When the topic of identifying skeletal remains arises, two world-renowned renowned forensic anthropologists immediately come to mind—Dr. Elizabeth A. Murray and Dr. Kathy Reichs. Both experts are at the top of their profession and are two of approximately 100 anthropologists certified as Diplomate by the American Board of Forensic Anthropology.

Law enforcement and other investigators around the world have relied on Drs. Murray and Reichs, as well as other forensic anthropologists, for their help with solving high-profile criminal cases, and to help identify recovered bones.

However, in many instances, on-the-scene law enforcement investigators don’t have speedy access to experienced experts, and they need to know right away if the bones they or someone else discovered are human. This immediate knowledge helps them decide whether the remains belong to a person, and if what they have before them could be a crime scene, or the found bones are those of an animal, which could be the remnants of a family pet, wild animal, or farm livestock.

Knowing the differences between the two bone types (animal and human) could mean a significant saving in costs and/or wasted time of valuable resources if the bones are of bovine origin, for example. If the remains are likely human then it’s time to initiate a full-blown criminal investigation with all the bells and whistles.

So, what do cops and other people with little or no training do when they need to quickly determine if bones are human or animal?

Well, they could turn to OsteoID, a new tool designed to help identify the type of skeletal remains.

Designed by Dr. Heather Garvin and her group from Des Moines University Osteopathic Medical Center, OsteoID is an easy-to-use online tool in which anyone can use simple measurements and morphological information to determine whether a particular bone is human. If not, OsteoID points the user to which animal species it belongs. It’s that simple, and best of all it’s free! Even better, it’s available to everyone, including authors who want and need this sort of detail in their next mystery or thriller.

Here’s how it works.

Users first view a series of high-quality photos to help determine the identity of the bone(s) in question (humerus, tibia, femur, etc.). Once identified, the user is prompted to enter basic measurements—bone length, etc.). The program then returns detailed photos and, when available, 3D surface models/images, of the potential species to allow for comparison.

The list of species included in the system includes (from the OsteoID website):

Mammals: Humans, Black Bear, Brown Bear, Cow, Elk, Moose, White-Tailed Deer, Mule Deer, Pig, Horse, Sheep, Goat, Coyote, Wolf, Domestic Dog, Domestic Cat, Grey Fox, Red Fox, Racoon, Opossum, Rabbit

Birds: Golden Eagle, Goose, Chicken, Duck, Turkey

Turtles: Box Turtle, Snapping Turtle

For more, please click here to visit the OsteoID website.


In 2012 Dr. Elizabeth Murray was a featured presenter at the Writers’ Police Academy. Her session included a discussion about skeletal remains and the tools associated with identification. She also provided information about NamUs (the National Missing and Unidentified Persons System) and some of its success stories. Since 1986, Dr. Murray has been involved in forensic and historic skeletal investigations worldwide.

In addition to working as a forensic anthropologist and professor of biology at the College of Mount St. Joseph in Cincinnati, Ohio (now retired), Dr. Murray is also the author of the books The Dozier School for Boys: Forensics, Survivors, and a Painful Past Death, and Corpses, Cadavers, and Other Grave Matters, a fascinating, enlightening nonfiction book for YA readers about the science of death. As an expert, Dr. Murray has also appeared on local and national television and in numerous documentary programs, such as Forensic Files and Skeleton Stories, and she’s featured in productions such as New Dominion Pictures’ series Buried Secrets.

To read about how Dr. Elizabeth Murray helped solve a complex murder case using core samples from a human skull, click here.


Dr. Kathy Reichs was a featured presenter at the 2013 Writers’ Police Academy. Her talk focused on how she transforms her real-life forensic experiences into fiction, in the form of books and the TV show Bones. Bones, of course, is based on Dr. Reichs’ career and her bestselling books of the same name, featuring protagonist Temperance Brennan. She was an executive producer of the show.

The following is from Dr. Reichs’ website:

“For years she consulted to the Office of the Chief Medical Examiner in North Carolina and to the Laboratoire de Sciences Judiciaires et de Médecine Légale for the province of Québec. Dr. Reichs has traveled to Rwanda to testify at the UN Tribunal on Genocide, and helped exhume a mass grave in Guatemala. As part of her work at JPAC (Formerly CILHI) she aided in the identification of war dead from World War II, Korea, and Southeast Asia. Dr. Reichs also assisted in the recovery of remains at the World Trade Center following the 9/11 terrorist attacks.”


It’s ALMOST TIME!

2024 Killer Con registration opens in January 2024.

Be ready to sign up because this is a KILLER event that’s not to be missed!

Visit a homicide scene and solve the case using tactics, tools, and techniques learned throughout the event.

2024 Killer Con Guest of Honor is internally bestselling author Charlaine Harris.

Click the link below to visit the Killer Con (Writers’ Police Academy) website to view the schedule of events, classes, instructors, and special guest presenters.

2024 Killer Con

Isotope fingerprinting can be used to analyze a single strand of human hair for the purpose of determining a person’s location during recent weeks, months, and sometimes years. Obviously, this type of geographical tracking can be extremely useful to law enforcement when investigating murder cases.

These particular isotopes are found in the DNA-free keratin protein shaft of a hair, and contain a sequential record of dietary and metabolic behaviors of the contributor.

Stable isotope analysis (SIA) uses, for example, stable carbon, nitrogen, and sulfur isotopes of human tissues to learn a victim’s dietary preferences.

Properties of various municipal water districts, even in cities and towns adjacent to one another, or within a large metropolitan city with more than a single water supply, can provide water that is isotopically distinct from one another and from other local water sources. Therefore, using unique stable oxygen and strontium isotope signatures, SIA reveals the source of an individual’s drinking water (a person drinks local water and the isotopic record of the water is captured and retained their hair).


There are many uses for Stable isotope analysis (SIA), including:

  • Food authenticity

  • Sports doping

  • Criminal forensics

  • Archaeology


When used in conjunction—stable carbon, nitrogen, and sulfur isotopes, along with stable oxygen and strontium isotopes—investigators are armed with a formidable geolocation tool for pinpointing a region of origin, or the path of recent travels of a murder victim. This is especially helpful when an investigation involves unidentified human remains.

Other Uses

Sample analysis of illegal drugs can reveal their sources (location), discovering whereabouts of clandestine laboratories, and even the trafficking routes used by dealers.

Stable isotope forensics is also used help to determine whether drugs, explosives, fibers, and other evidence share a mutual foundation or past. It’s utilized to differentiate counterfeit products such as pharmaceuticals and food products from authentic articles, and it’s used to determine if an athlete has used drugs to enhance their performance.

The World Anti-Doping Agency requires stable isotope analysis for doping analysis in sports. It’s also used to detect steroid abuse in cattle.

Analyzers, such as Elementar’s AnthrovisION, are the devices and included software used to determine the origin of a sample.


Isotopes

Scientists divide isotopes into two main types: radioactive and stable.

Stable Isotopes

Stable isotopes, those used in criminal forensics, sports doping, and archaeology have a stable proton-neutron combination and do not exhibit signs of decay/radiation.

The stable isotopes used in the testing/analyzing described in this article are oxygen, hydrogen, sulfur, nitrogen and carbon.

Radioactive Isotopes

When an atom has too many or too few neutrons, it is unstable and decays. As a result, these isotopes emit radiation that includes alpha, beta, and gamma rays.

Radioactive isotopes are used in medicine, agriculture, food industry, pest control, archeology. Radiocarbon dating uses the carbon-14 radioactive isotope. In medicine, radioactive gamma rays are used to detect tumors inside the human body. Exposing food to a controlled level of gamma rays kills many types of bacteria.

 

 

Female blowflies lay eggs, hundreds of them, on moist and juicy decaying matter that’s rich in microbes. These egg-laying sites include, among others, rotting food and the decomposing corpses of animals and humans.

Immediately after hatching, the creepy offspring of their fly parents—maggots—go to work using enzymes and bacteria to break down their food source into a mouthwatering broth.

Blowfly maggots consume their tasty meals much in the same way as gluttonous Sunday afternoon diners at all-you-can-five-dollar-buffets—heads down and without stopping to breathe.

Maggots, though, have an advantage over human buffet-eaters. They’re able to enjoy their feasts while simultaneously breathing through their specially adapted rear ends. Humans, however, are forced to come up for air at least once or twice during a roadside steakhouse feeding frenzy.

In addition to having poor table manners, maggots are a useful tool for homicide investigators. In fact, the first known instance of flies helping out in a murder case was during the 13th century, when Chinese judge Sung T’zu  investigated a fatal stabbing in a rice field.

Flies Don’t Lie

At the scene of the murder, judge Sung T’zu instructed each of the workers to lay down their sickles. Soon, attracted by the smell of blood, flies began landing on one of the sickles, but not the others. Sure, the murderer cleaned their weapon prior to the judge’s arrival, but the faint odor of the victim’s blood was still present. It was clear to T’zu who’d committed the killing. In 1247, T’zu wrote about the case in the book The Washing Away of Wrongs, the oldest known book on forensic medicine.

Today, in murder cases, a maggot’s rate of growth can help estimate time of death. For example, when detectives find maggots on a body that are in their early larvae stages, when they’re 5mm in length, officers then will have a pretty good idea that the victim has been deceased for only a day and a half, or so.

When maggots ingest human tissue as nourishment, they simultaneously absorb remnants of substances previously consumed by the deceased, such as illegal and prescription drugs, and poisons. Subsequently, traces of those substances are retained within the bodies and exoskeletons of the maggots.

An insect’s hard external skeleton is made of chitin, a substance that’s similar to the keratin protein from which hair is formed. Since an insect’s chitin stores consumed toxins for a long time, and blowfly maggots shed their exoskeletons twice as it passes through each of three larval stages, a toxicology analyses of those exoskeletons could be helpful in determining the drug use of the victim, poisoning as a murder weapon, and more. This is an especially important tool when working with skeletal remains. In fact, a forensic analysis of insects is more dependable than hair as a means to detect drug use immediately prior to death.

Mummy-“Flied”

How long are substances (toxins, etc.) retained in an insects exoskeleton? Shed fly puparial cases been used for toxicological studies of mummified bodies found weeks, months, an even years after death. Some scientists believe it’s possible to detect drugs in the insects associated with ancient skeletal remains. After all, cocaine has been discovered in the hair of 3,000-year-old Peruvian mummies, so why not the same for the bugs who once feasted on those bodies?

Most evidence, of course, comes from live maggots collected from the body at the crime scene. Those specimens are gathered by crime scene investigators and transported to a forensics laboratory for testing. The trick is keeping the wiggly maggots alive until an analysis is performed. Therefore, some scientists recommend that crime scene investigators stock cans of tuna as part of their evidence collection kits.

Pop the top on the can and maggots are then able to feed on the tuna until they’re properly secured and handled by a qualified forensic entomologist.

It’s also important to place maggots in a container with air holes (even though they breathe through their butts, they’ve still got to breathe to survive).

Now, who’s having tuna for lunch today?

Yum …

Footprints in the snow

“Neither snow nor rain nor heat nor gloom of night stays these couriers from the swift completion of their appointed rounds.”

The familiar phrase above is actually from an ancient Greek work of Herodotus describing the Persian system of mounted postal carriers. The phrase is also inscribed on the James Farley Post Office in New York City, and is sort of the unofficial creed of letter carriers across the country.

Another group of people who closely adhere to those words are criminals. Yes, this menagerie of lawbreakers—pickpockets, robbers, rapists, murderers, and the like—pay no attention to the weather when planning and plotting their devious acts against property and their fellow humans.

And, when the criminals do their dastardly deeds, even in bad weather such as the snowstorms we’re experiencing on the East Coast, law enforcement officers must do what it takes to bring the offenders to justice. Unfortunately, crime-solving often involves traipsing around the woods in the mud, snow, sleet, and freezing rain while trying to find a footprint or two.

One method of identifying and locating a bad guy is to do as they did back in the old west, and that’s to track the thugs back to their hideouts. Sure, following broken twigs and disturbed vegetation is one method. Finding and making castings of footprints and/or tire tracks in the dirt and dried mud is another.

But what about prints in the snow? After all, we know that casting materials generate heat, which causes snow to melt and deform the impressions left by footwear.

So how do investigators overcome the challenge of melting snow in and around footprints?

Well, our good friends at Sirchie have the perfect solution to the problem.

A squirt or two of Sirchie’s Snow Impression Wax provides an insulating medium between the heat-generating casting material and the surrounding snow. Once the spray contacts the snow it locks in the impression details while the casting material hardens.

Shake-N-Cast (center in photo below) is a kit containing a pre-measured water pouch and dental stone.

Apply pressure to break the water pouch and then shake to mix the two ingredients. No messy containers and no casting material on a detective’s shiny shoes. There’s enough material in a kit to cast an adult-size shoe up to 15″ long.

Metal casting frames are adjustable to fit all shoe sizes and most tire treads.

While we’re on the subject of impression evidence, the spray above—Dust and Dirt Hardener—is used to strengthen impression evidence (tire tracks, footwear impressions, etc.) found in loose or sandy soil.

The material keeps the soil intact under the weight of the casting material.

Finally, liquid silicone is often used for producing exact replicas of various impressions, including tire and footwear, jimmy marks, and even fingerprints.

Liquid Silicone is incredibly temperature tolerant, and can withstand cold down to -70F and heat to +500F.

Sirchie Silicone Casting Kit

The material sets within three to five minutes.

So there you go. Now your fictional CSI team need not worry about collecting evidence in the snow, or mud. Well, as long as they keep a can Sirchie’s Snow Impression Wax handy.

As the result of a DNA experiment on September 10, 1984, Alec Jeffreys discovered the technique of genetic fingerprinting. At the time, Jeffreys worked as a researcher and professor of genetics at the University of Leicester.

At 9.05 a.m. that September morning, the life of Alec Jeffreys changed forever, as did the entire world of criminal investigations and paternity cases. It was, as Jeffreys calls it, his “eureka moment.”

Jeffreys’ DNA fingerprinting was first used in a police forensic test to identify the killer of two teenagers, Lynda Mann and Dawn Ashworth. The two young women had been raped and murdered in 1983 and 1986 respectively.

A 17-year-old boy with learning difficulties—Richard Buckland—confessed to one of the killings but not the other.

The detective in charge of the case was skeptical of Buckland’s odd confession and his involvement, or lack of, in the second murder. The detective recently learned of Alec Jeffreys’ breakthrough discovery and figured, well, he thought he had nothing to lose so he contacted the scientist to ask if he thought his new technique could prove that Buckland had murdered both young women. The top cop was in for a surprise.

Jeffreys agreed to see what he could do and extracted DNA from Buckland’s blood and from semen taken from the dead girls’ bodies. Then he compared them, immediately seeing that the girls had been raped by the same man. However, Buckland’s DNA was completely different. He had not been in contact with either of the victims.

Police had the wrong man and, after three months in jail, Buckland was released from custody.

Detectives then came up with a wild plan. They decided to set up an operation to gather the DNA of every man in the area. Eight months later, after eight months of sampling and testing, 5,511 men had given blood samples. Only one man had refused to cooperate and after testing all those samples, still no match to the semen samples collected from the victims.

Among the over 5,000 men who provided blood samples was a 27-year-old baker and father of two young children named Colin Pitchfork. Three years earlier, police had questioned him about his movements on the evening that Lynda had been murdered. But nothing came of it.

In August 1987, over a year after the killing of Dawn, one of Colin Pitchfork’s coworkers was in a local pub having drinks with friends and somehow Pitchfork’s name entered their conversation. One member of the group, a man named Kelly, admitted that he’d impersonated Pitchfork and took the blood test on his behalf. Kelly told the group that Pitchfork asked him to do this for him because he’d already taken the test for another friend who had a criminal conviction and was afraid of taking the test a second time. So Kelly agreed. Pitchfork then doctored his passport by inserting Kelly’s photograph in place of his own and then drove Kelly to the test site where he waited outside while Kelly’s blood was drawn.

A few weeks later, one of the people in the pub passed along the information to a local policeman. Kelly was arrested and he confessed to the impersonation. By the end of the work day Pitchfork was also in custody. One of the detectives who questioned the Pitchfork asked him, “Why Dawn Ashworth?”

Pitchfork nonchalantly replied, “Opportunity. She was there and I was there.”


So this is how it all started. A drop of blood and a semen sample met a small electrical charge (see images of the process below). The result was a few blips on an x-ray film that resembled a grocery store product bar code. Each of us has one of those bar codes that is unique to us. And it was Professor Sir Alec Jeffreys discovered the secret to finding and reading those codes.

I knew of this incredible story and was reminded of it when Denene and I recently watched Code of a Killer, the television mini-series based on these events.

Joseph Wambaugh told the story in his 1989 best selling book The Blooding: The True Story of the Narborough Village Murders.

Finally, after watching the TV show I recommend taking a moment or two to watch Professor Sir Alec Jeffreys lecture about his discovery, and you may do so below.


DNA testing by electrophoresis (gel testing) … the process

Weighing the agar gel.

Mixing the gel with water.

Gel in chamber.

Forensic Facts

Injecting DNA into the gel.

Attaching electrodes to the chamber.

Introducing electric current to the gel.

Completed gel is placed onto an illuminator for viewing.

 Gel on illuminator.

*My thanks to Dr. Stephanie Smith for allowing me to hang out in her lab to take the above photos.

Completed gel showing DNA bands

DNA bands


DNA Facts

  • DNA is the acronym for deoxyribonucleic acid.
  • DNA is a double-helix molecule built from four nucleotides: adenine (A), thymine (T), guanine (G), and cytosine (C).
  • Every human being shares 99.9% of their DNA with every other human.
  • If you placed all the DNA molecules in your body end to end, the DNA would reach from the Earth to the Sun and back over 600 times!
  • Humans share 60% of our genes with fruit flies.
  • We share 98.7% of our DNA in common with chimpanzees and bonobos.
  • If you could type 60 words per minute, eight hours a day, it would take approximately 50 years to type the human genome.
  • Humans share 85% of our DNA with a mouse.
  • We also share 41% with a banana.
  • According to a study conducted at Princeton University, all humans, including Africans likely have a bit of Neanderthal in our DNA. This was a fascinating discovery since until these findings were released in 2020 it was believed that Africans did not have Neanderthal DNA.
  • Friedrich Miescher discovered DNA in 1869. However, it was not until 1943 that scientists came to understand that DNA was the genetic material in cells.

Okay, you’re at your desks with hands poised above the keyboard. Thoughts of murder, chaos, and of your 100th six-figure book deal churn inside your head like the winds of an F-5 twister that’s just touched down in a midwestern mobile home park. This. Is. Your Best. Story. And it is exciting.

Now it’s time for the call to action. The time when it’s your job duty to coax, draw, persuade, and perhaps even drag readers throughout the hero’s journey until they reach the final page of your book.

Along the way, of course, you’ll concoct dangers and thrills, twists and turns, and risks far more convoluted and sometimes more perilous than those undertaken by the average human. Readers do sometimes enjoy the fantasy of living life through the eyes of fictional characters, right? After all, being Jack Reacher or Kay Scarpetta for a few hours could be fun and thrilling.

So off you go, clacking away at the keyboard, transforming the tale you’ve spent months creating a saga, either on paper for you plotters or stored in your mind for those of you who’re pansters, that’ll sit on the top shelf in bookstores all around the world.

In your mind you picture the blurbs and promo ads sent out by your publisher and publicists. Each of them promise your fans “It’s THE book of a lifetime.” “A book you can’t put down until the final page is turned.” “Lock your doors before reading this thrilling ride into the unknown!”

“The crime of the century.”

“It’s THE PERFECT MURDER!”

Dr. Edmond Locard’s Exchange Principle

Creating a murder based upon terminological inexactitude, one that’s committed by a pretend villain in a make-believe world, a crime that’s to be solved by a fictional hero, can be a daunting task for many writers. This is especially so when the writer is clue-challenged when it comes to first-hand knowledge of actual death scenes. But help is on the way and it comes in the form of your imaginations, along with a little help from Dr. Edmond Locard.

So, whether you’re a panster or a plotter, my advice to you, the writer of twisted tales, is to carefully consider Dr. Locard’s Exchange Principle (see below) before writing the first word. Doing so could elevate your stories to levels you never thought were possible to achieve.

I know, you’ve done quite well in the past, but readers are changing. Their knowledge of forensics and police investigations is growing with each passing day and with with each new TV show featuring brilliant experts who really know their stuff. And those folks don’t hesitate to share their expertise with an eager viewing audience, an audience who’ll later pick up a book to read for enjoyment only to find that the author doesn’t know the difference between cordite and kryptonite. By the way, neither cordite nor kryptonite should appear in crime fiction set in modern times.

Cordite manufacturing CEASED somewhere around the end of WWII. I’ll say that again in case you weren’t listening, or in the event the radio was playing too loudly and caused you to miss it.

Cordite manufacturing CEASED somewhere around the end of WWII.

They don’t make the stuff anymore. It’s not used in modern ammunition. Nope. Not there. Don’t use it. Don’t make it.

So no, your cops can’t smell it! That’s not what’s hitting their noses when they enter a crime scene.

Getting “IT” Right

As a former police investigator, I’m often asked what I think would be the perfect murder and my response is typically quick and always the same … “there’s no such thing as a perfect murder.”

I say this because I’m a firm believer in Dr. Locard’s Exchange Principle, a theory stating that always, without fail, when two objects come into contact with one another, each of those objects take something from the other or leave something behind. According to Locard, “It is impossible for a criminal to act, especially considering the intensity of a crime, without leaving traces of this presence.”

Locard’s Principle was on my mind throughout every case I investigated. It helped me to maintain my focus on the tiniest of details so that nothing went overlooked, not even the smallest of fibers.

Therefore, writers must, and I emphasize the word MUST, consider keeping this simple rule of thumb in mind when creating crime scenes and scenes of crimes, IF you’re going for realism. You do know there’s a difference between a crime scene and a scene of a crime, right?

Crime Scenes

Crime Scene and scene of the crime are not always synonymous. A crime scene is anywhere evidence of a crime is found (a dumpster located five miles away where a killer dumped the murder weapon, or the killer’s home where he deposited his bloody clothes, where the body was found if removed from the scene of the crime, etc.). Scene of the Crime is the location where the actual crime took place (where the killer actually murdered his victim).

 

Crafting the Perfect Murder

We’ve all heard about the killer who stabs someone with an icicle, a murder weapon that melts, thus leaving no trace evidence. Well, this is far from the truth since the killer had to approach the victim and he/she had to leave the scene. Therefore, he either left something behind or he took something with him (soil on the shoes, DNA, etc.).

There is trace evidence of some sort everywhere in every crime scene—again, footprints, DNA, fibers, tiny shards of glass, blood, etc. The weak link in a case would be, unfortunately, the detective who doesn’t dig deep enough or long enough or hard enough to find the evidence. This is true in all cases. The evidence is ALWAYS there, somewhere, begging to be found. It’s up to the savvy detective to locate it.

Disposing of bodies in clandestine grave sites are a fantastic means to hide a big piece of evidence … the body. Still, the killer was at the scene of the crime, therefore he left evidence. He had to move the body to the burial site. More traces of evidence—footprints, toll receipts and images captured by cameras at toll booths, gas purchases, purchases of burial equipment, and on and on and on. And then there’s the hound dog who drags a human femur to his owner’s back doorstep. He, the killer had to arrive at and then leave the scene. Again, the evidence is there for the taking—tire tracks, footprints, a leaf, a unique plant seed, a hair, or mud stuck to the soles of his shoes, etc. The list is practically endless.

The Almost Perfect Crime

Embalming fluid

What if a killer committed the murder in a funeral home embalming room, a place that sees hundreds of dead bodies pass through its doors. It’s a place where death “evidence” is routinely and efficiently scrubbed away.

Think about it for a moment. A funeral home where tons of body fluids and DNA have the potential of co-mingling and are routinely cleaned away using chemicals that can and do eliminate the typical clues searched for by investigators.

Yep, blood, saliva, nitrous and other fluids are scrubbed from the room, and all other physical evidence (breaks in bones, gun shot and stab wounds, etc, are totally destroyed during cremation. It’s the perfect It’s the perfect spot for the perfect crime, right?

Well, not so fast. Remember Locard, “when two objects come into contact with one another, each of those objects will take something from the other or leave something behind.” The victim had to arrive at the funeral, therefore evidence of the trip there would generate some sort of evidence trail. However slight it may be, it’s there.

Still, an inexperienced investigator could miss the clues in a funeral home setting.

To make it even more difficult for the detective, there’s this …

Cremation: The Process

Coffin materials are generally selected so as to minimize pollution generated when cremation takes place. Non-combustable coffin do-dads are removed (handles, knobs, hinges, etc.). PVC, heavy metals, solvent-based paints and other toxic resins are also removed or not at all used.

Cremation containers should be completely enclosed, rigid, leak resistant, and definitely combustible. They may be made of cardboard or particle board, wooden, or even a those nice and shiny, highly polished caskets, as long as they’re combustible and non-toxic. Metal caskets cannot be cremated.

Implants of any types which contain power sources are removed from the remains. Also removed are prostheses, jewelry, and non-combustible parts of clothing.

Cremation takes anywhere from 30 minutes in the case of the very small, to over two hours. The human body contains between 65% and 85% water by weight, so a temperature high enough to facilitate the combustion process—up to 2,000 degrees F is where the cremation process typically occurs.

Not for the Squeamish!!

Combustion in the cremator occurs in two steps

  • The primary combustion in the main chamber. It’s here where tissue, organs, body fat, ligaments, tendons, and the casket itself burn off as gases.
  • The secondary chamber, where they continue to undergo combustion (bone fragments remain in the primary chamber). Inorganic particles, usually from the cremation container, settle on the floor of the secondary chamber.  The gases formed as a by-product of combustion—carbon dioxide, water, oxygen, etc.—discharge into the sky through a stack.

When complete, funeral home employees (or the villain of your story) sweep the remains into a tray where they’ll sit to cool. This step is similar to when grandma baked a pie and then allowed it to cool on the sill of an open window before slicing it into individual serving sizes.

Once sufficiently cool, the employee, or bad guy, sifts through the ashes to remove bit of metal, if any (evidence). Any bone fragments are pulverized until all until the remains are less than 1/8” in size.

The cremated and squashed remains are then transferred to a plastic bag and placed into an urn. Or, if this step involves a murderer, the remains would most likely wind up scattered in a field down by Old Man Kelsey’s creek.

The “Other” Cremation: Human Soup

Alkaline hydrolysis, AKA “water, or green cremation”, is a water-based dissolution process that uses alkaline chemicals, heat and pressure and agitation to speed up natural decomposition. Once complete, all that’s left behind is bone residue and a liquid … human soup. This “human broth” is, believe it or not, considered sterile and is simply discharged with into local sewer system and is then treated as any other wastewater product (the stuff that goes down the drains of your home).

Leftover bone material is then pulverized and placed into an urn. Since there is more leftover bone material than with cremation by fire, these remains require a larger urn. And, by the way, due to the larger amount of “leftovers,” it would be more difficult for the villain of your story, if this setting is your thing, is someone who most likely works in a funeral home, to hide the remains created by this method of cremation.

Still, these methods of hiding and/or destroying evidence are far more effective than merely shooting Bill Imdead and then leaving his corpse on the living room floor to be found by cleaning company workers.

The perfect murder? No, but pretty darn close.

*Someone who commits a murder inside a crematorium by hastily shoved the body into the cremation chamber, and then flees the scene, leaving the body to reduce to ashes, would leave behind a mound of clues—bone, teeth, jewelry, implants complete with serial numbers, etc. Sure, the majority of the body parts would be gone, but it would still speak to investigators … if they took time to listen.


Click the link below to discover …

6 WAYS TO TRANSFORM A BORING CRIME SCENE INTO FASCINATING FACTUAL FICTION

Any writer, reader, and fan of mysteries, thrillers, suspense, and other books and television shows and film that involves crime scene investigation, will most likely have heard of Luminol, the chemical that causes chemiluminescence.

Chemiluminescence, the vivid bluish glow we’ve seen on countless crime shows, occurs when Luminol contacts an oxidizing agent such as the hemoglobin found in blood. Other agents can cause a similar reaction (copper, bleach, etc.), but it is blood that causes the most vivid glow. And it is this reaction that is of particular interest both real and fictional investigators.

Even bloody footprints reveal themselves when exposed to luminol.

Sirchie, the world leader in crime scene investigation technology and products, describes Luminol as:

“Luminol is a chemiluminescent substance that can be used as a presumptive test for the presence of blood. Making use of the peroxidaselike activity of the heme portion of hemoglobin, Luminol produces a bluish-white light that can be viewed in total darkness. Invisible blood stains react with the Luminol reagent by luminescing—darkness is essential. It can also be photographed or videotaped with the aid of the SIRCHIE® KRIMESITE™ IMAGER. A very useful test for searching large areas for blood especially if the area has been cleaned up. Sensitivity:1:100,000.”

Sirchie’s LUMINOL8 Contents:
2- LUMINOL 8B bottles of solution, 8 oz. each
2- LUMINOL 8A packets of dry chemicals, Net. Wt. 14.5 gms
2- Spray Head Attachment

*Sirchie image


Blue Star

Sirchie’s BLUESTAR Forensic Kit “affords the Crime Scene Investigator a complete tool to determine the presence or absence of blood. The extreme sensitivity of BLUESTAR allows the detection of bloodstains down to 1:10,000 dilutions, including minute traces that have been washed off, with or without detergent. And unlike other blood reagents, total darkness is not required. With practice, it’s unlikely to get confused between blood and false positives as the luminescence is different in color, intensity and duration. Subsequent DNA Typing and ABO Typing is possible because BLUESTAR does not alter the DNA in suspect blood stains.” ~ Sirchie

*Above image ~ Sirchie


Luminol is a presumptive test, not a confirmatory test.

 

 

 

 

 

 

Luminol presents challenges, such as its potential to destroy DNA evidence when contacted, and its glow lasts for just mere seconds. Detectives must be quick with their photography skills!

Therefore, BGU Prof. Alina Karabchevsky, head of BGU’s Light-on-a-Chip Group, a member of the BGU Unit of Electro-Optical Engineering and the Ilse Katz Institute for Nanoscale Science and Technology, came up with a fantastic new idea … a device/chip that combines the use of luminol with gold or silver nanospheres.

Simply put, Dr. Karabchevsky invented a microfluidic chip that not only greatly increases the chemiluminescence intensity of luminol, but also extends its glow time. To sweeten the pot, the chip enables the detection of much smaller blood samples found at potential crime scenes.

“The method developed by BGU researchers will enable development of future detectors with improved sensitivity. We are currently looking for partners for further developing this promising patented invention,” said Netta Cohen, CEO, BGN Technologies.


What is a microfluidic chip?

Easy answer – a device (chip) that enables very small amount of liquid to be processed or visualized.

 

We all know how the story goes. A sly, blowhardish and extremely hungry wolf arrives at the front doors of the recently created homes of three very handy pigs, a trio of walking porkchops who’d built their individual abodes on prime pieces of suburban real estate.

The first pudgy, and not so construction-savvy pig fashioned his home from straw, and if you’ve watched HGTV lately you’ll recall that while inexpensive straw homes are susceptible to rot due to high moisture content, fire, and to the difficulty of obtaining homeowner insurance.

I imagine our first little porker thumbed his flat little nose at the rules, and safety, and bypassed the permitting process. I also believe he overlooked the possibility of wind damage and quickly learned of his error shortly after the wolf announced his presence on the front stoop.

“Little pig, little pig won’t you let me come in?” the mangy wolf cried out to pig number one.

“No, no, no, by the hair on my chinny, chin, chin,” said the worried hog.

Well, you know what happened next. The wolf, of course, huffed and puffed and in a matter of seconds enjoyed a tasty pulled pork appetizer.

The twisted and curly “tail” continues with the wolf’s forceful exhalations destroying pig number two’s stick-built home. As a result … pork roast for the entire Wolf family. And, as before, he’d gotten away without leaving a clue. Not even a paw print.

Then the murdering wolf, now deemed a serial killer by the local media, moved on to his next intended victim, the pig who lived in the brick rancher at the corner of Garlic and Rosemary Avenues.

Exasperated police almost captured the wolf thanks to a 911 call from the couple next door, Porky and Petunia, who’d seen the sneaky canine approaching pig number three’s doorstep. But, as bad luck would have it, the wolf escaped on foot, well, on four feet, actually.

The wolf was careless, though, during his third attempt at pig-killing. He’d forgotten it was the time of year when his species sheds their winter coats. Yep, you guessed it. Cops collected a few discarded hairs and subsequently rushed them to the lab where scientists immediately began testing them using an astonishing new process. They ‘d know the identity of the killer very soon. But this is fiction …

The Real Meat of the Story

Okay, the tale above is a bit stupid, I know. But I wrote it as a prelude to the true subject matter of the day—identifying a criminal suspect using his or her shed hairs found at a crime scene.

It’s fairly common knowledge that scientists and other lab experts, as well as law enforcement investigators and writers, are already familiar with the use of human hair from the head as a source used to identify people through DNA testing, etc. Suppose, though, that any hair from any part of the body could be used to identify the person who shed it, not just hairs from the head. To have this capability would be HUGE in the real world of crime-solving.

Sure, writers make up stuff like this all the time to help tie up loose ends in their books. After all, Jack Reacher, Bosch, DD Warren, and Tami Hoag’s Detectives Fourcade and Broussard, well, they’re unstoppable because their creators make it so. But actual cops must use actual evidence and actual crime-fighting tools and equipment to locate killers, such as the extensive catalog of items developed and manufactured by Sirchie.

But here in the world of genuine cops and murderers, the use of wishful thinking and fictional methods and procedures is not an option that’s available to local, state, and federal law enforcement.

However, thanks to a group of researchers, fiction is now a reality.

Yes, a groundbreaking technique of human identification using hairs from ANY part of the body is now possible. It’s the result of a yearlong study by researchers from Lawrence Livermore National Laboratory’s Forensic Science Center and Michigan State University.

The process interprets hair protein chemistry and how it effects protein marker identification.

Chemist Fanny Chu, a graduate student and researcher at MSU, along with other researchers involved in the Lawrence Livermore/Michigan State University study, took the hair testing process a step further by studying and comparing arm and pubic hair with head hair. The result—the hairs fundamentally presented the same data as head hair.

Additionally, the protein content of the hairs indicate whether a single hair is from a person’s head, arm, or pubic area, etc.

The team also learned that the protein content of pubic hair is appreciably greater than head and arm hair.

A single one-inch strand of hair has a unique pattern, much like DNA or fingerprints, that distinguish a person from among a population of 10 million people.

Fun Fact: Human hair proteins are chemically more stout than nuclear DNA. In fact, scientists have detected protein markers in human hair that’s more than 250 years old.


SIRCHIE

Sirchie products (mentioned above) are used by law enforcement professional worldwide. Additionally, they’re often seen in use by CSIs and detectives on popular television show/series.

In August, just a few weeks from today, writers, fans, and readers will have the opportunity to attend hands-on homicide investigation training sessions at Sirchie’s elite compound near Raleight, N.C. The event, MurderCON, is brought to you by the Writers’ Police Academy and Sirchie. It’s a rare opportunity to learn at a world-renowned facility in classes taught by some of the best instructors in the world. I cannot stress enough how extremely valuable attending MurderCon could be to the knowledge base of crime fiction writers.

The material offered at MurderCON is the identical material taught to top investigators from around the globe. Not only that, classes are scheduled at Sirchie’s facility, the source of crime scene investigation tools and equipment. It’s where ideas are conceived by researchers and are then brought to life by developers and scientists. Next, a team of experts fabricate assemble everything from fingerprint brushes and powders to fuming chambers, alternate light sources and even surveillance vehicles.

The subject material offered at MurderCon has never before been made available to the public.

Again, this is a RARE chance to go behind the scenes, affording you, the writer, to add better realism to your work by experiencing the touch, sight, smells, sounds, and even tastes associated with crime scene investigations. This is the key to activating the senses of your readers!!

We’ve nearly reached maximum capacity for the 2019 MurderCON event; therefore, registration will soon close. So again, I urge you to consider taking advantage of this unique opportunity. It’s a KILLER event!

Sign up today at:

MurderCON

See you in August!

In the grand scheme of murder, knives and guns pale in comparison to the instruments death that are nearly invisible to the human eye.

Long before man shaped the first stone into a weapon, viruses and bacteria quietly killed humans and animals, paying no attention to high they struck down. These tiny but deadly organisms are capable of shutting down the body’s entire operating system, and they can and often do destroy every single organ in the body.

A terrorist attack involving deadly viruses and bacteria is a threat that looms over the heads of government officials. After all, a single, minute particle of either anthrax, botulism, tularemia, bubonic plague, ricin, ebola, and hantavirus, for example, can be easily cultured and multiplied many times over. And, this process can be performed in any home in the country with minimal time, training, and equipment.

How easy? Well, a potential terrorist could simply order a starter bug from a laboratory supply company (a reference lab), much like a reader orders a book from Amazon. The bug is shipped to the buyer as a freeze-dried sample in the regular U.S. mail, or with any of the other popular shipping companies.

New Picture (2)

Growth of anthrax on plate containing sheep blood agar – Dept. of Labor image

Of course, reference lab customers must have proper credentials to place an order for anthrax. However, packages could easily be intercepted by people with ill-intentions against the U.S. and its citizens. After all, how difficult would it be for a potential terrorist to gain employment in the biotech industry (new drug discovery)? This is a field that’s comprised of scientists from across the globe, experts who work with these bugs on a daily basis and sometimes with very little accountability, if any, in some instances.

Many of these science-folks come to the U.S. from other countries and would be virtually undetectable as terrorists until it was too late. And, if all else failed for the terrorist, they could find the bacteria in its natural environment, readily growing on dead plant material and/or in fresh water or rainwater.

Anthrax is caused by a spore-forming bacteria, Bacillus anthracis.

Anthrax lesion on the neck – CDC image

Humans can become infected through skin contact, ingestion or inhalation of spores from infected animals or animal products. Anthrax can be delivered as a powder, such as in the cases of the letters mailed to U.S. officials. However, a better, more deadly method of delivery would be in aerosol form. Once the bacteria are inhaled, the disease progresses so rapidly that, once the symptoms began to appear, it would most likely be too late to prevent the victim’s death.

Symptoms of anthrax contamination

Symptoms of anthrax contamination include, skin infections, fever, chills, fluid in the lungs, difficulty breathing, nausea, weight loss, fever, diarrhea, and abdominal bleeding. Contrary to the belief of some people, inhaled anthrax contamination is not contagious. It cannot be passed from one person to another.

Anthrax lesion on the forearm – CDC image

Anthrax study requires that the work be conducted in a Biosafety Level 2 laboratory (BSL 2 labs are required to have waste contamination equipment on hand). However, if the study is to be performed on anthrax in aerosol form, a BSL 3 lab is required (BSL 3 labs require testing in enclosed equipment with high-tech ventilation systems. Access is limited to only those working on current experiments).

A 2008 anthrax investigation involving aggressive interview tactics by law enforcement investigators led to a bit of public protest. Former FBI agent and behavioral scientist Clint Van Zandt and I were featured on NPR’s Talk of the Nation to discuss those tactics.

You may remember Agent Van Zandt from his involvement in high-profile cases, such as Waco/David Koresh, Timothy McVeigh, and The Unabomber. And, well, you know me …

*Above images – CDC.gov

Regarding DNA and saliva, I’d like to note that it is indeed possible to expel DNA when coughing or sneezing. However, the fact that it’s possible doesn’t mean it’s always found, just that it could be. And, if found, it could be the DNA of someone other than than a suspect or victim, such as cop or lab scientist who was involved in the collection or testing of the evidence. Here’s why …

First, in the lab, to tell the difference between saliva and sputum, scientists look for epithelial cells. These cells have a nucleus, and within a nucleus DNA is found. Saliva is almost always present in the mouth, especially when we are awake. When we sneeze saliva and the DNA contained within is expelled.

FYI – Lab scientist/techs scan collected sputum samples for the presence or absence of white blood cells. White blood cells, not red, indicate infection. The presence of epithelial cells from saliva indicates the sample is contaminated with saliva, which would result in improper test results. Sputum is tested for respiratory tract infections. 

By the way, red blood cells (erythrocytes) have/contain no nucleus nor do they contain mitochondria. Therefore, red blood cells do not contain DNA because there’s no nucleus in the cells.

Those of you who attended the WPA when world-renowned DNA expert Dr. Dan Krane presented a fantastic session on DNA evidence, may remember when he mentioned how DNA evidence is sometimes contaminated, such as using fingerprint brushes or gloves from one scene to process evidence in an entirely different location. DNA could be transferred using those items. He also pointed out instances where coughing or sneezing could distribute DNA to the surface of an item being processed. (Dr. Krane is a former colleague of my wife, Denene)

On with DNA and Sneezing

As an example of evidence contamination via sneezing, when discussing the Jon Benet Ramsey case, Dr. Krane says, “The DNA in tests could be there because of a contact that was weeks, months, even years before the crime occurred. It’s not possible to make inferences about the tissue source here. We can’t say that it came from semen or saliva or blood or anything. What if one of the medical examiners sneezed on one of these articles of clothing and it came into contact with the other one? There are just so many possibilities.”

Additionally, from another source, “It is extremely easy to contaminate biological samples; this can occur by failing to change gloves or clean instruments properly, failing to wipe down benches properly between testing, or by sneezing or even talking over a sample (Buckleton et al 2005:277).”

And, from the National Institute of Justice:

Contamination

Because extremely small samples of DNA can be used as evidence, greater attention to contamination issues is necessary when identifying, collecting, and preserving DNA evidence. DNA evidence can be contaminated when DNA from another source gets mixed with DNA relevant to the case. This can happen when someone sneezes or coughs over the evidence or touches his/her mouth, nose, or other part of the face and then touches the area that may contain the DNA to be tested.

To avoid contamination of evidence that may contain DNA, always take the following precautions:

  • Wear gloves. Change them often.
  • Use disposable instruments or clean them thoroughly before and after handling each sample.
  • Avoid touching the area where you believe DNA may exist.
  • Avoid talking, sneezing, and coughing over evidence.
  • Avoid touching your face, nose, and mouth when collecting and packaging evidence.
  • Air-dry evidence thoroughly before packaging.
  • Put evidence into new paper bags or envelopes, not into plastic bags. Do not use staples.

From the U.S. National Library of Medicine/National Institute of Heath/The National Center for Biotechnology Information (NCBI):

4.2. Contamination

For DNA studies, one of the greatest laboratory barriers is the contamination of genetic material from other sources (e.g., from the examiner and other biological evidence). Contamination may occur during the sexual contact (e.g., if there is more than one perpetrator), during the period between the sexual contact and the FME, during the FME, and in the laboratory. In order to avoid it, examiners should take special precautions to prevent cross-contamination between evidences. For this purpose, it is important:

  1. to work under aseptic conditions to avoid microbial contamination;
  2. to always use disposable supplies to ensure individual protection (e.g., gowns, powder-free gloves, mask, or other protective clothing) and to avoid direct contact with the samples;
  3. to ensure that the room where FME takes place is regularly cleaned before and after patient use;
  4. to avoid sneezing, coughing, or talking over the samples;

Dr. Krane is one of the world’s foremost DNA experts, testifying worldwide as an expert witness in well over 100 criminal trials, in which DNA evidence was presented, such as the Jon Benet Ramsey case. He’s been involved as a top expert in other high-profile cases such as the DC Snipers, OJ Simpson case, and the infamous Monica Lewinsky/Bill Clinton “blue dress,” to name only a few. Dan also developed software that’s used in genetic analyzers, the devices used by scientists who conduct DNA tests.

My other source, in addition to our good friend Dr. Dan Krane, is, of course, my resident renowned expert, Dr. Denene Lofland.

Denene received a Ph.D. in Pathology, with an emphasis in microbiology, from Virginia Commonwealth University School of Medicine. As a former biotech company director, Denene managed successful clinical projects that resulted in regulatory filings of four compounds and FDA approval for two new antimicrobial drugs for the treatment of pneumonia and cystic fibrosis. The drugs are currently on the market.

Denene supervised several projects, including government-sponsored research which required her to maintain a secret security clearance. Her areas of expertise include medical microbiology, bioterrorism, and new drug discovery development. She has published numerous articles in a variety of peer reviewed scientific journals, contributed to the thirteenth edition of Bailey and Scott’s Diagnostic Microbiology, a textbook standard used in colleges and universities, published an article about anthrax in Police One magazine, and she has an upcoming tale in the Writers’ Police Academy’s anthology, After Midnight, Tales From the Graveyard Shift (edited by Phoef Sutton with foreword by Lee Child) ~ Level Best Books, publisher

Currently, Denene is an Associate Professor of Medical and Molecular Sciences at the University of Delaware. She also taught medical microbiology to medical students at a medical college in California. In her early days, prior to becoming a mad scientist, she managed the lab in a large, major hospital.

Over the years, I was fortunate to have the experience of witnessing Denene and her teams, and Dr. Krane’s team, perform numerous DNA testings using both gel electrophoresis and DNA Sequencers/Genetic Analyzers. I was once treated to conducting a test of my own in one of Dr. Dan Krane’s labs, an entire DNA test from extraction of sample to final result. I ran the test on the DNA of a strawberry, but hey, the process is the same as when using human samples. The strawberry was innocent, by the way.

Again, the fact that DNA is present in saliva, it doesn’t mean DNA is always found when someone sneezes or coughs, or talks over evidence (it’s even been found in traces of saliva found on a public phone receiver), just that it’s possible and that it does occur.


DNA Testing: The Process

The first step in the testing process is to extract DNA from the evidence sample. To do so, the scientist adds chemicals to the sample, a process that ruptures cells. When the cells open up DNA is released and is ready for examination.

extract-dna.jpg

DNA is actually visible to the naked eye. The slimy glob in the center of the circle below is DNA.

new-picture-11.jpg

DNA is tested in devices like the one below. They’re called genetic analyzers. This particular device is located in one of Dr. Dan Krane’s laboratories.

new-picture-1.jpg

DNA is loaded into wells inside the genetic analyzer. There are 96 wells in the gray, rectangular block shown below (inside the analyzer).

new-picture-2.jpg

An electric current separates the DNA, sending it from the wells through narrow straw-like tubes called capillaries. During its journey through the analyzer, DNA passes by a laser. The laser causes the DNA loci (a gene’s position on a chromosome) to fluoresce as they pass by, which allows a tiny camera to capture their images.

The image below shows DNA’s path through the genetic analyzer (wells are on the left; capillaries are the arcing lines leading to laser and camera on the right).

new-picture-3.jpg

Capillaries

new-picture-4.jpg

Doctor Stephanie Smith points to the row of eight capillaries, one for each well in the corresponding line of wells (12 rows of 8 wells).

At the end of the testing, the equipment produces a graph/chart called an electropherogram.

Peaks on the graph depict the amount of DNA strands at each location. It is this unique pattern of peaks and valleys that scientist use to match or exclude suspects.

Or, in the case of paternity testing, to include or exclude someone as a parent.

The image below is an electropheragram showing the DNA of a strawberry.

new-picture-8.jpg

Electropheragams are printed and it is this document that’s examined by experts for use in the ID/comparisons of sample contributors, such as suspects and victims.

Remember above when we discusses sneezing, coughing, and/or talking over DNA evidence? Well, here’s a DNA test result (electropheragram) of a contaminated sample, a mixture of DNA found on the body of a rape victim. The evidence was contaminated to the point that it was impossible to tell/prove whether or not Contributors 1 or 2 were involved in the assault. Notice that the peaks in the mixture do not quite match either suspect’s DNA.

Electropheragram showing tested DNA of two subjects, and a mixture of DNA collected from a victim. Results showing a mixture make it difficult to point to any one suspect, or if someone other than the suspect and victim contaminated the sample.

The image below shows a clear match between the DNA of the victim and suspect. The suspect was clearly in contact, in some way, with the victim.

 

DNA Facts:

Identical twins have identical DNA.

Humans are genetically 99.9% identical. Only 0.1% of our genetic makeup is different.

It takes about eight hours for one cell to copy its own DNA.

Red blood cells do not contain DNA.

DNA is used to determine pedigree in livestock.

DNA is used to authenticate wine and caviar.

Detergent and Alcohol will not destroy DNA.

DNA can be transferred from article of clothing to another, even in a washing machine. This is called secondary and tertiary transfer.

DNA testing is not 100% accurate.

*My thanks to Dr. Stephanie Smith and Dr. Dan Krane for allowing me to hang out in their labs to take the above photos.

*Thanks, too, to the good folks at crimescenewriter for the idea for this post. 


Have you reserved your spot at MurderCon? If not, there’s still time to do. Sign up today to attend this rare hands-on training event!

In the meantime, here’s a peek at the 2019 MurderCon instructors and speakers. The lineup is stellar!

MurderCon Instructors