For me Behe is like the Jordan Peterson of bioscience.
What a rare find this book is for me. I have never seen a scientist with so many good qualities rolled into one. Maybe it is because he is close to my age and uses examples to which I can easily relate but hopefully all generations will find his almost common sense logic at least difficult to avoid.
The following were some highlights I noted.
Car comparisons were fine with me.
Loved the Sisyphus picture for Darwinists in this comparison.
I remember Tinkertoys so this was a great example for an old guy like me:
Reality does not support "fuzzy-minded" approaches:
I love the way Behe uses everyday examples (crank up that chain saw) to prove logical functioning of biochemical discoveries and functions such as this:
It is like sitting in on an experiment in an Orion lab while they discuss the process design:
The celebrations have not been forthcoming so far for a recognition of "design"...
Those random mutation fans should at least figure out "how it works in the first place".
How’s this for something produced from random mutation?
Behe is even modest enough to give credit for the his "irreducible complexity" to another earlier source here:
What a rare find this book is for me. I have never seen a scientist with so many good qualities rolled into one. Maybe it is because he is close to my age and uses examples to which I can easily relate but hopefully all generations will find his almost common sense logic at least difficult to avoid.
The following were some highlights I noted.
Car comparisons were fine with me.
In this chapter I have looked at three features of the immune system— clonal selection, antibody diversity, and the complement system—and demonstrated that each individually poses massive challenges to a putative step-by-step evolution. But showing that the parts can't be built step by step only tells part of the story, because the parts interact with each other. Just as a car without steering, or a battery, or a carburetor isn't going to do you much good, an animal that has a clonal selection system won't get much benefit out of it if there is no way to generate antibody diversity. A large repertoire of antibodies won't do much good if there is no system to kill invaders. A system to kill invaders won't do much good if there's no way to identify them. At each step we are stopped not only by local system problems, but also by requirements of the integrated system.
(Page 138).
Loved the Sisyphus picture for Darwinists in this comparison.
Diversity, recognition, destruction, toleration—all these and more interact with each other. Whichever way we turn, a gradualistic account of the immune system is blocked by multiple interwoven requirements. As scientists we yearn to understand how this magnificent mechanism came to be, but the complexity of the system dooms all Darwinian explanations to frustration. Sisyphus himself would pity us.
(Page 139).
I remember Tinkertoys so this was a great example for an old guy like me:
Like Tinkertoys, atoms can be put together to form many different shapes. A big difference is that the cell is a machine, however, so the mechanism to assemble the molecules of life must be automated. Imagine the complexity of a machine that could automatically assemble Tinkertoys into, say, the shape of a castle! The mechanism that the cell uses to make AMP is automated, and as expected, it is far from simple.
(Page 143).
Reality does not support "fuzzy-minded" approaches:
The point is to appreciate the complexity of the system, to see the number of steps involved, to notice the specificity of the reacting components. The formation of biological molecules does not happen in some fuzzy-minded Calvin and Hobbes way; it requires specific, highly sophisticated molecular robots to get the job done.
(Page 143).
I love the way Behe uses everyday examples (crank up that chain saw) to prove logical functioning of biochemical discoveries and functions such as this:
The need for regulation is obvious for machines we use in our daily lives. A chain saw that couldn't be turned off would be quite a hazard, and a car with no brakes and no neutral gear would be of little use. Biochemical systems are also machines we use in our daily lives (whether we think of them or not), and so they too have to be regulated.
(Page 157).
It is like sitting in on an experiment in an Orion lab while they discuss the process design:
Enzyme I requires an ATP energy pellet to transform ribose-5- phosphate (the foundation) into Intermediate II. The enzyme has
an area on its surface that can bind either ADP or GDP when there is an excess of those chemicals in the cell. The binding of ADP or GDP acts as a valve, decreasing the activity of the enzyme and slowing the synthesis of AMP. This makes good physiological sense: since ADP is the remains of a spent ATP (like a bullet shell after a gun has been fired), high concentrations of ADP in the cell means that the concentration of ATP, the cellular energy pellet, is low. Instead of making AMP, Intermediate I is then used as fuel to produce more ATP.
(Page 158).
The celebrations have not been forthcoming so far for a recognition of "design"...
The result of these cumulative efforts to investigate the cell—to investigate life at the molecular level—is a loud, clear, piercing cry of «design!» The result is so unambiguous and so significant that it musy be ranked as one of the greatest achievements in the history of science. The discovery rivals those of Newton and Einstein, Lavoisier and SchrÖdinger, Pasteur, and Darwin. The observation of the intelligent design of life is as momentous as the observation that the earth goes around the sun or that disease is caused by bacteria or that radiation is emitted in quanta. The magnitude of the victory, gained at such great cost through sustained effort over the course of decades, would be expected to send champagne corks flying in labs around the world. This triumph of science should evoke cries of «Eureka!» from ten thousand throats, should occasion much hand-slapping and high-fiving, and perhaps even be an excuse to take a day off.
But no bottles have been uncorked, no hands slapped. Instead, a curious, embarrassed silence surrounds the stark complexity of the cell. When the subject comes up in public, feet start to shuffle, and breathing gets a bit labored. In private people are a bit more relaxed; many explicitly admit the obvious but then stare at the ground, shake their heads, and let it go at that.
(Page 233).
Those random mutation fans should at least figure out "how it works in the first place".
It would take at least as much work to figure out how such a structure could evolve by random mutation and natural selection as it did to figure out how it works in the first place. At an absolute minimum that would be expected to result in hundreds of papers—both theoretical and experimental—many reviews, books, meetings, and more, all devoted to the question of how such an intricate structure could have evolved in a Darwinian fashion.
(Page 267).
How’s this for something produced from random mutation?
The ribosome can be readily broken down into two large pieces, called the 30S sub-unit and the 50S subunit.6 Incredibly, the ribosome is self-assembling. Experiments have shown that when ribosomes are separated into their components and then remixed, under the right conditions the components will spontaneously reform ribosomes.
(Page 291).
Behe is even modest enough to give credit for the his "irreducible complexity" to another earlier source here:
2.The term «irreducible complexity» occurred to me independently. However, I've since learned that the phrase was used earlier in Templets and the Explanation of Complex Patterns (Cambridge University Press, 1986) by Case Western Reserve University biologist Michael
(Page 307).