Wednesday, June 13, 2018
Tuesday, June 5, 2018
Cis-Lunar Gateways and the Advantages of Near Rectilinear Orbits
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| Computer illustration of Near Rectilinear Orbits between EML1 and EML2 (Credit: NASA). |
NASA appears to have settled on a Near Rectilinear L2 Halo Orbit (NRO) for its future Deep Space Habitat (DSH). NROs are a subset of of L1 or L2 halo orbits. NRO's have large amplitudes over either the north or south lunar poles with shorter periods that pass closely to the opposite pole. Station keeping at an NRO would require a delta-v of only 5 m/s per year. With an impulsive departure from LEO at about 3.124 km/s, a crewed spacecraft would reach an L2 NRO in about 5.33 days. Orbital capture would require a delta-v of 0.829 km/s.
An EML1 location for a DSH would only require a delta-v of 3.77 km/s and four days of travel time. But 2 days of travel time would be required for a journey from EML1 to Low Lunar Orbit (LLO). An NRO location, however, would only require 12 hours of travel time to LLO. So the surface of the Moon could be accessed from a NRO located Deep Space Hab in just 12 hours.
Possible Cis-Lunar Locations for a DSH (Deep Space Habitat)
EML1(Earth-Moon Lagrange Point One):
Travel time to and from LEO: ~4 days (3.77 km/s)
Station keeping: < 10 m/s per year
Travel time to and from LLO: ~ 2 days (0.750 km/s)
EML2 (Earth Moon Lagrange Point Two):
Travel time to and from LEO:~ 8 days from LEO (3.43 km/s)
Station keeping < 10 m/s per year
Travel time to and from LLO:~ 3 days to LLO (0.8 km/s)
DRO (Distant Retrograde Orbit):
Travel time to and from LEO: ~ 6 days
Station keeping: 0 m/s per year
Travel time to and from LLO: ~ 4 days (0.83 km/s)
NRO: (Near Rectilinear Halo Orbit):
Travel time to and from LEO:~5 days from LEO (3.95 km/s)
Station keeping: 5 m/s per year
Travel time to and from LLO:~ 12 hours to LLO (0.730 km/s)
Significantly shorter flight times from LEO to NRO could be achieved with higher delta-v levels that could easily be achieved by future reusable LOX/LH2 fueled spacecraft such as the ULA's XEUS and Lockheed Martin's MADV which could be used for round trip journeys to the lunar surface from a NRO and for transporting crews between LEO and NRO.
Links and References
Wednesday, May 16, 2018
Monday, May 14, 2018
US Electric Energy Production in 2017 by Source
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| Credit: US Energy Information Administration |
References and Links
What is U.S. electricity generation by energy source?
Thursday, May 10, 2018
The Mighty XEUS
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| ACES derived XEUS DTAL lunar crew lander (Credit: ULA) |
The XEUS could also be used to transport astronauts between propellant depots located at LEO and EML1 or EML2.
Beyond cis-lunar space, the XEUS vehicle could be used to access the surfaces of Mercury, asteroids in the asteroid belt such as Ceres, Vesta, and Psyche, Jupiter's moon, Callisto, and also the moons of Mars, Phobos and Deimos.
As a cargo transport operating out of EML1, the XEUS could deliver more than 50 tonnes of cargo to the lunar surface or transport more than 50 tonnes of water extracted from the lunar ice back to propellant producing water depots located at EML1 or EML2.
Deployed into Earth orbit by a Vulcan/ACES 68 launch vehicle in the early 2020s, the XEUS could give NASA, the DOD, other government space agencies, and even space tourist easy access to the surface of the Moon and back while helping to give humans access to other regions of the solar system.
Marcel F. Williams
Links and References
Friday, May 4, 2018
The Swamp Ape's Pad-to-Pad Precision Grip
by Marcel F. Williams
Primates, of course, are generally characterized by their grasping hands and feet. While the toes of human feet have lost their prehensile capability, the fingers of human hands have the most sophisticated manipulative ability of any primate. Humans are the only hominoid (humans and apes) primate capable of supplying the substantial force necessary for holding objects steadily and securely between the pads of the thumb and one or more fingers. This is called a pad-to-pad precision grip.
Fossil evidence suggest that early hominins (humans and their ancestors) such as Australopithecus also possessed a pad-to-pad precision grip.
In 1970, Clifford Jolly suggested that human manipulative capability may have paralleled those of the small object feeding gelada baboon (Theropithecus), a largely terrestrial East African primate that uses its pad-to-pad precision grip to feed on grasses and the seeds of grasses. Jolly suggested that such a folivorous diet in early hominin ancestors might also explain the reduction in hominin canine size.
But in 1977, marine biologist, Alister Hardy proposed an alternative hypothesis for the origin of the human pad-to-pad precision grip. He hypothesized that the hominin precision grip was originally an adaptation for the intensive exploitation of benthic invertebrates while wading bipedally in shallow water. In 1960, Alister Hardy suggested that the sensitive probing fingers of humans may have evolved in human ancestors adapted for the exploitation of shelfish and other benthic organisms. Hardy also proposed that bipedal wading for benthic organism was the selective reason for the evolution of obligatory bipedalism in the earliest hominins.
In 1999,
Oreopithecus has been vernacularly called the 'Swamp Ape' because of its apparent preference for swampy wetland environments. This late Miocene hominoid was also the earliest bipedal ape and lived in isolation from the European and African continents on an ancient Mediterranean island known as Tuscany-Sardinia. Rather abundant oreopithecine fossils have been found in lignite layers along with the fossil remains of freshwater mollusk, turtles, otters, and crocodiles (the possible predators involved in the deaths of the oreopithecine remains).
Paleontologist such as Birdsell, Harrison, and Rook have suggested that Oreopithecus may have exploited these aquatic plants as a food resource. And sedges, water lilies, reeds, cattail, pond- weeds, horestails, and
stoneworts, and other wetland plants which were also abundantly represented
in the fossil pollen spectrum.
Feeding on aquatic vegetation is certainly not unusual in modern primates and has been observed in lemurs, chimpanzees, gorillas, baboons, the Colobus monkeys and, of course, in humans. Groups of Colobus monkeys have been known to descended from trees and to travel to pools of open water in swampy areas in order to feed on aquatic vegetation. Western Gorillas are also known to wade bipedally into swamps to feed on aquatic plants, sometimes even using walking sticks to stay erect.
The short legs of Oreopithecus along with its peculiar feet which exhibit a widely abducted hallux suggest that the swamp apes were less adapted for terrestrial locomotion than in the early African hominins. The short hindlimbs and the pedal tripod formed by widely abducted hallux and the deviated metatarsals of Oreopithecus appear to be designed as a stable platform for efficient postural harvesting which would have been advantageous for wading for food items in shallow aquatic environments.
While the cranio-dental evidence strongly indicates that Oreopithecus was intensely herbivorous, the unusual amount of wear on the canines and incisors in addition to the thickness of the central incisors which bear a number of small mammelons, may suggest that aquatic vertebrates were also included in their diets. As earlier noted, freshwater mollusks were abundant in the ancient wetland environments that Oreopithecus frequented. Oreopithecus also possessed a hominin-like pad-to-pad precision grip which they could have utilized to apprehend aquatic invertebrates while using their fingers, canines and central incisors to pry open and scrape out the edible flesh of the hard shelled freshwater bivalves.
Sometime after 7.4 million years ago, sea levels began to fall in the Mediterranean creating land bridges to North Africa. Global sea levels fell to such an extent that eventually the Mediterranean Sea became completely isolated from in the inflow of marine waters from the Atlantic Ocean 6.1 million years ago.
The earliest African hominin, Sahelanthropus, appeared in the fossil record in North Africa sometime between 6.8 and 7.2 million years ago. While not much is known about the postcranial remains of Sahelanthropus, its craniodental morphology is remarkably similar to that of Oreopithecus bambolii.
Aquatic foraging in the wetland swamps of Tuscany-Sardinia would, therefore, explain the adaptive value of bipedal behavior, pad-to-pad precision grips and intense folivory in Oreopithecus and the origins of obligatory bipedalism, precision grips, and hyper-mastication in hominin evolution. And this would appear to be further evidence that Oreopithecus was the earliest bipedal human ancestor.
Links and References
Was the Swamp Ape Bipedal?
Our Earliest Ancestor
 |
| Skull of Oreopithecus (Credit: After Szalay and Berzi, 1973) |
Fossil evidence suggest that early hominins (humans and their ancestors) such as Australopithecus also possessed a pad-to-pad precision grip.
In 1970, Clifford Jolly suggested that human manipulative capability may have paralleled those of the small object feeding gelada baboon (Theropithecus), a largely terrestrial East African primate that uses its pad-to-pad precision grip to feed on grasses and the seeds of grasses. Jolly suggested that such a folivorous diet in early hominin ancestors might also explain the reduction in hominin canine size.
But in 1977, marine biologist, Alister Hardy proposed an alternative hypothesis for the origin of the human pad-to-pad precision grip. He hypothesized that the hominin precision grip was originally an adaptation for the intensive exploitation of benthic invertebrates while wading bipedally in shallow water. In 1960, Alister Hardy suggested that the sensitive probing fingers of humans may have evolved in human ancestors adapted for the exploitation of shelfish and other benthic organisms. Hardy also proposed that bipedal wading for benthic organism was the selective reason for the evolution of obligatory bipedalism in the earliest hominins.
Oreopithecus has been vernacularly called the 'Swamp Ape' because of its apparent preference for swampy wetland environments. This late Miocene hominoid was also the earliest bipedal ape and lived in isolation from the European and African continents on an ancient Mediterranean island known as Tuscany-Sardinia. Rather abundant oreopithecine fossils have been found in lignite layers along with the fossil remains of freshwater mollusk, turtles, otters, and crocodiles (the possible predators involved in the deaths of the oreopithecine remains).
Feeding on aquatic vegetation is certainly not unusual in modern primates and has been observed in lemurs, chimpanzees, gorillas, baboons, the Colobus monkeys and, of course, in humans. Groups of Colobus monkeys have been known to descended from trees and to travel to pools of open water in swampy areas in order to feed on aquatic vegetation. Western Gorillas are also known to wade bipedally into swamps to feed on aquatic plants, sometimes even using walking sticks to stay erect.
 |
| Human pad-to-pad precision grip (Credit: Alister Hardy, 1977) |
The short legs of Oreopithecus along with its peculiar feet which exhibit a widely abducted hallux suggest that the swamp apes were less adapted for terrestrial locomotion than in the early African hominins. The short hindlimbs and the pedal tripod formed by widely abducted hallux and the deviated metatarsals of Oreopithecus appear to be designed as a stable platform for efficient postural harvesting which would have been advantageous for wading for food items in shallow aquatic environments.
While the cranio-dental evidence strongly indicates that Oreopithecus was intensely herbivorous, the unusual amount of wear on the canines and incisors in addition to the thickness of the central incisors which bear a number of small mammelons, may suggest that aquatic vertebrates were also included in their diets. As earlier noted, freshwater mollusks were abundant in the ancient wetland environments that Oreopithecus frequented. Oreopithecus also possessed a hominin-like pad-to-pad precision grip which they could have utilized to apprehend aquatic invertebrates while using their fingers, canines and central incisors to pry open and scrape out the edible flesh of the hard shelled freshwater bivalves.
Sometime after 7.4 million years ago, sea levels began to fall in the Mediterranean creating land bridges to North Africa. Global sea levels fell to such an extent that eventually the Mediterranean Sea became completely isolated from in the inflow of marine waters from the Atlantic Ocean 6.1 million years ago.
The earliest African hominin, Sahelanthropus, appeared in the fossil record in North Africa sometime between 6.8 and 7.2 million years ago. While not much is known about the postcranial remains of Sahelanthropus, its craniodental morphology is remarkably similar to that of Oreopithecus bambolii.
Aquatic foraging in the wetland swamps of Tuscany-Sardinia would, therefore, explain the adaptive value of bipedal behavior, pad-to-pad precision grips and intense folivory in Oreopithecus and the origins of obligatory bipedalism, precision grips, and hyper-mastication in hominin evolution. And this would appear to be further evidence that Oreopithecus was the earliest bipedal human ancestor.
Was the Swamp Ape Bipedal?
Our Earliest Ancestor
Evidence of hominid-like precision grip capability in the hand of the Miocene ape Oreopithecus
The morphology of Oreopithecus bambolii pollical distal phalanx.
Oreopithecus was a bipedal ape after all: evidence from the iliac cancellous architecture.
Ape-like or hominid-like? The positional behavior of Oreopithecus bambolii reconsidered.
Cranio-dental evidence of a hominin-like hyper-masticatory apparatus in Oreopithecus bambolii. Was the swamp ape a human ancestor?
Thursday, April 5, 2018
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