Weird Science

Laser Microscope: A DIY Project

Polish ver­sion is here

The fol­lo­wing article was ori­gi­nally publi­shed in the jour­nal for edu­ca­tors Bio­lo­gia w Szkole (eng. Bio­logy in School) (3/2015):

Ilustracja

Ples M., Lase­rowy mikro­skop - Zrób to sam (eng. Laser Micro­scope: A DIY Pro­ject), Bio­lo­gia w Szkole (eng. Bio­logy in School), 3 (2015), Forum Media Pol­ska Sp. z o.o., pp. 60-62

Do It Your­self

I believe the micro­scope holds a very impor­tant place in every bio­lo­gist’s life. In fact, I would go so far as to say it occu­pies a spe­cial place. I say this not merely because it is such a use­ful tool for scien­ti­sts and edu­ca­tors. The micro­scope is also a sym­bol of scien­ti­fic curio­sity about nature’s myste­ries and the sub­se­qu­ent under­stan­ding of them. The abi­lity to peer into the micro-world has fasci­na­ted not just scien­ti­sts but also arti­sts. In 1858, the Scot­tish wri­ter Fitz James O'Brien pen­ned the famous short story “The Dia­mond Lens” [1], and nearly 40 years later, the Spa­nish pain­ter Joa­quín Sorolla y Bastida, wor­king in the Impres­sio­nist spi­rit, cre­a­ted “Por­trait of Dr Simarro at the micro­scope.”

Ilustracja

Joa­quín Sorolla y Bastida, Por­trait of Dr Simarro at the micro­scope, source: http://upload.wiki­me­dia.org/wiki­pe­dia/com­mons/d/da/Por­trait_of_Dr_Simarro_at_the_micro­scope.JPG, acces­sed: 05/23/2015

It is not easy to iden­tify the inven­tor of the micro­scope. Some cre­dit cer­tain achie­ve­ments to Roger Bacon [2], a 13th-cen­tury Fran­ci­scan phi­lo­so­pher, but this rema­ins uncon­fir­med. More com­monly, the first opti­cal micro­sco­pes are said to have been built aro­und 1590 by the Dutch­men Hans Jans­sen and his son, Zacha­rias. Howe­ver, the high cost and limi­ted capa­bi­li­ties of these devi­ces pre­ven­ted them from being used more widely. Ano­ther bre­ak­th­ro­ugh came in the 17th cen­tury, when the mer­chant Anto­nie van Leeu­wen­hoek impro­ved upon the micro­scope and began pro­du­cing it on a bro­a­der scale. Among his accom­pli­sh­ments as a natu­ra­list were his obse­rva­tions of red blood cells, sperm cells, muscle and bone struc­ture, as well as bac­te­ria and cilia­tes [3].

Since then, opti­cal micro­sco­pes have been vastly refi­ned, lea­ding to many disco­ve­ries not only in bio­logy but also in other fields that owe a great deal to these instru­ments. Micro­scopy itself has grown into a vast branch of know­ledge. Today, apart from opti­cal micro­sco­pes (inc­lu­ding flu­o­re­scence, pola­ri­za­tion, phase-con­trast, con­fo­cal, and others), we also reco­gnize elec­tron, aco­u­stic, and ato­mic-force micro­sco­pes, among others.

Not every school can afford even sim­ple micro­sco­pes and the other equ­ip­ment requ­i­red to use them. Hence, I would like to pre­sent a method for buil­ding a setup to obse­rve micro­or­ga­ni­sms at very low cost. This descrip­tion may prove help­ful not only to stu­dents and tea­chers but also to any­one enthu­sia­stic about science.

Con­struc­tion

An opti­cal micro­scope con­si­sts of seve­ral basic com­po­nents, inc­lu­ding an illu­mi­na­tor, a con­den­ser, a stage for the spe­ci­men, an objec­tive, a tube, and an eye­piece [4]. But there is a sim­pler way!

Buil­ding a sim­ple laser micro­scope does not requ­ire expen­sive or hard-to-obtain equ­ip­ment. You only need:

The hypo­der­mic nee­dle’s sharp tip must be blun­ted by grin­ding it down with a metal file or shar­pe­ning stone.

The laser might seem to be the most dif­fi­cult part to obtain. In rea­lity, we’re in luck, because a laser poin­ter (Photo.1) is enti­rely suf­fi­cient for this role. Howe­ver, it is not advi­sa­ble to use a poin­ter emit­ting red light, as the wave­length is too long and the resul­ting image is not very clear. More­o­ver, the human eye is rela­ti­vely less sen­si­tive to red light. For these rea­sons, I used a green laser poin­ter (λ=532 nm) with a radia­tion out­put under 10 mW.

Cau­tion: never aim laser light direc­tly at your eyes — this can cause per­ma­nent vision damage!

Photo.1 – The laser poin­ter used in the expe­ri­ment

A stand or labo­ra­tory clamps are help­ful for secu­ring all the parts but are not stric­tly neces­sary. Any sta­ble way of moun­ting the com­po­nents will do. As for the screen, you could use a pro­jec­tion screen, a whi­te­bo­ard, a wall, or even a bed­sheet.

The water con­ta­i­ning micro­or­ga­ni­sms can be taken from a sun­lit pond or from a stan­dard cul­ture of Para­me­cium cau­da­tum or ano­ther micro­or­ga­nism. Water from a vase in which flo­wers have stood for at least a few days can also be used.

All com­po­nents sho­uld be arran­ged accor­ding to the dia­gram (Fig.1).

Ilustracja
Fig.1 – Sche­ma­tic of the setup

The nee­dle is atta­ched to the syringe, which is fil­led with water con­ta­i­ning the micro­or­ga­ni­sms.

In this micro­scope, the dro­plet of water acts as the lens. It hangs from the blun­ted tip of the nee­dle and con­ta­ins the micro­or­ga­ni­sms we want to obse­rve. The laser beam direc­ted at the dro­plet refracts thro­ugh it, for­ming an image on the screen. The fini­shed setup is also shown in Photo.2.

Photo.2 – The com­ple­ted setup

The dro­plet sho­uld mea­sure a few mil­li­me­ters (about 0.12 in) in dia­me­ter. You can adjust its size by mani­pu­la­ting the syringe’s plun­ger. Sys­tem sta­bi­lity is cru­cial — if even minor vibra­tions occur, the dro­plet will fall, and you will have to form ano­ther.

Obse­rva­tions

The magni­fi­ca­tion depends on the dro­plet’s distance from the screen: the far­ther it is, the lar­ger the image and the gre­a­ter the magni­fi­ca­tion. Howe­ver, as magni­fi­ca­tion incre­a­ses, the image beco­mes dim­mer. At a distance of aro­und 2 m (6.56 ft), the image is fairly large (in my expe­ri­ments, about 0.5–1.0 m [1.64–3.28 ft] in dia­me­ter), altho­ugh dar­ke­ning the room often helps in this case.

It is easy to see elon­ga­ted algal cells (Photo.3A) and cilia­tes such as Para­me­cium cau­da­tum (Photo.3B) or Sty­lo­ny­chia, as well as other micro­or­ga­ni­sms.

Photo.3 – The resul­ting image; A – algal cells, B – Para­me­cium cau­da­tum

Para­me­cium are an excel­lent sub­ject for obse­rva­tion because they can be very mobile. Photo.4 shows a sequ­ence of ima­ges cap­tu­ring the rapid move­ment (with about 0.1 s between each shot) of seve­ral of these cilia­tes aga­inst a back­gro­und of algal cells.

Photo.4 – A sequ­ence of ima­ges sho­wing Para­me­cium cau­da­tum and elon­ga­ted algal cells.

Of course, the results obta­i­ned here are not ideal. Inter­fe­rence stri­pes are visi­ble, disrup­ting the image. A stan­dard school opti­cal micro­scope pro­vi­des bet­ter image qua­lity. Pho­tos.5 and 6 were taken using a sim­ple light micro­scope equ­ip­ped with a sui­ta­bly adap­ted low-cost web­cam. Cle­arly, even such stra­i­ght­for­ward solu­tions can pro­vide quite good visu­a­li­za­tion of sub­tle deta­ils — eno­ugh for tea­ching bio­logy.

Photo.5 – Spi­ro­gyra; the spi­ral chlo­ro­pla­sts are cle­arly visi­ble
Photo.6 – A ciliate of the genus Vor­ti­cella, sho­wing the con­trac­tile stalk used to attach to sur­fa­ces

Never­the­less, the extre­mely low cost and high edu­ca­tio­nal value make this laser-based setup well sui­ted for bio­logy or natu­ral science clas­sro­oms. Addi­tio­nally, the resul­ting image is quite 'three-dimen­sio­nal'. In con­trast to a regu­lar opti­cal micro­scope — where obse­rved micro­or­ga­ni­sms move only in the very limi­ted space between a slide and cover­slip (prac­ti­cally just two dimen­sions) — this setup allows you to obse­rve their move­ment in three-dimen­sio­nal space.

Good results can also be achie­ved by using a blue laser, since its shor­ter wave­length pro­du­ces a cle­a­rer image.

Refe­ren­ces:

All pho­to­gra­phs and illu­stra­tions were cre­a­ted by the author.

This text has under­gone sli­ght edi­to­rial modi­fi­ca­tions com­pa­red to the ver­sion publi­shed in the jour­nal to bet­ter suit online pre­sen­ta­tion.

Adden­dum

Sta­tic ima­ges can't fully convey the impres­sion left by the view achie­ved thro­ugh descri­bed method. That’s why I’ve also pre­pa­red a video, which you can watch below:

The second video pre­sents a simi­lar pro­ce­dure using a blue-light laser poin­ter:

Marek Ples

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