitude of MRCP was significantly reduced when the index finger produced the task in combination with other fingers when compared to when the index finger performed the task in isolation. CONCLUSIONS: Overall, the amount of the fingers' dependency on the uninvolved fingers (e.g. amount of enslaving) during isometric force production tasks was inversely related with the amplitude of MRCP indicating the contribution of central mechanisms to the enslaving phenomenon.

Adult↗
PubMed1994

Frequency and chronological distribution of dental enamel hypoplasia in enslaved African Americans: a test of the weaning hypothesis.

The dentition of 27 enslaved African Americans from archaeological sites in Maryland and Virginia were examined. All 17 males and 7 of the 10 females in this study exhibited enamel hypoplastic defects indicative of systemic nutritional and disease stresses interfering with amelogenesis. Estimates of the ages of occurrence of these defects show that most occur between 1.5 and 4.5 years of age, 0.5-3.75 years later than historically documented weaning age (9-12 months of age) in similar plantation populations. Comparisons are made with studies of dental enamel hypoplasia in contemporaneous enslaved and free African American populations, including our data on 75 individuals from the First African Baptist Church cemetery in Philadelphia. These populations were highly stressed. While there appears to be a modest effect of early weaning stress, no direct relationship of peak frequencies to weaning age can be shown. These data raise questions about the attribution of peak hypoplasia frequencies to age at weaning or "post-weaning" stresses in previous paleopathological studies. High hypoplasia frequencies during the middle years of enamel development are more likely the result of a combination of 1) multiple environmental stresses, 2) differences in hypoplastic susceptibility in enamel, and 3) random factors.

Black or African American↗
PubMed2005

Role of early experience in ant enslavement: a comparative analysis of a host and a non-host species.

BACKGROUND: Ants use the odour of the colony to discriminate nestmates. In some species, this odour is learned during the first days following emergence, and thus early experience has a strong influence on nestmate discrimination. Slave-making ants are social parasites that capture brood of other ant species to increase the worker force of their colony. After emerging in the slave-maker nest, slave workers work as if they were in their own colony. We tested the hypothesis that early experience allows the deception of commonly enslaved species, while non-host species use a different mechanism, which does not involve learning. RESULTS: Pupae of a host species, Temnothorax unifasciatus, and a non-host species, T. parvulus, were allowed to emerge in the presence of workers of one of two slave-maker species, Chalepoxenus muellerianus or Myrmoxenus ravouxi. When T. unifasciatus was exposed to slave-makers for 10 days following emergence, they were more aggressive towards their own sisters and groomed the slave-maker more. T. parvulus gave a less clear result: while workers behaved more aggressively towards their sisters when exposed early to C. muellerianus workers, this was not the case when exposed early to M. ravouxi workers. Moreover, T. parvulus workers allogroomed conspecific nestmates less than T. unifasciatus. Allogrooming activity might be very important for the slave-makers because they are tended by their slaves. CONCLUSION: Our findings show that early experience influences nestmate discrimination in the ant T. unifasciatus and can account for the successful enslavement of this species. However, the non-host species T. parvulus is less influenced by the early environment. This might help to explain why this species is never used by social parasites.

Journal Article↗
PubMed2002

The enslaved healers of eighteenth-century Saint Domingue.

Enslaved healers including herbalists, kaperlatas, hospitalières, infirmières, and accoucheuses existed and flourished in the medical world of Saint Domingue. They were responsible for the creation of an indigenous form of medicine on the island. Using Western, African, and Caribbean remedies, they treated their fellow slaves and white residents of the island. Slaves were more comfortable and more familiar with the care and techniques employed by the popular healers, especially the kaperlatas and the herbalists. Plantation managers took advantage of the labor of female medical workers in order to reap economic profits for their planter employers and for themselves. Lower-class whites, unable to afford and unwilling to consult mainstream medical care, sought the assistance of healers known as kaperlatas. Lastly, orthodox medical practitioners turned to slave healers, especially herbalists, to exploit the therapeutic knowledge that the slaves possessed and, in the case of enslaved midwives, to bring them more closely under the authority of European medical men.

Colonialism↗
PubMed2002

Nucleomorphs: enslaved algal nuclei.

Nucleomorphs of cryptomonad and chlorarachnean algae are the relict, miniaturised nuclei of formerly independent red and green algae enslaved by separate eukaryote hosts over 500 million years ago. The complete 551 kb genome sequence of a cryptomonad nucleomorph confirms that cryptomonads are eukaryote-eukaryote chimeras and greatly illuminates the symbiogenetic event that created the kingdom Chromista and their alveolate protozoan sisters. Nucleomorph membranes may, like plasma membranes, be more enduring after secondary symbiogenesis than are their genomes. Partial sequences of chlorarachnean nucleomorphs indicate that genomic streamlining is limited by the mutational difficulty of removing useless introns. Nucleomorph miniaturisation emphasises that selection can dramatically reduce eukaryote genome size and eliminate most non-functional nuclear non-coding DNA. Given the differential scaling of nuclear and nucleomorph genomes with cell size, it follows that most non-coding nuclear DNA must have a bulk-sequence-independent function related to cell volume.

Animals↗
PubMed2001

The highly reduced genome of an enslaved algal nucleus.

Chromophyte algae differ fundamentally from plants in possessing chloroplasts that contain chlorophyll c and that have a more complex bounding-membrane topology. Although chromophytes are known to be evolutionary chimaeras of a red alga and a non-photosynthetic host, which gave rise to their exceptional membrane complexity, their cell biology is poorly understood. Cryptomonads are the only chromophytes that still retain the enslaved red algal nucleus as a minute nucleomorph. Here we report complete sequences for all three nucleomorph chromosomes from the cryptomonad Guillardia theta. This tiny 551-kilobase eukaryotic genome is the most gene-dense known, with only 17 diminutive spliceosomal introns and 44 overlapping genes. Marked evolutionary compaction hundreds of millions of years ago eliminated nearly all the nucleomorph genes for metabolic functions, but left 30 for chloroplast-located proteins. To allow expression of these proteins, nucleomorphs retain hundreds of genetic-housekeeping genes. Nucleomorph DNA replication and periplastid protein synthesis require the import of many nuclear gene products across endoplasmic reticulum and periplastid membranes. The chromosomes have centromeres, but possibly only one loop domain, offering a means for studying eukaryotic chromosome replication, segregation and evolution.

Base Sequence↗
PubMed2006

Origin of mitochondria by intracellular enslavement of a photosynthetic purple bacterium.

Mitochondria originated by permanent enslavement of purple non-sulphur bacteria. These endosymbionts became organelles through the origin of complex protein-import machinery and insertion into their inner membranes of protein carriers for extracting energy for the host. A chicken-and-egg problem exists: selective advantages for evolving import machinery were absent until inner membrane carriers were present, but this very machinery is now required for carrier insertion. I argue here that this problem was probably circumvented by conversion of the symbiont protein-export machinery into protein-import machinery, in three phases. I suggest that the first carrier entered the periplasmic space via pre-existing beta-barrel proteins in the bacterial outer membrane that later became Tom40, and inserted into the inner membrane probably helped by a pre-existing inner membrane protein, thereby immediately providing the protoeukaryote host with photosynthesate. This would have created a powerful selective advantage for evolving more efficient carrier import by inserting Tom70 receptors. Massive gene transfer to the nucleus inevitably occurred by mutation pressure. Finally, pressure from harmful, non-selected gene transfer to the nucleus probably caused evolution of the presequence mechanism, and photosynthesis was lost.

Bacterial Proteins↗
PubMed2004

Adaptation and enslavement in endosymbiont-host associations.

The evolutionary persistence of symbiotic associations is a puzzle. Adaptation should eliminate cooperative traits if it is possible to enjoy the advantages of cooperation without reciprocating-a facet of cooperation known in game theory as the Prisoner's Dilemma. Despite this barrier, symbioses are widespread and may have been necessary for the evolution of complex life. The discovery of strategies such as tit-for-tat has been presented as a general solution to the problem of cooperation. However, this only holds for within-species cooperation, where a single strategy will come to dominate the population. In a symbiotic association each species may have a different strategy, and the theoretical analysis of the single-species problem is no guide to the outcome. We present basic analysis of two-species cooperation and show that a species with a fast adaptation rate is enslaved by a slowly evolving one. Paradoxically, the rapidly evolving species becomes highly cooperative, whereas the slowly evolving one gives little in return. This helps understand the occurrence of endosymbioses where the host benefits, but the symbionts appear to gain little from the association.

Animals↗
PubMed1997

Self-reinforcing spatial patterns enslave evolution in a host-parasitoid system.

Spatially structured models of host-parasitoid interactions exhibit self-structuring into spatial patterns such as spiral waves and turbulence. We discuss the consequences of these patterns in an eco-evolutionary model of host-parasitoid interactions with evolution of the parasitoids' ability to disperse towards dense populations of hosts (termed the aggregation strength). It turns out that the direction of, and the time-scale over which the evolutionary selection pressure acts depends on the type of spatial pattern a parasitoid finds itself in. Evolution tends to reinforce the existence of the prevalent local pattern. Moreover, there is also competition between the patterns that ultimately determines the eco-evolutionary attractor. It is the interaction between multiple processes across spatial and temporal scales that leads to the rich meso-scale behaviour. Predicting the evolutionary outcome from statistical measures and subprocesses is shown to give incorrect and conflicting answers. Comparison with the behaviours of the complex Ginzburg-Landau equation shows striking similarities on which we comment.

Animals↗
PubMed2000

Enslaved bacteria as new hope for plant biotechnologists.

The most distinguishing feature of the plant cell is a DNA-containing organelle that sets plants apart from all other organisms: the chloroplast. Compelling evidence supports an endosymbiotic origin for chloroplasts. According to this theory, chloroplasts are descendants of formerly free-living cyanobacterial ancestors which entered an endosymbiotic relationship with a pre-eukaryotic cell and were ultimately integrated into the metabolism of the host cell. Chloroplasts retain many prokaryotic features and their gene expression system still closely resembles that of their eubacterial ancestors. During the past decade, our knowledge about chloroplast biology has benefited immensely from a most remarkable methodological breakthrough: the development of transformation technologies for chloroplast genomes. Moreover, recent advances in the manipulation of higher plant chloroplast genomes have created unprecedented opportunities for the genetic engineering of plants and promise to overcome many of the problems associated with conventional transgenic technologies. This review describes the state of the art in genetic engineering of higher plant chloroplast genomes and highlights the tremendous potential of these technologies for the biotechnology of the future.

Biological Evolution↗